Suleyman Gulsuner

Infantile onset spinocerebellar ataxia caused by compound heterozygosity for Twinkle mutations and modeling of Twinkle mutations causing recessive disease

Tom Walsh, Augusto Morales, T. Walsh, 2016, Cold Spring Harbor molecular case studies.

Genomic analysis of inherited breast cancer among Palestinian women: Genetic heterogeneity and a founder mutation in TP53

Tom Walsh, Mohammad Salahat, T. Walsh, 2017, International journal of cancer.

Inherited Mutations in Women With Ovarian Carcinoma.

Tom Walsh, Nilsa C Ramirez, Robert S Mannel, 2016, JAMA oncology.

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.

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

Huseyin Boyaci, Katja Doerschner, Ergin Atalar, 2011, Genome research.