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 | 330 | 2011 |
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 | 86 | 2016 |
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 | 61 | 2019 |
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 | 53 | 2017 |
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 | 52 | 2016 |
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 | 33 | 2019 |
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 | 26 | 2022 |
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 | 22 | 2021 |
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 | 15 | 2020 |
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 | 8 | 2021 |
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 | 7 | 2022 |
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 | 3 | 2023 |
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 | 2 | 2015 |
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 | 2 | 2015 |
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 | 2 | 2011 |
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 | 1 | 2024 |
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 | | |