Publications

2003 publications of the Riazuddin and Ahmed labs.

Ahmed ZM, Morell RJ, Riazuddin S, Gropman A, Shaukat S, Ahmad MM, Mohiddin SA, Fananapazir L, Caruso RC, Husnain T, Khan SN, Riazuddin S, Griffith AJ, Friedman TB, Wilcox ER. (2003)
Mutations of MYO6 are associated with recessive deafness DFNB37.
Am J Hum Genet 72:1315–1322
Ben-Yosef T, Ness SL, Madeo AC, Bar-Lev A, Wolfman JH, Ahmed ZM, Desnick RJ, Avraham KB, Ostrer H, Oddoux C, Griffith AJ, Friedman TB. (2003)
A prevalent founder mutation of PCDH15 among deaf-blind Ashkenazi jews with Usher syndrome type 1.
N Engl J Med 348:1664-1670
Ahmed ZM, Riazuddin S, Ahmad J, Bernstein SL, Guo Y, Sabir MF, Sieving P, Riazuddin S, Griffith AJ, Friedman TB, Belyantseva IA, Wilcox ER. (2003)
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.
Hum Mol Genet 12(24):3215-3223
Park HJ, Shaukat S, Liu XZ, Hahn SH, Naz S, Ghosh M, Kim HN, Moon SK, Abe S, Tukamoto K, Riazuddin S, Kabra M, Erdenetungalag R, Radnaabazar J, Khan S, Pandya A, Usami SI, Nance WE, Wilcox ER, Riazuddin S, Griffith AJ. (2003)
Origin and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.
J Med Genet 40:242-48
Naz S, Alastii F, Mowjoodi A, Riazuddin S, Sanati MH, Friedman TB, Griffith AJ, Wilcox ER, Riazuddin S. (2003)
Distinctive audiometric profiles associated with DFNB21 alleles of TECTA.
J Med Genet 40:360-63