Rehan Sadiq Shaikh

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

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 · 105 citations

A simple method for preparing ultra-light graphene aerogel for rapid removal of U(VI) from aqueous solution

Donglin Zhao, Yangyang Wang, Siyu Zhao et al. · Environmental Pollution · 2019 · 54 citations

Materials Science, Graphene Nanomeshes, Chemical Engineering +9

Molecular genetic studies and delineation of the oculocutaneous albinism phenotype in the Pakistani population

Thomas Jaworek, Tasleem Kausar, Shannon Bell et al. · Orphanet Journal of Rare Diseases · 2012 · 50 citations · Full text

FUT2 Variants Confer Susceptibility to Familial Otitis Media

Regie Lyn P. Santos‐Cortez, Charlotte M. Chiong, Daniel N. Frank et al. · The American Journal of Human Genetics · 2018 · 46 citations · Full text

Pathogenesis, Genetic Epidemiology, Otolaryngology +5