Date Added to Catalog (since 11/25/08) PubMedID First Author Date Journal Link Study Disease/Trait Initial Sample Size Replication Sample Size Region Reported Gene(s) Strongest SNP-Risk Allele SNPs Risk Allele Frequency p-Value p-Value (text) OR or beta 95% CI (text) Platform [SNPs passing QC] CNV 11/20/2009 19875614 Paterson 29-Oct-09 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19875614?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 "A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both HbA1c and glucose" Type 1 diabetes "1,304 diabetics" "531 diabetics, up to 37,436 non-diabetics" NR NR NR NR NS NS NR NR "Affymetrix and Illumina [2,518,578] (imputed)" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Body mass index "Up to 3,925 European individuals" NR 3q28 NR rs1152846-G rs1152846 0.77 0.000003 (females +males)  0.09 [NR] kg decrease "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Body mass index "Up to 3,925 European individuals" NR 19q13.3 NR rs1878047-G rs1878047 0.37 0.000005 (females + males)  0.06 [NR] kg decrease "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Body mass index "Up to 3,925 European individuals" NR 19p13.3 NR rs3803915-C rs3803915 0.89 0.000005 (females + males)  0.13 [NR] kg decrease "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Body mass index "Up to 3,925 European individuals" NR 11q14.1 NR rs1458095-G rs1458095 0.9 0.000007 (females)  0.19 [NR] kg increase "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Body mass index "Up to 3,925 European individuals" NR 2q36.1 NR rs824931-G rs824931 0.35 0.000003 (females + males)  0.07 [NR] kg increase "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Body mass index "Up to 3,925 European individuals" NR 4q34.3 NR rs2383393-G rs2383393 0.63 0.000002 (males)  0.1 [NR] kg increase "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Body mass index "Up to 3,925 European individuals" NR 1p36.33 NR rs3934834-G rs3934834 0.8 6.00E-07 (females + males)  0.11 [NR] kg increase "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Body mass index "Up to 3,925 European individuals" NR 3p14.1 NR rs1024889-G rs1024889 0.28 0.000006 (males)  0.12 [NR] kg increase "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Body mass index "Up to 3,925 European individuals" NR 5q35.3 NR rs12517906-G rs12517906 0.85 0.000006 (females)  0.16 [NR] kg decrease "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Body mass index "Up to 3,925 European individuals" NR 9p22.3 NR rs1927702-G rs1927702 0.42 0.000006 (females)  0.08 [NR] kg increase "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Weight "Up to 3,925 European individuals" NR 18q11.2 NR rs1840440-G rs1840440 0.61 3.00E-07 (females)  2.16 [NR] kg increase "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Weight "Up to 3,925 European individuals" NR 17q24.1 NR rs7209395-G rs7209395 0.23 0.000003 (females + males)  1.75 [NR] kg increase "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Weight "Up to 3,925 European individuals" NR 13q12.12 NR rs2765086-G rs2765086 0.94 0.000006 (females)  3.86 [NR] kg decrease "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Weight "Up to 3,925 European individuals" NR 12p11.21 NR rs10844154-C rs10844154 0.54 0.000004 (females)  1.87 [NR] kg increase "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Weight "Up to 3,925 European individuals" NR 10q22.2 NR rs7919006-G rs7919006 0.95 0.000004 (females)  4 [NR] kg decrease "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Weight "Up to 3,925 European individuals" NR 10q22.1 NR rs1816002-G rs1816002 0.46 0.000008 (females)  2.08 [NR] kg increase "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Weight "Up to 3,925 European individuals" NR 3q28 NR rs1152846-G rs1152846 0.77 0.000006 (females + males)  1.7 [NR] kg decrease "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Weight "Up to 3,925 European individuals" NR 5q35.3 MGAT1 rs12517906-G rs12517906 0.85 7.00E-08 (females)  2.96 [NR] kg decrease "Illumina [318,237]" N 11/18/2009 19851299 Johansson 22-Oct-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19851299?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=4 Linkage and Genome-wide Association Analysis of Obesity-related Phenotypes: Association of Weight With the MGAT1 Gene Weight "Up to 3,925 European individuals" NR 9p13.3 NR rs10972341-G rs10972341 0.6 0.000009 (males)  2.32 [NR] kg increase "Illumina [318,237]" N 11/25/2009 19846067 Garriock 19-Oct-09 Biol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 A Genomewide Association Study of Citalopram Response in Major Depressive Disorder Treatment response to citalopram "Up to 883 responders, 608 non-responders" NR 21q21.3 EIF4A1P rs2830840-? rs2830840 0.46 0.000005 (remission)  1.47 [1.23-1.72] "Affymetrix [430,198]" N 11/25/2009 19846067 Garriock 19-Oct-09 Biol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 A Genomewide Association Study of Citalopram Response in Major Depressive Disorder Treatment response to citalopram "Up to 883 responders, 608 non-responders" NR 18q12.1 NOL4 rs7239368-? rs7239368 0.42 0.000009 (remission)  1.45 [1.22-1.69] "Affymetrix [430,198]" N 11/25/2009 19846067 Garriock 19-Oct-09 Biol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 A Genomewide Association Study of Citalopram Response in Major Depressive Disorder Treatment response to citalopram "Up to 883 responders, 608 non-responders" NR 7q36.3 UBE3C rs6966038-? rs6966038 0.19 5.00E-07 (response)  1.64 [1.35-1.99] "Affymetrix [430,198]" N 11/25/2009 19846067 Garriock 19-Oct-09 Biol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 A Genomewide Association Study of Citalopram Response in Major Depressive Disorder Treatment response to citalopram "Up to 883 responders, 608 non-responders" NR 7q36.3 UBE3C rs6966038-? rs6966038 0.2 4.00E-07 (remission)  1.68 [1.37-2.04] "Affymetrix [430,198]" N 11/25/2009 19846067 Garriock 19-Oct-09 Biol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 A Genomewide Association Study of Citalopram Response in Major Depressive Disorder Treatment response to citalopram "Up to 883 responders, 608 non-responders" NR 15q22.2 RORA rs809736-? rs809736 0.17 0.000008 (response)  1.52 [1.27-1.83] "Affymetrix [430,198]" N 11/25/2009 19846067 Garriock 19-Oct-09 Biol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 A Genomewide Association Study of Citalopram Response in Major Depressive Disorder Treatment response to citalopram "Up to 883 responders, 608 non-responders" NR 20q13.31 BMP7 rs6127921-? rs6127921 0.82 0.000003 (response)  1.64 [1.33-2.04] "Affymetrix [430,198]" N 11/25/2009 19846067 Garriock 19-Oct-09 Biol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19846067?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 A Genomewide Association Study of Citalopram Response in Major Depressive Disorder Treatment response to citalopram "Up to 883 responders, 608 non-responders" NR 20q13.31 BMP7 rs6127921-? rs6127921 0.81 0.000001 (remission)  1.75 [1.39-2.17] "Affymetrix [430,198]" N 11/12/2009 19850125 Kim 19-Oct-09 Neurobiol Dis http://www.ncbi.nlm.nih.gov/pubmed/19850125?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Common CYP7A1 Promoter Polymorphism Associated With Risk of Neuromyelitis Optica Neuromyelitis optica "53 Korean cases, 240 Korean controls" 40 Korean cases NR NR NR NR NS NS NR NR "Illumina [288,025]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 16p11.2 NR rs7186852-A rs7186852 0.08 3.00E-07 1.29 [1.17-1.42] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 6p21.32 HLA-DRB1 rs9271100-? rs9271100 NR 1.00E-12 1.9 [1.59-2.27] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 2p22.3 RASGRP3 rs13385731-A rs13385731 0.85 1.00E-15 1.43 [1.32-1.56] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 2q32.3 STAT4 rs7574865-A rs7574865 0.33 5.00E-42 1.51 [1.43-1.61] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 5q33.1 TNIP1 rs10036748-A rs10036748 0.76 2.00E-09 1.23 [1.15-1.33] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 6q21 "PRDM1, ATG5" rs548234-G rs548234 0.26 5.00E-12 1.25 [1.17-1.33] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 6q23.3 TNFAIP3 rs2230926-C rs2230926 0.04 1.00E-17 1.72 [1.52-1.94] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 7p12.2 IKZF1 rs4917014-A rs4917014 0.68 3.00E-23 1.39 [1.30-1.47] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 7q11.23 NR rs1167796-G rs1167796 0.71 2.00E-08 1.2 [1.12-1.28] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 7q32.1 IRF5 rs4728142-A rs4728142 0.13 8.00E-19 1.43 [1.32-1.54] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 8p23.1 BLK rs7812879-G rs7812879 0.76 2.00E-24 1.45 [1.35-1.56] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 10q11.22 "LRRC18, WDFY4" rs1913517-A rs1913517 0.29 7.00E-12 1.24 [1.17-1.32] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 11q23.3 NR rs4639966-G rs4639966 0.3 1.00E-16 1.29 [1.22-1.37] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 11q24.3 ETS1 rs6590330-A rs6590330 0.34 2.00E-25 1.37 [1.29-1.45) "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 12q24.32 SLC15A4 rs1385374-A rs1385374 0.2 2.00E-11 1.26 [1.18-1.35] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 16p11.2 NR rs7197475-A rs7197475 0.08 3.00E-08 1.31 [1.20-1.46] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 22q11.21 "HIC2, UBE2L3" rs131654-A rs131654 0.48 1.00E-16 1.28 [1.20-1.35] "Illumina [493,955]" N 11/9/2009 19838193 Han 18-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19838193?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=2 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus Systemic lupus erythematosus "1,047 Chinese Han cases, 1,205 Chinese Han controls" "3,152 Chinese Han cases, 7,050 Chinese Han controls" 1q25.1 TNFSF4 rs2205960-A rs2205960 0.27 3.00E-32 1.46 [1.37-1.56] "Illumina [493,955]" N 11/9/2009 19836008 Landi 15-Oct-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19836008?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=5 A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma Lung adenocarcinoma "5,739 European descent cases, 5,848 European descent controls" "7,561 European descent cases, 13,818 European descent controls" 6p21.33 "BAT3, APOM" rs3117582-C rs3117582 0.1 5.00E-12 1.22 [1.15-1.29] "Illumina [515,922]" N 11/9/2009 19836008 Landi 15-Oct-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19836008?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=5 A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma Lung adenocarcinoma "5,739 European descent cases, 5,848 European descent controls" "7,561 European descent cases, 13,818 European descent controls" 5p15.33 TERT rs2736100-G rs2736100 0.5 2.00E-10 1.12 [1.08-1.16] "Illumina [515,922]" N 11/9/2009 19836008 Landi 15-Oct-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19836008?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=5 A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma Lung adenocarcinoma "5,739 European descent cases, 5,848 European descent controls" "7,561 European descent cases, 13,818 European descent controls" 6p22.1 TRNAA-UGC rs4324798-A rs4324798 0.09 2.00E-08 1.16 [1.09-1.24] "Illumina [515,922]" N 11/9/2009 19836008 Landi 15-Oct-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19836008?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=5 A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma Lung adenocarcinoma "5,739 European descent cases, 5,848 European descent controls" "7,561 European descent cases, 13,818 European descent controls" 5p15.33 CLPTM1L rs31489-C rs31489 0.59 2.00E-10 1.12 [1.09-1.16] "Illumina [515,922]" N 11/9/2009 19836008 Landi 15-Oct-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19836008?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=5 A Genome-wide Association Study of Lung Cancer Identifies a Region of Chromosome 5p15 Associated with Risk for Adenocarcinoma Lung adenocarcinoma "5,739 European descent cases, 5,848 European descent controls" "7,561 European descent cases, 13,818 European descent controls" 15q25.1 "CHRNA3, CHRNA5" rs1051730-T rs1051730 0.35 2.00E-51 1.31 [1.27-1.36] "Illumina [515,922]" N 11/5/2009 19820699 Benyamin 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820699?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants in TMPRSS6 are associated with iron status and erythrocyte volume Serum markers of iron status "4,818 Australian siblings" "3,470 Dutch individuals" 22q12.3 TMPRSS6 rs855791-T rs855791 0.42 1.00E-10 (MCV)  0.13 [0.09-0.17] SD decrease "Illumina & Perlegen [427,037]" N 11/5/2009 19820699 Benyamin 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820699?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants in TMPRSS6 are associated with iron status and erythrocyte volume Serum markers of iron status "4,818 Australian siblings" "3,470 Dutch individuals" 6p22.1 HFE rs1800562-A rs1800562 0.08 2.00E-08 (MCV)  0.22 [0.14-0.30] SD increase "Illumina & Perlegen [427,037]" N 11/5/2009 19820699 Benyamin 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820699?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants in TMPRSS6 are associated with iron status and erythrocyte volume Serum markers of iron status "4,818 Australian siblings" "3,470 Dutch individuals" 6p22.1 HFE rs1800562-A rs1800562 0.08 5.00E-07 (Hgb)  0.2 [0.12-0.28] SD increase "Illumina & Perlegen [427,037]" N 11/5/2009 19820699 Benyamin 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820699?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants in TMPRSS6 are associated with iron status and erythrocyte volume Serum markers of iron status "4,818 Australian siblings" "3,470 Dutch individuals" 22q12.3 TMPRSS6 rs855791-T rs855791 0.42 5.00E-07 (Hgb)  0.1 [0.06-0.14] SD decrease "Illumina & Perlegen [427,037]" N 11/5/2009 19820698 Chambers 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820698?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels Hemoglobin levels "6,316 Europeans, 9,685 Indian Asians" "5,187 Europeans, 6,721 Indian Asians" 6p22.1 HFE rs198846-A rs198846 NR 1.00E-08 NR NR "Affymetrix, Illumina & Perlegen [NR]" N 11/5/2009 19820698 Chambers 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820698?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels Hemoglobin levels "6,316 Europeans, 9,685 Indian Asians" "5,187 Europeans, 6,721 Indian Asians" 22q12.3 TMPRSS6 rs855791-A rs855791 0.53 2.00E-13 0.13 [0.09-0.17] g/dl decrease "Affymetrix, Illumina & Perlegen [NR]" N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hematocrit "24,167 European ancestry individuals" "9,456 European ancestry individuals" 22q12.3 TMPRSS6 rs2413450-T rs2413450 NR 2.00E-13 0.17 [0.13-0.22] % decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hematocrit "24,167 European ancestry individuals" "9,456 European ancestry individuals" 12q24.12 "SH2B3, ATXN2" rs11065987-G rs11065987 NR 1.00E-12 0.17 [0.12-0.22] % decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hematocrit "24,167 European ancestry individuals" "9,456 European ancestry individuals" 10q21.3 HK1 rs16926246-T rs16926246 NR 1.00E-13 0.33 [0.24-0.42] % increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hematocrit "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6q23.3 "HBS1L, MYB" rs9483788-C rs9483788 NR 3.00E-15 0.22 [0.16-0.28] % increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hematocrit "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6p22.1 HFE rs1800562-A rs1800562 NR 2.00E-09 0.31 [0.21-0.41] % increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hematocrit "24,167 European ancestry individuals" "9,456 European ancestry individuals" 7q36.1 PRKAG2 rs10224002-G rs10224002 NR 6.00E-15 0.2 [0.15-0.25] % increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hematocrit "24,167 European ancestry individuals" "9,456 European ancestry individuals" 7q22.1 TFR2 rs7385804-C rs7385804 NR 4.00E-10 0.15 [0.10-0.20] % decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hematocrit "24,167 European ancestry individuals" "9,456 European ancestry individuals" 2p21 PRKCE rs10168349-C rs10168349 NR 4.00E-15 0.19 [0.14-0.23] % increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 12q24.12 TRAFD1 rs11065987-A rs11065987 NR 1.00E-11 0.06 [0.04-0.08] g/dl increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 20q13.2 TSHZ2 rs6013509-A rs6013509 NR 1.00E-10 0.06 [0.05-0.08] g/dl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6p22.1 HFE rs1800562-A rs1800562 NR 6.00E-19 0.16 [0.13-0.20] g/dl increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 2p21 PRKCE rs10495928-G rs10495928 NR 7.00E-13 0.06 [0.05-0.08] g/dl increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 22q12.3 TMPRSS6 rs855791-A rs855791 NR 3.00E-25 0.09 [0.07-0.11] g/dl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 10q21.3 HK1 rs16926246-T rs16926246 NR 2.00E-11 0.11 [0.08-0.14] g/dl increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 7q36.1 PRKAG2 rs10224002-G rs10224002 NR 3.00E-15 0.07 [0.05-0.09] g/dl increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 16p13.3 ITFG3 rs1122794-A rs1122794 NR 3.00E-10 0 [0.003-0.006] pg increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 9p24.1 RCL1 rs10758658-A rs10758658 NR 2.00E-14 0 [0.004-0.006] pg decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6p22.2 SLC17A3 rs1408272-G rs1408272 NR 4.00E-39 0.02 [0.01-0.02] pg decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 3q29 TFRC rs11915082-A rs11915082 NR 8.00E-13 0 [0.003-0.005] pg increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 19p13.13 GCDH rs11085824-G rs11085824 NR 1.00E-11 0 [0.003-0.005] pg decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6q24.1 CITED2 rs628751-C rs628751 NR 1.00E-17 0 [0.003-0.005] pg decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6q23.3 "HBS1L, MYB" rs7776054-G rs7776054 NR 7.00E-69 0.01 [0.009-0.0111] pg decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6p21.1 "CCND3, BYSL" rs9349205-A rs9349205 NR 8.00E-20 0.01 [0.004-0.006] pg decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular hemoglobin "24,167 European ancestry individuals" "9,456 European ancestry individuals" 22q12.3 TMPRSS6 rs2413450-T rs2413450 NR 9.00E-34 0.01 [0.0005-0.007] pg decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 10q11.21 8-Mar rs11239550-G rs11239550 NR 1.00E-10 0 [0.002-0.003] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 19p13.13 RTBDN rs7255045-A rs7255045 NR 2.00E-12 0 [0.002-0.004] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 22q13.33 ECGF1 rs131794-A rs131794 NR 1.00E-15 0 [0.003-0.005] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 2p16.1 BCL11A rs2540917-C rs2540917 NR 1.00E-14 0 [0.002-0.004] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6p22.1 HFE rs1800562-A rs1800562 NR 1.00E-46 0.01 [0.010-0.014] fl increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6p21.1 "CCND3, BYSL" rs9349205-A rs9349205 NR 1.00E-31 0.01 [0.004-0.006] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 14q23.3 FNTB rs4466998-A rs4466998 NR 5.00E-08 0 [0.001-0.003] fl increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 16p13.3 ITFG3 rs7189020-T rs7189020 NR 2.00E-12 0 [0.002-0.004] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 22q12.3 TMPRSS6 rs2413450-T rs2413450 NR 3.00E-41 0.01 [0.004-0.006] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 3q29 TFRC rs9859260-C rs9859260 NR 8.00E-14 0 [0.002-0.004] fl increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 4q12 KIT rs172629-G rs172629 NR 1.00E-15 0 [0.003-0.006] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6q21 CD164 rs9374080-C rs9374080 NR 4.00E-10 0 [0.002-0.003] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6q23.3 "HBS1L, MYB" rs4895441-G rs4895441 NR 7.00E-86 0.01 [0.007-0.009] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6q24.1 CITED2 rs643381-A rs643381 NR 5.00E-25 0 [0.003-0.005] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 7p12.2 IKZF1 rs12718597-A rs12718597 NR 5.00E-13 0 [0.002-0.004] fl increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 7q22.1 TFR2 rs7786877-G rs7786877 NR 3.00E-11 0 [0.002-0.004] fl increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Mean corpuscular volume "24,167 European ancestry individuals" "9,456 European ancestry individuals" 9p24.1 RCL1 rs10758658-A rs10758658 NR 3.00E-20 0 [0.003-0.005] fl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Other erythrocyte phenotypes "24,167 European ancestry individuals" "9,456 European ancestry individuals" 1q23.1 SPTA1 rs857721-A rs857721 NR 1.00E-10 (MCHC)  0 [0.001-0.002] g/dl decrease Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Other erythrocyte phenotypes "24,167 European ancestry individuals" "9,456 European ancestry individuals" 7q22.1 EPO rs2075671-A rs2075671 NR 1.00E-09 (RBC)  0 [0.005-0.009] 1 M cell/mm^3 increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Other erythrocyte phenotypes "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6q23.3 "HBS1L, MYB" rs9483788-G rs9483788 NR 1.00E-47 (RBC)  0 [0.012-0.016] 1 M cells/mm^3 increase Affymetrix & Illumina [~2.5 million](imputed) N 11/3/2009 19862010 Ganesh 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19862010?itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum&ordinalpos=1 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium Other erythrocyte phenotypes "24,167 European ancestry individuals" "9,456 European ancestry individuals" 6q23.3 "HBS1L, MYB" rs9373124-C rs9373124 NR 7.00E-14 (MCHC)  0 [0.002-0.003] g/dl decrease Affymetrix & Illumina [~2.5 million](imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 6q21 Intergenic rs4947019-G rs4947019 NR 0.000008 (MCV)  0.01 [0.003-0.011] fl decrease Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 12q24.13 PTPN11 rs11066301-G rs11066301 NR 8.00E-12 (PLT)  4.65 [3.32-5.98] 10^9/l increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 6p21.31 BAK1 rs210135-A rs210135 NR 4.00E-10 (PLT)  5.44 [3.74-7.14] 10^9/l increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 9p24.1 AK3 rs385893-C rs385893 NR 9.00E-17 (PLT)  6.26 [4.78-7.74] 10^9/l increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 17q12 "GSDMA, ORMDL3" rs17609240-G rs17609240 NR 9.00E-09 (WBC)  0.02 [0.01-0.03] 10^9/l increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 6p21.32 Intergenic rs2227139-G rs2227139 NR 1.00E-07 (WBC)  0.02 [0.01-0.03] 10^9/l increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 7q22.1 TFR2 rs7385804-C rs7385804 NR 5.00E-10 (RBC)  0.01 [0.004-0.008] 10^12/l increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 6q23.3 "HBS1L, MYB" rs9402686-A rs9402686 NR 7.00E-42 (MCV)  0.82 [0.70-0.94] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 22q12.3 FBX07 rs9609565-G rs9609565 NR 4.00E-10 (MCV)  0.37 [0.25-0.49] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 6p21.1 "BYSL, CCND3" rs11970772-T rs11970772 NR 7.00E-19 (MCV)  0.58 [0.44-0.70] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 6p22.1 HFE rs1800562-A rs1800562 NR 1.00E-23 (MCV)  1.41 [1.13-1.69] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Hematological parameters "4,627 European individuals" "9,316 European individuals" 22q12.3 TMPRSS6 rs5756506-C rs5756506 NR 1.00E-09 (MCH)  0.14 [0.10-0.18] pg increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 10q21.3 JMJD1C rs2393967-A rs2393967 NR 3.00E-21 0.01 [0.01-0.018] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 1q32.1 TMCC2 rs1668873-G rs1668873 NR 1.00E-20 0.01 [0.01-0.014] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 2p23.1 EHD3 rs647316-A rs647316 NR 3.00E-11 0.01 [0.006-0.014] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 18q22.2 CD226 rs893001-C rs893001 NR 1.00E-10 0.01 [0.007-0.015] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 5q33.3 NR rs1473247-C rs1473247 NR 3.00E-07 0.01 [0.004-0.012] fl decrease Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 20p12.1 NR rs6110278-T rs6110278 NR 4.00E-07 0.01 [0.005-0.013] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 12q13.13 NR rs10506328-A rs10506328 NR 5.00E-07 0.01 [0.004-0.012] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 11p15.5 BET1L rs11602954-G rs11602954 NR 1.00E-14 0.01 [0.009-0.017] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 1q24.3 DNM3 rs10914144-C rs10914144 NR 2.00E-14 0.01 [0.009-0.017] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 20p13 SIRPA rs6136489-T rs6136489 NR 8.00E-11 0.01 [0.006-0.014] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 15q22.2 TPM1 rs11071720-T rs11071720 NR 2.00E-08 0.01 [0.007-0.015] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 3p14.3 ARHGEF3 rs12485738-A rs12485738 NR 6.00E-31 0.02 [0.013-0.017] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 12q24.31 WDR66 rs7961894-T rs7961894 NR 3.00E-44 0.03 [0.027-0.035] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 17q11.2 TAOK1 rs2138852-T rs2138852 NR 1.00E-22 0.02 [0.012-0.020] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/30/2009 19820697 Soranzo 11-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19820697?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium Mean platelet volume "4,627 European individuals" "9,316 European individuals" 7q22.3 PIK3CG rs342293-G rs342293 NR 2.00E-33 0.02 [0.013-0.017] fl increase Affymetrix and Illumina [~2.11 million] (imputed) N 10/23/2009 19812673 Weiss 8-Oct-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19812673?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide linkage and association scan reveals novel loci for autism Autism "1,031 families with 1,553 affected offspring (multiple races/ethnicities)" "2,073 trios (multiple races/ethnicities)" 5p15.2 "SEMA5A, TAS2R1" rs10513025-? rs10513025 NR 3.00E-07 1.81 [NR] "Affymetrix [~365,000]" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 1p31.3 GPR177 rs2566755-C rs2566755 0.21 2.00E-12 0.1 [0.07-0.13] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 8q24.12 TNFRSF11B rs11995824-G rs11995824 0.55 7.00E-09 0.07 [0.05-0.09] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 6q25.1 ESR1 rs2941740-G rs2941740 0.43 2.00E-10 0.07 [0.05-0.09] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 1p36.12 ZBTB40 rs6426749-C rs6426749 0.17 9.00E-08 0.08 [0.05-0.11] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 17q21.31 HDAC5 rs228769-G rs228769 0.2 2.00E-08 0.08 [0.05-0.11] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 11p11.2 ARHGAP1 rs7932354-T rs7932354 0.29 4.00E-09 0.07 [0.05-0.09] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 3p22.1 CTNNB1 rs87938-A rs87938 0.45 8.00E-10 0.07 [0.05-0.09] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 17q21.31 CRHR1 rs9303521-T rs9303521 0.46 0.000004 0.06 [0.04-0.07] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 16q24.1 FOXL1 rs10048146-G rs10048146 0.19 2.00E-07 0.09 [0.06-0.12] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 11p15.2 SOX6 rs7117858-G rs7117858 0.2 6.00E-10 0.09 [0.06-0.12] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 7q21.3 FLJ42280 rs7781370-T rs7781370 0.34 5.00E-12 0.08 [0.06-0.10] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 5q14.3 MEF2C rs1366594-C rs1366594 0.45 1.00E-13 0.09 [0.07-0.11] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (hip) "19,195 European individuals" NR 4q22.1 MEPE rs1471403-T rs1471403 0.34 8.00E-07 0.06 [0.04-0.08] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 18q21.33 TNFRSF11A rs884205-A rs884205 0.27 9.00E-09 0.08 [0.05-0.11] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 2p16.2 SPTBN1 rs11898505-A rs11898505 0.34 2.00E-08 0.07 [0.05-0.09] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 12q13.13 SP7 rs2016266-G rs2016266 0.32 1.00E-08 0.07 [0.05-0.09] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 11q13.2 LRP5 rs599083-G rs599083 0.31 5.00E-08 0.07 [0.05-0.09] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 13q14.11 AKAP11 rs9533090-T rs9533090 0.5 5.00E-25 0.12 [0.10-0.14] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 8q24.12 TNFRSF11B rs2062377-T rs2062377 0.44 4.00E-16 0.09 [0.07-0.11] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 6q25.1 ESR1 rs2504063-A rs2504063 0.4 6.00E-11 0.08 [0.06-0.10] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 1p36.12 ZBTB40 rs7524102-G rs7524102 0.17 3.00E-10 0.09 [0.06-0.12] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 17q21.31 HDAC5 rs228769-G rs228769 0.2 0.000004 0.07 [0.04-0.10] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 17q21.31 CRHR1 rs9303521-T rs9303521 0.46 1.00E-08 0.07 [0.05-0.09] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 16q24.1 FOXL1 rs10048146-G rs10048146 0.19 2.00E-08 0.09 [0.06-0.12] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 11p13 DCDC5 rs16921914-A rs16921914 0.27 2.00E-09 0.08 [0.05-0.11] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 7q21.3 FLJ42280 rs4729260-G rs4729260 0.32 2.00E-10 0.08 [0.05-0.11] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 4q22.1 MEPE rs1471403-T rs1471403 0.34 2.00E-08 0.07 [0.05-0.09] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 7p14.1 STARD3NL rs1524058-T rs1524058 0.4 1.00E-09 0.07 [0.05-0.09] sd decrease "Affymetrix & Illumina [2,543,686](imputed)" N 10/16/2009 19801982 Rivadeneira 4-Oct-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19801982?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies Bone mineral density (spine) "19,195 European individuals" NR 1p31.3 GPR177 rs1430742-C rs1430742 0.21 3.00E-13 0.11 [0.07-0.14] sd increase "Affymetrix & Illumina [2,543,686](imputed)" N 11/4/2009 19798445 Hicks 2-Oct-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19798445?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic determinants of circulating sphingolipid concentrations in European populations Sphingolipid Concentrations "4,110 European individuals" NR 4p12 ATP10D rs10938494-A rs10938494 0.23 8.00E-19 (GluCer)  0.06 [0.04-0.07] unit increase "Illumina [318,237]" N 11/4/2009 19798445 Hicks 2-Oct-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19798445?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic determinants of circulating sphingolipid concentrations in European populations Sphingolipid Concentrations "4,110 European individuals" NR 11q12.3 FADS rs1000778-A rs1000778 0.32 7.00E-13 (SM 16:1)  0.62 [0.45-0.78] unit decrease "Illumina [318,237]" N 11/4/2009 19798445 Hicks 2-Oct-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19798445?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic determinants of circulating sphingolipid concentrations in European populations Sphingolipid Concentrations "4,110 European individuals" NR 14q23.2 SGPP1 rs7157785-A rs7157785 0.19 9.00E-66 (SM 14:0Mol%)  0 [0.001-0.002] mol % increase "Illumina [318,237]" N 11/4/2009 19798445 Hicks 2-Oct-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19798445?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic determinants of circulating sphingolipid concentrations in European populations Sphingolipid Concentrations "4,110 European individuals" NR 19p13.2 LASS4 rs7258249-G rs7258249 0.48 2.00E-27 (SM 18:1Mol%)  0 [0.0007-0.001] mol % increase "Illumina [318,237]" N 11/4/2009 19798445 Hicks 2-Oct-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19798445?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic determinants of circulating sphingolipid concentrations in European populations Sphingolipid Concentrations "4,110 European individuals" NR 20p12.1 SPTLC3 rs680379-A rs680379 0.34 8.00E-15 (Cer24:0)  0.1 [0.08-0.13] mol % increase "Illumina [318,237]" N 10/6/2009 19786962 Roeske 29-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19786962?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children Speech perception in dyslexia 200 dyslexic German children 186 dyslexic German children 10q26.3 NR rs4751178-G rs4751178 NR 0.000007 (MMNb)  NR NR "Illumina [297,086]" N 10/6/2009 19786962 Roeske 29-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19786962?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children Speech perception in dyslexia 200 dyslexic German children 186 dyslexic German children 4q32.1 "CTSO, TDO2, PDGFC" rs4234898-T rs4234898 NR 5.00E-08 (MMNb)  NR NR "Illumina [297,086]" N 10/6/2009 19779542 Nakanishi 25-Sep-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19779542?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1 Myopia (pathological) "297 Japanese cases, 934 Japanese controls" "533 Japanese cases, 977 Japanese controls" 11q24.1 "BLID, LOC399959" rs577948-G rs577948 0.52 2.00E-07 1.37 [1.21-1.54] "Illumina [411,777]" N 10/5/2009 19772629 Latourelle 22-Sep-09 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/19772629?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study for Onset Age in Parkinson Disease Parkinson disease (age of onset) "857 white familial cases, 440 white idiopathic cases" 747 Italian idiopathic cases 2p14 AAK1 rs7577851-T rs7577851 NR 0.000009 6.85 [NR] years younger "Illumina and Perlegen [1,861,750] (imputed)" N 10/5/2009 19772629 Latourelle 22-Sep-09 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/19772629?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study for Onset Age in Parkinson Disease Parkinson disease (age of onset) "857 white familial cases, 440 white idiopathic cases" 747 Italian idiopathic cases 11p13 "QSER1, PRRG4" rs10767971-T rs10767971 NR 5.00E-07 3.24 [NR] years older "Illumina and Perlegen [1,861,750] (imputed)" N 10/5/2009 19772629 Latourelle 22-Sep-09 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/19772629?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study for Onset Age in Parkinson Disease Parkinson disease (age of onset) "857 white familial cases, 440 white idiopathic cases" 747 Italian idiopathic cases 1q23.3 ATF6 rs10918270-A rs10918270 NR 0.000008 2.26 [NR] years younger "Illumina and Perlegen [1,861,750] (imputed)" N 10/5/2009 19772629 Latourelle 22-Sep-09 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/19772629?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study for Onset Age in Parkinson Disease Parkinson disease (age of onset) "857 white familial cases, 440 white idiopathic cases" 747 Italian idiopathic cases 15q12 OCA2 rs17565841-A rs17565841 NR 0.000003 2.84 [NR] years younger "Illumina and Perlegen [1,861,750] (imputed)" N 10/5/2009 19772629 Latourelle 22-Sep-09 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/19772629?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study for Onset Age in Parkinson Disease Parkinson disease (age of onset) "857 white familial cases, 440 white idiopathic cases" 747 Italian idiopathic cases 18q12.1 DSG3 rs1941184-C rs1941184 NR 0.000004 2.28 [NR] years younger "Illumina and Perlegen [1,861,750] (imputed)" N 10/5/2009 19767754 Gudmundsson 20-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility Prostate cancer "Up to 1,968 Icelandic cases, 35,382 Icelandic controls" "Up to 11,806 European descent cases, 12,387 European descent controls" 19q13.2 Intergenic rs8102476-C rs8102476 0.54 2.00E-11 1.12 [1.08-1.15] "Illumina [310,520]" N 10/5/2009 19767754 Gudmundsson 20-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility Prostate cancer "Up to 1,968 Icelandic cases, 35,382 Icelandic controls" "Up to 11,806 European descent cases, 12,387 European descent controls" 8q24.21 Intergenic rs445114-T rs445114 0.64 5.00E-10 1.14 [1.10-1.19] "Illumina [310,520]" N 10/5/2009 19767754 Gudmundsson 20-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility Prostate cancer "Up to 1,968 Icelandic cases, 35,382 Icelandic controls" "Up to 11,806 European descent cases, 12,387 European descent controls" 3q21.3 Intergenic rs10934853-A rs10934853 0.28 3.00E-10 1.12 [1.08-1.16] "Illumina [310,520]" N 10/5/2009 19767754 Gudmundsson 20-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility Prostate cancer "Up to 1,968 Icelandic cases, 35,382 Icelandic controls" "Up to 11,806 European descent cases, 12,387 European descent controls" 8q24.21 Intergenic rs16901979-A rs16901979 0.04 3.00E-14 1.8 [1.55-2.09] "Illumina [310,520]" N 10/5/2009 19767754 Gudmundsson 20-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility Prostate cancer "Up to 1,968 Icelandic cases, 35,382 Icelandic controls" "Up to 11,806 European descent cases, 12,387 European descent controls" 8q24.21 Intergenic rs1447295-A rs1447295 0.11 2.00E-19 1.58 [1.43-1.74] "Illumina [310,520]" N 10/5/2009 19767754 Gudmundsson 20-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility Prostate cancer "Up to 1,968 Icelandic cases, 35,382 Icelandic controls" "Up to 11,806 European descent cases, 12,387 European descent controls" 8q24.21 Intergenic rs16902094-G rs16902094 0.15 6.00E-15 1.21 [1.15-1.26] "Illumina [310,520]" N 10/5/2009 19767754 Gudmundsson 20-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility Prostate cancer "Up to 1,968 Icelandic cases, 35,382 Icelandic controls" "Up to 11,806 European descent cases, 12,387 European descent controls" 11q13.2 Intergenic rs11228565-A rs11228565 0.2 7.00E-12 1.23 [1.16-1.31] "Illumina [310,520]" N 10/5/2009 19767754 Gudmundsson 20-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19767754?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility Prostate cancer "Up to 1,968 Icelandic cases, 35,382 Icelandic controls" "Up to 11,806 European descent cases, 12,387 European descent controls" 17q12 Intergenic rs4430796-A rs4430796 0.52 0.000008 1.19 [1.10-1.28] "Illumina [310,520]" N 9/30/2009 19754311 Le Clerc 15-Sep-09 J Infect Dis http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03). AIDS "85 French cases, 2,049 French controls" NR 9p22.3 NR rs1556032-C rs1556032 0.49 0.000009 2.05 [1.48-2.84] "Illumina [291,119]" N 9/30/2009 19754311 Le Clerc 15-Sep-09 J Infect Dis http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03). AIDS "85 French cases, 2,049 French controls" NR 12p12.1 SOX5 rs1522232-C rs1522232 0.52 0.000002 2.22 [1.59-3.13] "Illumina [291,119]" N 9/30/2009 19754311 Le Clerc 15-Sep-09 J Infect Dis http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03). AIDS "85 French cases, 2,049 French controls" NR 1p13.3 Intergenic rs4118325-G rs4118325 0.81 6.00E-07 4.17 [2.17-8.33] "Illumina [291,119]" N 9/30/2009 19754311 Le Clerc 15-Sep-09 J Infect Dis http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03). AIDS "85 French cases, 2,049 French controls" NR 1q23.3 RXRG rs10800098-A rs10800098 0.05 0.000004 3.29 [2.08-5.20] "Illumina [291,119]" N 9/30/2009 19754311 Le Clerc 15-Sep-09 J Infect Dis http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03). AIDS "85 French cases, 2,049 French controls" NR 2q12.1 TGFBRAP1 rs1020064-G rs1020064 0.23 0.000007 2.94 [1.75-5.00] "Illumina [291,119]" N 9/30/2009 19754311 Le Clerc 15-Sep-09 J Infect Dis http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03). AIDS "85 French cases, 2,049 French controls" NR 8q22.3 Intergenic rs3108919-C rs3108919 0.27 0.000004 2.13 [1.56-2.91] "Illumina [291,119]" N 9/30/2009 19754311 Le Clerc 15-Sep-09 J Infect Dis http://www.ncbi.nlm.nih.gov/pubmed/19754311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study of a Rapid Progression Cohort Identifies New Susceptibility Alleles for AIDS (ANRS Genomewide Association Study 03). AIDS "85 French cases, 2,049 French controls" NR 9p23 Intergenic rs1360517-A rs1360517 0.06 0.000003 3.09 [2.00-4.78] "Illumina [291,119]" N 9/30/2009 19749758 Suppiah 13-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19749758?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy Response to Hepatitis C treatment "131 European ancestry responders, 162 European ancestry non-responders" "261 European responders, 294 European non-responders" 19q13.2 "IL28A, IL28B" rs8099917-G rs8099917 NR 9.00E-09 1.98 [1.57-2.52] "Illumina [311,159]" N 9/30/2009 19749757 Tanaka 13-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19749757?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C Response to Hepatitis C treatment "72 Japanese responders, 82 Japanese non-responders" "122 Japanese responders, 50 Japanese non-responders" 19q13.2 IL28B rs8099917-G rs8099917 0.12 3.00E-32 27.1 [14.6-50.3] "Affymetrix [621,220]" N 9/30/2009 19749422 Heinzen 11-Sep-09 J Alzheimers Dis http://www.ncbi.nlm.nih.gov/pubmed/19749422?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease Alzheimer's Disease "331 cases, 368 controls" NR 6q24.3 SASH1 rs9390537-? rs9390537 0.22 0.000008 NR NR "Illumima [~550,000]" N 9/30/2009 19749422 Heinzen 11-Sep-09 J Alzheimers Dis http://www.ncbi.nlm.nih.gov/pubmed/19749422?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease Alzheimer's Disease "331 cases, 368 controls" NR 13q13.2 RFC3 rs690705-? rs690705 0.25 6.00E-07 NR NR "Illumima [~550,000]" N 9/30/2009 19749422 Heinzen 11-Sep-09 J Alzheimers Dis http://www.ncbi.nlm.nih.gov/pubmed/19749422?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease Alzheimer's Disease "331 cases, 368 controls" NR 19q13.32 "TOMM40, APOE" rs2075650-? rs2075650 0.15 3.00E-11 NR NR "Illumima [~550,000]" N 9/30/2009 19749422 Heinzen 11-Sep-09 J Alzheimers Dis http://www.ncbi.nlm.nih.gov/pubmed/19749422?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease Alzheimer's Disease "331 cases, 368 controls" NR 10q24.31 PAX2 rs4509693-? rs4509693 0.18 0.000006 NR NR "Illumima [~550,000]" N 9/30/2009 19749422 Heinzen 11-Sep-09 J Alzheimers Dis http://www.ncbi.nlm.nih.gov/pubmed/19749422?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease Alzheimer's Disease "331 cases, 368 controls" NR 1p31.1 TTLL7 rs7539409-? rs7539409 0.18 0.000001 NR NR "Illumima [~550,000]" N 9/30/2009 19740415 Sha 9-Sep-09 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/19740415?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis Amyotrophic lateral sclerosis (interaction) "276 Caucasian cases, 271 Caucasian controls" NR NR NR NR NR NS NS NR NR "Illumina [549,062]" N 9/29/2009 19734902 Harold 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734902?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Alzheimer's disease "3,941 European ancestry cases, 7,848 European ancestry controls" "2,023 European ancestry cases, 2,340 European ancestry controls" 19q13.32 "APOE, TOMM40" rs2075650-? rs2075650 0.15 0 2.53 [2.37-2.71] "Illumina [529,205]" N 9/29/2009 19734902 Harold 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734902?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Alzheimer's disease "3,941 European ancestry cases, 7,848 European ancestry controls" "2,023 European ancestry cases, 2,340 European ancestry controls" 11q14.2 PICALM rs3851179-? rs3851179 0.63 1.00E-09 1.16 [1.11-1.22] "Illumina [529,205]" N 9/29/2009 19734902 Harold 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734902?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease Alzheimer's disease "3,941 European ancestry cases, 7,848 European ancestry controls" "2,023 European ancestry cases, 2,340 European ancestry controls" 8p21.1 CLU rs11136000-? rs11136000 0.6 9.00E-10 1.16 [1.11-1.22] "Illumina [529,205]" N 9/29/2009 19734903 Lambert 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease Alzheimer's disease "2,032 French cases, 5,328 French controls" "3,978 European cases, 3,297 European controls" 1q32.2 CR1 2-SNP haplotype "rs3818361,rs6656401" 0.18 3.00E-10 (AA)  1.22 [1.15-1.30] "Illumina [537,029]" N 9/29/2009 19734903 Lambert 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease Alzheimer's disease "2,032 French cases, 5,328 French controls" "3,978 European cases, 3,297 European controls" 19q13.32 APOE rs2075650-? rs2075650 0.9 2.00E-16 NR NR "Illumina [537,029]" N 9/29/2009 19734903 Lambert 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease Alzheimer's disease "2,032 French cases, 5,328 French controls" "3,978 European cases, 3,297 European controls" 8p21.1 CLU 3-SNP haplotype "rs2279590,rs11136000,rs9331888" 0.26 6.00E-10 (CCG)  1.22 [1.14-1.29] "Illumina [537,029]" N 9/29/2009 19734900 Rung 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia" Type 2 diabetes and other traits "679 French cases, 697 French controls" "5,579 European cases, 7,096 European controls" 8q24.11 SLC30A8 rs13266634-C rs13266634 0.68 8.00E-08 1.16 [1.10-1.22] "Illumina [392,365]" N 9/29/2009 19734900 Rung 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia" Type 2 diabetes and other traits "679 French cases, 697 French controls" "5,579 European cases, 7,096 European controls" 10q25.2 TCF7L2 rs7903146-T rs7903146 0.27 1.00E-30 1.48 [1.39-1.57] "Illumina [392,365]" N 9/29/2009 19734900 Rung 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia" Type 2 diabetes and other traits "679 French cases, 697 French controls" "5,579 European cases, 7,096 European controls" 6p22.3 CDKAL1 rs4712523-G rs4712523 0.32 2.00E-12 1.2 [1.14-1.26] "Illumina [392,365]" N 9/29/2009 19734900 Rung 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia" Type 2 diabetes and other traits "679 French cases, 697 French controls" "5,579 European cases, 7,096 European controls" 5q14.3 "LOC72901, CETN3" rs12518099-C rs12518099 0.23 7.00E-07 1.16 [1.10-1.22] "Illumina [392,365]" N 9/29/2009 19734900 Rung 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia" Type 2 diabetes and other traits "679 French cases, 697 French controls" "5,579 European cases, 7,096 European controls" 4p16.1 "WFS1, PPP2R2C" rs4689388-T rs4689388 0.57 1.00E-08 1.16 [1.10-1.21] "Illumina [392,365]" N 9/29/2009 19734900 Rung 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia" Type 2 diabetes and other traits "679 French cases, 697 French controls" "5,579 European cases, 7,096 European controls" 2q36.3 "LOC64673, IRS1" rs2943641-C rs2943641 0.63 9.00E-12 1.19 [1.13-1.25] "Illumina [392,365]" N 9/29/2009 19734901 van Es 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "2,323 European descent cases, 9,013 European descent controls" "2,532 European descent cases, 5,940 European descent controls" Xp22.32 NR rs5916687-? rs5916687 0.27 0.000003 1.22 [NR] "Illumina [292,768]" N 9/29/2009 19734901 van Es 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "2,323 European descent cases, 9,013 European descent controls" "2,532 European descent cases, 5,940 European descent controls" 11q22.1 NR rs2405657-? rs2405657 0.66 0.000003 1.19 [NR] "Illumina [292,768]" N 9/29/2009 19734901 van Es 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "2,323 European descent cases, 9,013 European descent controls" "2,532 European descent cases, 5,940 European descent controls" 9p21.2 NR rs774359-? rs774359 0.25 0.000003 1.19 [NR] "Illumina [292,768]" N 9/29/2009 19734901 van Es 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "2,323 European descent cases, 9,013 European descent controls" "2,532 European descent cases, 5,940 European descent controls" 9p21.2 "MOBKL2B, IFNK, C9orf72" rs2814707-? rs2814707 0.23 7.00E-09 1.22 [NR] "Illumina [292,768]" N 9/29/2009 19734901 van Es 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "2,323 European descent cases, 9,013 European descent controls" "2,532 European descent cases, 5,940 European descent controls" 12p12.3 NR rs9971637-? rs9971637 0.05 0.000002 1.48 [NR] "Illumina [292,768]" N 9/29/2009 19734901 van Es 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "2,323 European descent cases, 9,013 European descent controls" "2,532 European descent cases, 5,940 European descent controls" Xq13.3 NR rs5937496-? rs5937496 0.13 6.00E-07 1.38 [NR] "Illumina [292,768]" N 9/29/2009 19734901 van Es 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "2,323 European descent cases, 9,013 European descent controls" "2,532 European descent cases, 5,940 European descent controls" 19p13.11 UNC13A rs12608932-? rs12608932 0.34 3.00E-14 1.25 [NR] "Illumina [292,768]" N 9/29/2009 19734901 van Es 6-Sep-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19734901?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "2,323 European descent cases, 9,013 European descent controls" "2,532 European descent cases, 5,940 European descent controls" 9p21.2 "MOBKL2B, IFNK, C9orf72" rs3849942-? rs3849942 0.23 1.00E-08 1.23 [NR] "Illumina [292,768]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 17q21.32 Intergenic rs2326017-? rs2326017 0.3 3.00E-07 (SWM strategy)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 1q32.1 MDM4 rs12143943-? rs12143943 0.41 0.000005 (PAL8)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 14q23.2 MTHFD1 rs10498514-? rs10498514 0.02 8.00E-07 (SWM strategy)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 3q27.2 EHHADH rs7374394-? rs7374394 0.2 0.000002 (IED)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 18q22.1 "C18orf4, DSEL" rs2124349-? rs2124349 0.05 0.000004 (IED)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 3q26.32 Intergenic rs7612209-? rs7612209 0.4 0.000004 (IED)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 1p32.1 JUN rs4601609-? rs4601609 0.05 0.000005 (PRM)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 7q31.1 IMMP2L rs12531640-? rs12531640 0.13 0.000006 (IED)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 7p14.1 VPS41 rs11984145-? rs11984145 0.05 0.000006 (PAL8)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR Xp22.2 HCCS rs5934953-? rs5934953 0.02 1.00E-07 (PAL6)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 21q21.3 JAM2 rs17001239-? rs17001239 0.12 0.000002 (PRM)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 1q23.2 VANGL2 rs16832015-? rs16832015 0.01 0.000002 (IED)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 8q12.1 TOX rs960089-? rs960089 0.07 0.000006 (PAL6)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 9p22.2 SH3GL2 rs10810865-? rs10810865 0.13 0.000004 (PAL6)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 11q14.2 C11orf73 rs6592284-? rs6592284 0.21 0.000002 (IED)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 11p12 API5 rs10501293-? rs10501293 0.25 0.000005 (SWM Strategy)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 12q24.23 CCDC64 rs11064994-? rs11064994 0.06 0.000006 (PAL6)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 13q14.11 DNAJC15 rs1324015-? rs1324015 0.42 0.000009 (PC1)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 14q23.2 MTHFD1 rs2295639-? rs2295639 0.02 0.000005 (SWM Strategy)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 16q23.3 Intergenic rs4082514-? rs4082514 0.03 0.000003 (PC1)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 17q25.2 SEC14L1 rs3744064-? rs3744064 0.03 7.00E-07 (PAL6)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 20p12.3 PLCB1 rs6056209-? rs6056209 0.43 0.000002 (RVP)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 2q31.1 GORASP2 rs4668356-? rs4668356 0.06 0.000001 (PAL8)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 3p22.3 ARPP-21 rs6799705-? rs6799705 0.05 2.00E-07 (PAL8)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 3p25.1 GRIP2 rs9036-? rs9036 0.19 0.000003 (PAL6)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 5p15.31 Intergenic rs7729273-? rs7729273 0.2 0.000001 (SSP)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 7q31.1 IMMP2L rs10279573-? rs10279573 0.14 0.000003 (IED)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 7p15.1 CPVL rs2252521-? rs2252521 0.34 0.000005 (PAL8)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 1q41 FAM177B rs6683071-? rs6683071 0.2 0.000004 (PC1)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 18q12.3 RIT2 rs8085804-? rs8085804 0.37 0.000008 (VRM)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 15q23 CORO2B rs11856323-? rs11856323 0.08 1.00E-07 (PAL8)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 15q12 GABRB3 rs8043440-? rs8043440 0.17 0.000002 (SRM)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 21q11.2 NRIP1 rs2229741-? rs2229741 0.47 6.00E-07 (SRM)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 6p21.2 C6orf129 rs904251-? rs904251 0.38 0.000007 (SWM Strategy)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 8q24.13 FAM91A1 rs10481151-? rs10481151 0.14 4.00E-07 (PRM)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 19q12 TSHZ3 rs1078373-? rs1078373 0.37 0.000006 (SSP)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 12p13.1 GRIN2B rs2160519-? rs2160519 0.06 0.000002 (IED)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 11q13.5 CAPN5 rs3781684-? rs3781684 0.11 0.000007 (VRM)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 3q13.33 FBXO40 rs3772130-? rs3772130 0.23 0.000006 (PC1)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 3p22.1 MOBP rs816488-? rs816488 0.04 0.000004 (IED)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 4q28.1 FAT4 rs12639834-? rs12639834 0.36 0.000006 (SWM Strategy)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 16p12.1 Intergenic rs2203512-? rs2203512 0.14 3.00E-07 (PRM)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR Xp22.31 VCX3B rs7892812-? rs7892812 0.47 0.000008 (SSP)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 1p36.13 FAM131C rs9442235-? rs9442235 0.42 0.000006 (PC1)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 13q12.3 FLT1 rs17086609-? rs17086609 0.35 0.000005 (IED)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 15q21.3 UNC13C rs1897031-? rs1897031 0.18 0.000001 (PRM)  NR NR "Illumina [475,971]" N 10/2/2009 19734545 Need 4-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19734545?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Study of Common SNPs and CNVs in Cognitive Performance in the CANTAB battery Cognitive performance "1,295 individuals" NR 13q34 Intergenic rs767210-? rs767210 0.11 3.00E-07 (PAL6)  NR NR "Illumina [475,971]" N 9/28/2009 19729612 Paterson 3-Sep-09 Arterioscler Thromb Vasc Biol http://www.ncbi.nlm.nih.gov/pubmed/19729612?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Identifies the ABO Blood Group as a Major Locus Associated With Serum Levels of Soluble E-Selectin Serum soluble E-selectin 685 individuals with type 1 diabetes 477 nondiabetic siblings 9q34.2 ABO rs579459-C rs579459 0.2 1.00E-29 NR NR "Illumina [~841,000]" N 9/28/2009 19729412 Tonjes 3-Sep-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19729412?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variation in GPR133 is Associated with Height - Genome Wide Association Study in the Self-contained Population of Sorbs Height "929 Sorbian individuals, 2,986 Caucasian individuals" "2,772 German individuals" 12q24.33 GPR133 rs1569019-? rs1569019 NR 5.00E-08 0.95 [0.61-1.29] cm increase "Affymetrix [390,619]" N 9/28/2009 19727025 De Moor 2-Sep-09 Med Sci Sports Exerc http://www.ncbi.nlm.nih.gov/pubmed/19727025?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Exercise Behavior in Dutch and American Adults Exercise (leisure time) "1,644 Dutch individuals, 978 European individuals" NR 10q23.2 PAPSS2 rs10887741-T rs10887741 NR 0.000004 1.32 [1.17-1.49] Affymetrix and Perlegen [~1.6 million] (imputed) N 9/28/2009 19727025 De Moor 2-Sep-09 Med Sci Sports Exerc http://www.ncbi.nlm.nih.gov/pubmed/19727025?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Exercise Behavior in Dutch and American Adults Exercise (leisure time) "1,644 Dutch individuals, 978 European individuals" NR 18p11.32 C18orf2 rs8097348-G rs8097348 NR 0.000007 1.36 [1.19-1.56] Affymetrix and Perlegen [~1.6 million] (imputed) N 9/28/2009 19727025 De Moor 2-Sep-09 Med Sci Sports Exerc http://www.ncbi.nlm.nih.gov/pubmed/19727025?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Exercise Behavior in Dutch and American Adults Exercise (leisure time) "1,644 Dutch individuals, 978 European individuals" NR 2q33.1 DNAPTP6 rs12612420-A rs12612420 NR 0.000008 1.43 [1.22-1.67] Affymetrix and Perlegen [~1.6 million] (imputed) N 9/29/2009 19736353 Ising 1-Sep-09 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19736353?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression Response to antidepressant treatment 339 German individuals "1,193 German individuals" NR NR NR NR NS NS NR NR "Illumina [389,251] (pooled)" N 9/28/2009 19721433 McClay 1-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics Treatment response to antipsychotics 738 cases NR 6p21.33 Intergenic rs12526186-? rs12526186 NR 0.000003 (risperidone)  9 [NR] % of variance explained "Affymetrix & Perlegen [492,900]" N 9/28/2009 19721433 McClay 1-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics Treatment response to antipsychotics 738 cases NR 15q13.3 TRPM1 rs17815774-? rs17815774 NR 0.000003 (risperidone)  9 [NR] % of variance explained "Affymetrix & Perlegen [492,900]" N 9/28/2009 19721433 McClay 1-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics Treatment response to antipsychotics 738 cases NR 1q21.3 Intergenic rs10888501-? rs10888501 NR 0.000001 (olanzapine)  9 [NR] % of variance explained "Affymetrix & Perlegen [492,900]" N 9/28/2009 19721433 McClay 1-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics Treatment response to antipsychotics 738 cases NR 3q28 Intergenic rs7635839-? rs7635839 NR 0.000003 (olanzapine)  9 [NR] % of variance explained "Affymetrix & Perlegen [492,900]" N 9/28/2009 19721433 McClay 1-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics Treatment response to antipsychotics 738 cases NR 2q14.3 CNTNAP5 rs17727261-? rs17727261 NR 5.00E-07 (risperidone)  10 [NR] % of variance explained "Affymetrix & Perlegen [492,900]" N 9/28/2009 19721433 McClay 1-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics Treatment response to antipsychotics 738 cases NR 6p24.1 Intergenic rs1040994-? rs1040994 NR 0.000002 (olanzapine)  9 [NR] % of variance explained "Affymetrix & Perlegen [492,900]" N 9/28/2009 19721433 McClay 1-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics Treatment response to antipsychotics 738 cases NR 4p15.1 Intergenic rs17390445-? rs17390445 NR 1.00E-07 (ziprasidone)  17 [NR] % of variance explained "Affymetrix & Perlegen [492,900]" N 9/28/2009 19721433 McClay 1-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics Treatment response to antipsychotics 738 cases NR 9q33.3 Intergenic rs888219-? rs888219 NR 2.00E-07 (risperidone)  11 [NR] % of variance explained "Affymetrix & Perlegen [492,900]" N 9/28/2009 19721433 McClay 1-Sep-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19721433?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics Treatment response to antipsychotics 738 cases NR 12q23.1 ANKS1B rs7968606-? rs7968606 NR 3.00E-07 (olanzapine)  10 [NR] % of variance explained "Affymetrix & Perlegen [492,900]" N 9/10/2009 19723657 Spain 1-Sep-09 Cancer Res http://www.ncbi.nlm.nih.gov/pubmed/19723657?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Colorectal Cancer Risk Is Not Associated with Increased Levels of Homozygosity in a Population from the United Kingdom Colorectal cancer "921 white cases, 929 white controls" "1,214 white cases, 1,435 white controls" NR NR NR NR NS NS NR NR "Illumina [486,303]" N 9/9/2009 19724244 Laje 31-Aug-09 Pharmacogenet Genomics http://www.ncbi.nlm.nih.gov/pubmed/19724244?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of suicidal ideation emerging during citalopram treatment of depressed outpatients Response to antidepressant treatment "90 white cases, 90 white controls" "30 white cases, 1,652 white controls" NR NR NR NR NS NS NR NR "Illumina [100,864]" N 9/9/2009 19714205 Hancock 28-Aug-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19714205?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children Asthma (childhood onset) 492 Mexican trios 177 Mexican trios 9q21.31 "TLE4, CHCHD9" rs2378383-? rs2378383 0.78 7.00E-07 1.64 [1.32-2.04] "Illumina [520,767]" N 9/24/2009 19714249 Liu 28-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19714249?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males Obesity and osteoporosis "499 Caucasian males, 501 Caucasian females" "1,370 Caucasian males, 1,985 Caucasian females" 11p15.1 SOX6 rs4756846-T rs4756846 0.12 5.00E-07 "(BMI-BMD, males) " NR NR "Affymetrix [379,319]" N 9/24/2009 19714249 Liu 28-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19714249?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males Obesity and osteoporosis "499 Caucasian males, 501 Caucasian females" "1,370 Caucasian males, 1,985 Caucasian females" 11p15.1 SOX6 rs297325-T rs297325 0.23 4.00E-07 "(BMI-BMD, males) " NR NR "Affymetrix [379,319]" N 9/9/2009 19706858 Shuldiner 26-Aug-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19706858?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy Response to clopidogrel therapy 429 Amish individuals "140 white, 83 African American, and 4 unspecified individuals" NR NR NR NR NS NS NR NR "Affymetrix [400,230]" N 9/9/2009 19698717 Cui 18-Aug-09 Gastroenterology http://www.ncbi.nlm.nih.gov/pubmed/19698717?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk Esophageal cancer "188 Japanese cases, 938 Japanese controls" "699 Japanese cases, 1,482 Japanese controls" 4q23 "ADH6, ADH1B" rs1229984-G rs1229984 0.35 8.00E-24 1.79 [1.69-1.88] "Illumina [359,195]" N 9/9/2009 19698717 Cui 18-Aug-09 Gastroenterology http://www.ncbi.nlm.nih.gov/pubmed/19698717?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk Esophageal cancer "188 Japanese cases, 938 Japanese controls" "699 Japanese cases, 1,482 Japanese controls" 12q24.12 "BRAP, ALDH2" rs671-A rs671 0.36 3.00E-24 1.67 [1.58-1.76] "Illumina [359,195]" N 9/9/2009 19684573 Ge 16-Aug-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19684573?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance Response to Hepatitis C treatment "871 Caucasian, 191 African American, and 75 Hispanic participants" NR 4q34.3 Intergenic rs17067123-? rs17067123 NR 0.000008 (combined)  NR NR "Illumina [565,759]" N 9/9/2009 19684573 Ge 16-Aug-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19684573?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance Response to Hepatitis C treatment "871 Caucasian, 191 African American, and 75 Hispanic participants" NR 19q13.2 IL28B rs12979860-C rs12979860 0.72 1.00E-28 (combined)  2 [1.8-2.3] (European-Americans) "Illumina [565,759]" N 9/9/2009 19684573 Ge 16-Aug-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19684573?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance Response to Hepatitis C treatment "871 Caucasian, 191 African American, and 75 Hispanic participants" NR 6q21 AKD2 rs9400317-? rs9400317 NR 0.000007 (combined)  NR NR "Illumina [565,759]" N 9/4/2009 19684604 Papaemmanuil 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684604?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia" Acute lymphoblastic leukemia (childhood) "503 European pediatric cases, 1,438 European pediatric controls" "404 European pediatric cases, 960 European pediatric controls" 10q21.2 ARID5B rs7089424-C rs7089424 0.34 7.00E-19 1.65 [1.54-1.76] "Illumina [291,473]" N 9/4/2009 19684604 Papaemmanuil 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684604?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia" Acute lymphoblastic leukemia (childhood) "503 European pediatric cases, 1,438 European pediatric controls" "404 European pediatric cases, 960 European pediatric controls" 14q11.2 CEBPE rs2239633-G rs2239633 0.52 3.00E-07 1.34 [1.22-1.45] "Illumina [291,473]" N 9/4/2009 19684604 Papaemmanuil 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684604?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia" Acute lymphoblastic leukemia (childhood) "503 European pediatric cases, 1,438 European pediatric controls" "404 European pediatric cases, 960 European pediatric controls" 7p12.2 IKZF1 rs4132601-C rs4132601 0.28 1.00E-19 1.69 [1.58-1.81] "Illumina [291,473]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 12p13.32 C12orf5 rs10849033-G rs10849033 0.02 0.000009 2.55 [1.60-3.80] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 1q43 RYR2 rs7554607-A rs7554607 0.56 0.000002 1.49 [1.20-1.70] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 19q13.31 ZNF230 rs2191566-G rs2191566 0.28 4.00E-07 1.52 [1.20-1.70] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 6q24.1 Intergenic rs11155133-G rs11155133 0.01 3.00E-07 3.62 [2.10-6.00] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 12q24.22 KRTHB5 rs2089222-A rs2089222 0.03 8.00E-08 2.26 [1.60-3.0] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 7p12.2 "IKZF1, DDC" rs11978267-G rs11978267 0.27 8.00E-11 1.69 [1.40-1.90] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 10q21.2 ARID5B rs10821936-C rs10821936 0.34 1.00E-15 1.91 [1.60-2.20] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 18p11.32 Intergenic rs1879352-C rs1879352 0.16 0.000009 1.53 [1.20-1.80] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 10p11.21 PARD3 rs563507-A rs563507 0.04 0.000009 2 [1.40-2.70] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 1p31.1 SIAT7C rs10873876-T rs10873876 0.15 0.000004 1.55 [1.20-1.80] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 3q26.32 KCNMB2 rs9290663-T rs9290663 0.13 0.000006 1.58 [1.20-1.90] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 1q31.3 Intergenic rs6428370-G rs6428370 0.32 0.000007 1.43 [1.20-1.60] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 1q44 OR2C3 rs1881797-C rs1881797 0.18 0.000007 1.52 [1.20-1.80] "Affymetrix [307,944]" N 9/11/2009 19684603 Trevino 16-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19684603?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Germline genomic variants associated with childhood acute lymphoblastic leukemia Acute lymphoblastic leukemia (childhood) "317 European descent cases, 17,958 European descent controls" NR 2q36.1 KCNE4 rs12621643-T rs12621643 0.28 0.000003 1.48 [1.20-1.70] "Affymetrix [307,944]" N 9/4/2009 19680635 Alkelai 13-Aug-09 Psychopharmacology http://www.ncbi.nlm.nih.gov/pubmed/19680635?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients Response to antipsychotic treatment "199 cases, 198 controls" NR 2q24.3 FIGN rs12476047-C rs12476047 NR 0.000003 3.21 [1.97-5.25] "Affymetrix & Perlegen [495,172]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 1q21.3 "AL157404.18, S100A5" rs4845552-? rs4845552 NR 0.000006 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 14q22.1 "FRMD6, AL079307.7" rs11626056-? rs11626056 NR 0.000001 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 20q11.23 C20orf132 rs8115854-? rs8115854 NR 0.000002 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 20q11.23 RPN2 rs6031882-? rs6031882 NR 0.000006 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 20q13.31 ZBP1 rs2073145-? rs2073145 NR 0.000002 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 21q21.1 FDPSP rs1888414-? rs1888414 NR 2.00E-07 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 5q14.1 "AC104108.3, SCAMP1, LHFPL2" rs6881634-? rs6881634 NR 0.000002 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 5p14.1 Intergenic rs7727656-? rs7727656 NR 0.000008 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 5p15.1 AC026790.5 rs682748-? rs682748 NR 0.000008 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 5q21.3 EFNA5 rs10074258-? rs10074258 NR 2.00E-07 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 11q24.3 Intergenic rs6590322-? rs6590322 NR 0.000009 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 9q21.31 "RP11, 232A1.1" rs10867752-? rs10867752 NR 0.000003 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 9q21.13 PRUNE2 rs10781380-? rs10781380 NR 7.00E-07 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 7p21.3 Intergenic rs9918508-? rs9918508 NR 0.000008 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 5q14.1 ARSB rs337847-? rs337847 NR 0.000007 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 12q13.11 "ARID2, SFRS2IP" rs1373549-? rs1373549 NR 0.000008 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 12q14.3 CAND1 rs1082714-? rs1082714 NR 0.000005 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 7p12.2 "IKZF1, AC020743.7" rs10276619-? rs10276619 NR 0.000003 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 7q21.11 MAGI2 rs11525066-? rs11525066 NR 0.000003 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 13q31.1 Intergenic rs4773460-? rs4773460 NR 0.000002 NR NR "Illumina [516,645]" N 9/9/2009 19668339 Potkin 7-Aug-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19668339?