Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry.
Research Articles
Aggression in children and adolescents with ASD: prevalence and risk factors.
SFARI Gene: An evolving database for the autism research community.
Distinct subclasses of medium spiny neurons differentially regulate striatal motor behaviors.
Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior.
Dissociable brain mechanisms for processing social exclusion and rule violation.
Haploinsufficiency of the autism-associated SHANK3 gene leads to deficits in synaptic function, social interaction, and social communication.
Evaluation, diagnosis, and treatment of gastrointestinal disorders in individuals with ASDs: a consensus report.
Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders.
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