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

Por Ozcelik, Tayfun, Akarsu, Nurten, Uz, Elif, Caglayan, Safak, Gulsuner, Suleyman, Onat, Onur Emre, Tan, Meliha, Tan, Uner
Publicado em 2008

Reply to Herz et al. and Humphrey et al.: Genetic heterogeneity of cerebellar hypoplasia with quadrupedal locomotion

Por Ozcelik, Tayfun, Akarsu, Nurten, Uz, Elif, Caglayan, Safak, Gulsuner, Suleyman, Onat, Onur Emre, Tan, Meliha, Tan, Uner
Publicado em 2008

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

Por Patke, Alina, Murphy, Patricia J., Onat, Onur Emre, Krieger, Ana C., Özçelik, Tayfun, Campbell, Scott S., Young, Michael W.
Publicado no Cell (2017)

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

Por Unal Gulsuner, Hilal, Gulsuner, Suleyman, Mercan, Fatma Nazli, Onat, Onur Emre, Walsh, Tom, Shahin, Hashem, Lee, Ming K., Dogu, Okan, Kansu, Tulay, Topaloglu, Haluk, Elibol, Bulent, Akbostanci, Cenk, King, Mary-Claire, Ozcelik, Tayfun, Tekinay, Ayse B.
Publicado no Proc Natl Acad Sci U S A (2014)

Reply to Tzoulis et al.: Genetic and clinical heterogeneity of essential tremor

Por Unal Gulsuner, Hilal, Gulsuner, Suleyman, Mercan, Fatma Nazli, Onat, Onur Emre, Walsh, Tom, Shahin, Hashem, Lee, Ming K., Dogu, Okan, Kansu, Tulay, Topaloglu, Haluk, Elibol, Bulent, Akbostanci, Cenk, King, Mary-Claire, Ozcelik, Tayfun, Tekinay, Ayse B.
Publicado no Proc Natl Acad Sci U S A (2015)