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease Hippocampal atrophy "172 cases, 209 controls" NR 8q24.12 MAL2 rs1364705-? rs1364705 NR 0.000009 NR NR "Illumina [516,645]" N 9/4/2009 19664746 Tse 5-Aug-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19664746?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21. Nasopharyngeal carcinoma "277 Han Chinese cases, 285 Han Chinese controls" "635 Han Chinese cases, 1,640 Han Chinese controls" 6p22.1 GABBR1 rs29232-A rs29232 0.46 9.00E-17 1.67 [1.48-1.88] "Illumina [480,365]" N 9/4/2009 19664746 Tse 5-Aug-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19664746?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21. Nasopharyngeal carcinoma "277 Han Chinese cases, 285 Han Chinese controls" "635 Han Chinese cases, 1,640 Han Chinese controls" 6p21.33 HLA-A rs2517713-A rs2517713 0.62 4.00E-20 1.88 [1.65-2.15] "Illumina [480,365]" N 9/4/2009 19664746 Tse 5-Aug-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19664746?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association Study Reveals Multiple Nasopharyngeal Carcinoma-Associated Loci within the HLA Region at Chromosome 6p21. Nasopharyngeal carcinoma "277 Han Chinese cases, 285 Han Chinese controls" "635 Han Chinese cases, 1,640 Han Chinese controls" 6p22.1 HLA-F rs3129055-G rs3129055 0.31 7.00E-11 1.51 [1.34-1.71] "Illumina [480,365]" N 9/14/2009 19654303 Broderick 4-Aug-09 Cancer Res http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study Lung cancer "1,952 European cases, 1,438 European controls" "5,608 European cases, 6,767 European controls" 5p15.33 CLPTM1L rs4975616-? rs4975616 NR 3.00E-09 1.15 [1.10-1.20] "Illumina [511,919]" N 9/14/2009 19654303 Broderick 4-Aug-09 Cancer Res http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study Lung cancer "1,952 European cases, 1,438 European controls" "5,608 European cases, 6,767 European controls" 15q25.1 CHRNA3 rs8034191-? rs8034191 NR 3.00E-26 1.29 [1.23-1.35] "Illumina [511,919]" N 9/14/2009 19654303 Broderick 4-Aug-09 Cancer Res http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study Lung cancer "1,952 European cases, 1,438 European controls" "5,608 European cases, 6,767 European controls" 6p21.33 BAT3 rs3117582-? rs3117582 NR 4.00E-10 1.24 [1.16-1.33] "Illumina [511,919]" N 9/14/2009 19654303 Broderick 4-Aug-09 Cancer Res http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study Lung cancer "1,952 European cases, 1,438 European controls" "5,608 European cases, 6,767 European controls" 2p14 NR rs4254535-? rs4254535 NR 0.000005 1.12 [NR] "Illumina [511,919]" N 9/14/2009 19654303 Broderick 4-Aug-09 Cancer Res http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study Lung cancer "1,952 European cases, 1,438 European controls" "5,608 European cases, 6,767 European controls" 15q15.2 TGM5 rs748404-? rs748404 NR 0.000001 1.15 [1.09-1.20] "Illumina [511,919]" N 9/14/2009 19654303 Broderick 4-Aug-09 Cancer Res http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study Lung cancer "1,952 European cases, 1,438 European controls" "5,608 European cases, 6,767 European controls" 3p24.1 NR rs1530057-? rs1530057 NR 0.000003 1.26 [NR] "Illumina [511,919]" N 9/14/2009 19654303 Broderick 4-Aug-09 Cancer Res http://www.ncbi.nlm.nih.gov/pubmed/19654303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Deciphering the Impact of Common Genetic Variation on Lung Cancer Risk: A Genome-Wide Association Study Lung cancer "1,952 European cases, 1,438 European controls" "5,608 European cases, 6,767 European controls" 10q23.31 NR rs1926203-? rs1926203 NR 0.000001 1.12 [NR] "Illumina [511,919]" N 9/4/2009 19651812 Chambers 3-Aug-09 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19651812?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type-2 diabetes amongst Indian Asians and European whites Fasting plasma glucose "7,474 Indian Asian individuals" "4,462 European controls" 11q21 MTNR1B rs2166706-G rs2166706 0.46 2.00E-09 0.07 (0.04-0.09) mmol/L increase "Illumina [up to 544,390]" N 9/4/2009 19656524 Grant 3-Aug-09 J Pediatr http://www.ncbi.nlm.nih.gov/pubmed/19656524?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies a Locus for Nonsyndromic Cleft Lip with or without Cleft Palate on 8q24 Nonsyndromic cleft lip with or without cleft palate "111 European ancestry cases, 5,951 European ancestry controls" NR 8q24.21 Intergenic rs987525-? rs987525 0.22 9.00E-08 2.09 [1.59-2.76] "Illumina [495,858]" N 9/4/2009 19656524 Grant 3-Aug-09 J Pediatr http://www.ncbi.nlm.nih.gov/pubmed/19656524?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies a Locus for Nonsyndromic Cleft Lip with or without Cleft Palate on 8q24 Nonsyndromic cleft lip with or without cleft palate "111 European ancestry cases, 5,951 European ancestry controls" NR 18q22.3 Intergenic rs17085106-? rs17085106 0.018 4.00E-08 4.07 [2.37-7.00] "Illumina [495,858]" N 9/4/2009 19648918 Amundadottir 2-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19648918?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer Pancreatic cancer "1,771 European ancestry cases, 1,805 European ancestry controls" "2,120 European ancestry cases, 2,127 European ancestry controls" 9q34.2 ABO rs505922-T rs505922 0.35 5.00E-08 1.2 [1.12-1.28] "Illumina [558,542]" N 9/4/2009 19648919 Song 2-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19648919?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2 Ovarian cancer "1,817 European ancestry cases, 2,353 European ancestry controls" "6,944 European ancestry cases, 9,477 European ancestry controls" 9p22.2 "BNC2, LOC648570, CNTLN" rs3814113-T rs3814113 0.68 5.00E-19 1.22 [1.16-1.27] "Illumina [up to ~2,000,000] (imputed)" N 8/21/2009 19648920 Wu 2-Aug-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19648920?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer Bladder cancer "969 Caucasian cases, 957 Caucasian controls" "5,698 US and European cases, 38,633 US and European controls" 8q24.3 PSCA rs2294008-T rs2294008 0.46 2.00E-10 1.15 [1.10-1.20] "Illumina [556,429]" N 9/4/2009 19667218 Comabella 1-Aug-09 Arch Neurol http://www.ncbi.nlm.nih.gov/pubmed/19667218?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide scan of 500,000 single-nucleotide polymorphisms among responders and nonresponders to interferon beta therapy in multiple sclerosis" Response to interferon beta therapy "53 responders, 53 non-responders" "49 responders, 45 non-responders" NR NR NR NR NS NS NR NR "Affymetrix [428,867](pooled)" N 8/21/2009 19625618 Nakano 22-Jul-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19625618?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Three susceptible loci associated with primary open-angle glaucoma identified by genome-wide association study in a Japanese population Glaucoma (primary open-angle) "418 Japanese cases, 300 Japanese controls" "409 Japanese cases, 448 Japanese controls" NR NR NR NR NS NS NR NR "Affymetrix [331,838]" N 8/21/2009 19620980 Skibola 20-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19620980?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics variants at 6p21.33 are associated with susceptibility to follicular lymphoma Follicular lymphoma "189 European ancestry cases, 592 European controls" "456 European ancestry cases, 2,785 European ancestry controls" 6p21.33 "STG, PSORS1" rs6457327-C rs6457327 0.62 5.00E-11 1.69 [1.43-2.00] "Illumina [~500,000] (pooled)" N 8/12/2009 19609347 Adeyemo 17-Jul-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19609347?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study of Hypertension and Blood Pressure in African Americans Hypertension "509 African American cases, 508 African American controls" "366 West African cases, 614 West African controls" 15q22.1 ALDH1A2 rs1550576-? rs1550576 0.86 0.000003 1.92 [NR] "Affymetrix [808,465]" N 8/12/2009 19609347 Adeyemo 17-Jul-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19609347?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study of Hypertension and Blood Pressure in African Americans Hypertension "509 African American cases, 508 African American controls" "366 West African cases, 614 West African controls" 4q23 ADH7 rs991316-T rs991316 0.45 0.000005 1.62 [NR] "Affymetrix [808,465]" N 8/4/2009 19597492 Benjamin 13-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19597492?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry Atrial fibrillation "3,413 cases, 37,105 referents" "2,145 cases, 4,073 controls" 1p36.22 "MTHFR, NPPA" rs17375901-T rs17375901 0.053 6.00E-07 1.26 Affymetrix & Illumina [~2.5 million] (imputed) N 8/4/2009 19597492 Benjamin 13-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19597492?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry Atrial fibrillation "3,413 cases, 37,105 referents" "2,145 cases, 4,073 controls" 16q22.3 ZFHX3 rs2106261-T rs2106261 0.174 2.00E-15 1.25 Affymetrix & Illumina [~2.5 million] (imputed) N 8/4/2009 19597492 Benjamin 13-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19597492?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry Atrial fibrillation "3,413 cases, 37,105 referents" "2,145 cases, 4,073 controls" 4q25 PITX2 rs17042171-A rs17042171 0.12 4.00E-63 1.65 Affymetrix & Illumina [~2.5 million] (imputed) N 7/30/2009 19597491 Gudbjartsson 13-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19597491?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke Atrial fibrillation "2,385 European cases, 33,752 European controls" "up to 2,427 European cases, 3,379 European controls" 16q22.3 ZFHX3 rs7193343-T rs7193343 NR 1.00E-10 1.21 [1.14-1.29] "Illumina [303,136]" N 7/30/2009 19597491 Gudbjartsson 13-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19597491?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke Atrial fibrillation "2,385 European cases, 33,752 European controls" "up to 2,427 European cases, 3,379 European controls" 4q25 Intergenic rs2200733-? rs2200733 0.12 1.00E-14 1.42 [NR] "Illumina [303,136]" N 7/24/2009 19587794 Nolte 9-Jul-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19587794?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies Cardiac repolarisation "3,558 Caucasian individuals" "29,527 Caucasian individuals" 6q22.31 "SLC35F1, C6orf204, PLN" rs11153730-C rs11153730 0.5 2.00E-29 0.09 [NR] unit increase "Affymetrix & Illumina [~2,399,142] (imputed)" N 7/24/2009 19587794 Nolte 9-Jul-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19587794?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies Cardiac repolarisation "3,558 Caucasian individuals" "29,527 Caucasian individuals" 1q23.3 "OLFML2B, NOS1AP" rs12143842-T rs12143842 0.25 1.00E-83 0.18 [NR] unit increase "Affymetrix & Illumina [~2,399,142] (imputed)" N 7/24/2009 19584900 Tonjes 8-Jul-09 Eur J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19584900?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in Germany Body mass index and fat mass 948 Sorbian individuals NR NR NR NR NR NS NS NR NR "Affymetrix [390,619]" N 8/7/2009 19584346 Vasan 8-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data Aortic root size "12,612 European ancestry individuals" "4,094 European ancestry individuals" 12p12.2 PDE3A rs10770612-G rs10770612 0.19 2.00E-08 0.03 [0.02-0.04] cm increase Affymetrix & Illumina [~2.5 million] (imputed) N 8/7/2009 19584346 Vasan 8-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data Aortic root size "12,612 European ancestry individuals" "4,094 European ancestry individuals" 12q14.3 HMGA2 rs4026608-C rs4026608 0.38 2.00E-09 0.03 [0.02-0.04] cm decrease Affymetrix & Illumina [~2.5 million] (imputed) N 8/7/2009 19584346 Vasan 8-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data Aortic root size "12,612 European ancestry individuals" "4,094 European ancestry individuals" 15q24.1 LOXL1 rs893817-G rs893817 0.34 0.000003 0.02 [0.01-0.03] cm increase Affymetrix & Illumina [~2.5 million] (imputed) N 8/7/2009 19584346 Vasan 8-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data Aortic root size "12,612 European ancestry individuals" "4,094 European ancestry individuals" 5q23.2 "CCDC100, PPIC" rs17470137-A rs17470137 0.29 1.00E-11 0.03 [0.02-0.04] cm increase Affymetrix & Illumina [~2.5 million] (imputed) N 8/7/2009 19584346 Vasan 8-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data Aortic root size "12,612 European ancestry individuals" "4,094 European ancestry individuals" 1p21.2 PALMD rs7543130-A rs7543130 0.49 1.00E-07 0.03 [0.02-0.04] cm increase Affymetrix & Illumina [~2.5 million] (imputed) N 8/7/2009 19584346 Vasan 8-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data Aortic root size "12,612 European ancestry individuals" "4,094 European ancestry individuals" 17p13.3 "SMG6, SRR, TSR1, SGSM2" rs10852932-T rs10852932 0.36 2.00E-11 0.03 [0.02-0.04] cm increase Affymetrix & Illumina [~2.5 million] (imputed) N 8/7/2009 19584346 Vasan 8-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data Cardiac structure and function "12,612 European ancestry individuals" "4,094 European ancestry individuals" 16q23.1 WWOX rs2059238-A rs2059238 0.22 0.000003 (LV wall thickness)  0.02 [0.01-0.03] cm decrease Affymetrix & Illumina [~2.5 million] (imputed) N 8/7/2009 19584346 Vasan 8-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data Cardiac structure and function "12,612 European ancestry individuals" "4,094 European ancestry individuals" 10q23.1 GRID1 rs7910620-G rs7910620 0.01 7.00E-07 (LV wall thickness)  0.17 [0.11-0.23] cm increase Affymetrix & Illumina [~2.5 million] (imputed) N 8/7/2009 19584346 Vasan 8-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data Cardiac structure and function "12,612 European ancestry individuals" "4,094 European ancestry individuals" 5q22.1 SLC25A46 rs17132261-T rs17132261 0.02 9.00E-07 (LV wall thickness)  0.06 [0.04-0.08] cm increase Affymetrix & Illumina [~2.5 million] (imputed) N 8/7/2009 19584346 Vasan 8-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19584346?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Variants Associated with Cardiac Structure and Function: A Meta-analysis and Replication of Genome-wide Association Data Cardiac structure and function "12,612 European ancestry individuals" "4,094 European ancestry individuals" 6q22.31 "SLC35F1, C6orf204, PLN" rs89107-G rs89107 0.5 1.00E-09 (LV internal diastolic dimensions)  0.03 [0.02-0.04] cm decrease Affymetrix & Illumina [~2.5 million] (imputed) N 7/16/2009 19578364 Bishop 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578364?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies three loci associated with melanoma risk Melanoma "1,539 European ancestry cases, 3,917 European ancestry controls" "2,312 European ancestry cases, 1,867 European ancestry controls" 16q24.3 MC1R rs4785763-A rs4785763 0.32 6.00E-22 1.36 [1.28-1.45] "Illumina [~317,000]" N 7/16/2009 19578364 Bishop 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578364?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies three loci associated with melanoma risk Melanoma "1,539 European ancestry cases, 3,917 European ancestry controls" "2,312 European ancestry cases, 1,867 European ancestry controls" 9p21.3 CDKN2A rs7023329-A rs7023329 0.5 4.00E-07 1.18 [1.10-1.25] "Illumina [~317,000]" N 7/16/2009 19578364 Bishop 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578364?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies three loci associated with melanoma risk Melanoma "1,539 European ancestry cases, 3,917 European ancestry controls" "2,312 European ancestry cases, 1,867 European ancestry controls" 11q14.3 TYR rs1393350-A rs1393350 0.27 2.00E-14 1.29 [1.21-1.38] "Illumina [~317,000]" N 7/16/2009 19578364 Bishop 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578364?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies three loci associated with melanoma risk Melanoma "1,539 European ancestry cases, 3,917 European ancestry controls" "2,312 European ancestry cases, 1,867 European ancestry controls" 22q13.1 Intergenic rs2284063-? rs2284063 0.37 2.00E-09 1.2 [1.14-1.28] "Illumina [~317,000]" N 7/16/2009 19578364 Bishop 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578364?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies three loci associated with melanoma risk Melanoma "1,539 European ancestry cases, 3,917 European ancestry controls" "2,312 European ancestry cases, 1,867 European ancestry controls" 16q24.3 MC1R rs258322-A rs258322 0.09 3.00E-27 1.67 [1.52-1.83] "Illumina [~317,000]" N 7/13/2009 19578365 Falchi 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578365?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi Cutaneous nevi "1,524 European twins" "4,107 European individuals" 22q13.1 PLA2G6 rs2284063-G rs2284063 0.35 3.00E-08 0.08 [-0.002-0.16] decrease in log nevus count "Illumina [297,108]" N 7/13/2009 19578365 Falchi 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578365?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi Cutaneous nevi "1,524 European twins" "4,107 European individuals" 9p21.3 MTAP rs4636294-A rs4636294 0.48 3.00E-15 0.2 [0.13-0.27] increase in log nevus count "Illumina [297,108]" N 7/12/2009 19578367 Shete 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies five susceptibility loci for glioma Glioma "1,878 cases, 3,670 controls" "2,545 cases, 2,953 controls" 5p15.33 TERT rs2736100-G rs2736100 0.49 2.00E-17 1.27 [1.19-1.37] "Illumina [454,576]" N 7/12/2009 19578367 Shete 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies five susceptibility loci for glioma Glioma "1,878 cases, 3,670 controls" "2,545 cases, 2,953 controls" 8q24.21 CCDC26 rs891835-G rs10464870 0.78 8.00E-11 1.24 [1.17-1.30] "Illumina [454,576]" N 7/12/2009 19578367 Shete 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies five susceptibility loci for glioma Glioma "1,878 cases, 3,670 controls" "2,545 cases, 2,953 controls" 20q13.33 RTEL1 rs6010620-G rs6010620 0.23 3.00E-12 1.28 [1.21-1.35] "Illumina [454,576]" N 7/12/2009 19578367 Shete 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies five susceptibility loci for glioma Glioma "1,878 cases, 3,670 controls" "2,545 cases, 2,953 controls" 9p21.3 "CDKN2A, CDKN2B" rs4977756-G rs4977756 0.6 7.00E-15 1.24 [1.19-1.30] "Illumina [454,576]" N 7/12/2009 19578367 Shete 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies five susceptibility loci for glioma Glioma "1,878 cases, 3,670 controls" "2,545 cases, 2,953 controls" 8q24.21 CCDC26 rs4295627-G rs4295627 0.83 2.00E-18 1.36 [1.29-1.43] "Illumina [454,576]" N 7/12/2009 19578367 Shete 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies five susceptibility loci for glioma Glioma "1,878 cases, 3,670 controls" "2,545 cases, 2,953 controls" 5p15.33 TERT rs2853676-A rs2853676 0.73 4.00E-14 1.26 [1.20-1.32] "Illumina [454,576]" N 7/12/2009 19578367 Shete 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578367?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies five susceptibility loci for glioma Glioma "1,878 cases, 3,670 controls" "2,545 cases, 2,953 controls" 11q23.3 PHLDB1 rs498872-T rs498872 0.69 1.00E-08 1.18 [1.13-1.24] "Illumina [454,576]" N 7/12/2009 19578366 Wrensch 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578366?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility Glioma (high-grade) "692 high-grade cases, 3,992 controls" "176 high-grade cases, 174 controls" 20q13.33 RTEL1 rs6010620-G rs6010620 0.77 3.00E-09 1.52 [1.32-1.75] "Illumina [326,506]" N 7/12/2009 19578366 Wrensch 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578366?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility Glioma (high-grade) "692 high-grade cases, 3,992 controls" "176 high-grade cases, 174 controls" 20q13.33 RTEL1 rs4809324-C rs4809324 0.1 2.00E-09 1.6 [1.37-1.87] "Illumina [326,506]" N 7/12/2009 19578366 Wrensch 5-Jul-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19578366?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility Glioma (high-grade) "692 high-grade cases, 3,992 controls" "176 high-grade cases, 174 controls" 9p21.3 Intergenic rs1412829-C rs1412829 0.39 2.00E-10 1.42 [1.27-1.58] "Illumina [326,506]" N 7/24/2009 19578179 Teichert 4-Jul-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19578179?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of acenocoumarol maintenance dosage Acenocoumarol maintenance dosage "1,451 Caucasian individuals" 287 Caucasian individuals 10q23.33 CYP2C18 rs12772169-? rs12772169 NR 8.00E-12 NR NR "Illumina [~550,000]" N 7/24/2009 19578179 Teichert 4-Jul-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19578179?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of acenocoumarol maintenance dosage Acenocoumarol maintenance dosage "1,451 Caucasian individuals" 287 Caucasian individuals 3q22.3 CNTN4 rs10935268-? rs10935268 NR 8.00E-07 NR NR "Illumina [~550,000]" N 7/24/2009 19578179 Teichert 4-Jul-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19578179?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of acenocoumarol maintenance dosage Acenocoumarol maintenance dosage "1,451 Caucasian individuals" 287 Caucasian individuals 19p13.12 CYP4F2 rs2108622-? rs2108622 NR 3.00E-10 NR NR "Illumina [~550,000]" N 7/24/2009 19578179 Teichert 4-Jul-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19578179?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of acenocoumarol maintenance dosage Acenocoumarol maintenance dosage "1,451 Caucasian individuals" 287 Caucasian individuals 10q23.33 CYP2C19 rs12767583-? rs12767583 NR 3.00E-07 NR NR "Illumina [~550,000]" N 7/12/2009 19567438 Elliott 1-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19567438?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease C-reactive protein "17,967 European and Indian Asian men and women" "13,615 European and Indian Asian men and women" 1q23.2 CRP rs7553007-A rs7553007 NR 8.00E-44 20.7 [18.9-23.4] % decrease "Affymetrix, Illumina & Perlegen [~1.4 million] (imputed)" N 7/12/2009 19567438 Elliott 1-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19567438?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease C-reactive protein "17,967 European and Indian Asian men and women" "13,615 European and Indian Asian men and women" 1q21.3 IL6R rs4537545-T rs4537545 NR 2.00E-14 11.5 [8.5-14.4] % decrease "Affymetrix, Illumina & Perlegen [~1.4 million] (imputed)" N 7/12/2009 19567438 Elliott 1-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19567438?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease C-reactive protein "17,967 European and Indian Asian men and women" "13,615 European and Indian Asian men and women" 19q13.32 "APOE, APOCI, APOCII" rs4420638-G rs4420638 NR 5.00E-27 21.8 [18.1-25.3] % decrease "Affymetrix, Illumina & Perlegen [~1.4 million] (imputed)" N 7/12/2009 19567438 Elliott 1-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19567438?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease C-reactive protein "17,967 European and Indian Asian men and women" "13,615 European and Indian Asian men and women" 1p31.3 LEPR rs6700896-T rs6700896 NR 3.00E-14 14.8 [12.0-17.6] % decrease "Affymetrix, Illumina & Perlegen [~1.4 million] (imputed)" N 7/12/2009 19567438 Elliott 1-Jul-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19567438?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease C-reactive protein "17,967 European and Indian Asian men and women" "13,615 European and Indian Asian men and women" 12q24.31 HNF1A rs1183910-T rs1183910 NR 1.00E-30 13.8 [10.9-16.6] % decrease "Affymetrix, Illumina & Perlegen [~1.4 million] (imputed)" N 7/24/2009 19570815 Estrada 1-Jul-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19570815?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation Height "10,074 European individuals" "6,912 European individuals" 22q13.1 "SGSM3, MKL1" rs5757949-T rs5757949 NR 0.000004 NR NR "Affymetrix, Illumina & Perlegen [2,228,850] (imputed)" N 7/24/2009 19570815 Estrada 1-Jul-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19570815?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation Height "10,074 European individuals" "6,912 European individuals" 2q37.1 "DIS3L2, ALPP, NPPC" rs6717918-T rs6717918 0.78 3.00E-09 0.44 [0.20-0.68] cm increase "Affymetrix, Illumina & Perlegen [2,228,850] (imputed)" N 7/24/2009 19570815 Estrada 1-Jul-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19570815?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation Height "10,074 European individuals" "6,912 European individuals" 11q14.1 "TMEM126B, TMEM126A" rs10898392-T rs10898392 NR 0.000003 NR NR "Affymetrix, Illumina & Perlegen [2,228,850] (imputed)" N 7/24/2009 19570815 Estrada 1-Jul-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19570815?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation Height "10,074 European individuals" "6,912 European individuals" 5p13.3 "C5orf23, NPR3" rs10472828-C rs10472828 0.56 3.00E-07 0.22 [0.04-0.40] cm increase "Affymetrix, Illumina & Perlegen [2,228,850] (imputed)" N 7/24/2009 19570815 Estrada 1-Jul-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19570815?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation Height "10,074 European individuals" "6,912 European individuals" 22q13.1 "TNRC6B, ADSL" rs139909-T rs139909 0.68 2.00E-07 0.25 [0.03-0.47] cm increase "Affymetrix, Illumina & Perlegen [2,228,850] (imputed)" N 7/13/2009 19571811 International Schizophrenia Consortium 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571811?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Schizophrenia "3,322 European descent cases, 3,587 European descent controls" "4,692 European descent cases, 15,493 European descent controls" 18q21.2 TCF4 rs17594526-T rs17594526 0.03 1.00E-07 1.44 "Affymetrix [739,995]" N 7/13/2009 19571811 International Schizophrenia Consortium 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571811?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Schizophrenia "3,322 European descent cases, 3,587 European descent controls" "4,692 European descent cases, 15,493 European descent controls" 1p21.3 PTBP2 rs7544736-G rs7544736 0.18 6.00E-07 1.25 "Affymetrix [739,995]" N 7/13/2009 19571811 International Schizophrenia Consortium 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571811?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Schizophrenia "3,322 European descent cases, 3,587 European descent controls" "4,692 European descent cases, 15,493 European descent controls" 3q26.33 FXR1 rs6782299-T rs6782299 0.73 1.00E-07 1.1 "Affymetrix [739,995]" N 7/13/2009 19571811 International Schizophrenia Consortium 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571811?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Schizophrenia "3,322 European descent cases, 3,587 European descent controls" "4,692 European descent cases, 15,493 European descent controls" 6p22.1 MHC rs13194053-T rs13194053 0.86 1.00E-08 1.22 "Affymetrix [739,995]" N 7/10/2009 19571809 Shi 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571809?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants on chromosome 6p22.1 are associated with schizophrenia Schizophrenia "2,681 European ancestry cases, 2,653 European ancestry controls, 1,286 African American cases, 973 African American controls" "5,327 European ancestry cases, 16,424 European ancestry controls" 6p22.1 "SLC17A1, SLC17A3, BTN3A2, BTN2A2, BTN3A1, HIST1H2AG, HIST1H2BJ, PRSS16, POM121L2, ZNF184" rs13194053-T rs13194053 0.82 1.00E-08 (EA)  1.28 [NR] "Affymetrix [up to 843,798]" N 7/10/2009 19571809 Shi 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571809?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants on chromosome 6p22.1 are associated with schizophrenia Schizophrenia "2,681 European ancestry cases, 2,653 European ancestry controls, 1,286 African American cases, 973 African American controls" "5,327 European ancestry cases, 16,424 European ancestry controls" 6p21.32 HLA-DQA1 rs9272219-G rs9272219 0.72 7.00E-08 (EA)  1.14 [NR] "Affymetrix [up to 843,798]" N 7/10/2009 19571808 Stefansson 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants conferring risk of schizophrenia Schizophrenia "2,663 European cases, 13,498 European controls" "10,282 European cases, 21,093 European controls" 5q21.1 SLCO6A1 rs1502844-C rs1502844 NR 0.000001 1.09 [NR] "Illumina [314,868]" N 7/10/2009 19571808 Stefansson 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants conferring risk of schizophrenia Schizophrenia "2,663 European cases, 13,498 European controls" "10,282 European cases, 21,093 European controls" 2p16.1 VRK2 rs2312147-C rs2312147 NR 3.00E-07 1.09 [NR] "Illumina [314,868]" N 7/10/2009 19571808 Stefansson 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants conferring risk of schizophrenia Schizophrenia "2,663 European cases, 13,498 European controls" "10,282 European cases, 21,093 European controls" 18q21.2 TCF4 rs9960767-C rs9960767 0.06 4.00E-09 1.23 [NR] "Illumina [314,868]" N 7/10/2009 19571808 Stefansson 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants conferring risk of schizophrenia Schizophrenia "2,663 European cases, 13,498 European controls" "10,282 European cases, 21,093 European controls" 6p21.32 "MHC, NOTCH4" rs3131296-G rs3131296 0.87 2.00E-10 1.19 [NR] "Illumina [314,868]" N 7/10/2009 19571808 Stefansson 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants conferring risk of schizophrenia Schizophrenia "2,663 European cases, 13,498 European controls" "10,282 European cases, 21,093 European controls" 9q33.1 Intergenic rs1572299-A rs1572299 NR 0.000004 1.08 [NR] "Illumina [314,868]" N 7/10/2009 19571808 Stefansson 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants conferring risk of schizophrenia Schizophrenia "2,663 European cases, 13,498 European controls" "10,282 European cases, 21,093 European controls" 11q24.2 NRGN rs12807809-T rs12807809 0.83 2.00E-09 1.15 [NR] "Illumina [314,868]" N 7/10/2009 19571808 Stefansson 1-Jul-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19571808?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants conferring risk of schizophrenia Schizophrenia "2,663 European cases, 13,498 European controls" "10,282 European cases, 21,093 European controls" 6p22.1 "MHC, PRSS16" rs6932590-T rs6932590 0.78 1.00E-12 1.16 [NR] "Illumina [314,868]" N 7/24/2009 19581569 Treutlein 1-Jul-09 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of alcohol dependence Alcohol dependence "476 German cases, 1,358 German controls" "1,024 German cases, 996 German controls" 5q32 PPP2R2B rs1864982-A rs1864982 0.13 0.000003 1.36 [1.20-1.55] "Illumina [524,396]" N 7/24/2009 19581569 Treutlein 1-Jul-09 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of alcohol dependence Alcohol dependence "476 German cases, 1,358 German controls" "1,024 German cases, 996 German controls" 6q25.1 ESR1 rs6902771-C rs6902771 0.51 0.000008 1.24 [1.13-1.36] "Illumina [524,396]" N 7/24/2009 19581569 Treutlein 1-Jul-09 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of alcohol dependence Alcohol dependence "476 German cases, 1,358 German controls" "1,024 German cases, 996 German controls" Xp22.2 Intergenic rs12388359-T rs12388359 0.11 0.000004 1.61 [1.32-2.00] "Illumina [524,396]" N 7/24/2009 19581569 Treutlein 1-Jul-09 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of alcohol dependence Alcohol dependence "476 German cases, 1,358 German controls" "1,024 German cases, 996 German controls" 2q35 PECR rs7590720-G rs7590720 0.29 1.00E-08 1.35 [1.22-1.49] "Illumina [524,396]" N 7/24/2009 19581569 Treutlein 1-Jul-09 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of alcohol dependence Alcohol dependence "476 German cases, 1,358 German controls" "1,024 German cases, 996 German controls" 4q26 "CAST, ERAP1" rs13150562-G rs13150562 0.68 0.000007 1.27 [1.14-1.41] "Illumina [524,396]" N 7/24/2009 19581569 Treutlein 1-Jul-09 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19581569?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of alcohol dependence Alcohol dependence "476 German cases, 1,358 German controls" "1,024 German cases, 996 German controls" 14q24.2 Intergenic rs36563-A rs36563 0.15 0.000005 1.33 [1.18-1.50] "Illumina [524,396]" N 7/1/2009 19561606 Thorleifsson 28-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19561606?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density Kidney stones "1,507 Icelandic cases, 34,033 Icelandic controls" "1,520 Icelandic cases, 4,726 Icelandic controls, 746 Dutch cases, 3,751 Dutch controls" 21q22.13 CLDN14 rs219780-C rs219780 0.79 4.00E-12 1.25 [1.17-1.33] "Illumina [303,120]" N 7/1/2009 19557197 Heard-Costa 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium Waist circumference "31,373 Caucasian individuals" "38,641 Caucasian individuals" 16q12.2 FTO rs1558902-? rs1558902 NR 5.00E-19 NR NR "Affymetrix & Illumina [up to 512,349]" N 7/1/2009 19557197 Heard-Costa 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium Waist circumference "31,373 Caucasian individuals" "38,641 Caucasian individuals" 6p12.2 PKHD1 rs1555967-? rs1555967 NR 0.000003 NR NR "Affymetrix & Illumina [up to 512,349]" N 7/1/2009 19557197 Heard-Costa 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium Waist circumference "31,373 Caucasian individuals" "38,641 Caucasian individuals" 12q13.13 "FAIM2, BCDIN3D" rs7138803-? rs7138803 NR 8.00E-07 NR NR "Affymetrix & Illumina [up to 512,349]" N 7/1/2009 19557197 Heard-Costa 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium Waist circumference "31,373 Caucasian individuals" "38,641 Caucasian individuals" 11p15.4 OVCH2 rs7932813-? rs7932813 NR 0.000005 NR NR "Affymetrix & Illumina [up to 512,349]" N 7/1/2009 19557197 Heard-Costa 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium Waist circumference "31,373 Caucasian individuals" "38,641 Caucasian individuals" 18q21.32 MC4R rs489693-? rs489693 NR 4.00E-07 NR NR "Affymetrix & Illumina [up to 512,349]" N 7/1/2009 19557197 Heard-Costa 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium Waist circumference "31,373 Caucasian individuals" "38,641 Caucasian individuals" 14q31.1 NRXN3 rs10146997-G rs10146997 NR 5.00E-08 0.65 [NR] cm increase "Affymetrix & Illumina [up to 512,349]" N 7/1/2009 19557197 Heard-Costa 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557197?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium Waist circumference "31,373 Caucasian individuals" "38,641 Caucasian individuals" 5p14.3 CDH12 rs4701252-? rs4701252 NR 0.000002 NR NR "Affymetrix & Illumina [up to 512,349]" N 7/1/2009 19557161 Lindgren 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557161?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution Adiposity "38,580 European-ancestry individuals" "Up to 102,064 European-ancestry individuals" 6p12.3 TFAP2B rs987237-G rs987237 0.164 2.00E-11 (WC)  0.04 [0.03-0.05] z-score unit increase "Affymetrix & Illumina [2,573,738] (imputed)" N 7/1/2009 19557161 Lindgren 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557161?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution Adiposity "38,580 European-ancestry individuals" "Up to 102,064 European-ancestry individuals" 1q42.3 TBCE rs6429082-C rs6429082 0.46 3.00E-07 (WC)  NR NR "Affymetrix & Illumina [2,573,738] (imputed)" N 7/1/2009 19557161 Lindgren 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557161?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution Adiposity "38,580 European-ancestry individuals" "Up to 102,064 European-ancestry individuals" 1q41 LYPLAL1 rs2605100-G rs2605100 0.692 3.00E-08 (WHR in women)  0.04 [0.03-0.05] z-score unit increase "Affymetrix & Illumina [2,573,738] (imputed)" N 7/1/2009 19557161 Lindgren 26-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19557161?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution Adiposity "38,580 European-ancestry individuals" "Up to 102,064 European-ancestry individuals" 8p23.1 MSRA rs7826222-G rs7826222 0.183 9.00E-09 (WC)  0.04 [0.03-0.05] z-score unit increase "Affymetrix & Illumina [2,573,738] (imputed)" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 4q26 TRAM1L1 rs10433903-T rs10433903 0.66 0.000003 1.33 [1.19-1.52] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 2p16.1 RTN4 rs6726292-G rs6726292 0.73 0.000001 1.39 [1.22-1.59] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 10q22.1 PRF1 rs10999409-T rs10999409 0.45 0.000005 1.3 [1.16-1.45] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 10p11.21 ZNF248 rs7474896-T rs7474896 0.14 9.00E-07 1.46 [1.25-1.69] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 6p21.31 ITPR3 rs999943-T rs999943 0.72 0.000001 1.37 [1.20-1.56] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 6p21.31 MLN rs2274459-A rs2274459 0.17 0.000006 1.38 [1.20-1.58] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 11p14.2 MUC15 rs12295638-C rs12295638 0.1 0.000004 1.49 [1.26-1.77] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 16q12.2 FTO rs9941349-T rs9941349 0.43 6.00E-12 1.48 [1.33-1.66] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 3p24.3 RAFTLIN rs12635698-C rs12635698 0.15 0.000005 1.41 [1.21-1.63] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 3p24.2 RARB rs1435703-T rs1435703 0.06 0.000004 1.66 [1.34-2.06] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 20p12.1 C20orf133 rs6110577-C rs6110577 0.16 0.000005 1.4 [1.21-1.61] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 5q23.3 FBN2 rs374748-G rs374748 0.11 0.000004 1.47 [1.25-1.73] "Illumina [457,251]" N 7/1/2009 19553259 Cotsapas 24-Jun-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19553259?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common BMI-associated variants confer risk of extreme obesity Obesity (extreme) "775 Caucasian cases, 3,197 Caucasian controls" NR 2q33.3 FLJ20309 rs7603514-A rs7603514 0.2 0.000008 1.36 [1.19-1.56] "Illumina [457,251]" N 6/30/2009 19525955 Bahlo 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Multiple sclerosis "1,618 European ancestry cases, 3,413 European ancestry controls" "2,256 European ancestry cases, 2,310 European ancestry controls" 20q13.12 CD40 rs6074022-G rs6074022 0.25 1.00E-07 1.2 [NR] "Illumina [302,098]" N 6/30/2009 19525955 Bahlo 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Multiple sclerosis "1,618 European ancestry cases, 3,413 European ancestry controls" "2,256 European ancestry cases, 2,310 European ancestry controls" 16p12.1 NR rs8049603-T rs8049603 0.2 0.000001 1.19 [NR] "Illumina [302,098]" N 6/30/2009 19525955 Bahlo 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Multiple sclerosis "1,618 European ancestry cases, 3,413 European ancestry controls" "2,256 European ancestry cases, 2,310 European ancestry controls" 8q24.21 "ASAP1, DDEF1" rs6984045-C rs6984045 0.02 0.000002 1.59 [NR] "Illumina [302,098]" N 6/30/2009 19525955 Bahlo 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Multiple sclerosis "1,618 European ancestry cases, 3,413 European ancestry controls" "2,256 European ancestry cases, 2,310 European ancestry controls" 10p15.1 IL2RA rs2104286-G rs2104286 0.73 0.000007 1.16 [NR] "Illumina [302,098]" N 6/30/2009 19525955 Bahlo 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Multiple sclerosis "1,618 European ancestry cases, 3,413 European ancestry controls" "2,256 European ancestry cases, 2,310 European ancestry controls" 1p13.1 CD58 rs1335532-A rs1335532 0.87 1.00E-07 1.28 [NR] "Illumina [302,098]" N 6/30/2009 19525955 Bahlo 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Multiple sclerosis "1,618 European ancestry cases, 3,413 European ancestry controls" "2,256 European ancestry cases, 2,310 European ancestry controls" 1p22.1 "EVI5, RPL5" rs6604026-G rs6604026 0.28 0.000003 1.17 [NR] "Illumina [302,098]" N 6/30/2009 19525955 Bahlo 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Multiple sclerosis "1,618 European ancestry cases, 3,413 European ancestry controls" "2,256 European ancestry cases, 2,310 European ancestry controls" 6p21.32 HLA-DRB1 rs9271366-G rs9271366 0.15 0 2.78 [NR] "Illumina [302,098]" N 6/30/2009 19525955 Bahlo 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 Multiple sclerosis "1,618 European ancestry cases, 3,413 European ancestry controls" "2,256 European ancestry cases, 2,310 European ancestry controls" 12q14.1 "METTL1, CYP27B1" rs703842-A rs703842 0.67 5.00E-11 1.23 [NR] "Illumina [302,098]" N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 5p13.2 IL7R rs6897932-C rs6897932 0.75 0.000002 1.12 [1.02-1.23] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 2q22.1 CXCR4 rs882300-C rs882300 0.61 1.00E-07 1.19 [1.09-1.30] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 12p13.31 TNFRSF1A rs1800693-C rs1800693 0.45 2.00E-11 1.2 [1.10-1.31] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 10p15.1 IL2RA rs2104286-T rs2104286 0.76 9.00E-08 1.15 [1.04-1.27] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 1p13.1 CD58 rs2300747-A rs2300747 0.88 3.00E-10 1.3 [1.14-1.47] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 6p21.32 HLA-DRB1 rs3135388-A rs3135388 0.22 0 2.75 [2.46-3.07] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 6p22.1 HLA-B rs2523393-A rs2523393 0.59 1.00E-17 1.28 [1.18-1.39] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 3q25.33 IL12A rs4680534-C rs4680534 0.37 0.000006 1.12 [1.02-1.22] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 10q22.3 ZMIZ1 rs1250540-G rs1250540 0.35 0.000002 1.12 [1.02-1.22] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 12q24.31 MPHOSPH9 rs1790100-G rs1790100 0.24 7.00E-07 1.11 [1.00-1.22] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 5p13.1 PTGER4 rs6896969-C rs6896969 0.62 2.00E-07 1.1 [1.01-1.20] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 16p13.13 CLEC16A rs11865121-C rs11865121 0.69 2.00E-07 1.15 [1.04-1.25] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 12p13.31 TNFRSF1A rs4149584-T rs4149584 0.022 0.000005 1.58 [1.15-2.17] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 16q24.1 IRF8 rs17445836-G rs17445836 0.81 4.00E-09 1.25 [1.12-1.39] Affymetrix & Illumina [~2.56 million] (imputed) N 6/29/2009 19525953 De Jager 14-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19525953?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci" Multiple sclerosis "2,624 cases, 7,220 controls" "2,215 cases, 2,116 controls" 11q12.2 CD6 rs17824933-G rs17824933 0.25 4.00E-09 1.18 [1.07-1.30] Affymetrix & Illumina [~2.56 million] (imputed) N 6/26/2009 19525478 Malarstig 12-Jun-09 Blood http://www.ncbi.nlm.nih.gov/pubmed/19525478?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study Plasma homocysteine 387 individuals from 21 Spanish families "1,238 European individuals" NR NR NR NR NS NS NR NR "Illumina [283,437]" N 6/19/2009 19508998 Knauff 9-Jun-09 Hum Reprod http://www.ncbi.nlm.nih.gov/pubmed/19508998?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene Premature ovarian failure "99 Caucasian cases, 235 Caucasian controls" "60 Caucasian cases, 90 Caucasian controls" NR NR NR NR NS NS NR NR "Illumina [309,158]" N 6/19/2009 19508968 Zhai 8-Jun-09 J Med Genet http://www.ncbi.nlm.nih.gov/pubmed/19508968?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study suggests that a locus within the ataxin 2 binding protein 1 gene is associated with hand osteoarthritis: the Treat-OA consortium Osteoarthritis "1,804 Caucasian individuals" "3,266 Caucasian individuals" NR NR NR NR NS NS NR NR "Illumina [up to 535,188]" N 6/17/2009 19503088 Gregersen 7-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19503088?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis" Rheumatoid arthritis "2,418 cases, 4,504 controls" "2,604 cases, 2,882 controls" 2p16.1 REL rs13017599-A rs13017599 0.34 2.00E-12 1.21 [1.15-1.28] "Illumina [278,502]" N 6/17/2009 19503088 Gregersen 7-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19503088?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis" Rheumatoid arthritis "2,418 cases, 4,504 controls" "2,604 cases, 2,882 controls" 2q33.2 CTLA4 rs231735-T rs231735 0.51 6.00E-09 1.17 [1.11-1.23] "Illumina [278,502]" N 6/17/2009 19503088 Gregersen 7-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19503088?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis" Rheumatoid arthritis "2,418 cases, 4,504 controls" "2,604 cases, 2,882 controls" 8p23.1 BLK rs2736340-A rs2736340 0.24 6.00E-09 1.19 [1.13-1.27] "Illumina [278,502]" N 6/17/2009 19503088 Gregersen 7-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19503088?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis" Rheumatoid arthritis "2,418 cases, 4,504 controls" "2,604 cases, 2,882 controls" 1p13.2 PTPN22 rs2476601-? rs2476601 NR 2.00E-21 NR NR "Illumina [278,502]" N 6/17/2009 19503088 Gregersen 7-Jun-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19503088?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis" Rheumatoid arthritis "2,418 cases, 4,504 controls" "2,604 cases, 2,882 controls" 9q33.2 "TRAF1, C5" rs881375-? rs881375 NR 4.00E-08 NR NR "Illumina [278,502]" N 6/17/2009 19497516 Elmore 6-Jun-09 J Vasc Surg http://www.ncbi.nlm.nih.gov/pubmed/19497516?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association Abdominal aortic aneurysm "123 cases, 112 controls" "827 cases, 594 controls" NR NR NR NR NS NS NR NR "Affymetrix [306,330] (pooled)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 11q13.1 SLC22A12 rs505802-T rs505802 0.7 2.00E-09 0.06 [0.038-0.074] mg/dl decrease "Affymetrix and Illumina [2,493,963] (imputed)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 4q22.1 ABCG2 rs2231142-T rs2231142 0.11 1.00E-10 (women)  0.14 [0.096-0.181] mg/dl increase "Affymetrix and Illumina [2,493,963] (imputed)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 1q21.1 PDZK1 rs12129861-A rs12129861 0.46 3.00E-09 0.06 [0.042-0.083] mg/dl decrease "Affymetrix and Illumina [2,493,963] (imputed)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 2p23.3 GCKR rs780094-T rs780094 0.42 1.00E-09 0.05 [0.035-0.068] mg/dl increase "Affymetrix and Illumina [2,493,963] (imputed)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 4p16.1 SLC2A9 rs734553-T rs734553 0.77 0 (women)  0.4 [0.371-0.423] mg/dl increase "Affymetrix and Illumina [2,493,963] (imputed)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 6p22.2 SLC17A1 rs1183201-A rs1183201 0.48 3.00E-14 0.06 [0.459-0.078] mg/dl decrease "Affymetrix and Illumina [2,493,963] (imputed)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 6p22.2 "LRRC16A, SCGN" rs742132-A rs742132 0.7 9.00E-09 0.05 [0.036-0.072] mg/dl increase "Affymetrix and Illumina [2,493,963] (imputed)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 4p16.1 SLC2A9 rs734553-T rs734553 0.77 1.00E-41 (men)  0.22 [0.188-0.252] mg/dl increase "Affymetrix and Illumina [2,493,963] (imputed)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 11q13.1 SLC22A11 rs17300741-A rs17300741 0.51 7.00E-14 0.06 [0.046-0.078] mg/dl increase "Affymetrix and Illumina [2,493,963] (imputed)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 10q21.1 SLC16A9 rs12356193-A rs12356193 0.83 1.00E-08 0.08 [0.051-0.105] mg/dl increase "Affymetrix and Illumina [2,493,963] (imputed)" N 6/22/2009 19503597 Kolz 5-Jun-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19503597?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations" Serum uric acid "12,328 European males, 15,813 European females" NR 4q22.1 ABCG2 rs2231142-T rs2231142 0.11 2.00E-18 (men)  0.22 [0.171-0.270] mg/dl increase "Affymetrix and Illumina [2,493,963] (imputed)" N 6/16/2009 19488044 Smith 2-Jun-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19488044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of bipolar disorder in European American and African American individuals Bipolar disorder "1,001 Caucasian cases, 345 African American cases, 1,033 Caucasian controls, 670 African American controls" "1,749 Caucasian family members, 1,263 Caucasian cases, 431 Caucasian controls" 19q13.11 DPY19L3 rs2111504-T rs2111504 0.23 0.000002 (AA)  1.74 [NR] "Affymetrix [702,044]" N 6/15/2009 19483685 Daly 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin Drug-induced liver injury (flucloxacillin) "58 cases, 282 controls" NR 3q27.3 ST6GAL1 rs10937275-? rs10937275 0.09 1.00E-08 (B*5701 positive)  4.1 [NR] "Illumina [866,399]" N 6/15/2009 19483685 Daly 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin Drug-induced liver injury (flucloxacillin) "58 cases, 282 controls" NR 3q11.2 OR5H2 rs1497546-? rs1497546 0.02 2.00E-07 6.57 [NR] "Illumina [866,399]" N 6/15/2009 19483685 Daly 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin Drug-induced liver injury (flucloxacillin) "58 cases, 282 controls" NR 12q12 ALG10B rs6582630-? rs6582630 0.38 0.000001 2.82 [NR] "Illumina [866,399]" N 6/15/2009 19483685 Daly 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin Drug-induced liver injury (flucloxacillin) "58 cases, 282 controls" NR 9p21.2 C9org82 rs10812428-? rs10812428 0.31 0.000001 2.85 [NR] "Illumina [866,399]" N 6/15/2009 19483685 Daly 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin Drug-induced liver injury (flucloxacillin) "58 cases, 282 controls" NR 6p21.33 "HCP5, HLA-B" rs2395029-? rs2395029 0.05 9.00E-33 45 [19.4-105] "Illumina [866,399]" N 6/15/2009 19483685 Daly 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483685?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin Drug-induced liver injury (flucloxacillin) "58 cases, 282 controls" NR 15q26.2 MCTP2 rs4984390-? rs4984390 0.41 0.000004 3.27 [NR] "Illumina [866,399]" N 6/14/2009 19483682 Kanetsky 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483682?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer Testicular cancer "277 white, non-Hispanic cases, 919 non-Hispanic controls" "371 non-Hispanic cases + 204 sets of parents, 860 non-Hispanic controls" 12q21.32 KITLG rs4474514-A rs4474514 NR 6.00E-15 3.07 [2.29-4.13] "Affymetrix [611,254]" N 6/14/2009 19483681 Rapley 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of testicular germ cell tumor Testicular germ cell tumor "730 cases, 1,435 controls" "571 cases, 1,806 controls" 12q21.32 KITLG rs1508595-G rs995030 0.83 3.00E-30 2.69 [2.10-3.44] "Illumina [307,666]" N 6/14/2009 19483681 Rapley 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of testicular germ cell tumor Testicular germ cell tumor "730 cases, 1,435 controls" "571 cases, 1,806 controls" 4q24 Intergenic rs4699052-C rs4699052 0.61 2.00E-07 1.21 [1.05-1.39] "Illumina [307,666]" N 6/14/2009 19483681 Rapley 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of testicular germ cell tumor Testicular germ cell tumor "730 cases, 1,435 controls" "571 cases, 1,806 controls" 5q31.3 SPRY4 rs4624820-A rs4624820 0.54 3.00E-13 1.37 [1.19-1.58] "Illumina [307,666]" N 6/14/2009 19483681 Rapley 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of testicular germ cell tumor Testicular germ cell tumor "730 cases, 1,435 controls" "571 cases, 1,806 controls" 12q21.32 KITLG rs995030-G rs995030 0.8 1.00E-31 2.55 [2.05-3.19] "Illumina [307,666]" N 6/14/2009 19483681 Rapley 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of testicular germ cell tumor Testicular germ cell tumor "730 cases, 1,435 controls" "571 cases, 1,806 controls" 6p21.31 BAK1 rs210138-G rs210138 0.2 1.00E-13 1.5 [1.28-1.75] "Illumina [307,666]" N 6/14/2009 19483681 Rapley 31-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19483681?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of testicular germ cell tumor Testicular germ cell tumor "730 cases, 1,435 controls" "571 cases, 1,806 controls" 1q24.1 Intergenic rs4657482-A rs4657482 0.33 0.000002 1.14 [0.99-1.31] "Illumina [307,666]" N 6/14/2009 19478819 Ng 29-May-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19478819?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma. Nasopharyngeal carcinoma "111 Chinese cases, 260 Chinese controls" "168 Chinese cases, 252 Chinese controls" 3p22.2 ITGA9 rs189897-A rs189897 0.09 7.00E-08 3.18 [1.94-5.21] "Illumina [533,048]" N 6/16/2009 19478329 Aston 28-May-09 J Androl http://www.ncbi.nlm.nih.gov/pubmed/19478329?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia Male infertility "52 oligozoospermic Caucasian males, 40 non-obstructive azoospermic Caucasian males, 80 Caucasian male controls" NR 2q22.1 NXPH2 rs1399645-? rs1399645 0.02 9.00E-07 (azoospermia)  NR NR "Illumina [314,776]" N 6/16/2009 19478329 Aston 28-May-09 J Androl http://www.ncbi.nlm.nih.gov/pubmed/19478329?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia Male infertility "52 oligozoospermic Caucasian males, 40 non-obstructive azoospermic Caucasian males, 80 Caucasian male controls" NR 20q13.2 SALL4 rs6068020-? rs6068020 0.49 5.00E-07 (azoospermia)  NR NR "Illumina [314,776]" N 6/16/2009 19478329 Aston 28-May-09 J Androl http://www.ncbi.nlm.nih.gov/pubmed/19478329?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia Male infertility "52 oligozoospermic Caucasian males, 40 non-obstructive azoospermic Caucasian males, 80 Caucasian male controls" NR 3q11.2 ARL6 rs9814870-? rs9814870 0.15 7.00E-07 (oligozoospermia)  NR NR "Illumina [314,776]" N 6/16/2009 19478329 Aston 28-May-09 J Androl http://www.ncbi.nlm.nih.gov/pubmed/19478329?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia Male infertility "52 oligozoospermic Caucasian males, 40 non-obstructive azoospermic Caucasian males, 80 Caucasian male controls" NR 12p12.2 PDE3A rs10841496-? rs10841496 0.58 5.00E-07 (azoospermia)  NR NR "Illumina [314,776]" N 6/16/2009 19478329 Aston 28-May-09 J Androl http://www.ncbi.nlm.nih.gov/pubmed/19478329?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Study of Single Nucleotide Polymorphisms Associated with Azoospermia and Severe Oligozoospermia Male infertility "52 oligozoospermic Caucasian males, 40 non-obstructive azoospermic Caucasian males, 80 Caucasian male controls" NR 12p13.32 EFCAB4B rs10848911-? rs10848911 0.11 0.000004 (azoospermia)  NR NR "Illumina [314,776]" N 6/10/2009 19456320 Ma 28-May-09 Ann Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19456320?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study of autism reveals a common novel risk locus at 5p14.1 Autism "1,390 family members" "2,390 family members" 5p14.1 Intergenic rs10038113-T rs10038113 0.59 0.000003 1.33 [1.11-1.43] "Illumina [775,311]" N 6/14/2009 19465909 Jallow 24-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19465909?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and fine-resolution association anaylsis of malaria in West Africa Malaria "958 Gambian cases, 1,382 Gambian controls, all children" "1,087 Gambian cases, 2,376 Gambian controls, all children" 7p12.2 DDC rs1451375-? rs1451375 0.78 0.000006 1.33 [1.18-1.52] "Affymetrix [402,814]" N 6/14/2009 19465909 Jallow 24-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19465909?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and fine-resolution association anaylsis of malaria in West Africa Malaria "958 Gambian cases, 1,382 Gambian controls, all children" "1,087 Gambian cases, 2,376 Gambian controls, all children" 17p13.1 SCO1 rs6503319-T rs6503319 0.45 7.00E-07 1.21 [1.12-1.31] "Affymetrix [402,814]" N 6/14/2009 19465909 Jallow 24-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19465909?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and fine-resolution association anaylsis of malaria in West Africa Malaria "958 Gambian cases, 1,382 Gambian controls, all children" "1,087 Gambian cases, 2,376 Gambian controls, all children" 11p15.4 HBB rs11036238-? rs11036238 0.14 4.00E-11 1.59 [1.39-1.82] "Affymetrix [402,814]" N 6/4/2009 19461586 Norris 21-May-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19461586?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association Study and Follow-up Analysis of Adiposity Traits in Hispanic Americans: The IRAS Family Study Obesity-related traits 229 Hispanic family members 961 Hispanic family members NR NR NR NR NS NS NR NR "Illumina [309,200]" N 6/21/2009 19458352 Hirschfield 20-May-09 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants" Primary biliary cirrhosis "505 cases, 1,507 controls" "up to 526 cases, 1,206 controls" 3q26.1 IL12A rs6441286-G rs6441286 0.39 2.00E-14 1.54 [1.38-1.72] "Illumina [305,724]" N 6/21/2009 19458352 Hirschfield 20-May-09 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants" Primary biliary cirrhosis "505 cases, 1,507 controls" "up to 526 cases, 1,206 controls" 1p31.3 IL12RB2 rs3790567-A rs3790567 0.24 3.00E-11 1.51 [1.33-1.70] "Illumina [305,724]" N 6/21/2009 19458352 Hirschfield 20-May-09 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants" Primary biliary cirrhosis "505 cases, 1,507 controls" "up to 526 cases, 1,206 controls" 7q32.1 IRFS-TNPO3 rs10488631-G rs10488631 NR 2.00E-07 1.52 [1.30-1.78] "Illumina [305,724]" N 6/21/2009 19458352 Hirschfield 20-May-09 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants" Primary biliary cirrhosis "505 cases, 1,507 controls" "up to 526 cases, 1,206 controls" 6p21.3 "c6orf10, BTNL2, HLA-DQB1" 4-SNP haplotype-2 "rs2856683,rs9357152,rs2395148,rs3135363" 0.2 7.00E-10 (CACA)  NR NR "Illumina [305,724]" N 6/21/2009 19458352 Hirschfield 20-May-09 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants" Primary biliary cirrhosis "505 cases, 1,507 controls" "up to 526 cases, 1,206 controls" 3q26.1 ARF7 rs4679904-G rs4679904 0.72 0.000001 1.38 [1.21-1.57] "Illumina [305,724]" N 6/21/2009 19458352 Hirschfield 20-May-09 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants" Primary biliary cirrhosis "505 cases, 1,507 controls" "up to 526 cases, 1,206 controls" 6p21.32 "c6orf10, BTNL2, HLA-DQB1" 4-SNP haplotype-1 "rs3135363,rs2395148,rs2856683,rs9357152" 0.01 1.00E-10 (AACA)  NR NR "Illumina [305,724]" N 6/21/2009 19458352 Hirschfield 20-May-09 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/19458352?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Primary Biliary Cirrhosis Associated with HLA, IL12A, and IL12RB2 Variants" Primary biliary cirrhosis "505 cases, 1,507 controls" "up to 526 cases, 1,206 controls" 17q12 IKZF3 rs907092-A rs907092 0.45 0.000008 1.29 [1.15-1.44] "Illumina [305,724]" N 6/14/2009 19454037 Arnett 19-May-09 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/19454037?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: The HyperGEN Study Left ventricular mass "101 Caucasian cases, 101 Caucasian controls" "704 Caucasian siblings, 1,467 African American siblings" 7q21.11 CD36 rs10499859-? rs10499859 0.45 0.000003 (Caucasian)  0.09 [NR] (LVMI) "Affymetrix [96,258]" N 6/14/2009 19454037 Arnett 19-May-09 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/19454037?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: The HyperGEN Study Left ventricular mass "101 Caucasian cases, 101 Caucasian controls" "704 Caucasian siblings, 1,467 African American siblings" 5p13.2 RAI14 rs409045-? rs409045 0.38 8.00E-07 (Caucasian)  0 [NR] (LVMI) "Affymetrix [96,258]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 18q12.1 B4GALT6 rs10438933-G rs10438933 0.12 0.000001 (susceptibilty)  1.3 [NR] "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 21q21.1 NR rs2823962-? rs2823962 NR 0.000009 (survival)  NR NR "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 1p34.2 NT5C1A rs873917-T rs873917 0.29 0.000008 (susceptibilty)  1.16 [NR] "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 2q24.2 RBMS1 rs10192369-T rs10192369 0.47 0.000009 (susceptibilty)  1.17 [NR] "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 2p16.1 EFEMP1 rs7577894-T rs7577894 0.39 0.000001 (site of onset)  1.41 [NR] "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 2q24.3 SCN7A rs13015447-T rs13015447 0.34 0.000007 (site of onset)  1.41 [NR] "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 5q23.1 SEMA6A rs7702057-C rs7702057 0.03 0.000008 (site of onset)  2.05 [NR] "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 17q24.3 SLC39A11 rs8066857-C rs8066857 NR 0.000008 (site of onset)  1.48 [NR] "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 6p22.3 ATXN1 rs697739-A rs697739 NR 0.000004 (age of onset)  2.04 [1.18-2.90] years younger "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 3p26.3 CNTN4 rs2619566-G rs2619566 NR 0.000007 (age of onset)  3.03 [1.71-4.35] years younger "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 1q24.2 KIFAP3 rs1541160-C rs1541160 NR 2.00E-08 (survival)  0.58 [0.38-0.78] years older "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 7q36.1 ZNF746 rs855913-A rs855913 NR 4.00E-08 (survival)  1.08 [0.70-1.46] years older "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 5q23.2 CSNK1G3 rs11241713-T rs11241713 NR 0.000003 (survival)  0.79 [0.46-1.12] years older "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 1q24.2 SELL rs3177980-G rs3177980 NR 0.000004 (survival)  0.51 [0.46-0.56] years older "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 2p22.1 NR rs3099950-? rs3099950 NR 0.000008 (survival)  NR NR "Illumina [288,357]" N 6/4/2009 19451621 Landers 18-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19451621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "1,821 cases, 2,258 controls" "538 cases, 556 controls" 1q42.2 DISC1 rs16856202-A rs16856202 0.04 0.000008 (susceptibilty)  2 [NR] "Illumina [288,357]" N 6/4/2009 19448621 He 17-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Menarche and menopause (age at onset) "17,438 Caucasian women" NR 6q21 LIN28B rs314277-A rs314277 0.14 3.00E-13 (age at menarche)  0.16 [0.12-0.20] years older "Illumina [317,759]" N 6/4/2009 19448621 He 17-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Menarche and menopause (age at onset) "17,438 Caucasian women" NR 19q13.42 BRSK1 rs1172822-T rs1172822 0.37 2.00E-19 (age at natural menopause)  0.49 [0.38-0.60] years younger "Illumina [317,759]" N 6/4/2009 19448621 He 17-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Menarche and menopause (age at onset) "17,438 Caucasian women" NR 20p12.3 "TRMT6, MCM8" rs16991615-A rs16991615 0.06 1.00E-21 (age at natural menopause)  1.07 [0.85-1.29] years older "Illumina [317,759]" N 6/4/2009 19448621 He 17-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Menarche and menopause (age at onset) "17,438 Caucasian women" NR 6p24.2 "GCM2, SYCP2L" rs2153157-T rs2153157 0.49 5.00E-08 (age at natural menopause)  0.29 [0.19-0.39] years older "Illumina [317,759]" N 6/4/2009 19448621 He 17-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Menarche and menopause (age at onset) "17,438 Caucasian women" NR 5q35.2 UIMC1 rs365132-T rs365132 0.49 8.00E-14 (age at natural menopause)  0.39 [0.29-0.49] years older "Illumina [317,759]" N 6/4/2009 19448621 He 17-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448621?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Menarche and menopause (age at onset) "17,438 Caucasian women" NR 9q31.2 Intergenic rs7861820-C rs7861820 0.48 3.00E-09 (age at menarche)  0.09 [0.06-0.12] years younger "Illumina [317,759]" N 6/1/2009 19448623 Ong 17-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448623?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic variation in LIN28B is associated with the timing of puberty Menarche (age at onset) "4,714 women" "16,373 women" 6q21 LIN28B rs314276-C rs314276 0.33 4.00E-16 0.14 [0.11-0.17] years younger "Affymetrix [up to 390,631]" N 5/28/2009 19448620 Perry 17-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448620?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data identifies two loci influencing age at menarche Menarche (age at onset) "17,510 women" NR 6q21 LIN28B rs7759938-C rs7759938 0.33 7.00E-09 0.09 [0.05-0.13] years older Affymetrix & Illumina [~2.5 million] (imputed) N 5/28/2009 19448620 Perry 17-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448620?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data identifies two loci influencing age at menarche Menarche (age at onset) "17,510 women" NR 9q31.2 "TMEM38B, SLC44A1, FKTN, FSD1L, TAL2, ZNF462" rs2090409-A rs2090409 0.31 2.00E-09 0.1 [0.06-0.14] years younger Affymetrix & Illumina [~2.5 million] (imputed) N 6/1/2009 19448189 Perlis 15-May-09 Am J Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19448189?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genomewide Association Study of Response to Lithium for Prevention of Recurrence in Bipolar Disorder Response to lithium treatment in bipolar disorder "458 lithium-treated subjects, 719 non-lithium treated subjects" 359 subjects NR NR NR NR NS NS NR NR Affymetrix [~1.4 million] (imputed) N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 20p12.3 MCM8 rs236114-A rs236114 0.21 1.00E-10 0.5 [0.34-0.65] years older "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 19q13.42 "BRSK1, TMEM224, SUV420H2" rs1172822-T rs1172822 0.39 6.00E-11 0.39 [0.27-0.51] years younger "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 13q34 "LOC121793, ARHGEF7" rs7333181-A rs7333181 0.12 3.00E-08 0.52 [0.34-0.70] years older "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 11q25 NR rs4397868-? rs4397868 NR 3.00E-07 0.4 [0.25-0.55] years younger "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 7q22.3 NR rs17153527-? rs17153527 NR 4.00E-07 0.51 [0.31-0.71] years older "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 20p12.3 NR rs2326679-? rs2326679 NR 0.000002 0.32 [0.19-0.45] years older "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 16q24.2 NR rs4843747-? rs4843747 NR 2.00E-07 0.39 [0.24-0.54] years older "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 8p12 NR rs6468442-? rs6468442 NR 3.00E-07 0.39 [0.24-0.54] years younger "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 2q23.3 NR rs11889862-? rs11889862 NR 0.000002 0.36 [0.21-0.51] years younger "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 6p21.32 NR rs494620-? rs494620 NR 5.00E-07 0.3 [0.18-0.42] years older "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 9q21.31 NR rs2151145-? rs2151145 NR 1.00E-07 0.41 [0.26-0.56] years older "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 3q26.2 NR rs4955755-? rs4955755 NR 7.00E-07 0.34 [0.21-0.47] years older "Illumina [315,418]" N 5/28/2009 19448619 Stolk 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448619?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." Menopause (age at onset) "2,979 women" "2,560 women" 14q32.31 NR rs4906172-? rs4906172 NR 0.000003 0.36 [0.21-0.51] years younger "Illumina [315,418]" N 6/1/2009 19448622 Sulem 15-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19448622?