Onat OE - Search Results

1

Evaluation of X Chromosome Inactivation with Respect to HLA Genetic Susceptibility in Rheumatoid Arthritis and Systemic Sclerosis.

Kanaan SB, Onat OE, Balandraud N, Martin GV, Nelson JL, Azzouz DF, Auger I, Arnoux F, Martin M, Roudier J, Ozcelik T, Lambert NC. Kanaan SB, et al. Among authors: onat oe. PLoS One. 2016 Jun 29;11(6):e0158550. doi: 10.1371/journal.pone.0158550. eCollection 2016. PLoS One. 2016. PMID: 27355582 Free PMC article.

2

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

3

MDM2 T309G polymorphism is associated with bladder cancer.

Onat OE, Tez M, Ozçelik T, Törüner GA. Onat OE, et al. Anticancer Res. 2006 Sep-Oct;26(5A):3473-5. Anticancer Res. 2006. PMID: 17094469 Free article.

4

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: onat oe. 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

5

Multiscale analysis of SRY-positive 46,XX testicular disorder of sex development: Presentation of nine cases.

Akar OS, Gunes S, Abur U, Altundag E, Asci R, Onat OE, Ozcelik T, Ogur G. Akar OS, et al. Among authors: onat oe. Andrologia. 2020 Dec;52(11):e13739. doi: 10.1111/and.13739. Epub 2020 Sep 3. Andrologia. 2020. PMID: 32882067

6

Two males with SRY-positive 46,XX testicular disorder of sex development.

Gunes S, Asci R, Okten G, Atac F, Onat OE, Ogur G, Aydin O, Ozcelik T, Bagci H. Gunes S, et al. Among authors: onat oe. Syst Biol Reprod Med. 2013 Feb;59(1):42-7. doi: 10.3109/19396368.2012.731624. Epub 2012 Oct 30. Syst Biol Reprod Med. 2013. PMID: 23110663

7

Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion.

Onat OE, Gulsuner S, Bilguvar K, Nazli Basak A, Topaloglu H, Tan M, Tan U, Gunel M, Ozcelik T. Onat OE, et al. Eur J Hum Genet. 2013 Mar;21(3):281-5. doi: 10.1038/ejhg.2012.170. Epub 2012 Aug 15. Eur J Hum Genet. 2013. PMID: 22892528 Free PMC article.

8

Early postzygotic mutations contribute to de novo variation in a healthy monozygotic twin pair.

Dal GM, Ergüner B, Sağıroğlu MS, Yüksel B, Onat OE, Alkan C, Özçelik T. Dal GM, et al. Among authors: onat oe. J Med Genet. 2014 Jul;51(7):455-9. doi: 10.1136/jmedgenet-2013-102197. Epub 2014 Apr 24. J Med Genet. 2014. PMID: 24764354

9

Mutations in the very low-density lipoprotein receptor VLDLR cause cerebellar hypoplasia and quadrupedal locomotion in humans.

Ozcelik T, Akarsu N, Uz E, Caglayan S, Gulsuner S, Onat OE, Tan M, Tan U. Ozcelik T, et al. Among authors: onat oe. Proc Natl Acad Sci U S A. 2008 Mar 18;105(11):4232-6. doi: 10.1073/pnas.0710010105. Epub 2008 Mar 7. Proc Natl Acad Sci U S A. 2008. PMID: 18326629 Free PMC article.

10

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.

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