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Moeen Al-Sayed

Observed names: M Al-Sayed, M. D. AlSayed, Moeen A D Al-Sayed, Moeen Al Sayed, Moeen AlSayed, Moeen Alsayed, Moeen Al‐ Sayed, Moeen D. AlSayed
ORCID: 0000-0003-1995-8465
Observed ORCID: 0000-0003-1995-8465
OpenAlex ID: A5113714045
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
2019 · Dorota Monies, Mohammed Abouelhoda, et al. · The American Journal of Human Genetics · 298
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In search of triallelism in Bardet–Biedl syndrome
2012 · Leen Abu-Safieh, Shamsa Al-Anazi, et al. · European Journal of Human Genetics · 126
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Guidelines for acute management of hyperammonemia in the Middle East region
2016 · Majid Alfadhel, Fuad Al Mutairi, et al. · Therapeutics and Clinical Risk Management · 51
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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
2019 · Dorota Monies, Mohammed Abouelhoda, et al. · The American Journal of Human Genetics · 47
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Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency
2009 · Muhammad Faiyaz-Ul-Haque, Mohammed Al-Owain, et al. · European Journal of Pediatrics · 37
Genetic and phenotypic characterization of NKX6‐2‐related spastic ataxia and hypomyelination
2019 · V. Chelban, M. Alsagob, et al. · European Journal of Neurology · 25
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Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin
2011 · Faiqa Imtiaz, Mohamed S. Rashed, et al. · Molecular Genetics and Metabolism · 22
GM2 gangliosidosis in Saudi Arabia: Multiple mutations and considerations for future carrier screening
2011 · Namik Kaya, Mohammad Al‐ Owain, et al. · American Journal of Medical Genetics Part A · 20
Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs
2010 · R Shaheen, OY Al-Dirbashi, et al. · Clinical Genetics · 19
The phenotype, genotype, and outcome of infantile-onset Pompe disease in 18 Saudi patients
2018 · Zuhair N. Al-Hassnan, Ola A. Khalifa, et al. · Molecular Genetics and Metabolism Reports · 15
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Spectrum of bone marrow pathology and hematological abnormalities in methylmalonic acidemia
2018 · Nasir A. Bakshi, Talal Al‐Anzi, et al. · American Journal of Medical Genetics Part A · 15
Rapid Determination of Orotic Acid in Urine by Liquid Chromatography–Electrospray Tandem Mass Spectrometry
2003 · Mohamed S Rashed, Minnie Jacob, et al. · Clinical Chemistry · 14
Emergency management of critically ill adult patients with inherited metabolic disorders
2022 · Raashda A. Sulaiman, Abdulaziz Alali, et al. · The American Journal of Emergency Medicine · 7
Optic neuropathy in classical methylmalonic acidemia
2019 · Mohammed AlOwain, Ola Ali Khalifa, et al. · Ophthalmic Genetics · 7
Human subjects in clinical trials: Ethical considerations and concerns
2018 · Ahmad W, Moeen Al-Sayed · Journal of Translational Science · 6
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Early access experience with VPRIV®: Recommendations for ‘core data’ collection
2010 · Derralynn A. Hughes, Moeen Al-Sayed, et al. · Blood Cells Molecules and Diseases · 4
Clinical, radiological, and genetic characterization of SLC13A5 variants in Saudi families: Genotype phenotype correlation and brief review of the literature
2023 · Hanan AlQudairy, Hesham AlDhalaan, et al. · Frontiers in Pediatrics · 3
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Trappsol®Cyclo™ and NPC: Efficacy shown across individual 5D domains and utilization of future assessment tools to demonstrate clinically relevant outcomes
2025 · Caroline A. Hastings, Fatih S. Ezgu, et al. · Molecular Genetics and Metabolism · 1
Agreement within couples on choosing preimplantation genetic diagnosis versus pre-natal diagnosis: perspective from Saudi population.
2019 · Fawz AlHarthi, Moeen Al Sayed, et al. · Journal of Biochemical and Clinical Genetics · 1
Impact of long-term elosulfase alfa treatment on pulmonary function in patients with Morquio syndrome type A
2016 · Christian J. Hendriksz, Barbara K. Burton, et al. · Molecular Genetics and Metabolism · 1
Outcome of hematopoietic stem cell transplantation in 19 patients with alpha-mannosidosis
2025 · Robert Saho, Renata Formankova, et al. · Molecular Genetics and Metabolism
Trappsol® Cyclo™ (hpβCd) for the long-term treatment of Niemann Pick type C1: Efficacy and safety data from 4 clinical studies and the ongoing expanded access program
2025 · Caroline A. Hastings, Fatih S. Ezgu, et al. · Molecular Genetics and Metabolism
Clinical Characterization and Outcome of Menkes Disease in Saudi Patients
2023 · Moeen AlSayed, Zainab Al Masseri, et al. · SSRN Electronic Journal
Ethical solicitude in medical genetics as perceived from a genetic counselor's perspective in the tribal-based community of Saudi Arabia
2021 · Alya Qari, Moeen Al-Sayed, et al. · Journal of Biochemical and Clinical Genetics
Works count: 24
Citation count: 719
H-index: 12
I10-index: 12
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