Ikram Chekroun
Dubai, DU, United Arab Emirates
Last Updated: 09/26/2026
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Found 9 publications
Targeted long-read genomic and epigenomic profiling enhances timely comprehensive variant discovery in hypotonia and muscle weakness.
Journal: BMC medicine
Published: December 14, 2025
Citywide premarital genomic screening in a Middle Eastern population.
Journal: Nature medicine
Published: October 09, 2025
Premarital genomic screening in Arab populations of the Middle East.
Journal: Nature medicine
Published: January 09, 2025
Pathogenic variation underlying rare diseases in an Arab population: Implications for screening programs.
Journal: Genetics in medicine open
Published: December 04, 2024
FBXO22 deficiency defines a pleiotropic syndrome of growth restriction and multi-system anomalies associated with a unique epigenetic signature.
Journal: American journal of human genetics
Published: October 08, 2024
Genomics of rare diseases in the Greater Middle East.
Journal: Nature genetics
Published: September 23, 2024
Long read sequencing enhances pathogenic and novel variation discovery in patients with rare diseases.
Journal: Nature communications
Published: April 18, 2024
Spinal muscular atrophy genetic epidemiology and the case for premarital genomic screening in Arab populations.
Journal: Communications medicine
Published: January 13, 2024
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Last Updated: 09/26/2026