The genetic orchestra of autism and its intersections with epilepsy, intellectual disability, and ADHD
Year: 2026
Type: article
Abstract: Autism is a complex condition with marked phenotypic variability and a multifactorial etiology orchestrated by diverse genetic and environmental influences. In this review, we dissect what we refer to as autism's "genetic orchestra", spanning from the high-impact "soloists", de novo and ultra-rare variants with large effect sizes, to the "polyphonic background" of common variants which individually exert modest effects but collectively have significant impact. We examine how this orchestra wires neural circuits, with convergent biological pathways modulating synaptic function and chromatin remodeling. Although de novo, rare, and common variants are often studied independently, converging evidence supports a model whereby their influences are largely additive. This genetic orchestra is not condition-specific; autism frequently co-occurs with other neurodevelopmental and psychiatric conditions, reflecting substantial pleiotropy across both rare and common variant landscapes. Notably, ultra-rare variants tend to associate with co-occurring intellectual disability, ADHD, epilepsy, and psychiatric conditions highlighting their high phenotypic impact. Beyond genetics, layers of environmental and contextual factors further modulate clinical outcomes. In this framework, we also discuss the challenges of identifying genetic variants associated with autism through clinical genetic testing, where yields remain context-dependent, varying by sex and co-occurring conditions. Finally, we address current limitations and future directions in refining our understanding of autism's genetic basis.
Source: Biological Psychiatry
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $5,489
Funders: Simons Foundation Autism Research Initiative, European Commission, Agence Nationale de la Recherche, Institut Pasteur, Centre National de la Recherche Scientifique, Conseil National de la Recherche Scientifique, Université de Paris, Horizon 2020 Framework Programme, HORIZON EUROPE Framework Programme
Awards: Institut Robert-Debré du Cerveau de l’Enfant, G1806772070, Risk and Resilience in Developmental Diversity and Mental Health, G452649895, G4986414685, Institut Convergences pour l’étude de l’Emergence des Pathologies au Travers des Individus et des populatiONs, Autism Innovative Medicine Studies – 2 – Trials, Modifiers of phenotypic outcomes in individuals with SHANK3 haplo-insufficiency and mouse models, G6684035547, G6972650492, G7070717597, G7080048889, G7540829840, Comorbid Analysis of Neurodevelopmental Disorders and Epilepsy, G7907412252, G9001168358
OpenAlex ID: W7221169729
