Progress in understanding and treating SCN2A-mediated disorders.
Clinical
Neonatal transitions in social behavior and their implications for autism.
Visual perception in genetically characterized autism subpopulations
Caroline Robertson plans to assess alterations in binocular rivalry in two distinct genetic subgroups of autism: fragile X syndrome and 16p11.2 deletion syndrome. Findings from these studies will lead to a better understanding of how sensory-perception deficits relate to specific subtypes of autism and will help to stratify individuals based on therapies they might be likely to respond to.
Associations between familial rates of psychiatric disorders and de novo genetic mutations in autism.
Plasma anandamide concentrations are lower in children with autism spectrum disorder.
Subcortical brain and behavior phenotypes differentiate infants with autism versus language delay.
Child and family characteristics moderate agreement between caregiver and clinician report of autism symptoms.
Sex differences in autism spectrum disorder: A review
Differential attention to faces in infant siblings of children with autism spectrum disorder and associations with later social and language ability.
Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion.
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