P.S.N. Menon

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

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

Screening of families with autosomal recessive non‐syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario

M. Maheshwari, R. Vijaya, Manju Ghosh et al. · American Journal of Medical Genetics Part A · 2003 · 68 citations

Life Sciences, Genetics, Molecular Genetics +14

Characterisation of mutations and genotype–phenotype correlation in cystic fibrosis: Experience from India

Shivaram Shastri, Madhulika Kabra, Sushil Kumar Kabra et al. · Journal of Cystic Fibrosis · 2007 · 52 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12