Sulman Basit

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

Life Sciences, Molecular Genetics, Neuroscience +13

Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability

Saleh AlAsiri, Sulman Basit, Michelle A. Wood et al. · Journal of Clinical Investigation · 2014 · 236 citations

Medicine, Endocrinology, Genetics +17

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 KARS, Encoding Lysyl-tRNA Synthetase, Cause Autosomal-Recessive Nonsyndromic Hearing Impairment DFNB89

Regie Lyn P. Santos‐Cortez, Kwanghyuk Lee, Zahid Azeem et al. · The American Journal of Human Genetics · 2013 · 114 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

A Homozygous Nonsense Mutation in the Human Desmocollin-3 (DSC3) Gene Underlies Hereditary Hypotrichosis and Recurrent Skin Vesicles

Muhammad Ayub, Sulman Basit, Musharraf Jelani et al. · The American Journal of Human Genetics · 2009 · 90 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10