Onur Emre Onat

Mutation of the Human Circadian Clock Gene CRY1 in Familial Delayed Sleep Phase Disorder

Alina Patke, Patricia Murphy, Onur Emre Onat et al. · Cell · 2017 · 376 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

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

Onur Emre Onat, Süleyman Gülsüner, Kaya Bilgüvar et al. · European Journal of Human Genetics · 2012 · 137 citations · Full text

Life Sciences, Genetics, Neurology +14

Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease

Hilal Ünal Gülsüner, Süleyman Gülsüner, Fatma Nazlı Mercan et al. · Proceedings of the National Academy of Sciences · 2014 · 135 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Mutations in the very low-density lipoprotein receptor <i>VLDLR</i> cause cerebellar hypoplasia and quadrupedal locomotion in humans

Tayfun Özçelık, Nurten Akarsu, Elif Uz et al. · Proceedings of the National Academy of Sciences · 2008 · 107 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

The genetic structure of the Turkish population reveals high levels of variation and admixture

Meltem Ece Kars, A. Nazlı Başak, Onur Emre Onat et al. · Proceedings of the National Academy of Sciences · 2021 · 92 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15