Rabia Faridi

Mutational Spectrum of<i>MYO15A</i>and the Molecular Mechanisms of DFNB3 Human Deafness

Atteeq U. Rehman, Jonathan E. Bird, Rabia Faridi et al. · Human Mutation · 2016 · 84 citations · Full text

Genetics, Molecular Biology, Molecular Genetics +18

Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss

Élodie M. Richard, Regie Lyn P. Santos‐Cortez, Rabia Faridi et al. · Human Mutation · 2018 · 84 citations

Genetics, Genetic Epidemiology, Consanguineous Pakistani Families +20

Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2

Regie Lyn P. Santos‐Cortez, Rabia Faridi, Atteeq U. Rehman et al. · The American Journal of Human Genetics · 2016 · 51 citations · Full text

Genetic Disorder, Genetics, Audiology +10

Mutations of <i><scp>SGO2</scp></i> and <i><scp>CLDN14</scp></i> collectively cause coincidental Perrault syndrome

Rabia Faridi, Atteeq U. Rehman, Robert J. Morell et al. · Clinical Genetics · 2016 · 49 citations · Full text

Coincidental Perrault Syndrome, Rare Diseases, Genome Instability +13

FUNCTIONS OF PLANT’S BZIP TRANSCRIPTION FACTORS

Zulfiqar Ali, Syeda Samara Sarwat, Ihsan Karim et al. · The Pakistan Journal of Agricultural Sciences · 2016 · 37 citations · Full text