Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits

by Gaurav Thareja, Yasser Al-Sarraj, Aziz Belkadi, Maryam Almotawa, The Qatar Genome Program Research (QGPR) Consortium, Karsten Suhre, Omar M. E. Albagha
Published 2021-02-01

A Novel Missense Mutation in Causes Congenital Disorder of Glycosylation Type I (Cerebello-Ocular Syndrome)

by Yasser Al-Sarraj BSC, Tawfeg Ben-Omran MD, Mohammed Tolefat MBBS, Yosra Bejaoui MSc, Hatem El-Shanti MD, Marios Kambouris PhD
Published 2014-09-01

Heterozygous PDGFRB Mutation in a Three-generation Family with Autosomal Dominant Infantile Myofibromatosis

by Clemence Lepelletier, Yasser Al-Sarraj, Christine Bodemer, Hibbah Shaath, Sylvie Fraitag, Marios Kambouris, Dominique Hamel-Teillac, Hatem El Shanti, Smail Hadj-Rabia
Published 2017-04-01

Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families

by Yasser Al-Sarraj, Eman Al-Dous, Rowaida Z. Taha, Dina Ahram, Fouad Alshaban, Mohammed Tolfat, Hatem El-Shanti, Omar M.E. Albagha
Published 2021-05-01