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 · 365 citations · Full text

Sleep Disorders, Sleep Medicine, Sleep +10

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 · 136 citations · Full text

Cerebellar Atrophy, Quadrupedal Locomotion, Molecular Physiology +11

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 · 131 citations · Full text

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 · 105 citations · Full text

Neurogenomics, Genetics, Genetic Epidemiology +17

Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindred

Süleyman Gülsüner, Ayşe B. Tekinay, Katja Doerschner et al. · Genome Research · 2011 · 87 citations · Full text