Mohammed A. Aldahmesh
King Faisal Specialist Hospital & Research Centre(SA)
Publications by Year
Research Areas
Retinal Development and Disorders, Connexins and lens biology, Genetic and Kidney Cyst Diseases, Retinal Diseases and Treatments, Ocular Disorders and Treatments
Most-Cited Works
- → Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families(2014)467 cited
- → An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes(2015)245 cited
- → Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectual Disability, and Spastic Quadriplegia(2011)185 cited
- → Characterizing the morbid genome of ciliopathies(2016)162 cited
- → IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome(2014)141 cited
- → Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus(2013)129 cited
- → Mutations in LRPAP1 Are Associated with Severe Myopia in Humans(2013)128 cited
- → Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies(2015)109 cited
- → Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract(2016)88 cited
- Novel mutations in MERTK associated with childhood onset rod-cone dystrophy.(2010)