Atteeq U. Rehman

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Publications

Citations

1.8K

H-Index

Active since

2009

Affiliations

National Institute on Deafness and Other Communication Disorders(Current)

National Institutes of Health

University of the Punjab

Baylor College of Medicine

Centre of Excellence in Molecular Biology

Atteeq U. Rehman is an author at National Institute on Deafness and Other Communication Disorders specializing in life sciences, genetics, and molecular genetics.

ORCID

Publications per year

2009–2023

Publications

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

Life Sciences, Genetics, Molecular Genetics +10

Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79

Atteeq U. Rehman, Robert J. Morell, Inna A. Belyantseva et al. · The American Journal of Human Genetics · 2010 · 193 citations · Full text

Medicine, Genetics, Molecular Genetics +10

Functional Null Mutations of MSRB3 Encoding Methionine Sulfoxide Reductase Are Associated with Human Deafness DFNB74

Zubair M. Ahmed, Rizwan Yousaf, Byung Cheon Lee et al. · The American Journal of Human Genetics · 2010 · 120 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Loss-of-Function Mutations of ILDR1 Cause Autosomal-Recessive Hearing Impairment DFNB42

Guntram Borck, Atteeq U. Rehman, Kwanghyuk Lee et al. · The American Journal of Human Genetics · 2011 · 120 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86

Atteeq U. Rehman, Regie Lyn P. Santos‐Cortez, Robert J. Morell et al. · The American Journal of Human Genetics · 2014 · 87 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

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