Tarfa Al‐Sheddi

Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes

Hanan E. Shamseldin, Muneera Alshammari, Tarfa Al‐Sheddi et al. · Journal of Medical Genetics · 2012 · 180 citations

The genetic landscape of familial congenital hydrocephalus

Ranad Shaheen, Mohammed Adeeb Sebai, Nisha Patel et al. · Annals of Neurology · 2017 · 144 citations

Recessive Mutations in DOCK6, Encoding the Guanidine Nucleotide Exchange Factor DOCK6, Lead to Abnormal Actin Cytoskeleton Organization and Adams-Oliver Syndrome

Ranad Shaheen, Eissa Faqeih, Asma Sunker et al. · The American Journal of Human Genetics · 2011 · 139 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +6

Genomic and phenotypic delineation of congenital microcephaly

Ranad Shaheen, Sateesh Maddirevula, Nour Ewida et al. · Genetics in Medicine · 2018 · 120 citations · Full text

Developmental Anomaly, Developmental Biology, Brain Development +7

Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay

Moeenaldeen AlSayed, Hamad Alzaidan, Albandary AlBakheet et al. · The American Journal of Human Genetics · 2013 · 119 citations

Cognitive Delay, Mendelian Disorder, Speech Impairment +8