Wessam Sharaf-Eldin
10PUBLICATIONS
54CO-AUTHORS

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Publications (10)
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|Feb 16, 2026
Clinical Utility of Genetic Diagnosis in Drug-Resistant Epilepsy: Refining Classification and Guiding Therapy in an Egyptian Cohort.Wessam E Sharaf-Eldin, Nirmeen A Kishk, Noura R Eissa
|Dec 27, 2025
Loss of the maternal effect gene NLRP2 impairs embryonic and extra-embryonic development, revealing a novel genetic cause of congenital anomalies†.Momal Sharif, Zahra Anvar, Imen Chakchouk
|Apr 30, 2025
Analysis of Copy Number Variants Is an Important Consideration in Exome Sequencing.Asmaa K Amin, Sara H El-Dessouky, Marwa Abd Elmaksoud
|Feb 25, 2025
Malformations of Core M3 on α-Dystroglycan Are the Leading Cause of Dystroglycanopathies.Wessam Sharaf-Eldin
|Feb 01, 2025
Integrating Prenatal Exome Sequencing and Ultrasonographic Fetal Phenotyping for Assessment of Congenital Malformations: High Molecular Diagnostic Yield and Novel Phenotypic Expansions in a Consanguineous Cohort.Sara H El-Dessouky, Wessam E Sharaf-Eldin, Mona M Aboulghar
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Frequent Collaborators
5 joint publications
Maha Zaki
3 joint publications
Mahmoud Y Issa
3 joint publications
Ebtesam M Abdalla
1 joint publications
Mahmoud M Noureldeen
1 joint publications
Mohamed S Abdel-Hamid
1 joint publications
Sara H El-Dessouky
1 joint publications
Shahryar Alavi
1 joint publications
Heba A El-Awady
1 joint publications
Momal Sharif
1 joint publications
Zahra Anvar