Amal Y. Kentab

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 · 472 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield

Shams Anazi, Sateesh Maddirevula, Eissa Faqeih et al. · Molecular Psychiatry · 2016 · 260 citations

Life Sciences, Genetics, Molecular Genetics +17

Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly

Fowzan S. Alkuraya, Xuyu Cai, Carina Emery et al. · The American Journal of Human Genetics · 2011 · 222 citations · Full text

Life Sciences, Genetics, Neuroscience +12

Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes

Hanan E. Shamseldin, Muneera Alshammari, Tarfa Al‐Sheddi et al. · Journal of Medical Genetics · 2012 · 182 citations

Life Sciences, Genetics, Molecular Genetics +14

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

Life Sciences, Genetics, Molecular Genetics +17