| Association and linkage of DRD4 and DRD5 with attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children E Tahir, Y Yazgan, B Cirakoglu, F Ozbay, I Waldman, PJ Asherson Molecular psychiatry 5 (4), 396-404, 2000 | 244 | 2000 |
| Joint analysis of the DRD5 marker concludes association with attention-deficit/hyperactivity disorder confined to the predominantly inattentive and combined subtypes N Lowe, A Kirley, Z Hawi, P Sham, H Wickham, CJ Kratochvil, SD Smith, ... The American Journal of Human Genetics 74 (2), 348-356, 2004 | 242 | 2004 |
| Association study of a dopamine transporter polymorphism and attention deficit hyperactivity disorder in UK and Turkish samples S Curran, J Mill, E Tahir, L Kent, S Richards, A Gould, L Huckett, J Sharp, ... Molecular psychiatry 6 (4), 425-428, 2001 | 231 | 2001 |
| Association analysis of MAOA and COMT with neuroticism assessed by peers TC Eley, E Tahir, A Angleitner, K Harriss, J McClay, R Plomin, R Riemann, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 120 …, 2003 | 167 | 2003 |
| Functional effects of a tandem duplication polymorphism in the 5′ flanking region of the DRD4 gene UM D’Souza, C Russ, E Tahir, J Mill, P McGuffin, PJ Asherson, IW Craig Biological psychiatry 56 (9), 691-697, 2004 | 146 | 2004 |
| Familial Mediterranean fever in childhood: a single-center experience K Barut, S Sahin, A Adrovic, AB Sinoplu, G Yucel, G Pamuk, AK Aydın, ... Rheumatology international 38, 67-74, 2018 | 130 | 2018 |
| No association between low‐and high‐activity catecholamine‐methyl‐transferase (COMT) and attention deficit hyperactivity disorder (ADHD) in a sample of Turkish children E Tahir, S Curran, Y Yazgan, F Ozbay, B Cirakoglu, PJ Asherson American journal of medical genetics 96 (3), 285-288, 2000 | 77 | 2000 |
| Clinical, imaging and genotypical features of three deceased and five surviving cases with ADA2 deficiency S Sahin, A Adrovic, K Barut, S Ugurlu, ET Turanli, H Ozdogan, ... Rheumatology International 38, 129-136, 2018 | 73 | 2018 |
| Protein biomarkers for multiple sclerosis: semi-quantitative analysis of cerebrospinal fluid candidate protein biomarkers in different forms of multiple sclerosis T Avsar, D Korkmaz, M Tütüncü, NO Demirci, S Saip, M Kamasak, A Siva, ... Multiple Sclerosis Journal 18 (8), 1081-1091, 2012 | 57 | 2012 |
| Analysis of MEFV exon methylation and expression patterns in familial Mediterranean fever AK Kirectepe, O Kasapcopur, N Arisoy, G Celikyapi Erdem, G Hatemi, ... BMC Medical Genetics 12, 1-6, 2011 | 56 | 2011 |
| A linkage study of the N-methyl-D-aspartate receptor subunit gene loci and schizophrenia in southern African Bantu-speaking families BP Riley, E Tahir, S Rajagopalan, M Mogudi-Carter, S Faure, ... Psychiatric genetics 7 (2), 57-74, 1997 | 55 | 1997 |
| Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study İ Karacan, A Balamir, S Uğurlu, AK Aydın, E Everest, S Zor, MÖ Önen, ... Rheumatology international 39 (5), 911-919, 2019 | 51 | 2019 |
| Low Dimensional and Nanostructured Materials and Devices H Ünlü, NJM Horing, J Dabrowski Springer Science LCC, 2015 | 48 | 2015 |
| A twin study in Behçet's syndrome S Masatlioglu, E Seyahi, E Tahir Turanli, I Fresko, F Gogus, E Senates, ... Clinical & Experimental Rheumatology 28 (4), S62, 2010 | 44 | 2010 |
| Joint analysis of DRD5 marker concludes association with ADHD confined to the predominantly inattentive and combined subtypes N Lowe, A Kirley, Z Hawi, P Sham, H Wickham, CJ Kratochvil, SD Smith, ... Am J Hum Genet 74 (2), 348-56, 2004 | 38 | 2004 |
| Spectrum of the neurologic manifestations in childhood-onset cryopyrin-associated periodic syndrome H Kilic, S Sahin, C Duman, A Adrovic, K Barut, ET Turanli, SR Yildirim, ... European Journal of Paediatric Neurology 23 (3), 466-472, 2019 | 32 | 2019 |
| Evaluation of the genes for the adrenergic receptors α2A and α1C and Gilles de la Tourette Syndrome C Xu, F Ozbay, K Wigg, R Shulman, E Tahir, Y Yazgan, P Sandor, CL Barr American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 119 …, 2003 | 32 | 2003 |
| The prevalence of Behçet's syndrome, familial Mediterranean fever, HLA-B51 and MEFV gene mutations among ethnic Armenians living in Istanbul, Turkey E Seyahi, E Tahir Turanli, MS Mangan, G Celikyapi, V Oktay, D Çevirgen, ... Clinical & Experimental Rheumatology 28 (4), S67, 2010 | 31 | 2010 |
| Analysis of the dopamine beta hydroxylase gene in Gilles de la Tourette syndrome F Ozbay, KG Wigg, ET Turanli, P Asherson, Y Yazgan, P Sandor, CL Barr American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 141 …, 2006 | 30 | 2006 |
| Stable transmission and expression of the hepatitis B virus total genome in hybrid transgenic mice until F10 generation H Bagis, S Arat, HO Mercan, D Aktoprakligil, M Caner, ET Turanli, ... Journal of Experimental Zoology Part A: Comparative Experimental Biology 305 …, 2006 | 28 | 2006 |
Ozgur KasapcopurIstanbul University, Cerrahpasa Medical School, Turkeyistanbul.edu.tr üzerinde doğrulanmış e-posta adresine sahip
