Associated Papers
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Anderson EN et al.
American Journal of Human Genetics, 2026
De novo variants in KDM2A cause a syndromic neurodevelopmental disorder.
Anderson EN et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
Genome Sequencing Identifies 13 Novel Candidate Risk Genes for Autism Spectrum Disorder in a Qatari Cohort.
Ben-Mahmoud A et al.
International Journal of Molecular Sciences, 2024
The genetic landscape of autism spectrum disorder in the Middle Eastern population.
Al-Sarraj Y et al.
Frontiers in Genetics, 2024
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