Wasim Ahmad

Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene

Wasim Ahmad, Muhammad Faiyaz ul Haque, Valeria Brancolini et al. · Science · 1998 · 413 citations

WDR62 is associated with the spindle pole and is mutated in human microcephaly

Adeline K. Nicholas, Maryam Khurshid, Julie Désir et al. · Nature Genetics · 2010 · 286 citations · Full text

Spindle Pole, Molecular Neuroscience, Disease Mechanism +6

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 · 247 citations · Full text

Nonsyndromic Deafness Dfnb48, Type 1J, Signal Transduction +7

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

Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse

Muhammad Faiyaz ul Haque, Lily King, Deborah Krakow et al. · Nature Genetics · 1998 · 211 citations

Biology, Developmental Biology, Somatic Variant +10