Muhammad Ansar

Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways

Liyun Sang, Julie J. Miller, Kevin C. Corbit et al. · Cell · 2011 · 617 citations · Full text

Molecular Neuroscience, Disease Mechanism, Glioma +7

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

Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

Muzammil Ahmad Khan, Muhammad Rafiq, Abdul Noor et al. · The American Journal of Human Genetics · 2012 · 228 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +7

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

Ricardo Harripaul, Nasim Vasli, Muhammad Rafiq et al. · Molecular Psychiatry · 2017 · 177 citations

Mendelian Disorder, Novel Candidate Genes, Genetic Disorder +6