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 · 476 citations · Full text

Medicine, Genetics, Molecular Genetics +16

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 · 176 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

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

Medicine, Infectious Diseases, Pediatrics +17

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

Life Sciences, Audiology, Genetics +9

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

Medicine, Genetics, Molecular Genetics +11