Homozygous loss of autism-risk gene CNTNAP2 results in reduced local and long-range prefrontal functional connectivity.
Research Articles
Maternal immunoreactivity to herpes simplex virus 2 and risk of autism spectrum disorder in male offspring.
Retrograde synaptic inhibition is mediated by alpha-neurexin binding to the alpha2delta subunits of N-type calcium channels.
Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.
UBE3A loss increases excitability and blunts orientation tuning in the visual cortex of Angelman syndrome model mice.
Neurogenetic analysis of childhood disintegrative disorder.
The maternal interleukin-17a pathway in mice promotes autism-like phenotypes in offspring.
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