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The genetic structure of the Turkish population reveals high levels of variation and admixture.
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. Kars ME, et al. Among authors: ozcelik t. Proc Natl Acad Sci U S A. 2021 Sep 7;118(36):e2026076118. doi: 10.1073/pnas.2026076118. Proc Natl Acad Sci U S A. 2021. PMID: 34426522 Free PMC article.
Recessive LAMC3 mutations cause malformations of occipital cortical development.
Barak T, Kwan KY, Louvi A, Demirbilek V, Saygı S, Tüysüz B, Choi M, Boyacı H, Doerschner K, Zhu Y, Kaymakçalan H, Yılmaz S, Bakırcıoğlu M, Cağlayan AO, Oztürk AK, Yasuno K, Brunken WJ, Atalar E, Yalçınkaya C, Dinçer A, Bronen RA, Mane S, Ozçelik T, Lifton RP, Sestan N, Bilgüvar K, Günel M. Barak T, et al. Among authors: ozcelik t. Nat Genet. 2011 Jun;43(6):590-4. doi: 10.1038/ng.836. Epub 2011 May 15. Nat Genet. 2011. PMID: 21572413 Free PMC article.
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: ozcelik t. 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.
Disruption of HDX gene in premature ovarian failure.
Okten G, Gunes S, Onat OE, Tukun A, Ozcelik T, Kocak I. Okten G, et al. Among authors: ozcelik t. Syst Biol Reprod Med. 2013 Aug;59(4):218-22. doi: 10.3109/19396368.2013.769028. Epub 2013 Feb 26. Syst Biol Reprod Med. 2013. PMID: 23441923
234 results