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Genomic landscape of the Greater Middle East.
Özçelik T, Onat OE. Özçelik T, et al. Among authors: onat oe. Nat Genet. 2016 Aug 30;48(9):978-9. doi: 10.1038/ng.3652. Nat Genet. 2016. PMID: 27573686
Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred.
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. Gulsuner S, et al. Among authors: onat oe. Genome Res. 2011 Dec;21(12):1995-2003. doi: 10.1101/gr.126110.111. Epub 2011 Sep 1. Genome Res. 2011. PMID: 21885617 Free PMC article. Clinical Trial.
Human CRY1 variants associate with attention deficit/hyperactivity disorder.
Onat OE, Kars ME, Gül Ş, Bilguvar K, Wu Y, Özhan A, Aydın C, Başak AN, Trusso MA, Goracci A, Fallerini C, Renieri A, Casanova JL, Itan Y, Atbaşoğlu CE, Saka MC, Kavaklı İH, Özçelik T. Onat OE, et al. J Clin Invest. 2020 Jul 1;130(7):3885-3900. doi: 10.1172/JCI135500. J Clin Invest. 2020. PMID: 32538895 Free PMC article. Clinical Trial.
Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease.
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. Unal Gulsuner H, et al. Among authors: onat oe. Proc Natl Acad Sci U S A. 2014 Dec 23;111(51):18285-90. doi: 10.1073/pnas.1419581111. Epub 2014 Nov 24. Proc Natl Acad Sci U S A. 2014. PMID: 25422467 Free PMC article.
17 results