Concepedia

Sabiha Nazli

SN

Statistics

Publications

4

Citations

362

H-Index

4

Active since

2005

Affiliations

Centre of Excellence in Molecular Biology(Current)

National Institute on Deafness and Other Communication Disorders

National Institutes of Health

University of the Punjab

Sabiha Nazli is an author at Centre of Excellence in Molecular Biology specializing in life sciences, genetics, and molecular genetics.

Publications per year

2005–2015

4

Publications

4

Mutations of Human NARS2, Encoding the Mitochondrial Asparaginyl-tRNA Synthetase, Cause Nonsyndromic Deafness and Leigh Syndrome

Mariella Simon, Élodie M. Richard, Xinjian Wang et al. · PLoS Genetics · 2015 · 113 citations · Full text

, , +17

Mutations in TRIOBP, Which Encodes a Putative Cytoskeletal-Organizing Protein, Are Associated with Nonsyndromic Recessive Deafness

Saima Riazuddin, Shaheen N. Khan, Zubair M. Ahmed et al. · The American Journal of Human Genetics · 2005 · 110 citations · Full text

, , +10

Mutation spectrum of<i>MYO7A</i>and evaluation of a novel nonsyndromic deafness<i>DFNB2</i>allele with residual function

Saima Riazuddin, Sabiha Nazli, Zubair M. Ahmed et al. · Human Mutation · 2008 · 106 citations

, , +15

The autosomal recessive nonsyndromic deafness locus DFNB72 is located on chromosome 19p13.3

Qurat Ul Ain, Sabiha Nazli, Saima Riazuddin et al. · Human Genetics · 2007 · 33 citations

, , +11

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