Assoc. Prof. Esra Battaloglu, PhD

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Contents

Education

1989-1992 Ph.D. Bogaziçi University Faculty of Arts and Sciences Department of Biology

1987-1989 M.S. Bogaziçi University Faculty of Arts and Sciences Department of Biology

1982-1986 B.S. Middle East Technical University Department of Biology

1975-1982 High School T.E.D. Ankara Koleji


Professional Appointments

September 1993 - Present, Assistant Proffesor, Bogaziçi University Faculty of Arts and Sciences Department of Molecular Biology and Genetics

March-August 1993, Lecturer, Bogaziçi University Faculty of Arts and Sciences Department of Biology

1987-1993, Research Assistant, Bogaziçi University Faculty of Arts and Sciences Department of Biology


International Activities

September 1992-January 1993 Visiting Researcher, Birmingham University, ENGLAND, Department of Biochemistry, Project: 'E.coli Nitrat Redüktaz Geninin Klonlanmasö ve Dizi Analizi'

June-July 1992, Visiting Researcher, Guy's Hospital, ENGLAND, Pediatrical Research Unit.

June-July 1991, Visiting Researcher, University of California Los Angeles, A.B.D., Department of Pathology.

July 1990, Visiting Researcher, University of California Los Angeles, A.B.D., Department of Pathology.


Memberships

American Society of Human Genetics

European Charcot-Marie-Tooth Consortium


Publications

1. Genetic spectrum of hereditary neuropathies with onset in the first year of life.

Baets J, Deconinck T, De Vriendt E, Zimoń M, Yperzeele L, Van Hoorenbeeck K, Peeters K, Spiegel R, Parman Y, Ceulemans B, Van Bogaert P, Pou-Serradell A, Bernert G, Dinopoulos A, Auer-Grumbach M, Sallinen SL, Fabrizi GM, Pauly F, Van den Bergh P, Bilir B, Battaloglu E, Madrid RE, Kabzińska D, Kochanski A, Topaloglu H, Miller G, Jordanova A, Timmerman V, De Jonghe P. Brain. 2011 Sep;134(Pt 9):2664-76. Epub 2011 Aug 11. PMID: 21840889 Free PMC Article


2. Nerve conduction studies in Charcot-Marie-Tooth disease in a cohort from Turkey.

Deymeer F, Matur Z, Poyraz M, Battaloglu E, Oflazer-Serdaroglu P, Parman Y. Muscle Nerve. 2011 May;43(5):657-64. doi: 10.1002/mus.21932. Epub 2011 Mar 14. PMID: 21404297


3. Combination of myotonic dystrophy and hereditary motor and sensory neuropathy.

Kurt S, Karaer H, Kaplan Y, Akat I, Battaloglu E, Eruslu D, Basak AN. J Neurol Sci. 2010 Jan 15;288(1-2):197-9. Epub 2009 Oct 21. PMID: 19846120


4. Low dose vincristine-induced severe polyneuropathy in a Hodgkin lymphoma patient: a case report (vincristine-induced severe polyneuropathy).

Cil T, Altintas A, Tamam Y, Battaloğlu E, Isikdogan A. J Pediatr Hematol Oncol. 2009 Oct;31(10):787-9. PMID: 19770686


5. A multiplexed ARMS-PCR approach for the detection of common MECP2 mutations.

Baris I, Battaloglu E. Genet Test Mol Biomarkers. 2009 Feb;13(1):19-22. PMID: 19309269


6. Hereditary neuropathy with liability to pressure palsy (HNPP) in childhood: a case study emphasizing the relevance of detailed electrophysiological examination for suspected HNPP in the first decade.

Bayrak AO, Battaloglu E, Turker H, Baris I, Oztas G. Brain Dev. 2009 Jun;31(6):445-8. Epub 2008 Aug 29. PMID: 18760885


7. Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4.

Stendel C, Roos A, Deconinck T, Pereira J, Castagner F, Niemann A, Kirschner J, Korinthenberg R, Ketelsen UP, Battaloglu E, Parman Y, Nicholson G, Ouvrier R, Seeger J, De Jonghe P, Weis J, Krüttgen A, Rudnik-Schöneborn S, Bergmann C, Suter U, Zerres K, Timmerman V, Relvas JB, Senderek J. Am J Hum Genet. 2007 Jul;81(1):158-64. Epub 2007 May 24. PMID: 17564972 Free PMC Article


8. X-linked Charcot-Marie-Tooth disease and multiple sclerosis.

Parman Y, Ciftci F, Poyraz M, Halefoglu AM, Oge AE, Eraksoy M, Saruhan-Direskeneli G, Deymeer F, Battaloglu E. J Neurol. 2007 Jul;254(7):953-5. Epub 2007 Jan 30. No abstract available. PMID: 17468966


9. A novel missense mutation in human TTF-2 (FKHL15) gene associated with congenital hypothyroidism but not athyreosis.

Baris I, Arisoy AE, Smith A, Agostini M, Mitchell CS, Park SM, Halefoglu AM, Zengin E, Chatterjee VK, Battaloglu E. J Clin Endocrinol Metab. 2006 Oct;91(10):4183-7. Epub 2006 Aug 1. PMID: 16882747 Free Article


