Nurten Akarsu

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

Tayfun Ozcelik, Uner Tan, E. Uz, 2008, Proceedings of the National Academy of Sciences.

Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly

Naoto Endo, Peter Heutink, Minoru Shibata, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome

Han G. Brunner, Hülya Kayserili, Flemming Skovby, 2000, Nature Genetics.