1 Jul 2026
Phenotypic and genetic characterization of 64 Egyptian children with neuronal ceroid lipofuscinosisPublisher sitePediatric Neurology, Lysosomal Storage Disorders Research
UniversitiesMohamed S. Abdel‐Hamid
Active, last published 2026
In rna modifications and cancer
Mohamed S.
Abdel‐Hamid
Scholar“Research focused on RNA modifications and cancer and adjacent fields.”
National Human Genome Research Institute
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01 · About the work
What I study
ohamed S. Abdel‐Hamid is a researcher working on RNA modifications and cancer. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Mohamed's work has been cited 2,678 times across 3 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
RNA modifications and cancer×17Connective tissue disorders research×13Genomics and Rare Diseases×13Genetics and Neurodevelopmental Disorders×13RNA regulation and disease×12
04 · Where I am
Affiliations
Affiliation on published researchNational Human Genome Research InstituteDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
11 works23 Feb 2026
Improving quantity estimation in the construction industry: a case study approach to 5D BIM implementationPublisher siteInternational Journal of Construction Management, BIM and Construction Integration
3 Nov 2025
EPG5-Related Disorders in Seven New Patients: Refining the Phenotypic Spectrum and Insights on Phenotype-Genotype CorrelationsPublisher siteJournal of Molecular Neuroscience, Genomics and Rare Diseases
30 Sept 2025
<scp> <i>MINPP1</i> </scp> ‐Related Pontocerebellar Hypoplasia in Five New Patients: Identification of Three Novel Variants and Further Phenotype DelineationPublisher siteClinical Genetics, Fetal and Pediatric Neurological Disorders
17 Dec 2024Open access2cites
Biallelic <i>NDUFA13</i> variants lead to a neurodevelopmental phenotype with gradual neurological impairmentPublisher siteBrain Communications, Mitochondrial Function and Pathology
5 Nov 2024Open access1cites
Biallelic loss-of-function variants in GON4L cause microcephaly and brain structure abnormalitiesPublisher sitenpj Genomic Medicine, Genomics and Rare Diseases
1 Nov 2024
Risk assessment during construction stage for the heritage buildings rehabilitation in EgyptPublisher siteEngineering Research Journal, BIM and Construction Integration
19 Sept 2024Open access8cites
Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a severe developmental disorder spectrumPublisher siteGenetics in Medicine, Metabolism and Genetic Disorders
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