
Publications
Human CRY1 variants associate with attention deficit/hyperactivity disorder
Authors: Onat OE, Kars ME, Gul S, Bilguvar K, Wu Y, Ozhan A, Aydin C, Basak AN, Trusso MA, Goracci A, Fallerini C, Renieri A, Casanova JL, Itan Y, Atbasoglu CE, Saka MC, Kavakli H, Ozcelik T.
Journal: Journal of Clinical Investigation (JCI)
Year: 2020
DOI: 10.1172/JCI135500
PMID: 32538895

Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutation
Authors: Demirayak P, Onat OE, Gevrekci AO, Gulsuner S, Uysal H, Bilgen RS, Doerschner K, Ozcelik T, Boyaci H.
Journal: Diagnostic and Interventional Radiology (Diagn Interv Radiol)
Year: 2018
PMID: 30406765

Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder
Authors: Patke A, Murphy PJ, Onat OE, Krieger AC, Ozcelik T, Campbell SS, Young MW.
Journal: Cell Press
Year: 2017
DOI: 10.1016/j.cell.2017.03.027
PMID: 28388406

Meta-analysis of Commonly Mutated Genes in Leptomeningeal Carcinomatosis
Authors: Congur I, Koni E, Onat OE, Tokcaer Keskin Z.
Journal: PeerJ
Year: 2023
DOI: 10.7717/peerj.15250
PMID: 37096065

The genetic structure of the Turkish population reveals high levels of variation and admixture
Authors: Kars ME, Başak AN, Onat OE, Bilguvar K, Choi J, Itan Y, Çağlar C, Palvadeau R, Casanova JL, Cooper DN, Stenson PD, Yavuz A, Buluş H, Günel M, Friedman JM, Özçelik T.
Journal: Proceedings of the National Academy of Sciences (PNAS)
Year: 2021
PMID: 34426522

Multiscale analysis of SRY-positive 46,XX testicular disorder of sex development: Presentation of nine cases
Authors: Akar OS, Gunes S, Abur U, Altundag E, Asci R, Onat OE, Ozcelik T, Ogur G.
Journal: Andrologia
Year: 2020
DOI: 10.1111/and.13739
PMID: 3288206

Genomic landscape of the Greater Middle East

Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis
Authors: Kanaan SB, Onat OE, Balandraud N, Martin GV, Nelson JL, Azzouz DF, Auger I, Arnoux F, Martin M, Roudier J, Ozcelik T, Lambert NC.
Journal: PLoS One
Year: 2016
DOI: 10.1371/journal.pone.0158550
PMID: 27355582

Reply to Tzoulis et al.: Genetic and clinicalheterogeneity of essential tremor
Authors: Unal Gulsuner H, Gulsuner S, Mercan FN, Onat OE, Walsh T, Shahin H, Lee MK, Dogu O, Kansu T, Topaloglu H, Elibol B, Akbostanci C, King MC, Ozcelik T, Tekinay AB.
Journal: Proceedings of the National Academy of Sciences (PNAS)
Year: 2015
PMID: 25825780

Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease
Authors: Unal Gulsuner H, Gulsuner S, Mercan FN, Onat OE, Walsh T, Shahin H, Lee MK, Dogu O, Kansu T, Topaloglu H, Elibol B, Akbostanci C, King MC, Ozcelik T, Tekinay AB.
Journal: Proceedings of the National Academy of Sciences (PNAS)
Year: 2014
PMID: 25422467

Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair
Authors: Dal GM, Erguner B, Sagiroglu MS, Yuksel B, Onat OE, Alkan C, Ozcelik T.
Journal: Journal of Medical Genetics
Year: 2014
DOI: 10.1136/jmedgenet-2013-102197
PMID: 24764354

Disruption of HDX gene in premature ovarian failure
Authors: Okten G, Gunes S, Onat OE,, Tukun A, Ozcelik T, Kocak I.
Journal: Systems Biology in Reproductive Medicine (SBiRM)
Year: 2013
DOI: 10.3109/19396368.2013.769028
PMID: 23441923

Two males with SRY-positive 46,XX testicular disorder of sex development
Authors: Gunes S, Asci R, Okten G, Atac F, Onat OE, Ogur G, Aydin O, Ozcelik T, Bagci H.
Journal: Systems Biology in Reproductive Medicine (SBiRM)
Year: 2012
DOI: 10.3109/19396368.2012.731624
PMID: 23110663

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion
Authors: Onat OE, Gulsuner S, Bilguvar K, Nazli Basak A, Topaloglu H, Tan M, Tan U, Gunel M, Ozcelik T.
Journal: European Journal of Human Genetics
Year: 2012
PMID: 22892528

Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred
Authors: Gulsuner S, Tekinay AB, Doerschner K, Boyaci H, Bilguvar K, Unal H, Ors A, Onat OE, Atalar E, Basak AN, Topaloglu H, Kansu T, Tan M, Tan U, Gunel M, Ozcelik T.
Journal: Genome Research
Year: 2011
PMID: 21885617

Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotion
Authors: Ozcelik T, Akarsu N, Uz E, Caglayan S, Gulsuner S, Onat OE, Tan M, Tan U.
Journal: Proceedings of the National Academy of Sciences (PNAS)
Year: 2008
PMID: 18544652

Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans
Authors: Ozcelik T, Akarsu N, Uz E, Caglayan S, Gulsuner S, Onat OE, Tan M, Tan U
Journal: Proceedings of the National Academy of Sciences (PNAS)
Year: 2008
PMID: 18326629

MDM2 T309G polymorphism is associated with bladder cancer
Authors: Onat OE, Tez M, Ozcelik T, Toruner GA.
Journal: Anticancer Research
Year: 2006
Full Text: https://ar.iiarjournals.org/content/26/5A/3473
PMID: 17094469
