Early brain development in infants at high risk for autism spectrum disorder.
Research Articles
Diverse non-genetic, allele-specific expression effects shape genetic architecture at the cellular level in the mammalian brain.
Conditional ablation of neuroligin-1 in CA1 pyramidal neurons blocks LTP by a cell-autonomous NMDA receptor-independent mechanism.
Dynamics of BAF-Polycomb complex opposition on heterochromatin in normal and oncogenic states.
MECP2 regulates cortical plasticity underlying a learned behavior in adult female mice.
Homozygous loss of autism-risk gene CNTNAP2 results in reduced local and long-range prefrontal functional connectivity.
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.
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