Atteeq U. Rehman

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 · 238 citations · Full text

Mitochondrial Function, Genetic Disorder, Medicine +7

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

Mutated Gene, Genetic Disorder, Medicine +9

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

Signal Transduction, Genetics, Molecular Biology +6

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 · 119 citations · Full text

Genetics, Audiology, Auditory Physiology +7

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 · 86 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +7