P. Menon

The first two authors should be regarded as joint first authors

S. Riazuddin, Z. Ahmed, S. Riazuddin, 2002 .

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

H. Ostrer, B. Keats, S. Riazuddin, 2002, Nature Genetics.

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

J. Lupski, S. Riazuddin, Z. Ahmed, 2001, Human Genetics.

Detection of complex chromosomal rearrangements in a woman with repeated spontaneous abortions

M. Kabra, S. Dubey, R. Mathur, 2001, Acta obstetricia et gynecologica Scandinavica.

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

S. Riazuddin, Z. Ahmed, S. Riazuddin, 2002, Human Genetics.

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

M. Maheshwari, M. Kabra, M. Ghosh, 2003, American journal of medical genetics. Part A.

Is the spectrum of mutations in Indian patients with cystic fibrosis different?

M. Kabra, I. Verma, M. Ghosh, 2000, American journal of medical genetics.