Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders.
Research Articles
Associations between familial rates of psychiatric disorders and de novo genetic mutations in autism.
Allele-specific expression in a family quartet with autism reveals mono-to-biallelic switch and novel transcriptional processes of autism susceptibility genes.
Plasma anandamide concentrations are lower in children with autism spectrum disorder.
Subcortical brain and behavior phenotypes differentiate infants with autism versus language delay.
Neuron numbers increase in the human amygdala from birth to adulthood, but not in autism.
Child and family characteristics moderate agreement between caregiver and clinician report of autism symptoms.
Activity regulates cell death within cortical interneurons through a calcineurin-dependent mechanism.
Hierarchical genetic interactions between FOXG1 and LHX2 regulate the formation of the cortical hem in the developing telencephalon.
Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language.
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