Ibrahim Taha

6PUBLICATIONS
5CO-AUTHORS
Gene mappingEpigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Cardiology (incl. cardiovascular diseases)Vision science
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Publications (6)

|Jul 03, 2026
Ocular and Systemic Phenotyping of Bardet-Biedel Syndrome Type 7 (BBS7) in a Palestinian Male: Case Report and Literature Review.

|May 09, 2026
Electronegative electroretinography in inherited retinal disease: a systematic review of genotype-phenotype correlations.

|Apr 27, 2026
Homozygous Pathogenic Variant in Elongation Factor-Like 1 (EFL1) as a Causal Factor in Shwachman-Diamond Syndrome 2 in a Palestinian Child, With Distinct Ocular Manifestations.

|Dec 01, 2025
Assessment of Adherence to Iron Chelation Therapy Among Thalassemia Patients in Palestine.

Hamzeh Al Zabadi, Zein Ieran, Ibrahim Taha

|Jul 27, 2022
Phenotypic Variation in Two Siblings Affected with Shwachman-Diamond Syndrome: The Use of Expert Variant Interpreter (eVai) Suggests Clinical Relevance of a Variant in the KMT2A Gene.

Ibrahim Taha, Federica De Paoli, Selena Foroni

|Jul 27, 2022
Clinical and Molecular Characteristics of Diabetic Retinopathy and Its Severity Complications among Diabetic Patients: A Multicenter Cross-Sectional Study.

Hamzeh Al Zabadi, Ibrahim Taha, Rami Zagha

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Frequent Collaborators

2 joint publications

Hamzeh Al Zabadi

2 joint publications

Antonella Minelli

1 joint publications

Federica De Paoli

1 joint publications

Khaled R Beshtawi