Autism spectrum disorder (ASD) is a highly heritable, clinically diverse group of
neurodevelopmental disorders. Its genetic heterogeneity is remarkable, with more than 800 …

Autism spectrum disorders (ASD) are characterized by two seemingly unrelated symptom
domains—deficits in social interactions and restrictive, repetitive patterns of behavioral …

Autism spectrum disorder (ASD) is a common neurodevelopmental disorder with onset in
childhood. The mechanisms underlying ASD are unclear. In recent years, the role of …

Autism spectrum disorder (ASD) is a neurodevelopmental disorder with an unknown
molecular pathogenesis. A recent molecular focus has been the mutated neuroligin 3 …

Autism spectrum disorders (ASD) are a group of neurodevelopmental diseases. The cause
of ASD is unknown, but several genetic and non-genetic risk factors have been …

Autism spectrum disorder (ASD) has a major impact on the development and social
integration of affected individuals and is the most heritable of psychiatric disorders. An …

Researchers have now identified many highly penetrant genetic risk factors for autism
spectrum disorder (ASD). Some of these genes encode synaptic proteins, lending support to …

Autism spectrum disorders (ASD) are common heterogeneous neurodevelopmental
disorders with typical triad of symptoms: impaired social interaction, language and …

Cognitive defects in autism spectrum disorder (ASD) include socialization and
communication: key behavioral capacities that separate humans from other species. Here …

Autism and epilepsy are two associated disorders that are highly prevalent, share common
developmental origins, and demonstrate substantial heritability. In this review, cross …