Investigation of maternal genotype effects in autism by genome-wide association.
Research Articles
Modest impact on risk for autism spectrum disorder of rare copy number variants at 15q11.2, specifically breakpoints 1 to 2.
Eating in the absence of hunger but not loss of control behaviors are associated with 16p11.2 deletions.
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors.
Chromatin regulators, phenotypic robustness, and autism risk.
Loss of mTOR-dependent macroautophagy causes autistic-like synaptic pruning deficits
Largely typical patterns of resting-state functional connectivity in high-functioning adults with autism
Oxytocin-mediated GABA inhibition during delivery attenuates autism pathogenesis in rodent offspring.
Equivalent neural responses in children and adolescents with and without autism during judgments of affect.
The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism.
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