Mohammed A. Aldahmesh

Author

King Faisal Specialist Hospital & Research Centre ORCID

Also Known As

Aldahmesh, Mohammed, Hadeel Alsharif, M A Aldahmesh, M. A. Al-Dahmesh, M. A. Aldahmesh, M. Aldahmesh, M.A. Aldahmesh, MA Aldahmesh, Mohamed A. Aldahmesh, Mohammad A. Aldahmesh

Publications

3.9K

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre Alfaisal University King Khaled Eye Specialist Hospital King Saud University King Khalid University Hospital

About

Mohammed A. Aldahmesh is an author at King Faisal Specialist Hospital & Research Centre specializing in medicine, genetics, and ophthalmology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	21	1.5K
2	Public Health	3	3	193
3	Cell Biology	2	2	289
4	Biology	1	1	60
5	Biostatistics	1	1	63

Mohammed A. Aldahmesh

Publications

3.6K

Citations

H-Index

Page 1

	Year	Citations
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, Cell Reports	2014	465
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes Gabrielle Wheway, Miriam Schmidts, Dorus A. Mans, Nature Cell Biology Ciliopathy GenesFunctional GenomicsGliomaGeneticsGene Regulation	2015	245
Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectual Disability, and Spastic Quadriplegia Mohammed A. Aldahmesh, Jawahir Y. Mohamed, Hisham Alkuraya, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyElovl4 Cause Ichthyosis	2011	183
IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome Mohammed A. Aldahmesh, Yuanyuan Li, Amal Alhashem, Human Molecular Genetics	2014	140
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, Journal of Medical Genetics	2013	129
Mutations in LRPAP1 Are Associated with Severe Myopia in Humans Mohammed A. Aldahmesh, Arif O. Khan, Hisham Alkuraya, The American Journal of Human Genetics OphthalmologySevere MyopiaGenetic DisorderGeneticsPathology	2013	128
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies Nisha Patel, Mohammed A. Aldahmesh, Hisham Alkuraya, Genetics in Medicine Ocular DiseaseRetinaOphthalmologyGeneticsLocus Heterogeneity	2015	109
Novel mutations in MERTK associated with childhood onset rod-cone dystrophy. Donna S. Mackay, Robert Henderson, Panagiotis I. Sergouniotis, PubMed	2010	87
Clinical and molecular characterisation of Bardet–Biedl syndrome in consanguineous populations: the power of homozygosity mapping Leen Abu Safieh, Mohammed A. Aldahmesh, Hanan E. Shamseldin, Journal of Medical Genetics	2009	86
Identification of <i>ADAMTS18</i> as a gene mutated in Knobloch syndrome Mohammed A. Aldahmesh, Arif O. Khan, JawahirY Mohamed, Journal of Medical Genetics	2011	86

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