Aziza Chedrawi

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes

Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed et al. · Human Genetics · 2017 · 309 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population

Dorota Monies, Mohammed Abouelhoda, Mirna Assoum et al. · The American Journal of Human Genetics · 2019 · 283 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Autozygome and high throughput confirmation of disease genes candidacy

Sateesh Maddirevula, Fatema Alzahrani, Mohammed Al‐Owain et al. · Genetics in Medicine · 2018 · 118 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Loss of the Potassium Channel β‐Subunit Gene, <i>KCNAB2</i>, Is Associated with Epilepsy in Patients with 1p36 Deletion Syndrome

Heidi A. Heilstedt, Daniel L. Burgess, Anne E. Anderson et al. · Epilepsia · 2001 · 92 citations

Life Sciences, Genetics, Molecular Genetics +17

A novel X‐linked disorder with developmental delay and autistic features

Namik Kaya, Dilek Çolak, Albandary AlBakheet et al. · Annals of Neurology · 2011 · 74 citations

Life Sciences, Genetics, Molecular Genetics +17