Comprehensive analysis of the 16p11.2 deletion and null CNTNAP2 mouse models of autism spectrum disorder.
Research Articles
Arginine vasopressin is a blood-based biomarker of social functioning in children with autism.
Genotype to phenotype relationships in autism spectrum disorders.
PTEN mutations alter brain growth trajectory and allocation of cell types through elevated beta-catenin signaling.
Eye-tracking measurements of language processing: Developmental differences in children at high risk for ASD.
An expanded sequence context model broadly explains variability in polymorphism levels across the human genome.
Robust classification of protein variation using structural modelling and large-scale data integration.
CASPR2-reactive antibody cloned from a mother of an ASD child mediates an ASD-like phenotype in mice.
Brief report: Further examination of self-injurious behaviors in children and adolescents with autism spectrum disorders.
Mutations in human accelerated regions disrupt cognition and social behavior.
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