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche Menarche (age at onset) "15,297 Icelandic women" "10,040 Icelandic women" 6q21 "LIN28B, HACE1, E3 ubiquitin protein ligase 1, BVES, POPDC3" rs314280-T rs314280 0.48 2.00E-14 1.2 [0.9-1.5] months older "Illumina [304,226]" N 5/26/2009 19442274 Fei 14-May-09 Arthritis Res Ther http://www.ncbi.nlm.nih.gov/pubmed/19442274?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Identification of novel genetic susceptibility loci for Behcet's disease using a genome-wide association study Behcet's disease "152 cases, 170 controls" NR NR NR NR NR NS NS NR NR "Affymetrix [~500,000] (pooled)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 6p21.32 MHC rs9268645-? rs9268645 NR 1.00E-100 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 7p15.2 Intergenic rs7804356-? rs7804356 0.76 5.00E-09 1.14 [1.06-1.22] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 17p13.1 Intergenic rs16956936-? rs16956936 0.86 5.00E-07 1.09 [1.00-1.19] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 1p13.2 PTPN22 rs2476601-? rs2476601 NR 9.00E-85 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 2q24.2 IFIH1 rs1990760-? rs1990760 NR 7.00E-09 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 2q33.2 CTLA4 rs3087243-? rs3087243 NR 1.00E-15 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 4q27 IL2 rs4505848-? rs4505848 NR 5.00E-13 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 6q15 BACH2 rs11755527-? rs11755527 NR 5.00E-08 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 10p15.1 IL2RA rs12251307-? rs12251307 NR 1.00E-13 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 10p15.1 PRKCQ rs11258747-? rs11258747 NR 1.00E-07 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 11p15.5 INS rs7111341-? rs7111341 NR 4.00E-48 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 12q13.2 ERBB3 rs2292239-? rs2292239 NR 2.00E-25 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 12q24.12 SH2B3 rs3184504-? rs3184504 NR 3.00E-27 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 15q25.1 CTSH rs3825932-? rs3825932 NR 8.00E-08 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 16p13.13 CLEC16A rs12708716-? rs12708716 NR 2.00E-16 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 18p11.21 PTPN2 rs1893217-? rs1893217 NR 4.00E-15 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 21q22.3 UBASH3A rs11203203-? rs11203203 NR 2.00E-09 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 22q13.1 C1QTNF6 rs229541-? rs229541 NR 2.00E-07 NR NR "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 1q32.1 IL10 rs3024505-? rs3024505 0.83 2.00E-09 1.19 [1.10-1.30] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 4p15.2 Intergenic rs10517086-A rs10517086 0.3 5.00E-10 1.09 [1.02-1.17] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 6q22.32 C6orf173 rs9388489-G rs9388489 0.45 4.00E-13 1.17 [1.10-1.24] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 7p12.1 COBL rs4948088-? rs4948088 0.95 4.00E-08 1.3 [1.11-1.49] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 9p24.2 GLIS3 rs7020673-? rs7020673 0.5 5.00E-12 1.14 [1.08-1.20] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 10q23.31 C10orf59 rs10509540-? rs10509540 0.71 1.00E-28 1.33 [1.25-1.43] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 12p13.31 CD69 rs4763879-A rs4763879 0.37 2.00E-11 1.09 [1.02-1.16] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 14q24.1 Intergenic rs1465788-? rs1465788 0.71 2.00E-12 1.16 [1.10-1.25] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 14q32.2 Intergenic rs4900384-G rs4900384 0.29 4.00E-09 1.09 [1.02-1.16] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 16p11.2 IL27 rs4788084-G rs4788084 0.42 3.00E-13 1.09 [1.02-1.16] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 16q23.1 Intergenic rs7202877-G rs7202877 0.1 3.00E-15 1.28 [1.17-1.41] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 17q12 ORMDL3 rs2290400-? rs2290400 0.5 6.00E-13 1.15 [1.08-1.22] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 17q21.2 Intergenic rs7221109-? rs7221109 0.65 1.00E-09 1.05 [0.99-1.12] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 19q13.32 Intergenic rs425105-? rs425105 0.84 3.00E-11 1.16 [1.08-1.27] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 20p13 Intergenic rs2281808-? rs2281808 0.64 1.00E-11 1.11 [1.05-1.19] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 22q12.2 Intergenic rs5753037-T rs5753037 0.39 3.00E-16 1.1 [1.04-1.17] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" Xq28 Intergenic rs2664170-G rs2664170 0.32 8.00E-09 1.16 [1.07-1.24] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 1p31.3 PGM1 rs2269241-G rs2269241 0.19 4.00E-07 1.1 [1.02-1.18] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 2p25.1 Intergenic rs1534422-G rs1534422 0.46 0.000002 1.08 [1.02-1.15] "Affymetrix & Illumina [841,622] (imputed)" N 6/1/2009 19430480 Barrett 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430480?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes Type 1 diabetes "7,514 cases, 9,045 controls" "4,267 cases, 4,670 controls, 4,342 trios" 16p12.3 Intergenic rs12444268-A rs12444268 0.3 2.00E-07 1.1 [1.03-1.17] "Affymetrix & Illumina [841,622] (imputed)" N 5/27/2009 19430482 Kottgen 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Multiple loci associated with indices of renal function and chronic kidney disease Renal function and chronic kidney disease "19,877 individuals, up to 2,388 cases" "21,466 individuals, up to 1,932 cases" 16p12.3 UMOD rs12917707-T rs12917707 0.18 5.00E-16 (eGFRcrea)  0.02 [0.014-0.022] ml/min/1.73m2 increase Affymetrix & Illumina [~2.5 million] (imputed) N 5/27/2009 19430482 Kottgen 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Multiple loci associated with indices of renal function and chronic kidney disease Renal function and chronic kidney disease "19,877 individuals, up to 2,388 cases" "21,466 individuals, up to 1,932 cases" 16p12.3 UMOD rs12917707-G rs12917707 0.18 2.00E-12 (CKD)  1.25 [1.18-1.33] Affymetrix & Illumina [~2.5 million] (imputed) N 5/27/2009 19430482 Kottgen 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Multiple loci associated with indices of renal function and chronic kidney disease Renal function and chronic kidney disease "19,877 individuals, up to 2,388 cases" "21,466 individuals, up to 1,932 cases" 4q21.1 SHROOM3 rs17319721-A rs17319721 0.44 1.00E-12 (eGFRcrea)  0.01 [0.008-0.016] ml/min/1.73m2 decrease Affymetrix & Illumina [~2.5 million] (imputed) N 5/27/2009 19430482 Kottgen 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Multiple loci associated with indices of renal function and chronic kidney disease Renal function and chronic kidney disease "19,877 individuals, up to 2,388 cases" "21,466 individuals, up to 1,932 cases" 15q21.1 "SPATA5L1, GATM" rs2467853-G rs2467853 0.38 6.00E-14 (eGFRcrea)  0.01 [0.009-0.017] ml/min/1.73m2 decrease Affymetrix & Illumina [~2.5 million] (imputed) N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Diastolic blood pressure "29,136 individuals" "34,433 individuals" 12q21.33 ATP2B1 rs2681472-A rs2681472 0.83 1.00E-09 0.5 [0.34-0.66] mm Hg increase "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Diastolic blood pressure "29,136 individuals" "34,433 individuals" 15q24.1 "CSK, ULK3" rs6495122-A rs6495122 0.42 2.00E-10 0.4 [0.28-0.52] mm Hg increase "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Diastolic blood pressure "29,136 individuals" "34,433 individuals" 11p15.1 PLEKHA7 rs11024074-T rs11024074 0.72 0.000001 0.33 [0.19-0.47] mm Hg decrease "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Diastolic blood pressure "29,136 individuals" "34,433 individuals" 10p12.33 CACNB2 rs11014166-A rs11014166 0.66 1.00E-08 0.37 [0.25-0.49] mm Hg increase "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Diastolic blood pressure "29,136 individuals" "34,433 individuals" 12q24.21 "TBX3, TBX5" rs2384550-A rs2384550 0.35 4.00E-08 0.35 [0.23-0.47] mm Hg decrease "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Diastolic blood pressure "29,136 individuals" "34,433 individuals" 12q24.12 SH2B3 rs3184504-T rs3184504 0.48 3.00E-14 0.48 [0.36-0.60] mm Hg increase "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Diastolic blood pressure "29,136 individuals" "34,433 individuals" 3p22.1 ULK4 rs9815354-A rs9815354 0.17 3.00E-09 0.49 [0.33-0.65] mm Hg increase "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Hypertension "29,136 individuals" "34,433 individuals" 10p12.33 CACNB2 rs11014166-A rs11014166 0.66 6.00E-08 0.09 [0.05-0.13] increase in log odds "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Hypertension "29,136 individuals" "34,433 individuals" 20q13.32 "ZNF831, EDN3" rs16982520-A rs16982520 0.88 2.00E-07 0.13 [0.09-0.17] decrease in log odds "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Hypertension "29,136 individuals" "34,433 individuals" 12q21.33 ATP2B1 rs2681472-A rs2681472 0.83 2.00E-11 0.15 [0.11-0.19] increase in log odds "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Hypertension "29,136 individuals" "34,433 individuals" 8p23.1 MSRA rs11775334-A rs11775334 0.32 0.000004 0.08 [0.04-0.12] increase in log odds "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Systolic blood pressure "29,136 individuals" "34,433 individuals" 3q26.2 MDS1 rs448378-A rs448378 0.52 1.00E-07 0.51 [0.31-0.71] mm Hg decrease "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Systolic blood pressure "29,136 individuals" "34,433 individuals" 10p12.33 CACNB2 rs11014166-A rs11014166 0.66 7.00E-07 0.5 [0.30-0.70] mm Hg increase "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Systolic blood pressure "29,136 individuals" "34,433 individuals" 12q24.12 SH2B3 rs3184504-T rs3184504 0.48 5.00E-09 0.58 [0.38-0.78] mm Hg increase "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Systolic blood pressure "29,136 individuals" "34,433 individuals" 10q24.32 CYP17A1 rs1004467-A rs1004467 0.9 1.00E-10 1.05 [0.74-1.36] mm Hg increase "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Systolic blood pressure "29,136 individuals" "34,433 individuals" 12q21.33 ATP2B1 rs2681492-T rs2681492 0.8 4.00E-11 0.85 [0.60-1.10] mm Hg increase "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Systolic blood pressure "29,136 individuals" "34,433 individuals" 11p15.1 PLEKHA7 rs381815-T rs381815 0.26 2.00E-09 0.65 [0.43-0.87] mm Hg increase "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430479 Levy 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430479?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of blood pressure and hypertension Systolic blood pressure "29,136 individuals" "34,433 individuals" 1p36.22 CASZ1 rs12046278-T rs12046278 0.64 0.000005 0.53 [0.29-0.77] mm Hg decrease "Affymetrix & Illumina [2,533,153](imputed)" N 5/19/2009 19430483 Newton-Cheh 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies eight loci associated with blood pressure Diastolic blood pressure "34,433 individuals" "Up to 100,347 white individuals, up to 12,889 Indian Asian individuals" 4q21.21 "FGF5, PRDM8, c4orf22" rs16998073-T rs16998073 0.21 1.00E-21 0.5 [0.40-0.60] mm Hg increase "Affymetrix & Illumina [2,497,993] (imputed)" N 5/19/2009 19430483 Newton-Cheh 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies eight loci associated with blood pressure Diastolic blood pressure "34,433 individuals" "Up to 100,347 white individuals, up to 12,889 Indian Asian individuals" 3q26.2 MDS1 rs1918974-T rs1918974 0.54 8.00E-08 0.27 [0.17-0.37] mm Hg decrease "Affymetrix & Illumina [2,497,993] (imputed)" N 5/19/2009 19430483 Newton-Cheh 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies eight loci associated with blood pressure Diastolic blood pressure "34,433 individuals" "Up to 100,347 white individuals, up to 12,889 Indian Asian individuals" 17q21.32 "ZNF652, PHB" rs16948048-G rs16948048 0.39 5.00E-09 0.31 [0.21-0.41] mm Hg increase "Affymetrix & Illumina [2,497,993] (imputed)" N 5/19/2009 19430483 Newton-Cheh 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies eight loci associated with blood pressure Diastolic blood pressure "34,433 individuals" "Up to 100,347 white individuals, up to 12,889 Indian Asian individuals" 12q24.12 "ATXN2, SH2B3" rs653178-T rs653178 0.53 3.00E-18 0.46 [0.36-0.56] mm Hg decrease "Affymetrix & Illumina [2,497,993] (imputed)" N 5/19/2009 19430483 Newton-Cheh 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies eight loci associated with blood pressure Diastolic blood pressure "34,433 individuals" "Up to 100,347 white individuals, up to 12,889 Indian Asian individuals" 15q24.1 "CYP1A1, CYP1A2, CSK, LMAN1L, CPLX3, ARID3B" rs1378942-C rs1378942 0.36 1.00E-23 0.43 [0.35-0.51] mm Hg increase "Affymetrix & Illumina [2,497,993] (imputed)" N 5/19/2009 19430483 Newton-Cheh 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies eight loci associated with blood pressure Diastolic blood pressure "34,433 individuals" "Up to 100,347 white individuals, up to 12,889 Indian Asian individuals" 10q21.2 "c10orf107, TMEM26, RTKN2, RHOBTB1, ARID5B" rs1530440-T rs1530440 0.19 1.00E-09 0.39 [0.27-0.51] mm Hg decrease "Affymetrix & Illumina [2,497,993] (imputed)" N 5/19/2009 19430483 Newton-Cheh 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies eight loci associated with blood pressure Systolic blood pressure "34,433 individuals" "Up to 100,347 white individuals, up to 12,889 Indian Asian individuals" 17q21.31 "PLCD3, ACBD4, HEXIM1, HEXIM2" rs12946454-T rs12946454 0.28 1.00E-08 0.57 [0.37-0.77] mm Hg increase "Affymetrix & Illumina [2,497,993] (imputed)" N 5/19/2009 19430483 Newton-Cheh 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies eight loci associated with blood pressure Systolic blood pressure "34,433 individuals" "Up to 100,347 white individuals, up to 12,889 Indian Asian individuals" 1p36.22 "MTHFR, NPPA, CLCN6, NPPB, AGTRAP" rs17367504-G rs17367504 0.14 2.00E-13 0.85 [0.63-1.07] mm Hg decrease "Affymetrix & Illumina [2,497,993] (imputed)" N 5/19/2009 19430483 Newton-Cheh 10-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19430483?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies eight loci associated with blood pressure Systolic blood pressure "34,433 individuals" "Up to 100,347 white individuals, up to 12,889 Indian Asian individuals" 10q24.32 "CYP17A1, AS3MT, CNNM2, NT5C2" rs11191548-T rs11191548 0.91 7.00E-24 1.16 [0.92-1.40] mm Hg increase "Affymetrix & Illumina [2,497,993] (imputed)" N 5/21/2009 19430760 Rich 9-May-09 Diabetologia http://www.ncbi.nlm.nih.gov/pubmed/19430760?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS). Insulin response 229 family members 961 family members NR NR NR NR NS NS NR NR "Illumina [309,200]" N 5/20/2009 19426955 Himes 7-May-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19426955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene Asthma "422 cases, 1,533 controls" "3,750 white cases, 13,365 white controls, 592 white trios, 1,903 black cases, 2,432 black controls, 929 black family members" 5q12.1 PDE4D rs1588265-C rs1588265 0.29 3.00E-08 1.18 [1.08-1.30] "Illumina [518,230]" N 5/21/2009 19421330 Yang 7-May-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19421330?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan Hypertension (young onset) "175 Han Chinese cases, 175 Han Chinese controls" "833 Han Chinese cases, 833 Han Chinese controls" 2p22.3 "LOC344371, MYADML, FAM98A, RASGRP3" 4-SNP-haplotype "rs6729869,rs10495809,rs9308945,rs6711736" NR 3.00E-10 NR NR "Affymetrix [91,713]" N 5/19/2009 19419973 Sanna 6-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19419973?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia Bilirubin levels "4,300 individuals" "2,692 individuals" 12p12.2 SLC01B3 rs2117032-C rs2117032 0.47 3.00E-14 0.13 [0.08-0.18] SD increase "Affymetrix [362,129]" N 5/19/2009 19419973 Sanna 6-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19419973?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia Bilirubin levels "4,300 individuals" "2,692 individuals" Xq28 G6PD rs766420-G rs766420 0.18 9.00E-09 0.18 [0.12-0.24] SD decrease "Affymetrix [362,129]" N 5/19/2009 19419973 Sanna 6-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19419973?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia Bilirubin levels "4,300 individuals" "2,692 individuals" 2q37.1 UGT1A1 rs887829-T rs887829 0.3 1.00E-69 0.57 [0.50-0.63] SD decrease "Affymetrix [362,129]" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 8p12 NR rs6990255-T rs6990255 0.95 0.000006 1.33 [1.18-1.51] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 9q34.13 NR rs2905072-A rs2905072 0.77 0.000006 1.21 [1.11-1.32] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 11q13.1 NR rs2242663-T rs2242663 0.25 0.000001 1.2 [1.11-1.29] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 17q21.33 NR rs1035050-T rs1035050 0.4 0.000009 1.17 [1.09-1.25] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 19p13.3 NR rs7250872-T rs7250872 0.69 0.000002 1.21 [1.12-1.31] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 15q23 NR rs6494849-A rs6494849 0.12 0.000007 1.23 [1.13-1.35] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 3p21.1 "ITIH1, NEK4" rs1042779-A rs1042779 0.63 2.00E-07 1.19 [1.11-1.27] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 4q12 KIT rs2537859-T rs2537859 0.6 0.000004 1.16 [1.09-1.24] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 5q15 MCTP1 rs17418283-C rs17418283 0.28 1.00E-07 1.21 [1.13-1.30] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 1p32.1 NF1A rs472913-C rs472913 0.5 2.00E-07 1.18 [1.11-1.25] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 2p12 CTNNA2 rs13409348-G rs13409348 0.24 0.000003 1.2 [1.11-1.29] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 2q11.2 Intergenic rs6733011-G rs6733011 0.46 0.000003 1.17 [1.10-1.25] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/14/2009 19416921 Scott 5-May-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19416921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry Bipolar disorder "3,683 cases, 14,507 controls" NR 3q26.1 NR rs7427021-G rs7427021 0.56 0.000005 1.16 [1.09-1.24] "Affymetrix and Illumina [2,366,197] (imputed)" N 5/12/2009 19414484 Johnson 4-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association meta-analysis for total serum bilirubin levels Serum bilirubin levels "9,264 individuals" NR 2p11.2 KRCC1 rs12714207-T rs12714207 0.03 5.00E-07 0.03 [0.01-0.05] umol/l decrease in log(tbil) "Affymetrix & Illumina [2,555,103] (imputed)" N 5/12/2009 19414484 Johnson 4-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association meta-analysis for total serum bilirubin levels Serum bilirubin levels "9,264 individuals" NR 2q37.1 UGT1A1 rs6742078-T rs6742078 0.32 0 0.23 [0.21-0.25] umol/l increase in log(tbil) "Affymetrix & Illumina [2,555,103] (imputed)" N 5/12/2009 19414484 Johnson 4-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association meta-analysis for total serum bilirubin levels Serum bilirubin levels "9,264 individuals" NR 11p15.4 SLC22A18 rs16928809-A rs16928809 0.09 1.00E-07 0.06 [0.04-0.08] umol/l increase in log(tbil) "Affymetrix & Illumina [2,555,103] (imputed)" N 5/12/2009 19414484 Johnson 4-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association meta-analysis for total serum bilirubin levels Serum bilirubin levels "9,264 individuals" NR 12p12.1 "SLCO1B1,LST-3TM12,SLCO1A2" rs4149056-C rs4149056 0.15 7.00E-13 0.05 [0.03-0.07] umol/l increase in log(tbil) "Affymetrix & Illumina [2,555,103] (imputed)" N 5/12/2009 19414484 Johnson 4-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association meta-analysis for total serum bilirubin levels Serum bilirubin levels "9,264 individuals" NR 4q28.1 Intergenic rs1986655-A rs1986655 0.17 0.000002 0.02 [0.00-0.04] umol/l decrease in log(tbil) "Affymetrix & Illumina [2,555,103] (imputed)" N 5/12/2009 19414484 Johnson 4-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association meta-analysis for total serum bilirubin levels Serum bilirubin levels "9,264 individuals" NR 7q21.11 SEMA3C rs4236644-A rs4236644 0.26 0.000002 0.02 [0.00-0.04] umol/l decrease in log(tbil) "Affymetrix & Illumina [2,555,103] (imputed)" N 5/12/2009 19414484 Johnson 4-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association meta-analysis for total serum bilirubin levels Serum bilirubin levels "9,264 individuals" NR 13q34 ARHGEF7 rs4773330-A rs4773330 0.12 0.000008 0.04 [0.02-0.06] umol/l decrease in log(tbil) "Affymetrix & Illumina [2,555,103] (imputed)" N 5/12/2009 19414484 Johnson 4-May-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19414484?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association meta-analysis for total serum bilirubin levels Serum bilirubin levels "9,264 individuals" NR 6p22.1 HIST1H2BC rs12206204-T rs12206204 0.02 8.00E-07 0.18 [0.10-0.26] umol/l increase in log(tbil) "Affymetrix & Illumina [2,555,103] (imputed)" N 5/7/2009 19412175 Capasso 3-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19412175?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants in BARD1 influence susceptibility to high-risk neuroblastoma Neuroblastoma (high-risk) "397 cases, 2,043 controls" "189 cases, 1,178 controls" 2q35 BARD1 rs6435862-G rs6435862 0.29 9.00E-18 1.68 [1.49-1.90] "Illumina [462,866]" N 5/7/2009 19412176 Hallmayer 3-May-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19412176?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Narcolepsy is strongly associated with the T-cell receptor alpha locus Narcolepsy "807 Caucasian cases, 1,074 Caucasian controls" "363 Caucasian cases, 355 Caucasian controls, 561 Asian cases, 605 Asian controls, 133 African American cases, 144 African American controls" 14q11.2 "TRA-alpha, TRAJ10" rs1154155-C rs1154155 0.14 3.00E-22 1.69 [1.52-1.88] "Affymetrix [549,596]" N 5/7/2009 19401414 Takeuchi 29-Apr-09 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population Type 2 diabetes "519 Japanese cases, 503 Japanese controls" "5,629 Japanese cases, 7,370 Japanese controls" 11p15.5 KCNQ1 rs2237892-C rs2237892 0.59 1.00E-26 1.33 [1.27-1.41] "Illumina [482,625]" N 5/7/2009 19401414 Takeuchi 29-Apr-09 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population Type 2 diabetes "519 Japanese cases, 503 Japanese controls" "5,629 Japanese cases, 7,370 Japanese controls" 3q27.2 IGF2BP2 rs4402960-T rs4402960 0.31 0.000001 1.14 [1.08-1.21] "Illumina [482,625]" N 5/7/2009 19401414 Takeuchi 29-Apr-09 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population Type 2 diabetes "519 Japanese cases, 503 Japanese controls" "5,629 Japanese cases, 7,370 Japanese controls" 8q24.11 SLC30A8 rs13266634-C rs13266634 0.57 2.00E-14 1.22 [1.16-1.28] "Illumina [482,625]" N 5/7/2009 19401414 Takeuchi 29-Apr-09 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population Type 2 diabetes "519 Japanese cases, 503 Japanese controls" "5,629 Japanese cases, 7,370 Japanese controls" 9p21.3 "CDKN2A, CDKN2B" rs2383208-A rs2383208 0.55 2.00E-29 1.34 [1.27-1.41] "Illumina [482,625]" N 5/7/2009 19401414 Takeuchi 29-Apr-09 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population Type 2 diabetes "519 Japanese cases, 503 Japanese controls" "5,629 Japanese cases, 7,370 Japanese controls" 10q22.33 HHEX rs1111875-C rs1111875 0.28 7.00E-12 1.21 [1.15-1.28] "Illumina [482,625]" N 5/7/2009 19401414 Takeuchi 29-Apr-09 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population Type 2 diabetes "519 Japanese cases, 503 Japanese controls" "5,629 Japanese cases, 7,370 Japanese controls" 10q25.2 TCF7L2 rs7903146-T rs7903146 0.04 8.00E-12 1.54 [1.36-1.74] "Illumina [482,625]" N 5/7/2009 19401414 Takeuchi 29-Apr-09 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19401414?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Confirmation of multiple risk loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population Type 2 diabetes "519 Japanese cases, 503 Japanese controls" "5,629 Japanese cases, 7,370 Japanese controls" 6p22.3 CDKAL1 rs4712523-G rs4712523 0.41 7.00E-20 1.27 [1.21-1.33] "Illumina [482,625]" N 5/11/2009 19404256 Wang 28-Apr-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19404256?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common genetic variants on 5p14.1 associate with autism spectrum disorders Autism "3,101 family members, 1,204 cases, 6,491 controls" "1,390 family members, 108 cases, 540 controls" 5p14.1 "CDH10,CDH9" rs4307059-T rs4307059 0.61 2.00E-10 1.19 [NR] "Illumina [474,019]" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Biomedical quantitative traits "8,842 Korean individuals" "7,861 Korean individuals" 16q12.2 FTO rs9939609-A rs9939609 0.13 2.00E-07 (BMI)  0.24 [0.14-0.32] kg/m2 increase "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Biomedical quantitative traits "8,842 Korean individuals" "7,861 Korean individuals" 7q31.31 FAM3C rs7776725-C rs7776725 0.13 1.00E-11 (BD-RT)  NR NR "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Biomedical quantitative traits "8,842 Korean individuals" "7,861 Korean individuals" 7q31.31 FAM3C rs7776725-C rs7776725 0.13 0.000002 (BD-TT)  NR NR "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Biomedical quantitative traits "8,842 Korean individuals" "7,861 Korean individuals" 6q22.31 LOC644502 rs12110693-A rs12110693 0.49 2.00E-09 (pulse rate)  0.66 [0.45-0.87] beats per minute increase "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Biomedical quantitative traits "8,842 Korean individuals" "7,861 Korean individuals" 12q21.33 ATP2B1 rs17249754-A rs17249754 0.37 0.000003 (DBP)  0.63 [0.37-0.89] mm Hg decrease "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Biomedical quantitative traits "8,842 Korean individuals" "7,861 Korean individuals" 12q21.33 ATP2B1 rs17249754-A rs17249754 0.37 1.00E-07 (SBP)  1.06 [0.67-1.45] mm Hg decrease "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Biomedical quantitative traits "8,842 Korean individuals" "7,861 Korean individuals" 1q32.2 "CD46, LOC148696" rs12731740-T rs12731740 0.1 3.00E-09 (pulse rate)  1.09 [0.72-1.44] beats per minute increase "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Biomedical quantitative traits "8,842 Korean individuals" "7,861 Korean individuals" 12q24.13 C12orf51 rs2074356-T rs2074356 0.15 8.00E-12 (waist-hip ratio)  0.01 [0.004-0.008] decrease "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Height "8,842 Korean individuals" "7,861 Korean individuals" 1p12 Intergenic rs17038182-C rs17038182 0.42 5.00E-07 0.3 [0.18-0.42] cm decrease "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Height "8,842 Korean individuals" "7,861 Korean individuals" 3q23 ZBTB38 rs10513137-A rs10513137 0.26 6.00E-12 0.46 [0.33-0.59] cm increase "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Height "8,842 Korean individuals" "7,861 Korean individuals" 2p16.1 EFEMP1 rs3791675-G rs3791675 0.22 2.00E-09 0.42 [0.28-0.56] cm increase "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Height "8,842 Korean individuals" "7,861 Korean individuals" 6p21.31 HMGA1 rs6918981-G rs6918981 0.21 3.00E-08 0.4 [0.26-0.54] cm increase "Affymetrix [2,156,535] (imputed)" N 5/5/2009 19396169 Cho 26-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19396169?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits Height "8,842 Korean individuals" "7,861 Korean individuals" 8q12.1 PLAG1 rs13273123-G rs13273123 0.07 1.00E-09 0.71 [0.48-0.94] cm decrease "Affymetrix [2,156,535] (imputed)" N 4/23/2009 19369658 Ikram 15-Apr-09 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/19369658?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Studies of Stroke Stroke "19,602 Caucasian individuals" "3,004 African American individuals, 652 Caucasian cases, 3,613 Caucasian controls" 12p13.33 NINJ2 rs12425791-A rs12425791 0.19 1.00E-09 (ischemic stroke)  1.29 [1.19-1.41] "Affymetrix & Illumina [2,194,468]" N 4/22/2009 19367585 Poduslo 14-Apr-09 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/19367585?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome screen of successful aging without cognitive decline identifies LRP1B by haplotype analysis Aging "89 cases, 227 controls" NR 2q22.1 LRP1B rs12474609-? rs12474609 NR 6.00E-09 NR NR "Affymetrix [469,218]" N 5/5/2009 19359809 Hiura 10-Apr-09 Circ J http://www.ncbi.nlm.nih.gov/pubmed/19359809?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Identification of Genetic Markers Associated With High-Density Lipoprotein-Cholesterol by Genome-Wide Screening in a Japanese Population LDL cholesterol 900 Japanese individuals "1,810 Japanese individuals" 16q13 CETP rs3764261-A rs3764261 0.2 3.00E-12 6.2 mg/dl increase "Illumina [368,274]" N 4/22/2009 19359265 Mangino 8-Apr-09 J Med Genet http://www.ncbi.nlm.nih.gov/pubmed/19359265?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length Telomere length "1,625 women" "1,165 individuals" 18q12.2 "BRUNOL4, VPS34" rs2162440-G rs2162440 NR 0.000003 106 [62.88-149.12] base pairs shorter "Illumina [~314,075]" N 4/14/2009 19349984 Esparza-Gordillo 6-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19349984?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A common variant on chromosome 11q13 is associated with atopic dermatitis Atopic dermatitis "939 cases, 975 controls, 1,097 family members" "2,637 cases, 3,957 controls" 11q13.5 C11orf30 rs7927894-A rs7927894 0.36 8.00E-10 1.22 [1.15-1.30] "Affymetrix [342,303]" N 4/16/2009 19349983 Kamatani 6-Apr-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19349983?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians Hepatitis B "179 Japanese cases, 934 Japanese controls" "1,599 Japanese cases, 2,821 Japanese controls, 308 Thai cases, 546 Thai controls" 6p21.32 HLA-DPB1 rs9277535-G rs9277535 0.56 6.00E-39 1.75 [1.61-1.92] "Illumina [499,544]" N 5/11/2009 19403135 Yamada 5-Apr-09 Atherosclerosis http://www.ncbi.nlm.nih.gov/pubmed/19403135?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study Ischemic stroke "131 cases, 135 controls" "776 cases, 5,205 controls" NR NR NR NR NS NS NR NR "Affymetrix [~520,000]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 4q31.22 HHIP rs1812175-? rs1812175 0.49 0.000004 0.06 [0.03-0.09] SD decrease "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 14q24.3 TMED10 rs910316-? rs910316 0.15 1.00E-07 0.05 [0.03-0.07] SD increase "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 13q14.3 DLEU7 rs3118914-? rs3118914 0.39 4.00E-10 0.08 [0.05-0.11] SD decrease "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 7p22.2 GNA12 rs1182188-? rs1182188 0.27 3.00E-09 0.07 [0.04-0.10] SD increase "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 6q24.1 GPR126 rs6570507-? rs6570507 0.42 4.00E-11 0.08 [0.06-0.10] SD decrease "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 6p21.33 HLA-B rs13437082-? rs13437082 0.13 5.00E-08 0.07 [0.04-0.10] SD decrease "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 1p36.11 CATSPER4 rs11809207-? rs11809207 0.23 6.00E-08 0.07 [0.04-0.10] SD increase "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 4p15.32 LCORL rs6830062-? rs6830062 0.23 5.00E-09 0.1 [0.07-0.13] SD increase "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 7q21.2 CDK6 rs2282978-? rs2282978 0.08 1.00E-08 0.06 [0.04-0.08] SD decrease "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 9p13.3 WDR40A rs7871764-? rs7871764 0.44 0.000002 0.06 [0.03-0.09] SD increase "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 8q12.1 PLAG1 rs7815788-? rs7815788 0.39 0.000005 0.07 [0.04-0.10] SD decrease "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 20q11.22 UQCC rs6088813-? rs6088813 0.11 1.00E-13 0.09 [0.07-0.11] SD decrease "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 15q25.2 ADAMTSL3 rs4842838-? rs4842838 0.32 3.00E-08 0.06 [0.04-0.07] SD decrease "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 12q14.3 HMGA2 rs8756-? rs8756 0.17 5.00E-14 0.08 [0.06-0.10] SD decrease "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 7p15.1 JAZF1 rs849141-? rs849141 0.23 3.00E-11 0.08 [0.06-0.10] SD increase "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 6p21.31 "HMGA1,C6orf106" rs1776897-? rs1776897 0.49 8.00E-11 0.12 [0.08-0.16] SD increase "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 6p22.1 HIST1H1D rs10946808-? rs10946808 0.43 6.00E-12 0.07 [0.04-0.10] SD increase "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 5p13.3 NPR3 rs10472828-? rs10472828 0.26 3.00E-07 0.06 [0.04-0.08] SD decrease "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 3q23 ZBTB38 rs6763931-? rs6763931 0.35 3.00E-12 0.07 [0.05-0.09] SD increase "Illumina [229,216]" N 4/22/2009 19343178 Soranzo 3-Apr-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19343178?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size Height "12,611 individuals" "7,187 individuals" 4q21.21 PRKG2 rs710841-? rs710841 0.12 2.00E-08 0.07 [0.04-0.10] SD increase "Illumina [229,216]" N 4/13/2009 19340012 Nan 2-Apr-09 J Invest Dermatol http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry Tanning "2,287 women" 870 controls 14q32.2 Intergenic rs17094273-A rs17094273 NR 9.00E-08 0.2 [0.12-0.28] increase in tanning ability score "Illumina [528,173]" N 4/13/2009 19340012 Nan 2-Apr-09 J Invest Dermatol http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry Tanning "2,287 women" 870 controls 5p13.3 MATP rs35391-T rs35391 NR 3.00E-10 0.44 [0.30-0.58] decrease in tanning ability score "Illumina [528,173]" N 4/13/2009 19340012 Nan 2-Apr-09 J Invest Dermatol http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry Tanning "2,287 women" 870 controls 5q33.1 PPARGC1B rs32579-A rs32579 NR 0.000004 0.11 [0.07-0.15] decrease in tanning ability score "Illumina [528,173]" N 4/13/2009 19340012 Nan 2-Apr-09 J Invest Dermatol http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry Tanning "2,287 women" 870 controls 12q13.13 LOC440100 rs7969151-A rs7969151 0.21 0.000002 0.13 [0.07-0.19] increase in tanning ability score "Illumina [528,173]" N 4/13/2009 19340012 Nan 2-Apr-09 J Invest Dermatol http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry Tanning "2,287 women" 870 controls 11q14.3 TYR rs1393350-A rs1393350 NR 2.00E-13 0.19 [0.13-0.25] increase in tanning ability score "Illumina [528,173]" N 4/13/2009 19340012 Nan 2-Apr-09 J Invest Dermatol http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry Tanning "2,287 women" 870 controls 6p25.3 EXOC2 rs12210050-T rs12210050 NR 5.00E-14 0.22 [0.16-0.28] increase in tanning ability score "Illumina [528,173]" N 4/13/2009 19340012 Nan 2-Apr-09 J Invest Dermatol http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry Tanning "2,287 women" 870 controls 21q22.3 PRDM15 rs7279297-G rs7279297 NR 0.000003 0.12 [0.06-0.18] decrease in tanning ability score "Illumina [528,173]" N 4/13/2009 19340012 Nan 2-Apr-09 J Invest Dermatol http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry Tanning "2,287 women" 870 controls 16q24.3 MC1R rs154659-C rs154659 NR 7.00E-08 0.14 [0.08-0.20] increase in tanning ability score "Illumina [528,173]" N 4/13/2009 19340012 Nan 2-Apr-09 J Invest Dermatol http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry Tanning "2,287 women" 870 controls 11q14.3 GRM5 rs10831496-G rs10831496 NR 5.00E-09 0.14 [0.10-0.18] decrease in tanning ability score "Illumina [528,173]" N 4/13/2009 19340012 Nan 2-Apr-09 J Invest Dermatol http://www.ncbi.nlm.nih.gov/pubmed/19340012?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry Tanning "2,287 women" 870 controls 16q24.3 MC1R rs11648785-T rs11648785 NR 3.00E-09 0.14 [0.10-0.18] decrease in tanning ability score "Illumina [528,173]" N 4/3/2009 19330030 Thomas 29-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) Breast cancer "1,145 cases, 1,142 controls" "8,625 cases, 9,657 controls" 2q35 Intergenic rs13387042-A rs13387042 0.51 2.00E-08 1.25 [1.15-1.37] "Illumina [528,173]" N 4/3/2009 19330030 Thomas 29-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) Breast cancer "1,145 cases, 1,142 controls" "8,625 cases, 9,657 controls" 5q11.2 MAP3K1 rs16886165-G rs16886165 0.15 5.00E-07 1.23 [1.12-1.35] "Illumina [528,173]" N 4/3/2009 19330030 Thomas 29-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) Breast cancer "1,145 cases, 1,142 controls" "8,625 cases, 9,657 controls" 14q24.1 RAD51L1 rs999737-C rs999737 0.76 2.00E-07 1.06 [1.01-1.14] "Illumina [528,173]" N 4/3/2009 19330030 Thomas 29-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) Breast cancer "1,145 cases, 1,142 controls" "8,625 cases, 9,657 controls" 1p11.2 Intergenic rs11249433-C rs11249433 0.39 7.00E-10 1.16 [1.09-1.24] "Illumina [528,173]" N 4/3/2009 19330030 Thomas 29-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) Breast cancer "1,145 cases, 1,142 controls" "8,625 cases, 9,657 controls" 10q26.13 FGFR2 rs2981579-T rs2981579 0.41 2.00E-10 1.17 [1.07-1.27] "Illumina [528,173]" N 4/3/2009 19330030 Thomas 29-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19330030?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1) Breast cancer "1,145 cases, 1,142 controls" "8,625 cases, 9,657 controls" 16q12.1 TOX3 rs3803662-T rs3803662 0.27 1.00E-09 1.16 [1.07-1.27] "Illumina [528,173]" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 3p22.2 SCN5A rs12053903-C rs12053903 0.34 1.00E-14 1.23 [0.88-1.57] msec decrease "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 1q23.3 NOS1AP rs12029454-A rs12029454 0.15 3.00E-45 2.98 [2.63-3.32] msec increase "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 17q12 "LIG3,RFFL" rs2074518-T rs2074518 0.46 6.00E-12 1.05 [0.71-1.39] msec decrease "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 1q23.3 NOS1AP rs16857031-G rs16857031 0.14 1.00E-34 2.63 [2.28-2.97] msec increase "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 7q36.1 KCNH2 rs2968864-C rs2968864 0.25 8.00E-16 1.4 [1.06-1.74] msec decrease "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 7q36.1 KCNH2 rs4725982-T rs4725982 0.22 5.00E-16 1.58 [1.23-1.92] msec increase "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 1p36.31 "RNF207,NPHP4, CHDS, ACOT7, PLEKHG5, KLH21" rs846111-C rs846111 0.28 1.00E-16 1.75 [1.41-2.09] msec increase "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 11p15.5 KCNQ1 rs12576239-T rs12576239 0.13 1.00E-15 1.75 [1.41-2.09] msec increase "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 6q22.31 "c6orf204,SLC35F1, PLN, ASF1A" rs11756438-A rs11756438 0.47 5.00E-22 1.4 [1.06-1.74] msec increase "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 16q21 "CNOT1,GINS3, NDRG4, SLC38A7, GOT2" rs37062-G rs37062 0.24 3.00E-25 1.75 [1.41-2.09] msec decrease "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 11p15.5 KCNQ1 rs2074238-T rs2074238 0.06 3.00E-17 7.88 [6.16-9.59] msec decrease "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 1q23.3 NOS1AP rs12143842-T rs12143842 0.26 2.00E-78 3.15 [2.81-3.49] msec increase "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 3/31/2009 19305408 Newton-Cheh 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305408?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci influence QT interval duation in the QTGEN Study QT interval "13,685 individuals" "15,854 individuals" 16p13.13 "LITAF,CLEC16A, SNN, ZC3H7A, TNFRSF17" rs8049607-T rs8049607 0.49 5.00E-15 1.23 [0.88-1.57] msec increase "Affymetrix and Illumina [up to 2,543,686] (imputed)" N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 1q23.3 NOS1AP rs4657178-T rs4657178 0.33 7.00E-33 2.19 [1.76-2.62] ms increase Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 1q24.2 ATP1B1 rs10919071-A rs10919071 0.87 1.00E-15 2.05 [1.48-2.62] ms increase Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 1p36.31 RNF207 rs846111-C rs846111 0.29 4.00E-16 1.49 [1.00-1.98] ms increase Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 11p15.5 KCNQ1 rs12296050-T rs12296050 0.2 3.00E-17 1.44 [0.95-1.93] ms increase Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 16p13.13 LITAF rs8049607-T rs8049607 0.46 6.00E-15 1.25 [0.81-1.69] ms increase Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 17q24.3 KCNJ2 rs17779747-T rs17779747 0.35 6.00E-12 1.02 [0.53-1.51] ms decrease Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 16q21 NDRG4 rs7188697-A rs7188697 0.74 7.00E-25 1.66 [1.20-2.12] ms increase Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 7q36.1 KCNH2 rs2968863-T rs2968863 0.29 2.00E-15 1.35 [0.90-1.80] ms decrease Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 6q22.31 PLN rs11970286-T rs11970286 0.44 2.00E-24 1.64 [1.25-2.03] ms increase Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 6q22.31 PLN rs12210810-C rs12210810 0.06 2.00E-17 3.13 [2.29-3.97] ms decrease Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 1q23.3 NOS1AP rs12143842-T rs12143842 0.24 2.00E-78 2.88 [2.43-3.33] ms increase Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19305409 Pfeufer 22-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19305409?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at ten loci modulate the QT interval duration in the QTSCD Study QT interval "15,842 individuals" "up to 13,602 individuals" 3p22.2 SCN5A rs11129795-A rs11129795 0.23 5.00E-14 1.27 [0.82-1.72] ms decrease Affymetrix and Illumina [unsure] (imputed) N 4/2/2009 19304780 Org 20-Mar-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19304780?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations Hypertension "364 cases, 590 controls" "1,043 cases, 1,769 controls" 16q23.3 CDH13 rs11646213-T rs11646213 0.6 0.000008 1.28 [1.15-1.43] "Affymetrix [395,912]" N 3/31/2009 19300482 Pillai 20-Mar-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19300482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci Chronic Obstructive Pulmonary Disease "823 cases, 810 controls" "2,840 family members, 389 cases, 472 controls" 15q25.1 "CHRNA3,CHRNA4,CHRNA5, IREB2, PSMA4, NP_001013641.2,Q9UD29" rs8034191-C rs8034191 0.33 1.00E-10 1.4 [1.18-1.67] "Ilumina [493,609]" N 3/31/2009 19300482 Pillai 20-Mar-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19300482?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study in Chronic Obstructive Pulmonary Disease (COPD): Identification of Two Major Susceptibility Loci Chronic Obstructive Pulmonary Disease "823 cases, 810 controls" "2,840 family members, 389 cases, 472 controls" 4q31.22 HHIP rs1828591-? rs1828591 NR 1.00E-07 1.38 [1.17-1.63] "Ilumina [493,609]" N 3/30/2009 19300499 Takeuchi 20-Mar-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19300499?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose" Warfarin maintenance dose "1,053 individuals" 588 individuals 10q23.33 CYP2C9 rs1799853-? rs1799853 0.11 1.00E-31 0.54 [0.45-0.63] mg/week decrease "Illumina [325,997]" N 3/30/2009 19300499 Takeuchi 20-Mar-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19300499?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose" Warfarin maintenance dose "1,053 individuals" 588 individuals 16p11.2 VKORC1 rs9923231-T rs9923231 0.4 0 0.97 [0.91-1.02] mg/week decrease "Illumina [325,997]" N 3/30/2009 19300499 Takeuchi 20-Mar-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19300499?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose" Warfarin maintenance dose "1,053 individuals" 588 individuals 10q23.33 CYP2C9 rs1057910-? rs1057910 0.07 3.00E-79 1.11 [1.00-1.22] mg/week decrease "Illumina [325,997]" N 3/30/2009 19300499 Takeuchi 20-Mar-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19300499?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "A Genome-Wide Association Study Confirms VKORC1, CYP2C9, and CYP4F2 as Principal Genetic Determinants of Warfarin Dose" Warfarin maintenance dose "1,053 individuals" 588 individuals 19p13.12 CYP4F2 rs2108622-? rs2108622 0.24 3.00E-10 0.21 [0.14-0.27] mg/week increase "Illumina [325,997]" N 3/31/2009 19300500 Wilk 20-Mar-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19300500?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study of Pulmonary Function Measures in the Framingham Heart Study Pulmonary function measures "7,691 individuals" 835 individuals 4q31.22 HHIP rs13147758-G rs13147758 0.39 8.00E-11 0.1 [NR] % increase in FEV1/FVC ratio "Affymetrix [2,540,223] (imputed)" N 4/1/2009 19303062 Tanaka 18-Mar-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19303062?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations" Folate pathway vitamin levels "2,934 individuals" 686 individuals 11q12.1 TCN1 rs526934-A rs526934 0.67 0.000002 (vitamin B12)  27.62 [11.65-43.59] pg/mL increase Affymetrix and Illumina [~2.5 million] (imputed) N 4/1/2009 19303062 Tanaka 18-Mar-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19303062?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations" Folate pathway vitamin levels "2,934 individuals" 686 individuals 19q13.33 FUT2 rs602662-A rs602662 0.53 3.00E-20 (vitamin B12)  49.77 [37.09-62.45] pg/ml increase Affymetrix and Illumina [~2.5 million] (imputed) N 4/1/2009 19303062 Tanaka 18-Mar-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19303062?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations" Folate pathway vitamin levels "2,934 individuals" 686 individuals 3p14.1 PRICKLE2 rs153734-T rs153734 0.84 0.000007 (folate)  0.29 [0.13-0.45] ng/ml increase Affymetrix and Illumina [~2.5 million] (imputed) N 4/1/2009 19303062 Tanaka 18-Mar-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19303062?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations" Folate pathway vitamin levels "2,934 individuals" 686 individuals 1p36.12 ALPL rs4654748-C rs4654748 0.5 8.00E-18 (vitamin B6)  1.45 [0.90-2.00] ng/ml decrease Affymetrix and Illumina [~2.5 million] (imputed) N 4/1/2009 19303062 Tanaka 18-Mar-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19303062?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide Association Study of Vitamin B6, Vitamin B12, Folate, and Homocysteine Blood Concentrations" Folate pathway vitamin levels "2,934 individuals" 686 individuals 10p13 CUBN rs11254363-A rs11254363 0.7 0.000001 (vitamin B12)  21.49 [7.71-35.27] pg/mL decrease Affymetrix and Illumina [~2.5 million] (imputed) N 3/31/2009 19287384 Kilpivaara 15-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19287384?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms Myeloproliferative neoplasms "324 cases, 2,999 controls" NR 9p24.1 JAK2 rs10974944-? rs10974944 NR 4.00E-20 3.1 [2.40-4.00] "Affymetrix [62,775]" N 3/31/2009 19287509 Cui 14-Mar-09 Mol Med http://www.ncbi.nlm.nih.gov/pubmed/19287509?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome Wide Association Study of Determinants of Anti-cyclic Citrullinated Peptide Antibody Titer in Adults with Rheumatoid Arthritis Anti-cyclic Citrullianted Peptide Antibody 531 individuals with rheumatoid arthritis 849 individuals with rheumatoid arthritis 6p21.32 "HLA-DRA, HLA-DR3,BTNL2" rs1980493-? rs1980493 0.13 5.00E-07 NR NR "Affymetrix [97,248]" N 3/29/2009 19282985 Liu 13-Mar-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19282985?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche Menarche (age at onset) 477 women "854 siblings, 762 women, 1,387 Chinese women" NR NR NR NR NS NS NR NR "Affymetrix [379,319]" N 3/30/2009 19278955 Tregouet 10-Mar-09 Blood http://www.ncbi.nlm.nih.gov/pubmed/19278955?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common susceptibility allele are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach Venous thromboembolism "419 cases, 1,228 controls" "1,757 cases, 1,480 controls" 9q34.2 ABO rs505922-C rs505922 0.35 4.00E-15 1.81 [1.56-2.11] "Illumina [291,872]" N 3/28/2009 19270707 Birnbaum 8-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19270707?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 Nonsyndromic cleft lip with or without cleft palate "224 cases, 383 controls" "246 cases, 954 controls" 1q32.2 IRF6 rs642961-A rs642961 NR 0.000002 NR NR "Illumina [521,176]" N 3/28/2009 19270707 Birnbaum 8-Mar-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19270707?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 Nonsyndromic cleft lip with or without cleft palate "224 cases, 383 controls" "246 cases, 954 controls" 8q24.21 "PVT1, GSDMC" rs987525-A rs987525 0.2 3.00E-24 2.57 [2.02-3.26] "Illumina [521,176]" N 3/24/2009 19268274 Liu 4-Mar-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19268274?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association and Replication Studies Identified TRHR as an Important Gene for Lean Body Mass Body mass (lean) "1,000 individuals" "1,488 individuals, 1,972 family members, 2,955 Chinese individuals" 8q23.1 TRHR rs7832552-T rs7832552 0.32 4.00E-10 0.1 [0.04-0.16] kg increase "Affymetrix [379,319]" N 3/24/2009 19268276 Vink 4-Mar-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19268276?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association Study of Smoking Initiation and Current Smoking Smoking behavior "3,540 individuals" "6,405 individuals, 824 twin pairs" NR NR NR NR NS NS NR NR "Perlegen [427,037]" N 3/28/2009 19259986 Hattori 2-Mar-09 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/19259986?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Preliminary genome-wide association study of bipolar disorder in the Japanese population Bipolar disorder "107 cases, 107 controls" "395 cases, 409 controls" NR NR NR NR NS NS NR NR "Affymetrix [88,671]" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 3q13.12 BBX rs6437740-? rs6437740 0.24 2.00E-07 (CPD)  0.1 [NR] fewer cigarettes per day "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 16p13.2 Intergenic rs3112740-? rs3112740 0.86 0.000006 (CPDBI)  2.16 [NR] "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 19p12 ZNF505 rs10411195-? rs10411195 0.03 0.000006 (CPD)  0.21 [NR] fewer cigarettes per day "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR Xq23 TRPC5 rs7050529-? rs7050529 0.07 0.000006 (CPD)  0.06 [NR] fewer cigarettes per day "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 17p13.2 CAMKK1 rs758642-? rs758642 0.34 0.000007 (CPD)  0.08 [NR] more cigarettes per day "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 3q27.2 Intergenic rs6444087-? rs6444087 0.26 0.000009 (EVNV)  1.28 [NR] "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 1p22.3 AK002179 rs7553864-? rs7553864 0.39 0.000003 (SMKDU)  0.08 [NR] more years "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 13q33.1 Intergenic rs912969-? rs912969 0.07 0.000008 (SMKDU)  0.14 [NR] fewer years "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 4q28.1 Intergenic rs950063-? rs950063 0.39 0.000009 (SMKDU)  0.08 [NR] fewer years "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 5q14.3 LOC133789 rs933688-? rs933688 0.17 0.000006 (EVNV)  1.48 [NR] "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 14q24.1 ACTN1 rs2268983-? rs2268983 0.51 0.000007 (CPDBI)  1.52 [NR] "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR Xp11.3 MAOA rs3027409-? rs3027409 0.95 0.000007 (CPDBI)  1.73 [NR] "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 7p15.2 Intergenic rs886716-? rs886716 0.69 0.000008 (CPDBI)  1.52 [NR] "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 18q11.2 CABLES1 rs11082304-? rs11082304 0.49 0.000006 (SMKAGE)  0.03 [NR] years older "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 4q31.1 SET7 rs17050782-? rs17050782 0.21 0.000008 (SMKAGE)  0.03 [NR] years older "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 1p35.2 Intergenic rs910696-? rs910696 0.31 0.000003 (CPD)  0.08 [NR] more cigarettes per day "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 3q24 Intergenic rs800082-? rs800082 0.42 0.000003 (PKYRS)  0.12 [NR] more pack years "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 12q21.2 Intergenic rs1402279-? rs1402279 0.95 0.000005 (EVNV)  1.51 [NR] "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 9p21.2 Intergenic rs1889899-? rs1889899 0.37 0.000006 (EVNV)  1.26 [NR] "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 9q31.1 Intergenic rs10989661-? rs10989661 0.74 0.000006 (CIGSTAT)  1.68 [NR] "Illumina [~518,000] (pooled)" N 4/1/2009 19247474 Caporaso 27-Feb-09 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/19247474?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide and candidate gene association study of cigarette smoking behaviors Smoking behavior "4,611 individuals (2,617 smokers)" NR 12q21.33 Intergenic rs1847461-? rs1847461 0.94 0.000008 (CIGSTAT)  1.8 [NR] "Illumina [~518,000] (pooled)" N 3/18/2009 19252134 Pezzolesi 27-Feb-09 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19252134?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association Scan for Diabetic Nephropathy Susceptibility Genes in Type 1 Diabetes Mellitus Diabetic nephropathy "820 cases, 885 controls" "1,304 individuals" NR NR NR NR NS NS NR NR "Affymetrix [359,193]" N 3/18/2009 19242412 Gu 25-Feb-09 Nature http://www.ncbi.nlm.nih.gov/pubmed/19242412?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease Cystic fibrosis severity "160 severe lung disease patients, 160 mild lung disease patients (all homozygous for CFTR deltaF508 variant)" "101 severe lung disease patients, 381 mild lung disease patients, 1,118 family members" NR NR NR NR NS NS NR NR "Affymetrix [100,198] (pooled)" N 3/18/2009 19249006 Xiong 25-Feb-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19249006?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association and Follow-Up Replication Studies Identified ADAMTS18 and TGFBR3 as Bone Mass Candidate Genes in Different Ethnic Groups Bone mineral density "1,000 white individuals" "4,925 white individuals, 350 Chinese hip fracture cases, 350 Chinese controls, 2,955 Chinese individuals, 908 West African men" 16q23.1 ADAMTS18 rs11864477-C rs11864477 0.12 2.00E-08 (hip BMD)  1 % [NR] of variance explained "Affymetrix [379,319]" N 3/18/2009 19249006 Xiong 25-Feb-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19249006?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association and Follow-Up Replication Studies Identified ADAMTS18 and TGFBR3 as Bone Mass Candidate Genes in Different Ethnic Groups Bone mineral density "1,000 white individuals" "4,925 white individuals, 350 Chinese hip fracture cases, 350 Chinese controls, 2,955 Chinese individuals, 908 West African men" 1p22.2 TGFBR3 rs17131547-A rs17131547 0.01 0.000001 (spine BMD)  1.2 % [NR] of variance explained "Affymetrix [379,319]" N 3/1/2009 19230858 Schrauwen 18-Feb-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19230858?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-wide Analysis Identifies Genetic Variants in the RELN Gene Associated with Otosclerosis Otosclerosis "302 cases, 302 controls" "847 cases, 872 controls" 7q22.1 RELN rs3914132-? rs3914132 0.23 2.00E-08 1.54 [1.32-1.79] "Illumina [~555,000] (pooled)" N 5/7/2009 19389651 Smith 15-Feb-09 Heart Rhythm http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae Electrocardiographic conduction measures "1,262 Kosraen individuals" NR 3p22.2 SCN5A rs7638909-G rs7638909 0.4 0.000002 (PR interval)  4.8 [2.84-6.76] ms increase "Affymetrix [338,049]" N 5/7/2009 19389651 Smith 15-Feb-09 Heart Rhythm http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae Electrocardiographic conduction measures "1,262 Kosraen individuals" NR 2q31.1 Intergenic rs2461751-G rs2461751 0.44 0.000008 (PR interval)  4.54 [2.58-6.50] ms increase "Affymetrix [338,049]" N 5/7/2009 19389651 Smith 15-Feb-09 Heart Rhythm http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae Electrocardiographic conduction measures "1,262 Kosraen individuals" NR 3p22.2 SCN5A rs2070488-A rs2070488 0.33 0.000004 (PR interval)  5 [2.84-7.16] ms decrease "Affymetrix [338,049]" N 5/7/2009 19389651 Smith 15-Feb-09 Heart Rhythm http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae Electrocardiographic conduction measures "1,262 Kosraen individuals" NR 4p16.1 MSX1 rs2008242-? rs2008242 0.15 0.000003 (PR segment)  NR NR "Affymetrix [338,049]" N 5/7/2009 19389651 Smith 15-Feb-09 Heart Rhythm http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae Electrocardiographic conduction measures "1,262 Kosraen individuals" NR 1q32.1 NR rs7512898-? rs7512898 0.41 0.000005 (PR segment)  NR NR "Affymetrix [338,049]" N 5/7/2009 19389651 Smith 15-Feb-09 Heart Rhythm http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae Electrocardiographic conduction measures "1,262 Kosraen individuals" NR 4q31.3 NR rs17030434-? rs17030434 0.43 0.000005 (P wave duration)  NR NR "Affymetrix [338,049]" N 5/7/2009 19389651 Smith 15-Feb-09 Heart Rhythm http://www.ncbi.nlm.nih.gov/pubmed/19389651?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae Electrocardiographic conduction measures "1,262 Kosraen individuals" NR 6p12.2 NR rs283566-? rs283566 0.16 0.000009 (P wave duration)  NR NR "Affymetrix [338,049]" N 2/28/2009 19219042 Zheng 15-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19219042?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1 Breast cancer "1,505 Chinese cases, 1,522 Chinese controls" "1,554 Chinese cases, 1,576 Chinese controls" 6q25.1 C6orf97 rs2046210-A rs2046210 0.37 2.00E-15 1.29 [1.21-1.37] "Affymetrix [up to 607,728]" N 2/28/2009 19221038 Soranzo 12-Feb-09 Blood http://www.ncbi.nlm.nih.gov/pubmed/19221038?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "A novel variant on chromosome 7Q22.3 associated with mean platelet volume, counts and function" Mean platelet volume "1,221 individuals" "7,365 individuals" 7q22.3 Intergenic rs342293-G rs342293 0.45 1.00E-24 0.02 [0.014-0.018] log fl increase "Affymetrix [361,352]" N 3/1/2009 19198612 Erdmann 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198612?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New susceptibility locus for coronary artery disease on chromosome 3q22.3 Coronary artery disease "6,990 cases, 8,955 controls" "12,417 cases, 12,411 controls" 12q24.31 "HNF1A,C12orf43" rs2259816-T rs2259816 0.36 5.00E-07 1.08 [1.05-1.11] "Affymetrix [567,119]" N 3/1/2009 19198612 Erdmann 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198612?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New susceptibility locus for coronary artery disease on chromosome 3q22.3 Coronary artery disease "6,990 cases, 8,955 controls" "12,417 cases, 12,411 controls" 3q22.3 MRAS rs9818870-T rs9818870 0.15 7.00E-13 1.15 [1.11-1.19] "Affymetrix [567,119]" N 3/1/2009 19198610 Gudbjartsson 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction Plasma eosinophil count "9,392 individuals" "12,118 individuals" 2q12.1 IL1RL1 rs1420101-A rs1420101 0.41 5.00E-14 (European)  6.4 [4.7-8.1] % standard unit increase "Illumina [312,179]" N 3/1/2009 19198610 Gudbjartsson 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction Plasma eosinophil count "9,392 individuals" "12,118 individuals" 12q24.12 SH2B3 rs3184504-T rs3184504 0.38 7.00E-19 (European)  7.6 [5.9-9.3] % standard unit increase "Illumina [312,179]" N 3/1/2009 19198610 Gudbjartsson 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction Plasma eosinophil count "9,392 individuals" "12,118 individuals" 5q31.1 IL5 rs4143832-C rs4143832 0.16 1.00E-10 (European)  7.1 [4.9-9.2] % standard unit increase "Illumina [312,179]" N 3/1/2009 19198610 Gudbjartsson 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction Plasma eosinophil count "9,392 individuals" "12,118 individuals" 6p21.32 MHC rs2269426-T rs2269426 0.76 0.000003 (European)  4.6 [2.7-6.6] % standard unit increase "Illumina [312,179]" N 3/1/2009 19198610 Gudbjartsson 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction Plasma eosinophil count "9,392 individuals" "12,118 individuals" 2q34 IKZF2 rs12619285-G rs12619285 0.74 5.00E-10 (European)  6.3 [4.3-8.3] % standard unit increase "Illumina [312,179]" N 3/1/2009 19198610 Gudbjartsson 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction Plasma eosinophil count "9,392 individuals" "12,118 individuals" 5q22.1 "WDR36, TSLP" rs2416257-G rs2416257 0.85 0.000001 (European)  6.1 [3.7-8.6] % standard unit increase "Illumina [312,179]" N 3/1/2009 19198610 Gudbjartsson 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198610?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction Plasma eosinophil count "9,392 individuals" "12,118 individuals" 3q21.3 GATA2 rs4857855-T rs4857855 0.82 9.00E-17 (European)  9.4 [7.2-11.6] % standard unit increase "Illumina [312,179]" N 3/1/2009 19198609 Kathiresan 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial infarction (early onset) "2,967 cases, 3,075 controls" "9,746 cases, 9,746 controls" 1p32.3 PCSK9 rs11206510-T rs11206510 0.81 1.00E-08 1.15 [1.10-1.21] Affymetrix [~2.5 million] (imputed) N 3/1/2009 19198609 Kathiresan 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial infarction (early onset) "2,967 cases, 3,075 controls" "9,746 cases, 9,746 controls" 19p13.2 LDLR rs1122608-G rs1122608 0.75 2.00E-09 1.15 [1.10-1.20] Affymetrix [~2.5 million] (imputed) N 3/1/2009 19198609 Kathiresan 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial infarction (early onset) "2,967 cases, 3,075 controls" "9,746 cases, 9,746 controls" 21q22.11 "SLC5A3, MRPS6, KCNE2" rs9982601-T rs9982601 0.13 6.00E-11 1.2 [1.14-1.27] Affymetrix [~2.5 million] (imputed) N 3/1/2009 19198609 Kathiresan 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial infarction (early onset) "2,967 cases, 3,075 controls" "9,746 cases, 9,746 controls" 10q11.21 CXCL12 rs1746048-C rs1746048 0.84 7.00E-09 1.17 [1.11-1.24] Affymetrix [~2.5 million] (imputed) N 3/1/2009 19198609 Kathiresan 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial infarction (early onset) "2,967 cases, 3,075 controls" "9,746 cases, 9,746 controls" 9p21.3 "CDKN2A, CDKN2B" rs4977574-G rs4977574 0.56 3.00E-44 1.29 [1.25-1.34] Affymetrix [~2.5 million] (imputed) N 3/1/2009 19198609 Kathiresan 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial infarction (early onset) "2,967 cases, 3,075 controls" "9,746 cases, 9,746 controls" 6p24.1 PHACTR1 rs12526453-C rs12526453 0.65 1.00E-09 1.12 [1.08-1.17] Affymetrix [~2.5 million] (imputed) N 3/1/2009 19198609 Kathiresan 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial infarction (early onset) "2,967 cases, 3,075 controls" "9,746 cases, 9,746 controls" 2q33.1 WDR12 rs6725887-C rs6725887 0.14 1.00E-08 1.17 [1.11-1.23] Affymetrix [~2.5 million] (imputed) N 3/1/2009 19198609 Kathiresan 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial infarction (early onset) "2,967 cases, 3,075 controls" "9,746 cases, 9,746 controls" 1p13.3 "CELSR2, PSRC1, SORT1" rs646776-T rs646776 0.81 8.00E-12 1.19 [1.13-1.26] Affymetrix [~2.5 million] (imputed) N 3/1/2009 19198609 Kathiresan 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198609?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial infarction (early onset) "2,967 cases, 3,075 controls" "9,746 cases, 9,746 controls" 1q41 MIA3 rs17465637-C rs17465637 0.72 1.00E-09 1.14 [1.10-1.19] Affymetrix [~2.5 million] (imputed) N 4/1/2009 19198611 Tregouet 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198611?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease Coronary artery disease "1,926 cases, 2,938 controls" "7,073 cases, 7,325 controls" 6q25.3 "SLC22A3,LPAL2,LPA" 4-SNP haplotype-1 "rs7767084,rs10755578,rs2048327,rs3127599" 0.16 1.00E-09 (CTTG)  1.2 [1.13-1.28] "Affymetrix [~500,000]" N 4/1/2009 19198611 Tregouet 8-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198611?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease Coronary artery disease "1,926 cases, 2,938 controls" "7,073 cases, 7,325 controls" 6q25.3 "SLC22A3,LPAL2,LPA" 4-SNP haplotype-2 "rs2048327,rs3127599,rs7767084,rs10755578" 0.02 4.00E-15 (CCTC)  1.82 [1.57-2.12] "Affymetrix [~500,000]" N 2/28/2009 19198613 Gudmundsson 6-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198613?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations Thyroid cancer "192 cases, 37,196 controls" "432 cases, 1,727 controls" 14q13.3 NKX2-1 rs944289-T rs944289 0.57 2.00E-09 1.37 [1.24-1.52] "Illumina [304,083]" N 2/28/2009 19198613 Gudmundsson 6-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19198613?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations Thyroid cancer "192 cases, 37,196 controls" "432 cases, 1,727 controls" 9q22.33 FOXE1 rs965513-A rs965513 0.34 2.00E-27 1.75 [1.59-1.94] "Illumina [304,083]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 12q24.31 SPPL3 rs1039302-T rs1039302 0.36 0.000005 (CRP)  0.21 [NR] mg/L increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 12p13.33 "ENSG00000118975, FKBP4" rs10848704-C rs10848704 0.35 0.000002 (TSH)  0.29 [NR] mIU/L decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 5q35.3 MGAT1 rs655601-A rs655601 0.47 0.000005 (HDL-C)  0.23 [NR] mg/dL increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 19q13.32 "MGC2650, BLOC1S3, XTP7" rs2159324-T rs2159324 0.44 4.00E-07 (LDL-C)  0.21 [NR] mg/dL decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 5q13.3 "COL4A3BP, HMGCR" rs3846663-T rs3846663 0.39 0.000001 (LDL-C)  0.21 [NR] mg/dL increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 10p15.3 ADARB2 rs6560749-T rs6560749 0.14 0.000002 (BMI)  0.32 [NR] kg/m2 decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 7p14.1 Intergenic rs10486715-A rs10486715 0.07 0.000003 (height)  0.44 [NR] inch decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 3q25.33 SCHIP1 rs2222328-C rs2222328 0.32 8.00E-07 (WC)  0.22 [NR] inch decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 9p21.3 Intergenic rs613391-G rs613391 0.49 0.000005 (WC)  0.2 [NR] inch increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 9p21.3 Intergenic rs2225614-C rs2225614 0.5 0.000003 (weight)  0.21 [NR] lb. decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 2q22.2 ARHGAP15 rs10928195-C rs10928195 0.08 0.000004 (weight)  0.36 [NR] lb. decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 7q34 TRIM24 rs1874326-G rs1874326 0.47 0.000009 (weight)  0.22 [NR] lb. increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 20q13.12 Intergenic rs6066084-A rs6066084 0.06 0.000002 (% body fat)  0.85 [NR] % increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 10p15.3 ADARB2 rs6560749-T rs6560749 0.14 0.000008 (% body fat)  0.34 [NR] % decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 6p22.3 Intergenic rs10498712-G rs10498712 0.25 0.000009 (HDL-C)  0.23 [NR] mg/dL increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 19q13.32 "MGC2650, BLOC1S3, XTP7" rs2159324-T rs2159324 0.44 0.000002 (CRP)  0.19 [NR] mg/L decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 19q13.32 "TOMMM40, APOC2, APOE, APOC4, APOC1" rs4420638-G rs4420638 0.21 3.00E-07 (TC)  0.28 [NR] mg/dL increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 5q13.3 "COL4A3BP, HMGCR" rs3846663-T rs3846663 0.39 0.000006 (TC)  0.19 [NR] mg/dL increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 10p13 ITGA8 rs7895372-G rs7895372 0.04 0.000006 (TC)  0.35 [NR] mg/dL decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 7p21.3 Intergenic rs17157663-A rs17157663 0.32 0.000009 (TC)  0.18 [NR] mg/dL decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 11q23.3 Intergenic rs7396835-T rs7396835 0.32 1.00E-09 (TG)  0.23 [NR] mg/dL increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 4q21.21 Intergenic rs10518224-A rs10518224 0.23 0.000007 (TG)  0.19 [NR] mg/dL increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 19q13.32 "TOMM40, APOC2, APOE, APOC4, APOC1" rs4420638-G rs4420638 0.21 0.000005 (TG)  0.22 [NR] mg/dL increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 10p12.33 CACNB2 rs7069923-C rs7069923 0.49 0.000001 (SBP)  0.19 [NR] mm Hg increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 7q36.3 UBE3C rs2527866-C rs2527866 0.23 0.000003 (SBP)  0.27 [NR] mm Hg decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 5q35.1 Intergenic rs254893-A rs254893 0.06 0.000006 (DBP)  0.58 [NR] mm Hg decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 10p13 CUBN rs10508517-A rs10508517 0.43 0.000006 (DBP)  0.18 [NR] mm Hg decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 9q22.33 "HEMGN, C9ORF156" rs755109-C rs755109 0.23 0.000001 (TSH)  0.31 [NR] mIU/L decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 7p22.2 SDK1 rs6462411-C rs6462411 0.2 0.000001 (TSH)  0.36 [NR] mIU/L decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 19q13.32 "TOMM40, APOC2, APOE, APOC4, APOC1" rs4420638-G rs4420638 0.21 0.000002 (CRP)  0.28 [NR] mg/L decrease "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 2p23.3 "ENSG0000173957, UBXD4, FKBP1B, FLJ21945" rs7561273-A rs7561273 0.35 0.000006 (CRP)  0.22 [NR] mg/L decrease] "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 12q24.13 Intergenic rs11066587-G rs11066587 0.16 0.000005 (CRP)  0.26 [NR] mg/L increase "Affymetrix [408,775]" N 10/15/2009 19197348 Lowe 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197348?