Manju Ghosh

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

Risk factors for severe acute lower respiratory tract infection in under-five children.

Shobha Broor, Rudra Pandey, Manju Ghosh et al. · PubMed · 2001 · 155 citations

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

Noncoding Mutations of HGF Are Associated with Nonsyndromic Hearing Loss, DFNB39

Julie M. Schultz, Shaheen N. Khan, Zubair M. Ahmed et al. · The American Journal of Human Genetics · 2009 · 120 citations · Full text

Genetics, Audiology, Pathology +9