Copy number variations and cognitive phenotypes in unselected populations.
Research Articles
Modeling a model: Mouse genetics, 22q11.2 deletion syndrome, and disorders of cortical circuit development.
Children with 7q11.23 duplication syndrome: Psychological characteristics.
miRNA-target chimeras reveal miRNA 3′-end pairing as a major determinant of Argonaute target specificity.
Altered neuronal and circuit excitability in fragile X syndrome.
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment.
An acetylcholine-activated microcircuit drives temporal dynamics of cortical activity.
Methyl-CpG binding protein 2 regulates microglia and macrophage gene expression in response to inflammatory stimuli.
Mutations in SLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelination.
Replicated linear association between DUF1220 copy number and severity of social impairment in autism.
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