6 Apr 2026
EGP1K: Whole-Genome Sequencing of 1,024 Egyptians Characterizes Population Structure and Genetic DiversityPublisher sitebioRxiv (Cold Spring Harbor Laboratory), Genetic Associations and Epidemiology
UniversitiesMohamed A. Elmonem
Active, last published 2026
In biomedical research and pathophysiology
Mohamed A.
Elmonem
Scholar“Research focused on Biomedical Research and Pathophysiology and adjacent fields.”
Cairo University
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01 · About the work
What I study
ohamed A. Elmonem is a researcher working on Biomedical Research and Pathophysiology. A fuller summary will appear once they update their profile.
02 · Reach
Publication output and reach
Mohamed's work has been cited 21,235 times across 5 active years. Bars show publications per year; the line shows cumulative citation totals across publications first appearing in each year.
03 · Research focus
Topics
Biomedical Research and Pathophysiology×26Neonatal Health and Biochemistry×14Metabolism and Genetic Disorders×12Amino Acid Enzymes and Metabolism×11Lysosomal Storage Disorders Research×10
04 · Where I am
Affiliations
Affiliation on published researchCairo UniversityDrawn from the institution listed on this researcher’s published work.
Research themes (UN SDGs)
05 · Selected work
Recent publications
11 works27 Mar 2026Open access
Fibroblast growth factor 21 and growth differentiation factor 15 as biomarkers for oxidative stress in children with methylmalonic acidemiaPublisher siteBMC Pediatrics, Metabolism and Genetic Disorders
10 Mar 2026Open access
Editorial: Newborn screening for inborn errors of metabolism volume IIPublisher siteFrontiers in Pediatrics, Metabolism and Genetic Disorders
17 Sept 2025Open access44cites
The global, regional, and national burden attributable to low bone mineral density, 1990–2020: an analysis of a modifiable risk factor from the Global Burden of Disease Study 2021Publisher siteThe Lancet Rheumatology, Bone health and osteoporosis research
22 May 2025Open access4cites
Whole genome sequencing identifies monogenic disease in 56.1% of families with early-onset steroid-resistant nephrotic syndromePublisher siteHuman Genetics, Renal Diseases and Glomerulopathies
5 Jun 2024Open access4cites
Egypt Genome: Towards an African new genomic eraPublisher siteJournal of Advanced Research, Genomics and Rare Diseases
29 Apr 202415cites
The Egypt Genome ProjectPublisher siteNature Genetics, Paleopathology and ancient diseases
25 Mar 2024Open access8cites
<i>RTN2</i> deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticityPublisher siteBrain, Hereditary Neurological Disorders
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