M. Almuriekhi

Biallelic Mutations in TMTC3, Encoding a Transmembrane and TPR-Containing Protein, Lead to Cobblestone Lissencephaly.

J. Al-Aama, K. Campbell, E. Dikoglu, 2016, American journal of human genetics.

Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features.

Z. Nawaz, T. Shintani, M. Noda, 2015, Cell reports.

Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome

Z. Nawaz, V. Tropepe, J. Nadaf, 2015, Journal of Medical Genetics.

Whole exome sequencing unravels disease‐causing genes in consanguineous families in Qatar

Z. Nawaz, J. Majewski, J. Schwartzentruber, 2014, Clinical genetics.