Rabia Faridi - Concepedia

Author

Rabia Faridi

National Institute on Deafness and Other Communication Disorders ORCID

Also Known As

Faridi, Rabia, R FARIDI, R. Faridi, Rabia Faridi Faridi, Rabia Faridi

Publications

700

Citations

H-Index

Concepts

All Affiliations

National Institute on Deafness and Other Communication Disorders National Institutes of Health University of the Punjab Jinnah Postgraduate Medical Center Centre of Excellence in Molecular Biology

About

Rabia Faridi is an author at National Institute on Deafness and Other Communication Disorders specializing in medicine, genetics, and auditory research.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	316
2	Arts	2	2	135
3	Health Sciences	1	1	84
4	Biology	1	1	13
5	Microbiology	1	1	13

Rabia Faridi

Publications

444

Citations

H-Index

Page 1

	Year	Citations
Mutational Spectrum of<i>MYO15A</i>and the Molecular Mechanisms of DFNB3 Human Deafness Atteeq U. Rehman, Jonathan E. Bird, Rabia Faridi, Human Mutation GeneticsMolecular BiologyMolecular GeneticsDisease Gene IdentificationHair Cells	2016	84
Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss Élodie M. Richard, Regie Lyn P. Santos‐Cortez, Rabia Faridi, Human Mutation GeneticsGenetic EpidemiologyConsanguineous Pakistani FamiliesPathologyGene Discovery	2018	84
Autosomal-Recessive Hearing Impairment Due to Rare Missense Variants within S1PR2 Regie Lyn P. Santos‐Cortez, Rabia Faridi, Atteeq U. Rehman, The American Journal of Human Genetics Genetic DisorderGeneticsAudiologyAuditory PhysiologyRare Missense Variants	2016	51
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, Clinical Genetics Coincidental Perrault SyndromeRare DiseasesGenome InstabilityMendelian DisorderGenetic Disorder	2016	49
FUNCTIONS OF PLANT’S BZIP TRANSCRIPTION FACTORS Zulfiqar Ali, Syeda Samara Sarwat, Ihsan Karim, The Pakistan Journal of Agricultural Sciences	2016	37
Mutational and phenotypic spectra of <i>KCNE1</i> deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome Rabia Faridi, Risa Tona, Alessandra Brofferio, Human Mutation Cardiac MuscleLange‐nielsen SyndromeGeneticsSudden DeathMolecular Biology	2018	35
Vestibular <scp>phenotype‐genotype</scp> correlation in a cohort of 90 patients with Usher syndrome Talah Wafa, Rabia Faridi, Kelly King, Clinical Genetics	2020	35
Variants of <scp> <i>LRP2</i> </scp> , encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy Rabia Faridi, Rizwan Yousaf, Shoujun Gu, Clinical Genetics	2023	23
Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness Risa Tona, Iván A. López, Cristina Fenollar‐Ferrer, Genes	2020	18
Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria Adebolajo A. Adeyemo, Rabia Faridi, Parna Chattaraj, European Journal of Human Genetics	2021	15

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