Zakia Abdelhamed

A meckelin–filamin A interaction mediates ciliogenesis

Matthew Adams, Roslyn Simms, Zakia Abdelhamed et al. · Human Molecular Genetics · 2011 · 107 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +12

Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects

Kamron N. Khan, Clare V. Logan, Martin McKibbin et al. · Human Molecular Genetics · 2011 · 94 citations · Full text

Ocular Disease, Genetics, Molecular Genetics +20

Homozygous Mutations in PXDN Cause Congenital Cataract, Corneal Opacity, and Developmental Glaucoma

Kamron N. Khan, Adam K Rudkin, David Parry et al. · The American Journal of Human Genetics · 2011 · 79 citations · Full text

Homozygous Mutations, Congenital Cataract-microcornea, Ocular Disease +13

A mutation in <i>Ccdc39</i> causes neonatal hydrocephalus with abnormal motile cilia development in mice

Zakia Abdelhamed, Shawn M. Vuong, Lauren M. Hill et al. · Development · 2018 · 78 citations · Full text

Differential requirements of tubulin genes in mammalian forebrain development

Elizabeth Bittermann, Zakia Abdelhamed, Ryan P. Liegel et al. · PLoS Genetics · 2019 · 62 citations · Full text

Genetics, Cytoskeleton, Molecular Genetics +18