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List of works by Rabia Faridi

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

scientific article published on 19 January 2016

Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria

scientific article published in 2021

Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss

article

Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness

scientific article published on 24 September 2020

Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness

scientific article

Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome

scientific article published on 12 December 2018

Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.

scientific article

Variants of <scp><i>LRP2</i></scp>, encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy

scientific article published in 2023

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