Anas M. Alazami

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

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 · 254 citations

Intellectual Impairment, Medicine, Genetics +6

TLE6 mutation causes the earliest known human embryonic lethality

Anas M. Alazami, Salma Awad, Serdar Coşkun et al. · Genome biology · 2015 · 216 citations · Full text

Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by <i>TMEM38B</i> mutation

Ranad Shaheen, Anas M. Alazami, Muneera Alshammari et al. · Journal of Medical Genetics · 2012 · 139 citations

Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome

Anas M. Alazami, Amr Al‐Saif, Abdulaziz Alsemari et al. · The American Journal of Human Genetics · 2008 · 136 citations · Full text

Developmental Biology, Mendelian Disorder, Genetic Disorder +7