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae Quantitative traits "Up to 2,906 Micronesian individuals" NR 6q16.2 Intergenic rs6909430-G rs6909430 0.08 0.000008 (TSH)  0.49 [NR] mIU/L decrease "Affymetrix [408,775]" N 8/21/2009 19197363 Need 6-Feb-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19197363?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide investigation of SNPs and CNVs in schizophrenia Schizophrenia "871 European ancestry cases, 863 European ancestry controls" "1,460 European ancestry cases, 12,995 European ancestry controls" NR NR NR NR NS NS NR NR "Illumina [312,565] (pooled)" N 2/27/2009 19196962 Garcia-Barcelo 5-Feb-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19196962?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease Hirschsprung's disease "181 Chinese cases, 346 Chinese controls" "190 Chinese cases, 510 Chinese controls" 8p12 NRG1 rs16879552-G rs16879552 0.39 2.00E-08 1.68 [1.40-2.00] "Affymetrix [293,836]" N 2/27/2009 19196962 Garcia-Barcelo 5-Feb-09 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19196962?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease Hirschsprung's disease "181 Chinese cases, 346 Chinese controls" "190 Chinese cases, 510 Chinese controls" 10q21.1 "RET, GALNACT-2, RASGEF1A" rs2742234-T rs2742234 NR 4.00E-18 NR NR "Affymetrix [293,836]" N 3/31/2009 19193627 Chio 4-Feb-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19193627?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "553 cases, 2,338 controls" "3,149 cases, 3,335 controls" NR NR NR NR NS NS NR NR "Illumina [545,066]" N 2/27/2009 19188921 Liu 3-Feb-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19188921?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analyses suggested a novel mechanism for smoking behavior regulated by IL15 Smoking behavior "417 Caucasian males, 423 Caucasian females" "412 African American males, 839 African American females, 3,491 Caucasian males, 4,132 Caucasian females" NR NR NR NR NS NS NR NR "Affymetrix [379,319]" N 2/28/2009 19187332 Kim 1-Feb-09 Clin Exp Allergy http://www.ncbi.nlm.nih.gov/pubmed/19187332?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis Asthma (toluene diisocyanate-induced) "84 Korean cases, 263 Korean controls" NR 10q21.3 CTNNA3 rs10762058-G rs10762058 0.25 0.000006 5 [2.36-10.6] "Affymetrix [312,978]" N 2/28/2009 19187332 Kim 1-Feb-09 Clin Exp Allergy http://www.ncbi.nlm.nih.gov/pubmed/19187332?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis Asthma (toluene diisocyanate-induced) "84 Korean cases, 263 Korean controls" NR 13q12.13 Intergenic rs9319321-T rs9319321 0.29 0.000003 5.2 [2.47-10.92] "Affymetrix [312,978]" N 2/28/2009 19187332 Kim 1-Feb-09 Clin Exp Allergy http://www.ncbi.nlm.nih.gov/pubmed/19187332?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis Asthma (toluene diisocyanate-induced) "84 Korean cases, 263 Korean controls" NR 9p21.3 Intergenic rs16937883-G rs16937883 0.02 0.000007 5.29 [2.41-11.61] "Affymetrix [312,978]" N 2/27/2009 19207018 Kim 1-Feb-09 Pharmacogenomics http://www.ncbi.nlm.nih.gov/pubmed/19207018?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of acute post-surgical pain in humans Pain "60 females, 52 males" NR 19p12 "LOC400680, ZNF429" rs2562456-? rs2562456 NR 2.00E-10 (onset time of analgesia)  NR NR "Affymetrix [374,975]" N 2/27/2009 19207018 Kim 1-Feb-09 Pharmacogenomics http://www.ncbi.nlm.nih.gov/pubmed/19207018?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of acute post-surgical pain in humans Pain "60 females, 52 males" NR 11q23.3 NR rs17122021-? rs17122021 NR 7.00E-07 (maximum post-operative pain rating)  NR NR "Affymetrix [374,975]" N 2/27/2009 19207018 Kim 1-Feb-09 Pharmacogenomics http://www.ncbi.nlm.nih.gov/pubmed/19207018?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of acute post-surgical pain in humans Pain "60 females, 52 males" NR 1p21.3 NR rs6693882-? rs6693882 NR 0.000002 (post-operative pain onset time)  NR NR "Affymetrix [374,975]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 14q32.13 "LOC122509, FAM14B" rs7157940-? rs7157940 0.46 0.000003 (weight)  0.12 [0.07-0.17] kg increase "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 2q31.1 Intergenic rs7590983-? rs7590983 0.05 0.000006 (BMI)  0.46 [0.26-0.66] kg/m2 increase "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 7q22.1 ZNF498 rs7792939-? 0.15 0.000006 (hip circumference)  0.26 [0.15-0.37] mm increase "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 5q33.3 SGCD rs157350-? 0.11 0.000006 (hip circumference)  0.31 [0.18-0.44] mm decrease "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 5q33.2 "AMPA1, GRIA1" rs12658202-? rs12658202 0.45 0.000009 (height)  0.11 [0.06-0.16] mm increase "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 2p22.3 CRIM1 rs1863080-? rs1863080 0.1 0.000008 (brachial circumference)  0.31 [0.17-0.45] mm increase "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 7q22.1 ZNF498 rs7792939-? 0.15 0.000004 (weight)  0.26 [0.15-0.37] kg increase "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 7q22.1 ZNF498 rs7792939-? "rs7792939,rs7792939,rs7792939" 0.15 0.000005 (brachial circumference)  0.26 [0.15-0.37] mm increase "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 5q33.3 SGCD rs157350-? rs157350 0.11 0.000004 (brachial circumference)  0.31 [0.18-0.44] mm decrease "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 13q14.3 XTP498 rs7792939-? rs7792939 0.28 0.000006 (brachial circumference)  0.17 [0.10-0.24] mm increase "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 16p11.2 SEZ6L2 rs4787483-? rs4787483 0.34 0.000002 (waist cirumference)  0.16 [0.09-0.23] mm increase "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 14q23.3 MAX rs7158173-? rs7158173 0.48 0.000004 (waist circumference)  0.11 [0.06-0.16] mm decrease "Illumina [316,730]" N 3/30/2009 19260139 Polasek 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260139?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of anthropometric traits in Korcula Island, Croatia" Anthropometric traits 898 individuals NR 1p36.32 Intergenic rs7513590-? rs7513590 0.1 0.000005 (height)  0.31 [0.17-0.45] mm decrease "Illumina [316,730]" N 2/25/2009 19182806 Stefansson 1-Feb-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19182806?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variant in the sequence of the LINGO1 gene confers risk of essential tremor Essential tremor "452 cases, 14,378 controls" "300 cases, 1,419 controls" 15q24.3 LINGO1 rs9652490-G rs9652490 0.23 1.00E-09 1.55 [1.35-1.79] "Illumina [305,624]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 6q16.3 GRIK2 rs12207601-G rs12207601 0.16 0.000002 (fibrinogen)  0.26 [0.15-0.37] g/L decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 21q22.3 PKNOX1 rs2839619-G "rs2839619,rs2839619" 0.4 0.000008 (total cholesterol)  0.13 [0.07-0.19] mmol/L increase "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 12q24.23 KSR2 rs10444502-C rs10444502 0.28 0.000006 (total cholesterol)  0.17 [0.10-0.24] mmol/L decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR Xp22.31 Neuroligin 4 rs7885458-G rs7885458 0.24 0.000003 (fibrinogen)  0.23 [0.13-0.33] g/L decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 4p16.1 SLC2A9 rs13129697-C rs13129697 0.25 1.00E-09 (uric acid)  0.29 [0.21-0.37] umol/l decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 18q12.3 SLC14A2 rs10502868-G rs10502868 0.08 0.000007 (albumin)  0.04 [0.21-0.51] g/L decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 4q13.1 LPHN3 rs4599440-A rs4599440 0.23 0.000002 (HDL cholesterol)  0.2 [0.12-0.28] mmol/L increase "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 12q12 Intergenic rs871392-A rs871392 0.15 0.000003 (HDL cholesterol)  0.26 [0.15-0.37] mmol/L decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 16q13 CETP rs7499892-A rs7499892 0.16 0.000009 (HDL cholesterol)  0.24 [0.14-0.34] mmol/L decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 12q24.23 KSR2 rs4767631-A rs4767631 0.31 6.00E-07 (LDL cholesterol)  0.12 [0.11-0.23] mmol/L decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 21q22.3 PKNOX1 rs2839619-G 0.4 0.000008 (LDL cholesterol)  0.13 [0.08-0.18] mmol/L increase "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 4q23 RAP1GDS1 rs10516430-A rs10516430 0.28 0.000006 (triglycerides)  0.16 [0.09-0.23] mmol/L decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 4q12 USP46 rs346923-A rs346923 0.13 0.000002 (triglycerides)  0.28 [0.17-0.39] mmol/L decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 4q31.23 NR3C2 rs1490453-A rs1490453 0.17 0.000003 (fibrinogen)  0.25 [0.15-0.35] g/L increase "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 20p12.1 PCSK2 rs6044777-A rs6044777 0.17 0.000008 (fibrinogen)  0.23 [0.13-0.33] g/L increase "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR 12q21.33 Intergenic rs10777332-A rs10777332 0.11 0.000005 (total cholesterol)  0.24 [0.14-0.34] mmol/L decrease "Illumina [316,730]" N 3/31/2009 19260141 Zemunik 1-Feb-09 Croat Med J http://www.ncbi.nlm.nih.gov/pubmed/19260141?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genome-wide association study of biochemical traits in Korcula Island, Croatia" Biochemical measures 898 individuals NR Xq23 ZCCHC16 rs5982533-G rs5982533 0.22 0.000007 (triglycerides)  0.23 [0.13-0.33] mmol/L decrease "Illumina [316,730]" N 2/25/2009 19181680 Timpson 30-Jan-09 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19181680?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants in the region around Osterix are associated with bone mineral density and growth in childhood Bone mineral density "1,418 children, 135 adults" "3,875 children" NR NR NR NR NS NS NR NR "Illumina [up to 315,807]" N 2/28/2009 19185284 Ferrucci 29-Jan-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19185284?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study" Plasma carotenoid and tocopherol levels "1,191 individuals" "2,751 individuals" 16q23.2 BCMO1 rs6564851-G rs6564851 0.39 2.00E-24 (beta-carotene)  0.15 [0.120-0.177] umol/L increase "Illumina [~500,451] (pooled)" N 2/28/2009 19185284 Ferrucci 29-Jan-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19185284?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study" Plasma carotenoid and tocopherol levels "1,191 individuals" "2,751 individuals" 11q23.3 APOA5 rs12272004-A rs12272004 0.07 8.00E-10 (alpha-tocopherol)  0.07 [0.049-0.095] umol/L increase "Illumina [~500,451] (pooled)" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 10p14 Intergenic rs10508343-A rs10508343 0.04 0.000008 3.81 [1.40-10.40] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 10q26.12 intergenic rs2901286-A rs2901286 0.03 0.000004 4.66 [1.58-13.7] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 7p21.2 DGKB rs6971925-T rs6971925 0.02 0.000003 13.91 [2.72-70.92] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 11p15.1 intergenic rs7128311-C rs7128311 0.03 0.000005 13.9 [2.72-71.1] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 11q21 MAML2 rs7115578-A rs7115578 0.64 0.000008 1.86 [1.23-2.79] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 10p12.33 ST8SIA6 rs359312-T rs359312 0.04 9.00E-08 3.91 [1.52-10.10] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 4q31.21 IL15 rs17007695-C rs17007695 0.1 9.00E-07 2.67 [1.53-4.68] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 7p14.2 ELMO1 rs4723619-C rs4723619 0.07 0.000003 3.01 [1.50-6.03] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 6q25.3 intergenic rs35229355-T rs35229355 0.03 0.000005 7.24 [2.46-21.30] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 5p13.2 LMBRD2 rs267759-A rs267759 0.05 0.000007 3.23 [1.52-6.87] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 2q33.1 C2orf47 rs1569175-T rs1569175 0.11 9.00E-07 2.73 [1.52-4.93] "Affymetrix [476,796]" N 2/26/2009 19176441 Yang 28-Jan-09 JAMA http://www.ncbi.nlm.nih.gov/pubmed/19176441?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia Treatment response for acute lymphoblastic leukemia 487 children NR 20q13.12 NCOA3 rs6125048-T rs6125048 0.04 0.000002 2.73 [1.08-6.88] "Affymetrix [476,796]" N 2/6/2009 19169254 Nair 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways Psoriasis "1,359 cases, 1,400 controls" "5,048 cases, 5,041 controls" 1p31.3 IL23R rs2201841-G rs2201841 0.3 3.00E-08 1.13 [NR] Perlegen [~2.5 million] (imputed) N 2/6/2009 19169254 Nair 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways Psoriasis "1,359 cases, 1,400 controls" "5,048 cases, 5,041 controls" 12q13.2 "IL23A, STAT2" rs2066808-A rs2066808 0.93 1.00E-09 1.34 [NR] Perlegen [~2.5 million] (imputed) N 2/6/2009 19169254 Nair 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways Psoriasis "1,359 cases, 1,400 controls" "5,048 cases, 5,041 controls" 6q23.3 TNFAIP3 rs610604-G rs610604 0.32 9.00E-12 1.19 [NR] Perlegen [~2.5 million] (imputed) N 2/6/2009 19169254 Nair 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways Psoriasis "1,359 cases, 1,400 controls" "5,048 cases, 5,041 controls" 5q33.1 TNIP1 rs17728338-A rs17728338 0.054 1.00E-20 1.59 [NR] Perlegen [~2.5 million] (imputed) N 2/6/2009 19169254 Nair 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways Psoriasis "1,359 cases, 1,400 controls" "5,048 cases, 5,041 controls" 6p21.33 HLA-C rs12191877-T rs12191877 0.15 1.00E-100 2.64 [NR] Perlegen [~2.5 million] (imputed) N 2/6/2009 19169254 Nair 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways Psoriasis "1,359 cases, 1,400 controls" "5,048 cases, 5,041 controls" 5q31.1 IL13 rs20541-G rs20541 0.79 5.00E-15 1.27 [NR] Perlegen [~2.5 million] (imputed) N 2/6/2009 19169254 Nair 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways Psoriasis "1,359 cases, 1,400 controls" "5,048 cases, 5,041 controls" 5q33.3 IL12B rs2082412-G rs2082412 0.8 2.00E-28 1.44 [NR] Perlegen [~2.5 million] (imputed) N 2/6/2009 19169254 Nair 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169254?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways Psoriasis "1,359 cases, 1,400 controls" "5,048 cases, 5,041 controls" 9q34.13 TSC1 rs1076160-T rs1076160 0.48 0.000006 1.09 [NR] Perlegen [~2.5 million] (imputed) N 2/7/2009 19169255 Zhang 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169255?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21 Psoriasis "1,139 Chinese cases, 1,132 Chinese controls" "5,721 Chinese cases, 7,340 Chinese controls" 1q21.3 "LCE3D, LCE3A" rs4085613-A rs4085613 0.43 7.00E-30 1.32 [1.25-1.39] "Illumina [494,902]" N 2/7/2009 19169255 Zhang 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169255?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21 Psoriasis "1,139 Chinese cases, 1,132 Chinese controls" "5,721 Chinese cases, 7,340 Chinese controls" 5q33.3 IL12B rs3213094-A rs3213094 0.45 3.00E-26 1.28 [1.23-1.35] "Illumina [494,902]" N 2/7/2009 19169255 Zhang 25-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19169255?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21 Psoriasis "1,139 Chinese cases, 1,132 Chinese controls" "5,721 Chinese cases, 7,340 Chinese controls" 6p21.33 MHC rs1265181-? rs1265181 NR NS NS 22.62 "Illumina [494,902]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 19q13.33 Intergenic rs3810265-? rs3810265 0.07 0.000004 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 20p13 SMOX rs16989303-? rs16989303 0.21 0.000006 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 1q32.1 PKP1 rs860554-? rs860554 0.05 5.00E-08 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 6q25.1 PLEKHG1 rs9372078-? rs9372078 0.11 5.00E-07 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 8p21.1 CLU rs17466684-? rs17466684 0.09 7.00E-07 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 12p13.31 TMEM16B rs12579350-? rs12579350 0.01 4.00E-09 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 12q24.33 Intergenic rs7299940-? rs7299940 0.29 0.000007 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 3p26.1 GRM7 rs3749380-? rs3749380 0.25 0.000002 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 14q23.1 Intergenic rs4901869-? rs4901869 0.02 0.000006 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 21q21.1 USP25 rs2823455-? rs2823455 0.03 0.000009 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 1p13.3 Intergenic rs12061304-? rs12061304 0.1 0.000001 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 12q13.13 CALCOCO1 rs941184-? rs941184 0.03 3.00E-07 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 13q32.1 Intergenic rs9302001-? rs9302001 0.2 3.00E-07 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 17q25.1 SDK2 rs3816995-? rs3816995 0.03 2.00E-07 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 5q21.1 Intergenic rs4702982-? rs4702982 0.16 0.000006 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 6p12.3 TNFRSF21 rs2103868-? rs2103868 0.26 0.000005 NR NR "Affymetrix [253,903]" N 2/26/2009 19165232 Otowa 23-Jan-09 J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19165232?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of panic disorder in the Japanese population Panic disorder "200 Japanese cases, 200 Japanese controls" NR 12q12 Intergenic rs2731006-? rs2731006 0.29 0.000004 NR NR "Affymetrix [253,903]" N 2/25/2009 19165155 Ling 22-Jan-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19165155?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Linkage and Association Anaylses to Identify Genes Influencing Adiponectin Levels: The GEMS Study Adiponectin levels "997 cases, 989 controls" NR 5q35.2 Intergenic rs7722022-? rs7722022 NR 0.000009 NR NR "Affymetrix [398,625]" N 2/25/2009 19165155 Ling 22-Jan-09 Obesity http://www.ncbi.nlm.nih.gov/pubmed/19165155?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Linkage and Association Anaylses to Identify Genes Influencing Adiponectin Levels: The GEMS Study Adiponectin levels "997 cases, 989 controls" NR 3q27.3 ADIPOQ rs6773957-A rs6773957 0.37 5.00E-08 NR NR "Affymetrix [398,625]" N 3/3/2009 19151714 Meyre 18-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19151714?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations Obesity "695 obese adults, 685 obese children, 731 lean adults, 685 lean children" "1,171 obese adults, 896 obese children, 1,114 lean adults, 1,297 lean children, 4,417 adults, 5,291 children" 18q21.32 MC4R rs17782313-C rs17782313 0.18 5.00E-15 (children)  1.22 [1.05-1.40] "Illumina [308,846]" N 3/3/2009 19151714 Meyre 18-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19151714?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations Obesity "695 obese adults, 685 obese children, 731 lean adults, 685 lean children" "1,171 obese adults, 896 obese children, 1,114 lean adults, 1,297 lean children, 4,417 adults, 5,291 children" 18q11.2 NPC1 rs1805081-A rs1805081 0.56 3.00E-07 (children)  1.33 [1.08-1.75] "Illumina [308,846]" N 3/3/2009 19151714 Meyre 18-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19151714?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations Obesity "695 obese adults, 685 obese children, 731 lean adults, 685 lean children" "1,171 obese adults, 896 obese children, 1,114 lean adults, 1,297 lean children, 4,417 adults, 5,291 children" 16q23.2 MAF rs1424233-A rs1424233 0.43 4.00E-13 (children)  1.12 [1.00-1.24] "Illumina [308,846]" N 3/3/2009 19151714 Meyre 18-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19151714?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations Obesity "695 obese adults, 685 obese children, 731 lean adults, 685 lean children" "1,171 obese adults, 896 obese children, 1,114 lean adults, 1,297 lean children, 4,417 adults, 5,291 children" 10p13 PTER rs10508503-C rs10508503 0.91 2.00E-07 (children)  1.56 [1.10-2.78] "Illumina [308,846]" N 3/3/2009 19151714 Meyre 18-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19151714?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations Obesity "695 obese adults, 685 obese children, 731 lean adults, 685 lean children" "1,171 obese adults, 896 obese children, 1,114 lean adults, 1,297 lean children, 4,417 adults, 5,291 children" 16q12.2 FTO rs1421085-C rs1421085 0.4 1.00E-28 (children)  1.39 [1.27-1.51] "Illumina [308,846]" N 1/21/2009 19148276 Tanaka 16-Jan-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19148276?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study Plasma levels of polyunsaturated fatty acids "1,210 individuals" "1,076 individuals" NR NR NR NR NS NS NR NR "Illumina [495,343]" N 2/27/2009 19136949 Carrasquillo 11-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19136949?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease Alzheimer's disease "844 cases, 1,255 controls" "1,547 cases, 1,209 controls" Xq21.31 PCDH11X rs2573905-? rs2573905 0.46 2.00E-07 1.29 [1.17-1.42] "Illumina [313,504]" N 1/21/2009 19132087 Burgner 9-Jan-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19132087?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study identifies novel and functionally related susceptibility loci for Kawasaki disease Kawasaki disease "107 cases, 134 controls" "583 cases, 1,357 family members" 3q26.31 NAALADL2 rs17531088-T rs17531088 0.44 0.000001 1.43 [1.32-1.53] "Affymetrix [223,922]" N 1/21/2009 19132087 Burgner 9-Jan-09 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19132087?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study identifies novel and functionally related susceptibility loci for Kawasaki disease Kawasaki disease "107 cases, 134 controls" "583 cases, 1,357 family members" 16q22.3 ZFHX3 rs7199343-T rs7199343 0.3 0.000002 1.56 [1.33-1.92] "Affymetrix [223,922]" N 2/25/2009 19125160 Feulner 7-Jan-09 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19125160?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Examination of the current top candidate genes for AD in a genome-wide association study Alzheimer's disease "491 cases, 479 controls" NR 19q13.32 "TOMM40, APOE" rs157580-? rs157580 NR 1.00E-40 NR NR "Illumina [~550,000]" N 1/21/2009 19124843 Ober 7-Jan-09 J Lipid Res http://www.ncbi.nlm.nih.gov/pubmed/19124843?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of plasma Lp(a)levels Identifies multiple genes on chromosome 6q Plasma Lp (a) levels 357 individuals "1,054 individuals" 6q25.3 LPA rs6919346-? rs6919346 0.16 4.00E-11 0.66 [mg/dl decrease] "Affymetrix [290,327]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 12q15 "IFNG, IL26, IL22" rs1558744-A rs1558744 0.38 3.00E-12 1.35 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 7q31.1 "SLC26A3, DLD, LAMB1" rs2158836-A rs2158836 0.35 0.000007 1.21 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 7q31.1 Intergenic rs4730273-? rs4730273 0.7 0.000005 1.22 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 6p21.32 "BTNL2, HLA-DRA, HLA-DRB5, HLA-DRB1, HLA-DQA1, HLA-DQB1" rs2395185-? rs2395185 0.67 1.00E-16 1.52 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 12q15 IL26 rs2870946-G rs2870946 0.055 5.00E-07 1.54 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 7q31.1 "SLC26A3, DLD, LAMB1" rs4730276-? rs4730276 0.39 0.000009 1.22 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 1p36.13 RNF186 rs3806308-? rs3806308 0.63 7.00E-09 1.28 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 1p36.13 "OTUD3, PLA2G2E" rs6426833-G rs6426833 0.54 5.00E-13 1.37 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 1p31.3 IL23R rs10889677-A rs10889677 0.3 1.00E-08 1.29 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 7q31.1 "SLC26A3, DLD, LAMB1" rs4598195-? rs4598195 0.54 0.000001 1.23 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 9q21.32 Intergenic rs668853-G rs668853 0.39 0.000002 1.2 "Illumina [280,748]" N 1/21/2009 19122664 Silverberg 4-Jan-09 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19122664?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Ulcerative colitis "1,022 cases, 2,503 controls" "1,387 cases, 1,115 controls" 1p31.3 IL23R rs11209026-? rs11209026 0.93 1.00E-08 1.79 "Illumina [280,748]" N 1/21/2009 19118814 Beecham 3-Jan-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19118814?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease Alzheimer's disease "492 cases, 496 controls" "238 cases, 220 controls" 1q42.2 DISC1 rs12044355-? rs12044355 NR 0.000009 NR NR Illumina [~2.5 million] (imputed) N 1/21/2009 19118814 Beecham 3-Jan-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19118814?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease Alzheimer's disease "492 cases, 496 controls" "238 cases, 220 controls" 12q13.11 FAM113B rs11610206-? rs11610206 NR 3.00E-07 NR NR Illumina [~2.5 million] (imputed) N 1/21/2009 19118814 Beecham 3-Jan-09 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19118814?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease Alzheimer's disease "492 cases, 496 controls" "238 cases, 220 controls" 19q13.31 ZNF224 rs2061333-? rs2061333 NR 0.000002 NR NR Illumina [~2.5 million] (imputed) N 2/27/2009 19116933 Hinks 1-Jan-09 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/19116933?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis Arthritis (juvenile idiopathic) "279 cases, 184 controls" "up to 654 cases, 1,847 controls" 1p13.1 VTCN1 rs12046117-? rs12046117 0.09 0.000001 1.58 [1.29-1.94] "Affymetrix [88,862]" N 1/16/2009 19115949 Limou 1-Jan-09 J Infect Dis http://www.ncbi.nlm.nih.gov/pubmed/19115949?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study of an AIDS-Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02). AIDS progression "275 HIV positive patients, 1,438 controls" 626 patients 6p21.33 "HCP5, MICB, MCCD1, BAT1, LTB, TNF" rs2395029-G rs2395029 0.03 3.00E-19 3.47 [2.39-5.04] "Illumina [291,119]" N 1/16/2009 19115949 Limou 1-Jan-09 J Infect Dis http://www.ncbi.nlm.nih.gov/pubmed/19115949?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study of an AIDS-Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02). AIDS progression "275 HIV positive patients, 1,438 controls" 626 patients 6p21.33 HLA-C rs10484554-T rs10484554 0.13 6.00E-08 NR NR "Illumina [291,119]" N 1/16/2009 19115949 Limou 1-Jan-09 J Infect Dis http://www.ncbi.nlm.nih.gov/pubmed/19115949?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Study of an AIDS-Nonprogression Cohort Emphasizes the Role Played by HLA Genes (ANRS Genomewide Association Study 02). AIDS progression "275 HIV positive patients, 1,438 controls" 626 patients 6p21.33 "ZNRD1, RNF39" rs8321-G rs8321 NR 5.00E-07 NR NR "Illumina [291,119]" N 2/26/2009 19117981 Sun 1-Jan-09 Cancer Res http://www.ncbi.nlm.nih.gov/pubmed/19117981?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variants at 22q13 are associated with prostate cancer risk Prostate cancer "1,235 aggressive cases, 1,599 controls" "3,629 aggressive cases, 4,255 non-aggressive cases, 5,738 controls" 22q13.1 TNRC6B rs9623117-C rs9623117 0.21 5.00E-07 1.18 [1.11-1.26] Affymetrix and Illumina [~2 million] (imputed) N 1/14/2009 19114987 Zhang 31-Dec-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19114987?ordinalpos=17&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Singleton deletions throughout the genome increase risk of bipolar disorder Bipolar disorder "1,001 cases, 1,033 controls" NR Pending Pending Pending Pending Pending Pending Pending Pending "Affymetrix [51,757 CNVs]" Y 1/14/2009 19114657 Wang 29-Dec-08 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/19114657?ordinalpos=13&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Whole-genome association study identifies STK39 as a hypertension susceptibility gene Blood pressure 542 individuals "6,583 individuals" 2q24.3 STK39 rs6749447-G rs6749447 0.28 2.00E-07 1.9 [1.2-2.6] mm Hg increase in DBP "Affymetrix [79,447]" N 1/14/2009 19110211 Meisinger 24-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19110211?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study identifies three loci associated with mean platelet volume Mean platelet volume "1,606 individuals" "8,617 individuals" 3p14.3 ARHGEF3 rs12485738-A rs12485738 0.3 4.00E-27 0.02 [0.01-0.02] per log fl increase "Affymetrix [335,152]" N 1/14/2009 19110211 Meisinger 24-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19110211?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study identifies three loci associated with mean platelet volume Mean platelet volume "1,606 individuals" "8,617 individuals" 12q24.31 WDR66 rs7961894-A rs7961894 0.11 7.00E-48 0.03 [0.03-0.04] per log fl increase "Affymetrix [335,152]" N 1/14/2009 19110211 Meisinger 24-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19110211?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study identifies three loci associated with mean platelet volume Mean platelet volume "1,606 individuals" "8,617 individuals" 17q11.2 TAOK1 rs2138852-C rs2138852 0.47 7.00E-28 0.02 [0.01-0.02] per log fl decrease "Affymetrix [335,152]" N 2/4/2009 19107115 Muglia 23-Dec-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19107115?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts Major depressive disorder "1,359 cases, 1,782 controls" NR 12p13.32 CCND2 rs4238010-G rs4238010 0.02 0.000006 1.72 "Illumina and Affymetrix [494,678] (imputed)" N 6/22/2009 19096518 Pare 19-Dec-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19096518?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study" Glycated hemoglobin levels "14,618 Caucasian women" 455 Caucasian men and women 10q21.3 HK1 rs7072268-A rs7072268 0.5 2.00E-25 0.05 [NR] % increase "Illumina [337,343]" N 6/22/2009 19096518 Pare 19-Dec-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19096518?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study" Glycated hemoglobin levels "14,618 Caucasian women" 455 Caucasian men and women 8q24.11 SLC30A8 rs13266634-A rs13266634 0.3 5.00E-08 0.02 [NR] % decrease "Illumina [337,343]" N 6/22/2009 19096518 Pare 19-Dec-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19096518?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study" Glycated hemoglobin levels "14,618 Caucasian women" 455 Caucasian men and women 7p13 GCK rs730497-A rs730497 0.17 6.00E-12 0.03 [NR] % increase "Illumina [337,343]" N 6/22/2009 19096518 Pare 19-Dec-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19096518?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study" Glycated hemoglobin levels "14,618 Caucasian women" 455 Caucasian men and women 2q24.3 G6PC2 rs1402837-A rs1402837 0.23 5.00E-10 0.02 [NR] % increase "Illumina [337,343]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.2 LRRC16A rs2274089-? rs2274089 NR 0.000005 (serum iron)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.1 HFE rs1800562-? rs1800562 NR 4.00E-11 (serum iron)  0.66 [0.46-0.86] SD increase "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.1 HFE rs1800562-? rs1800562 NR 1.00E-10 (serum transferrin)  0.68 [0.48-0.88] SD decrease "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 3q22.1 TF rs3811647-? rs3811647 NR 3.00E-15 (serum transferrin)  0.46 [0.34-0.58] SD decrease "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.2 LRRC16 rs2274089-? rs2274089 NR 3.00E-07 (serum transferrin)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 3q22.1 TOPBP1 rs2718812-? rs2718812 NR 0.000001 (serum transferrin)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR Xq24 KLHL13 rs2430212-? rs2430212 NR 0.000002 (serum transferrin)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.2 SLC17A1 rs17270561-? rs17270561 NR 5.00E-07 (transferrin saturation)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.2 SCGN rs932316-? rs932316 NR 0.000009 (transferrin saturation)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 411 family members NR 3q22.1 TF rs1830084-A rs1830084 0.36 1.00E-09 (serum transferrin)  0.43 [NR] SD increase "Affymetrix [100,846]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 411 family members NR 14q23.2 Q6ZUR9 rs973968-? rs973968 NR 0.000003 (transferrin saturation)  NR NR "Affymetrix [100,846]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 411 family members NR 6q22.33 RSPO3 rs972275-? rs972275 NR 0.000002 (serum ferritin)  NR NR "Affymetrix [100,846]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 22q12.3 TMPRSS6 rs4820268-? rs4820268 NR 0.000006 (serum iron)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 3q22.1 TF rs1867504-? rs1867504 NR 0.000002 (serum transferrin)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 11p14.3 LUZP2 rs10500991-? rs10500991 NR 0.000002 (serum transferrin)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.1 HFE rs1800562-? rs1800562 NR 4.00E-15 (transferrin saturation)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.1 HIST1H2BJ rs13194491-? rs13194491 NR 1.00E-08 (transferrin saturation)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.1 BTN1A1 rs13194984-? rs13194984 NR 6.00E-08 (transferrin saturation)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.2 LRRC16 rs2274089-? rs2274089 NR 8.00E-07 (transferrin saturation)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 2p14 Q6ZNG6 rs1457451-? rs1457451 NR 0.000003 (transferrin saturation)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6p22.1 TRIM38 rs12216125-? rs12216125 NR 0.000004 (transferrin saturation)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 5p12 GHR rs13188386-? rs13188386 NR 0.000008 (transferrin saturation)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 6q25.3 WTAP rs4516970-? rs4516970 NR 0.000001 (serum ferritin)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 7p14.1 Q4KMW4 rs29880-? rs29880 NR 0.000007 (serum ferritin)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 5q14.1 ARSB rs2052550-? rs2052550 NR 0.000008 (serum ferritin)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 18q22.2 Intergenic rs2660917-? rs2660917 NR 0.000008 (serum ferritin)  NR NR "Illumina [315,887]" N 1/14/2009 19084217 Benyamin 17-Dec-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19084217?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels Serum markers of iron status 459 twin pairs NR 3q22.1 TF rs1799852-? rs1799852 0.09 0.000005 (serum transferrin)  0.43 [0.25-0.61] SD decrease "Illumina [315,887]" N 1/14/2009 19074352 Pollin 17-Dec-08 Science http://www.ncbi.nlm.nih.gov/pubmed/19074352?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection Triglycerides 809 individuals 698 individuals 11q23.3 "APOA1, APOC3, APOA4, APOA5, DSCAML1" rs10892151-A rs10892151 0.028 3.00E-29 NR NR "Affymetrix [381,934]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (hip) "6,865 individuals" "8,510 individuals" 6q25.1 ESR1 rs1038304-G rs1038304 0.47 4.00E-10 0.08 [0.06-0.11] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (hip) "6,865 individuals" "8,510 individuals" 1p36.12 Intergenic rs7524102-A rs7524102 0.82 1.00E-16 0.15 [0.11-0.18] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (hip) "6,865 individuals" "8,510 individuals" 2q12.1 NR rs6735786-C rs6735786 0.64 0.000002 0.07 [0.04-0.09] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (hip) "6,865 individuals" "8,510 individuals" 17q21.31 SOST rs1513670-A rs1513670 0.37 2.00E-08 0.08 [0.05-0.10] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (hip) "6,865 individuals" "8,510 individuals" Xq21.2 NR rs2710057-T rs2710057 0.67 0.000001 0.07 [0.04-0.09] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (hip) "6,865 individuals" "8,510 individuals" 17q21.31 C17orf53 rs227584-T rs227584 0.73 9.00E-07 0.07 [0.04-0.10] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (hip) "6,865 individuals" "8,510 individuals" 3p22.1 NR rs10490823-G rs10490823 0.46 0.000009 0.06 [0.03-0.09] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (hip) "6,865 individuals" "8,510 individuals" 11p11.2 LRP4 rs1007738-A rs1007738 0.77 7.00E-07 0.08 [0.05-0.11] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (spine) "6,865 individuals" "8,510 individuals" 21q11.2 NR rs1006899-A rs1006899 0.84 0.000006 0.09 [0.05-0.13] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (spine) "6,865 individuals" "8,510 individuals" 2p22.2 LOC344382 rs4670779-T rs4670779 0.32 0.000004 0.07 [0.04-0.10] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (spine) "6,865 individuals" "8,510 individuals" 1p36.12 Intergenic rs6696981-G rs6696981 0.86 2.00E-08 0.12 [0.08-0.16] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (spine) "6,865 individuals" "8,510 individuals" 2p16.2 SPTBN1 rs11898505-G rs11898505 0.68 0.000004 0.07 [0.04-0.10] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (spine) "6,865 individuals" "8,510 individuals" 6q25.1 "C6orf97, ESR1" rs6929137-A rs6929137 0.3 2.00E-10 0.1 [0.07-0.13] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (spine) "6,865 individuals" "8,510 individuals" 12q13.13 OSX rs10876432-A rs10876432 0.73 1.00E-07 0.08 [0.05-0.11] SD decrease "Illumina [305,051]" N 1/16/2009 19079262 Styrkarsdottir 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079262?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum New sequence variants associated with bone mineral density Bone mineral density (spine) "6,865 individuals" "8,510 individuals" 13q14.11 RANKL rs9594759-T rs9594759 0.62 2.00E-17 0.12 [0.09-0.15] SD decrease "Illumina [305,051]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 1p21.3 NR rs10783050-C rs10783050 0.36 0.000004 2.6 [1.50-3.70] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 19q13.11 "KCTD15, CHST8" rs29941-C rs29941 0.69 7.00E-12 4.18 [2.98-5.38] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 18q21.32 MC4R rs12970134-A rs12970134 0.3 1.00E-12 4.38 [3.16-5.60] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 16q12.2 FTO rs8050136-A rs8050136 0.41 1.00E-47 8.04 [6.96-9.12] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 11p14.1 BDNF rs925946-T rs925946 0.34 9.00E-10 3.85 [2.62-5.08] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 11p14.1 BDNF rs7481311-T rs7481311 0.24 0.000008 3.15 [1.78-4.52] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 3q27.2 "SFRS10, ETV5, DGKG" rs7647305-C rs7647305 0.77 7.00E-11 4.42 [3.09-5.75] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 2p25.3 TMEM18 rs7561317-G rs7561317 0.84 4.00E-17 6.12 [4.69-7.55] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 1p31.1 NEGR1 rs2568958-A rs2568958 0.58 1.00E-11 3.77 [2.67-4.87] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 16q12.2 FTO rs6499640-A rs6499640 0.41 4.00E-13 5.25 [3.82-6.68] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 16p11.2 "SH2B1, ATP2A1" rs7498665-G rs7498665 0.44 3.00E-10 3.63 [2.49-4.77] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 12q13.13 "BCDIN3D, FAIM2" rs7138803-A rs7138803 0.37 1.00E-07 3.28 [2.06-4.50] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 11p14.1 BDNF rs6265-G rs6265 0.85 5.00E-10 4.58 [3.07-6.09] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Body mass index "80,969 individuals" "11,036 individuals" 1q25.2 "SEC16B, RASAL2" rs10913469-C rs10913469 0.2 6.00E-08 3.36 [2.14-4.58] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 1p31.1 NEGR1 rs2568958-A rs2568958 0.58 2.00E-08 3.37 [2.19-4.55] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 1p21.3 NR rs1973993-C rs1973993 0.63 0.000001 2.71 [1.61-3.81] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 5q23.2 NR rs2115172-A rs2115172 0.57 0.000002 2.71 [1.59-3.83] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 16q12.2 FTO rs6499640-A rs6499640 0.65 6.00E-14 5.5 [4.07-6.93] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 19q13.11 "KCTD15, CHST8" rs29941-C rs29941 0.69 5.00E-09 3.73 [2.48-4.98] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 18q21.32 MC4R rs12970134-A rs12970134 0.3 5.00E-13 4.66 [3.41-5.91] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 16q12.2 FTO rs8050136-A rs8050136 0.41 5.00E-36 7.05 [5.95-8.15] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 11p14.1 BDNF rs7481311-T rs7481311 0.24 0.000003 3.5 [2.03-4.97] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 1q25.2 "SEC16B, RASAL2" rs10913469-C rs10913469 0.2 1.00E-08 3.82 [2.51-5.13] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 16p11.2 "SH2B1, ATP2A1" rs7498665-G rs7498665 0.44 1.00E-09 3.69 [2.51-4.87] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 13q12.2 NR rs7336332-G rs7336332 0.15 0.000001 4.01 [2.40-5.62] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 12q13.13 "BCDIN3D, FAIM2" rs7138803-A rs7138803 0.37 2.00E-07 3.27 [2.05-4.49] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 11p14.1 BDNF rs6265-G rs6265 0.85 2.00E-07 4 [2.47-5.53] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 11p14.1 BDNF rs925946-T rs925946 0.34 4.00E-09 3.8 [2.55-5.05] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 2p25.3 TMEM18 rs7561317-G rs7561317 0.84 2.00E-18 6.47 [5.02-7.92] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 3q27.2 "SFRS10, ETV5, DGKG" rs7647305-C rs7647305 0.77 4.00E-09 4 [2.67-5.33] % SD "Illumina [305,846]" N 1/15/2009 19079260 Thorleifsson 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079260?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity Weight "80,969 individuals" "11,036 individuals" 6p21.33 "AIF1, NCR3" rs2844479-T rs2844479 0.68 2.00E-08 3.58 [2.33-4.83] % SD "Illumina [305,846]" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 4p13 GNPDA2 rs10938397-G rs10938397 0.45 3.00E-16 0.19 [0.13-0.25] kg/m2 "Illumina and Affymetrix [2,399,588] (imputed)" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 18q21.32 MC4R rs17782313-C rs17782313 0.21 5.00E-18 0.2 [0.12-0.28] kg/m2 increase "Illumina and Affymetrix [2,399,588] (imputed)" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 2p25.3 TMEM18 rs6548238-C rs6548238 0.84 1.00E-18 0.26 [0.19-0.34] kg/m2 increase "Illumina and Affymetrix [2,399,588] (imputed)" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 16q12.2 FTO rs9939609-A rs9939609 0.41 4.00E-51 0.33 [0.27-0.39] kg/m2 increase "Illumina and Affymetrix [2,399,588] (imputed)" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 11p11.2 MTCH2 rs10838738-G rs10838738 0.34 5.00E-09 0.07 [0.01-0.13] kg/m2 increase "Illumina and Affymetrix [2,399,588] (imputed)" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 19q13.11 KCTD15 rs11084753-G rs11084753 0.67 2.00E-08 0.06 [-0.01-0.13] kg/m2 increase "Illumina and Affymetrix [2,399,588] (imputed)" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 15q25.2 RKHD3 rs12324805-C rs12324805 0.31 0.000007 NR NR "Illumina and Affymetrix [2,399,588] (imputed)" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 20p12.3 BMP2 rs2145270-T rs2145270 0.65 0.000006 NR NR "Illumina and Affymetrix [2,399,588] (imputed)" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 11p15.4 STK33 rs10769908-C rs10769908 0.53 0.000001 NR NR "Illumina and Affymetrix [2,399,588] (imputed)" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 1p31.1 NEGR1 rs2815752-A rs2815752 0.62 6.00E-08 0.1 [0.04-0.16] kg/m2 increase "Illumina and Affymetrix [2,399,588] (imputed)" N 1/12/2009 19079261 Willer 14-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19079261?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Body mass index "32,387 individuals" "59,092 individuals" 16p11.2 SH2B1 rs7498665-G rs7498665 0.41 5.00E-11 0.15 [0.08-0.21] kg/m2 increase "Illumina and Affymetrix [2,399,588] (imputed)" N 2/5/2009 19081515 Mead 11-Dec-08 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/19081515?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study Creutzfeldt-Jakob disease "117 CJD cases, 3,083 controls" "506 sCJD cases, 28 iCJD cases, 151 Kuru cases, 125 Kuru-resistant cases, up to 1,137 controls" 8q21.13 STMN2 rs1460163-A rs1460163 NR 6.00E-08 NR NR "Affymetrix [288,908]" N 2/5/2009 19081515 Mead 11-Dec-08 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/19081515?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study Creutzfeldt-Jakob disease "117 CJD cases, 3,083 controls" "506 sCJD cases, 28 iCJD cases, 151 Kuru cases, 125 Kuru-resistant cases, up to 1,137 controls" 20p13 PRNP rs1799990-A rs1799990 NR 2.00E-21 NR NR "Affymetrix [288,908]" N 1/6/2009 19065144 Sullivan 9-Dec-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/19065144?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo Major depressive disorder "1,738 cases, 1,802 controls" "6,079 cases, 5,893 controls" NR NR NR NR NS NS NR NR "Perlegen [435,291]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 19q13.32 "TOMM40, APOE" rs2075650-G rs2075650 0.15 3.00E-19 0.14 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 2p21 ABCG5 rs6756629-G rs6756629 0.92 2.00E-11 0.15 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 1p36.11 TMEM57 rs10903129-G rs10903129 0.54 5.00E-10 0.06 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 2p24.1 APOB rs693-G rs693 0.52 9.00E-23 0.1 [NR] SD decrease "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 11q12.2 "FADS2, FADS3" rs174570-G rs174570 0.83 2.00E-10 0.09 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 19p13.2 LDLR rs2228671-G rs2228671 0.88 9.00E-24 0.16 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 15q22.1 LIPC rs1532085-G rs1532085 0.59 4.00E-07 0.05 [NR] SD decrease "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 11q23.3 "APOA1, APOA4, APOA5, APOC3" rs12272004-C rs12272004 0.93 7.00E-07 0.11 [NR] SD decrease "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 8q24.13 TRIB1 rs6987702-G rs6987702 0.29 3.00E-09 0.07 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 7p15.3 DNAH11 rs12670798-G rs12670798 0.24 9.00E-07 0.06 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 5q13.3 HMGCR rs3846662-G rs3846662 0.44 3.00E-19 0.09 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 1p13.3 CELSR2 rs646776-G rs646776 0.22 9.00E-22 0.13 [NR] SD decrease "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 18q21.1 LIPG rs4939883-G rs4939883 0.83 2.00E-11 0.07 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 19p13.11 NCAN rs2304130-G rs2304130 0.07 2.00E-15 0.15 [NR] SD decrease "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts "Cholesterol, total" "22,562 individuals" NR 1p31.3 DOCK7 rs10889353-C rs10889353 0.32 4.00E-12 0.08 [NR] SD decrease "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts HDL cholesterol "21,412 individuals" NR 16q13 CETP rs1532624-C rs1532624 0.57 9.00E-94 0.21 [NR] SD decrease "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts HDL cholesterol "21,412 individuals" NR 2p24.1 APOB rs6754295-C rs6754295 0.25 4.00E-08 0.07 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts HDL cholesterol "21,412 individuals" NR 11p11.2 "MADD, FOLH1" rs7395662-G rs7395662 0.61 6.00E-11 0.07 [NR] SD decrease "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts HDL cholesterol "21,412 individuals" NR 8p21.3 LPL rs2083637-G rs2083637 0.26 6.00E-18 0.11 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts HDL cholesterol "21,412 individuals" NR 19q13.32 "TOMM40, APOE" rs157580-G rs157580 0.33 4.00E-07 0.06 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts HDL cholesterol "21,412 individuals" NR 9q31.1 ABCA1 rs3905000-G rs3905000 0.86 9.00E-13 0.11 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts HDL cholesterol "21,412 individuals" NR 11q12.2 "FADS2, FADS3" rs174570-G rs174570 0.83 0.000004 0.06 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts HDL cholesterol "21,412 individuals" NR 15q22.1 LIPC rs1532085-G rs1532085 0.59 1.00E-35 0.13 [NR] SD decrease "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts HDL cholesterol "21,412 individuals" NR 18q21.1 LIPG rs4939883-G rs4939883 0.83 2.00E-11 0.1 [NR] SD increase "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts HDL cholesterol "21,412 individuals" NR 16q22.1 "CTCF, PRMT8" rs2271293-G rs2271293 0.87 8.00E-16 0.13 [NR] SD decrease "Illumina and Affymetrix [up to ~600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 19q13.32 "TOMM40, APOE" rs157580-G rs157580 0.33 2.00E-19 0.11 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 11q12.2 "FADS2, FADS3" rs174570-G rs174570 0.83 4.00E-13 0.11 [NR] SD increase "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 2p24.1 APOB rs693-G rs693 0.52 4.00E-17 0.1 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 1p31.3 DOCK7 rs10889353-C rs10889353 0.32 0.000008 0.06 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 1p13.3 CELSR2 rs646776-G rs646776 0.22 8.00E-23 0.16 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 5q13.3 HMGCR rs3846662-G rs3846662 0.44 2.00E-11 0.08 [NR] SD increase "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 8q24.13 TRIB1 rs6987702-G rs6987702 0.29 0.000003 0.07 [NR] SD increase "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 11q23.3 "APOA1, APOA4, APOA5, APOC3" rs12272004-C rs12272004 0.93 5.00E-13 0.18 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 2p21 ABCG5 rs6756629-G rs6756629 0.92 3.00E-10 0.16 [NR] SD increase "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 7p15.3 DNAH11 rs12670798-G rs12670798 0.24 6.00E-09 0.09 [NR] SD increase "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 19p13.2 LDLR rs2228671-G rs2228671 0.88 4.00E-14 0.14 [NR] SD increase "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts LDL cholesterol "17,797 individuals" NR 19p13.11 NCAN rs2304130-G rs2304130 0.07 0.000003 0.12 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Triglycerides "17,815 individuals" NR 8p21.3 LPL rs10096633-G rs10096633 0.88 2.00E-18 0.17 [NR] SD increase "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Triglycerides "17,815 individuals" NR 2p23.3 GCKR rs780094-G rs780094 0.63 3.00E-20 0.1 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Triglycerides "17,815 individuals" NR 2p24.1 APOB rs6754295-C rs6754295 0.25 3.00E-08 0.08 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Triglycerides "17,815 individuals" NR 1p31.3 DOCK7 rs1167998-C rs1167998 0.32 2.00E-12 0.09 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Triglycerides "17,815 individuals" NR 11q23.3 "APOA1, APOA4, APOA5, APOC3" rs12272004-C rs12272004 0.93 5.00E-13 0.18 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Triglycerides "17,815 individuals" NR 19p13.11 NCAN rs2304130-G rs2304130 0.07 0.000003 0.1 [NR] SD decrease "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Triglycerides "17,815 individuals" NR 7q11.23 MLXIPL rs2240466-G rs2240466 0.87 1.00E-12 0.14 [NR] SD increase "Illumina and Affymetrix [up to 600,000]" N 1/12/2009 19060911 Aulchenko 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts Triglycerides "17,815 individuals" NR 19q13.32 "TOMM40, APOE" rs439401-G rs439401 0.68 2.00E-09 0.09 [NR] SD increase "Illumina and Affymetrix [up to 600,000]" N 1/7/2009 19060909 Bouatia-Naji 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060909?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk Fasting plasma glucose "2,151 individuals" "6,332 cases, 9,132 controls" 11q21 MTNR1B rs1387153-T rs1387153 0.29 2.00E-36 0.07 [0.05-0.08] mmol/l increase "Illumina [308,846]" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 9q31.1 ABCA1 rs1883025-T rs1883025 0.26 1.00E-09 0.08 [0.04-0.12] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 1q42.13 GALNT2 rs4846914-G rs4846914 0.4 4.00E-08 0.05 [0.01-0.09] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 16q22.1 LCAT rs2271293-A rs2271293 0.11 9.00E-13 0.07 [0.01-0.13] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 16q13 CETP rs173539-T rs173539 0.32 4.00E-75 0.25 [0.21-0.29] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 8p21.3 LPL rs12678919-G rs12678919 0.1 2.00E-34 0.23 [0.17-0.29] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 15q22.1 LIPC rs10468017-T rs10468017 0.3 8.00E-23 0.1 [0.06-0.14] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 18q21.1 LIPG rs4939883-T rs4939883 0.17 7.00E-15 0.14 [0.10-0.18] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 11q23.3 "APOA1, APOC3, APOA4, APOA5" rs964184-G rs964184 0.14 1.00E-12 0.17 [0.11-0.23] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 12q24.11 "MMAB,MVK" rs2338104-C rs2338104 0.45 1.00E-10 0.07 [0.03-0.11] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 11q12.2 "FADS1, FADS2, FADS3" rs174547-C rs174547 0.33 2.00E-12 0.09 [0.05-0.13] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 9p22.3 TTC39B rs471364-C rs471364 0.12 3.00E-10 0.08 [0.02-0.14] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 20q13.2 HNF4A rs1800961-T rs1800961 0.03 8.00E-10 0.19 [0.09-0.29] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 20q13.12 PLTP rs7679-C rs7679 0.19 4.00E-09 0.07 [0.03-0.11] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia HDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 19p13.2 ANGPTL4 rs2967605-T rs2967605 0.16 1.00E-08 0.12 [0.04-0.20] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 5q13.3 HMGCR rs3846663-T rs3846663 0.38 8.00E-12 0.07 [0.03-0.11] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 19p13.11 "NCAN, CILP2, PBX4" rs10401969-C rs10401969 0.06 2.00E-08 0.05 [-0.03-0.13] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 19p13.2 LDLR rs6511720-T rs6511720 0.1 2.00E-26 0.26 [0.18-0.34] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 19q13.32 "APOE, APOC1, APOC4, APOC2" rs4420638-G rs4420638 0.16 4.00E-27 0.29 [0.17-0.41] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 2p24.1 APOB rs515135-T rs515135 0.2 5.00E-29 0.16 [0.12-0.20] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 12q24.31 HNF1A rs2650000-A rs2650000 0.36 2.00E-08 0.07 [0.03-0.11] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 1p13.3 "CELSR2, PSRC1, SORT1" rs12740374-T rs12740374 0.21 2.00E-42 0.23 [0.19-0.27] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 2p21 ABCG8 rs6544713-T rs6544713 0.32 2.00E-20 0.15 [0.11-0.19] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 5q33.3 "TIMD4, HAVCR1" rs1501908-G rs1501908 0.37 1.00E-11 0.07 [0.03-0.11] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 20q12 MAFB rs6102059-T rs6102059 0.32 4.00E-09 0.06 [0.03-0.10] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia LDL cholesterol "19,840 individuals" "Up to 20,623 individuals" 1p32.3 PCSK9 rs11206510-C rs11206510 0.19 4.00E-08 0.09 [0.05-0.13] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 8p23.1 "XKR6, AMAC1L2" rs7819412-G rs7819412 0.48 3.00E-08 0.04 [0.001-0.08] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 11q12.2 "FADS1, FADS2, FADS3" rs174547-C rs174547 0.33 2.00E-14 0.06 [0.02-0.10] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 1p31.3 ANGPTL3 rs10889353-C rs10889353 0.33 3.00E-07 0.05 [0.01-0.09] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 20q13.12 PLTP rs7679-C rs7679 0.19 7.00E-11 0.07 [0.03-0.11] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 19p13.11 "NCAN,CILP2,PBX4" rs17216525-T rs17216525 0.07 4.00E-11 0.11 [0.05-0.17] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 7q11.23 MLXIPL rs714052-G rs714052 0.12 3.00E-15 0.16 [0.10-0.22] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 8q24.13 TRIB1 rs2954029-T rs2954029 0.44 3.00E-19 0.11 [0.07-0.15] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 2p23.3 GCKR rs1260326-T rs1260326 0.45 2.00E-31 0.12 [0.08-0.16] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 8p21.3 LPL rs12678919-G rs12678919 0.1 2.00E-41 0.25 [0.19-0.31] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 11q23.3 "APOA1, APOC3, APOA4, APOA5" rs964184-G rs964184 0.14 4.00E-62 0.3 [0.24-0.36] SD increase "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060906 Kathiresan 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060906?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at 30 loci contribute to polygenic dyslipidemia Triglycerides "19,840 individuals" "Up to 20,623 individuals" 2p24.1 APOB rs7557067-G rs7557067 0.22 9.00E-12 0.08 [0.04-0.12] SD decrease "Affymetrix and Illumina [~2,600,000] (imputed)" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population HDL cholesterol "4,763 individuals" NR 11p11.2 NR1H3 rs7120118-G rs7120118 0.42 4.00E-08 0.04 [0.03-0.05] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population HDL cholesterol "4,763 individuals" NR 16q22.1 LCAT rs255049-G rs255049 0.22 3.00E-08 0.05 [0.03-0.07] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population HDL cholesterol "4,763 individuals" NR 17p13.3 Intergenic rs9891572-A rs9891572 0.16 2.00E-07 0.05 [0.048-0.051] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population HDL cholesterol "4,763 individuals" NR 16q13 CETP rs3764261-A rs3764261 0.28 7.00E-29 0.09 [0.08-0.11] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population HDL cholesterol "4,763 individuals" NR 15q22.1 LIPC rs1532085-A rs1532085 0.44 2.00E-10 0.05 [0.03-0.06] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population LDL cholesterol "4,763 individuals" NR 1q32.2 CR1L rs4844614-A rs4844614 0.32 2.00E-07 0.1 [0.06-0.14] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population LDL cholesterol "4,763 individuals" NR 1p13.3 "CELSR2, PSRC1, SORT1" rs646776-G rs646776 0.21 2.00E-12 0.16 [0.11-0.20] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population LDL cholesterol "4,763 individuals" NR 19q13.32 APO cluster rs157580-G rs157580 0.29 5.00E-08 0.11 [0.07-0.15] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population LDL cholesterol "4,763 individuals" NR 19p13.2 LDLR rs11668477-G rs11668477 0.18 2.00E-07 0.13 [0.08-0.17] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population LDL cholesterol "4,763 individuals" NR 11q12.2 "FADS1, FADS2" rs174546-A rs174546 0.44 1.00E-07 0.1 [0.06-0.13] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population LDL cholesterol "4,763 individuals" NR 2p24.1 APOB rs693-A rs693 0.41 3.00E-11 0.12 [0.09-0.16] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population LDL cholesterol "4,763 individuals" NR Xq12 AR rs5031002-A rs5031002 0.02 2.00E-07 0.3 [0.18-0.41] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 10q23.31 PANK1 rs11185790-A rs11185790 0.21 3.00E-07 (INS)  0.31 [0.18-0.44] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 11q21 MTNR1B rs1447352-G rs1447352 0.42 6.00E-08 (GLU)  0.05 [0.03-0.06] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 2p24.1 APOB rs673548-A rs673548 0.27 2.00E-08 (TG)  0.08 [0.05-0.11] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 2p23.3 GCKR rs1260326-A rs1260326 0.35 4.00E-10 (TG)  0.09 [0.06-0.12] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 8p21.3 LPL rs10096633-A rs10096633 0.098 5.00E-08 (TG)  0.12 [0.07-0.17] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 15q14 Intergenic rs2624265-G rs2624265 0.42 4.00E-07 (TG)  0.07 [0.04-0.10] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 12q24.31 LEF1 rs2650000-A rs2650000 0.45 3.00E-11 (CRP)  0.4 [0.25-0.55] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 2q24.3 "G6PC2, ABCB11" rs560887-A rs560887 0.31 6.00E-10 (GLU)  0.06 [0.04-0.07] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 7p21.2 Intergenic rs10244051-C rs10244051 0.46 1.00E-07 (GLU)  0.05 [0.03-0.06] mmol/l increase "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 1q23.2 CRP rs2794520-A rs2794520 0.36 3.00E-22 (CRP)  0.47 [0.32-0.62] mmol/l decrease "Illumina [329,091]" N 1/12/2009 19060910 Sabatti 7-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060910?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Other metabolic traits "4,763 individuals" NR 1p31.3 LEPR rs12753193-G rs12753193 0.45 4.00E-07 (CRP)  0.13 [-0.02-0.27] mmol/l decrease "Illumina [329,091]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 14q23.2 Intergenic rs1514928-? rs1514928 NR 0.000003 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 16q22.1 HAS3 rs8047014-? rs8047014 NR 0.000004 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 19q13.43 ZNF544 rs260461-? rs260461 NR 0.000008 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 22q12.3 Intergenic rs130575-? rs130575 NR 0.000005 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 2q14.3 Intergenic rs17367118-? rs17367118 NR 0.000009 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 2q24.1 Intergenic rs1918172-? rs1918172 NR 0.000005 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 3p24.3 Intergenic rs11719664-? rs11719664 NR 0.000002 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 8q24.3 NAPRT1 rs2290416-? rs2290416 NR 0.000009 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 4q13.3 EREG rs1350666-? rs1350666 NR 0.000008 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 1q41 Intergenic rs1018040-? rs1018040 NR 0.000005 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 3p14.1 FOXP1 rs17651978-? rs17651978 NR 0.000006 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 2q21.2 FLJ34870 rs7577925-? rs7577925 NR 0.000003 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 12p11.22 Intergenic rs522958-? rs522958 NR 0.000001 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 2q14.1 Intergenic rs272000-? rs272000 NR 0.000009 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 3p14.2 FHIT rs6791644-? rs6791644 NR 0.000008 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 2p21 OXER1 rs930421-? rs930421 NR 0.000006 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 1p31.2 Intergenic rs4147141-? rs4147141 NR 0.000006 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 11p13 Intergenic rs10767942-? rs10767942 NR 0.000008 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Attention deficit hyperactivity disorder 909 trios NR 13q32.3 CLYBL rs7992643-? rs7992643 NR 0.000005 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 14q23.1 Intergenic rs1335515-C rs1335515 NR 0.000008 (earlier onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 20q13.13 SULF2 rs4810685-C rs4810685 NR 0.000007 (earlier onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 7q31.1 Intergenic rs6968385-T rs6968385 NR 0.000002 (earlier onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 11p15.1 Intergenic rs874426-C rs874426 NR 0.000004 (earlier onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 2q36.3 Intergenic rs1517484-C rs1517484 NR 5.00E-07 (earlier onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 3p22.3 Intergenic rs9845475-G rs9845475 NR 0.000004 (later onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 3q29 Intergenic rs3892715-C rs3892715 NR 0.000006 (earlier onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 5q35.3 ADAMTS2 rs10039254-A rs10039254 NR 0.000008 (later onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 6q15 Intergenic rs806276-A rs806276 NR 3.00E-07 (later onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 8q23.3 Intergenic rs17658378-A rs17658378 NR 0.000009 (later onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18937294 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18937294?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder (time to onset) 930 trios NR 9p23 Intergenic rs1325154-C rs1325154 NR 0.000005 (later onset)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 6p22.3 Intergenic rs1202199-? rs1202199 NR 0.000009 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 6p22.3 Intergenic rs41441749-? rs41441749 NR 0.000001 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 21q21.3 GRIK1 rs363512-? rs363512 NR 0.000004 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 9p24.3 DMRT2 rs17641078-? rs17641078 NR 0.000005 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 3q26.1 Intergenic rs6808138-? "rs6808138,rs6808138" NR 0.000005 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 2p21 OXER1 rs6719977-? rs6719977 NR 0.000002 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 18q22.1 Intergenic rs13353224-? rs13353224 NR 0.000009 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 3q26.1 Intergenic rs6808138-? rs6808138 NR 0.000008 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 8p21.3 LPL rs7816032-? rs7816032 NR 0.000002 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 12p11.22 Intergenic rs522958-? rs522958 NR 8.00E-07 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 1q41 Intergenic rs1018040-? rs1018040 NR 0.000008 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 1p13.2 Intergenic rs11590090-? rs11590090 NR 0.000003 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 19q13.43 LOC390980 rs2014572-? rs2014572 NR 0.000007 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Hyperactive-impulsive symptoms 909 trios NR 15q14 MEIS2 rs8041675-? rs8041675 NR 0.000004 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 9q21.31 Intergenic rs2769967-? rs2769967 NR 0.000003 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 7q36.3 Intergenic rs10227331-? rs10227331 NR 0.000004 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 16q23.1 Intergenic rs13330107-? rs13330107 NR 0.000009 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 16q12.1 ZNF423 rs17281813-? rs17281813 NR 0.000003 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 15q26.1 SLCO3A1 rs7495052-? rs7495052 NR 0.000003 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 11q22.3 Intergenic rs10895959-? rs10895959 NR 0.000003 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 8q21.11 Intergenic rs12679254-? rs12679254 NR 0.000002 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 15q13.1 Intergenic rs1471225-? rs1471225 NR 0.000008 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 15q25.1 IL16 rs7172689-? rs7172689 NR 0.000004 (count)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 12q24.22 Intergenic rs478597-? rs478597 NR 0.000008 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 13q12.12 Intergenic rs17079773-? rs17079773 NR 0.000005 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 8p11.21 Intergenic rs11786458-? rs11786458 NR 0.000009 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 1p31.2 Intergenic rs4650135-? rs4650135 NR 0.000005 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 9q22.32 Intergenic rs11790994-? rs11790994 NR 2.00E-07 (binary)  NR NR "Perlegen [429,981]" N 5/7/2009 18821565 Lasky-Su 5-Dec-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821565?