Khalid Fakhro

27PUBLICATIONS
120CO-AUTHORS
GenomicsEpigenetics (incl. genome methylation and epigenomics)NeonatologyGene expression (incl. microarray and other genome-wide approaches)Gene mapping
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Publications (27)

|Jan 13, 2026
The biomedical landscape of genomic structural variation in the qatari population.

Elbay Aliyev, Najeeb Syed, Alessia Visconti

|Dec 30, 2025
Functional Interpretation of a Novel Homozygous METTL5 Variant Associated with ADHD and Neurodevelopmental Abnormalities: A Case Report and Literature Review.

Sheema Hashem, Saba F Elhag, Ajaz A Bhat

|Jun 13, 2025
Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder.

Aljazi Al-Maraghi, Rulan Shaath, Katherine Ford

|May 05, 2025
Near-complete Middle Eastern genomes refine autozygosity and enhance disease-causing and population-specific variant discovery.

Mohammadmersad Ghorbani, Shabir Moosa, Zenab Siddig

|Feb 03, 2025
Genomics of rare diseases in the Greater Middle East.

Ikram Chekroun, Shruti Shenbagam, Mohamed A Almarri

|Jun 28, 2024
Rare variants at KCNJ2 are associated with LDL-cholesterol levels in a cross-population study.

Niccolò Rossi, Najeeb Syed, Alessia Visconti

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Frequent Collaborators

9 joint publications

Waleed Aamer

8 joint publications

Elbay Aliyev

5 joint publications

Younes Mokrab

3 joint publications

Fowzan S Alkuraya