KDM5A mutations identified in autism spectrum disorder using forward geneticsLauretta El Hayek, Maria H. Chahrour, İslam Oğuz Tuncay et al.|eLife|2020Cited by 63
Elucidating the clinical and molecular spectrum of SMARCC2-associated NDD in a cohort of 65 affected individualsElisabeth Bosch, E. Grau Garcia, Bernt Popp et al.|Genetics in Medicine|2023Cited by 16
De novo variants in KDM2A cause a syndromic neurodevelopmental disorderEric N. Anderson, Ivan Ivanovski, Karen Stals et al.|Universität Zürich, ZORA|2026Cited by 0