Reciprocal copy number variations at 22q11.2 produce distinct and convergent neurobehavioral impairments relevant for schizophrenia and autism spectrum disorder.
Research Articles
Autism risk in offspring can be assessed through quantification of male sperm mosaicism.
Distinct pathogenic genes causing intellectual disability and autism exhibit a common neuronal network hyperactivity phenotype.
A MEG study of acute arbaclofen (STX-209) administration.
Aberrant calcium channel splicing drives defects in cortical differentiation in Timothy syndrome.
FMRP has a cell-type-specific role in CA1 pyramidal neurons to regulate autism-related transcripts and circadian memory.
IL-17a promotes sociability in mouse models of neurodevelopmental disorders.
The network structure of irritability and aggression in individuals with autism spectrum disorder.
Exploring the familial role of social responsiveness differences between savant and non-savant children with autism.
Abnormal auditory mismatch fields in children and adolescents with 16p11.2 deletion and 16p11.2 duplication.
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