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Rabia Faridi
Rabia Faridi
NIDCD, NIH
Verified email at nih.gov
Title
Cited by
Cited by
Year
Oncogenic potential of Human Papillomavirus (HPV) and its relation with cervical cancer
R Faridi, A Zahra, K Khan, M Idrees
Virology Journal 8, 1-8, 2011
3302011
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness
AU Rehman, JE Bird, R Faridi, M Shahzad, S Shah, K Lee, SN Khan, ...
Human mutation 37 (10), 991-1003, 2016
862016
Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss
EM Richard, RLP Santos‐Cortez, R Faridi, AU Rehman, K Lee, ...
Human mutation 40 (1), 53-72, 2019
612019
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome
R Faridi, AU Rehman, RJ Morell, PL Friedman, L Demain, S Zahra, ...
Clinical genetics 91 (2), 328-332, 2017
532017
Autosomal-recessive hearing impairment due to rare missense variants within S1PR2
RLP Santos-Cortez, R Faridi, AU Rehman, K Lee, M Ansar, X Wang, ...
The American Journal of Human Genetics 98 (2), 331-338, 2016
522016
Mutational and phenotypic spectra of KCNE1 deficiency in Jervell and Lange‐Nielsen Syndrome and Romano‐Ward Syndrome
R Faridi, R Tona, A Brofferio, M Hoa, R Olszewski, I Schrauwen, ...
Human mutation 40 (2), 162-176, 2019
332019
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder
R Faridi, A Rea, C Fenollar-Ferrer, RT O’Keefe, S Gu, Z Munir, AA Khan, ...
Human Genetics 141 (3), 805-819, 2022
262022
Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome
TT Wafa, R Faridi, KA King, C Zalewski, R Yousaf, JM Schultz, RJ Morell, ...
Clinical Genetics 99 (2), 226-235, 2021
222021
Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness
R Tona, IA Lopez, C Fenollar-Ferrer, R Faridi, C Anselmi, AA Khan, ...
Genes 11 (10), 1122, 2020
152020
Variants of human CLDN9 cause mild to profound hearing loss
M Ramzan, C Philippe, IA Belyantseva, Y Nakano, C Fenollar‐Ferrer, ...
Human mutation 42 (10), 1321-1335, 2021
82021
Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria
A Adeyemo, R Faridi, P Chattaraj, R Yousaf, R Tona, S Okorie, ...
European Journal of Human Genetics 30 (1), 42-52, 2022
72022
Variants of LRP2, encoding a multifunctional cell‐surface endocytic receptor, associated with hearing loss and retinal dystrophy
R Faridi, R Yousaf, S Gu, S Inagaki, AE Turriff, K Pelstring, B Guan, A Naik, ...
Clinical genetics 103 (6), 699-703, 2023
32023
PERILS OF EUTROPHICATION AND SPATIO-TEMPORAL DYNAMICS OF LAKE KALAR KAHAR, POTOHAR PLEATUE, SALT RANGE, PAKISTAN.
K KHAN, M Ikram, R FARIDI, R Amjad
Science International 27 (4), 2015
22015
Genetics of yield components for drought tolerant wheat (Triticum aestivum L.) genotypes
S Ashraf, I Khaliq, S Malook, SA Qasrani, S Jabeen, R Faridi, HM Ahmad, ...
Int. J. Biol. Sci 6, 21-34, 2015
22015
Climate Change Effect On The Hunza Lake And Geomorphologic Status Of The Hunza River Basin, Gilgit-Baltistan, Pakistan
K Khan, CM Ashraf, R Faridi
14th World Lake Conference, Austin 31, 2011
22011
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome.
R Faridi, P Stratton, N Salmeri, RJ Morell, AA Khan, MA Usmani, ...
Clinical Genetics, 2024
12024
Bulk segregant analysis of tomato to identify polymorphism associated with tomato-Phytoplasma solani interaction using RNA-sequencing data
MA Sarwar, SH Khan, R Faridi, M Jamil, DJ Norman, GS Ali, Z Afzal
2023
Deafness DFNB110 associated with a human MAP3K1 recessive variant recapitulates hearing loss of Map3k1 kinase deficient mice
R Faridi, R Yousaf, S Inagaki, R Olszewski, S Gu, RJ Morell, E Wilson, ...
2023
Molecular Characterization of Syndromic and Nonsyndromic forms of Deafness using Molecular Genetic Approaches
R Faridi
University of the Punjab, Lahore, 2018
2018
Influence of Different Dosages of Electron Beam Irradiation on Microbial Load and Physiochemical Attributes of Radix Ophiopogonis (Ophiopogon Japonicas)
DK Manghwani, MK Rathore, D Wang, AM Abeera, MB Mahmooda, ...
Available at SSRN 4820174, 0
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