Tenesha N. Smith

Mutations in the Gene Encoding Tight Junction Claudin-14 Cause Autosomal Recessive Deafness DFNB29

Edward R. Wilcox, Quianna Burton, Sadaf Naz et al. · Cell · 2001 · 437 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +7

OTOF Encodes Multiple Long and Short Isoforms: Genetic Evidence That the Long Ones Underlie Recessive Deafness DFNB9

Shin’ichiro Yasunaga, M’hamed Grati, Sébastien Chardenoux et al. · The American Journal of Human Genetics · 2000 · 203 citations · Full text

Developmental Biology, Short Isoforms, Genetic Disorder +11

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

Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome

Nikki Liburd, Manju Ghosh, Saima Riazuddin et al. · Human Genetics · 2001 · 148 citations · Full text

Mendelian Disorder, Genetic Disorder, Novel Mutations +6

Dominant modifier DFNM1 suppresses recessive deafness DFNB26

Saima Riazuddin, Caley M. Castelein, Zubair M. Ahmed et al. · Nature Genetics · 2000 · 139 citations

Mendelian Disorder, Genetic Disorder, Genetics +5