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations Inattentive symptoms 909 trios NR 1p31.2 Intergenic rs4147141-? rs4147141 NR 0.000008 (binary)  NR NR "Perlegen [429,981]" N 1/15/2009 19056611 Timpson 3-Dec-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls" 11p15.1 KCNJ11 rs5219-? rs5219 NR 1.00E-09 (non-obese)  1.25 [1.16-1.34] "Affymetrix [393,453]" N 1/15/2009 19056611 Timpson 3-Dec-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls" 11p15.1 KCNJ11 rs5219-? rs5219 NR 5.00E-07 (obese)  1.19 [1.11-1.27] "Affymetrix [393,453]" N 1/15/2009 19056611 Timpson 3-Dec-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls" 16q12.2 FTO rs8050136-? rs8050136 NR 2.00E-17 (obese)  1.3 [1.23-1.39] "Affymetrix [393,453]" N 1/15/2009 19056611 Timpson 3-Dec-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls" 8q24.11 SLC30A8 rs13266634-? rs13266634 NR 0.000007 (non-obese)  1.18 [1.10-1.27] "Affymetrix [393,453]" N 1/15/2009 19056611 Timpson 3-Dec-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls" 10q25.2 TCF7L2 rs7903146-? rs7903146 NR 9.00E-30 (non-obese)  1.49 [1.39-1.59] "Affymetrix [393,453]" N 1/15/2009 19056611 Timpson 3-Dec-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls" 9p21.3 CDKN2B rs10811661-? rs10811661 NR 7.00E-07 (non-obese)  1.26 [1.15-1.38] "Affymetrix [393,453]" N 1/15/2009 19056611 Timpson 3-Dec-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls" 10q25.2 TCF7L2 rs7903146-? rs7903146 NR 6.00E-16 (obese)  1.31 [1.23-1.40] "Affymetrix [393,453]" N 1/15/2009 19056611 Timpson 3-Dec-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/19056611?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome wide association data Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls" 6p22.3 CDKAL rs10946398-? rs10946398 NR 7.00E-07 (non-obese)  1.18 [1.11-1.26] "Affymetrix [393,453]" N 1/12/2009 19047183 Friedman 1-Dec-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19047183?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum grm7 variants confer susceptibility to age-related hearing impairment Hearing impairment "846 cases, 846 controls" "63 cases, 67 controls" NR NR NR NR NS NS NR NR "Affymetrix [506,627] (pooled)" N 2/26/2009 19060907 Prokopenko 1-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060907?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in MTNR1B influence fasting glucose levels Fasting plasma glucose "35,812 individuals" NR 11q21 MTNR1B rs10830963-G rs10830963 0.28 3.00E-50 0.07 [0.06-0.08] mmol/l increase "Affymetrix, Illumina and Perlegen [up to 2,557,249] (imputed)" N 2/26/2009 19060907 Prokopenko 1-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060907?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in MTNR1B influence fasting glucose levels Fasting plasma glucose "35,812 individuals" NR 7p13 GCK rs4607517-A rs4607517 0.18 1.00E-25 0.06 [0.05-0.07] mmol/l increase "Affymetrix, Illumina and Perlegen [up to 2,557,249] (imputed)" N 2/26/2009 19060907 Prokopenko 1-Dec-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19060907?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in MTNR1B influence fasting glucose levels Fasting plasma glucose "35,812 individuals" NR 2q24.3 G6PC2 rs560887-C rs560887 0.7 1.00E-57 0.06 [0.05-0.07] mmol/l increase "Affymetrix, Illumina and Perlegen [up to 2,557,249] (imputed)" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 12q24.21 Intergenic rs2194980-? rs2194980 0.33 3.00E-07 (Tyrosine)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 15q26.1 SV2B rs886144-? rs886144 0.38 2.00E-07 (SM)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 6q25.1 C6orf71 rs1591830-? rs1591830 0.32 1.00E-07 (sugar)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 6q12 Intergenic rs9354308-? rs9354308 0.37 3.00E-07 (serotonin)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 3p25.3 ATP2B2 rs6807064-? rs6807064 0.29 1.00E-07 (phenylalanine)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 6q26 PARK2 rs992037-? rs992037 0.35 1.00E-07 (Lysine)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 2p14 PLEK rs9309413-? rs9309413 0.45 2.00E-09 (SM)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 11q12.2 FADS1 rs174548-? rs174548 0.28 5.00E-08 (PC)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 15q22.1 LIPC rs4775041-? rs4775041 0.28 1.00E-07 (PE)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 3q22.3 Intergenic rs1382269-? rs1382269 0.47 5.00E-07 (SM)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 3q28 FGF12 rs4453795-? rs4453795 0.41 4.00E-07 (PC)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 4q13.1 Intergenic rs10517480-? rs10517480 0.31 2.00E-07 (PC)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 7q31.1 Intergenic rs10953730-? rs10953730 0.35 2.00E-07 (acylcarnitine)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 16p13.2 A2BP1 rs9924951-? rs9924951 0.41 5.00E-07 (PC)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 13q31.3 GPC5 rs17267292-? rs17267292 0.28 1.00E-07 (Docosahexaonic acid)  NR NR "Affymetrix [187,454]" N 12/24/2008 19043545 Gieger 28-Nov-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/19043545?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genetics Meets Metabolomics: A Genome-Wide Association Study of Metabolite Profiles in Human Serum Serum metabolites 284 males NR 10p11.21 ANKRD30A rs1148259-? rs1148259 0.42 3.00E-09 (SM)  NR NR "Affymetrix [187,454]" N 12/9/2008 18957941 Terracciano 24-Nov-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18957941?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan for five major dimensions of personality Personality dimensions "3,972 individuals" "3,903 individuals" 2p22.1 THUMPD2 rs2540226-T rs2540226 0.53 0.000003 (agreeableness)  0.13 [NR] SD increase "Affymetrix [362,129]" N 12/9/2008 18957941 Terracciano 24-Nov-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18957941?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan for five major dimensions of personality Personality dimensions "3,972 individuals" "3,903 individuals" 19q13.31 ZNF180 rs644148-G rs644148 0.5 0.000008 (extraversion)  0.14 [NR] SD increase "Affymetrix [362,129]" N 12/9/2008 18957941 Terracciano 24-Nov-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18957941?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan for five major dimensions of personality Personality dimensions "3,972 individuals" "3,903 individuals" 4q12 CLOCK rs6832769-A rs6832769 0.73 0.000002 (agreeableness)  0.14 [NR] SD decrease "Affymetrix [362,129]" N 12/9/2008 18957941 Terracciano 24-Nov-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18957941?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan for five major dimensions of personality Personality dimensions "3,972 individuals" "3,903 individuals" Xp11.3 FUNDC1 rs6610953-G rs6610953 0.85 0.000006 (openness)  0.15 [NR] SD increase "Affymetrix [362,129]" N 12/9/2008 18957941 Terracciano 24-Nov-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18957941?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan for five major dimensions of personality Personality dimensions "3,972 individuals" "3,903 individuals" 19q13.31 ZNF180 rs644148-G rs644148 0.5 9.00E-07 (openness)  0.15 [NR] SD increase "Affymetrix [362,129]" N 1/7/2009 19030899 Lei 23-Nov-08 Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/19030899?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci Height 618 Chinese individuals "2,953 Chinese individuals" 9q22.23 ZNP510 rs10816533-C rs10816533 0.29 0.000002 NR NR "Affymetrix [281,533]" N 1/6/2009 19023125 Potkin 20-Nov-08 Schizophr Bull http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype Brain imaging in schizophrenia (interaction) "64 cases, 74 cases" NR 3p12.3 "ROBO2, ROBO1" rs9836484-? rs9836484 0.32 0.000004 NR NR "Illumina [302,783]" N 1/6/2009 19023125 Potkin 20-Nov-08 Schizophr Bull http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype Brain imaging in schizophrenia (interaction) "64 cases, 74 cases" NR 6q16.2 POU3F2 rs9491640-? rs9491640 0.06 0.000009 NR NR "Illumina [302,783]" N 1/6/2009 19023125 Potkin 20-Nov-08 Schizophr Bull http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype Brain imaging in schizophrenia (interaction) "64 cases, 74 cases" NR 3q26.2 TNIK rs2088885-? rs2088885 0.47 0.000006 NR NR "Illumina [302,783]" N 1/6/2009 19023125 Potkin 20-Nov-08 Schizophr Bull http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype Brain imaging in schizophrenia (interaction) "64 cases, 74 cases" NR 5q23.2 "CTXN3, SLC12A2" rs245201-? rs245201 0.32 9.00E-08 NR NR "Illumina [302,783]" N 1/6/2009 19023125 Potkin 20-Nov-08 Schizophr Bull http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype Brain imaging in schizophrenia (interaction) "64 cases, 74 cases" NR 2q37.3 GPC1 rs1574192-? rs1574192 0.38 0.000004 NR NR "Illumina [302,783]" N 1/6/2009 19023125 Potkin 20-Nov-08 Schizophr Bull http://www.ncbi.nlm.nih.gov/pubmed/19023125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A Genome-Wide Association Study of Schizophrenia Using Brain Activation as a Quantitative Phenotype Brain imaging in schizophrenia (interaction) "64 cases, 74 cases" NR 14q32.32 TRAF3 rs10133111-? rs10133111 0.2 0.000005 NR NR "Illumina [302,783]" N 12/1/2008 19011631 COGENT Study 16-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19011631?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer Colorectal cancer "1,902 cases, 1,929 controls" "4,878 cases, 4,914 controls" 19q13.11 RHPN2 rs10411210-C rs10411210 0.9 5.00E-09 1.15 [1.10-1.20] "Illumina [up to 548,586]" N 12/1/2008 19011631 COGENT Study 16-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19011631?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer Colorectal cancer "1,902 cases, 1,929 controls" "4,878 cases, 4,914 controls" 14q22.2 BMP4 rs4444235-C rs4444235 0.46 8.00E-10 1.11 [1.08-1.15] "Illumina [up to 548,586]" N 12/1/2008 19011631 COGENT Study 16-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19011631?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer Colorectal cancer "1,902 cases, 1,929 controls" "4,878 cases, 4,914 controls" 16q22.1 CDH1 rs9929218-A rs9929218 0.29 1.00E-08 1.1 [1.06-1.12] "Illumina [up to 548,586]" N 12/1/2008 19011631 COGENT Study 16-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/19011631?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer Colorectal cancer "1,902 cases, 1,929 controls" "4,878 cases, 4,914 controls" 20p12.3 Intergenic rs961253-A rs961253 0.36 2.00E-10 1.12 [1.08-1.16] "Illumina [up to 548,586]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Brain lesion load "791 cases, 883 controls" NR 6q25.3 IGF2R rs6917747-? rs6917747 0.15 0.000007 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Brain lesion load "791 cases, 883 controls" NR 14q12 NUBPL rs2039485-? rs2039485 0.22 0.000006 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Brain lesion load "791 cases, 883 controls" NR 19p13.11 CPAMD8 rs11666377-? rs11666377 0.14 0.000007 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Brain lesion load "791 cases, 883 controls" NR 2q37.1 CHRND rs2602397-? rs2602397 0.45 0.000004 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis "978 cases, 883 controls" NR 3q23 SLC25A36 rs908821-? rs908821 0.71 0.000003 1.37 [NR] "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis "978 cases, 883 controls" NR 2q14.2 EN1 rs651477-? rs651477 0.26 0.000007 1.38 [NR] "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis "978 cases, 883 controls" NR 4q35.1 MGC45800 rs7672826-? rs7672826 0.34 0.000008 1.37 [NR] "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis "978 cases, 883 controls" NR 3q24 ZIC1 rs1841770-? rs1841770 0.53 0.000008 1.34 [NR] "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis "978 cases, 883 controls" NR 13q31.3 GPC5 rs9523762-? rs9523762 0.35 0.000001 1.36 [NR] "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis "978 cases, 883 controls" NR 20p13 C20orf46 rs397020-? rs397020 0.52 8.00E-07 1.41 [NR] "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis "978 cases, 883 controls" NR 8p23.2 CSMD1 rs1529316-? rs1529316 0.47 0.000002 1.36 [NR] "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis "978 cases, 883 controls" NR 9p22.2 SH3GL2 rs1755289-? rs1755289 0.61 0.000003 1.35 [NR] "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis "978 cases, 883 controls" NR 2p25.1 DDEF2 rs1109670-? rs1109670 0.26 0.000009 1.38 [NR] "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis "978 cases, 883 controls" NR 12q12 PDZRN4 rs1458175-? rs1458175 0.49 0.000002 1.34 [NR] "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (age of onset) "978 cases, 883 controls" NR 18q21.31 WDR7 rs1557351-? rs1557351 0.22 0.000004 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (age of onset) "978 cases, 883 controls" NR 11q14.2 RAB38 rs1386330-? rs1386330 0.13 0.000002 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (age of onset) "978 cases, 883 controls" NR 5q33.2 SGCD rs4704970-? rs4704970 0.2 0.000007 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (age of onset) "978 cases, 883 controls" NR 1q25.2 C1orf125 rs12047808-? rs12047808 0.13 0.000006 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (age of onset) "978 cases, 883 controls" NR 8q13.3 KCNB2 rs2116078-? rs2116078 0.48 0.000003 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (age of onset) "978 cases, 883 controls" NR 7q22.1 RELN rs17157903-? rs17157903 0.14 0.000003 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (age of onset) "978 cases, 883 controls" NR 2q21.2 FLJ34870 rs1437898-? rs1437898 0.4 0.000008 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (age of onset) "978 cases, 883 controls" NR 9q21.13 RFK rs2842483-? rs2842483 0.29 0.000005 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 6p23 JARID2 rs6941421-? rs6941421 0.24 0.000006 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 16q22.3 C16orf47 rs7191888-? rs7191888 0.17 0.000006 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 7q31.2 MET rs10243024-? rs10243024 0.23 0.000006 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 11q23.3 MGC13125 rs180358-? rs180358 0.23 0.000006 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 4q13.2 CENPC1 rs10518025-? rs10518025 0.14 0.000004 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 7p21.3 C1GALT1 rs10259085-? rs10259085 0.46 0.000004 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 19p13.2 ACP5 rs7253363-? rs7253363 0.05 0.000009 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 18q22.3 CBLN2 rs337718-? rs337718 0.29 0.000009 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 19q13.42 NLRP11 rs299175-? rs299175 0.46 0.000004 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 4q28.3 LOC132321 rs1478091-? rs1478091 0.06 0.000002 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Multiple sclerosis (severity) "794 cases, 883 controls" NR 3q25.32 FLJ16641 rs12638253-? rs12638253 0.47 0.000002 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Normalized brain volume "753 cases, 883 controls" NR 12p11.21 BICD1 rs261902-? rs261902 0.16 0.000004 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Normalized brain volume "753 cases, 883 controls" NR 10p11.23 SVIL rs1927457-? rs1927457 0.31 0.000008 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Normalized brain volume "753 cases, 883 controls" NR 10q25.2 MXI1 rs716595-? rs716595 0.08 0.000008 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Normalized brain volume "753 cases, 883 controls" NR 6q21 FOXO3 rs9480865-? rs9480865 0.16 0.000007 NR NR "Illumina [551,642]" N 1/16/2009 19010793 Baranzini 14-Nov-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/19010793?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Normalized brain volume "753 cases, 883 controls" NR 5q35.1 KCNIP1 rs11957313-? rs11957313 0.13 0.000009 NR NR "Illumina [551,642]" N 12/9/2008 18997785 Aulchenko 9-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18997785?ordinalpos=&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.SmartSearch&log$=citationsensor Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis Multiple sclerosis "45 cases, 195 controls" "2,634 cases, 2,930 controls" 1p36.22 KIF1B rs10492972-C rs10492972 0.27 3.00E-10 1.34 [1.23-1.48] "Affymetrix [~250,000]" N 12/1/2008 18997786 Bilguvar 9-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18997786?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Susceptibility loci for intracranial aneurysm in European and Japanese populations Intracranial aneurysm "1,580 European cases, 6,276 European controls" "495 Japanese cases, 676 Japanese controls" 8q11.23 SOX17 rs10958409-A rs10958409 0.15 1.00E-10 1.36 [1.24-1.49] "Illumina [289,271]" N 12/1/2008 18997786 Bilguvar 9-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18997786?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Susceptibility loci for intracranial aneurysm in European and Japanese populations Intracranial aneurysm "1,580 European cases, 6,276 European controls" "495 Japanese cases, 676 Japanese controls" 9q21.3 "CDKN2A, CDKN2B" rs1333040-T rs1333040 0.55 1.00E-10 1.29 [1.19-1.40] "Illumina [289,271]" N 12/1/2008 18997786 Bilguvar 9-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18997786?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Susceptibility loci for intracranial aneurysm in European and Japanese populations Intracranial aneurysm "1,580 European cases, 6,276 European controls" "495 Japanese cases, 676 Japanese controls" 8q11.23-q12.1 SOX17 rs9298506-A rs9298506 0.81 2.00E-09 1.35 [1.22-1.49] "Illumina [289,271]" N 12/1/2008 18997786 Bilguvar 9-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18997786?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Susceptibility loci for intracranial aneurysm in European and Japanese populations Intracranial aneurysm "1,580 European cases, 6,276 European controls" "495 Japanese cases, 676 Japanese controls" 2q33.1 "BOLL, PLCL1" rs700651-G rs700651 0.35 4.00E-08 1.24 [1.15-1.34] "Illumina [289,271]" N 12/30/2008 19009022 Drgon 9-Nov-08 Mol Med http://www.ncbi.nlm.nih.gov/pubmed/19009022?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome wide association for nicotine dependence and smoking cessation success in NIH research volunteers Nicotine dependence "220 cases, 260 controls" "2,271 cases, 1,868 controls" NR NR NR NR NS NS NR NR "Affymetrix [~600,00] (pooled)" N 12/9/2008 18985386 Pankratz 6-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18985386?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide association study for susceptibility genes contributing to familial Parkinson disease Parkinson's disease (familial) "857 cases, 867 controls" "262 cases, 260 controls" 4p16.3 "GAK, DGKQ" rs1564282-T rs1564282 0.09 7.00E-07 1.7 [NR] "Illumina [328,189]" N 12/9/2008 18987618 Cronin 5-Nov-08 Eur J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18987618?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSu Screening for replication of genome-wide SNP associations in sporadic AL Amyotrophic lateral sclerosis "958 cases, 932 controls" "309 cases, 404 controls" 7q36.2 DPP6 rs10260404-C rs10260404 0.35 0.000003 1.37 [1.20-1.56] "Illumina [287,522]" N 12/1/2008 18980221 Neale 3-Nov-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18980221?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide association scan of attention deficit hyperactivity disorder Attention deficit hyperactivity disorder 909 trios NR NR NR NR NR NS NS NR NR "Perlegen [438,784]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 10p15.1 IL2RA rs12251307-T rs12251307 NR 0.000002 NR NR "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 22q13.1 C1QTNF6 rs229541-T rs229541 0.43 2.00E-08 1.04 [0.97-1.12] "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 6p21.32 HLA rs9272346-G rs9272346 NR 6.00E-129 NR NR "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 2q33.2 CTLA4 rs3087243-A rs3087243 NR 8.00E-11 NR NR "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 16p13.13 "C16orf75, PRM3, TNP2" rs416603-T rs416603 0.44 0.000003 1.06 [1.01-1.12] "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 15q25.1 CTSH rs3825932-C rs3825932 0.32 3.00E-15 1.16 [1.10-1.22] "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 10p15.1 PRKCQ rs947474-G rs947474 0.19 4.00E-09 1.1 [1.03-1.18] "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 6q15 BACH2 rs11755527-G rs11755527 0.47 5.00E-12 1.13 [1.08-1.19] "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 2p23.3 Intergenic rs2165738-C rs2165738 0.27 0.000004 1.07 [1.01-1.13] "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 18p11.21 PTPN2 rs2542151-C rs2542151 NR 9.00E-08 NR NR "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 12q24.13 C12orf30 rs17696736-G rs17696736 NR 6.00E-18 NR NR "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 12q13.2 ERBB3 rs2292239-A rs2292239 NR 3.00E-16 NR NR "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 16p13.13 CLEC16A rs12708716-G rs12708716 NR 7.00E-13 NR NR "Affymetrix [up to 335,565]" N 11/25/2008 18978792 Cooper 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978792?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci Type 1 diabetes "3,561 cases, 4,646 controls" "6,225 cases, 6,946 controls, 3,064 trios" 1p13.2 PTPN22 rs6679677-A rs6679677 NR 1.00E-40 NR NR "Affymetrix [up to 335,565]" N 12/9/2008 18978790 McKay 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978790?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Lung cancer susceptibility locus at 5p15.33 Lung cancer "2,971 cases, 3,746 controls" "2,899 cases, 5,573 controls" 5p15.33 "TERT, CLPTM1" rs402710-C rs402710 NR 0.000004 1.18 [1.12-1.24] "Illumina [315,194]" N 12/9/2008 18978790 McKay 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978790?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Lung cancer susceptibility locus at 5p15.33 Lung cancer "2,971 cases, 3,746 controls" "2,899 cases, 5,573 controls" 15q25.1 Intergenic rs1051730-A rs1051730 NR 1.00E-15 1.35 [1.25-1.45] "Illumina [315,194]" N 11/25/2008 18978787 Wang 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978787?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common 5p15.33 and 6p21.33 variants influence lung cancer risk Lung cancer "1,952 cases, 1,438 controls" "7,579 cases, 8,236 controls" 6p21.33 "BAT3,MSH5" rs3117582-C rs3117582 NR 5.00E-10 1.24 [1.16-1.33] "Illumina [223,891]" N 11/25/2008 18978787 Wang 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978787?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common 5p15.33 and 6p21.33 variants influence lung cancer risk Lung cancer "1,952 cases, 1,438 controls" "7,579 cases, 8,236 controls" 5p15.33 CLPTM1L rs401681-G rs401681 NR 8.00E-09 1.15 [1.09-1.19] "Illumina [223,891]" N 11/25/2008 18978787 Wang 2-Nov-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18978787?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common 5p15.33 and 6p21.33 variants influence lung cancer risk Lung cancer "1,952 cases, 1,438 controls" "7,579 cases, 8,236 controls" 15q25.1 NR rs8042374-? rs8042374 NR 8.00E-12 NR NR "Illumina [223,891]" N 12/9/2008 18976728 Bertram 29-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18976728?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE Alzheimer's disease "941 affected individuals, 404 unaffected individuals" "1,767 affected individuals, 838 unaffected individuals" 14q31.2 Intergenic rs11159647-? rs11159647 NR 0.000002 NR NR "Affymetrix [484,522]" N 12/9/2008 18976728 Bertram 29-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18976728?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide Association Analysis Reveals Putative Alzheimer's Disease Susceptibility Loci in Addition to APOE Alzheimer's disease "941 affected individuals, 404 unaffected individuals" "1,767 affected individuals, 838 unaffected individuals" 19q13.33 CD33 rs3826656-? rs3826656 NR 0.000006 NR NR "Affymetrix [484,522]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 7q31.1 "FLJ31818, GPR85" rs10229603-C rs10229603 0.31 0.000005 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 12q21.2 PAWR rs7297018-A rs7297018 0.19 0.000004 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 13q12.2 "GSX1, PDX1" rs9512900-C rs9512900 0.37 0.000009 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 13q33.3 "LIG4, ABHD13" rs10492664-C rs10492664 0.84 0.000001 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 1q42.13 LOC729257 rs701157-C rs701157 0.45 0.000004 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 16q21 Intergenic rs1381102-A rs1381102 0.4 0.000006 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 1q25.3 "RGL1, GLT25D2" rs10797919-G rs10797919 0.59 0.000009 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 10p14 A2BP1 rs1291846-T rs1291846 0.19 0.000009 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 15q26.2 SPATA8 rs4533251-T rs4533251 0.15 0.000004 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 11q24.2 KIRREL3 rs1557488-T rs1557488 0.18 0.000005 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 14q12 Intergenic rs1951082-T rs1951082 0.43 0.000005 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 12q15 C12orf28 rs789560-G rs789560 0.87 0.000007 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 4q13.3 "AMOTL1, CWC15, JMJD2D" rs10831284-G rs10831284 0.13 0.000002 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 18q21.31 ATP8B1 rs7236632-A rs7236632 0.86 0.000006 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 16q22.3 "PKD1L3, KIAA0174, DHODH" rs16973500-C rs16973500 0.86 0.000007 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 16q23.2 "PKD1L2, C16orf46" rs4889240-T rs4889240 0.45 0.000007 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 21q21.1 Intergenic rs2826340-T rs2826340 0.17 0.000002 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 1p35.2 Intergenic rs2180233-C rs2180233 0.31 0.000009 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 1q23.1 "ETV3L, ETV3" rs6427356-G rs6427356 0.28 0.000008 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 2p22.3 Intergenic rs6733379-G rs6733379 0.28 0.000004 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 2p12 Intergenic rs7595103-A rs7595103 0.64 0.000007 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 2q33.1 "FLJ39061, FZD7" rs1521882-A rs1521882 0.82 0.000008 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 5q31.1 C5orf15 rs1644305-A rs1644305 0.41 0.000008 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 8q22.3 YWHAZ rs931812-C rs931812 0.74 0.000005 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 9p24.1 PTPRD rs10815798-A rs10815798 0.48 0.000006 NR NR "Perlegen [378,332]" N 12/9/2008 18951430 Anney 24-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18951430?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study Attention deficit hyperactivity disorder and conduct disorder 938 affected trios NR 10p15.2 PITRM1 rs2764980-A rs2764980 0.51 0.000009 NR NR "Perlegen [378,332]" N 12/1/2008 18952825 Johansson 24-Oct-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/18952825?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis Height "3,925 individuals" "38,091 individuals" 7p15.1 JAZF1 rs1635852-A rs1635852 NR 9.00E-10 0.25 [0.17-0.33] cm taller Illumina [NR] N 12/9/2008 18941528 Comabella 22-Oct-08 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/18941528?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms" Multiple sclerosis "242 cases, 242 controls" "375 cases, 375 controls" 6p21.32 HLA-DRB1 rs3129934-T rs3129934 NR 9.00E-11 3.3 [2.3-4.9] "Affymetrix [428,867] (pooled)" N 11/25/2008 18849994 Hillmer 12-Oct-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18849994?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Susceptibility variants for male-pattern baldness on chromosome 20p11 Male-pattern baldness "296 cases, 347 controls" "319 cases, 234 controls" 20p11.22 "PAX1, BQ013595, BE789145" rs2180439-C rs2180439 0.43 3.00E-15 1.82 [1.45-2.30] "Illumina [531,695]" N 11/25/2008 18849991 Richards 12-Oct-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18849991?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Male-pattern baldness susceptibility locus at 20p11 Male-pattern baldness "578 cases, 547 controls" "1,351 cases, 2,485 controls" Xq12 AR rs6625163-A rs6625163 NR 5.00E-11 3.3 [2.31-4.71] "Affymetrix [370,102]" N 11/25/2008 18849991 Richards 12-Oct-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18849991?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Male-pattern baldness susceptibility locus at 20p11 Male-pattern baldness "578 cases, 547 controls" "1,351 cases, 2,485 controls" 20p11.22 PAX1 rs1160312-A rs1160312 0.43 1.00E-14 (males)  1.6 [1.42-1.80] (males) "Affymetrix [370,102]" N 11/25/2008 18849993 Stacey 12-Oct-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18849993?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits Basal cell carcinoma (cutaneous) "930 cases, 33,117 controls" "1,216 cases, 2,844 controls" 1q42.13 RHOU rs801114-G rs801114 0.33 6.00E-12 1.28 [1.19-1.37] "Illumina [304,083]" N 11/25/2008 18849993 Stacey 12-Oct-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18849993?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits Basal cell carcinoma (cutaneous) "930 cases, 33,117 controls" "1,216 cases, 2,844 controls" 1p36.13 "PADI4, PADI6,RCC2, ARHGEF10L" rs7538876-A rs7538876 0.35 4.00E-12 1.28 [1.19-1.37] "Illumina [304,083]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 10q21.3 POU2F1 rs9803659-C rs9803659 NR 0.000004 (ALT)  0.03 [0.018-0.042] U/L decrease "Affymetrix and Illumina [up to 496,032]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 9q34.2 ADAMTS13 rs4962153-A rs4962153 NR 8.00E-21 (ALP)  0.06 [0.048-0.072] U/L decrease "Affymetrix and Illumina [up to 496,032]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 22q13.31 "PNPLA3, SAMM50" rs2281135-T rs2281135 0.18 8.00E-16 (ALT)  0.06 [0.046-0.074] U/L increase "Affymetrix and Illumina [up to 496,032]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 6p22.2 GPLD1 rs9467160-A rs9467160 0.24 1.00E-11 (ALP)  0.03 [0.024-0.044] U/L increase "Affymetrix and Illumina [up to 496,032]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 10q24.31 JMJD1C rs12355784-A rs12355784 0.48 5.00E-10 (ALP)  0.03 [0.017-0.033] U/L increase "Affymetrix and Illumina [up to 496,032]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 1p36.12 "NBPF3, ALPL, RAP1GAP" rs1780324-T rs1780324 0.43 7.00E-15 (ALP)  0.03 [0.023-0.039] U/L increase "Affymetrix and Illumina [up to 496,032]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 9p34.2 ABO rs657152-T rs657152 0.39 2.00E-30 (ALP)  0.05 [0.039-0.055] U/L decrease "Affymetrix and Illumina [up to 496,032]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 22q11.23 "GGT1, C22orf36" rs4820599-G rs4820599 0.31 4.00E-11 (GGT)  0.01 [0.005-0.009] U/L increase "Affymetrix and Illumina [up to 496,032]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 10q24.2q "CPN1, CHUK, ERLIN1" rs11597390-A rs11597390 0.36 2.00E-08 (ALT)  0.04 [0.025-0.053] U/L decrease "Affymetrix and Illumina [up to 496,032]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 12q24.2 "HNF1A, C12orf27, C12orf43" rs1169313-C rs1169313 0.38 2.00E-10 (GGT)  0.01 [0.003-0.007] U/L decrease "Affymetrix and Illumina [up to 496,032]" N 12/1/2008 18940312 Yuan 10-Oct-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18940312?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes Plasma levels of liver enzymes "7,751 European white individuals" "4,704 European white and Indian Asian individua" 10q21.2 REEP3 rs10761779-G rs10761779 0.49 7.00E-10 (ALP)  0.03 [0.017-0.033] U/L increase "Affymetrix and Illumina [up to 496,032]" N 11/25/2008 18840781 Grant 7-Oct-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/18840781?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes Type 1 diabetes "563 cases, 1,146 controls, 483 case-parents trios" "636 families, 3,303 cases, 4,673 controls" 6q15 BACH2 rs3757247-A rs3757247 NR 1.00E-06 1.13 [1.08-1.19] "Illumina [up to 1,000,000]" N 11/25/2008 18840781 Grant 7-Oct-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/18840781?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes Type 1 diabetes "563 cases, 1,146 controls, 483 case-parents trios" "636 families, 3,303 cases, 4,673 controls" 9p24.2 GLIS3 rs10758593-A rs10758593 NR 0.000003 1.13 [1.07-1.19] "Illumina [up to 1,000,000]" N 11/25/2008 18840781 Grant 7-Oct-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/18840781?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes Type 1 diabetes "563 cases, 1,146 controls, 483 case-parents trios" "636 families, 3,303 cases, 4,673 controls" 15q14 RASGRP1 rs8035957-C rs8035957 NR 4E-06 1.14 [1.08-1.21] "Illumina [up to 1,000,000]" N 11/25/2008 18840781 Grant 7-Oct-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/18840781?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes Type 1 diabetes "563 cases, 1,146 controls, 483 case-parents trios" "636 families, 3,303 cases, 4,673 controls" 21q22.3 UBASH3A rs9976767-C rs9976767 NR 2.00E-08 1.16 [1.10-1.22] "Illumina [up to 1,000,000]" N 11/25/2008 18840781 Grant 7-Oct-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/18840781?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Follow up analysis of genome-wide association data identifies novel loci for type 1 diabetes Type 1 diabetes "563 cases, 1,146 controls, 483 case-parents trios" "636 families, 3,303 cases, 4,673 controls" 1p22.3 EDG7 rs1983853-? rs1983853 NR 2E-06 1.2 [1.11-1.29] "Illumina [up to 1,000,000]" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 10q24.1 TLL2 rs10786284-? rs10786284 NR 0.000002 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 5q22.2 REEP5 rs469727-? rs469727 NR 0.000008 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 2p25.3 MYT1L rs2241685-? rs2241685 NR 0.000008 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 13q31.3 GPC6 rs7995215-? rs7995215 NR 1.00E-08 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 15q23 ITGA11 rs7164335-? rs7164335 NR 1.00E-07 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 20q11.22 MMP24 rs1555322-? rs1555322 NR 0.000004 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 2q33.3 CRYGC rs2242073-? rs2242073 NR 0.000008 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 12q23.3 NT5DC3 rs4964805-? rs4964805 NR 0.000005 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 7p15.1 CREB5 rs2237349-? rs2237349 NR 0.000005 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 16q24.1 ATP2C2 rs10514604-? rs10514604 NR 8.00E-07 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 6p21.1 TFEB rs2842643-? rs2842643 NR 0.000003 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 17p13.2 ITGAE rs220470-? rs220470 NR 1.00E-07 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 6p21.1 SUPT3H rs3799977-? rs3799977 NR 0.000005 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 16q23.3 CDH13 rs11646411-? rs11646411 NR 0.000007 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 10q25.1 C10orf79 rs515910-? rs515910 NR 0.000004 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 22q11.22 PPM1F rs412050-? rs412050 NR 0.000006 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 9q34.11 DNM1 rs2502731-? rs2502731 NR 0.000002 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 1p35.1 CSMD2 rs2281597-? rs2281597 NR 5.00E-07 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 9q33.1 ASTN2 rs10983238-? rs10983238 NR 1.00E-07 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 15q26.1 AK094352 rs7175404-? rs7175404 NR 6.00E-07 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 9q34.13 C9orf98 rs11243897-? rs11243897 NR 6.00E-08 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 2q14.2 MGC33657 rs2587695-? rs2587695 NR 3.00E-07 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 3p22.1 MOBP rs864643-? rs864643 NR 1.00E-08 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 5q13.2 MAP1B rs2199161-? rs2199161 NR 0.000002 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 10q22.1 UNC5B rs16928529-? rs16928529 NR 0.000004 NR NR "Affymetrix [504,219](pooled)" N 5/7/2009 18839057 Lesch 7-Oct-08 J Neural Transm http://www.ncbi.nlm.nih.gov/pubmed/18839057?ordinalpos=16&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies Attention deficit hyperactivity disorder "343 cases, 304 controls" NR 15q26.1 MAN2A2 rs2677744-? rs2677744 NR 0.000001 NR NR "Affymetrix [504,219](pooled)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan Attention deficit hyperactivity disorder symptoms (interaction) 909 trios NR 3q27.2 Intergenic rs10049246-G rs10049246 0.59 0.000008 "(int, MW) " 0.6 [NR] unit increase "Perlegen [429,981]" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan Attention deficit hyperactivity disorder symptoms (interaction) 909 trios NR 11q21 PIWIL4 rs2212361-C rs2212361 0.26 9.00E-07 "(int, MW) " 0.97 [NR] unit decrease "Perlegen [429,981]" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan Attention deficit hyperactivity disorder symptoms (interaction) 909 trios NR 21q21.1 Intergenic rs2825388-A rs2825388 0.4 0.000008 "(int, MC) " 1.06 [NR] unit increase "Perlegen [429,981]" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan Attention deficit hyperactivity disorder symptoms (interaction) 909 trios NR 8p23.2 Intergenic rs4875598-G rs4875598 0.34 0.000009 "(int, MW) " 0.94 [NR] unit decrease "Perlegen [429,981]" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan Attention deficit hyperactivity disorder symptoms (interaction) 909 trios NR 14q24.3 Intergenic rs2360997-C rs2360997 0.86 0.000008 "(int, MW) " 1.3 [NR] unit decrease "Perlegen [429,981]" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan Attention deficit hyperactivity disorder symptoms (interaction) 909 trios NR 13q12.3 Intergenic rs1161463-C rs1161463 0.79 0.000002 "(int, MW) " 1.72 [NR] unit decrease "Perlegen [429,981]" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=9&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? an exploration using a genome wide association scan Attention deficit hyperactivity disorder symptoms (interaction) 909 trios NR 6p21.2 KIF6 rs4714261-T rs4714261 0.17 0.000002 "(int, MW) " 0.95 [NR] unit increase "Perlegen [429,981]" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 17q22 Intergenic rs8073783-C rs8073783 0.49 0.000008 "(int, MW) " 1.76 [NR] unit decrease "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 18q12.3 Intergenic rs17664267-T rs17664267 0.19 0.000007 "(int, MW) " 1.39 [NR] unit increase "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 1q22 RIT1 rs2282301-A rs2282301 0.23 0.000007 "(int, MW) " 2.88 [NR] unit increase "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 10q22.3 Intergenic rs2395528-T rs2395528 0.23 0.000006 "(int, MW) " 1.46 [NR] unit decrease "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 3p25.3 SLC6A1 rs9990174-T rs9990174 0.33 0.000006 "(int, MW) " 2.52 [NR] unit decrease "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 8p23.1 MFHAS1 rs332034-A rs332034 0.85 0.000006 "(int, MW) " 1.05 [NR] unit increase "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 4q23 ADH1C rs1789891-A rs1789891 0.14 0.000003 "(int, MW) " 1.47 [NR] unit increase "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 16p13.3 A2BP1 rs6500744-C rs6500744 0.53 0.000003 "(int, MW) " 0.91 [NR] unit increase "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 5q21.1 Intergenic rs13188771-A rs13188771 0.17 0.000002 "(int, MW) " 4.24 [NR] unit decrease "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 11q23.2 ZBTB16 rs17116334-T rs17116334 0.16 0.000009 "(int, MC) " 1.3 [NR] unit increase "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 6p15 Intergenic rs16880441-G rs16880441 0.08 0.000009 "(int, MC) " 1.63 [NR] unit increase "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 15q26.2 Intergenic rs4321143-G rs4321143 0.28 0.000007 "(int, MC) " 1.13 [NR] unit increase "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 4q22.1 PPM1K rs893971-T rs893971 0.6 0.000007 "(int, MC) " 1.15 [NR] unit decrease "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 2p21 Intergenic rs719593-T rs719593 0.86 0.000005 "(int, MC) " 2.05 [NR] unit decrease "Perlegen [429,901)" N 12/9/2008 18846501 Sonuga-Barke 7-Oct-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18846501?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan Conduct disorder (interaction) 909 trios NR 2p22.2 Intergenic rs604381-A rs604381 0.32 0.000008 "(int, MW) " 1.26 [NR] unit increase "Perlegen [429,901)" N 11/25/2008 18836448 Franke 5-Oct-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18836448?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility" Ulcerative colitis "1,167 cases, 777 controls" "1,855 cases, 3,091 controls" 1q32.1 IL10 rs3024505-T rs3024505 0.15 1.00E-12 1.46 [1.31-1.62] "Affymetrix [355,262]" N 11/25/2008 18836448 Franke 5-Oct-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18836448?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility" Ulcerative colitis "1,167 cases, 777 controls" "1,855 cases, 3,091 controls" 6p21.32 "HLA-DRA, BTNL2" rs9268877-T rs9268877 0.45 6.00E-18 1.45 [1.33-1.58] "Affymetrix [355,262]" N 10/14/2009 19802338 Chasman 1-Oct-08 Circ Cardiovasc Genet http://www.ncbi.nlm.nih.gov/pubmed/19802338?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum "Genetic loci associated with plasma concentration of LDL-C, HDL-C, triglycerides, ApoA1, and ApoB among 6382 Caucasian women in genome-wide analysis with replication" Lipid traits "6,382 Caucasian women" 970 Caucasian individuals NR NR NR NR NS NS NR NR "Illumina [314,518]" N 11/25/2008 18834626 Dehghan 1-Oct-08 Lancet http://www.ncbi.nlm.nih.gov/pubmed/18834626?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study Serum urate "11,847 individuals" "14,867 individuals" 4p16.1 SLC2A9 rs16890979-T rs16890979 0.23 0 (whites)  0.34 [0.30-0.38] SD decrease in serum uric acid level "Affymetrix and Illumina [up to 530,683]" N 11/25/2008 18834626 Dehghan 1-Oct-08 Lancet http://www.ncbi.nlm.nih.gov/pubmed/18834626?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study Serum urate "11,847 individuals" "14,867 individuals" 6p22.2 SLC17A3 rs1165205-? rs1165205 0.47 4.00E-29 (whites)  0.09 [0.07-0.11] SD decrease in serum uric acid level "Affymetrix and Illumina [up to 530,683]" N 11/25/2008 18834626 Dehghan 1-Oct-08 Lancet http://www.ncbi.nlm.nih.gov/pubmed/18834626?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study Serum urate "11,847 individuals" "14,867 individuals" 4q22.1 ABCG2 rs2231142-? rs2231142 0.11 3.00E-60 (whites)  0.24 [0.20-0.28] SD increase in serum uric acid level "Affymetrix and Illumina [up to 530,683]" N 12/9/2008 18991354 Gretarsdottir 1-Oct-08 Ann Neurol http://www.ncbi.nlm.nih.gov/pubmed/18991354?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke Ischemic stroke "1,661 cases, 10,815 controls" "4,576 cases, 19,343 controls" 4q25 NR rs2200733-T rs2200733 0.11 2.00E-10 1.26 [1.17-1.35] "Illumina [310,881]" N 11/25/2008 18835860 Mushiroda 1-Oct-08 J Med Genet http://www.ncbi.nlm.nih.gov/pubmed/18835860?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis Idiopathic pulmonary fibrosis "159 Japanese cases, 934 Japanese controls" "83 Japanese cases, 535 Japanese controls" 5p15.33 TERT rs2736100-A rs2736100 0.41 3.00E-08 2.11 [1.61-2.78] "Illumina [214,508]" N 11/25/2008 18823527 Abraham 29-Sep-08 BMC Med Genomics http://www.ncbi.nlm.nih.gov/pubmed/18823527?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study for late-onset Alzheimer's disease using DNA pooling Alzheimer's disease "1,082 cases, 1,239 controls" "1,400 additional controls" 19q13.32 "PVRL2, TOMM40, APOE" rs6859-A rs6859 NR 6.00E-14 NR NR "Illumina [561,494] (pooled)" N 11/25/2008 18823527 Abraham 29-Sep-08 BMC Med Genomics http://www.ncbi.nlm.nih.gov/pubmed/18823527?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A genome-wide association study for late-onset Alzheimer's disease using DNA pooling Alzheimer's disease "1,082 cases, 1,239 controls" "1,400 additional controls" 22q13.33 CPT1B rs727153-C rs727153 0.17 0.000003 1.63 [1.37-1.95] "Illumina [561,494] (pooled)" N 11/25/2008 18820697 Miyagawa 28-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18820697?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variant between CPT1B and CHKB associated with susceptibility to narcolepsy Narcolepsy "222 Japanese cases, 389 Japanese controls" "748 cases, 994 controls" 22q13.33 CPT1B rs5770917-C rs5770917 0.17 6.00E-08 1.63 [1.37-1.95] "Affymetrix [249,133]" N 11/25/2008 18821564 Mick 26-Sep-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821564?ordinalpos=&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.SmartSearch&log$=citationsensor Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder Attention deficit hyperactivity disorder 187 children NR 5p15.31 Intergenic rs11134178-T rs11134178 0.05 0.000003 NR NR "Affymetrix [319,722]" N 11/25/2008 18821564 Mick 26-Sep-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18821564?ordinalpos=&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.SmartSearch&log$=citationsensor Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder Attention deficit hyperactivity disorder 187 children NR 22q13.31 Intergenic rs9627183-C rs9627183 0.03 0.000003 NR NR "Affymetrix [319,722]" N 12/9/2008 18802019 Burkhardt 18-Sep-08 Arterioscler Thromb Vasc Biol http://www.ncbi.nlm.nih.gov/pubmed/18802019?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common SNPs in HMGCR in Micronesians and Whites Associated With LDL-Cholesterol Levels Affect Alternative Splicing of Exon13 LDL cholesterol "2,346 Micronesian individuals" "1,464 European white cases, 1,467 European white controls" 19q13.32 "APOE, APOC1, APOC4, APOC2" rs4420638-? rs4420638 NR 2.00E-07 NR NR "Affymetrix [~500,000]" N 12/9/2008 18802019 Burkhardt 18-Sep-08 Arterioscler Thromb Vasc Biol http://www.ncbi.nlm.nih.gov/pubmed/18802019?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common SNPs in HMGCR in Micronesians and Whites Associated With LDL-Cholesterol Levels Affect Alternative Splicing of Exon13 LDL cholesterol "2,346 Micronesian individuals" "1,464 European white cases, 1,467 European white controls" 5q13.3 HMGCR rs7703051-A rs7703051 0.41 1.00E-08 18 [NR] % SD increase "Affymetrix [~500,000]" N 11/25/2008 18780872 Liu 17-Sep-08 J Natl Cancer Inst http://www.ncbi.nlm.nih.gov/pubmed/18780872?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Familial Aggregation of Common Sequence Variants on 15q24-25.1 in Lung Cancer Lung cancer "194 cases, 219 controls" "3,878 cases, 4,831 controls" 15q25.1 "LOC123688, PSMA4, CHRNA3, CHRNA5, CHRNB4" rs8034191-G rs8034191 NR 1.00E-08 1.38 [1.17-1.64] "Affymetrix [up to 722,376]" N 11/25/2008 18794855 Kiemeney 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794855?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variant on 8q24 confers susceptibility to urinary bladder cancer Urinary bladder cancer "1,803 cases, 34,336 controls" "2,165 cases, 3,800 controls" 8q24.21 "MYC, BC042052" rs9642880-T rs9642880 0.45 9.00E-12 1.22 [1.15-1.29] "Illumina [302,140]" N 11/25/2008 18794855 Kiemeney 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794855?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Sequence variant on 8q24 confers susceptibility to urinary bladder cancer Urinary bladder cancer "1,803 cases, 34,336 controls" "2,165 cases, 3,800 controls" 3q28 TP63 rs710521-A rs710521 0.73 1.00E-07 1.19 [1.12-1.27] "Illumina [302,140]" N 11/25/2008 18794853 Raychaudhuri 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at CD40 and other loci confer risk of rheumatoid arthritis Rheumatoid arthritis "3,393 cases, 12,460 controls" "3,929 cases, 5,807 controls" 1p13.2 PTPN22 rs6679677-? rs6679677 0.1 6.00E-42 1.79 [1.65-1.94] "Illumina [818,728] Affymetrix [~340,000] (imputed)" N 11/25/2008 18794853 Raychaudhuri 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at CD40 and other loci confer risk of rheumatoid arthritis Rheumatoid arthritis "3,393 cases, 12,460 controls" "3,929 cases, 5,807 controls" 6p21.32 HLA-DRB1 rs6457620-? rs6457620 0.5 0 2.55 [2.40-2.71] "Illumina [818,728] Affymetrix [~340,000] (imputed)" N 11/25/2008 18794853 Raychaudhuri 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at CD40 and other loci confer risk of rheumatoid arthritis Rheumatoid arthritis "3,393 cases, 12,460 controls" "3,929 cases, 5,807 controls" 6q23.3 "OLIG3, TNFIP3" rs6920220-? rs6920220 0.22 2.00E-09 1.24 [1.16-1.32] "Illumina [818,728] Affymetrix [~340,000] (imputed)" N 11/25/2008 18794853 Raychaudhuri 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at CD40 and other loci confer risk of rheumatoid arthritis Rheumatoid arthritis "3,393 cases, 12,460 controls" "3,929 cases, 5,807 controls" 7q21.2 CDK6 rs42041-G rs42041 0.24 4E-06 1.11 [NR] "Illumina [818,728] Affymetrix [~340,000] (imputed)" N 11/25/2008 18794853 Raychaudhuri 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at CD40 and other loci confer risk of rheumatoid arthritis Rheumatoid arthritis "3,393 cases, 12,460 controls" "3,929 cases, 5,807 controls" 12q13.3 KIF5A-PIP4K2C rs1678542-C rs1678542 0.37 9.00E-08 1.12 [NR] "Illumina [818,728] Affymetrix [~340,000] (imputed)" N 11/25/2008 18794853 Raychaudhuri 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at CD40 and other loci confer risk of rheumatoid arthritis Rheumatoid arthritis "3,393 cases, 12,460 controls" "3,929 cases, 5,807 controls" 1p36.32 MMEL1-TNFRSF14 rs3890745-T rs3890745 0.33 1.00E-07 1.12 [NR] "Illumina [818,728] Affymetrix [~340,000] (imputed)" N 11/25/2008 18794853 Raychaudhuri 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at CD40 and other loci confer risk of rheumatoid arthritis Rheumatoid arthritis "3,393 cases, 12,460 controls" "3,929 cases, 5,807 controls" 10p15.1 PRKCQ rs4750316-G rs4750316 0.2 4E-06 1.14 [NR] "Illumina [818,728] Affymetrix [~340,000] (imputed)" N 11/25/2008 18794853 Raychaudhuri 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at CD40 and other loci confer risk of rheumatoid arthritis Rheumatoid arthritis "3,393 cases, 12,460 controls" "3,929 cases, 5,807 controls" 20q13.12 CD40 rs4810485-G rs4810485 0.25 8.00E-09 1.15 [NR] "Illumina [818,728] Affymetrix [~340,000] (imputed)" N 11/25/2008 18794853 Raychaudhuri 14-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18794853?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants at CD40 and other loci confer risk of rheumatoid arthritis Rheumatoid arthritis "3,393 cases, 12,460 controls" "3,929 cases, 5,807 controls" 9p13.3 CCL21 rs2812378-G rs2812378 0.34 3.00E-08 1.12 [NR] "Illumina [818,728] Affymetrix [~340,000] (imputed)" N 11/25/2008 18760390 Huyghe 12-Sep-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18760390?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait Hearing impairment "1,081 individuals" NR NR NR NR NR NS NS NR NR "Affymetrix [169,154]" N 11/25/2008 18776929 Liu 8-Sep-08 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/18776929?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study Hip bone size "501 women, 499 men" "1,216 women" 2q33.1 PLCL1 rs7595412-A rs7595412 0.89 2E-06 5 [NR] cm2 increase in hip bone size on women "Affymetrix [306,823]" N 11/25/2008 18776911 Hazra 7-Sep-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18776911?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Common variants of FUT2 are associated with plasma vitamin B12 levels Plasma level of vitamin B12 "1,658 women" "1,059 women" 19q13.3 FUT2 rs492602-G rs492602 0.49 5.00E-17 0.09 [0.07-0.11] pg/ml decrease "Illumina [528,134]" N 11/25/2008 18759275 McArdle 1-Sep-08 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish Serum uric acid "408 women, 460 men" NR 4p16.1 "GLUT9, WDR1" rs16890979-? rs16890979 NR 1.00E-11 0.44 [0.32-0.56] mg/dl decrease in uric serum levels "Affymetrix [361,034]" N 11/25/2008 18759275 McArdle 1-Sep-08 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish Serum uric acid "408 women, 460 men" NR 13q33.1 NR rs4771450-? rs4771450 NR 2E-06 0.23 [NR] mg/dl decrease in uric acid levels "Affymetrix [361,034]" N 11/25/2008 18759275 McArdle 1-Sep-08 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish Serum uric acid "408 women, 460 men" NR 2q31.1 NR rs4668338-? rs4668338 NR 0.000003 4.29 [NR] mg/dl decrease in uric acid levels "Affymetrix [361,034]" N 11/25/2008 18759275 McArdle 1-Sep-08 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish Serum uric acid "408 women, 460 men" NR 13q14.11 NR rs17065323-? rs17065323 NR 4E-06 4.29 [NR] mg/dl decrease in uric acid levels "Affymetrix [361,034]" N 11/25/2008 18759275 McArdle 1-Sep-08 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish Serum uric acid "408 women, 460 men" NR 20p12.3 NR rs6085920-? rs6085920 NR 0.000006 0.4 [NR] mg/dl decrease in uric acid levels "Affymetrix [361,034]" N 11/25/2008 18759275 McArdle 1-Sep-08 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish Serum uric acid "408 women, 460 men" NR 3p24.3 NR rs6442522-? rs6442522 NR 0.000005 0.05 [NR] mg/dl increase in uric acid levels "Affymetrix [361,034]" N 11/25/2008 18759275 McArdle 1-Sep-08 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/18759275?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish Serum uric acid "408 women, 460 men" NR 5q31.3 NR rs3776331-? rs3776331 NR 8E-06 0.3 [NR] mg/dl increase in uric acid levels "Affymetrix [361,034]" N 11/25/2008 18762592 van den Oord 1-Sep-08 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18762592?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Analysis Followed by a Replication Study Implicates a Novel Candidate Gene for Neuroticism Neuroticism "1,227 individuals" "1,880 individuals" 14q21.3 MAMDC1 rs12883384-? rs12883384 NR 7.00E-07 NR NR "Affymetrix [420,287]" N 11/25/2008 18762592 van den Oord 1-Sep-08 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18762592?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Analysis Followed by a Replication Study Implicates a Novel Candidate Gene for Neuroticism Neuroticism "1,227 individuals" "1,880 individuals" 7p21.3 NXPH1 rs2349775-? rs2349775 NR 7E-06 NR NR "Affymetrix [420,287]" N 11/25/2008 18762592 van den Oord 1-Sep-08 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18762592?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide Association Analysis Followed by a Replication Study Implicates a Novel Candidate Gene for Neuroticism Neuroticism "1,227 individuals" "1,880 individuals" 8q24.23 AK127771 rs2705293-? rs2705293 NR 0.000006 NR NR "Affymetrix [420,287]" N 11/25/2008 18758461 Di Bernardo 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia Chronic lymphocytic leukemia "505 cases, 1,438 controls" "1,024 cases, 1,677 controls" 2q13 "ACOXL,BCL2L11" rs17483466-G rs17483466 0.2 2.00E-10 1.39 [1.25-1.53] "Illumina [345,665]" N 11/25/2008 18758461 Di Bernardo 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia Chronic lymphocytic leukemia "505 cases, 1,438 controls" "1,024 cases, 1,677 controls" 19q13.32 "PRKD2,STRN4" rs11083846-A rs11083846 0.22 4.00E-09 1.35 [1.22-1.49] "Illumina [345,665]" N 11/25/2008 18758461 Di Bernardo 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia Chronic lymphocytic leukemia "505 cases, 1,438 controls" "1,024 cases, 1,677 controls" 11q24.1 GRAMD1B rs735665-A rs735665 0.21 4.00E-12 1.45 [1.31-1.61] "Illumina [345,665]" N 11/25/2008 18758461 Di Bernardo 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia Chronic lymphocytic leukemia "505 cases, 1,438 controls" "1,024 cases, 1,677 controls" 2q37.1 "SP140, SP110" rs13397985-G rs13397985 0.19 6.00E-10 1.41 [1.26-1.57] "Illumina [345,665]" N 11/25/2008 18758461 Di Bernardo 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia Chronic lymphocytic leukemia "505 cases, 1,438 controls" "1,024 cases, 1,677 controls" 15q23 Intergenic rs7176508-A rs7176508 0.37 5.00E-12 1.37 [1.26-1.50] "Illumina [345,665]" N 11/25/2008 18758461 Di Bernardo 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia Chronic lymphocytic leukemia "505 cases, 1,438 controls" "1,024 cases, 1,677 controls" 6p25.3 IRF4 rs872071-G rs872071 0.54 2.00E-20 1.54 [1.41- 1.69] "Illumina [345,665]" N 11/25/2008 18758464 Kugathasan 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease Inflammatory bowel disease "1,011 cases, 4,250 controls" "1,922 cases, 14,124 controls" 20q13.33 TNFRSF6B rs2315008-G rs2315008 0.69 9.00E-15 1.36 [1.05-1.76] Illumina [NR] N 11/25/2008 18758464 Kugathasan 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease Inflammatory bowel disease "1,011 cases, 4,250 controls" "1,922 cases, 14,124 controls" 21q22.2 PSMG1 rs2836878-? rs2836878 0.72 4.00E-12 1.41 [1.08-1.84] Illumina [NR] N 11/25/2008 18758464 Kugathasan 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease Inflammatory bowel disease "1,011 cases, 4,250 controls" "1,922 cases, 14,124 controls" 1p31.3 IL23R rs11209026-? rs11209026 0.94 7.00E-11 2.56 [1.92-3.45] Illumina [NR] N 11/25/2008 18758464 Kugathasan 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease Inflammatory bowel disease "1,011 cases, 4,250 controls" "1,922 cases, 14,124 controls" 16q12.1 NOD2 rs5743289-T rs5743289 0.17 4.00E-10 1.46 [1.29-1.64] Illumina [NR] N 11/25/2008 18758464 Kugathasan 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease Inflammatory bowel disease "1,011 cases, 4,250 controls" "1,922 cases, 14,124 controls" 9q32 TNFSF15 rs6478109-? rs6478109 0.69 3.00E-08 1.36 [1.22-1.52] Illumina [NR] N 11/25/2008 18758464 Kugathasan 31-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18758464?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease Inflammatory bowel disease "1,011 cases, 4,250 controls" "1,922 cases, 14,124 controls" 6p21.32 HLA-DQA1 rs477515-? rs477515 0.69 1.00E-08 1.38 [1.23-1.54] Illumina [NR] N 11/25/2008 18729187 Galvan 26-Aug-08 Int J Cancer http://www.ncbi.nlm.nih.gov/pubmed/18729187?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A polygenic model with common variants may predict lung adenocarcinoma risk in humans Lung adenocarcinoma "482 cases, 522 controls" NR NR NR NR NR NS NS NR NR "Illumina [~318,000] (pooled)" N 11/25/2008 18846228 Weidinger 22-Aug-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18846228?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Scan on Total Serum IgE Levels Identifies FCER1A as Novel Susceptibility Locus Serum IgE levels "1,530 individuals" "9,769 individuals" 5q31.1 RAD50 rs2040704-? rs2040704 0.23 4.00E-08 13.9 [NR] % increase "Affymetrix [353,569]" N 11/25/2008 18846228 Weidinger 22-Aug-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18846228?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genome-Wide Scan on Total Serum IgE Levels Identifies FCER1A as Novel Susceptibility Locus Serum IgE levels "1,530 individuals" "9,769 individuals" 1q23.2 FCER1A rs2251746-C rs2251746 0.26 2.00E-20 19.2 [NR] % decrease "Affymetrix [353,569]" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 11q14.1 NR rs12290811-A rs12290811 0.15 4E-06 1.2 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 2q11.2 Intergenic rs2314398-? rs2314398 0.69 0.000003 1.17 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 15q14 "C15orf53, RASGRP1" rs12899449-? rs12899449 0.72 4.00E-07 1.2 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 10q21.2 ANK3 rs10994336-T rs10994336 0.05 9.00E-09 1.45 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 12q13.12 CACNA1C rs1006737-A rs1006737 0.32 7.00E-08 1.18 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 10q22.3 NR rs703965-? rs703965 0.54 8E-06 1.15 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 3p26.2 NR rs1601875-? rs1601875 0.5 7E-06 1.14 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 18p11.32 NR rs7226677-G rs7226677 0.12 7E-06 1.24 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 15q25.1 NR rs2278702-? rs2278702 0.83 0.000006 1.21 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 11q24.2 NR rs544368-T rs544368 0.12 0.000006 1.22 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 9q31.3 NR rs7042161-? rs7042161 0.65 0.000006 1.15 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 1p21.2 NR rs1948368-? rs1948368 0.51 0.000006 1.15 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 3p24.3 NR rs11720452-? rs11720452 0.58 0.000005 1.15 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 14q11.2 NR rs12436436-C rs12436436 0.08 0.000005 1.3 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 14q13.1 NR rs8015959-T rs8015959 0.02 0.000005 1.59 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 3p24.3 NR rs3821396-A rs3821396 0.11 0.000005 1.23 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 9q33.3 NR rs4130590-? rs4130590 0.56 0.000003 1.16 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 6q25.2 NR rs17082664-G rs17082664 0.13 4E-06 1.22 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 15q14 NR rs16966460-G rs16966460 0.1 4E-06 1.26 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 3p22.3 NR rs4380451-? rs4380451 0.73 4E-06 1.18 [NR] "Affymetrix [1,769,948] imputed" N 11/25/2008 18711365 Ferreira 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711365?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder Bipolar disorder "4,387 cases, 6,209 controls" NR 9p13.3 NR rs216345-T rs216345 0.37 4E-06 1.15 [NR] "Affymetrix [1,769,948] imputed" N 4/10/2009 18711366 Unoki 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711366?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations Type 2 diabetes "194 Japanese cases, 1,558 Japanese controls" "4,924 cases, 2,618 controls (Japanese), 1433 cases, 1,735 controls (Singaporean), 3,891 cases, 4,888 controls (Danish)" 6p22.3 CDKAL1 rs4712524-G rs4712524 0.42 3.00E-10 1.22 [1.15-1.31] "Affymetrix [207,097]" N 4/10/2009 18711366 Unoki 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711366?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations Type 2 diabetes "194 Japanese cases, 1,558 Japanese controls" "4,924 cases, 2,618 controls (Japanese), 1433 cases, 1,735 controls (Singaporean), 3,891 cases, 4,888 controls (Danish)" 3q27.2 IGF2BP2 rs6769511-C rs6769511 0.32 1.00E-09 1.23 [1.15-1.31] "Affymetrix [207,097]" N 4/10/2009 18711366 Unoki 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711366?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations Type 2 diabetes "194 Japanese cases, 1,558 Japanese controls" "4,924 cases, 2,618 controls (Japanese), 1433 cases, 1,735 controls (Singaporean), 3,891 cases, 4,888 controls (Danish)" 11p15.4 KCNQ1 rs2237897-C rs2237897 0.61 1.00E-16 1.33 [1.24-1.41] "Affymetrix [207,097]" N 4/3/2009 18711367 Yasuda 17-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18711367?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus Type 2 diabetes "187 Japanese cases, 1,504 Japanese controls" "6,552 Asian cases, 6,621 Asian controls, 2,830 cases, 3,740 controls (Swedish)" 11p15.5 KCNQ1 rs2237892-C rs2237892 0.61 2.00E-42 1.4 [1.34-1.47] "Invader [82,343]" N 11/25/2008 18685109 Shlien 12-Aug-08 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/18685109?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome TP53 carriage "53 carriers, 70 controls" 770 individuals Pending Pending Pending Pending Pending Pending Pending Pending "Affymetrix [3,884 CNVs]" Y 11/25/2008 18690218 Hofmann 10-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18690218?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis Sarcoidosis "499 cases, 490 controls" "1,649 cases, 1,832 controls" NR NR NR NR NS NS NR NR "Affymetrix [375,771]" N 11/25/2008 18677312 Graham 1-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus Systemic lupus erythematosus "431 cases, 2,155 controls" 740 trios 2q32.3 STAT4 rs3821236-? rs3821236 0.19 8.00E-11 1.49 [NR] "Affymetrix [313,238]" N 11/25/2008 18677312 Graham 1-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus Systemic lupus erythematosus "431 cases, 2,155 controls" 740 trios 4q28.3 Intergenic rs2313132-? rs2313132 0.12 8E-06 NR NR "Affymetrix [313,238]" N 11/25/2008 18677312 Graham 1-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus Systemic lupus erythematosus "431 cases, 2,155 controls" 740 trios 17p12 Intergenic rs12949531-? rs12949531 0.22 8E-06 NR NR "Affymetrix [313,238]" N 11/25/2008 18677312 Graham 1-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus Systemic lupus erythematosus "431 cases, 2,155 controls" 740 trios 8p23.1 BLK rs2618476-? rs2618476 0.26 2.00E-08 1.29 [NR] "Affymetrix [313,238]" N 11/25/2008 18677312 Graham 1-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus Systemic lupus erythematosus "431 cases, 2,155 controls" 740 trios 16p11.2 ITGAM rs11150610-? rs11150610 0.42 2E-06 NR NR "Affymetrix [313,238]" N 11/25/2008 18677312 Graham 1-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus Systemic lupus erythematosus "431 cases, 2,155 controls" 740 trios 6q23.3 TNFAIP3 rs5029939-? rs5029939 0.03 3.00E-12 2.28 [NR] "Affymetrix [313,238]" N 11/25/2008 18677312 Graham 1-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus Systemic lupus erythematosus "431 cases, 2,155 controls" 740 trios 10q11.22 c10orf64 rs11101442-? rs11101442 0.32 0.000003 NR NR "Affymetrix [313,238]" N 11/25/2008 18677312 Graham 1-Aug-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677312?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus Systemic lupus erythematosus "431 cases, 2,155 controls" 740 trios 2p16.3 Intergenic rs17039212-? rs17039212 0.1 0.000009 NR NR "Affymetrix [313,238]" N 11/25/2008 18668548 Julia 1-Aug-08 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/18668548?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility Rheumatoid arthritis "400 cases, 400 controls" "410 cases, 394 controls" 18q23 SALL3 rs2002842-A rs2002842 0.49 0.000006 1.61 [NR] "Illumina [299,918]" N 11/25/2008 18668548 Julia 1-Aug-08 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/18668548?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility Rheumatoid arthritis "400 cases, 400 controls" "410 cases, 394 controls" 6p21.32 "HLA-DQA1, HLA-DQA2" rs6457617-? rs6457617 NR 1.00E-09 NR NR "Illumina [299,918]" N 11/25/2008 18677311 O'Donovan 30-Jul-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of loci associated with schizophrenia by genome-wide association and follow-up Schizophrenia "479 cases, 2,937 controls" "6,666 cases, 9,897 controls" 16p13.12 Intergenic rs7192086-T rs7192086 0.24 0.000006 1.12 [NR] "Affymetrix [362,532]" N 11/25/2008 18677311 O'Donovan 30-Jul-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of loci associated with schizophrenia by genome-wide association and follow-up Schizophrenia "479 cases, 2,937 controls" "6,666 cases, 9,897 controls" 11p14.1 Intergenic rs1602565-C rs1602565 0.11 0.000003 1.16 [NR] "Affymetrix [362,532]" N 11/25/2008 18677311 O'Donovan 30-Jul-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18677311?