Edward Cohn

GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study

Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann et al. · The American Journal of Human Genetics · 2005 · 551 citations · Full text

Genetic Disorder, Genetics, Audiology +9

Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children

William J. Kimberling, Michael S. Hildebrand, A. Eliot Shearer et al. · Genetics in Medicine · 2010 · 268 citations · Full text

Early Diagnosis, Pediatric Otolaryngology, Pediatric Audiology +10

Clinical Studies of Families With Hearing Loss Attributable to Mutations in the Connexin 26 Gene (GJB2/DFNB1)

Edward Cohn, Philip M. Kelley, Thomas W. Fowler et al. · PEDIATRICS · 1999 · 201 citations

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele

Renée Varga, Matthew R. Avenarius, Philip M. Kelley et al. · Journal of Medical Genetics · 2005 · 166 citations · Full text

Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss

Edward Cohn, Philip M. Kelley · American Journal of Medical Genetics · 1999 · 141 citations