Ilyas Ahmad

Loss of Cav1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness

Shahid Mahmood Baig, Alexandra Koschak, Andreas Lieb et al. · Nature Neuroscience · 2010 · 313 citations

Congenital Deafness, Channelopathies, Human Channelopathy +5

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

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

A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia

Mahmood Rasool, Jens Schuster, Muhammad Aslam et al. · Journal of Human Genetics · 2008 · 33 citations · Full text

Biology, Genetic Disorder, Genetics +7