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of loci associated with schizophrenia by genome-wide association and follow-up Schizophrenia "479 cases, 2,937 controls" "6,666 cases, 9,897 controls" 2q32.1 ZNF804A rs1344706-T rs1344706 0.59 2.00E-07 1.12 [NR] "Affymetrix [362,532]" N 11/25/2008 18660810 Schormair 27-Jul-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18660810?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome Restless legs syndrome "628 cases, 1,644 controls" "1,835 cases, 3,111 controls" 9p24.1 PTPRD rs1975197-T rs1975197 0.16 6.00E-09 1.31 [1.20-1.44] "Affymetrix [208,733]" N 11/25/2008 18660810 Schormair 27-Jul-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18660810?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome Restless legs syndrome "628 cases, 1,644 controls" "1,835 cases, 3,111 controls" 9p23 PTPRD rs4626664-A rs4626664 0.12 6.00E-10 1.44 [1.31-1.59] "Affymetrix [208,733]" N 11/25/2008 18650507 The SEARCH Collaborative Group 23-Jul-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18650507?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum SLCO1B1 Variants and Statin-Induced Myopathy--A Genomewide Study Response to statin therapy "85 cases, 90 controls" "19,856 individuals" 12p12.1 SLCO1B1 rs4149056-C rs4149056 0.13 2.00E-09 4.5 [2.60-7.70] "Illumina [316,184]" N 11/25/2008 18723019 Franke 21-Jul-08 Gastroenterology http://www.ncbi.nlm.nih.gov/pubmed/18723019?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study anaylsis in sarcoidosis and Crohn disease unravels a common susceptibility locus on 10p12.2 Crohn's disease and Sarcoidosis (combined) "382 CD cases, 398 SA cases, 394 controls" "660 CD cases, 657 SA cases, 1,091 controls" 10p12.2 C10orf67 rs1398024-A rs1398024 0.25 0.000004 1.23 [1.04-1.45] "Affymetrix [83,360]" N 11/25/2008 18615156 Liu 10-Jul-08 Mol Med http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis Treatment response to TNF antagonists 89 cases NR 9p21.2 IFNK rs7046653-A rs7046653 0.26 5.00E-07 NR NR "Illumina [283,348]" N 11/25/2008 18615156 Liu 10-Jul-08 Mol Med http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis Treatment response to TNF antagonists 89 cases NR 20q12 MAFB rs6028945-T rs6028945 0.12 2.00E-07 NR NR "Illumina [283,348]" N 11/25/2008 18615156 Liu 10-Jul-08 Mol Med http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis Treatment response to TNF antagonists 89 cases NR 7q21.3 PON1 rs854555-A rs854555 0.34 2E-06 NR NR "Illumina [283,348]" N 11/25/2008 18615156 Liu 10-Jul-08 Mol Med http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis Treatment response to TNF antagonists 89 cases NR 4p15.1 CENTD1 rs437943-G rs437943 0.33 4E-06 NR NR "Illumina [283,348]" N 11/25/2008 18615156 Liu 10-Jul-08 Mol Med http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis Treatment response to TNF antagonists 89 cases NR 1p22.3 LMO4 rs983332-A rs983332 0.21 0.000005 NR NR "Illumina [283,348]" N 11/25/2008 18615156 Liu 10-Jul-08 Mol Med http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis Treatment response to TNF antagonists 89 cases NR 6q26 QKI rs10945919-G rs10945919 0.32 3.00E-07 NR NR "Illumina [283,348]" N 11/25/2008 18615156 Liu 10-Jul-08 Mol Med http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis Treatment response to TNF antagonists 89 cases NR 20p11.21 CST5 rs6138150-T rs6138150 0.84 0.000003 NR NR "Illumina [283,348]" N 11/25/2008 18615156 Liu 10-Jul-08 Mol Med http://www.ncbi.nlm.nih.gov/pubmed/18615156?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in Rheumatoid Arthritis Treatment response to TNF antagonists 89 cases NR 2q24.3 LASS6 rs13393173-A rs13393173 0.12 4E-06 NR NR "Illumina [283,348]" N 11/25/2008 18604267 Pare 4-Jul-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18604267?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women" Soluble ICAM-1 "4,570 women" "2,008 women" 9q34.2 ABO rs507666-G rs507666 0.2 5.00E-29 17.73 [NR] umol/L decrease "Illumina [336,108]" N 11/25/2008 18604267 Pare 4-Jul-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18604267?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women" Soluble ICAM-1 "4,570 women" "2,008 women" 19p13.2 ICAM1 rs1799969-G rs1799969 0.12 4.00E-47 28.19 [NR] umol/L decrease "Illumina [336,108]" N 11/25/2008 18604267 Pare 4-Jul-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18604267?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women" Soluble ICAM-1 "4,570 women" "2,008 women" 19p13.2 ICAM1 rs5498-A rs5498 0.43 5.00E-25 13.22 [NR] umol/L increase "Illumina [336,108]" N 11/25/2008 18604267 Pare 4-Jul-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18604267?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women" Soluble ICAM-1 "4,570 women" "2,008 women" 19p13.2 ICAM1 rs281437-? rs281437 0.3 3.00E-10 10.1 [NR] umol/L increase "Illumina [336,108]" N 11/25/2008 18601904 Bae 2-Jul-08 Biochem Biophys Res Commun http://www.ncbi.nlm.nih.gov/pubmed/18601904?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population Subarachnoid aneurysmal hemorrhage "203 cases, 294 controls" NR Pending Pending Pending Pending Pending Pending Pending Pending "Illumina [317,503]" Y 11/25/2008 18594024 Sarasquete 1-Jul-08 Blood http://www.ncbi.nlm.nih.gov/pubmed/18594024?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis Osteonecrosis of the jaw "21 cases, 64 controls" NR 10q23.33 CYP2C8 rs1934951-T rs1934951 0.12 1.00E-06 12.75 [3.7-43.5] "Affymetrix [339,972]" N 11/25/2008 18591461 Turner 30-Jun-08 Hypertension http://www.ncbi.nlm.nih.gov/pubmed/18591461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic Response to diuretic therapy "194 blacks, 195 whites" NR 12q15 "LYZ, YEATS4, FRS2" 3-SNP haplotype "rs317689,rs315135,rs7297610" NR 0.000006 NR NR "Affymetrix [up to 102,334]" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 2q37.1 ATG16L1 rs3828309-G rs3828309 0.53 2.00E-32 1.25 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 16q12.1 NOD2 rs2066847-C rs2066847 0.02 3.00E-24 3.99 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 10q24.2 NKX2-3 rs11190140-T rs11190140 0.48 3.00E-16 1.2 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 9q32 TNFSF15 rs4263839-G rs4263839 0.68 3.00E-10 1.22 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 5q33.1 IRGM rs11747270-G rs11747270 0.09 3.00E-16 1.33 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 5q31.1 Intergenic rs2188962-T rs2188962 0.43 2.00E-18 1.25 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 5p13.1 PTGER4 rs4613763-C rs4613763 0.13 7.00E-27 1.32 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 10q21.2 ZNF365 rs10995271-C rs10995271 0.39 4.00E-20 1.25 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 13q14.11 Unknown rs3764147-G rs3764147 0.22 2.00E-13 1.25 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 5q33.3 IL12B rs10045431-C rs10045431 0.71 4.00E-13 1.11 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 6q27 CCR6 rs2301436-T rs2301436 0.46 1.00E-12 1.21 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 17q21.2 STAT3 rs744166-A rs744166 0.57 7.00E-12 1.18 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 6q21 Unknown rs7746082-C rs7746082 0.29 2.00E-10 1.17 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 3p21.31 MST1 rs3197999-A rs3197999 0.27 1.00E-12 1.2 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 18p11.21 PTPN2 rs2542151-G rs2542151 0.15 5.00E-17 1.35 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 1p31.3 IL23R rs11465804-T rs11465804 0.93 7.00E-63 2.5 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 1p13.2 PTPN22 rs2476601-G rs2476601 0.9 1.00E-08 1.31 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 1q23.2 ITLN1 rs2274910-C rs2274910 0.68 1.00E-09 1.14 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 1q24.3 Intergenic rs9286879-G rs9286879 0.24 2.00E-09 1.19 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 1q32.1 Intergenic rs11584383-T rs11584383 0.7 1.00E-11 1.18 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 6p22.3 CDKAL1 rs6908425-C rs6908425 0.78 9.00E-10 1.21 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 7p12.2 Intergenic rs1456893-A rs1456893 0.68 5.00E-09 1.2 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 8q24.13 Intergenic rs1551398-A rs1551398 0.62 5.00E-09 1.08 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 9p24.1 JAK2 rs10758669-C rs10758669 0.35 3.00E-09 1.12 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 10p11.21 Intergenic rs17582416-G rs17582416 0.35 2.00E-09 1.16 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 11q13.5 C11orf30 rs7927894-T rs7927894 0.39 1.00E-09 1.16 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 12q12 "LRRK2, MUC19" rs11175593-T rs11175593 0.02 3.00E-10 1.54 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 17q12 ORMDL3 rs2872507-A rs2872507 0.47 5.00E-09 1.12 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 21q21.1 Intergenic rs1736135-T rs1736135 0.57 7.00E-09 1.18 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18587394 Barrett 29-Jun-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18587394?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide assocation defines more than 30 distinct susceptibility loci for Crohn's disease Crohn's disease "3,230 cases 4,829 controls" "1,339 trios, 2,325 cases, 1,809 controls" 21q22.3 ICOSLG rs762421-G rs762421 0.39 1.00E-09 1.13 [NR] "Affymetrix and Illumina [635,547] (imputed)" N 11/25/2008 18576341 Behrens 24-Jun-08 Arthritis Rheum http://www.ncbi.nlm.nih.gov/pubmed/18576341?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis Arthritis (juvenile idiopathic) "130 cases 1,952 controls" NR 6p21.32 HLA-DRB1 rs2395148-? rs2395148 NR 2.00E-10 5.37 [3.02-9.56] "Illumina [524,684]" N 11/25/2008 18451265 Bouatia-Naji 19-Jun-08 Science http://www.ncbi.nlm.nih.gov/pubmed/18451265?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Polymorphism Within the G6PC2 Gene is Associated with Fasting Plasma Glucose Levels Fasting plasma glucose 654 normoglycemic individuals "9,353 individuals" 2q24.3 G6PC2 rs560887-A rs560887 0.3 4.00E-23 0.06 [0.05-0.08] mmol/l decrease "Illumina [392,935]" N 11/25/2008 18535201 Cooper 5-Jun-08 Blood http://www.ncbi.nlm.nih.gov/pubmed/18535201?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose Warfarin maintenance dose 181 individuals 374 individuals 12p13.33 CACNA1C rs216013-? rs216013 NR 9.00E-07 NR NR "Illumina [538,629]" N 11/25/2008 18535201 Cooper 5-Jun-08 Blood http://www.ncbi.nlm.nih.gov/pubmed/18535201?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose Warfarin maintenance dose 181 individuals 374 individuals 10q23.33 CYP2C9 rs4086116-? rs4086116 NR 6.00E-12 NR NR "Illumina [538,629]" N 11/25/2008 18535201 Cooper 5-Jun-08 Blood http://www.ncbi.nlm.nih.gov/pubmed/18535201?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose Warfarin maintenance dose 181 individuals 374 individuals 16p11.2 VKORC1 rs10871454-? rs10871454 NR 5.00E-34 NR NR "Illumina [538,629]" N 11/25/2008 18521185 Chen 4-Jun-08 J Clin Invest http://www.ncbi.nlm.nih.gov/pubmed/18521185?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels Fasting plasma glucose "5,088 nondiabetic individuals" "18,436 nondiabetic individuals" 2q24.3 "G6PC2,ABCB11" rs563694-C rs563694 0.34 4.00E-07 NR NR "Illumina [315,635]" N 11/25/2008 18519826 Uhl 4-Jun-08 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18519826?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Molecular genetics of successful smoking cessation: convergent genome-wide association study results Smoking cessation "241 cases, 309 controls" NR NR NR NR NR NS NS NR NR "Affymetrix [~500,000] (pooled)" N 11/25/2008 18521090 Lavedan 3-Jun-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18521090?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of the NPAS3gene and five other loci with response of the antipsychotic iloperidone identified in a whole genome association study Response to iloperidone treatment (PANSS-T score) 106 individuals 104 individuals NR NR NR NR NS NS NR NR "Affymetrix [334,563]" N 11/25/2008 18521091 Volpi 3-Jun-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia Response to iloperidone treatment (QT prolongation) 183 individuals NR 2q31.3 CERKL rs993648-T rs993648 NR 0.000003 NR NR "Affymetrix [339,272]" N 11/25/2008 18521091 Volpi 3-Jun-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia Response to iloperidone treatment (QT prolongation) 183 individuals NR 10q23.1 NRG3 rs4933824-T rs4933824 NR 2E-06 NR NR "Affymetrix [339,272]" N 11/25/2008 18521091 Volpi 3-Jun-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia Response to iloperidone treatment (QT prolongation) 183 individuals NR 15q26.1 SLCO3A1 rs3924426-T rs3924426 NR 2E-06 NR NR "Affymetrix [339,272]" N 11/25/2008 18521091 Volpi 3-Jun-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia Response to iloperidone treatment (QT prolongation) 183 individuals NR 4q32.3 PALLD rs17054392-C rs17054392 NR 0.000003 NR NR "Affymetrix [339,272]" N 11/25/2008 18521091 Volpi 3-Jun-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia Response to iloperidone treatment (QT prolongation) 183 individuals NR 18q12.2 BRUNOL4 rs4799915-T rs4799915 NR 0.000003 NR NR "Affymetrix [339,272]" N 11/25/2008 18521091 Volpi 3-Jun-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18521091?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia Response to iloperidone treatment (QT prolongation) 183 individuals NR 14q12 NUBPL rs7142881-A rs7142881 NR 2E-06 NR NR "Affymetrix [339,272]" N 11/25/2008 18488026 Brown 18-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18488026?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common sequence variants on 20q11.22 confer melanoma susceptibility Melanoma "864 cases, 864 controls" "1,230 cases, 1,251 controls" 20q11.22 CDC91L1 rs910873-T rs910873 0.09 1.00E-15 1.75 [1.53-2.01] "Illumina [535,150] (pooled)" N 11/25/2008 18488028 Sulem 18-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Two newly identified genetic determinants of pigmentation in Europeans Blond vs. brown hair color "5,130 individuals" "3,330 individuals" 11q13.2 TPCN2 rs35264875-T rs35264875 0.22 4.00E-30 2.49 [1.96-3.15] "Illumina [316,515]" N 11/25/2008 18488028 Sulem 18-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Two newly identified genetic determinants of pigmentation in Europeans Blue vs. green eyes "5,130 individuals" "3,330 individuals" 9p23 TYRP1 rs1408799-C rs1408799 0.75 6.00E-17 1.4 [1.25-1.57] "Illumina [316,515]" N 11/25/2008 18488028 Sulem 18-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Two newly identified genetic determinants of pigmentation in Europeans Burning and freckling "5,130 individuals" "3,330 individuals" 20q11.22 ASIP rs1015362-G + rs4911414-T "rs1015362,rs4911414" 0.08 6.00E-37 2.56 [2.06-3.18] "Illumina [316,515]" N 11/25/2008 18488028 Sulem 18-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Two newly identified genetic determinants of pigmentation in Europeans Freckles "5,130 individuals" "3,330 individuals" 20q11.22 ASIP rs1015362-G + rs4911414-T "rs1015362,rs4911414" 0.08 8.00E-29 1.95 [1.65-2.32] "Illumina [316,515]" N 11/25/2008 18488028 Sulem 18-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Two newly identified genetic determinants of pigmentation in Europeans Red vs. non-red hair color "5,130 individuals" "3,330 individuals" 20q11.22 ASIP rs1015362-G + rs4911414-T "rs1015362,rs4911414" 0.08 3.00E-09 1.76 [1.34-2.31] "Illumina [316,515]" N 11/25/2008 18488028 Sulem 18-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18488028?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Two newly identified genetic determinants of pigmentation in Europeans Skin sensitivity to sun "5,130 individuals" "3,330 individuals" 20q11.22 ASIP rs1015362-G + rs4911414-T "rs1015362,rs4911414" 0.08 2.00E-24 1.76 [1.49-2.08] "Illumina [316,515]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. blond hair color "2,287 women" "up to 8,465 individuals" 5p13.3 MATP rs28777-C rs28777 NR 1.00E-17 0.46 [0.36-0.56] decrease in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. blond hair color "2,287 women" "up to 8,465 individuals" 15q13.1 Intergenic rs8033165-T rs8033165 NR 5.00E-11 0.12 [0.08-0.16] increase in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. blond hair color "2,287 women" "up to 8,465 individuals" 14q32.12 SLC24A4 rs12896399-G rs12896399 NR 8.00E-21 0.18 [0.14-0.22] increase in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. blond hair color "2,287 women" "up to 8,465 individuals" 15q13.1 HERC2 rs12913832-A rs12913832 NR 4.00E-103 0.44 [0.40-0.48] decrease in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. blond hair color "2,287 women" "up to 8,465 individuals" 6p25.3 IRF4 rs12203592-T rs12203592 NR 7.00E-127 0.35 [0.33-0.37] decrease in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. blond hair color "2,287 women" "up to 8,465 individuals" 15q13.1 OCA2 rs11855019-G rs11855019 NR 2.00E-24 0.28 [0.22-0.34] decrease in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. blond hair color "2,287 women" "up to 8,465 individuals" 6p25.3 EXOC2 rs6918152-A rs6918152 NR 6.00E-08 0.11 [0.07-0.15] increase in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. red hair color "2,287 women" "up to 8,465 individuals" 15q13.1 HERC2 rs12913832-A rs12913832 NR 1.00E-77 0.44 [0.40-0.48] decrease in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. red hair color "2,287 women" "up to 8,465 individuals" 6p25.3 EXOC2 rs6918152-A rs6918152 NR 5.00E-07 0.11 [0.07-0.15] increase in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. red hair color "2,287 women" "up to 8,465 individuals" 5p13.3 MATP rs28777-C rs28777 NR 9.00E-14 0.46 [0.34-0.58] decrease in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. red hair color "2,287 women" "up to 8,465 individuals" 16q24.3 MC1R rs258322-T rs258322 NR 2.00E-23 0.36 [0.28-0.44] increase in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. red hair color "2,287 women" "up to 8,465 individuals" 6p25.3 IRF4 rs12203592-T rs12203592 NR 9.00E-28 0.31 [0.25-0.36] decrease in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. red hair color "2,287 women" "up to 8,465 individuals" 15q13.1 Intergenic rs8033165-T rs8033165 NR 2.00E-12 0.15 [0.11-0.19] increase in hair color score "Illumina [528,173]" N 11/25/2008 18483556 Han 16-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18483556?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Novel Alleles Associated with Hair Color and Skin Pigmentation Black vs. red hair color "2,287 women" "up to 8,465 individuals" 15q13.1 OCA2 rs11855019-G rs11855019 NR 6.00E-20 0.29 [0.23-0.35] decrease in hair color score "Illumina [528,173]" N 11/25/2008 18463370 Maris 9-May-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18463370?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Chromosome 6p22 Locus Associated with Clinically Aggressive Neuroblastoma Neuroblastoma "1,032 cases, 2,043 controls" "720 cases, 2,128 controls" 6p22.3 "FLJ22536, FLJ44180" rs6939340-G rs6939340 0.5 9.00E-15 1.37 [1.27-1.49] "Illumina [464,934]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 12q12 "PDZRN4,CNTN1" rs1880887-? rs1880887 0.03 1.00E-10 (Alkaline phosphatase)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 12q24.11 ATP2A2 rs11065611-? rs11065611 0.06 1.00E-07 (Alpha-1 globulin)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 12q24.33 GPR133 rs10466868-? rs10466868 0.12 1.00E-06 (Erythropoeitin)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 13q12.11 FGF3 rs17369571-? rs17369571 0.16 1.00E-07 (IL1RA)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 13q12.2 SACS rs4770433-? rs4770433 0.4 4E-06 (IL12)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 15q15.2 CDAN1 rs16957063-? rs16957063 0.01 5.00E-07 (Ft4)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 15q21.1 DUT rs11637235-? rs11637235 0.28 0.000003 (Adiponectin)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 16q23.2 BCM01 rs4889294-? rs4889294 0.47 5.00E-07 (IL1B)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 17p12 HS3ST3B1 rs3848445-? rs3848445 0.05 8.00E-09 (Ft3)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 17q25.3 C17orf62 rs9303029-? rs9303029 0.08 4.00E-07 (Free IGF1)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 18q11.2 OSBPL1A rs9635963-? rs9635963 0.18 2.00E-07 (SHBG)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 18q12.1 DSC3 rs2729409-? rs2729409 0.26 0.000003 (Parathyroid hormone)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 19p13.2 ANGPTL6 rs8109578-? rs8109578 0.08 4.00E-07 (TSH)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 11q23.1 IL18 rs2250417-A rs2250417 0.44 7.00E-13 (IL18)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 1q21.3 IL6R rs4129267-C rs4129267 0.37 2.00E-57 (sIL-6R)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 17q12 CCL4L2 rs4796217-T rs4796217 0.34 4.00E-21 (MIPb)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 6q26 LPA rs7770628-T rs7770628 0.49 4.00E-10 (LPA)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 22q11.23 GGT1 rs5751901-T rs5751901 0.39 2.00E-07 (GGT1)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 9q34.2 ABO rs505922-? rs505922 0.34 7.00E-40 (TNFA)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 17p13.1 SHBG rs6761-? rs6761 0.31 3.00E-07 (SHBG)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 1q23.2 CRP rs12093699-? rs12093699 0.29 0.000006 (CRP)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 2q13 IL1RN rs6761276-? rs6761276 0.37 7E-06 (IL1RA)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 1p21.1 COL11A rs10874639-? rs10874639 0.12 0.000003 (Fibrinogen)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 1q21.1 CHD1L rs4950322-? rs4950322 0.21 2.00E-07 (Resistin)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 1q21.1 CHD1L rs4950322-? rs4950322 0.21 7.00E-07 (Hgb)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 2p15 LOC51057 rs11683229-? rs11683229 0.15 0.000006 (IL6)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 2p13.3 DYSF rs2900976-? rs2900976 0.3 1.00E-06 (Albumin)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 2p12 CTNNA2 rs11695685-? rs11695685 0.3 5.00E-07 (IL10)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 2p11.2 SH2D6 rs7577642-? rs7577642 0.27 7E-06 (sIL-6R)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 2q23.1 EPC2 rs10191411-? rs10191411 0.32 4E-06 (IL8)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 3p12.3 ROBO1 rs9834373-? rs9834373 0.17 4E-06 (GP130)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 5q35.1 DOCK2 rs169082-? rs169082 0.48 1.00E-06 (Leptin)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 6p21.33 HLA-C rs9461688-? rs9461688 0.31 4E-06 (IL18)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 6q11.1 KHDRBS2 rs6455128-? rs6455128 0.19 3.00E-07 (GOT (AST))  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 6q22.31 GJA1 rs4541776-? rs4541776 0.33 2E-06 (GGT)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 6q23.2 EYA4 rs9402515-? rs9402515 0.09 1.00E-06 (Alpha-2 macroglobulin)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 6q24.3 SASH1 rs6930337-? rs6930337 0.06 1.00E-06 (insulin)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 7p21.3 NXPH1 rs1285407-? rs1285407 0.35 1.00E-06 (TGF-b1)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 8q21.11 "GDAP1,PI15" rs6472866-? rs6472866 0.42 8.00E-07 (myoglobin)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 8q24.21 FAM49B rs10092658-? rs10092658 0.07 0.000006 (Aldolase)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 9q22.2 "GADD45G,DIRAS2" rs2081670-? rs2081670 0.15 0.000003 (MIP-1b)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 9q31.2 TMEM38B rs4742971-? rs4742971 0.11 8.00E-07 (GPT (ALT))  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 10p12.33 CACNB2 rs7076247-? rs7076247 0.37 0.000006 (CRP)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 10p11.21 "FZD8,ANKRD30A" rs1779876-? rs1779876 0.1 0.000003 (Lipoprotein A)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 11p15.5 KCNQ1 rs2237878-? rs2237878 0.07 0.000001 (Lactic dehydrogenase)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 11q14.1 DLG2 rs3885683-? rs3885683 0.11 8E-06 (MCP1)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 11q23.3 PAFAH1B2 rs7112513-? rs7112513 0.13 6.00E-09 (Soluble transferrin receptor)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 11q24.2 KIRREL3 rs1939992-? rs1939992 0.26 1.00E-06 (Total IGF-1)  NR NR "Illumina [496,032]" N 11/25/2008 18464913 Melzer 9-May-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18464913?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs) Protein quantitative trait loci "1,200 individuals" NR 12p12.3 EPS8 rs17415853-? rs17415853 0.02 7.00E-07 (Ferritin)  NR NR "Illumina [496,032]" N 11/25/2008 18463975 Kibriya 8-May-08 Breast Cancer Res Treat http://www.ncbi.nlm.nih.gov/pubmed/18463975?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum A pilot genome-wide association study of early-onset breast cancer Breast cancer "30 cases, 30 controls" NR 2q37.1 GLG1 3-SNP haplotype 1 rs10871290 0.34 4.00E-07 NR NR "Affymetrix [200,220]" N 11/25/2008 18471798 Valdes 8-May-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18471798?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide Association Scan Identifies a Prostaglandin-Endoperoxide Synthase 2 Variant Involved in Risk of Knee Osteoarthritis Knee osteoarthritis "357 cases, 285 controls" "1,177 cases, 2,372 controls" 2q33.3 PARD3B rs1207421-? rs1207421 0.09 0.000006 1.46 [1.24-1.73] "Illumina [413,461]" N 11/25/2008 18471798 Valdes 8-May-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18471798?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide Association Scan Identifies a Prostaglandin-Endoperoxide Synthase 2 Variant Involved in Risk of Knee Osteoarthritis Knee osteoarthritis "357 cases, 285 controls" "1,177 cases, 2,372 controls" 1q31.1 "PTGS2, PLA2G4A" rs4140564-? rs4140564 0.05 0.000003 1.59 [1.31-1.94] "Illumina [413,461]" N 11/25/2008 18454146 Chambers 4-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18454146?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common genetic variation near MC4R is associated with waist circumference and insulin resistance Waist circumference and related phenotypes "2,684 Asian Indian men" "11,955 Asian Indian and European individuals" 2p23.3 GCKR rs1260326-? rs1260326 NR 4.00E-08 (triglycerides)  NR NR "Illumina [308,067]" N 11/25/2008 18454146 Chambers 4-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18454146?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common genetic variation near MC4R is associated with waist circumference and insulin resistance Waist circumference and related phenotypes "2,684 Asian Indian men" "11,955 Asian Indian and European individuals" 18q21.32 MC4R rs12970134-A rs12970134 0.36 2.00E-09 (waist circumference)  0.88 [0.59-1.17] cm increase "Illumina [308,067]" N 11/25/2008 18454146 Chambers 4-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18454146?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common genetic variation near MC4R is associated with waist circumference and insulin resistance Waist circumference and related phenotypes "2,684 Asian Indian men" "11,955 Asian Indian and European individuals" 16q13 CETP rs3764261-? rs3764261 NR 1.00E-27 (HDL cholesterol)  NR NR "Illumina [308,067]" N 11/25/2008 18454146 Chambers 4-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18454146?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common genetic variation near MC4R is associated with waist circumference and insulin resistance Waist circumference and related phenotypes "2,684 Asian Indian men" "11,955 Asian Indian and European individuals" 8p21.3 LPL rs2083637-? rs2083637 NR 0.000005 (HDL cholesterol)  NR NR "Illumina [308,067]" N 11/25/2008 18454148 Loos 4-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18454148?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Common variants near MC4R are associated with fat mass, weight and risk of obesity" Body mass index "16,876 individuals" "60,352 individuals" 16q12.2 FTO rs1121980-? rs1121980 NR 4.00E-08 0.06 [0.04-0.08] unit increase in log(BMI) "Affymetrix [344,883]" N 11/25/2008 18454148 Loos 4-May-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18454148?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Common variants near MC4R are associated with fat mass, weight and risk of obesity" Body mass index "16,876 individuals" "60,352 individuals" 18q21.32 MC4R rs17782313-C rs17782313 0.24 3.00E-15 0.05 [0.04-0.06] unit increase in log(BMI) "Affymetrix [344,883]" N 11/25/2008 18449908 Poduslo 30-Apr-08 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/18449908?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome Screen of Late-Onset Alzheimer's Extended Pedigrees Identifies TRPC4AP by Haplotype Analysis Alzheimer's disease "29 siblings from 2 affected families, 60 unrelated controls" "199 patients, 85 spouses" NR NR NR NR NS NS NR NR "Affymetrix [469,218]" N 11/25/2008 18455228 Richards 29-Apr-08 Lancet http://www.ncbi.nlm.nih.gov/pubmed/18455228?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study" Bone mineral density "2,094 women" "6,463 individuals" 8q24.12 TNFRSF11B rs4355801-A rs4355801 0.53 8.00E-10 0.09 [NR] SD decrease "Illumina [314,075]" N 11/25/2008 18455228 Richards 29-Apr-08 Lancet http://www.ncbi.nlm.nih.gov/pubmed/18455228?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study" Bone mineral density "2,094 women" "6,463 individuals" 11q13.2 LRP5 rs3736228-T rs3736228 0.14 6.00E-12 0.13 [NR] SD decrease "Illumina [314,075]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (hip) "5,861 individuals" "7,925 individuals" 18q21.33 RANK rs3018362-A rs3018362 0.35 1.00E-06 0.07 [0.04-0.10] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (hip) "5,861 individuals" "7,925 individuals" 13q14.11 RANKL rs9594738-T rs9594738 0.56 2.00E-08 0.1 [0.06-0.13] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (hip) "5,861 individuals" "7,925 individuals" 1p36.12 ZBTB40 rs7524102-A rs7524102 0.82 5.00E-16 0.15 [0.11-0.19] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (hip) "5,861 individuals" "7,925 individuals" 6q25.1 ESR1 rs1038304-G rs1038304 0.47 5.00E-09 0.08 [0.06-0.11] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (hip) "5,861 individuals" "7,925 individuals" 8q24.12 OPG rs6993813-C rs6993813 0.5 3.00E-11 0.09 [0.07-0.12] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (hip) "5,861 individuals" "7,925 individuals" 6q25.1 "ESR1, C6orf97" rs4870044-T rs4870044 0.28 2.00E-07 0.08 [0.05-0.11] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (spine) "5,861 individuals" "7,925 individuals" 13q14.11 RANKL rs9594759-T rs9594759 0.62 2.00E-21 0.17 [0.14-0.21] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (spine) "5,861 individuals" "7,925 individuals" 8q24.12 OPG rs6469804-A rs6469804 0.51 7.00E-15 0.12 [0.09-0.15] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (spine) "5,861 individuals" "7,925 individuals" 6p25.1 ESR1 rs4870044-T rs4870044 0.28 2.00E-11 0.11 [0.08-0.14] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (spine) "5,861 individuals" "7,925 individuals" 6p21.32 "MHC, C6orf10" rs3130340-T rs3130340 0.79 1.00E-07 0.1 [0.06-0.13] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (spine) "5,861 individuals" "7,925 individuals" 1p36.12 ZBTB40 rs7524102-A rs7524102 0.82 9.00E-09 0.11 [0.07-0.15] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (spine) "5,861 individuals" "7,925 individuals" 6q25.1 "ESR1, C6orf97" rs1038304-G rs1038304 0.47 4.00E-11 0.1 [0.07-0.13] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (spine) "5,861 individuals" "7,925 individuals" 2p16.2 SPTBN1 rs11898505-G rs11898505 0.67 8.00E-07 0.08 [0.05-0.11] SD decrease "Illumina [301,019]" N 11/25/2008 18445777 Styrkarsdottir 29-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18445777?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple Genetic Loci for Bone Mineral Density and Fractures Bone mineral density (spine) "5,861 individuals" "7,925 individuals" 6q25.1 "ESR1, C6orf97" rs1999805-C rs1999805 0.44 2.00E-08 0.09 [0.06-0.12] SD decrease "Illumina [301,019]" N 11/25/2008 18369103 Walsh 25-Apr-08 Science http://www.ncbi.nlm.nih.gov/pubmed/18369103?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia Schizophrenia "150 cases, 268 controls" "83 children, 154 parents" Pending Pending Pending Pending Pending Pending Pending Pending "Illumina [~550,000]" Y 11/25/2008 18439552 Reiner 24-Apr-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18439552?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Polymorphisms of the HNF1A Gene Encoding Hepatocyte Nuclear Factor-1 Alpha are Associated with C-Reactive Protein C-reactive protein 909 individuals "5,106 individuals" 19q13.32 APOE rs2075650-? rs2075650 NR 1.00E-07 NR NR "Illumina [317,000]" N 11/25/2008 18439552 Reiner 24-Apr-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18439552?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Polymorphisms of the HNF1A Gene Encoding Hepatocyte Nuclear Factor-1 Alpha are Associated with C-Reactive Protein C-reactive protein 909 individuals "5,106 individuals" 1q23.2 CRP rs11265260-? rs11265260 NR 7E-06 NR NR "Illumina [317,000]" N 11/25/2008 18439552 Reiner 24-Apr-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18439552?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Polymorphisms of the HNF1A Gene Encoding Hepatocyte Nuclear Factor-1 Alpha are Associated with C-Reactive Protein C-reactive protein 909 individuals "5,106 individuals" 12q24.31 HNF1A rs1169310-A rs1169310 0.38 2.00E-08 0.13 [0.08-0.17] mg/l decrease in log(CRP) level "Illumina [317,000]" N 11/25/2008 18439548 Ridker 24-Apr-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study" C-reactive protein "6,345 women" NR 12q24.31 HNF1A rs7310409-A rs7310409 NR 7.00E-17 0.15 [NR] mg/dl decrease "Illumina [336,108]" N 11/25/2008 18439548 Ridker 24-Apr-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study" C-reactive protein "6,345 women" NR 2p23.3 GCKR rs780094-A rs780094 NR 7.00E-15 0.14 [NR] mg/dl increase "Illumina [336,108]" N 11/25/2008 18439548 Ridker 24-Apr-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study" C-reactive protein "6,345 women" NR 12q23.2 Unknown rs10778213-G rs10778213 NR 1.00E-10 0.12 [NR] mg/dl decrease "Illumina [336,108]" N 11/25/2008 18439548 Ridker 24-Apr-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study" C-reactive protein "6,345 women" NR 1q21.3 IL6R rs8192284-? rs8192284 NR 2.00E-08 0.1 [NR] mg/dl decrease "Illumina [336,108]" N 11/25/2008 18439548 Ridker 24-Apr-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study" C-reactive protein "6,345 women" NR 1p31.3 LEPR rs1892534-A rs1892534 NR 7.00E-21 0.17 [NR] mg/dl decrease "Illumina [336,108]" N 11/25/2008 18439548 Ridker 24-Apr-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study" C-reactive protein "6,345 women" NR 1q23.2 CRP rs3091244-? rs3091244 NR 6.00E-28 0.2 [NR] mg/dl increase "Illumina [336,108]" N 11/25/2008 18439548 Ridker 24-Apr-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18439548?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Loci Related to Metabolic-Syndrome Pathways Including LEPR, HNF1A, IL6R, and GCKR Associate with Plasma C-Reactive Protein: The Women's Genome Health Study" C-reactive protein "6,345 women" NR 19q13.32 APOE rs769449-? rs769449 NR 9.00E-21 0.26 [NR] mg/dl decrease "Illumina [336,108]" N 11/25/2008 18403759 Ober 9-Apr-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18403759?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Effect of Variation in CHI31 on Serum YKL-40 Level, Risk of Asthma, and Lung Function" YKL-40 levels 632 individuals 206 children 1q32.1 CHI3L1 rs4950928-G rs4950928 0.29 1.00E-13 0.3 [NR] ng/ml decrease "Affymetrix [290,325]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 7p22.2 GNA12 rs798544-G rs798544 0.72 7.00E-15 5.9 [6.03-8.77] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6q24.1 GPR126 rs3748069-A rs3748069 0.74 5.00E-14 6.5 [5.44-9.36] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 4q31.22 HHIP rs1812175-C rs1812175 0.86 1.00E-11 8.3 [5.95-10.65] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6p24.3 BMP6 rs12198986-A rs12198986 0.5 2.00E-11 6.8 [4.84-8.76] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 1q21.2 "Histone class 2A,MTMR11, SV2A, SF3B4" rs11205277-G rs11205277 0.44 1.00E-10 5.1 [3.53-6.67] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 1q24.3 DNM3 rs678962-G rs678962 0.22 3.00E-08 5.4 [3.44-7.36] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6q21 "LIN28B, HACE1, BVES, POPDC3" rs314268-C rs314268 0.34 8.00E-07 4.6 [2.84-6.36] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6q21 "PPIL6, CD164, SMPD2,MNICAL1,ZBTB24" rs9487094-G rs9487094 0.69 4E-06 4.7 [2.74-6.66] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6q22.32 C6orf173 rs1490388-T rs1490388 0.42 6.00E-07 4.8 [2.84-6.76] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6q22.33-6q23.1 "L3MBTL3, SAMD3" rs6899976-G rs6899976 0.28 0.000006 3.8 [2.23-5.37] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 9q22.1 "SPIN1, CCRK" rs2814828-T rs2814828 0.25 9.00E-07 5.4 [3.24-7.56] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 9q32 COL27A1 rs946053-T rs946053 0.52 2.00E-07 4.4 [2.83-5.97] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 12p13.2 ETV6 rs2187642-A rs2187642 0.39 2E-06 4.6 [2.64-6.56] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 12p12.2 "PDE3A, SLCO1C1, SLCO1B3" rs11611208-A rs11611208 0.06 2E-06 11.4 [6.7-16.1] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 12q15 "LYZ,YEATS4,FRS2,CPSF6,CCT2,LRRC10" rs11177669-A rs11177669 0.31 0.000003 4.5 [2.54-6.46] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 12q22 "SOCS2, MRPL42, CRADD, UBE2N" rs3825199-C rs3825199 0.24 2.00E-07 6.2 [3.85-8.55] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 13q14.3 DLEU7 rs1239947-G rs1239947 0.35 8E-06 3.8 [2.23-5.37] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 15q25.2 "ADAMTSL3, SH3GL3" rs2554380-T rs2554380 0.78 9.00E-07 4.5 [2.74-6.26] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 16q24.1 "ZDHHC7, CRISPLD2, USP10" rs2326458-C rs2326458 0.26 8.00E-07 5.1 [3.14-7.06] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 17q23.3 "MAP3K3, WDR68, LYK5, MT1F" rs7209435-C rs7209435 0.27 7.00E-07 4.8 [2.84-6.76] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 19p13.2 "ADAMTS10, MYO1F, PRAM1, OR2Z1" rs7249094-G rs7249094 0.59 1.00E-06 4.3 [2.54-6.06] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 22q11.23 "BCR, GNAZ, RTDR1, IGLL1" rs5751614-A rs5751614 0.49 0.000006 4.3 [2.34-6.26] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" Xq21.1 ITM2A rs1474563-T rs1474563 0.58 0.000003 3.5 [1.93-5.07] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 20q11.22 "UQCC, GDF5, CEP250, EIF6, MMP24" rs6088792-T rs6088792 0.26 8.00E-07 4.7 [2.74-6.66] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 14q32.12 "TRIP11, FBLN5, ATXN3, CPSF2" rs7153027-A rs7153027 0.52 1.00E-10 5.7 [3.94-7.46] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 1q25.3 "C1orf19,GLT25D2" rs2274432-T rs2274432 0.37 8.00E-09 5.3 [3.54-7.06] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 2p16.1 "EFEMP1, PNPT1" rs3791679-T rs3791679 0.81 6.00E-11 5.8 [4.04-7.56] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 4p15.32 "LCORL, NCAPG" rs6830062-T rs6830062 0.89 1.00E-10 6.3 [4.34-8.26] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6p22.1 "Histone class 1,Butyrophilin genes" rs10946808-A rs10946808 0.7 6.00E-10 5.6 [3.84-7.36] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6p21.32 HLA class III rs185819-T rs185819 0.52 3.00E-08 5.2 [3.44-6.96] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6p21.31 "HMGA1, LBH" rs1776897-C rs1776897 0.07 1.00E-08 8.8 [5.66-11.94] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6p21.31 "ANKS1A, TCP11, ZNF76, DEF6,SCUBE3" rs4713858-G rs4713858 0.86 4.00E-08 6.8 [4.45-9.15] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 7q21.2 "CDK6, PEX1, GATAD1, ERVWE1" rs2282978-C rs2282978 0.29 1.00E-08 5.8 [3.84-7.76] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 8q12.1 "PLAG1, MOS, CHCHD7,RDHE2, RPS20,LYN, TGS1, PENK" rs10958476-C rs10958476 0.23 7.00E-08 5.4 [3.44-7.36] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 8q21.11 "PXMP3, ZFHX4" rs7846385-C rs7846385 0.27 5.00E-08 5 [3.24-6.76] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 9q31.2 ZNF462 rs4743034-A rs4743034 0.23 2.00E-08 5.3 [3.54-7.06] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 12q14.3 HMGA2 rs8756-C rs8756 0.52 2.00E-16 6.6 [5.03-8.17] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 15q26.3 ADAMTS17 rs4533267-A rs4533267 0.28 3.00E-08 5.6 [3.64-7.56] % SD taller % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 17q11.2 "CRLF3, ATAD5, CENTA2, RNF135" rs3760318-C rs3760318 0.63 2.00E-09 6 [4.04-7.96] % SD taller % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 17q22 "NOG, DGKE, TRIM25, COIL, RISK" rs4794665-A rs4794665 0.48 1.00E-07 3.6 [2.23-4.97] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 17q23.2 "BCAS3, NACA2, TBX2, TBX4" rs757608-T rs757608 0.35 6.00E-08 4.4 [2.83-5.97] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 18q11.2 "CABLES1, RBBP8, C18orf45" rs4800148-A rs4800148 0.79 4.00E-09 6.4 [4.24-8.56] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 20p12.3 BMP2 rs967417-C rs967417 0.53 2.00E-08 4.3 [2.73-5.87] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 2p23.3 "ADCY3, RBJ, POMC, DNMT3A, DTNB" rs6733301-G rs6733301 0.87 8.00E-07 7.5 [4.56-10.44] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 2q35 "IHH, CRYBA2, FEV, SLC23A3, TUBA1" rs1052483-C rs1052483 0.91 1.00E-06 6.9 [4.16-9.64] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 2q37.1 "NPPC, DIS3L2, COPS7B, PDE6D, PTMA" rs749052-A rs749052 0.94 1.00E-06 8.7 [5.17-12.23] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 3q26.2 "GOLIM4, SERPINI1" rs4345115-T rs4345115 0.63 7E-06 4.4 [2.44-6.36] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 4q21.21 "BMP3, PRKG2, RASGEF1B" rs710841-A rs710841 0.27 2E-06 5 [3.04-6.96] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 5q31.1 "PITX1, PCBD2, CATSPER3, TXNDC15,DDX46, CAMLG" rs31198-T rs31198 0.75 8E-06 4.8 [2.64-6.96] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6p22.3 "NUP153, CAP2, KIF13A" rs12199222-T rs12199222 0.33 7.00E-07 4.4 [2.64-6.16] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 6p12.3 "SUPT3H, RUNX2" rs9395066-C rs9395066 0.48 8E-06 3.5 [1.93-5.07] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391951 Gudbjartsson 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391951?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Many sequence variants affecting diversity of adult human height Height "30,968 individuals" "8,541 individuals" 3q23 ZBTB38 rs6763931-A rs6763931 0.45 1.00E-27 7.4 [6.03-8.77] % SD taller "Illumina and Affymetrix [up to 304,226]" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 14q13.3 NKX2-1 rs17104630-G rs17104630 0.04 8E-06 0.42 [0.61-1.10] cm shorter "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 12q14.3 HMGA2 rs1042725-T rs1042725 0.49 3.00E-20 0.48 [0.58-1.09] cm shorter "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 20q11.22 "GDF5,UQCC" rs6060369-C rs6060369 0.36 1.00E-16 0.44 [0.34-0.72] cm taller "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 6q21 LIN28B rs314277-A rs314277 0.13 1.00E-08 0.41 [0.26-0.59] cm taller "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 19p13.3 DOT1L rs12986413-T rs12986413 0.45 3.00E-08 0.31 [0.21-0.46] cm taller "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 15q25.2 "SH3GL3,ADAMTSL3" rs2562784-G rs2562784 0.17 6.00E-08 0.34 [0.21-0.48] cm taller "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 8q12.1 "CHCHD7,RDHE2" rs9650315-T rs9650315 0.13 4.00E-07 0.43 [0.59-1.07] cm shorter "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 7q21.2 CDK6 rs2040494-C rs2040494 0.5 4.00E-07 0.26 [0.36-0.65] cm shorter "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 7q36.3 WDR60 rs2730245-G rs2730245 0.33 3.00E-07 0.32 [0.19-0.44] cm taller "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 9q34.11 FUBP3 rs7466269-G rs7466269 0.33 8.00E-07 0.27 [0.38-0.69] cm shorter "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 9q33.1 PAPPA rs7869550-G rs7869550 0.24 1.00E-06 0.33 [0.45-0.82] cm shorter "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 3q23 ZBTB38 rs724016-G rs724016 0.48 8.00E-22 0.37 [0.29-0.45] cm taller "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 6q24.3 GPR126 rs4896582-A rs4896582 0.27 2.00E-18 0.38 [0.28-0.48] cm shorter "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 6q22.1 HIST1H1D rs10946808-G rs10946808 0.28 4.00E-17 0.36 [0.26-0.46] cm shorter "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 4q31.22 HHIP rs1492820-G rs1492820 0.48 1.00E-11 0.29 [0.21-0.37] cm shorter "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 14q32.12 "TRIP11,ATXN3" rs8007661-T rs8007661 0.3 6.00E-10 0.42 [0.30-0.54] cm shorter "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 17q22 ANKFN1 rs12449568-C rs12449568 0.47 2E-06 0.25 [0.15-0.35] cm taller "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391950 Lettre 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391950?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ten loci associated with height highlights new biological pathways in human growth Height "15,821 individuals" "13,671 individuals" 16p13.3 RAB40C rs763014-C rs763014 0.43 0.000005 0.24 [0.12-0.29] cm taller "Affymetrix and Illumina [2,260,683] (imputed)" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 15q25.2 ADAMTSL3 rs10906982-A rs10906982 0.48 2.00E-08 0.05 [0.02-0.07] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 13q14.3 DLEU7 rs3116602-G rs3116602 0.21 7.00E-09 0.04 [0.00-0.07] SD shorter - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 1q42.13 ZNF678 rs1390401-A rs1390401 0.18 5.00E-09 0.04 [0.01-0.08] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 4q31.22 HHIP rs6854783-A rs6854783 0.43 2.00E-09 0.06 [0.03-0.08] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 12q22 SOCS2 rs11107116-G rs11107116 0.23 6.00E-10 0.04 [0.01-0.07] SD shorter - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 1p12 SPAG17 rs12735613-A rs12735613 0.24 4.00E-11 0.08 [0.05-0.11] SD shorter - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 9q22.32 PTCH1 rs10512248-G rs10512248 0.31 4.00E-11 0.05 [0.02-0.07] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 6p21.31 C6orf106 rs2814993-A rs2814993 0.15 4.00E-12 0.09 [0.05-0.13] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 3q23 ZBTB38 rs6440003-A rs6440003 0.44 2.00E-24 0.07 [0.04-0.09] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 7q21.2 CDK6 rs2282978-C rs2282978 0.33 8.00E-23 0.09 [0.06-0.12] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 12q14.3 HMGA2 rs1042725-C rs1042725 0.49 3.00E-18 0.05 [0.03-0.08] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 20q11.22 GDF5 rs6060373-G rs6060373 0.38 2.00E-17 0.08 [0.05-0.11] SD shorter - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 4p15.32 LCORL rs16896068-A rs16896068 0.16 2.00E-13 0.07 [0.03-0.11] SD shorter - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 1p34.2 SCMH1 rs6686842-C rs6686842 0.44 2.00E-08 0.05 [0.02-0.08] SD shorter - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 2q35 IHH rs6724465-A rs6724465 0.1 2.00E-08 0.06 [0.02-0.10] SD shorter - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 3q22.2 "ANAPC13,CEP63" rs10935120-A rs10935120 0.33 7.00E-08 0.06 [0.03-0.09] SD shorter - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 15q26.1 ACAN rs8041863-A rs8041863 0.47 8.00E-08 0.04 [0.01-0.06] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 18q21.1 DYM rs8099594-A rs8099594 0.35 3.00E-07 0.05 [0.02-0.08] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 6q22.32 LOC387103 rs4549631-C rs4549631 0.5 5.00E-13 0.06 [0.03-0.08] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18391952 Weedon 6-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18391952?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies 20 loci that influence adult height Height "13,665 individuals" "16,482 individuals" 2p16.1 EFEMP1 rs3791675-C rs3791675 0.23 2.00E-12 0.09 [0.05-0.12] SD taller - among males "Affymetrix [402,951]" N 11/25/2008 18369459 Liu 4-Apr-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18369459?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease Loci Psoriasis "218 cases, 519 controls" "1,153 cases, 1,217 controls" 13q13 COG6 rs7993214-? rs7993214 0.65 2E-06 1.41 [1.22-1.61] "Illumina [305,983]" N 11/25/2008 18369459 Liu 4-Apr-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18369459?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease Loci Psoriasis "218 cases, 519 controls" "1,153 cases, 1,217 controls" 6p21.33 HLA-C rs2395029-C rs2395029 0.03 2.00E-26 4.1 [3.10-5.30] "Illumina [305,983]" N 11/25/2008 18369459 Liu 4-Apr-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18369459?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease Loci Psoriasis "218 cases, 519 controls" "1,153 cases, 1,217 controls" 6p21.33 HLA-C rs10484554-T rs10484554 0.15 2.00E-39 2.8 [2.40-3.30] "Illumina [305,983]" N 11/25/2008 18385676 Amos 3-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18385676?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1 Lung cancer "1,154 cases, 1,137 controls" "2,724 cases, 3,694 controls" 3q28 IL1RAP rs7626795-G rs7626795 NR 8E-06 1.16 [1.05-1.28] "Illumina [317,498]" N 11/25/2008 18385676 Amos 3-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18385676?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1 Lung cancer "1,154 cases, 1,137 controls" "2,724 cases, 3,694 controls" 1q23.2 CRP rs2808630-G rs2808630 NR 7E-06 1.22 [1.10-1.35] "Illumina [317,498]" N 11/25/2008 18385676 Amos 3-Apr-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18385676?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1 Lung cancer "1,154 cases, 1,137 controls" "2,724 cases, 3,694 controls" 15q25.1 "CHRNA3, CHRNA5, PSMA4, LOC123688" rs8034191-G rs8034191 NR 3.00E-18 1.3 [1.15-1.47] "Illumina [317,498]" N 11/25/2008 18385738 Hung 3-Apr-08 Nature http://www.ncbi.nlm.nih.gov/pubmed/18385738?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A susceptibility locus for lung cancer maps to nicotinic acteylcholine receptor subunit genes on 15q25 Lung cancer "1,926 cases, 2,522 controls" "2,513 cases, 4,752 controls" 15q25.1 "CHRNA3,CHRNA5, CHRNB4, PSMA4, LOC123688" rs8034191-C rs8034191 0.34 5.00E-20 1.3 [1.23-1.37] "Illumina [310,023]" N 11/25/2008 18385739 Thorgeirsson 3-Apr-08 Nature http://www.ncbi.nlm.nih.gov/pubmed/18385739?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "A variant associated with nicotine dependence, lung cancer and peripheral arterial disease" Nicotine dependence "10,995 smokers" "4,848 smokers" 15q25.1 "CHRNA3,CHRNA5,CHRNB4" rs1051730-T rs1051730 0.35 6.00E-20 0.1 [0.08-0.12] increase in cigarettes per day "Illumina [306,207]" N 11/25/2008 18372901 Tenesa 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372901?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21 Colorectal cancer "981 cases, 1,002 controls" "16,476 cases, 15,351 controls" 8q24.21 "POU5FIP1, HsG57825, DQ515897" rs7014346-A rs7014346 0.18 9.00E-26 1.19 [1.15-1.23] "Illumina [541,628]" N 11/25/2008 18372901 Tenesa 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372901?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21 Colorectal cancer "981 cases, 1,002 controls" "16,476 cases, 15,351 controls" 11q23.1 Intergenic rs3802842-C rs3802842 0.43 6.00E-10 1.11 [1.08-1.15] "Illumina [541,628]" N 11/25/2008 18372901 Tenesa 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372901?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21 Colorectal cancer "981 cases, 1,002 controls" "16,476 cases, 15,351 controls" 18q21.1 SMAD7 rs4939827-T rs4939827 0.17 8.00E-28 1.2 [1.16-1.24] "Illumina [541,628]" N 11/25/2008 18372905 Tomlinson 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372905?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3 Colorectal cancer "922 cases, 927 controls" "17,872 cases, 17,526 controls" 10p14 Intergenic rs10795668-A rs10795668 0.67 3.00E-13 1.12 [1.10-1.16] "Illumina [547,647]" N 11/25/2008 18372905 Tomlinson 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372905?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3 Colorectal cancer "922 cases, 927 controls" "17,872 cases, 17,526 controls" 15q13.3 Intergenic rs4779584-? rs4779584 0.19 5.00E-07 1.23 [1.14-1.34] "Illumina [547,647]" N 11/25/2008 18372905 Tomlinson 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372905?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3 Colorectal cancer "922 cases, 927 controls" "17,872 cases, 17,526 controls" 18q21.1 SMAD7 rs4939827-? rs4939827 0.53 2E-06 1.18 [1.10-1.25] "Illumina [547,647]" N 11/25/2008 18372905 Tomlinson 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372905?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3 Colorectal cancer "922 cases, 927 controls" "17,872 cases, 17,526 controls" 8q24.21 Intergenic rs6983267-? rs6983267 0.48 7.00E-11 1.24 [1.17-1.33] "Illumina [547,647]" N 11/25/2008 18372905 Tomlinson 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372905?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies colorectal cancer susceptibility loci on chromosome 10p14 and 8q23.3 Colorectal cancer "922 cases, 927 controls" "17,872 cases, 17,526 controls" 8q23.3 EIF3H rs16892766-A rs16892766 0.07 3.00E-18 1.27 [1.20-1.34] "Illumina [547,647]" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 10q23.33 HHEX rs5015480-C rs5015480 NR 7.00E-08 1.17 [1.11-1.24] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 9p21.3 "CDKN2A,CDKN2B" rs7020996-C rs7020996 NR 2.00E-07 1.26 [1.15-1.38] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 1p12 "NOTCH2, ADAM30" rs10923931-T rs10923931 0.11 4.00E-08 1.13 [1.08-1.17] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 12q13.2 DCD rs1153188-A rs1153188 0.73 2.00E-07 1.08 [1.05-1.11] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 6p21.1 VEGFA rs9472138-T rs9472138 0.28 4E-06 1.06 [1.04-1.09] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 3p25.2 "SYN2, PPARG" rs17036101-G rs17036101 0.93 2.00E-07 1.15 [1.10-1.21] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 3q27.2 IGF2BP2 rs4402960-T rs4402960 NR 8.00E-08 1.17 [1.10-1.25] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 11p15.1 KCNJ11 rs5215-C rs5215 NR 4.00E-07 1.16 [1.09-1.23] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 10q25.2 TCF7L2 rs7903146-T rs7903146 NR 3.00E-23 1.37 [1.28-1.47] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 16q12.2 FTO rs8050136-A rs8050136 NR 7E-06 1.15 [1.09-1.22] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 7p15.1 JAZF1 rs864745-T rs864745 0.5 5.00E-14 1.1 [1.07-1.13] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 10p13 "CDC123,CAMK1D" rs12779790-G rs12779790 0.18 1.00E-10 1.11 [1.07-1.14] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 12q21.1 "TSPAN8,LGR5" rs7961581-C rs7961581 0.27 1.00E-09 1.09 [1.06-1.12] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 6p22.3 CDKAL1 rs6931514-G rs6931514 NR 1.00E-11 1.25 [1.17-1.33] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 3p14.1 ADAMTS9 rs4607103-C rs4607103 0.76 1.00E-08 1.09 [1.06-1.12] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18372903 Zeggini 30-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18372903?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes Type 2 diabetes "4,549 cases, 5,579 controls" "24,194 cases, 55,598 controls" 2p21 THADA rs7578597-T rs7578597 0.9 1.00E-09 1.15 [1.10-1.20] "Affymetrix and Illumina [2,202,892] (imputed)" N 11/25/2008 18360741 Butcher 25-Mar-08 Behav Genet http://www.ncbi.nlm.nih.gov/pubmed/18360741?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum The Nature of Nuture: A Genomewide Association Scan for Family Chaos Environmental confusion in the home "469 children from low chaos families,369 children from high chaos families" "3,529 children" NR NR NR NR NS NS NR NR "Affymetrix [117,062] (pooled)" N 11/25/2008 18364390 Capon 25-Mar-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/18364390?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene Psoriasis "318 cases, 288 controls" "2,361 cases, 1,927 controls" 6p21.33 HLA-C rs3134792-? rs3134792 NR 1.00E-09 NR NR "Illumina [~408,000] (pooled)" N 11/25/2008 18364390 Capon 25-Mar-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/18364390?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene Psoriasis "318 cases, 288 controls" "2,361 cases, 1,927 controls" 20q13.13 SPATA2 rs495337-? rs495337 NR 1.00E-08 1.25 [1.12-1.39] "Illumina [~408,000] (pooled)" N 11/25/2008 18347602 Sullivan 18-Mar-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide association for schizophrenia in the CATIE study: results of stage 1 Schizophrenia "738 cases, 733 controls" NR 13q12.2 Intergenic rs9512730-? rs9512730 0.26 0.000005 1.52 [NR] "Affymetrix [492,900]" N 11/25/2008 18347602 Sullivan 18-Mar-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide association for schizophrenia in the CATIE study: results of stage 1 Schizophrenia "738 cases, 733 controls" NR 15q25.3 AGBL1 rs16977195-? rs16977195 0.03 2E-06 6.01 [NR] "Affymetrix [492,900]" N 11/25/2008 18347602 Sullivan 18-Mar-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide association for schizophrenia in the CATIE study: results of stage 1 Schizophrenia "738 cases, 733 controls" NR 1q31.1 Intergenic rs10911902-? rs10911902 0.17 2E-06 1.79 [NR] "Affymetrix [492,900]" N 11/25/2008 18347602 Sullivan 18-Mar-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide association for schizophrenia in the CATIE study: results of stage 1 Schizophrenia "738 cases, 733 controls" NR 1p36.22 Intergenic rs4846033-? rs4846033 0.01 4E-06 2.87 [NR] "Affymetrix [492,900]" N 11/25/2008 18347602 Sullivan 18-Mar-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide association for schizophrenia in the CATIE study: results of stage 1 Schizophrenia "738 cases, 733 controls" NR 16p12.2 "ACSM1, BUCS1" rs151222-? rs151222 0.08 0.000006 2.1 [NR] "Affymetrix [492,900]" N 11/25/2008 18347602 Sullivan 18-Mar-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18347602?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Genomewide association for schizophrenia in the CATIE study: results of stage 1 Schizophrenia "738 cases, 733 controls" NR Xq28 Intergenic rs2159767-? rs2159767 0.62 7E-06 1.33 [NR] "Affymetrix [492,900]" N 11/25/2008 18326623 Gold 11-Mar-08 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/18326623?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33 Breast cancer "249 cases, 299 controls (Ashkenazi Jewish, non-BRCA1/2 carriers)" "1,193 cases, 1,166 controls (Ashkenazi Jewish, non-BRCA1/2 carriers)" 6q22.33 "ECHDC1,RNF146" rs2180341-G rs2180341 0.21 3.00E-08 1.41 [1.25-1.59] "Affymetrix [150,080]" N 11/25/2008 18332876 Kirov 11-Mar-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18332876?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study in 574 schizophrenia trios using DNA pooling Schizophrenia "574 cases, 605 controls, 1,148 parents of cases" NR 12q24.23 CCDC60 rs11064768-A rs11064768 0.91 1.00E-06 NR NR "Illumina [~550,000] (pooled)" N 11/25/2008 18327256 Doring 9-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18327256?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum SLC2A9 influences uric acid concentrations with pronounced sex-specific effects Serum urate "1,644 individuals" "9,947 individuals" 4p16.1 SLC2A9 rs7442295-C rs7442295 0.4 3.00E-70 0.35 [NR] mg/dl decrease in uric acid "Affymetrix [335,152]" N 11/25/2008 18327257 Vitart 9-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18327257?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout" Serum urate 794 individuals 706 individuals 4p16.1 SLC2A9 rs737267-C rs737267 0.31 3.00E-09 0.88 [NR] uM decrease in uric acid [females only] "Illumina [308,140]" N 11/25/2008 18325910 Liu 5-Mar-08 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/18325910?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scans identified CTNNBL1 as a novel gene for obesity Obesity "1,000 individuals" "896 obese individuals, 2,916 lean individuals" NR NR NR NR NS NS NR NR "Affymetrix [379,319]" N 11/25/2008 18317468 Sklar 4-Mar-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18317468?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Whole-genome association study of bipolar disorder Bipolar disorder "1,461 cases, 2,008 controls" "409 trios, 365 cases, 351 controls" NR NR NR NR NS NS NR NR "Affymetrix [372,193]" N 11/25/2008 18311140 Hunt 2-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified genetic risk variants for celiac disease related to the immune response Celiac disease "767 cases, 1,422 controls" "1,643 cases, 3,406 controls" 6q25.3 TAGAP rs1738074-A rs1738074 NR 7.00E-08 1.21 [1.13-1.30] "Illumina [310,605]" N 11/25/2008 18311140 Hunt 2-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified genetic risk variants for celiac disease related to the immune response Celiac disease "767 cases, 1,422 controls" "1,643 cases, 3,406 controls" 4q27 "KIAA1109, ADAD1, IL2, IL21" rs6822844-C rs6822844 0.81 3.00E-13 1.44 [1.30-1.58] "Illumina [310,605]" N 11/25/2008 18311140 Hunt 2-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified genetic risk variants for celiac disease related to the immune response Celiac disease "767 cases, 1,422 controls" "1,643 cases, 3,406 controls" 12q24.12 "SH2B3, ATXN2" rs653178-G rs653178 0.48 8.00E-08 1.21 [1.13-1.30] "Illumina [310,605]" N 11/25/2008 18311140 Hunt 2-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified genetic risk variants for celiac disease related to the immune response Celiac disease "767 cases, 1,422 controls" "1,643 cases, 3,406 controls" 3p21.31 "CCR1, CCR3" rs6441961-A rs6441961 0.3 3.00E-07 1.21 [1.13-1.30] "Illumina [310,605]" N 11/25/2008 18311140 Hunt 2-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified genetic risk variants for celiac disease related to the immune response Celiac disease "767 cases, 1,422 controls" "1,643 cases, 3,406 controls" 1q31.2 RGS1 rs2816316-C rs2816316 NR 3.00E-11 1.39 [1.26-1.53] "Illumina [310,605]" N 11/25/2008 18311140 Hunt 2-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified genetic risk variants for celiac disease related to the immune response Celiac disease "767 cases, 1,422 controls" "1,643 cases, 3,406 controls" 2q12.1 "IL1RL1,IL18R1,IL18RAP, SLC9A4" rs13015714-C rs13015714 NR 4.00E-09 1.28 [1.18-1.39] "Illumina [310,605]" N 11/25/2008 18311140 Hunt 2-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified genetic risk variants for celiac disease related to the immune response Celiac disease "767 cases, 1,422 controls" "1,643 cases, 3,406 controls" 3q25.33 "IL12A, SCHIP1" rs17810546-G rs17810546 NR 1.00E-09 1.35 [1.23-1.49] "Illumina [310,605]" N 11/25/2008 18311140 Hunt 2-Mar-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18311140?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified genetic risk variants for celiac disease related to the immune response Celiac disease "767 cases, 1,422 controls" "1,643 cases, 3,406 controls" 3q28 LPP rs1464510-A rs1464510 NR 5.00E-09 1.23 [1.15-1.32] "Illumina [310,605]" N 11/25/2008 18316681 Uhl 1-Mar-08 Arch Gen Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18316681?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association for methamphetamine dependence: convergent results from 2 samples Methamphetamine dependence "240 cases, 340 controls" NR NR NR NR NR NS NS NR NR "Affymetrix [up to 466,883] (pooled)" N 11/25/2008 18313986 Blauw 29-Feb-08 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/18313986?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Copy-number variation in sporadic amyotrophic lateral sclerosis: a genome-wide screen Amyotrophic lateral sclerosis "406 cases, 404 controls" NR Pending Pending Pending Pending Pending Pending Pending Pending "Illumina [317,503]" Y 11/25/2008 18282107 Shifman 15-Feb-08 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/18282107?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-Wide Association Identifies a Common Variant in the Reelin Gene That Increases the Risk of Schizophrenia Only in Women Schizophrenia "660 cases, 2,271 controls" "2,274 cases, 4,401 controls" 7q22.1 RELN rs7341475-G rs7341475 0.62 9.00E-07 1.58 [1.31-1.89] "Affymetrix [510,552]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 8q24.21 Intergenic rs6983267-G rs6983267 0.49 9.00E-13 1.42 [NR] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 8q24.21 Intergenic rs1016343-T rs1016343 0.18 1.00E-07 1.37 [NR] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 8q24.21 Intergenic rs4242384-C rs4242384 0.09 3.00E-16 1.88 [NR] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 17q12 HNF1B rs7501939-C rs7501939 0.57 9.00E-12 1.41 [NR] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 17q24.3 Intergenic rs1859962-G rs1859962 0.46 1.00E-06 1.26 [NR] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" Xp11.22 "NUDT10, NUDT11" rs5945619-C rs5945619 0.36 2.00E-09 1.19 [1.07-1.31] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 3p12.1 SLC22A3 rs2660753-T rs2660753 0.11 3.00E-08 1.18 [1.06-1.31] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 10q11.23 MSMB rs10993994-T rs10993994 0.4 9.00E-29 1.25 [1.17-1.34] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 7q21.3 LMTK2 rs6465657-C rs6465657 0.46 1.00E-09 1.12 [1.05-1.20] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 6q25.3 SLC22A3 rs9364554-T rs9364554 0.29 6.00E-10 1.17 [1.08-1.26] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 11q13.2 Intergenic rs7931342-G rs7931342 0.51 2.00E-12 1.19 [1.11-1.27] "Illumina [541,129]" N 11/25/2008 18264097 Eeles 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264097?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple newly identified loci associated with prostate cancer susceptibility Prostate cancer "1,854 cases, 1,894 controls" "3,268 cases, 3,366 controls" 19q13.33 KLK3 rs2735839-G rs2735839 0.85 2.00E-18 1.2 [1.10-1.33] "Illumina [541,129]" N 11/25/2008 18264098 Gudmundsson 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264098?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer Prostate cancer "1,854 cases, 21,372 controls" "8,239 cases, 7,590 controls" 2p15 EHBP1 rs721048-A rs721048 0.19 8.00E-09 1.15 [1.10-1.21] "Illumina [310,520]" N 11/25/2008 18264098 Gudmundsson 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264098?