Ghada Y El-Kamah

4PUBLICATIONS
12CO-AUTHORS
Major global burdens of diseaseEpigenetics (incl. genome methylation and epigenomics)Early English languagesGene mapping
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Publications (4)

|May 13, 2026
Mapping Current and Emerging Laboratory Techniques for Haemoglobinopathy Carrier Detection and Prevention: A Narrative Review from the HELIOS Action.

|Apr 28, 2023
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families.

Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher

|Aug 08, 2019
Genetic assessment of ten Egyptian patients with Sjögren-Larsson syndrome: expanding the clinical spectrum and reporting a novel ALDH3A2 mutation.

Khalda Amr, Hala T El-Bassyouni, Samira Ismail

|May 31, 2019
Whole exome sequencing identifies a new mutation in the SLC19A2 gene leading to thiamine-responsive megaloblastic anemia in an Egyptian family.

Khalda Amr, Patrycja Pawlikowska, Said Aoufouchi

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Frequent Collaborators

1 joint publications

Said Aoufouchi

1 joint publications

Filippo Rosselli

1 joint publications

Norafiza Mohd Yasin

1 joint publications

Sotiroula Chatzimatthaiou