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Disease Markers|June 20, 2015
Association of PRPS1 Mutations with Disease PhenotypesRahul Mittal, Kunal Patel, Jeenu Mittal, et al.
American Journal of Otolaryngology|September 22, 2023
Chemosensory function recovery in COVID-19 patients: A cross-sectional studyAria Nawab, Aura Acosta, Corinna G Levine, et al.
Genetic Testing and Molecular Biomarkers|January 25, 2011
Mutation screening of the GJA7 (Cx45) gene in a large international series of probands with nonsyndromic hearing impairmentXiao Mei Ouyang, Denise Yan, Idil Aslan, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 3, 2020
MITF Is Mutated in Type 1 Waardenburg Syndrome With Unusual PhenotypeWu Li, Yong Feng, Hongsheng Chen, et al.
Genetic Testing and Molecular Biomarkers|September 29, 2020
Screening Consanguineous Families for Hearing Loss Using the MiamiOtoGenes PanelAbhiraami Kannan-Sundhari, Denise Yan, Kolsoum Saeidi, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|December 2, 2014
Immunity genes and susceptibility to otitis media: a comprehensive reviewRahul Mittal, Giannina Robalino, Robert Gerring, et al.
Children (Basel, Switzerland)|February 27, 2026
Increasing Genetic Testing Uptake Through Workflow Optimization: A Quality Improvement Study in Pediatric Hearing LossJennifer Coto, Julia Anne Morris, Valerie Yunis, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|December 3, 2014
Role of innate immunity in the pathogenesis of otitis mediaRahul Mittal, Joyson Kodiyan, Robert Gerring, et al.
The Laryngoscope|August 19, 2025
RNA Sequencing Provides Insight Into Idiopathic Subglottic StenosisMursalin M Anis, Anthony J Griswold, Ahmed M S Soliman, et al.
Journal of Human Genetics|November 3, 2009
Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type IIDenise Yan, Xiaomei Ouyang, D Michael Patterson, et al.
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