Muhammad Sajid Hussain

Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy

Carol-Anne Martin, Ilyas Ahmad, Anna Klingseisen et al. · Nature Genetics · 2014 · 178 citations · Full text

Centriole Biogenesis, Ocular Disease, Developmental Biology +8

A Truncating Mutation of CEP135 Causes Primary Microcephaly and Disturbed Centrosomal Function

Muhammad Sajid Hussain, Shahid Mahmood Baig, Sascha Neumann et al. · The American Journal of Human Genetics · 2012 · 171 citations · Full text

Developmental Biology, Genetic Disorder, Autophagy +8

Mutations in multiple components of the nuclear pore complex cause nephrotic syndrome

Daniela A. Braun, Svjetlana Lovric, David Schapiro et al. · Journal of Clinical Investigation · 2018 · 138 citations · Full text

Glomerular Disease, Genetics, Renal Pathology +22

CDK6 associates with the centrosome during mitosis and is mutated in a large Pakistani family with primary microcephaly

Muhammad Sajid Hussain, Shahid Mahmood Baig, Sascha Neumann et al. · Human Molecular Genetics · 2013 · 120 citations · Full text

Microtubule Organization, Cytogenetics, Genetics +19

Seeing clearly: the dominant and recessive nature of<i>FOXE3</i>in eye developmental anomalies

Robert J. Osborne, Martin Farrall, Alexander W. Wyatt et al. · Human Mutation · 2009 · 88 citations

Eye Anomalies, Developmental Anomaly, Ocular Disease +15