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer Prostate cancer "1,854 cases, 21,372 controls" "8,239 cases, 7,590 controls" Xp11.22 "NUDT10, NUDT11, LOC340602, GSPT2, MAGED1" rs5945572-A rs5945572 0.35 4.00E-13 1.23 [1.16-1.30] "Illumina [310,520]" N 11/25/2008 18264096 Thomas 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple loci identified in a genome-wide association study of prostate cancer Prostate cancer "1,172 cases, 1,157 controls" "3,941 cases, 3,964 controls" 10q11.23 MSMB rs10993994-T rs10993994 0.4 7.00E-13 1.16 [1.04-1.29] "Illumina [527,869]" N 11/25/2008 18264096 Thomas 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple loci identified in a genome-wide association study of prostate cancer Prostate cancer "1,172 cases, 1,157 controls" "3,941 cases, 3,964 controls" 8q24.21 Intergenic rs4242382-A rs4242382 0.12 3.00E-19 1.66 [1.47-1.87] "Illumina [527,869]" N 11/25/2008 18264096 Thomas 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple loci identified in a genome-wide association study of prostate cancer Prostate cancer "1,172 cases, 1,157 controls" "3,941 cases, 3,964 controls" 17q12 HNF1B rs4430796-A rs4430796 0.54 1.00E-09 1.18 [1.04-1.32] "Illumina [527,869]" N 11/25/2008 18264096 Thomas 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple loci identified in a genome-wide association study of prostate cancer Prostate cancer "1,172 cases, 1,157 controls" "3,941 cases, 3,964 controls" 7p15.2 JAZF1 rs10486567-G rs10486567 0.77 2E-06 1.12 [1.02-1.25] "Illumina [527,869]" N 11/25/2008 18264096 Thomas 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple loci identified in a genome-wide association study of prostate cancer Prostate cancer "1,172 cases, 1,157 controls" "3,941 cases, 3,964 controls" 11q13.2 Intergenic rs10896449-G rs10896449 0.52 2.00E-09 1.1 [0.98-1.23] "Illumina [527,869]" N 11/25/2008 18264096 Thomas 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple loci identified in a genome-wide association study of prostate cancer Prostate cancer "1,172 cases, 1,157 controls" "3,941 cases, 3,964 controls" 10q26.13 CTBP2 rs4962416-C rs4962416 0.27 2.00E-07 1.17 [1.05-1.30] "Illumina [527,869]" N 11/25/2008 18264096 Thomas 10-Feb-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18264096?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Multiple loci identified in a genome-wide association study of prostate cancer Prostate cancer "1,172 cases, 1,157 controls" "3,941 cases, 3,964 controls" 8q24.21 Intergenic rs6983267-G rs6983267 0.53 7.00E-12 1.28 [1.15-1.45] "Illumina [527,869]" N 11/25/2008 18262040 Sandhu 9-Feb-08 Lancet http://www.ncbi.nlm.nih.gov/pubmed/18262040?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum LDL-cholesterol concentrations: a genome-wide association study LDL cholesterol "11,685 individuals" "5,036 individuals" 19q13.32 APOC1 rs4420638-G rs4420638 0.18 1.00E-20 0.06 [0.04-0.08] mmol/L increase "Affymetrix and Illumina [up to 461,986]" N 11/25/2008 18262040 Sandhu 9-Feb-08 Lancet http://www.ncbi.nlm.nih.gov/pubmed/18262040?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum LDL-cholesterol concentrations: a genome-wide association study LDL cholesterol "11,685 individuals" "5,036 individuals" 2p24.1 APOB rs562338-T rs562338 0.2 1.00E-09 0.04 [0.02-0.06] mmol/L decrease "Affymetrix and Illumina [up to 461,986]" N 11/25/2008 18262040 Sandhu 9-Feb-08 Lancet http://www.ncbi.nlm.nih.gov/pubmed/18262040?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum LDL-cholesterol concentrations: a genome-wide association study LDL cholesterol "11,685 individuals" "5,036 individuals" 1p13.3 "CELSR2,PSRC1" rs599839-G rs599839 0.19 1.00E-33 0.16 [0.14-0.18] mmol/L decrease "Affymetrix and Illumina [up to 461,986]" N 11/25/2008 18245381 Uda 5-Feb-08 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/18245381?rdinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia Fetal hemoglobin levels "4,305 individuals" 521 individuals 2p15 BCL11A rs1186868-T rs1186868 0.2 7.00E-35 0.48 [NR] SD decrease in HbF "Affymetrix [362,129]" N 11/25/2008 18245381 Uda 5-Feb-08 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/18245381?rdinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia Fetal hemoglobin levels "4,305 individuals" 521 individuals 11p15.4 HBB rs4910742-A rs4910742 0.07 1.00E-21 0.58 [NR] SD decrease in HbF "Affymetrix [362,129]" N 11/25/2008 18239089 Kong 2-Feb-08 Science http://www.ncbi.nlm.nih.gov/pubmed/18239089?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence Variants in the RNF212 Gene Associate with Genomewide Recombination Rate Recombination rate (females) "1,702 women" "1,663 women" 4p16.3 "RNF212,SPON2" rs1670533-C rs1670533 0.23 (men and women combined) 2.00E-12 88.2 [63.7-112.7] cM increase "Illumina [309,241]" N 11/25/2008 18239089 Kong 2-Feb-08 Science http://www.ncbi.nlm.nih.gov/pubmed/18239089?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence Variants in the RNF212 Gene Associate with Genomewide Recombination Rate Recombination rate (males) "1,887 men" "1,248 men" 4p16.3 "RNF212,SPON2" rs3796619-T rs3796619 0.33 (men and women combined) 3.00E-24 70.7 [84.3-57.1] cM decrease "Illumina [309,241]" N 12/11/2008 18227835 Berrettini 29-Jan-08 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/18227835?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_DefaultReportPanel.Pubmed_RVDocSum Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking Nicotine dependence "7,481 individuals" ~2000 individuals NR NR NR NR NS NS NR NR "Affymetrix [460,959]" N 11/25/2008 18252221 Kayser 24-Jan-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18252221?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene Iris color "1,406 individuals" "8,273 individuals" 15q13.1 HERC2 rs916977-? rs916977 NR 1.00E-43 NR NR "Affymetrix and Illumina [up to ~500,000] (pooled)" N 11/25/2008 18067574 Butcher 22-Jan-08 Genes Brain Behav http://www.ncbi.nlm.nih.gov/pubmed/18067574?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays General cognitive ability "458 low g, 402 high g twin children (unrelated)" "3,195 twin children (unrelated)" NR NR NR NR NS NS NR NR "Affymetrix [449,127]" N 11/25/2008 18204446 Harley 20-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci" Systemic lupus erythematosus "720 female cases, 2,337 female controls" "1,846 female cases, 1,825 female controls" 16p11.2 ITGAM rs9888739-T rs9888739 0.13 2.00E-23 1.62 [1.47-1.78] "Illumina [317,501]" N 11/25/2008 18204446 Harley 20-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci" Systemic lupus erythematosus "720 female cases, 2,337 female controls" "1,846 female cases, 1,825 female controls" 6p21.33 HLA region rs3131379-A rs3131379 0.1 2.00E-52 2.36 [2.11-2.64] "Illumina [317,501]" N 11/25/2008 18204446 Harley 20-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci" Systemic lupus erythematosus "720 female cases, 2,337 female controls" "1,846 female cases, 1,825 female controls" 3p14.3 PXK rs6445975-C rs6445975 0.28 7.00E-09 1.25 [1.16-1.35] "Illumina [317,501]" N 11/25/2008 18204446 Harley 20-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci" Systemic lupus erythematosus "720 female cases, 2,337 female controls" "1,846 female cases, 1,825 female controls" 1q25.1 Intergenic rs10798269-? rs10798269 0.64 1.00E-07 1.22 [1.14-1.32] "Illumina [317,501]" N 11/25/2008 18204446 Harley 20-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci" Systemic lupus erythematosus "720 female cases, 2,337 female controls" "1,846 female cases, 1,825 female controls" 11p15.5 KIAA1542 rs4963128-? rs4963128 0.34 3.00E-10 1.28 [1.18-1.37] "Illumina [317,501]" N 11/25/2008 18204446 Harley 20-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18204446?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci" Systemic lupus erythematosus "720 female cases, 2,337 female controls" "1,846 female cases, 1,825 female controls" 7q32.1 "IRF5, TNPO3" rs12537284-A rs12537284 0.13 4.00E-19 1.54 [1.40-1.70] "Illumina [317,501]" N 11/25/2008 18204098 Hom 20-Jan-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX Systemic lupus erythematosus "1,311 cases, 3,340 controls" "793 cases, 857 controls" 1p31.3 NEGR1 rs12141391-A rs12141391 0.02 7E-06 NR NR "Illumina [502,033]" N 11/25/2008 18204098 Hom 20-Jan-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX Systemic lupus erythematosus "1,311 cases, 3,340 controls" "793 cases, 857 controls" 9q34.13 NTNG2 rs11243676-A rs11243676 0.07 0.000003 NR NR "Illumina [502,033]" N 11/25/2008 18204098 Hom 20-Jan-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX Systemic lupus erythematosus "1,311 cases, 3,340 controls" "793 cases, 857 controls" 5p12 GHR rs979233-T rs979233 0.46 4E-06 NR NR "Illumina [502,033]" N 11/25/2008 18204098 Hom 20-Jan-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX Systemic lupus erythematosus "1,311 cases, 3,340 controls" "793 cases, 857 controls" 18q22.3 SOCS6 rs17083844-A rs17083844 0.03 0.000006 NR NR "Illumina [502,033]" N 11/25/2008 18204098 Hom 20-Jan-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX Systemic lupus erythematosus "1,311 cases, 3,340 controls" "793 cases, 857 controls" 8p23.1 "C8orf13, BLK" rs13277113-A rs13277113 0.23 1.00E-10 1.39 [1.28-1.51] "Illumina [502,033]" N 11/25/2008 18204098 Hom 20-Jan-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX Systemic lupus erythematosus "1,311 cases, 3,340 controls" "793 cases, 857 controls" 6p21.32 HLA-DQA1 rs2187668-A rs2187668 0.11 3.00E-21 NR NR "Illumina [502,033]" N 11/25/2008 18204098 Hom 20-Jan-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX Systemic lupus erythematosus "1,311 cases, 3,340 controls" "793 cases, 857 controls" 7q32.1 "IRF5, TNPO3" rs10488631-C rs10488631 0.12 2.00E-11 NR NR "Illumina [502,033]" N 11/25/2008 18204098 Hom 20-Jan-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX Systemic lupus erythematosus "1,311 cases, 3,340 controls" "793 cases, 857 controls" 2q32.3 STAT4 rs7574865-T rs7574865 0.23 9.00E-14 NR NR "Illumina [502,033]" N 11/25/2008 18204098 Hom 20-Jan-08 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/18204098?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX Systemic lupus erythematosus "1,311 cases, 3,340 controls" "793 cases, 857 controls" 16p11.2 "ITGAM, ITGAX" rs11574637-C rs11574637 0.19 3.00E-11 1.33 [1.22-1.46] "Illumina [502,033]" N 11/25/2008 18204447 Kozyrev 20-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18204447?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus Systemic lupus erythematosus "279 cases, 515 controls" "1,757 cases, 1,540 controls" 4q24 BANK1 rs10516487-G rs10516487 0.77 4.00E-10 1.38 [1.25-1.53] "Affymetrix [85,042]" N 11/25/2008 18198356 Hakonarson 15-Jan-08 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/18198356?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study Type 1 diabetes "467 trios, 561 cases, 1,143 controls" "549 families, 364 trios" 12q13.2 "RAB5B, SUOX, IKZF4, ERBB3, CDK2" rs1701704-C rs1701704 0.35 9.00E-10 1.25 [1.12-1.40] "Illumina [543,071]" N 11/25/2008 18195134 Byun 14-Jan-08 Arch Neurol http://www.ncbi.nlm.nih.gov/pubmed/18195134?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-Wide Pharmacogenomic Analysis of the Response to Interferon Beta Therapy in Multiple Sclerosis Response to interferon beta therapy 206 multiple sclerosis cases NR NR NR NR NR NS NS NR NR "Affymetrix [~100,000] (pooled)" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" HDL cholesterol "2,758 individuals" "18,544 individuals" 8p21.3 LPL rs328-G rs328 0.09 9.00E-23 0.17 [0.13-0.21]% SD higher "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" HDL cholesterol "2,758 individuals" "18,544 individuals" 1q42.13 GALNT2 rs4846914-G rs4846914 0.4 2.00E-13 0.07 [0.05-0.09] % SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" HDL cholesterol "2,758 individuals" "18,544 individuals" 9q31.1 ABCA1 rs3890182-A rs3890182 0.13 3.00E-10 0.1 [0.06-0.14]% SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" HDL cholesterol "2,758 individuals" "18,544 individuals" 16q13 CETP rs1800775-C rs1800775 0.51 1.00E-73 0.18 [0.16-0.20]% SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" HDL cholesterol "2,758 individuals" "18,544 individuals" 18q21.1 "LIPG, ACAA2" rs2156552-A rs2156552 0.18 2.00E-07 0.07 [0.05-0.09]% SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" HDL cholesterol "2,758 individuals" "18,544 individuals" 15q22.1 LIPC rs1800588-T rs1800588 0.21 2.00E-32 0.14 [0.12-0.16]% SD higher "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" LDL cholesterol "2,758 individuals" "18,544 individuals" 1p32.3 PCSK9 rs11591147-T rs11591147 0.01 2.00E-44 0.47 [0.41-0.53] % SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" LDL cholesterol "2,758 individuals" "18,544 individuals" 19p13.2 LDLR rs6511720-T rs6511720 0.1 2.00E-51 0.26 [0.22-0.30] % SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" LDL cholesterol "2,758 individuals" "18,544 individuals" 5q13.3 HMGCR rs12654264-T rs12654264 0.39 1.00E-20 0.1 [0.08-0.12] % SD higher "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" LDL cholesterol "2,758 individuals" "18,544 individuals" 19p13.11 "CILP2, PBX4" rs16996148-T rs16996148 0.1 3.00E-08 0.1 [0.06-0.14] % SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" LDL cholesterol "2,758 individuals" "18,544 individuals" 1p13.3 "CELSR2,PSRC1,SORT1" rs646776-C rs646776 0.24 3.00E-29 0.16 [0.14-0.18] % SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" LDL cholesterol "2,758 individuals" "18,544 individuals" 2p24.1 APOB rs693-A rs693 0.48 1.00E-21 0.12 [0.10-0.14] % SD higher "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" LDL cholesterol "2,758 individuals" "18,544 individuals" 19q13.32 "APOE, APOC1, APOC4, APOC2" rs4420638-G rs4420638 0.2 1.00E-60 0.19 [0.15-0.23] % SD higher "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" Triglycerides "2,758 individuals" "18,544 individuals" 8q24.13 TRIB1 rs17321515-G rs17321515 0.49 4.00E-17 0.08 [0.06-0.10] % SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" Triglycerides "2,758 individuals" "18,544 individuals" 7q11.23 "BCL7B, TBL2, MLXIPL" rs17145738-T rs17145738 0.13 7.00E-22 0.14 [0.25-0.53] % SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" Triglycerides "2,758 individuals" "18,544 individuals" 11q23.3 "APOA1, APOC3, APOA4, APOA5, ZNF259, BUD13" rs28927680-G rs28927680 0.07 2.00E-17 0.26 [0.20-0.32]% SD higher "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" Triglycerides "2,758 individuals" "18,544 individuals" 2p24.1 APOB rs693-A rs693 0.48 2.00E-07 0.08 [0.04-0.12]% SD higher "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" Triglycerides "2,758 individuals" "18,544 individuals" 1p31.3 "ANGPTL3, DOCK7, ATG4C" rs12130333-T rs12130333 0.22 2.00E-08 0.11 [0.07-0.15] % SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" Triglycerides "2,758 individuals" "18,544 individuals" 8p21.3 LPL rs328-G rs328 0.09 2.00E-28 0.19 [0.15-0.23]% SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" Triglycerides "2,758 individuals" "18,544 individuals" 1q42.13 GALNT2 rs4846914-G rs4846914 0.4 7.00E-15 0.08 [0.06-0.10] % SD higher "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" Triglycerides "2,758 individuals" "18,544 individuals" 19p13.11 "CILP2, PBX4" rs16996148-T rs16996148 0.1 4.00E-09 0.1 [0.06-0.14] % SD lower "Affymetrix [389,878]" N 11/25/2008 18193044 Kathiresan 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193044?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans" Triglycerides "2,758 individuals" "18,544 individuals" 2p23.3 GCKR rs780094-T rs780094 0.34 3.00E-14 0.13 [0.09-0.17]% SD higher "Affymetrix [389,878]" N 11/25/2008 18193046 Kooner 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193046?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides Triglycerides "2,011 individuals" "10,536 individuals" 8p21.3 "LPL, C8orf35, SLC18A1" rs326-A rs326 0.78 5.00E-12 6.6 [3.66-9.54] % higher "Perlegen [up to 216,774]" N 11/25/2008 18193046 Kooner 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193046?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides Triglycerides "2,011 individuals" "10,536 individuals" 11q23.3 "APOA1,KIAA0999,LOC645044" rs2075292-G rs2075292 0.24 5.00E-08 8.7 [5.76-11.64] % higher "Perlegen [up to 216,774]" N 11/25/2008 18193046 Kooner 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193046?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides Triglycerides "2,011 individuals" "10,536 individuals" 11q23.3 "LOC440069, MGC13125" rs1558861-C rs1558861 0.18 2.00E-26 17 [13.28-20.72] % higher "Perlegen [up to 216,774]" N 11/25/2008 18193046 Kooner 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193046?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides Triglycerides "2,011 individuals" "10,536 individuals" 7q11.23 MLXIPL rs3812316-C rs3812316 0.95 1.00E-10 10.5 [5.3-17.7]% higher "Perlegen [up to 216,774]" N 11/25/2008 18193045 Sanna 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193045?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common variants in the GDF5-UQCC region are associated with variation in human height Height "6,669 individuals" "28,801 individuals" 5q14.1 HOMER1 rs10078095-C rs10078095 0.22 0.000003 0.9 [NR] cm taller "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193045 Sanna 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193045?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common variants in the GDF5-UQCC region are associated with variation in human height Height "6,669 individuals" "28,801 individuals" 20q11.22 BFZB rs6060369-C rs6060369 0.44 2.00E-16 0.44 [NR] cm taller "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193045 Sanna 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193045?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common variants in the GDF5-UQCC region are associated with variation in human height Height "6,669 individuals" "28,801 individuals" 4q12 PDGFRA rs17690232-C rs17690232 0.8 4.00E-07 0.86 [NR] cm taller "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193045 Sanna 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193045?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common variants in the GDF5-UQCC region are associated with variation in human height Height "6,669 individuals" "28,801 individuals" 15q26.1 POLG rs4932217-A rs4932217 0.58 8.00E-07 0.66 [NR] cm taller "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193045 Sanna 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193045?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common variants in the GDF5-UQCC region are associated with variation in human height Height "6,669 individuals" "28,801 individuals" 3q23 ZBTB38 rs724016-G rs724016 0.36 1.00E-06 0.61 [NR] cm taller "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease HDL cholesterol "8,656 individuals" "11,399 individuals" 16q13 CETP rs9989419-G rs9989419 0.65 3.00E-31 1.72 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease HDL cholesterol "8,656 individuals" "11,399 individuals" 16q13 CETP rs1864163-G rs1864163 0.8 7.00E-39 4.12 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease HDL cholesterol "8,656 individuals" "11,399 individuals" 1q42.13 GALNT2 rs2144300-T rs2144300 0.6 3.00E-14 1.11 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease HDL cholesterol "8,656 individuals" "11,399 individuals" 18q21.1 LIPG rs2156552-T rs2156552 0.84 6.00E-12 1.2 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease HDL cholesterol "8,656 individuals" "11,399 individuals" 9q31.1 ABCA1 rs4149268-C rs4149268 0.64 1.00E-10 0.82 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease HDL cholesterol "8,656 individuals" "11,399 individuals" 15q22.1 LIPC rs4775041-C rs4775041 0.33 3.00E-20 1.38 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease HDL cholesterol "8,656 individuals" "11,399 individuals" 8p21.3 LPL rs10503669-A rs10503669 0.1 4.00E-19 2.09 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease HDL cholesterol "8,656 individuals" "11,399 individuals" 12q24.11 "MVK,MMAB" rs2338104-G rs2338104 0.45 3.00E-08 0.48 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease HDL cholesterol "8,656 individuals" "11,399 individuals" 16q22.1 LCAT rs255052-A rs255052 0.17 1.00E-07 0.74 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease HDL cholesterol "8,656 individuals" "11,399 individuals" 16q13 CETP rs3764261-A rs3764261 0.31 2.00E-57 3.47 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease LDL cholesterol "8,589 individuals" "7,440-10,783 individuals" 19p13.11 "NCAN,CILP2" rs16996148-G rs16996148 0.89 3.00E-09 3.32 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease LDL cholesterol "8,589 individuals" "7,440-10,783 individuals" 2p24.1 APOB rs562338-G rs562338 0.82 6.00E-22 4.89 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease LDL cholesterol "8,589 individuals" "7,440-10,783 individuals" 19q13.32 "APOE,APOC1,APOC4" rs4420638-G rs4420638 0.18 3.00E-43 6.61 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease LDL cholesterol "8,589 individuals" "7,440-10,783 individuals" 1p32.3 PCSK9 rs11206510-T rs11206510 0.81 4.00E-11 3.04 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease LDL cholesterol "8,589 individuals" "7,440-10,783 individuals" 19p13.2 LDLR rs6511720-G rs6511720 0.9 4.00E-26 9.17 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease LDL cholesterol "8,589 individuals" "7,440-10,783 individuals" 6p21.32 B3GALT4 rs2254287-G rs2254287 0.38 5.00E-08 1.91 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease LDL cholesterol "8,589 individuals" "7,440-10,783 individuals" 1p13.3 "CELSR2,PSRC1,SORT1" rs599839-A rs599839 0.77 6.00E-33 5.48 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease Triglycerides "8,684 individuals" "5,312-9,707 individuals" 15q22.1 LIPC rs4775041-C rs4775041 0.33 2.00E-08 3.62 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000]] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease Triglycerides "8,684 individuals" "5,312-9,707 individuals" 19p13.3 "NCAN,CILP2" rs16996148-G rs16996148 0.92 3.00E-09 6.1 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000]] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease Triglycerides "8,684 individuals" "5,312-9,707 individuals" 7q11.23 MLXIPL rs17145738-C rs17145738 0.84 2.00E-12 8.21 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000]] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease Triglycerides "8,684 individuals" "5,312-9,707 individuals" 1p31.3 ANGPTL3 rs1748195-C rs1748195 0.7 2.00E-10 7.12 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000]] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease Triglycerides "8,684 individuals" "5,312-9,707 individuals" 1q42.13 GALNT2 rs2144300-C rs2144300 0.4 8.00E-07 4.25 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000]] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease Triglycerides "8,684 individuals" "5,312-9,707 individuals" 8q24.13 TRIB1 rs17321515-A rs17321515 0.56 7.00E-13 6.42 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000]] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease Triglycerides "8,684 individuals" "5,312-9,707 individuals" 11q23.3 "APOA5, APOA4, APOC3, APOA1" rs12286037-T rs12286037 0.06 1.00E-26 25.82 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000]] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease Triglycerides "8,684 individuals" "5,312-9,707 individuals" 8p21.3 LPL rs10503669-C rs10503669 0.9 4.00E-22 11.57 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000]] (imputed)" N 11/25/2008 18193043 Willer 13-Jan-08 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18193043?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Newly identified loci that influence lipid concentrations and risk of coronary artery disease Triglycerides "8,684 individuals" "5,312-9,707 individuals" 2p23.3 GCKR rs780094-T rs780094 0.39 6.00E-32 8.59 [NR] mg/dl higher "Illumina and Affymetrix [~2,261,000]] (imputed)" N 11/25/2008 18179892 Wallace 10-Jan-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18179892?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia LDL cholesterol "1,955 hypertensive individuals" "2,033 individuals in 519 families; 1,461 twins (1/pair selected randomly)" 11q23.3 "APOA1,APOC3,APOA5" rs6589566-G rs6589566 0.06 3.00E-11 NR NR "Affymetrix [400,496]" N 11/25/2008 18179892 Wallace 10-Jan-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18179892?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia LDL cholesterol "1,955 hypertensive individuals" "2,033 individuals in 519 families; 1,461 twins (1/pair selected randomly)" 2p23.3 GCKR rs780094-T rs780094 0.39 5.00E-07 NR NR "Affymetrix [400,496]" N 11/25/2008 18179892 Wallace 10-Jan-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18179892?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia LDL cholesterol "1,955 hypertensive individuals" "2,033 individuals in 519 families; 1,461 twins (1/pair selected randomly)" 1p13.3 "CELSR2,PSRC1" rs599839-G rs599839 0.24 1.00E-07 0.95 [0.93-0.97] "Affymetrix [400,496]" N 11/25/2008 18179892 Wallace 10-Jan-08 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/18179892?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia Serum urate "1,955 hypertensive individuals" "2,033 individuals in 519 families; 1,461 twins (1/pair selected randomly)" 4p16.1 "SLC2A9,WDR1" rs7442295-A rs7442295 0.79 2.00E-15 0.02 [0.02-0.03] mMol/L higher "Affymetrix [400,496]" N 11/25/2008 18159244 Hinney 26-Dec-07 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/18159244?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome Wide Association (GWA) Study for Early Onset Extreme Obesity Supports the Role of Fat Mass and Obesity Associated Gene (FTO) Variants Obesity (early onset extreme) "487 young cases, 442 controls" "2,269 individuals in 644 families" 16q12.2 FTO rs1121980-T rs1121980 0.41 1.00E-07 1.66 [1.37-2.01] "Affymetrix [440,794]" N 11/25/2008 18073375 Duggan 19-Dec-07 J Natl Cancer Inst http://www.ncbi.nlm.nih.gov/pubmed/18073375?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP Prostate cancer "1,235 cases, 1,599 controls" "1,242 cases, 917 controls" NR NR NR NR NS NS NR NR "Illumina & Affymetrix [60,275]" N 11/25/2008 18084291 van Es 16-Dec-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18084291?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "737 cases, 721 controls" "1,030 cases, 1,195 controls" 7q36.2 DPP6 rs10260404-C rs10260404 0.35 5.00E-08 1.3 [1.18-1.43] "Illumina [311,946]" N 11/25/2008 18084291 van Es 16-Dec-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18084291?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "737 cases, 721 controls" "1,030 cases, 1,195 controls" 15q22.1 LIPC rs3825776-? rs3825776 0.29 0.000009 1.34 [1.20-1.46] "Illumina [311,946]" N 11/25/2008 18084291 van Es 16-Dec-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/18084291?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "737 cases, 721 controls" "1,030 cases, 1,195 controls" 2p24.2 Intergenic rs7580332-? rs7580332 0.45 0.000009 1.22 [1.09-1.35] "Illumina [311,946]" N 11/25/2008 18057069 Cronin 7-Dec-07 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/18057069?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of sporadic ALS in a homogenous Irish population Amyotrophic lateral sclerosis "221 cases, 211 controls" "737 cases, 721 controls" 7q36.2 DPP6 rs10260404-? rs10260404 0.37 0.000003 1.37 [1.20-1.56] "Illumina [497,917]" N 11/25/2008 18075462 Suzuki 17-Nov-07 Pharmacogenet Genomics http://www.ncbi.nlm.nih.gov/pubmed/18075462?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A novel genetic marker for coronary spasm in women from a genome-wide single nucleotide polymorphism analysis Coronary spasm "50 Japanese female cases, 50 Japanese female controls" "151 Japanese female cases, 160 Japanese female controls" 14q21.1 Intergenic rs10498345-T rs10498345 0.3 9.00E-07 2.33 [1.64-3.23] "Affymetrix [97,552]" N 11/25/2008 17998437 Li 12-Nov-07 Arch Neurol http://www.ncbi.nlm.nih.gov/pubmed/17998437?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease Alzheimer's disease "753 cases, 736 controls" "418 cases, 249 controls" 19q13.32 "APOE, APOC" rs4420638-? rs4420638 NR 2.00E-44 NR NR "Affymetrix [469,438]" N 11/25/2008 17997608 Li 9-Nov-07 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/17997608?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum The GLUT9 Gene Is Associated with Serum Uric Acid Levels in Sardinia and Chianti Cohorts Serum urate "4,305 Sardinian individuals" "1,301 Tuscan individuals" 4p16.1 GLUT9 rs6855911-A rs6855911 0.74 2.00E-16 0.32 [NR] mg/dl higher "Affymetrix [362,129]" N 11/25/2008 17982456 Plenge 4-Nov-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17982456?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Two independent alleles at 6q23 associated with risk of rheumatoid arthritis Rheumatoid arthritis "397 cases, 1,211 Framingham individuals" "2,283 cases, 3,258 controls" 6q23.3 "TNFAIP3, OLIG3" rs10499194-C rs10499194 0.71 1.00E-09 1.33 [1.15-1.52] "Affymetrix [79,853]" N 11/25/2008 17982456 Plenge 4-Nov-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17982456?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Two independent alleles at 6q23 associated with risk of rheumatoid arthritis Rheumatoid arthritis "397 cases, 1,211 Framingham individuals" "2,283 cases, 3,258 controls" 6q23.3 "TNFAIP3, OLIG3" rs6920220-? rs6920220 0.2 1.00E-07 1.22 [NR] "Affymetrix [79,853]" N 11/25/2008 17975299 Webster 1-Nov-07 Neurodegener Dis http://www.ncbi.nlm.nih.gov/pubmed/17975299?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sorl1 as an Alzheimer's disease predisposition gene? Alzheimer's disease "664 cases, 422 controls" NR 19q13.32 APOE rs4420638-? rs4420638 NR 1.00E-39 NR NR "Affymetrix [~502,627]" N 11/25/2008 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genetic determinants of hair, eye and skin pigmentation in Europeans" Blond vs. brown hair color "2,986 individuals" "3,932 individuals" 14q32.12 SLC24A4 rs12896399-T rs12896399 0.44 1.00E-48 2.56 [2.12-3.09] "Illumina [317,511]" N 11/25/2008 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genetic determinants of hair, eye and skin pigmentation in Europeans" Blond vs. brown hair color "2,986 individuals" "3,932 individuals" 16q24.3 MC1R rs1805007-T rs1805007 0.08 2.00E-13 2.34 [1.69-3.24] "Illumina [317,511]" N 11/25/2008 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genetic determinants of hair, eye and skin pigmentation in Europeans" Blond vs. brown hair color "2,986 individuals" "3,932 individuals" 15q13.1 OCA2 rs1667394-A rs1667394 0.88 6.00E-35 4.94 [3.16-7.71] "Illumina [317,511]" N 11/25/2008 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genetic determinants of hair, eye and skin pigmentation in Europeans" Blond vs. brown hair color "2,986 individuals" "3,932 individuals" 12q21.33 KITLG rs12821256-C rs12821256 0.14 4.00E-30 2.32 [1.86-2.92] "Illumina [317,511]" N 2/16/2009 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum+E2 "Genetic determinants of hair, eye and skin pigmentation in Europeans" Blue vs. brown eyes "2,986 individuals" "3,932 individuals" 15q13.1 OCA2 rs1667394-A rs1667394 0.88 0 29.43 [21.47-40.35] "Illumina [317,511]" N 11/25/2008 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genetic determinants of hair, eye and skin pigmentation in Europeans" Blue vs. green eyes "2,986 individuals" "3,932 individuals" 11q14.3 TYR rs1393350-A rs1393350 0.23 3.00E-12 1.52 [1.28-1.81] "Illumina [317,511]" N 11/25/2008 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genetic determinants of hair, eye and skin pigmentation in Europeans" Blue vs. green eyes "2,986 individuals" "3,932 individuals" 14q32.12 SLC24A4 rs12896399-T rs12896399 0.4 4.00E-38 2.06 [1.76-2.42] "Illumina [317,511]" N 11/25/2008 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genetic determinants of hair, eye and skin pigmentation in Europeans" Blue vs. green eyes "2,986 individuals" "3,932 individuals" 15q13.1 OCA2 rs1667394-A rs1667394 0.98 2.00E-53 6.74 [4.61-9.83] "Illumina [317,511]" N 11/25/2008 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genetic determinants of hair, eye and skin pigmentation in Europeans" Freckles "2,986 individuals" "3,932 individuals" 11q14.3 TYR rs1042602-C rs1042602 0.67 2.00E-11 1.32 [1.17-1.49] "Illumina [317,511]" N 11/25/2008 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genetic determinants of hair, eye and skin pigmentation in Europeans" Freckles "2,986 individuals" "3,932 individuals" 16q24.3 MC1R rs1805007-T rs1805007 0.05 1.00E-96 4.37 [3.56-5.37] "Illumina [317,511]" N 11/25/2008 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genetic determinants of hair, eye and skin pigmentation in Europeans" Freckles "2,986 individuals" "3,932 individuals" 6p25.3 "SEC5L1,IRF4" rs1540771-A rs1540771 0.42 4.00E-18 1.4 [1.26-1.57] "Illumina [317,511]" N 2/16/2009 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum+E2 "Genetic determinants of hair, eye and skin pigmentation in Europeans" Red vs non-red hair color "2,986 individuals" "3,932 individuals" 16q24.3 MC1R rs1805007-T rs1805007 NR 0 12.47 [9.37-16.60] "Illumina [317,511]" N 2/16/2009 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum+E2 "Genetic determinants of hair, eye and skin pigmentation in Europeans" Skin sensitivity to sun "2,986 individuals" "3,932 individuals" 11q14.3 TYR rs1393350-A rs1393350 0.27 2E-06 1.26 [1.11-1.43] "Illumina [317,511]" N 2/16/2009 17952075 Sulem 21-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17952075?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum+E2 "Genetic determinants of hair, eye and skin pigmentation in Europeans" Skin sensitivity to sun "2,986 individuals" "3,932 individuals" 16q24.3 MC1R rs1805007-T rs1805007 0.06 2.00E-55 2.94 [2.42-3.58] "Illumina [317,511]" N 11/25/2008 17999355 Stokowski 15-Oct-07 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/17999355?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genomewide association study of skin pigmentation in a South Asian population Skin pigmentation 363 with maxL* < 56 and 374 with maxL* > 63; 20% tails of distribution "116 low maxL*, 115 high maxL* individuals" 15q21.1 SLC24A5 rs1834640-G rs1834640 0.08 1.00E-50 12.5 [8.33-20.0] "Perlegen [1,502,205] (pooled)" N 11/25/2008 17999355 Stokowski 15-Oct-07 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/17999355?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genomewide association study of skin pigmentation in a South Asian population Skin pigmentation 363 with maxL* < 56 and 374 with maxL* > 63; 20% tails of distribution "116 low maxL*, 115 high maxL* individuals" 11q14.3 TYR rs1042602-C rs1042602 0.84 4.00E-10 4.36 [2.64-7.20] "Perlegen [1,502,205] (pooled)" N 11/25/2008 17999355 Stokowski 15-Oct-07 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/17999355?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genomewide association study of skin pigmentation in a South Asian population Skin pigmentation 363 with maxL* < 56 and 374 with maxL* > 63; 20% tails of distribution "116 low maxL*, 115 high maxL* individuals" 5p13.3 SLC45A2 rs16891982-C rs16891982 0.83 3.00E-11 4.86 [2.88-8.21] "Perlegen [1,502,205] (pooled)" N 11/25/2008 17934461 Broderick 14-Oct-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17934461?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk Colorectal cancer "940 cases, 965 controls" "7,473 cases, 5,984 controls" 18q21.1 SMAD7 rs4939827-T rs4939827 0.52 1.00E-12 1.16 [1.09-1.27] "Illumina [547,647]" N 11/25/2008 17911428 Cervino 8-Oct-07 Ann NY Acad Sci http://www.ncbi.nlm.nih.gov/pubmed/17911428?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide study of lupus: preliminary analysis and data release Lupus "51 cases, 114 controls" NR NR NR NR NR NS NS NR NR "Affymetrix [241,701]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 1q23.2 "FCER1A,OR10J3" rs2494250-? rs2494250 NR 1.00E-14 (MCP1)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 14q23.2 Intergenic rs8005745-? rs8005745 NR 4E-06 (CD40L)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 1q23.2 CRP rs2794520-? rs2794520 NR 3.00E-08 "(CRP average 2,6,7) " NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 1p31.1 Intergenic rs7552393-? rs7552393 NR 5.00E-07 (TNFA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 19q12 ZNF536 rs746961-? rs746961 NR 8.00E-07 (CRP6)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 4q31.1 "CLGN, ELMOD2" rs17532515-? rs17532515 NR 1.00E-06 (Bilirubin)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 9q21.32 Intergenic rs1998303-? rs1998303 NR 0.000001 (AAT)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 1q23.2 IGSF4B rs10489849-? rs10489849 NR 0.000001 (MCP1)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 15q21.3 Intergenic rs10518765-? rs10518765 NR 1.00E-06 (AlkPhos)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 10q26.2 "PTPRE, MKI67" rs2387326-? rs2387326 NR 1.00E-06 (VitKPhylloq)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 5q23.2 Intergenic rs1119582-? rs1119582 NR 1.00E-06 "(CRP average 2,6,7) " NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 6q15 Intergenic rs10485165-? rs10485165 NR 1.00E-06 (VitD25OH)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 6q21 Intergenic rs1417352-? rs1417352 NR 2E-06 (ANP6)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 10q21.1 Intergenic rs583012-? rs583012 NR 2E-06 (CRP2)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 7p13 Intergenic rs1486139-? rs1486139 NR 2E-06 (ANP6)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 13q14.11 Intergenic rs10492681-? rs10492681 NR 2E-06 (ALT2)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 13q21.1 Intergenic rs10507577-? rs10507577 NR 0.000003 (VitD25OH)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 11q23.2 DRD2 rs1079596-? rs1079596 NR 0.000003 (ANP6)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 1q23.2 IGSF4B rs1474747-? rs1474747 NR 0.000003 (MCP1)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 7p21.3 Intergenic rs7778619-? rs7778619 NR 0.000003 (CD40L)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903293 Benjamin 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903293?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with select biomarker traits in the Framingham Heart Study Select biomarker traits "1,012 individuals (Framingham)" NR 1q23.2 OR10J1 rs4128725-? rs4128725 NR 4.00E-12 (MCP1)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903300 Fox 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903300?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project Body mass index "1,341 individuals (Framingham)" NR 7q32.3 Intergenic rs1106683-? rs1106683 NR 1.00E-07 NR NR "Affymetrix [70,897]" N 11/25/2008 17903300 Fox 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903300?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project Body mass index "1,341 individuals (Framingham)" NR 7q23.3 Intergenic rs1106684-? rs1106684 NR 2E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903300 Fox 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903300?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project Body mass index "1,341 individuals (Framingham)" NR 13q21.32 Intergenic rs1333026-? rs1333026 NR 8E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903300 Fox 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903300?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project Waist circumference traits "1,341 individuals (Framingham)" NR 8q21.1 GDAP1 rs4471028-? rs4471028 NR 2.00E-07 NR NR "Affymetrix [70,897]" N 11/25/2008 17903300 Fox 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903300?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project Waist circumference traits "1,341 individuals (Framingham)" NR 3q13.31 Intergenic rs1875517-? rs1875517 NR 2E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903308 Gottlieb 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903308?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association of sleep and circadian phenotypes Sleep duration 738 individuals (Framingham) NR 3p22.1 MYR1P rs6599077-? rs6599077 NR 1.00E-07 NR NR "Affymetrix [70,897]" N 11/25/2008 17903308 Gottlieb 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903308?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association of sleep and circadian phenotypes Sleep duration 738 individuals (Framingham) NR 13q21.2 Intergenic rs10492604-? rs10492604 NR 4E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903308 Gottlieb 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903308?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association of sleep and circadian phenotypes Sleepiness 738 individuals (Framingham) NR 5q11.2 PDE4D rs1823068-? rs1823068 NR 3.00E-08 (sleepiness)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903308 Gottlieb 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903308?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association of sleep and circadian phenotypes Sleepiness 738 individuals (Framingham) NR 8q13.3 EYA1 rs2218488-? rs2218488 NR 0.000003 (sleepiness)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903292 Hwang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study Cystatin C "810-1,010 individuals depending on measure (Framingham)" NR 20p11.21 "CST9L, CST9, CST3" rs1158167-? rs1158167 NR 9.00E-09 NR NR "Affymetrix [70,897]" N 11/25/2008 17903292 Hwang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study Thyroid stimulating hormone "810-1,010 individuals depending on measure (Framingham)" NR 7p15.3 Intergenic rs6977660-? rs6977660 NR 4E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903292 Hwang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study Thyroid stimulating hormone "810-1,010 individuals depending on measure (Framingham)" NR 6q21 HACE1 rs9322817-? rs9322817 NR 7E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903292 Hwang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study Thyroid stimulating hormone "810-1,010 individuals depending on measure (Framingham)" NR 7p15.3 RAPGEF5 rs10499559-? rs10499559 NR 8E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903292 Hwang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study Urinary albumin excretion "810-1,010 individuals depending on measure (Framingham" NR 11q23.2 FAM55B rs1712790-? rs1712790 NR 2E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903292 Hwang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903292?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study Urinary albumin excretion "810-1,010 individuals depending on measure (Framingham" NR 21q21.3 Intergenic rs9305354-? rs9305354 NR 8E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903299 Kathiresan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903299?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study Blood lipid traits "1,087 individuals (Framingham)" "~8,100 individuals" NR NR NR NR NS NS NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Bone mineral density "1,141 individuals (Framingham)" NR 13q21.31 Intergenic rs9317284-? rs9317284 NR 2.00E-07 (FNBMDm)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Bone mineral density "1,141 individuals (Framingham)" NR 4p16.1 Intergenic rs9291683-? rs9291683 NR 2E-06 (BUA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Bone mineral density "1,141 individuals (Framingham)" NR 20q11.23 CTNNBL1 rs4811196-? rs4811196 NR 1.00E-06 (TRBMDf)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Bone mineral density "1,141 individuals (Framingham)" NR 16q23.3 Intergenic rs4087296-? rs4087296 NR 3.00E-07 (TRBMDf)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Bone mineral density "1,141 individuals (Framingham)" NR 12q21.1 Intergenic rs10506701-? rs10506701 NR 1.00E-06 (TRBMD)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Bone mineral density "1,141 individuals (Framingham)" NR 10p15.2 Intergenic rs2165468-? rs2165468 NR 1.00E-06 (FNBMDm)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Bone mineral density "1,141 individuals (Framingham)" NR 7q35 CNTNAP2 rs2214681-? rs2214681 NR 0.000003 (BUA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Bone mineral density "1,141 individuals (Framingham)" NR 3p24.1 RBMS3 rs10510628-? rs10510628 NR 0.000003 (TRBMDm)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 5q13.2 ZNF366 rs10515148-? rs10515148 NR 6.00E-07 (NeckZ1rf)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 12q21.31 Intergenic rs10506821-? rs10506821 NR 2.00E-07 (ShaftW1f)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 5q14.3 GPR98 rs10514345-? rs10514345 NR 2.00E-07 (NeckZ1)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 11q14.1 Intergenic rs1452928-? rs1452928 NR 7.00E-07 (ShaftW1f)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 12p13.31 VAMP1 rs10492096-? rs10492096 NR 0.000003 (ShaftZ1rf)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 13q13.3 Intergenic rs1590305-? rs1590305 NR 0.000003 (NeckZ1rm)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 18q12.1 Intergenic rs4131805-? rs4131805 NR 2E-06 (NSAm)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 3q12.3 Intergenic rs991258-? rs991258 NR 5.00E-07 (ShaftW1)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 3p14.1 Intergenic rs922948-? rs922948 NR 2E-06 (ShaftW1f)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 1p11.2 Intergenic rs6600671-? rs6600671 NR 6.00E-07 (NeckZ1rf)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 3p24.3 KCNH8 rs2053506-? rs2053506 NR 4E-06 (NeckZ1)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 6p24.1 PHACTR1 rs4715166-? rs4715166 NR 0.000003 (NeckW1rf)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 3p14.3 ERC2 rs2054989-? rs2054989 NR 6.00E-07 (NeckW1rf)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 5p14.1 Intergenic rs2548003-? rs2548003 NR 2.00E-07 (NeckZ1rf)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 8p12 NRG1 rs10503887-? rs10503887 NR 2.00E-07 (ShaftZ1R)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903296 Kiel 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903296?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with bone mass and geometry in the Framingham Heart Study Hip geometry "1,141 individuals (Framingham)" NR 11q23.2 Intergenic rs638882-? rs638882 NR 4E-06 (NeckZ1rf)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903304 Larson 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903304?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes Atrial fibrillation "1,341-1,345 individuals, depending on measure (Framingham)" NR 11q22.1 CNTN5 rs10501920-? rs10501920 NR 0.000009 NR NR "Affymetrix [70,897]" N 11/25/2008 17903304 Larson 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903304?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes Atrial fibrillation "1,341-1,345 individuals, depending on measure (Framingham)" NR 15q23 Intergenic rs4776472-? rs4776472 NR 0.000008 NR NR "Affymetrix [70,897]" N 11/25/2008 17903304 Larson 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903304?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes Atrial fibrillation "1,341-1,345 individuals, depending on measure (Framingham)" NR 13q14 Intergenic rs958546-? rs958546 NR 0.000005 NR NR "Affymetrix [70,897]" N 11/25/2008 17903304 Larson 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903304?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes Heart failure "1,341-1,345 individuals, depending on measure (Framingham" NR 10q25.3 KIAA1598 rs740363-? rs740363 NR 0.000009 NR NR "Affymetrix [70,897]" N 11/25/2008 17903304 Larson 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903304?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes Major CVD "1,341-1,345 individuals, depending on measure (Framingham)" NR 6p24.1 Intergenic rs499818-? rs499818 NR 7E-06 (major CVD)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Blood pressure "644-1,327 individuals, depending on measure (Framingham)" NR 14q24.3 Intergenic rs935334-? rs935334 NR 0.000003 (DBP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Blood pressure "644-1,327 individuals, depending on measure (Framingham)" NR 8q13.3 Intergenic rs1963982-? rs1963982 NR 0.000003 (DBP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Blood pressure "644-1,327 individuals, depending on measure (Framingham)" NR 1p31.3 Intergenic rs10493340-? rs10493340 NR 2E-06 (SBP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Blood pressure "644-1,327 individuals, depending on measure (Framingham)" NR 2q36.3 "CCL20, WDR69" rs7591163-? rs7591163 NR 3.00E-07 (DBPLTA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Blood pressure "644-1,327 individuals, depending on measure (Framingham)" NR 16q23.3 CDH13 rs3096277-? rs3096277 NR 1.00E-09 (SBPLTA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Blood pressure "644-1,327 individuals, depending on measure (Framingham)" NR 6q15 Intergenic rs2509458-? rs2509458 NR 7E-06 (DBP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Blood pressure "644-1,327 individuals, depending on measure (Framingham)" NR 14q24.3 C14orf118 rs2121070-? rs2121070 NR 0.000005 (DBP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Blood pressure "644-1,327 individuals, depending on measure (Framingham)" NR 5q22.1 CAMK4 rs10491334-? rs10491334 NR 4E-06 (DBP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Blood pressure "644-1,327 individuals, depending on measure (Framingham)" NR 3p26.3 CNTN4 rs4370013-? rs4370013 NR 4E-06 (DBP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 6q25.2 SYNE1 rs1322512-? rs1322512 NR 8E-06 (MAP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 5q14.3 MEF2C rs770189-? rs770189 NR 0.000003 (CB-PWV)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 7q33 EXOC4 rs10488172-? rs10488172 NR 8E-06 (RWLTA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 3q24 SLC9A9 rs1371924-? rs1371924 NR 4E-06 (RWLTA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 1q25.1 TNR rs3766680-? rs3766680 NR 4E-06 (FWLTA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 17p12 HS3ST3A1 rs10521232-? rs10521232 NR 4E-06 (CF-PWVLTA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 2q14.3 CNTNAP5 rs1367248-? rs1367248 NR 0.000003 (CF-PWVLTA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 13q13.3 GPC6 rs6492654-? rs6492654 NR 2E-06 (RWLTA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 8p22 VPS37A rs3793427-? rs3793427 NR 2E-06 (FWLTA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 3p24.1 TGFBR2 rs3773643-? rs3773643 NR 2.00E-07 (MAPLTA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 20q13.13 PREX1 rs6063312-? rs6063312 NR 2E-06 (RW)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 9q31.2 Intergenic rs7042864-? rs7042864 NR 0.000006 (CB-PWV)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903302 Levy 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903302?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness Tonometry "644-1,327 individuals, depending on measure (Framingham" NR 3p22.3 Intergenic rs10514688-? rs10514688 NR 0.000006 (CB-PWV)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study Aging traits "1,345 individuals (Framingham)" NR 12p11.22 Intergenic rs1463605-? rs1463605 NR 7.00E-08 (biologic age)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study Aging traits "1,345 individuals (Framingham)" NR 7q21.11 Intergenic rs2371208-? rs2371208 NR 0.000003 (age at death)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study Aging traits "1,345 individuals (Framingham)" NR 2p12 Intergenic rs10496262-? rs10496262 NR 3.00E-07 (age at natural menopause)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study Aging traits "1,345 individuals (Framingham)" NR 2q24.1 GALNT13 rs958672-? rs958672 NR 2E-06 (age at natural menopause)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study Aging traits "1,345 individuals (Framingham)" NR 1q42.3 GNG4 rs291353-? rs291353 NR 0.000006 (age at natural menopause)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study Aging traits "1,345 individuals (Framingham)" NR 11q14.3 Intergenic rs1528753-? rs1528753 NR 8.00E-08 (age at death)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study Aging traits "1,345 individuals (Framingham)" NR 2p12 Intergenic rs10496265-? rs10496265 NR 1.00E-08 (age at natural menopause)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study Aging traits "1,345 individuals (Framingham)" NR 3q25.31 KCNAB1 rs3772255-? rs3772255 NR 8E-06 (biologic age)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study Aging traits "1,345 individuals (Framingham)" NR 15q25.3 KLHL25 rs7176093-? rs7176093 NR 7E-06 (biologic age)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study Aging traits "1,345 individuals (Framingham)" NR 12q24.23 CCDC60 rs7137869-? rs7137869 NR 6.00E-07 (walking speed exam 7)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. Morbidity-free survival "1,345 individuals (Framingham)" NR 16q21 Intergenic rs2639889-? rs2639889 NR 9.00E-07 NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. Morbidity-free survival "1,345 individuals (Framingham)" NR 6p24.3 Intergenic rs10484246-? rs10484246 NR 8.00E-08 NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. Morbidity-free survival "1,345 individuals (Framingham)" NR 5p15.32 Intergenic rs32566-? rs32566 NR 2.00E-09 NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. Morbidity-free survival "1,345 individuals (Framingham)" NR 8p22 Intergenic rs4831837-? rs4831837 NR 5.00E-07 NR NR "Affymetrix [70,897]" N 11/25/2008 17903295 Lunetta 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903295?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. Morbidity-free survival "1,345 individuals (Framingham)" NR 1q24.2 DPT rs1412337-? rs1412337 NR 2.00E-09 NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Diabetes (incident) "1,087 individuals (Framingham)" NR 2q32.3 TMEFF2 rs10497721-? rs10497721 NR 7.00E-07 NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Diabetes related insulin traits "1,087 individuals (Framingham)" NR 7p15.1 CPVL rs10486607-? rs10486607 NR 8E-06 (HbA1C)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Diabetes related insulin traits "1,087 individuals (Framingham)" NR 13q21.33 Intergenic rs2066219-? rs2066219 NR 0.000009 (ISI_0-120)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Diabetes related insulin traits "1,087 individuals (Framingham)" NR 14q12 Intergenic rs2877832-? rs2877832 NR 2E-06 (FI)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Diabetes related insulin traits "1,087 individuals (Framingham)" NR 14q12 Intergenic rs2877832-? rs2877832 NR 0.000003 (HOMA-IR)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Fasting plasma glucose "1,087 individuals (Framingham)" NR 3p24.1 Intergenic rs10510634-? rs10510634 NR 0.000005 (tFPG)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Fasting plasma glucose "1,087 individuals (Framingham)" NR 8p11.21 ZMAT4 rs2722425-? rs2722425 NR 2.00E-08 (tFPG)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Fasting plasma glucose "1,087 individuals (Framingham)" NR 4q27 PRDM5 rs180730-? rs180730 NR 0.000005 (FPG)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Fasting plasma glucose "1,087 individuals (Framingham)" NR 8p11.21 ZMAT4 rs2722425-? rs2722425 NR 0.000009 (FPG)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Fasting plasma glucose "1,087 individuals (Framingham)" NR 5q23.3 Intergenic rs7731657-? rs7731657 NR 7E-06 (tFPG)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903298 Meigs 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903298?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association with diabetes-related traits in the Framingham Heart Study Fasting plasma glucose "1,087 individuals (Framingham)" NR 4q27 PRDM5 rs180730-? rs180730 NR 0.000006 (tFPG)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Breast cancer "1,345 individuals (Framingham)" NR 13q32.1 ABCC4 rs1926657-? rs1926657 NR 2E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Breast cancer "1,345 individuals (Framingham)" NR 7q11.22 Intergenic rs10263639-? rs10263639 NR 0.000003 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Breast cancer "1,345 individuals (Framingham)" NR 12q21.1 Intergenic rs1154865-? rs1154865 NR 7.00E-07 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Breast cancer "1,345 individuals (Framingham)" NR 18q21.2 Intergenic rs1978503-? rs1978503 NR 1.00E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Breast cancer "1,345 individuals (Framingham)" NR 5q34 Intergenic rs6556756-? rs6556756 NR 5.00E-07 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Breast cancer "1,345 individuals (Framingham)" NR 15q21.1 FBN1 rs1876206-? rs1876206 NR 0.000006 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Breast cancer "1,345 individuals (Framingham)" NR 17q21.33 COL1A1 rs2075555-? rs2075555 NR 8.00E-08 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Breast cancer "1,345 individuals (Framingham)" NR 2p16.1 Intergenic rs10490113-? rs10490113 NR 0.000005 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Breast cancer "1,345 individuals (Framingham)" NR 21q21.3 GRIK1 rs458685-? rs458685 NR 0.000006 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Prostate cancer "1,345 individuals (Framingham)" NR 3q24 Intergenic rs345013-? rs345013 NR 0.000005 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Prostate cancer "1,345 individuals (Framingham)" NR 5q14.3 HAPLN1 rs4466137-? rs4466137 NR 0.000003 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Prostate cancer "1,345 individuals (Framingham)" NR 6p12.2 PKHD1 rs10498792-? rs10498792 NR 0.000003 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Prostate cancer "1,345 individuals (Framingham)" NR 13q33.1 Intergenic rs1529276-? rs1529276 NR 2E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903305 Murabito 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903305?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study Prostate cancer "1,345 individuals (Framingham)" NR 3p22.2 CTDSPL rs9311171-? rs9311171 NR 2E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903306 Newton-Cheh 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903306?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study Electrocardiographic traits "548-1,175 individuals, depending on measure (Framingham)" NR 13q12.2 RPL21 rs10507380-? rs10507380 NR 8E-06 (QT interval)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903306 Newton-Cheh 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903306?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study Electrocardiographic traits "548-1,175 individuals, depending on measure (Framingham)" NR 2q22.1 Intergenic rs882300-? rs882300 NR 3.00E-07 (PR interval)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903306 Newton-Cheh 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903306?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study Heart rate variability traits "548-1,175 individuals, depending on measure (Framingham)" NR 4q34 NEIL3 rs1395479-? rs1395479 NR 7E-06 (LF/HF)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903306 Newton-Cheh 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903306?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study Heart rate variability traits "548-1,175 individuals, depending on measure (Framingham)" NR 13q13.3 DCAMKL1 rs9315385-? rs9315385 NR 8E-06 (TP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Coronary artery calcification "673-984 individuals, depending on measure (Framingham)" NR 1p22.2 Intergenic rs2390582-? rs2390582 NR 1.00E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Coronary artery calcification "673-984 individuals, depending on measure (Framingham)" NR 14q24.2 NUMB rs10483853-? rs10483853 NR 0.000006 NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Coronary artery calcification "673-984 individuals, depending on measure (Framingham)" NR 12q23.2 DR1M rs10507130-? rs10507130 NR 7E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Subclinical atherosclerosis traits (other) "673-984 individuals, depending on measure (Framingham)" NR 5p15.2 DNAH5 rs2896103-? rs2896103 NR 0.000005 (ABI)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Subclinical atherosclerosis traits (other) "673-984 individuals, depending on measure (Framingham)" NR 11q14.3 Intergenic rs1350445-? rs1350445 NR 0.000009 (ABI)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Subclinical atherosclerosis traits (other) "673-984 individuals, depending on measure (Framingham)" NR 4q28.1 Intergenic rs1320267-? rs1320267 NR 7E-06 (ABI)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Subclinical atherosclerosis traits (other) "673-984 individuals, depending on measure (Framingham)" NR 1q31.1 Intergenic rs1400544-? rs1400544 NR 0.000006 (CCA IMT)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Subclinical atherosclerosis traits (other) "673-984 individuals, depending on measure (Framingham)" NR 5p15.2 DNAH5 rs1502050-? rs1502050 NR 0.000009 (ABI)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Subclinical atherosclerosis traits (other) "673-984 individuals, depending on measure (Framingham)" NR 10q11.22 LRRC18 rs3849150-? rs3849150 NR 2E-06 (AAC)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Subclinical atherosclerosis traits (other) "673-984 individuals, depending on measure (Framingham)" NR 2q33.2 ABI2 rs1376877-? rs1376877 NR 4.00E-07 (ICA IMT)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903303 O'Donnell 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903303?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study Subclinical atherosclerosis traits (other) "673-984 individuals, depending on measure (Framingham)" NR 5p15.2 DNAH5 rs7715811-? rs7715811 NR 0.000006 (ABI)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 12p11.1 Intergenic rs9300212-? rs9300212 NR 8E-06 (WRAT)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 9q22.2 DIRAS2 rs1831521-? rs1831521 NR 8E-06 (Nam)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 2q22.1 Intergenic rs934299-? rs934299 NR 0.000009 (F3)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 1p22.2 Intergenic rs2179965-? rs2179965 NR 1.00E-06 (F3)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 4q13.2 Intergenic rs1155865-? rs1155865 NR 2E-06 (Nam)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 21q21.3 Intergenic rs2832077-? rs2832077 NR 2E-06 (F3)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 6p23 Intergenic rs6914079-? rs6914079 NR 2E-06 (F2)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 1q42.2 TARBP1 rs10489896-? rs10489896 NR 0.000006 (F2)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 11q25 NCAPD3 rs1031381-? rs1031381 NR 0.000006 (F3)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 17q22 PPM1E rs9303401-? rs9303401 NR 0.000005 (NAM)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 11q14.1 Intergenic rs530965-? rs530965 NR 4E-06 (Nam)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 12q23.3 "POLR3B, RFX4" rs3891355-? rs3891355 NR 0.000003 (Sim)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 5q32 Intergenic rs9325032-? rs9325032 NR 0.000003 (F2)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Cognitive test performance 705 individuals (Framingham) NR 14q24.3 Intergenic rs2352904-? rs2352904 NR 2E-06 (F2)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Volumetric brain MRI 705 individuals (Framingham) NR 4q31.3 Intergenic rs360929-? rs360929 NR 0.000009 (ALTHBV)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Volumetric brain MRI 705 individuals (Framingham) NR 20q13.33 CDH4 rs1970546-? rs1970546 NR 4.00E-08 (ATCBV)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Volumetric brain MRI 705 individuals (Framingham) NR 11q23.2 NNMT rs2847476-? rs2847476 NR 0.000003 (ALLV)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Volumetric brain MRI 705 individuals (Framingham) NR 11p13 EHF rs5028798-? rs5028798 NR 0.000003 (ATBV)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903297 Seshadri 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903297?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study Volumetric brain MRI 705 individuals (Framingham) NR 11q22.1 CNTN5 rs952700-? rs952700 NR 0.000006 (AFBV)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Echocardiographic traits "1,238 individuals (Framingham)" NR 4p15.31 SLIT2 rs1379659-? rs1379659 NR 1.00E-07 (LVDD)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Echocardiographic traits "1,238 individuals (Framingham)" NR 1p31.3 PDE4B rs10493389-? rs10493389 NR 7E-06 (LAD)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Echocardiographic traits "1,238 individuals (Framingham)" NR 2q36.1 Intergenic rs10498091-? rs10498091 NR 0.000006 (LVM)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Echocardiographic traits "1,238 individuals (Framingham)" NR 1q31.1 FAM5C rs1935881-? rs1935881 NR 0.000006 (LAD)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Echocardiographic traits "1,238 individuals (Framingham)" NR 8q13.3 KCNB2 rs10504543-? rs10504543 NR 0.000005 (LVSD)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Echocardiographic traits "1,238 individuals (Framingham)" NR 4p15.31 SLIT2 rs666088-? rs666088 NR 0.000005 (LVDD)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Echocardiographic traits "1,238 individuals (Framingham)" NR 6q15 SPACA1 rs366676-? rs366676 NR 2E-06 (LVFS)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Echocardiographic traits "1,238 individuals (Framingham)" NR 5q14.3 Intergenic rs4920799-? rs4920799 NR 7E-06 (LVDD)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Endothelial function traits "1,238 individuals (Framingham)" NR 10q24.33 OBFC1 rs3814219-? rs3814219 NR 9.00E-07 (BABF)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Exercise treadmill test traits "1,238 individuals (Framingham)" NR 11q22.3 Intergenic rs746463-? rs746463 NR 0.000005 (P3MRSBP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Exercise treadmill test traits "1,238 individuals (Framingham)" NR 8p12 WRN rs2553268-? rs2553268 NR 0.000006 (S2ESBP)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Exercise treadmill test traits "1,238 individuals (Framingham)" NR 4q25 NOLA1 rs6847149-? rs6847149 NR 0.000003 (S2EHR)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903301 Vasan 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903301?