Saima Riazuddin

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Julie M. Bork, Linda Peters, Saima Riazuddin et al. · The American Journal of Human Genetics · 2001 · 551 citations · Full text

Developmental Biology, Allelic Mutations, Mendelian Disorder +7

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

Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

Zubair M. Ahmed, Saima Riazuddin, Steven L. Bernstein et al. · The American Journal of Human Genetics · 2001 · 412 citations · Full text

Genetic Disorder, Genetics, Pathogenesis +4

The Tip-Link Antigen, a Protein Associated with the Transduction Complex of Sensory Hair Cells, Is Protocadherin-15

Zubair M. Ahmed, Richard J. Goodyear, Saima Riazuddin et al. · Journal of Neuroscience · 2006 · 297 citations · Full text

Tricellulin Is a Tight-Junction Protein Necessary for Hearing

Saima Riazuddin, Zubair M. Ahmed, Alan S. Fanning et al. · The American Journal of Human Genetics · 2006 · 282 citations · Full text

Audiology, Auditory Physiology, Cytoskeleton +10