Ali Alsarhan

This study evaluates genomic diagnostic yield and clinical impact in rare disease patients from the Middle East, finding higher yields with sequencing than microarrays and highlighting diagnostic delays due to limited access.

This study identifies rare genetic variants in MIS-C patients from the Middle East, linking them to disease onset and treatment resistance.

This study performs genomic analysis on pediatric rheumatology patients in the Middle East, finding that comprehensive sequencing identifies pathogenic variants in multiple genes, with MEFV and IFIH1 being significant contributors.