Author

Ehab Tous

King Faisal Specialist Hospital & Research CentreORCID 0009-0002-2329-7268Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Ahmet YeşilyurtiD· 1 shared Amira Nabil· 1 shared Annarita ScardamagliaiD· 1 shared Bader AlhaddadiD· 1 shared David P. MurphyiD· 1 shared Ebtessam Abdalla· 1 shared Eleanor Self· 1 shared Eyyüp ÜçtepeiD· 1 shared

Activity by Year

2026-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ahmet YeşilyurtORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicineThe American Journal of Human GeneticsPeer-reviewedJan 21, 2026

MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathy

Heba Morsy, Hyeonho Kim, Gyubin Jang…·Reza Maroofian

This study identifies homozygous loss-of-function MDGA2 variants in individuals with developmental and epileptic encephalopathy, establishing MDGA2 as a novel gene for this condition.

1 citation

humanstatistical model

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