Arabandi Ramesh

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Julie M. Bork, Linda Peters, Saima Riazuddin et al. · The American Journal of Human Genetics · 2001 · 551 citations · Full text

Developmental Biology, Allelic Mutations, Mendelian Disorder +7

Mutations in a Novel Gene, TMIE, Are Associated with Hearing Loss Linked to the DFNB6 Locus

Sadaf Naz, Chantal Giguère, David C. Kohrman et al. · The American Journal of Human Genetics · 2002 · 143 citations · Full text

Developmental Biology, Novel Gene, Genetic Disorder +10

Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human

Nikoletta Charizopoulou, Andrea Lelli, Margit Schraders et al. · Nature Communications · 2011 · 118 citations · Full text

Functional consequences of novel connexin 26 mutations associated with hereditary hearing loss

Ram S. Mani, Aparna Ganapathy, Rajeev Jalvi et al. · European Journal of Human Genetics · 2008 · 83 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +12

Mutations of the<i>RDX</i>gene cause nonsyndromic hearing loss at the<i>DFNB24</i>locus

Shahid Y. Khan, Zubair M. Ahmed, Muhammad Imran Shabbir et al. · Human Mutation · 2007 · 83 citations · Full text

Genetic Disorder, Natural Sciences, Genetics +12