Tenesha N. Smith

The first two authors should be regarded as joint first authors

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

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.

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

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

Dominant modifier DFNM1 suppresses recessive deafness DFNB26

S. Riazuddin, Z. Ahmed, S. Riazuddin, 2000, Nature Genetics.

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

S. Riazuddin, S. Riazuddin, A. Griffith, 2001, Cell.

A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome type 2.

A. Lalwani, E. Wilcox, C. Wang, 1998, Molecular and cellular probes.

OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.

C. Petit, S. Chardenoux, T. Friedman, 2000, American journal of human genetics.