Mustafa A. Salih
King Abdulaziz City for Science and Technology(SA)University of Babylon(IQ)King Saud University(SA)Sudan International University(SD)Baylor Medical Center at Garland(US)Heart Hospital Baylor Plano(US)
Publications by Year
Research Areas
Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders, Muscle Physiology and Disorders, Genomic variations and chromosomal abnormalities, Hereditary Neurological Disorders
Most-Cited Works
- → Mutation of TDP1, encoding a topoisomerase I–dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy(2002)522 cited
- → Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families(2014)467 cited
- → Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2(2000)457 cited
- → Mutations in a Human ROBO Gene Disrupt Hindbrain Axon Pathway Crossing and Morphogenesis(2004)384 cited
- → Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development(2005)303 cited
- → The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes(2017)300 cited