| Mutation of the human circadian clock gene CRY1 in familial delayed sleep phase disorder A Patke, PJ Murphy, OE Onat, AC Krieger, T Özçelik, SS Campbell, ... Cell 169 (2), 203-215. e13, 2017 | 350 | 2017 |
| Mitochondrial serine protease HTRA2 p. G399S in a kindred with essential tremor and Parkinson disease H Unal Gulsuner, S Gulsuner, FN Mercan, OE Onat, T Walsh, H Shahin, ... Proceedings of the National Academy of Sciences 111 (51), 18285-18290, 2014 | 157 | 2014 |
| Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion O Emre Onat, S Gulsuner, K Bilguvar, A Nazli Basak, H Topaloglu, M Tan, ... European Journal of Human Genetics 21 (3), 281-285, 2013 | 125 | 2013 |
| Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans T Ozcelik, N Akarsu, E Uz, S Caglayan, S Gulsuner, OE Onat, M Tan, ... Proceedings of the National Academy of Sciences 105 (11), 4232-4236, 2008 | 123 | 2008 |
| Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred S Gulsuner, AB Tekinay, K Doerschner, H Boyaci, K Bilguvar, H Unal, ... Genome Research 21 (12), 1995-2003, 2011 | 84 | 2011 |
| MDM2 T309G polymorphism is associated with bladder cancer OE Onat, M Tez, T Özçelik, GA Törüner Anticancer research 26 (5A), 3473-3475, 2006 | 69 | 2006 |
| The genetic structure of the Turkish population reveals high levels of variation and admixture ME Kars, AN Başak, OE Onat, K Bilguvar, J Choi, Y Itan, C Çağlar, ... Proceedings of the National Academy of Sciences 118 (36), e2026076118, 2021 | 58 | 2021 |
| Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair GM Dal, B Ergüner, MS Sağıroğlu, B Yüksel, OE Onat, C Alkan, T Özçelik Journal of medical genetics 51 (7), 455-459, 2014 | 52 | 2014 |
| Human CRY1 variants associate with attention deficit/hyperactivity disorder OE Onat, ME Kars, Ş Gül, K Bilguvar, Y Wu, A Özhan, C Aydın, AN Başak, ... The Journal of Clinical Investigation 130 (7), 3885-3900, 2023 | 39 | 2023 |
| Two males with SRY-positive 46, XX testicular disorder of sex development S Gunes, R Asci, G Okten, F Atac, OE Onat, G Ogur, O Aydin, T Ozcelik, ... Systems biology in reproductive medicine 59 (1), 42-47, 2013 | 35 | 2013 |
| Evaluation of X chromosome inactivation with respect to HLA genetic susceptibility in rheumatoid arthritis and systemic sclerosis SB Kanaan, OE Onat, N Balandraud, GV Martin, JL Nelson, DF Azzouz, ... PLoS One 11 (6), e0158550, 2016 | 33 | 2016 |
| Genomic landscape of the Greater Middle east T Özçelik, OE Onat Nature Genetics 48 (9), 978-979, 2016 | 19 | 2016 |
| Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation P Demirayak, OE Onat, AÖ Gevrekci, S Gülsüner, H Uysal, R Bilgen, ... Diagnostic and Interventional Radiology 24 (6), 392, 2018 | 15 | 2018 |
| Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotion T Ozcelik, N Akarsu, E Uz, S Caglayan, S Gulsuner, OE Onat, M Tan, ... Proceedings of the National Academy of Sciences 105 (23), E32-E33, 2008 | 10 | 2008 |
| Multiscale analysis of SRY‐positive 46, XX testicular disorder of sex development: Presentation of nine cases OS Akar, S Gunes, U Abur, E Altundag, R Asci, OE Onat, T Ozcelik, ... Andrologia 52 (11), e13739, 2020 | 8 | 2020 |
| Disruption of HDX gene in premature ovarian failure G Okten, S Gunes, OE Onat, A Tukun, T Ozcelik, I Kocak Systems biology in reproductive medicine 59 (4), 218-222, 2013 | 6 | 2013 |
| Meta-analysis of commonly mutated genes in leptomeningeal carcinomatosis I Congur, E Koni, OE Onat, ZT Keskin PeerJ 11, e15250, 2023 | 1 | 2023 |
| Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor H Unal Gulsuner, S Gulsuner, FN Mercan, OE Onat, T Walsh, H Shahin, ... Proceedings of the National Academy of Sciences 112 (18), E2269-E2269, 2015 | 1 | 2015 |
| A7. 9 Does Telomere Shortening in Women with Rheumatoid Arthritis Predict X Chromosome Inactivation Bias? SB Kanaan, OE Onat, N Balandraud, DF Azzouz, J Roudier, T Ozcelik, ... Annals of the Rheumatic Diseases 72 (Suppl 1), A51-A51, 2013 | 1 | 2013 |
| Identification of ATP8A2 Gene Mutation in a Consaguineous Family Segregating Cerebellar Atrophy and Quadrupedal Gait OE Onat PQDT-Global, 2012 | | 2012 |
