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Nature Genetics|August 31, 2016
Genomic landscape of the Greater Middle EastTayfun Özçelik, Onur Emre OnatAnnals of the New York Academy of Sciences|July 11, 2026
Escape From X-Chromosome Inactivation Enables Survival in a Male With an Unbalanced X;19 TranslocationOnur Emre Onat, Tayfun OzcelikAnticancer Research|November 11, 2006
MDM2 T309G polymorphism is associated with bladder cancerOnur Emre Onat, Mesut Tez, Tayfun Ozçelik, et al.Peerj|April 25, 2023
Meta-analysis of commonly mutated genes in leptomeningeal carcinomatosisIrem Congur, Ekin Koni, Onur Emre Onat, et al.Systems Biology in Reproductive Medicine|February 28, 2013
Disruption of HDX gene in premature ovarian failureGülsen Okten, Sezgin Gunes, Onur Emre Onat, et al.Journal of Medical Genetics|April 26, 2014
Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pairGülşah M Dal, Bekir Ergüner, Mahmut S Sağıroğlu, et al.Proceedings of the National Academy of Sciences of the United States of America|March 11, 2008
Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humansTayfun Ozcelik, Nurten Akarsu, Elif Uz, et al.Andrologia|September 4, 2020
Multiscale analysis of SRY-positive 46,XX testicular disorder of sex development: Presentation of nine casesOmer Salih Akar, Sezgin Gunes, Ummet Abur, et al.Cell|April 8, 2017
Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase DisorderAlina Patke, Patricia J Murphy, Onur Emre Onat, et al.European Journal of Human Genetics : EJHG|August 16, 2012
Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotionOnur Emre Onat, Suleyman Gulsuner, Kaya Bilguvar, et al.Pageof 2