Akademik Kadro

Prof. Dr. Eda Tahir Turanlı

Akademik dereceler ve çalışma deneyimi

Yrd Doç. Dr. – İstanbul Teknik Üniversitesi, Fen-Edebiyat Fakültesi, Moleküler Biyoloji ve Genetik Bölümü , İstanbul, 2005-

Misafir Öğretim Elemanı – İstanbul Teknik Üniversitesi, Fen-Edebiyat Fakültesi, Moleküler Biyoloji ve Genetik Bölümü, İstanbul, 2004-2005.

Öğretim Görevlisi – Boğaziçi Üniversitesi, Fen-Edebiyat Fakültesi, Moleküler Biyoloji ve Genetik Bölümü, İstanbul, 2001-2003.

Doktora – Marmara Üniversitesi, Sağlık Bilimleri Enstiitüsü, Tıbbi Biyoloji ve Genetik Bölümü, İstanbul, 2000.

Uzman Araştırmacı – TÜBİTAK, Gen Mühendisliği ve Biyoteknoloji Araştırma Merkezi, Gebze- Kocaeli (1997-2001)

Yüksek Lisans – University of London, Imperial College of Science and Technology, St Mary’s Medical School, Londra, UK, MSc. İnsan Moleküler Genetiği, 1995.

Lisans – University of Nottingham, Queen’s Medical Hospital, Department of Genetics, Nottingham, UK, BSc. Genetik, 1994

Yurt dışı çalışma deneyimi:

1998-1999: University of London, King’s College, Social, Genetic and Developmental  Pshyciatry Research Center, London, UK- Visiting Scientist, Short-term EMBO Fellow

1999-2000: University of London, King’s College, Social, Genetic and Developmental  Pshyciatry Research Center, London, UK, Researcher)

İlgi alanları

Enflammasyonda epigenetik mekanizmaların araştırılması

Multipl Skleroz hastalığının modellenmesi ve biyobelirteç analizleri

Kompleks hastalıkların genetik unsurlarının araştırılması, asosiyasyon ve bağlantı analizleri

Yayınlar

Avsar T, Korkmaz D, Tütüncü M, Demirci NO, Saip S, Kamasak M, Siva A, Turanli ET. Protein biomarkers for multiple sclerosis: semi-quantitative analysis of cerebrospinal fluid candidate protein biomarkers in different forms of multiple sclerosis. Multiple Sclerosis, 2012 (Epub)

Asli K Kirectepe, Ozgur Kasapcopur , Nil Arisoy, Gokce Celikyapi, Gulen Hatemi, Huri Ozdogan and Eda Tahir Turanli. Analysis of MEFV exon methylation and expression patterns in familial Mediterranean fever. Submitted October (2011).BMC Medical Genetics 12:105.

Asli K Kirectepe, Gokce Celikyapi Erdem, Nevcin Senturk, Nil Arisoy, Gulen Hatemi, Huri Ozdogan, Ozgur Kasapcopur and Eda Tahir Turanli (2011). Increased expression of exon 2 deleted MEFV transcript in Familial Mediterranean Fever Patients. International Journal of Immunogenetics 38, 327-329

Emire Seyahi, Eda Tahir Turanli, Mehmet Serhat Mangan, Gökçe Çelikyapı, Veysel Oktay, Dilşen Çevirgen, Duygu Kuzuoğlu, Şuşan Muratyan and Hasan Yazıcı. The Prevalence of Behçet’s Syndrome, Familial Mediterranean Fever, HLA-B51 and MEFV gene mutations among Ethnic Armenians living in Istanbul, Turkey. Clinical and Experimental Rheumatology, 2010,28,4,Suppl.60, pages 67-75.

Seval Masatlıoğlu, Emire Seyahi, Eda Tahir Turanli, Izzet Fresko, Feride Göğüs, Ebubekir Senates, Oğuz Savra ve Hasan Yazıcı. A twin study in Behçet`s syndrome. Clinical and Experimental Rheumatology, 2010,28,4,Suppl.60, pages 62-66.

Emire Seyahi, Eda Tahir Turanli, Mehmet Serhat Mangan, Gökçe Çelikyapı, Veysel Oktay, Dilşen Çevirgen, Duygu Kuzuoğlu, Şuşan Muratyan and Hasan Yazıcı. The Prevalence of Behçet’s Syndrome, Familial Mediterranean Fever, HLA-B51 and MEFV gene mutations among Ethnic Armenians living in Istanbul, Turkey. Gönderildi 2010, Arthritis & Rheumatism.

