Yavuz Oktay
Yavuz Oktay
Izmir Biomedicine and Genome Center (iBG) / Dokuz Eylul University
Verified email at - Homepage
Cited by
Cited by
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
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
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
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
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
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
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
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
RdRp mutations are associated with SARS-CoV-2 genome evolution
D Eskier, G Karakülah, A Suner, Y Oktay
PeerJ 8, e9587, 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
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
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
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
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
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
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
Confirmation of TACO1 as a Leigh syndrome disease gene in two additional families
Y Oktay, S Güngör, L Zeltner, S Wiethoff, L Schöls, E Sonmezler, E Yilmaz, ...
Journal of neuromuscular diseases 7 (3), 301-308, 2020
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
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
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
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