Maternal loss of UBE3A impairs experience-driven dendritic spine maintenance in the developing visual cortex.
Research Articles
Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder.
A systematic variant annotation approach for ranking genes associated with autism spectrum disorders.
Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.
Loss and gain of MeCP2 cause similar hippocampal circuit dysfunction that is rescued by deep brain stimulation in a Rett syndrome mouse model.
Putative microcircuit-level substrates for attention are disrupted in mouse models of autism.
Visualizing the origins of selfish de novo mutations in individual seminiferous tubules of human testes.
Auditory processing in noise is associated with complex patterns of disrupted functional connectivity in autism spectrum disorder.
DIXDC1 contributes to psychiatric susceptibility by regulating dendritic spine and glutamatergic synapse density via GSK3 and Wnt/beta-catenin signaling.
Adult restoration of SHANK3 expression rescues selective autistic-like phenotypes.
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