10. A large family with Charcot-Marie-Tooth Type 1a and Type 2 diabetes mellitus.

Koç F, Sarica Y, Yerdelen D, Baris I, Battaloglu E, Sert M. Int J Neurosci. 2006 Feb;116(2):103-14. PMID: 16393877


11. Voltage-gated sodium channel expression and potentiation of human breast cancer metastasis.

Fraser SP, Diss JK, Chioni AM, Mycielska ME, Pan H, Yamaci RF, Pani F, Siwy Z, Krasowska M, Grzywna Z, Brackenbury WJ, Theodorou D, Koyutürk M, Kaya H, Battaloglu E, De Bella MT, Slade MJ, Tolhurst R, Palmieri C, Jiang J, Latchman DS, Coombes RC, Djamgoz MB. Clin Cancer Res. 2005 Aug 1;11(15):5381-9. Erratum in: Clin Cancer Res. 2005 Nov 15;11(22):8224. PMID: 16061851 Free Article


12. Clinicopathological and genetic study of early-onset demyelinating neuropathy.

Parman Y, Battaloglu E, Baris I, Bilir B, Poyraz M, Bissar-Tadmouri N, Williams A, Ammar N, Nelis E, Timmerman V, De Jonghe P, Najafov A, Deymeer F, Serdaroglu P, Brophy PJ, Said G. Brain. 2004 Nov;127(Pt 11):2540-50. Epub 2004 Oct 6. Erratum in: Brain. 2007 Jul;130(7):1972. Necefov, Ayaz [corrected to Najafov, Ayaz]. PMID: 15469949 Free Article


13. Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene.

Bissar-Tadmouri N, Nelis E, Züchner S, Parman Y, Deymeer F, Serdaroglu P, De Jonghe P, Van Gerwen V, Timmerman V, Schröder JM, Battaloglu E. Neurology. 2004 May 11;62(9):1522-5. PMID: 15136675


14. Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.

Züchner S, Mersiyanova IV, Muglia M, Bissar-Tadmouri N, Rochelle J, Dadali EL, Zappia M, Nelis E, Patitucci A, Senderek J, Parman Y, Evgrafov O, Jonghe PD, Takahashi Y, Tsuji S, Pericak-Vance MA, Quattrone A, Battaloglu E, Polyakov AV, Timmerman V, Schröder JM, Vance JM. Nat Genet. 2004 May;36(5):449-51. Epub 2004 Apr 4. No abstract available. Erratum in: Nat Genet. 2004 Jun;36(6):660. Battologlu E [corrected to Battaloglu E]. PMID: 15064763


15. Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy.

Senderek J, Bergmann C, Stendel C, Kirfel J, Verpoorten N, De Jonghe P, Timmerman V, Chrast R, Verheijen MH, Lemke G, Battaloglu E, Parman Y, Erdem S, Tan E, Topaloglu H, Hahn A, Müller-Felber W, Rizzuto N, Fabrizi GM, Stuhrmann M, Rudnik-Schöneborn S, Züchner S, Michael Schröder J, Buchheim E, Straub V, Klepper J, Huehne K, Rautenstrauss B, Büttner R, Nelis E, Zerres K. Am J Hum Genet. 2003 Nov;73(5):1106-19. Epub 2003 Oct 21. PMID: 14574644 Free PMC Article


16. Charcot-Marie-Tooth disease associated with Type 2 diabetes mellitus.

Celik M, Forta H, Parman Y, Bissar-Tadmouri N, Demirkirkan K, Battaloglu E. Diabet Med. 2001 Aug;18(8):685-6. No abstract available. PMID: 11553211


17. Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians.

Onengüt S, Kavaslar GN, Battaloğlu E, Serdaroğlu P, Deymeer F, Ozdemir C, Calafell F, Tolun A. Ann Hum Genet. 2000 Jan;64(Pt 1):33-40. PMID: 11388892


18. Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patients.

Bissar-Tadmouri N, Parman Y, Boutrand L, Deymeer F, Serdaroglu P, Vandenberghe A, Battaloglu E. Clin Genet. 2000 Nov;58(5):396-402. PMID: 11140841


19. Two novel mutations in the MPZ gene coding region in Charcot-Marie-Tooth type 1 patients of Turkish origin: S54P, [I30del; GVYI29ins].

Bissar-Tadmouri N, Gulsen-Parman Y, Latour P, Deymeer F, Serdaroglu P, Vandenberghe A, Battaloglu E. Hum Mutat. 1999 Nov;14(5):449. No abstract available. PMID: 10533074


20. DNA analysis in Turkish Duchenne/Becker muscular dystrophy families.

Battaloğlu E, Telatar M, Deymeer F, Serdaroğlu P, Kuseyri F, Ozdemir C, Apak M, Tolun A. Hum Genet. 1992 Aug;89(6):635-9. PMID: 1355068


21. Carrier detection by DNA analysis in Duchenne muscular dystrophy families.

Battaloğlu E, Telatar M, Deymeer F, Serdaroğlu P, Ozdemir C, Kuseyri F, Apak MY, Tolun A. Turk J Pediatr. 1992 Apr-Jun;34(2):79-92. PMID: 1440954

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