Author

Haytham Hussien

Alexandria University

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Fowzan Sami AlkurayaiD· 2 shared Heba MorsyiD· 2 shared Henry HouldeniD· 2 shared Joseph G. GleesoniD· 2 shared Maha Saad ZakiiD· 2 shared Reza MaroofianiD· 2 shared Shahryar AlaviiD· 2 shared Abdolmajid Omrani· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Fowzan Sami AlkurayaORCID

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Author profile →

2 papers

Recent·Most cited

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

Heba Morsy, Hyeonho Kim, Gyubin Jang, Maha Saad Zaki, Mariasavina Severino, Ibrahim M. Abdelrazek, Haytham Hussien, Eleanor Self, Raidah Albaradie, Khadijah Bakur, Zahra Firoozfar, Stéphanie Efthymiou, Mahmoud M. Noureldeen, Amira Nabil, Javeria Raza Alvi, , 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.

The American Journal of Human Genetics · Jan 21, 2026Peer-reviewedGenetic & Genomic Medicine

Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy and periventricular calcifications

Erik Rosenhahn, Thomas James O’Brien, Maha Saad Zaki, Ina Sorge, Dagmar Wieczorek, Kevin M. Rostasy, Antonio Vitobello, Sophie Nambot, Fowzan Sami Alkuraya, Mais O. Hashem, Amal Mohammed Alhashem, Brahim M. Tabarki, Abdullah Alamri, Ayat H. Al Safar, Dalal Bubshait, , Konrad Platzer

The American Journal of Human Genetics · Jul 12, 2022Peer-reviewedGenetic & Genomic Medicine