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Elife|November 9, 2021
Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndromeSaumil Sethna, Wadih M Zein, Sehar Riaz, et al.
BMC Medicine|January 8, 2025
Pharmacological treatment in autism: a proposal for guidelines on common co-occurring psychiatric symptomsMariah A Manter, Kirstin B Birtwell, James Bath, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|March 20, 2012
Immune response in melanoma: an in-depth analysis of the primary tumor and corresponding sentinel lymph nodeMichelle W Ma, Ratna C Medicherla, Meng Qian, et al.
American Journal of Human Genetics|December 23, 2006
Tricellulin is a tight-junction protein necessary for hearingSaima Riazuddin, Zubair M Ahmed, Alan S Fanning, et al.
Frontiers in Aging|December 19, 2023
Examining provider perceptions and practices for comprehensive geriatric assessment among cancer survivors: a qualitative study with an implementation science focusAaron T Seaman, Julia H Rowland, Samantha J Werts, et al.
Human Mutation|January 18, 2007
Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locusShahid Y Khan, Zubair M Ahmed, Muhammad I Shabbir, et al.
European Journal of Human Genetics : EJHG|November 27, 2021
Genomic analysis of childhood hearing loss in the Yoruba population of NigeriaAdebolajo Adeyemo, Rabia Faridi, Parna Chattaraj, et al.
Clinical Genetics|September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.
Clinical Genetics|October 22, 2020
Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndromeTalah T Wafa, Rabia Faridi, Kelly A King, et al.
Genes|September 29, 2020
Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving DeafnessRisa Tona, Ivan A Lopez, Cristina Fenollar-Ferrer, et al.
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