Dilip Deshmukh

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

Kiyoto Kurima, Linda Peters, Yandan Yang et al. · Nature Genetics · 2002 · 471 citations · Full text

Novel Gene, Genetic Disorder, Genetics +15

Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC

Zubair M. Ahmed, Tenesha N. Smith, Saima Riazuddin et al. · Human Genetics · 2002 · 175 citations · Full text

Mendelian Disorder, Allelic Mutations, Genetic Disorder +6

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

A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (<i>dn</i>) locus

Pawan Kumar Jain, Kunihiro Fukushima, Dilip Deshmukh et al. · Human Molecular Genetics · 1995 · 67 citations

Genetic Mapping Refines DFNB3 to 17p11.2, Suggests Multiple Alleles of DFNB3, and Supports Homology to the Mouse Model shaker-2

Yong Liang, Aihui Wang, Frank J. Probst et al. · The American Journal of Human Genetics · 1998 · 65 citations · Full text

Mouse Model Shaker-2, Developmental Biology, Supports Homology +10