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Paper Details

Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort.
PLoS Genet
3
2023
COL5A1, HMMR, Loss or absence of hearing, Mendelian hearing, Mendelian hearing loss, Mendelian hearing loss genes, NNT, RAPGEF3, TCOF1, age-related hearing loss, candidate genes, congenital deafness, hearing loss, human, syndromic form of congenital hearing loss
Author NameAffiliation
Binglan LiStanford University
Daniel J RaderPerelman School of Medicine, University of Pennsylvania
Daniel J RaderPerelman School of Medicine, University of Pennsylvania
Daniel J RaderInstitute for Translational Medicine and Therapeutics, Perelman School of Medicine, University of Pennsylvania
Marylyn D RitchiePerelman School of Medicine, University of Pennsylvania
Marylyn D RitchieInstitute for Biomedical Informatics, Perelman School of Medicine, University of Pennsylvania
Marylyn D RitchiePerelman School of Medicine, University of Pennsylvania
Marylyn D RitchieInstitute for Biomedical Informatics, Perelman School of Medicine, University of Pennsylvania
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