Saad AlShahwan

Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families

Anas M. Alazami, Nisha Patel, Hanan E. Shamseldin et al. · Cell Reports · 2014 · 472 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

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

Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase

Valeria Massa, Erika Fernández‐Vizarra, Saad AlShahwan et al. · The American Journal of Human Genetics · 2008 · 193 citations · Full text

Life Sciences, Genetics, Neuroscience +13

Characterizing the morbid genome of ciliopathies

Ranad Shaheen, Katarzyna Szymańska, Basudha Basu et al. · Genome biology · 2016 · 165 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Genomic and phenotypic delineation of congenital microcephaly

Ranad Shaheen, Sateesh Maddirevula, Nour Ewida et al. · Genetics in Medicine · 2018 · 124 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14