Naveed Wasif

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

Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3)

Zahid Azeem, Musharraf Jelani, Gul Naz et al. · Human Genetics · 2008 · 49 citations

Signal Transduction, G Protein-coupled Receptor, Genetic Disorder +9

Whole exome sequencing identified a novel zinc-finger gene <i>ZNF141</i> associated with autosomal recessive postaxial polydactyly type A

Umme Kalsoom, Eva Klopocki, Naveed Wasif et al. · Journal of Medical Genetics · 2012 · 47 citations · Full text

Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families

Naveed Wasif, Syed Kamran‐ul‐Hassan Naqvi, Sulman Basit et al. · Human Genetics · 2010 · 40 citations

Pakistani Families, Genetic Disorder, Genetics +7

A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family

Sulman Basit, Syed Kamran‐ul‐Hassan Naqvi, Naveed Wasif et al. · BMC Medical Genetics · 2008 · 39 citations · Full text