Nabil Moghrabi

Deficient 17β-Hydroxysteroid Dehydrogenase Type 2 Expression in Endometriosis: Failure to Metabolize 17β-Estradiol¹

Khaled Zeitoun, Kazuto Takayama, Hironobu Sasano et al. · The Journal of Clinical Endocrinology & Metabolism · 1998 · 312 citations · Full text

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 · 296 citations · Full text

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 · 276 citations · Full text

Sequencing, Next-generation Sequencing, Genetics +8

A Role for the deep orange and carnation Eye Color Genes in Lysosomal Delivery in Drosophila

Evgueni A. Sevrioukov, Jing-Ping He, Nabil Moghrabi et al. · Molecular Cell · 1999 · 206 citations · Full text

Biology, Genetics, Genomic Mechanism +7

Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias

Douglas J. Clarke, Nabil Moghrabi, Gemma Monaghan et al. · Clinica Chimica Acta · 1997 · 139 citations

Allelic Variant, Mendelian Disorder, Genetic Disorder +9