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Mohammed A. Aldahmesh | Researchclopedia

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Mohammed A. Aldahmesh

King Faisal Specialist Hospital & Research Centre ORCID

94

Works

3,960

Citations

37

h-index

65

i10-index

Research Topics

Retinal Development and Disorders Connexins and lens biology Genetic and Kidney Cyst Diseases

Affiliations

King Faisal Specialist Hospital & Research Centre2006–2025

Southampton General Hospital2006–2006

King Saud University2011–2011

University of Southampton2005–2006

Top Works

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

Anas M. Alazami,Nisha Patel,et al.

2014467 citations

Retinal Diseases and Treatments

Ocular Disorders and Treatments

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

Gabrielle Wheway,Miriam Schmidts,et al.

2015245 citations

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

Mohammed A. Aldahmesh,Jawahir Y. Mohamed,et al.

2011185 citations

Characterizing the morbid genome of ciliopathies

Ciliopathy WorkingGroup,Ranad Shaheen,et al.

2016162 citations

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

Mohammed A. Aldahmesh,Yuanyuan Li,et al.

2014141 citations

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

Anas M. Alazami,Hadia Hijazi,et al.

2013129 citations

Mutations in LRPAP1 Are Associated with Severe Myopia in Humans

Mohammed A. Aldahmesh,Arif O. Khan,et al.

2013128 citations

Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies

Nisha Patel,Mohammed A. Aldahmesh,et al.

2015109 citations

Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract

Nisha Patel,Deepti Anand,et al.

201688 citations