Mohammed A. Aldahmesh

Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families

Anas M. Alazami, Nisha Patel, Hanan E. Shamseldin et al. · Cell Reports · 2014 · 465 citations · Full text

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes

Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans et al. · Nature Cell Biology · 2015 · 245 citations · Full text

Ciliopathy Genes, Functional Genomics, Glioma +10

Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectual Disability, and Spastic Quadriplegia

Mohammed A. Aldahmesh, Jawahir Y. Mohamed, Hisham Alkuraya et al. · The American Journal of Human Genetics · 2011 · 183 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +6

IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome

Mohammed A. Aldahmesh, Yuanyuan Li, Amal Alhashem et al. · Human Molecular Genetics · 2014 · 140 citations · Full text

Mutation in <i>ADAT3</i>, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus

Anas M. Alazami, Hadia Hijazi, Mohammed S. Al‐Dosari et al. · Journal of Medical Genetics · 2013 · 129 citations