Saima Anwar

Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

Saima Riazuddin, Inna A. Belyantseva, Arnaud P. J. Giese et al. · Nature Genetics · 2012 · 247 citations · Full text

Nonsyndromic Deafness Dfnb48, Type 1J, Signal Transduction +7

SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis

Saima Anwar, Saima Riazuddin, Zubair M. Ahmed et al. · Journal of Human Genetics · 2009 · 98 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7

Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome

Zubair M. Ahmed, Saima Riazuddin, Sandar Aye et al. · Human Genetics · 2008 · 95 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +9

Molecular Basis of DFNB73: Mutations of BSND Can Cause Nonsyndromic Deafness or Bartter Syndrome

Saima Riazuddin, Saima Anwar, Martin Fischer et al. · The American Journal of Human Genetics · 2009 · 86 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2–q13.3

Shahid Y. Khan, Saima Riazuddin, Muhammad Tariq et al. · Human Genetics · 2006 · 30 citations

Chromosome 11Q13.2–q13.3, Mendelian Disorder, Genetic Disorder +4