| Multiple organ pathology, metabolic abnormalities and impaired homeostasis of reactive oxygen species in Epas1−/− mice M Scortegagna, K Ding, Y Oktay, A Gaur, F Thurmond, LJ Yan, BT Marck, ... Nature genetics 35 (4), 331-340, 2003 | 624 | 2003 |
| UCP2 regulates energy metabolism and differentiation potential of human pluripotent stem cells J Zhang, I Khvorostov, JS Hong, Y Oktay, L Vergnes, E Nuebel, ... The EMBO journal 30 (24), 4860-4873, 2011 | 554 | 2011 |
| PNPASE regulates RNA import into mitochondria G Wang, HW Chen, Y Oktay, J Zhang, EL Allen, GM Smith, KC Fan, ... Cell 142 (3), 456-467, 2010 | 387 | 2010 |
| Cardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner membrane SM Claypool, Y Oktay, P Boontheung, JA Loo, CM Koehler The Journal of cell biology 182 (5), 937-950, 2008 | 371 | 2008 |
| HIF-2α regulates murine hematopoietic development in an erythropoietin-dependent manner M Scortegagna, K Ding, Q Zhang, Y Oktay, MJ Bennett, M Bennett, ... Blood 105 (8), 3133-3140, 2005 | 292 | 2005 |
| The HIF family member EPAS1/HIF-2α is required for normal hematopoiesis in mice M Scortegagna, MA Morris, Y Oktay, M Bennett, JA Garcia Blood 102 (5), 1634-1640, 2003 | 280 | 2003 |
| Hypoxia-inducible factor 2α regulates expression of the mitochondrial aconitase chaperone protein frataxin Y Oktay, E Dioum, S Matsuzaki, K Ding, LJ Yan, RG Haller, LI Szweda, ... Journal of Biological Chemistry 282 (16), 11750-11756, 2007 | 112 | 2007 |
| Determinants of resistance to chemotherapy and ionizing radiation in breast cancer stem cells A Pavlopoulou, Y Oktay, K Vougas, M Louka, CE Vorgias, AG Georgakilas Cancer letters 380 (2), 485-493, 2016 | 89 | 2016 |
| RdRp mutations are associated with SARS-CoV-2 genome evolution D Eskier, G Karakülah, A Suner, Y Oktay PeerJ 8, e9587, 2020 | 68 | 2020 |
| Mutations of SARS-CoV-2 nsp14 exhibit strong association with increased genome-wide mutation load D Eskier, A Suner, Y Oktay, G Karakülah PeerJ 8, e10181, 2020 | 50 | 2020 |
| Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas CB Akyerli, Ş Yüksel, Ö Can, EZ Erson-Omay, Y Oktay, E Coşgun, ... Journal of neurosurgery 128 (4), 1102-1114, 2018 | 34 | 2018 |
| IDH-mutant glioma specific association of rs55705857 located at 8q24.21 involves MYC deregulation Y Oktay, E Ülgen, Ö Can, CB Akyerli, Ş Yüksel, Y Erdemgil, IM Durası, ... Scientific Reports 6, 27569, 2016 | 32 | 2016 |
| UCP 2 regulates energy metabolism and differentiation potential of human pluripotent stem cells J Zhang, I Khvorostov, JS Hong, Y Oktay, L Vergnes, E Nuebel, ... The EMBO journal 35 (8), 899-899, 2016 | 26 | 2016 |
| High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases S Hiz Kurul, Y Oktay, A Töpf, NZ Szabó, S Güngör, A Yaramis, ... Brain 145 (4), 1507-1518, 2022 | 21 | 2022 |
| Mutation density changes in SARS-CoV-2 are related to the pandemic stage but to a lesser extent in the dominant strain with mutations in spike and RdRp D Eskier, A Suner, G Karakülah, Y Oktay PeerJ 8, e9703, 2020 | 19 | 2020 |
| Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss EM Richard, S Bakhtiari, APL Marsh, R Kaiyrzhanov, M Wagner, S Shetty, ... The American Journal of Human Genetics 108 (10), 2006-2016, 2021 | 18 | 2021 |
| Confirmation of TACO1 as a Leigh syndrome disease gene in two additional families Y Oktay, S Güngör, L Zeltner, S Wiethoff, L Schoels, E Sonmezler, ... Journal of neuromuscular diseases 7 (3), 301-308, 2020 | 17 | 2020 |
| Whole exome sequencing–based analysis to identify DNA damage repair deficiency as a major contributor to gliomagenesis in adult diffuse gliomas E Ülgen, Ö Can, K Bilguvar, Y Oktay, CB Akyerli, AE Danyeli, MC Yakıcıer, ... Journal of Neurosurgery 132 (5), 1435-1446, 2019 | 17 | 2019 |
| Different selection dynamics of S and RdRp between SARS-CoV-2 genomes with and without the dominant mutations N Koçhan, D Eskier, A Suner, G Karakülah, Y Oktay Infection, Genetics and Evolution 91, 104796, 2021 | 16 | 2021 |
| Improved diagnosis of rare disease patients through systematic detection of runs of homozygosity L Matalonga, S Laurie, A Papakonstantinou, D Piscia, E Mereu, G Bullich, ... The Journal of Molecular Diagnostics 22 (9), 1205-1215, 2020 | 16 | 2020 |
