Muhammad Rafiq

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

Towards a comprehensive structural variation map of an individual human genome

Andy Wing Chun Pang, Jeffrey R. MacDonald, Dalila Pinto et al. · Genome biology · 2010 · 353 citations · Full text

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

Genome assembly comparison identifies structural variants in the human genome

Razi Khaja, Junjun Zhang, Jeffrey R. MacDonald et al. · Nature Genetics · 2006 · 164 citations · Full text

Genetics, Genome Structure, Molecular Biology +8