Eda Tahir Turanli , Tanju Beger, Deniz Erdincler, Aslı Cungurlu, Sinem Karaman, Esra Karaca, Selcuk Dasdemir, Murat Bolayirli and Hasan Yazici (2009). MEFV mutations in an elderly population: An Association with E148Q mutation and Romatoid Factor levels. Clinical and Experimental Rheumatology, Vol 27: 340-343.

Ozbay F, Wigg KG, Turanli ET, Asherson P, Yazgan Y, Sandor P, Barr CL. Analysis of the dopamine beta hydroxylase gene in Gilles de la tourette syndrome (2006). Am J Med Genet B Neuropsychiatr Genet. Vol 141(6):673-7.

Bagis H, Arat S, Mercan HO, Aktoprakligil D, Caner M, Turanli ET, Baysal K, Turgut G, Sekmen S, Cirakoglu B. Stable transmission and expression of the hepatitis B virus total genome in hybrid transgenic mice until F10 generation (2006).J Exp Zoolog A Comp Exp Biol. Vol 305(5):420-7.

Lowe N, Kirley A, Hawi Z, Sham P, Vickham H, Kratochvil CJ, Smith SD, Lee SY, Levy F, Kent L, Middle F Rohde LA, Roman T, Tahir E, Yazgan Y, Asherson P, Mill J, Thapar A, Payton A, Todd RD, Stephens T, Ebstein RP, Manor I, Barr JL, Wigg KG, Sinke RJ, Buitelaar JK, Smalley SL, Nelson SF, Biederman J, Faraone SV, Gill M. (2004). Joint analysis of the DRD5 marker concludes association with attention deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes. Am J Hum Genet 74 (2): 348-56.

UM D’Souza, C Russ, E Tahir, C Browes, Mill J, P McGuffin, PJ Asherson and IW Craig. Functional Effects of a Tandem Duplication Polymorphism in the 5’flanking region of the DRD4 gene (2004). Biological Psychiatry Vol 56:691-697.

Thalia C. Eley, Eda Tahir, Alois Angleitner, Kaveri Harriss, Joseph McClay, Robert Plomin, Rainer Riemann, Frank Spinath, and Ian Craig. Association analysis of MAOA and COMT with neuroticism (2003). American Journal of Medical Genetics (Neuropsychiatric Genetics) Vol 120B(1):90-6.

Chun Xu, Fatih Ozbay, Karen Wigg, Rayzie Shulman, Eda Tahir, Yanki Yazgan, Cathy L. Barr, and The Tourette Syndrome Association Genetic Consortium. Evaluation of the Genes for the Adrenergic Receptors 2A and 1C and Gilles de la Tourette Syndrome (2003). American Journal of Medical Genetics (Neuropsychiatric Genetics). Vol 119B(1):54-9

Sarah Curran, Jonathan Mill, Eda Tahir, Lindsey Kent, Sandra Richards, Alison Gould, Louise Huckett, Jonathan Sharp, Claire Batten, Shamira Fernando, Fatih Ozbay, Yanki Yazgan, Emily Simanoff, Margaret Thompson, Eric Taylor and Philip Asherson. Association study of a dopamine transporter polymorphism and Attention Deficit Hyperactivity Disorder in UK and Turkish samples (2001). Molecular Psychiatry 6: 425-428.

Tahir E, Yazgan Y, Cirakoglu B, Ozbay F, Waldman I and Asherson P J. Association and Linkage of DRD4 and DRD5 with attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children (2000). Molecular Psychiatry.5: 396-404.

Tahir E, Curran S, Yazgan Y, Ozbay F, Cirakoglu B and Asherson P J. No association between low and high activity catecholamine-methyl-transferase (COMT) and Attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children (2000). American Journal of Medical Genetics (Neuropsychiatric Genetics ) 96: 285-288.

The ADHD Molecular Genetics Network (2000). Collaborative Possibilities for Molecular Genetic Studies of Attention Deficit Hyperactivity Disorder: Report From an International Conference. American Journal of Medical Genetics (Neuropsychiatric Genetics) 96: 251-257.

Riley BP, Tahir E, Rajagopalan S, Mogudi-Carter M, Fauré S, Weissenbach J, Jenkins T and Williamson R (1997). A linkage study of the N-methyl-D-aspartate receptor subunit gene loci and schizophrenia in southern African Bantu-speaking families. Psychiatric Genetics 7: 57-74.

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