Saima Riazuddin
University of Maryland, Baltimore(US)Cincinnati Children's Hospital Medical Center(US)Johns Hopkins University(US)Johns Hopkins Medicine(US)University of Cincinnati Medical Center(US)
Publications by Year
Research Areas
Hearing, Cochlea, Tinnitus, Genetics, Connexins and lens biology, Vestibular and auditory disorders, Retinal Development and Disorders, Ear Surgery and Otitis Media
Most-Cited Works
- → Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23(2001)552 cited
- → Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function(2002)473 cited
- → Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F(2001)413 cited
- → The Tip-Link Antigen, a Protein Associated with the Transduction Complex of Sensory Hair Cells, Is Protocadherin-15(2006)297 cited
- → Tricellulin Is a Tight-Junction Protein Necessary for Hearing(2006)282 cited
- → Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48(2012)247 cited