Tahir Naeem Khan

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

Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features

Paweł Stankiewicz, Tahir Naeem Khan, Przemysław Szafrański et al. · The American Journal of Human Genetics · 2017 · 111 citations · Full text

Developmental Anomaly, Chromatin, Developmental Biology +13

De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder

Sébastien Küry, Thomas Besnard, Frédéric Ebstein et al. · The American Journal of Human Genetics · 2017 · 107 citations · Full text

Molecular Neuroscience, Developmental Biology, De Novo Disruption +12

Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia

Claire Guissart, Xénia Latypova, Paul Rollier et al. · The American Journal of Human Genetics · 2018 · 81 citations · Full text

Molecular Neuroscience, Neurological Disorder, Genetic Disorder +13

Evidence for autosomal recessive inheritance in SPG3A caused by homozygosity for a novel ATL1 missense mutation

Tahir Naeem Khan, Joakim Klar, Muhammad Tariq et al. · European Journal of Human Genetics · 2014 · 48 citations · Full text

Autosomal Recessive Inheritance, Allelic Variant, Developmental Biology +7