Ahmed K Saad
4PUBLICATIONS
15CO-AUTHORS
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Publications (4)
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|Jan 07, 2025
Lethal Phenotype and Expansion of the Clinical Spectrum of Biallelic Loss of Function Variant in SENP7 Gene Unveiled by Whole Exome Sequencing.Ahmed K Saad, Nagwa H Hassan, Hala N Soliman
|Dec 05, 2024
Fetal Phenotyping and Whole Exome Sequencing for 12 Egyptian Families With Serine Biosynthesis Defect: Novel Clinical and Allelic Findings With a Founder Effect.Sara H El-Dessouky, Wessam E Sharaf-Eldin, Mona M Aboulghar
|May 09, 2023
Novel LSS variants in alopecia and intellectual disability syndrome: New case report and clinical spectrum of LSS-related rare disease traits.Hasnaa M Elbendary, Dana Marafi, Ahmed K Saad
|Feb 05, 2021
Neurodevelopmental disorder in an Egyptian family with a biallelic ALKBH8 variant.Ahmed K Saad, Dana Marafi, Tadahiro Mitani
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Frequent Collaborators
3 joint publications
Maha S Zaki
2 joint publications
Dana Marafi
2 joint publications
Davut Pehlivan
2 joint publications
Jennifer E Posey
2 joint publications
James R Lupski
2 joint publications
Sara H El-Dessouky
1 joint publications
Haowei Du
1 joint publications
Jawid M Fatih
1 joint publications
Zeynep Coban-Akdemir
1 joint publications
Richard A Gibbs
