Concepedia

Shaheen N. Khan

SN

Statistics

Publications

80

Citations

5.7K

H-Index

39

Active since

2001

Affiliations

Centre of Excellence in Molecular Biology(Current)

University of the Punjab

Allama Iqbal Medical College

University of Health Sciences Lahore

National Institutes of Health

Shaheen N. Khan is an author at Centre of Excellence in Molecular Biology specializing in genetics, molecular genetics, and life sciences.

Publications per year

2001–2018

80

Publications

80

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

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Null Mutations in LTBP2 Cause Primary Congenital Glaucoma

Manir Ali, Martin McKibbin, Adam Booth et al. · The American Journal of Human Genetics · 2009 · 325 citations · Full text

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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

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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 · 249 citations · Full text

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Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Emma M. Jenkinson, Atteeq U. Rehman, Tom Walsh et al. · The American Journal of Human Genetics · 2013 · 245 citations · Full text

, , +10

1–5 of 80