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Mohammed A. Aldahmesh

Observed names: Aldahmesh, Mohammed, Aldahmesh, Mohammed Abdullah A, M A Aldahmesh, M. A. Al-Dahmesh, M. A. Aldahmesh, M. Aldahmesh, M.A. Aldahmesh, MA Aldahmesh, Mohamed A. Aldahmesh, Mohammad A. Aldahmesh, Mohammad Aldahmesh, Mohammed A Aldahmesh, Mohammed Al-Dahmesh, Mohammed Aldahmesh, Mohammed A. Aldahmesh
ORCID: 0000-0003-0130-9029
Observed ORCID: 0000-0003-0130-9029
OpenAlex ID: A5000221925
Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families
2014 · Anas M. Alazami, Nisha Patel, et al. · Cell Reports · 459
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An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
2015 · Gabrielle Wheway, Miriam Schmidts, et al. · Nature Cell Biology · 235
Recessive Mutations in ELOVL4 Cause Ichthyosis, Intellectual Disability, and Spastic Quadriplegia
2011 · Mohammed A. Aldahmesh, Jawahir Y. Mohamed, et al. · The American Journal of Human Genetics · 186
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Characterizing the morbid genome of ciliopathies
2016 · Ciliopathy WorkingGroup, Ranad Shaheen, et al. · Genome biology · 171
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IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome
2014 · M. A. Aldahmesh, Y. Li, et al. · Human Molecular Genetics · 140
Mutations in LRPAP1 Are Associated with Severe Myopia in Humans
2013 · Mohammed A. Aldahmesh, Arif O. Khan, et al. · The American Journal of Human Genetics · 121
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Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus
2013 · Anas M Alazami, Hadia Hijazi, et al. · Journal of Medical Genetics · 114
Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies
2015 · Nisha Patel, Mohammed A. Aldahmesh, et al. · Genetics in Medicine · 112
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Novel mutations in MERTK associated with childhood onset rod-cone dystrophy.
2010 · Donna S Mackay, Robert H Henderson, et al. · PubMed Central · 90
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract
2016 · Nisha Patel, Deepti Anand, et al. · Human Genetics · 87
The distinct ophthalmic phenotype of Knobloch syndrome in children
2012 · Arif O Khan, Mohammed A Aldahmesh, et al. · British Journal of Ophthalmology · 86
Identification of ADAMTS18 as a gene mutated in Knobloch syndrome
2011 · Mohammed A Aldahmesh, Arif O Khan, et al. · Journal of Medical Genetics · 86
Clinical and molecular characterisation of Bardet–Biedl syndrome in consanguineous populations: the power of homozygosity mapping
2009 · L Abu Safieh, M A Aldahmesh, et al. · Journal of Medical Genetics · 86
Molecular characterization of retinitis pigmentosa in Saudi Arabia.
2009 · Mohammed A Aldahmesh, Leen Abu Safieh, et al. · PubMed Central · 82
Identification of a truncation mutation of acylglycerol kinase (AGK) gene in a novel autosomal recessive cataract locus
2012 · Mohammed A. Aldahmesh, Arif O. Khan, et al. · Human Mutation · 70
Recessive Congenital Total Cataract with Microcornea and Heterozygote Carrier Signs Caused by a Novel Missense CRYAA Mutation (R54C)
2007 · Arif O. Khan, Mohammad A. Aldahmesh, et al. · American Journal of Ophthalmology · 66
Prevalence and functionality of paucimorphic and privateMC4Rmutations in a large, unselected European British population, scanned by meltMADGE
2006 · Khalid K. Alharbi, Emmanuel Spanakis, et al. · Human Mutation · 66
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Biometric and Molecular Characterization of Clinically Diagnosed Posterior Microphthalmos
2012 · Sawsan R. Nowilaty, Arif O. Khan, et al. · American Journal of Ophthalmology · 64
Autozygosity Mapping with Exome Sequence Data
2012 · Ian M. Carr, Sanjeev Bhaskar, et al. · Human Mutation · 64
The Syndrome of Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus (MMCAT) Is Caused by Mutations inADAMTS18
2013 · Mohammed A. Aldahmesh, Muneera J. Alshammari, et al. · Human Mutation · 61
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Genomic analysis of pediatric cataract in Saudi Arabia reveals novel candidate disease genes
2012 · Mohammed A. Aldahmesh, Arif O. Khan, et al. · Genetics in Medicine · 61
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Homozygous null mutation in ODZ3 causes microphthalmia in humans
2012 · Mohammed A. Aldahmesh, Jawahir Y. Mohammed, et al. · Genetics in Medicine · 61
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Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma - a distinct phenotype caused by recessive LTBP2 mutations.
2011 · Arif O Khan, Mohammed A Aldahmesh, et al. · Europe PMC (PubMed Central) · 61
Allelic heterogeneity in inbred populations: The Saudi experience with Alström syndrome as an illustrative example
2009 · Mohamed A. Aldahmesh, Leen Abu‐Safieh, et al. · American Journal of Medical Genetics Part A · 54
Congenital glaucoma and CYP1B1: an old story revisited
2018 · Hessa S. Alsaif, Arif O. Khan, et al. · Human Genetics · 53
Works count: 102
Citation count: 3,934
H-index: 37
I10-index: 64
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