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study" Exercise treadmill test traits "1,238 individuals (Framingham)" NR 1q43 RYR2 rs2819770-? rs2819770 NR 4E-06 (S2EHR)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Mean forced vital capacity from 2 exams "1,097-1,222 individuals, depending on measure (Framingham)" NR 4q25 Intergenic rs10516541-? rs10516541 NR 4E-06 (meanfvc)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Mean forced vital capacity from 2 exams "1,097-1,222 individuals, depending on measure (Framingham)" NR 7q21.3 COL1A2 rs441051-? rs441051 NR 2E-06 (meanfvc)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Pulmonary function traits (other) "1,097-1,222 individuals, depending on measure (Framingham)" NR 15q26.1 FLJ32831 rs1455782-? rs1455782 NR 4E-06 (ppfvc)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Pulmonary function traits (other) "1,097-1,222 individuals, depending on measure (Framingham)" NR 15q11.2 SNRPN rs3867498-? rs3867498 NR 1.00E-06 (fev1slope)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Pulmonary function traits (other) "1,097-1,222 individuals, depending on measure (Framingham)" NR 21q22.3 ADARB1 rs2838815-? rs2838815 NR 0.000003 (meanratio)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Pulmonary function traits (other) "1,097-1,222 individuals, depending on measure (Framingham)" NR 7q34 Intergenic rs357394-? rs357394 NR 0.000009 (ppfvc)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Pulmonary function traits (other) "1,097-1,222 individuals, depending on measure (Framingham)" NR 17p12 CDRT4 rs2906966-? rs2906966 NR 8E-06 (ppfev1)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Pulmonary function traits (other) "1,097-1,222 individuals, depending on measure (Framingham)" NR 1q21.3 IL6R rs4129267-? rs4129267 NR 7E-06 (ppfef)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Pulmonary function traits (other) "1,097-1,222 individuals, depending on measure (Framingham)" NR 14q23.1 Intergenic rs808225-? rs808225 NR 7E-06 (ppfefrat)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Pulmonary function traits (other) "1,097-1,222 individuals, depending on measure (Framingham)" NR 14q22.1 NID2 rs730532-? rs730532 NR 0.000006 (ppfef)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Pulmonary function traits (other) "1,097-1,222 individuals, depending on measure (Framingham)" NR 2q36.3 RHBDD1 rs3820928-? rs3820928 NR 0.000005 (ppfev1)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903307 Wilk 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903307?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Framingham Heart Study genome-wide association: results for pulmonary function measures Pulmonary function traits (other) "1,097-1,222 individuals, depending on measure (Framingham)" NR 8q11.22 SNTG1 rs310558-? rs310558 NR 0.000005 (ppratio)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Factor VII "1,000 individuals (Framingham)" NR 7p22.2 Intergenic rs10488360-? rs10488360 0.3 7E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Factor VII "1,000 individuals (Framingham)" NR 1p36.32 Intergenic rs966321-? rs966321 0.47 8E-06 NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Factor VII "1,000 individuals (Framingham)" NR 13q34 "MCF2L, AB116074, AK092739, AK123267, AB0023600, F7, CR603372, F10, PROZ" rs561241-? rs561241 0.12 5.00E-16 NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Factor VII "1,000 individuals (Framingham)" NR 3p26.1 Intergenic rs4591494-? rs4591494 0.19 0.000009 NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 6q25.1 MAP3K7IP2 rs727979-? rs727979 0.14 8E-06 (RBCC)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 20p12.3 Intergenic rs6108011-? rs6108011 0.28 0.000006 (RBCC)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 14q21.3 MAMDC1 rs7159841-? rs7159841 0.21 2.00E-07 (Viscosity)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 1q23.2 "OR10J1,OR10J5" rs4133289-? rs4133289 0.19 2.00E-07 (Hgb)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 5q21.3 Intergenic rs4460176-? rs4460176 0.29 0.000003 (PAI-1)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 1p31.1 NEGR1 rs10493485-? rs10493485 0.29 2E-06 (tPA)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 11q24.1 Intergenic rs565229-? rs565229 0.1 4E-06 (pltcoll)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 14q32.2 Intergenic rs10484128-? rs10484128 0.15 0.000006 (pltadp)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 11q11 "OR5AP2, OR5AR1, OR9G1, OR9G4" rs1397048-? rs1397048 0.4 7.00E-08 (MCH)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 10p11.21 ANKRD30A rs1200821-? rs1200821 0.47 0.000006 (MCH)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 5q21.1 Intergenic rs1829883-? rs1829883 0.41 0.000006 (MCH)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 8q24.13 Intergenic rs7844723-? rs7844723 0.45 2E-06 (Hgb)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 2p16.2 Intergenic rs2357013-? rs2357013 0.45 0.000006 (Hgb)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 6q25.1 Intergenic rs636864-? rs636864 0.21 0.000006 (RBCC)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 4p15.33 Intergenic rs10489087-? rs10489087 0.13 0.000005 (RBCC)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 2p16.2 Intergenic rs1160297-? rs1160297 0.43 1.00E-06 (Hgb)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 12q14.2 Intergenic rs10506458-? rs10506458 0.13 0.000005 (pltcoll)  NR NR "Affymetrix [70,897]" N 11/25/2008 17903294 Yang 19-Sep-07 BMC Med Genet http://www.ncbi.nlm.nih.gov/pubmed/17903294?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study Hemostatic factors and hematological phenotypes "1,000 individuals (Framingham" NR 1p34.3 "FLJ11730, BC016328" rs9253-? rs9253 0.18 4E-06 (RBCC)  NR NR "Affymetrix [70,897]" N 11/25/2008 17848626 Florez 10-Sep-07 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/17848626?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets Type 2 diabetes and 6 quantitative traits "1,087 family members" "1,465 unrelated individuals; 2,175 cases and 2,412 controls" NR NR NR NR NS NS NR NR "Affymetrix [66,543]" N 11/25/2008 17846125 Hanson 10-Sep-07 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/17846125?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A search for variants associated with young-onset type 2 diabetes in American Indians in a 100K genotyping array Type 2 diabetes "300 cases, 334 controls, 121 nondiabetic siblings, 140 diabetic siblings" "1,207 cases, 1,627 controls" NR NR NR NR NS NS NR NR "Affymetrix [80,044]" N 11/25/2008 17846124 Hayes 10-Sep-07 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/17846124?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies Type 2 diabetes "281 cases, 280 controls" "~1,979 cases, ~3,092 controls" NR NR NR NR NS NS NR NR "Affymetrix [88,142]" N 11/25/2008 17846126 Rampersaud 10-Sep-07 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/17846126?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations Type 2 diabetes "124 cases, 295 controls" "2,142 cases, 2,117 controls" NR NR NR NR NS NS NR NR "Affymetrix [82,485]" N 11/25/2008 17827064 van Es 7-Sep-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17827064?ordinalpos=13&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study Amyotrophic lateral sclerosis "737 cases, 721 controls" "1,030 cases, 1,195 controls" 12p11 ITPR2 rs2306677-? rs2306677 0.07 0.000003 1.58 [1.30-1.91] "Illumina [311,946]" N 11/25/2008 17804836 Plenge 5-Sep-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17804836?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study Rheumatoid arthritis "1,493 cases, 1,831 controls" "1,053 cases, 1,858 controls" 1p13.2 PTPN22 rs2476601-? rs2476601 0.1 2.00E-11 1.72 [NR] "Illumina [297,086]" N 11/25/2008 17804836 Plenge 5-Sep-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17804836?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study Rheumatoid arthritis "1,493 cases, 1,831 controls" "1,053 cases, 1,858 controls" 9q34 TRAF1-C5 rs3761847-G rs3761847 0.41 4.00E-14 1.32 [1.23-1.42] "Illumina [297,086]" N 11/25/2008 17804836 Plenge 5-Sep-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17804836?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study Rheumatoid arthritis "1,493 cases, 1,831 controls" "1,053 cases, 1,858 controls" 6p21.32 HLA-DRB1 rs660895-? rs660895 0.21 1.00E-108 3.62 [NR] "Illumina [297,086]" N 11/25/2008 17804789 Raelson 5-Sep-07 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/17804789?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci Crohn's disease 382 trios "750 cases, 828 controls, 521 trios" 16q12.1 NOD2 rs5743289-? rs5743289 NR 6.00E-17 NR NR "Perlegen [164,279]" N 11/25/2008 17804789 Raelson 5-Sep-07 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/17804789?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci Crohn's disease 382 trios "750 cases, 828 controls, 521 trios" 1p31.3 IL23R 17 marker haplotype-1 "rs11465802,rs2064689,rs2902440,rs1343151,rs10889676,rs9988642,rs12567232,rs6669582,rs10789230,rs11209026,rs11465804,rs11209003,rs11209002,rs1004819,rs2201841,rs10889677" 0.23 1.00E-08 1.38 [1.23-1.53] "Perlegen [164,279]" N 11/25/2008 17804789 Raelson 5-Sep-07 Proc Natl Acad Sci USA http://www.ncbi.nlm.nih.gov/pubmed/17804789?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci Crohn's disease 382 trios "750 cases, 828 controls, 521 trios" 1p31.3 IL23R 17 marker haplotype-2 "rs11209002,rs2064689,rs1004819,rs2902440,rs11465802,rs2201841,rs11465804,rs11209026,rs1343151,rs10889676,rs10889677,rs9988642,rs12567232,rs6669582,rs10789230,rs11209003" 0.97 2.00E-07 2.56 [1.75-3.70] "Perlegen [164,279]" N 11/25/2008 17767159 Menzel 2-Sep-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17767159?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 F-cell distribution 179 adults in upper and lower 5% 90 adults 2p15.1 BCL11A rs1427407-? rs1427407 0.14 6.00E-31 13.1 [NR] % of variance explained "Illumina [308,015]" N 11/25/2008 17767159 Menzel 2-Sep-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17767159?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 F-cell distribution 179 adults in upper and lower 5% 90 adults 6q23.3 Intergenic rs9399137-? rs9399137 0.23 3.00E-36 15.8 [NR] % of variance explained "Illumina [308,015]" N 11/25/2008 17767159 Menzel 2-Sep-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17767159?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 F-cell distribution 179 adults in upper and lower 5% 90 adults 11p15.5 HBB NR NR 0.33 2.00E-38 10.2 [NR] % of variance explained "Illumina [308,015]" N 11/25/2008 17767157 Weedon 2-Sep-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17767157?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A common variant of HMGA2 is associated with adult and childhood height in the general population Height "4,921 individuals" "29,098 individuals (19,064 adults)" 12q14.3 HMGA2 rs1042725-C rs1042725 0.51 6.00E-16 0.4 [NR] cm per copy in adult height "Affymetrix [364,301]" N 11/25/2008 17690259 Thorleifsson 9-Aug-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17690259?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma Glaucoma (exfoliation) "75 cases, 14,474 controls" "254 cases, 198 controls" 15q24.1 LOXL1 rs3825942-G rs3825942 0.85 3.00E-21 20.1 [10.80-37.41] "Illumina [304,250]" N 11/25/2008 17684544 Franke 8-Aug-07 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/17684544?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Systematic association mapping identifies NELL1 as a novel IBD disease gene Crohn's disease "393 cases, 399 controls" "1,248 trios, 2,920 cases, 1,961 controls" 5p13.1 PTGER4 rs1992660-? rs1992660 0.39 4.00E-07 1.42 [1.24-1.67] "Affymetrix [92,387]" N 11/25/2008 17684544 Franke 8-Aug-07 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/17684544?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Systematic association mapping identifies NELL1 as a novel IBD disease gene Crohn's disease "393 cases, 399 controls" "1,248 trios, 2,920 cases, 1,961 controls" 11p15.1 NELL1 rs1793004-? rs1793004 0.27 0.000003 1.3 [1.12-1.52] "Affymetrix [92,387]" N 11/25/2008 17684544 Franke 8-Aug-07 PLoS ONE http://www.ncbi.nlm.nih.gov/pubmed/17684544?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Systematic association mapping identifies NELL1 as a novel IBD disease gene Crohn's disease "393 cases, 399 controls" "1,248 trios, 2,920 cases, 1,961 controls" 16q12.1 CARD15 rs2076756-? rs2076756 0.27 1.00E-21 1.71 [1.42-2.05] "Affymetrix [92,387]" N 11/25/2008 17671248 Dunckley 1-Aug-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17671248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Whole-genome analysis of sporadic amyotrophic lateral sclerosis Amyotrophic lateral sclerosis "386 cases, 542 controls" "901 cases, 1,025 controls" NR NR NR NR NS NS NR NR "Affymetrix and Illumina [776,955]" N 11/25/2008 17653210 Maeda 1-Aug-07 Kidney Int Suppl http://www.ncbi.nlm.nih.gov/pubmed/17653210?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population Diabetic nephropathy "94 cases, 94 controls" NR 7p14.2 ELMO1 rs741301-? rs741301 NR 8E-06 2.67 [1.71-4.16] "NR [~80,000]" N 11/25/2008 17667963 Shifman 31-Jul-07 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/17667963?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A whole genome association study of neuroticism using DNA pooling Neuroticism "1,038 cases, 1,016 controls" "831 cases, 702 controls" 5q11.2 PDE4D rs702543-A rs702543 0.55 2E-06 1.27 [1.15-1.40] "Affymetrix [452,574] (pooled)" N 11/25/2008 17660530 Hafler 29-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Risk alleles for multiple sclerosis identified by a genomewide study Multiple sclerosis "931 trios, 2,431 controls" "609 trios, 2,322 cases, 2,987 controls" 6p21.32 HLA-DRA rs3135388-A rs3135388 0.23 9.00E-81 1.99 [1.84-2.15] "Affymetrix [334,923]" N 11/25/2008 17660530 Hafler 29-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Risk alleles for multiple sclerosis identified by a genomewide study Multiple sclerosis "931 trios, 2,431 controls" "609 trios, 2,322 cases, 2,987 controls" 10p15.1 IL2RA rs12722489-C rs12722489 0.85 3.00E-08 1.25 [1.11-1.36] "Affymetrix [334,923]" N 11/25/2008 17660530 Hafler 29-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Risk alleles for multiple sclerosis identified by a genomewide study Multiple sclerosis "931 trios, 2,431 controls" "609 trios, 2,322 cases, 2,987 controls" 5p13.2 IL7RA rs6897932-C rs6897932 0.75 3.00E-07 1.18 [1.11-1.26] "Affymetrix [334,923]" N 11/25/2008 17660530 Hafler 29-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Risk alleles for multiple sclerosis identified by a genomewide study Multiple sclerosis "931 trios, 2,431 controls" "609 trios, 2,322 cases, 2,987 controls" 16p13 KIAA0350 rs6498169-G rs6498169 0.37 4E-06 1.14 [1.08-1.21] "Affymetrix [334,923]" N 11/25/2008 17660530 Hafler 29-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Risk alleles for multiple sclerosis identified by a genomewide study Multiple sclerosis "931 trios, 2,431 controls" "609 trios, 2,322 cases, 2,987 controls" 1p22 RPL5 rs6604026-C rs6604026 0.29 8E-06 1.15 [1.08-1.22] "Affymetrix [334,923]" N 11/25/2008 17660530 Hafler 29-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17660530?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Risk alleles for multiple sclerosis identified by a genomewide study Multiple sclerosis "931 trios, 2,431 controls" "609 trios, 2,322 cases, 2,987 controls" 9q33 DBC1 rs10984447-A rs10984447 0.77 8E-06 1.17 [1.09-1.25] "Affymetrix [334,923]" N 11/25/2008 17611496 Moffatt 26-Jul-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17611496?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma Asthma "994 cases, 1,243 controls" "2,320 cases, 3,301 controls" 17q12 ORMDL3 rs7216389-T rs7216389 0.52 9.00E-11 1.45 [1.17-1.81] "Illumina [307,328]" N 11/25/2008 17658951 Scuteri 20-Jul-07 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/17658951?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits Obesity-related traits "4,741 individuals" "3,205 individuals" 16q12.2 FTO rs9930506-A rs9930506 0.54 9.00E-07 (BMI)  0.13 [NR] SD lower (BMI) "Affymetrix [362,129]" N 11/25/2008 17658951 Scuteri 20-Jul-07 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/17658951?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits Obesity-related traits "4,741 individuals" "3,205 individuals" 16q12.2 FTO rs9930506-A rs9930506 0.54 3.00E-08 (hip)  0.16 [NR] SD lower (hip) "Affymetrix [362,129]" N 11/25/2008 17658951 Scuteri 20-Jul-07 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/17658951?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-Wide Association Scan Shows Genetic Variants in the FTO Gene Are Associated with Obesity-Related Traits Obesity-related traits "4,741 individuals" "3,205 individuals" 16q12.2 FTO rs9930506-A rs9930506 0.54 9.00E-07 (weight)  0.12 [NR] SD lower (weight) "Affymetrix [362,129]" N 11/25/2008 17641165 Fellay 19-Jul-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17641165?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A whole-genome association study of major determinants for host control of HIV-1 HIV1 viral setpoint 486 patients 140 patients NR NR NR NR NS NS NR NR "Illumina [535,101]" N 11/25/2008 17634447 Stefansson 19-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17634447?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genetic risk factor for periodic limb movements in sleep Restless legs syndrome "306 cases, 15,664 controls" "311 cases, 1,895 controls" 6p21.2 BTBD9 rs3923809-A rs3923809 0.66 1.00E-17 1.9 [1.50-2.20] "Illumina [306,937]" N 11/25/2008 17634449 Samani 18-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genomewide association analysis of coronary artery disease Coronary disease "1,926 cases, 2,938 controls" "875 cases, 1,644 controls" 9p21.3 Intergenic rs1333049-C rs1333049 0.47 3.00E-19 1.36 [1.27-1.46] "Affymetrix [377,857]" N 11/25/2008 17634449 Samani 18-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genomewide association analysis of coronary artery disease Coronary disease "1,926 cases, 2,938 controls" "875 cases, 1,644 controls" 1q41 MIA3 rs17465637-C rs17465637 0.29 1.00E-06 1.2 [1.12-1.30] "Affymetrix [377,857]" N 11/25/2008 17634449 Samani 18-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genomewide association analysis of coronary artery disease Coronary disease "1,926 cases, 2,938 controls" "875 cases, 1,644 controls" 15q22.33 SMAD3 rs17228212-C rs17228212 0.3 2.00E-07 1.21 [1.13-1.30] "Affymetrix [377,857]" N 11/25/2008 17634449 Samani 18-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genomewide association analysis of coronary artery disease Coronary disease "1,926 cases, 2,938 controls" "875 cases, 1,644 controls" 1p13.3 PSRC1 rs599839-A rs599839 0.23 4.00E-09 1.29 [1.18-1.40] "Affymetrix [377,857]" N 11/25/2008 17634449 Samani 18-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genomewide association analysis of coronary artery disease Coronary disease "1,926 cases, 2,938 controls" "875 cases, 1,644 controls" 10q11.21 CXCL12 rs501120-T rs501120 0.13 9.00E-08 1.33 [1.20-1.48] "Affymetrix [377,857]" N 11/25/2008 17634449 Samani 18-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genomewide association analysis of coronary artery disease Coronary disease "1,926 cases, 2,938 controls" "875 cases, 1,644 controls" 2q36.3 pseudogene rs2943634-C rs2943634 0.65 2.00E-07 1.21 [1.13-1.30] "Affymetrix [377,857]" N 11/25/2008 17634449 Samani 18-Jul-07 N Engl J Med http://www.ncbi.nlm.nih.gov/pubmed/17634449?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genomewide association analysis of coronary artery disease Coronary disease "1,926 cases, 2,938 controls" "875 cases, 1,644 controls" 6q25.1 MTHFD1L rs6922269-A rs6922269 0.25 3.00E-08 1.23 [1.15-1.33] "Affymetrix [377,857]" N 11/25/2008 17637780 Winkelmann 18-Jul-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17637780?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions Restless legs syndrome "401 cases, 1,644 controls" "1,158 cases, 1,178 controls" 15q23 "MAP2K5, LBXCOR1" rs12593813-G rs12593813 0.67 1.00E-15 1.5 [1.36-1.66] "Affymetrix [236,758]" N 11/25/2008 17637780 Winkelmann 18-Jul-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17637780?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions Restless legs syndrome "401 cases, 1,644 controls" "1,158 cases, 1,178 controls" 2p14 MEIS1 rs2300478-G rs2300478 0.24 3.00E-28 1.74 [1.57-1.92] "Affymetrix [236,758]" N 11/25/2008 17637780 Winkelmann 18-Jul-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17637780?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions Restless legs syndrome "401 cases, 1,644 controls" "1,158 cases, 1,178 controls" 6p21.2 BTBD9 rs9296249-T rs9296249 0.76 4.00E-18 1.67 [1.49-1.89] "Affymetrix [236,758]" N 11/25/2008 17632509 Buch 15-Jul-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17632509?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease Gallstones "280 cases, 360 controls" "2,000 cases, 1,202 controls" 2p21 ABCG8 rs11887534-C rs11887534 0.1 1.00E-14 2.2 [1.80-2.60] "Affymetrix [382,492]" N 11/25/2008 17632545 Hakonarson 15-Jul-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17632545?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene Type 1 diabetes "467 trios, 561 cases, 1,143 controls" "2,350 individuals in 549 families; 390 trios" 16p13.13 KIAA0350 rs2903692-G rs2903692 0.62 7.00E-11 1.54 [1.32-1.79] "Illumina [543,071]" N 11/25/2008 17632545 Hakonarson 15-Jul-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17632545?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene Type 1 diabetes "467 trios, 561 cases, 1,143 controls" "2,350 individuals in 549 families; 390 trios" 1p13.2 PTPN22 rs2476601-A rs2476601 0.09 1.00E-07 1.8 [1.44-2.24] "Illumina [543,071]" N 11/25/2008 17632545 Hakonarson 15-Jul-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17632545?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene Type 1 diabetes "467 trios, 561 cases, 1,143 controls" "2,350 individuals in 549 families; 390 trios" 6p21.32 HLA-E rs2647044-A rs2647044 0.13 1.00E-16 8.3 [6.97-9.89] "Illumina [543,071]" N 11/25/2008 17632545 Hakonarson 15-Jul-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17632545?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene Type 1 diabetes "467 trios, 561 cases, 1,143 controls" "2,350 individuals in 549 families; 390 trios" 11p15.5 INS rs1004446-C rs1004446 0.65 4.00E-09 1.61 [1.37-1.89] "Illumina [543,071]" N 11/25/2008 17618284 Tomlinson 8-Jul-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17618284?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21 Colorectal cancer "930 cases, 960 controls" "7,334 cases, 5,246 controls" 8q24.21 Intergenic rs6983267-G rs6983267 0.49 1.00E-14 1.27 [1.16-1.39] "Illumina [547,647]" N 11/25/2008 17618283 Zanke 8-Jul-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17618283?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24 Colorectal cancer "1,257 cases, 1,336 controls" "6,223 cases, 6,443 controls" 8q24.21 ORF DQ515897 rs10505477-A rs10505477 0.5 3.00E-11 1.17 [1.12-1.23] "Illumina and Affymetrix [99,632]" N 11/25/2008 17603472 Gudbjartsson 1-Jul-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17603472?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Variants conferring risk of atrial fibrillation on chromosome 4q25 Atrial fibrillation/atrial flutter "550 cases, 4,476 controls" "3,363 cases, 17,616 controls" 4q25 "PITX2,ENPEP" rs2200733-T rs2200733 0.11 3.00E-41 1.72 [1.59-1.86] "Illumina [316,515]" N 11/25/2008 17603472 Gudbjartsson 1-Jul-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17603472?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Variants conferring risk of atrial fibrillation on chromosome 4q25 Atrial fibrillation/atrial flutter "550 cases, 4,476 controls" "3,363 cases, 17,616 controls" 4q25 "PITX2,ENPEP" rs10033464-T rs10033464 0.08 7.00E-11 1.39 [1.26-1.53] "Illumina [316,515]" N 11/25/2008 17603485 Gudmundsson 1-Jul-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17603485?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes" Prostate cancer "1,501 cases, 11,290 controls" "1,992 cases, 3,058 controls" 17q12 TCF2 rs4430796-A rs4430796 0.49 1.00E-11 1.22 [1.15-1.30] "Illumina [310,520]" N 11/25/2008 17603485 Gudmundsson 1-Jul-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17603485?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes" Prostate cancer "1,501 cases, 11,290 controls" "1,992 cases, 3,058 controls" 17q24.3 Intergenic rs1859962-G rs1859962 0.46 3.00E-10 1.2 [1.14-1.27] "Illumina [310,520]" N 11/25/2008 17668382 Salonen 26-Jun-07 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/17668382?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium Type 2 diabetes "500 cases, 497 controls" "2,573 cases, 2,776 controls" 10q25.2 TCF7L2 rs7903146-A rs7903146 NR 5.00E-08 1.71 [1.41-2.08] "Illumina [315,917]" N 11/25/2008 17668382 Salonen 26-Jun-07 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/17668382?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium Type 2 diabetes "500 cases, 497 controls" "2,573 cases, 2,776 controls" 2q12.1 Intergenic rs6712932-? rs6712932 NR 0.000006 1.52 [1.27-1.82] "Illumina [315,917]" N 11/25/2008 17558408 van Heel 10-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17558408?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 Celiac disease "778 cases, 1,422 controls" "991 cases, 1,489 controls" 6p21.32 HLA-DQA1 rs2187668-A rs2187668 0.14 1.00E-19 7.04 [6.08-8.15] "Illumina [310,605]" N 11/25/2008 17558408 van Heel 10-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17558408?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 Celiac disease "778 cases, 1,422 controls" "991 cases, 1,489 controls" 4q27 "KIAA1109,TENR,IL2,IL21" rs6822844-G rs6822844 0.82 1.00E-14 1.59 [1.41-1.75] "Illumina [310,605]" N 11/25/2008 17553421 Reiman 7-Jun-07 Neuron http://www.ncbi.nlm.nih.gov/pubmed/17553421?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers Alzheimer's disease (late onset) "446 cases, 290 controls" "415 cases, 260 controls" 11q14.1 GAB2 rs2373115-G rs2373115 0.7 1.00E-10 4.06 [2.81-14.69] "Affymetrix [312,316]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Bipolar disorder "1,868 cases, 2,938 controls" NR 16p12.1 "PALB2,NDUFAB1,DCTN5" rs420259-A rs420259 0.72 6.00E-08 2.08 [1.60-2.71] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Bipolar disorder "1,868 cases, 2,938 controls" NR 3q27 NR rs683395-G rs683395 0.08 0.000005 1.47 [1.26-1.71] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Bipolar disorder "1,868 cases, 2,938 controls" NR 6p21 NR rs6458307-? rs6458307 0.69 4E-06 1.19 [1.04-1.33] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Bipolar disorder "1,868 cases, 2,938 controls" NR 2q37 NR rs2953145-C rs2953145 0.23 7E-06 1.84 [1.31-2.58] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Bipolar disorder "1,868 cases, 2,938 controls" NR 14q23.1 NR rs10134944-T rs10134944 0.09 7E-06 1.45 [1.24-1.68] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Bipolar disorder "1,868 cases, 2,938 controls" NR 20p13 NR rs3761218-C rs3761218 0.64 7E-06 1.03 [1.15-1.23] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Bipolar disorder "1,868 cases, 2,938 controls" NR 14q32.33 NR rs11622475-C rs11622475 0.3 8E-06 1.13 [0.89-1.44] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Coronary disease "1,926 cases, 2,938 controls" (see Samani 2007) 22q12 NR rs688034-T rs688034 0.31 4E-06 1.11 [0.99-1.25] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Coronary disease "1,926 cases, 2,938 controls" (see Samani 2007) 16q23 NR rs8055236-G rs8055236 0.2 0.000006 1.91 [1.33-2.74] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Coronary disease "1,926 cases, 2,938 controls" (see Samani 2007) 1q43 NR rs17672135-C rs17672135 0.87 2E-06 1.43 [1.23-1.64] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Coronary disease "1,926 cases, 2,938 controls" (see Samani 2007) 9p21.3 "CDKN2A,CDKN2B" rs1333049-C rs1333049 0.47 1.00E-13 1.47 [1.27-1.70] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 2q37.1 ATG16L1 rs10210302-T rs10210302 0.48 5.00E-14 1.19 [1.01-1.41] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 5p13.1 Intergenic rs17234657-G rs17234657 0.13 2.00E-12 1.54 [1.34-1.76] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 10q21.2 Intergenic rs10761659-G rs10761659 0.46 2E-06 1.23 [1.05-1.45] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 5q31.1 Intergenic rs6596075-C rs6596075 0.17 0.000003 1.55 [1.00-2.39] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 6p21 NR rs9469220-A rs9469220 0.48 2E-06 1.14 [0.98-1.32] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 1p31.3 IL23R rs11805303-T rs11805303 0.68 6.00E-12 1.39 [1.22-1.58] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 16q12.1 NOD2 rs17221417-G rs17221417 0.29 4.00E-11 1.29 [1.13-1.46] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 10q24.2 NKX2-3 rs10883365-G rs10883365 0.48 6.00E-08 1.2 [1.03-1.39] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 7q36.1 NR rs7807268-G rs7807268 0.46 4E-06 1.38 [1.20-1.60] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 10p15.1 NR rs6601764-C rs6601764 0.41 0.000009 1.16 [1.01-1.33] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 5q33.1 IRGM rs1000113-T rs1000113 0.07 3.00E-07 1.54 [1.31-1.82] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 18p11.21 PTPN2 rs2542151-G rs2542151 0.16 2.00E-07 1.3 [1.14-1.48] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Crohn's disease "1,748 cases, 2,938 controls" (see Parkes 2007) 3p21.31 "BSN, MST1" rs9858542-A rs9858542 0.28 4.00E-08 1.09 [0.96-1.24] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Hypertension "1,952 cases, 2,938 controls" NR 15q26 NR rs2398162-A rs2398162 0.26 0.000006 1.31 [1.03-1.67] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Hypertension "1,952 cases, 2,938 controls" NR 1q43 "RYR2,CHRM3,ZP4" rs2820037-T rs2820037 0.14 8.00E-07 1.54 [1.03-2.31] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Rheumatoid arthritis "1,860 cases, 2,938 controls" NR 6p21.32 MHC rs6457617-T rs6457617 0.49 5.00E-75 2.36 [1.97-2.84] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Rheumatoid arthritis "1,860 cases, 2,938 controls" NR 1p13.2 PTPN22 rs6679677-A rs6679677 0.1 6.00E-25 1.98 [1.72-2.27] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Rheumatoid arthritis "1,860 cases, 2,938 controls" NR 6p21.32 HLA-DRB1 rs615672-? rs615672 NR 8.00E-27 NR NR "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Rheumatoid arthritis "1,860 cases, 2,938 controls" NR 7q32.3 Intergenic rs11761231-C rs11761231 0.62 4.00E-07 (sex-differentiated)  1.32 [NR] (women) "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Rheumatoid arthritis "1,860 cases, 2,938 controls" NR 22q13 NR rs743777-G rs743777 0.29 1.00E-06 1.09 [0.97-1.24] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Rheumatoid arthritis "1,860 cases, 2,938 controls" NR 4p15.2 NR rs3816587-C rs3816587 0.41 0.000009 1.09 [0.96-1.25] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Rheumatoid arthritis "1,860 cases, 2,938 controls" NR 21q22 NR rs2837960-G rs2837960 0.17 2E-06 1.05 [0.93-1.20] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 1 diabetes "1,963 cases, 2,938 controls" (see Todd 2007) 6p21.32 MHC rs9272346-G rs9272346 0.61 0 5.49 [4.83-6.24] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 1 diabetes "1,963 cases, 2,938 controls" (see Todd 2007) 1p13.2 PTPN22 rs6679677-A rs6679677 0.1 5.00E-26 1.82 [1.59-2.09] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 1 diabetes "1,963 cases, 2,938 controls" (see Todd 2007) 5q31.1 NR rs17166496-G rs17166496 0.61 0.000005 1.3 [1.15-1.47] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 1 diabetes "1,963 cases, 2,938 controls" (see Todd 2007) 12p13.31 NR rs3764021-C rs3764021 0.47 5.00E-08 1.57 [1.38-1.79] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 1 diabetes "1,963 cases, 2,938 controls" (see Todd 2007) 4q27 NR rs17388568-A rs17388568 0.26 0.000003 1.26 [1.11-1.42] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 1 diabetes "1,963 cases, 2,938 controls" (see Todd 2007) 12q13.2 ERBB3 rs11171739-C rs11171739 0.42 1.00E-11 1.34 [1.17-1.54] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 1 diabetes "1,963 cases, 2,938 controls" (see Todd 2007) 12q24.13 "SH2B3,LNK,TRAFD1,PTPN1" rs17696736-G rs17696736 0.42 2.00E-14 1.34 [1.16-1.53] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 1 diabetes "1,963 cases, 2,938 controls" (see Todd 2007) 16p13.13 KIAA0350 rs12708716-A rs12708716 0.65 5.00E-07 1.19 [0.97-1.45] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 1 diabetes "1,963 cases, 2,938 controls" (see Todd 2007) 12p13 NR rs11052552-G rs11052552 0.49 7.00E-07 1.49 [1.28-1.73] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 1 diabetes "1,963 cases, 2,938 controls" (see Todd 2007) 4q27 NR rs6534347-A rs6534347 0.35 2E-06 1.3 [1.10-1.55] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 2 diabetes "1,924 cases, 2,938 controls" (see Zeggini 2007) 10q25.2 TCF7L2 rs4506565-T rs4506565 0.32 5.00E-12 1.36 [1.20-1.54] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 2 diabetes "1,924 cases, 2,938 controls" (see Zeggini 2007) 4q27 NR rs7659604-T rs7659604 0.38 0.000009 1.35 [1.19-1.54] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 2 diabetes "1,924 cases, 2,938 controls" (see Zeggini 2007) 12q13 NR rs12304921-G rs12304921 0.15 7E-06 2.5 [1.53-4.09] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 2 diabetes "1,924 cases, 2,938 controls" (see Zeggini 2007) 12q15 NR rs1495377-G rs1495377 0.5 7E-06 1.28 [1.11-1.49] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 2 diabetes "1,924 cases, 2,938 controls" (see Zeggini 2007) 3p14 NR rs358806-? rs358806 0.8 0.000003 1.16 [1.03-1.33] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 2 diabetes "1,924 cases, 2,938 controls" (see Zeggini 2007) 6p22.3 CDKAL1 rs9465871-C rs9465871 0.18 3.00E-07 1.18 [1.04-1.34] "Affymetrix [469,557]" N 11/25/2008 17554300 WTCCC 7-Jun-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17554300?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls" Type 2 diabetes "1,924 cases, 2,938 controls" (see Zeggini 2007) 16q12.2 FTO rs9939609-A rs9939609 0.4 2.00E-07 1.34 [1.17-1.52] "Affymetrix [469,557]" N 11/25/2008 17554261 Parkes 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility Crohn's disease "1,748 cases, 2,938 controls" "1,182 cases, 2,024 controls" 10q24.2 NKX2-3 rs10883365-? rs10883365 0.48 4.00E-10 1.18 [1.05-1.32] see WTCCC N 11/25/2008 17554261 Parkes 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility Crohn's disease "1,748 cases, 2,938 controls" "1,182 cases, 2,024 controls" 5q33.1 IRGM rs13361189-? rs13361189 0.08 2.00E-10 1.38 [1.15-1.66] see WTCCC N 11/25/2008 17554261 Parkes 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility Crohn's disease "1,748 cases, 2,938 controls" "1,182 cases, 2,024 controls" 3p21.31 MST1 rs9858542-? rs9858542 0.29 5.00E-08 1.17 [1.14-1.31] see WTCCC N 11/25/2008 17554261 Parkes 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility Crohn's disease "1,748 cases, 2,938 controls" "1,182 cases, 2,024 controls" 1q31.2 Intergenic rs10801047-? rs10801047 0.08 3.00E-08 1.47 [1.22-1.76] see WTCCC N 11/25/2008 17554261 Parkes 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility Crohn's disease "1,748 cases, 2,938 controls" "1,182 cases, 2,024 controls" 18p11.21 PTPN2 rs2542151-? rs2542151 0.18 3.00E-08 1.15 [1.00-1.32] see WTCCC N 11/25/2008 17554261 Parkes 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility Crohn's disease "1,748 cases, 2,938 controls" "1,182 cases, 2,024 controls" 1q24.3 Intergenic rs12035082-? rs12035082 0.4 2.00E-07 1.14 [1.02-1.27] see WTCCC N 11/25/2008 17554261 Parkes 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility Crohn's disease "1,748 cases, 2,938 controls" "1,182 cases, 2,024 controls" 5q33.3 IL12B rs6887695-? rs6887695 0.32 0.000009 1.26 [1.12-1.41] see WTCCC N 11/25/2008 17554261 Parkes 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility Crohn's disease "1,748 cases, 2,938 controls" "1,182 cases, 2,024 controls" 5p13.1 Intergenic rs9292777-? rs9292777 0.4 3.00E-18 1.34 [1.20-1.50] see WTCCC N 11/25/2008 17554261 Parkes 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554261?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility Crohn's disease "1,748 cases, 2,938 controls" "1,182 cases, 2,024 controls" 21q22.2 Intergenic rs2836754-? rs2836754 0.35 5.00E-07 1.15 [1.03-1.28] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 18p11.21 PTPN2 rs2542151-C rs2542151 0.16 1.00E-14 1.3 [1.22-1.40] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 18q22.2 CD226 rs763361-A rs763361 0.47 1.00E-08 1.16 [1.10-1.22] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 1p13.2 PTPN22 rs2476601-T rs2476601 0.09 2.00E-80 1.98 [1.82-2.15] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 2q24.2 IFIH1 rs1990760-A rs1990760 0.6 2.00E-11 1.18 [1.11-1.23] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 5p13.2 CAPSL rs1445898-G rs1445898 0.55 8E-06 1.12 [1.06-1.19] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 5p13.2 IL7R rs6897932-G rs6897932 0.71 8E-06 1.12 [1.06-1.19] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 2p11.2 "AFF3, LOC150577" rs9653442-G rs9653442 0.46 0.000005 1.11 [1.05-1.17] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 1p13.2 "PHTF1, PTPN22" rs6679677-A rs6679677 0.1 8.00E-24 1.89 [1.67-2.13] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 11p15.5 INS rs3741208-T rs3741208 0.38 2.00E-07 1.25 [1.15-1.35] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 12q24.13 C12orf30 rs17696736-G rs17696736 0.42 2.00E-16 1.22 [1.15-1.28] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 12q13.2 ERBB3 rs2292239-A rs2292239 0.34 2.00E-20 1.28 [1.21-1.35] see WTCCC N 11/25/2008 17554260 Todd 6-Jun-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17554260?ordinalpos=11&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes Type 1 diabetes "1,963 cases, 2,938 controls" "2997 trios, 4,000 cases, 5,000 controls" 16p13.13 KIAA0350 rs12708716-A rs12708716 0.68 3.00E-18 1.23 [1.16-1.30] see WTCCC N 11/25/2008 17529967 Easton 27-May-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies novel breast cancer susceptibility loci Breast cancer "390 cases, 364 controls" "26,646 cases, 24,889 controls" 10q26.13 FGFR2 rs2981582-G rs2981582 0.38 2.00E-76 1.26 [1.23-1.30] "Perlegen [205,586]" N 11/25/2008 17529967 Easton 27-May-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies novel breast cancer susceptibility loci Breast cancer "390 cases, 364 controls" "26,646 cases, 24,889 controls" 5q11.2 MAP3K1 rs889312-A rs889312 0.28 7.00E-20 1.13 [1.10-1.16] "Perlegen [205,586]" N 11/25/2008 17529967 Easton 27-May-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies novel breast cancer susceptibility loci Breast cancer "390 cases, 364 controls" "26,646 cases, 24,889 controls" 5p12 Intergenic rs981782-C rs981782 0.53 0.000009 1.04 [1.01-1.08] "Perlegen [205,586]" N 11/25/2008 17529967 Easton 27-May-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies novel breast cancer susceptibility loci Breast cancer "390 cases, 364 controls" "26,646 cases, 24,889 controls" 8q24.21 Intergenic rs13281615-T rs13281615 0.4 5.00E-12 1.08 [1.05-1.11] "Perlegen [205,586]" N 11/25/2008 17529967 Easton 27-May-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies novel breast cancer susceptibility loci Breast cancer "390 cases, 364 controls" "26,646 cases, 24,889 controls" 11p15.5 LSP1 rs3817198-T rs3817198 0.3 3.00E-09 1.07 [1.04-1.11] "Perlegen [205,586]" N 11/25/2008 17529967 Easton 27-May-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17529967?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies novel breast cancer susceptibility loci Breast cancer "390 cases, 364 controls" "26,646 cases, 24,889 controls" 16q12.1 "TNCR9,LOC643714" rs3803662-C rs3803662 0.25 1.00E-36 1.2 [1.16-1.24] "Perlegen [205,586]" N 11/25/2008 17529973 Hunter 27-May-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17529973?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer Breast cancer "1,145 cases, 1,142 controls" "1,176 cases, 2,072 controls" 10q26.13 FGFR2 rs1219648-G rs1219648 0.4 1.00E-10 1.2 [1.07-1.42] "Illumina [528,173]" N 11/25/2008 17529974 Stacey 27-May-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17529974?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer Breast cancer "1,599 cases, 11,546 controls" "2,934 cases, 5,967 controls" 2q35 Intergenic rs13387042-A rs13387042 0.5 1.00E-13 1.2 [1.14-1.26] "Illumina [311,524]" N 11/25/2008 17529974 Stacey 27-May-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17529974?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer Breast cancer "1,599 cases, 11,546 controls" "2,934 cases, 5,967 controls" 16q12.1 TNRC9 rs3803662-T rs3803662 0.27 6.00E-19 1.28 [1.21-1.35] "Illumina [311,524]" N 11/25/2008 17505501 Kindmark 15-May-07 Pharmacogenomics J http://www.ncbi.nlm.nih.gov/pubmed/17505501?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis Response to ximelagatran treatment "74 cases, 130 controls" "10 cases, 16 controls" 6p21.3 HLA-DRB1 DRB1*07 NR 0.000009 4.41 [2.20-8.87] "Perlegen [~266,722]" N 11/25/2008 17486107 Baum 8-May-07 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/17486107?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder Bipolar disorder "461 cases, 563 controls" "772 cases, 876 controls" 13q14.11 DGKH rs1012053-A rs1012053 0.84 2.00E-08 1.59 [1.35-1.87] "Illumina [555,235] (pooled)" N 11/25/2008 17434096 Matarin 6-May-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17434096?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release Stroke "259 cases, 269 controls" NR 18p11.2 IMPA2 rs7506045-? rs7506045 0.1 7.00E-07 5.39 [2.77-10.5] "Illumina [408,803]" N 11/25/2008 17434096 Matarin 6-May-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17434096?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release Stroke "259 cases, 269 controls" NR 7p21 Intergenic rs10486776-? rs10486776 0.1 0.000006 5.62 [2.66-11.9] "Illumina [408,803]" N 11/25/2008 17434096 Matarin 6-May-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17434096?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release Stroke "259 cases, 269 controls" NR 6q21 AIM1 rs783396-? rs783396 0.9 0.000009 2.17 [1.47-3.13] "Illumina [408,803]" N 11/25/2008 17434096 Matarin 6-May-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17434096?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release Stroke "259 cases, 269 controls" NR 13q21.1 Intergenic rs9536591-? rs9536591 0.1 0.000006 1.92 [1.41-2.63] "Illumina [408,803]" N 11/25/2008 17478679 Helgadottir 3-May-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17478679?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A common variant on chromosome 9p21 affects the risk of myocardial infarction Myocardial infarction "1,607 cases, 6,728 controls" "2,980 cases, 6,309 controls" 9p21.3 "CDKN2A,CDKN2B" rs10757278-G rs10757278 0.45 1.00E-20 1.28 [1.22-1.35] "Illumina [305,953]" N 11/25/2008 17478681 McPherson 3-May-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17478681?ordinalpos=12&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A common allele on chromosome 9 associated with coronary heart disease Coronary disease "322 cases, 312 controls" "3,984 cases, 19,807 controls" NR NR NR NR NS NS NR NR "Perlegen [72,864]" N 11/25/2008 17470457 Huentelman 30-Apr-07 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/17470457?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance Episodic memory 341 young adults 472 young adults NR NR NR NR NS NS NR NR "Affymetrix [~502,627] (pooled)" N 2/13/2009 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Triglycerides "up to 5,217 individuals" NR 19q13.32 APOE cluster rs4420638-G rs4420638 0.22 3.00E-13 (LDL)  2.4 % [NR] of variance explained "Affymetrix [386,731]" N 2/13/2009 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Triglycerides "up to 5,217 individuals" NR 2p24.1 APOB rs693-A rs693 0.49 7.00E-07 (LDL)  NR NR "Affymetrix [386,731]" N 2/13/2009 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Triglycerides "up to 5,217 individuals" NR 16q13 CETP rs1800775-C rs1800775 0.47 3.00E-13 (HDL)  2.1 % [NR] of variance explained "Affymetrix [386,731]" N 2/13/2009 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Triglycerides "up to 5,217 individuals" NR 8p21.3 LPL rs328-T rs328 0.1 5.00E-07 (TG)  1 % [NR] of variance explained "Affymetrix [386,731]" N 2/13/2009 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Triglycerides "up to 5,217 individuals" NR 16q13 CETP rs1800775-C rs1800775 0.44 0.000003 (apoA-1)  1.6 % [NR] of variance explained "Affymetrix [386,731]" N 11/25/2008 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Type 2 diabetes "1,464 cases, 1,467 controls" "5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 8q24.11 SLC30A8 rs13266634-C rs13266634 0.65 5.00E-08 (DGI+FUSION+WTCCC)  1.12 [1.07-1.16] "Affymetrix [386,731]" N 11/25/2008 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Type 2 diabetes "1,464 cases, 1,467 controls" "5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 3p25.2 PPARG rs1801282-C rs1801282 0.86 0.000002 (DGI+FUSION+WTCCC)  1.14 [1.08-1.20] "Affymetrix [386,731]" N 11/25/2008 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Type 2 diabetes "1,464 cases, 1,467 controls" "5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 10q23.33 HHEX rs1111875-C rs1111875 0.53 6.00E-10 (DGI+FUSION+WTCCC)  1.13 [1.08-1.17] "Affymetrix [386,731]" N 11/25/2008 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Type 2 diabetes "1,464 cases, 1,467 controls" "5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 6p22.3 CDKAL1 rs7754840-C rs7754840 0.31 4.00E-11 (DGI+FUSION+WTCCC)  1.12 [1.08-1.16] "Affymetrix [386,731]" N 11/25/2008 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Type 2 diabetes "1,464 cases, 1,467 controls" "5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 10q25.2 TCF7L2 rs7903146-T rs7903146 0.26 2.00E-31 1.38 [1.31-1.46] "Affymetrix [386,731]" N 11/25/2008 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Type 2 diabetes "1,464 cases, 1,467 controls" "5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 3q27.2 IGF2BP2 rs4402960-T rs4402960 0.29 2.00E-09 1.17 [1.11-1.23] "Affymetrix [386,731]" N 11/25/2008 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Type 2 diabetes "1,464 cases, 1,467 controls" "5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 9p21.3 "CDKN2A,CDKN2B" rs10811661-T rs10811661 0.83 5.00E-08 1.2 [1.12-1.28] "Affymetrix [386,731]" N 11/25/2008 17463246 Saxena 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463246?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels Type 2 diabetes "1,464 cases, 1,467 controls" "5,065 cases, 5,785 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 11p15.1 KCNJ11 rs5219-T rs5219 0.47 1.00E-07 1.15 [1.09-1.21] "Affymetrix [386,731]" N 11/25/2008 17463248 Scott 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants Type 2 diabetes "1,161 cases, 1,174 controls" "1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 3q27.2 IGF2BP2 rs4402960-T rs4402960 0.3 9.00E-16 (DGI+FUSION+WTCCC)  1.14 [1.11-1.18] "Illumina [315,635]" N 11/25/2008 17463248 Scott 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants Type 2 diabetes "1,161 cases, 1,174 controls" "1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 6p22.3 CDKAL1 rs7754840-C rs7754840 0.36 4.00E-11 (DGI+FUSION+WTCCC)  1.12 [1.08-1.16] "Illumina [315,635]" N 11/25/2008 17463248 Scott 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants Type 2 diabetes "1,161 cases, 1,174 controls" "1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 9p21.3 "CDKN2A,CDKN2B" rs10811661-T rs10811661 0.85 8.00E-15 (DGI+FUSION+WTCCC)  1.2 [1.14-1.25] "Illumina [315,635]" N 11/25/2008 17463248 Scott 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants Type 2 diabetes "1,161 cases, 1,174 controls" "1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 11p12 Intergenic rs9300039-C rs9300039 0.89 6.00E-08 1.48 [1.28-1.71] "Illumina [315,635]" N 11/25/2008 17463248 Scott 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants Type 2 diabetes "1,161 cases, 1,174 controls" "1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 16q12.2 FTO rs8050136-A rs8050136 0.38 1.00E-12 (DGI+FUSION+WTCCC)  1.17 [1.12-1.22] "Illumina [315,635]" N 11/25/2008 17463248 Scott 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants Type 2 diabetes "1,161 cases, 1,174 controls" "1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 11p15.1 KCNJ11 rs5219-T rs5219 0.46 7.00E-11 (DGI+FUSION+WTCCC)  1.14 [1.10-1.19] "Illumina [315,635]" N 11/25/2008 17463248 Scott 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants Type 2 diabetes "1,161 cases, 1,174 controls" "1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 10q23.33 HHEX rs1111875-C rs1111875 0.52 6.00E-10 (DGI+FUSION+WTCCC)  1.13 [1.09-1.17] "Illumina [315,635]" N 11/25/2008 17463248 Scott 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants Type 2 diabetes "1,161 cases, 1,174 controls" "1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 8q24.11 SLC30A8 rs13266634-C rs13266634 0.61 5.00E-08 (DGI+FUSION+WTCCC)  1.12 [1.07-1.16] "Illumina [315,635]" N 11/25/2008 17463248 Scott 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants Type 2 diabetes "1,161 cases, 1,174 controls" "1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 3p25.2 PPARG rs1801282-C rs1801282 0.82 0.000002 (DGI+FUSION+WTCCC)  1.14 [1.08-1.20] "Illumina [315,635]" N 11/25/2008 17463248 Scott 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463248?ordinalpos=1&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants Type 2 diabetes "1,161 cases, 1,174 controls" "1,215 cases, 1,258 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 10q25.2 TCF7L2 rs7903146-T rs7903146 0.18 1.00E-08 1.34 [1.21-1.49] "Illumina [315,635]" N 11/25/2008 17460697 Steinthorsdottir 26-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17460697?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A variant in CDKAL1 influences insulin response and risk of type 2 diabetes Type 2 diabetes "1,399 EA cases, 5,275 EA controls" "2,437 EA cases, 7,287 EA controls" 10q25.2 TCF7L2 rs7903146-? rs7903146 0.3 2.00E-10 1.38 [NR] "Illumina [313,179 SNPs; 339,846 2-SNP haplotypes]" N 11/25/2008 17460697 Steinthorsdottir 26-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17460697?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A variant in CDKAL1 influences insulin response and risk of type 2 diabetes Type 2 diabetes "1,399 EA cases, 5,275 EA controls" "2,437 EA cases, 7,287 EA controls" 6p22.3 CDKAL1 rs7756992-G rs7756992 0.26 8.00E-09 1.2 [1.13-1.27] "Illumina [313,179 SNPs; 339,846 2-SNP haplotypes]" N 11/25/2008 17460697 Steinthorsdottir 26-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17460697?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A variant in CDKAL1 influences insulin response and risk of type 2 diabetes Type 2 diabetes "1,399 EA cases, 5,275 EA controls" "2,437 EA cases, 7,287 EA controls" 8q24.11 SLC30A8 rs13266634-C rs13266634 0.67 0.000003 1.15 [1.08-1.22] "Illumina [313,179 SNPs; 339,846 2-SNP haplotypes]" N 11/25/2008 17463249 Zeggini 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 16q12.2 FTO rs8050136-A rs8050136 0.4 7.00E-14 1.23 [1.18-1.32] "Affymetrix [393,453]" N 11/25/2008 17463249 Zeggini 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 3p25.2 PPARG rs1801282-C rs1801282 NR 0.000002 (DGI+FUSION+WTCCC)  1.14 [1.08-1.20] "Affymetrix [393,453]" N 11/25/2008 17463249 Zeggini 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 9p21.3 "CDKN2A, CDKN2B" rs564398-T rs564398 0.56 0.000001 1.13 [1.08-1.19] "Affymetrix [393,453]" N 11/25/2008 17463249 Zeggini 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 9p21.3 "CDKN2A, CDKN2B" rs10811661-T rs10811661 0.83 0.000005 1.19 [1.11-1.28] "Affymetrix [393,453]" N 11/25/2008 17463249 Zeggini 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 10q25.2 TCF7L2 rs7901695-C rs7901695 NR 1.00E-48 (DGI+FUSION+WTCCC)  1.37 [1.31-1.43] "Affymetrix [393,453]" N 11/25/2008 17463249 Zeggini 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 10q23.33 HHEX rs5015480-C rs5015480 0.57 0.000005 1.13 [1.07-1.19] "Affymetrix [393,453]" N 11/25/2008 17463249 Zeggini 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 6p22.3 CDKAL1 rs10946398-C rs10946398 0.32 1.00E-08 1.16 [1.10-1.22] "Affymetrix [393,453]" N 11/25/2008 17463249 Zeggini 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 3q27.2 IGF2BP2 rs4402960-T rs4402960 0.32 9.00E-16 (DGI+FUSION+WTCCC)  1.14 [1.11-1.18] "Affymetrix [393,453]" N 11/25/2008 17463249 Zeggini 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 8q24.11 SLC30A8 rs13266634-C rs13266634 0.69 5.00E-08 (DGI+FUSION+WTCCC)  1.12 [1.07-1.16] "Affymetrix [393,453]" N 11/25/2008 17463249 Zeggini 26-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17463249?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes Type 2 diabetes "1,924 cases, 2,938 controls" "3,757 cases, 5,346 controls (also includes meta-analysis from DGI+FUSION+WTCCC)" 11p15.1 KCNJ11 rs5215-C rs5215 NR 5.00E-11 (DGI+FUSION+WTCCC)  1.14 [1.10-1.19] "Affymetrix [393,453]" N 11/25/2008 17435756 Rioux 15-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17435756?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis Crohn's disease "946 cases, 977 controls" "530 trios, 353 cases, 207 controls" 1p31.3 IL23R rs7517847-? rs7517847 0.4 3.00E-12 NR NR "Illumina [304,413]" N 11/25/2008 17435756 Rioux 15-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17435756?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis Crohn's disease "946 cases, 977 controls" "530 trios, 353 cases, 207 controls" 2q37.1 ATG16L1 rs2241880-G rs2241880 0.55 1.00E-13 1.45 [1.27-1.64] "Illumina [304,413]" N 11/25/2008 17435756 Rioux 15-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17435756?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis Crohn's disease "946 cases, 977 controls" "530 trios, 353 cases, 207 controls" 10q21.2 Intergenic rs224136-? rs224136 0.81 1.00E-10 1.67 [NR] "Illumina [304,413]" N 11/25/2008 17435756 Rioux 15-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17435756?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis Crohn's disease "946 cases, 977 controls" "530 trios, 353 cases, 207 controls" 16q12.1 CARD15 rs2076756-? rs2076756 0.24 7.00E-14 NR NR "Illumina [304,413]" N 11/25/2008 17434869 Frayling 12-Apr-07 Science http://www.ncbi.nlm.nih.gov/pubmed/17434869?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity Body mass index "10,657 adults" "19,424 adults, 10,172 children" 16q12.2 FTO rs9939609-A rs9939609 0.39 2.00E-20 0.36 [NR] kg/m2 per copy in adults "Affymetrix [490,032]" N 11/25/2008 17407593 Uhl 3-Apr-07 BMC Genetics http://www.ncbi.nlm.nih.gov/pubmed/17407593?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Molecular genetics of nicotine dependence and abstinence: whole genome association using 520,000 SNPs" Nicotine dependence "134 cases, 320 controls" NR NR NR NR NR NS NS NR NR "Affymetrix [~520,000] (pooled)" N 11/25/2008 17474819 Coon 1-Apr-07 J Clin Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/17474819?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease Alzheimer's disease (late onset) "664 cases, 422 controls" NR 19q13.32 APOE rs4420638-? rs4420638 NR 1.00E-39 4.01 [NR] "Affymetrix [~502,627]" N 11/25/2008 17401366 Gudmundsson 1-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17401366?ordinalpos=26&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24 Prostate cancer "1,453 cases, 3,064 controls" "1,210 EA cases, 2,445 EA controls; 373 AA cases, 372 AA controls" 8q24.21 Intergenic rs1447295-A rs1447295 0.09 6.00E-18 1.6 [1.43-1.77] "Illumina [316,515]" N 11/25/2008 17401366 Gudmundsson 1-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17401366?ordinalpos=26&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24 Prostate cancer "1,453 cases, 3,064 controls" "1,210 EA cases, 2,445 EA controls; 373 AA cases, 372 AA controls" 8q24.21 Intergenic HapC 0.02 (EA) 3.00E-15 (EA)  2.1 [1.75-2.53] (EA) "Illumina [316,515]" N 11/25/2008 17401366 Gudmundsson 1-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17401366?ordinalpos=26&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24 Prostate cancer "1,453 cases, 3,064 controls" "1,210 EA cases, 2,445 EA controls; 373 AA cases, 372 AA controls" 8q24.21 Intergenic rs16901979-A rs16901979 0.03 (EA) 1.00E-12 (EA)  1.79 [1.53-2.11] (EA) "Illumina [316,515]" N 11/25/2008 17395743 Hanson 1-Apr-07 Diabetes http://www.ncbi.nlm.nih.gov/pubmed/17395743?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study End-stage renal disease "105 cases, 102 controls" NR 8q24.21 PVT1 rs2648875-A rs2648875 0.53 2E-06 2.97 [1.90-4.65] "Affymetrix [115,352]" N 11/25/2008 17401363 Yeager 1-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17401363?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of prostate cancer identifies a second risk locus at 8q24 Prostate cancer "1,172 cases, 1,157 controls" "3,124 cases, 3,142 controls" 8q24.21 Intergenic rs6983267-G rs6983267 0.5 9.00E-13 1.26 [1.13-1.41] "Illumina [538,548]" N 11/25/2008 17401363 Yeager 1-Apr-07 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/17401363?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide association study of prostate cancer identifies a second risk locus at 8q24 Prostate cancer "1,172 cases, 1,157 controls" "3,124 cases, 3,142 controls" 8q24.21 Intergenic rs1447295-A rs1447295 0.11 2.00E-14 1.43 [1.29-1.59] "Illumina [538,548]" N 11/25/2008 17522711 Lencz 20-Mar-07 Mol Psychiatry http://www.ncbi.nlm.nih.gov/pubmed/17522711?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia Schizophrenia "178 cases, 144 controls" NR "Xp22.33,Yp11.32" "CSF2RA,IL3RA" rs4129148-C rs4129148 NR 4.00E-07 3.23 [2.04-5.15] "Affymetrix [439,511]" N 11/25/2008 17357082 Melquist 8-Mar-07 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/17357082?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms" Progressive supranuclear palsy "288 cases, 344 controls" "213 cases, 391 controls" NR NR NR NR NS NS NR NR "Affymetrix [428,867]" N 11/25/2008 17447842 Libioulle 5-Mar-07 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/17447842?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4 Crohn's disease "547 cases, 928 controls" "1,266 cases, 559 controls, 428 trios" 1p31.3 IL23R rs11209026-? rs11209026 0.92 2.00E-18 2.92 [NR] "Illumina [302,451]" N 11/25/2008 17447842 Libioulle 5-Mar-07 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/17447842?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4 Crohn's disease "547 cases, 928 controls" "1,266 cases, 559 controls, 428 trios" 5p13.1 Intergenic rs1373692-? rs1373692 0.59 2.00E-12 1.46 [NR] "Illumina [302,451]" N 11/25/2008 17447842 Libioulle 5-Mar-07 PLoS Genet http://www.ncbi.nlm.nih.gov/pubmed/17447842?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4 Crohn's disease "547 cases, 928 controls" "1,266 cases, 559 controls, 428 trios" 16q12.1 CARD15 rs5743289-? rs5743289 NR 1.00E-06 NR NR "Illumina [302,451]" N 11/25/2008 17362836 Schymick 20-Feb-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data Amyotrophic lateral sclerosis "276 cases, 276 controls" NR 10q26.13 Intergenic rs4363506-? rs4363506 NR 7.00E-07 1.9 [1.50-2.40] "Illumina [549,062]" N 11/25/2008 17362836 Schymick 20-Feb-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data Amyotrophic lateral sclerosis "276 cases, 276 controls" NR 2p24 Intergenic rs16984239-? rs16984239 NR 2E-06 2.1 [1.50-3.00] "Illumina [549,062]" N 11/25/2008 17362836 Schymick 20-Feb-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data Amyotrophic lateral sclerosis "276 cases, 276 controls" NR 8q24.2 Intergenic rs12680546-? rs12680546 NR 0.000003 1.67 [1.25-2.00] "Illumina [549,062]" N 11/25/2008 17362836 Schymick 20-Feb-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data Amyotrophic lateral sclerosis "276 cases, 276 controls" NR 20q13.2 ZFP64 rs6013382-? rs6013382 NR 0.000005 1.43 [1.11-1.67] "Illumina [549,062]" N 11/25/2008 17362836 Schymick 20-Feb-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data Amyotrophic lateral sclerosis "276 cases, 276 controls" NR 4q31.3 KlAA1727 rs11099864-? rs11099864 NR 0.000009 1 [0.80-1.40] "Illumina [549,062]" N 11/25/2008 17362836 Schymick 20-Feb-07 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17362836?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data Amyotrophic lateral sclerosis "276 cases, 276 controls" NR 9q31.3 SUSD1 rs2782931-? rs2782931 NR 0.000006 1.11 [0.91-1.43] "Illumina [549,062]" N 11/25/2008 17293876 Sladek 11-Feb-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17293876?ordinalpos=24&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies novel risk loci for type 2 diabetes Type 2 diabetes "661 cases, 614 controls" "2,617 cases, 2,894 controls" 8q24.11 SLC30A8 rs13266634-C rs13266634 0.7 6.00E-08 1.18 [0.69-1.67] "Illumina [392,935]" N 11/25/2008 17293876 Sladek 11-Feb-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17293876?ordinalpos=24&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies novel risk loci for type 2 diabetes Type 2 diabetes "661 cases, 614 controls" "2,617 cases, 2,894 controls" 10q25.3 TCF7L2 rs7903146-T rs7903146 0.3 2.00E-34 1.65 "[1.28, 2.02]" "Illumina [392,935]" N 11/25/2008 17293876 Sladek 11-Feb-07 Nature http://www.ncbi.nlm.nih.gov/pubmed/17293876?ordinalpos=24&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies novel risk loci for type 2 diabetes Type 2 diabetes "661 cases, 614 controls" "2,617 cases, 2,894 controls" 10q23.33 HHEX rs1111875-G rs1111875 0.6 0.000003 1.19 [0.82-1.56] "Illumina [392,935]" N 11/25/2008 17223258 Spinola 16-Jan-07 Cancer Lett http://www.ncbi.nlm.nih.gov/pubmed/17223258?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide single nucleotide polymorphism analysis of lung cancer risk detects the KLF6 gene Lung cancer "338 Italian lung adenocarcinoma cases, 335 Italian controls" 265 Norwegian non-small lung carcinoma cases 356 Norwegian controls NR NR NR NR NS NS NR NR "Affymetrix [~116,204] (pooled)" N 11/25/2008 17158188 Bierut 7-Dec-06 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/17158188?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Novel genes identified in a high-density genome wide association study for nicotine dependence Nicotine dependence "1,050 cases, 879 controls" NR 21q22.2 NR rs2836823-T rs2836823 0.4 2E-06 1.46 [1.23-1.73] Perlegen [2.4 million] (pooled) N 11/25/2008 17158188 Bierut 7-Dec-06 Hum Mol Genet http://www.ncbi.nlm.nih.gov/pubmed/17158188?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Novel genes identified in a high-density genome wide association study for nicotine dependence Nicotine dependence "1,050 cases, 879 controls" NR 10q21.3 CTNNA3 rs4142041-G rs4142041 0.34 0.000006 1.14 [0.97-1.35] Perlegen [2.4 million] (pooled) N 11/25/2008 17099884 Liu 5-Dec-06 Am J Med Genet B Neuropsychiatr Genet http://www.ncbi.nlm.nih.gov/pubmed/17099884?ordinalpos=7&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum "Addiction molecular genetics: 639,401 SNP whole genome association identifies many ""cell adhesion"" genes" Addiction "980 cases, 680 controls" NR NR NR NR NR NS NS NR NR "Affymetrix [639,401]" N 11/25/2008 17068223 Duerr 26-Oct-06 Science http://www.ncbi.nlm.nih.gov/pubmed/17068223?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies IL23R as an inflammatory bowel disease gene Inflammatory bowel disease "547 cases, 548 controls" "401 cases, 433 controls, 883 families, 1,119 affected offspring" 1p31.3 IL23R rs11209026-A rs11209026 0.93 4.00E-11 3.84 [2.33-6.66] "Illumina [308,332]" N 11/25/2008 17068223 Duerr 26-Oct-06 Science http://www.ncbi.nlm.nih.gov/pubmed/17068223?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies IL23R as an inflammatory bowel disease gene Inflammatory bowel disease "547 cases, 548 controls" "401 cases, 433 controls, 883 families, 1,119 affected offspring" 1p31.3 IL23R rs7517847-C rs7517847 0.56 4.00E-13 1.61 [1.35-1.92] "Illumina [308,332]" N 11/25/2008 17068223 Duerr 26-Oct-06 Science http://www.ncbi.nlm.nih.gov/pubmed/17068223?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A genome-wide association study identifies IL23R as an inflammatory bowel disease gene Inflammatory bowel disease "547 cases, 548 controls" "401 cases, 433 controls, 883 families, 1,119 affected offspring" 16q12.1 CARD15 rs2076756-? rs2076756 NR 5.00E-10 NR NR "Illumina [308,332]" N 11/25/2008 17053149 Papassotiropoulos 20-Oct-06 Science http://www.ncbi.nlm.nih.gov/pubmed/17053149?ordinalpos=4&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Common Kibra alleles are associated with human memory performance Memory performance 341 individuals 680 individuals NR NR NR NR NS NS NR NR "Affymetrix [178,390]" N 11/25/2008 17053108 DeWan 19-Oct-06 Science http://www.ncbi.nlm.nih.gov/pubmed/17053108?ordinalpos=5&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum HTRA1 promoter polymorphism in wet age-related macular degeneration Age-related macular degeneration (wet) "96 Southeast Asian cases, 130 Southeast Asian controls" NR 10q26 HTRA1 rs11200638-A rs11200638 NR 8.00E-12 1.6 [0.71-3.61] "Affymetrix [97,824]" N 11/25/2008 17052657 Fung 28-Sep-06 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17052657?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data Parkinson's disease "267 cases, 270 controls" NR 10q11.21 Intergenic rs1480597-? rs1480597 NR 2E-06 2.5 [1.67-3.33] "Illumina [408,803]" N 11/25/2008 17052657 Fung 28-Sep-06 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17052657?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data Parkinson's disease "267 cases, 270 controls" NR 4q13.2 BRDG1 rs2242330-? rs2242330 NR 2E-06 2 [1.43-2.50] "Illumina [408,803]" N 11/25/2008 17052657 Fung 28-Sep-06 Lancet Neurol http://www.ncbi.nlm.nih.gov/pubmed/17052657?ordinalpos=2&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data Parkinson's disease "267 cases, 270 controls" NR 11q14 DLG2 rs10501570-? rs10501570 NR 7E-06 5 [2.00-12.50] "Illumina [408,803]" N 11/25/2008 16648850 Arking 30-Apr-06 Nat Genet http://www.ncbi.nlm.nih.gov/pubmed/16648850?ordinalpos=10&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization QT interval prolongation "100 > 445ms, 100 < 386ms" "200 > 85th pct, 200 < 15th pct, 7,817 cohort members" 1q23.3 NOS1AP rs10494366-? rs10494366 0.36 1.00E-10 4.9 - 7.90 [NR] msec difference between homozygotes "Affymetrix [88,500]" N 11/25/2008 16614226 Herbert 14-Apr-06 Science http://www.ncbi.nlm.nih.gov/pubmed/16614226?ordinalpos=8&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum A common genetic variant is associated with adult and childhood obesity Obesity 694 offspring "3,489 cases, 6,392 controls, 361 trios" NR NR NR NR NS NS NR NR "Affymetrix [86,604]" N 11/25/2008 16252231 Maraganore 9-Sep-05 Am J Hum Genet http://www.ncbi.nlm.nih.gov/pubmed/16252231?ordinalpos=6&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum High-resolution whole-genome association study of Parkinson disease Parkinson's disease 443 sib pairs "332 cases, 332 controls" 5p15.2 SEMA5A rs7702187-? rs7702187 NR 8E-06 1.74 [1.36-2.24] "Perlegen [198,345]" N 11/25/2008 15761122 Klein 10-Mar-05 Science http://www.ncbi.nlm.nih.gov/pubmed/15761122?ordinalpos=3&itool=EntrezSystem2.PEntrez.Pubmed.Pubmed_ResultsPanel.Pubmed_RVDocSum Complement factor H polymorphism in age-related macular degeneration Age-related macular degeneration "96 cases, 50 controls" NR 1q31 CFH rs380390-C rs380390 0.70 (HapMap CEU) 4.00E-08 4.6 [2.0-11] "Affymetrix [103,611]" N