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 · 557 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

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

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 · 414 citations · Full text

Life Sciences, Genetics, Molecular Genetics +6

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 · 300 citations · Full text

Health Professions, Cell Biology, Molecular Biology +16

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 · 284 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +12