Khalid Adnan Fakhro

The paper develops a machine learning-based T1D risk model tailored to Middle Eastern populations, showing improved performance over existing models in this region.

This study identifies RSS as a recyclinopathy caused by dysfunction in the Commander endosomal recycling pathway, linking it to multiple tissue malformations.

This study surveys healthcare professionals in the Middle East to understand challenges and perspectives on genetic counseling and testing, finding cultural and resource-related barriers and positive patient attitudes.

The paper improves T2D risk prediction using ensemble learning with multi-trait polygenic risk scores in the Qatar Biobank cohort.

This study identifies 135 ASD-associated protein-coding genes using whole-genome sequencing data from 11,312 individuals and exome sequencing from over 18,000 trios, with a false discovery rate of 80%.

The Qatar Genome Program sequenced 6,045 individuals, identifying 88 million variants, including novel ones, and revealed genetic structure and disease-related markers in the Qatari population.