Differences in social brain function in autism spectrum disorder are linked to the serotonin transporter.
Preprints
Atlas of functional connectivity relationships across rare and common genetic variants, traits, and psychiatric conditions.
Prevalence of returnable genetic results based on recognizable phenotypes among children with autism spectrum disorder.
The ciliary gene INPP5E confers dorsal telencephalic identity to human cortical organoids by negatively regulating sonic hedgehog signalling.
Association of CDH11 with ASD revealed by matched-gene co-expression analysis and mouse behavioral studies.
A normative model representing autistic individuals amidst autism spectrum disorders phenotypic heterogeneity.
Generation of fate patterns via intercellular forces.
Microglia complement signaling promotes neuronal elimination and normal brain functional connectivity.
fmr1 mutation interacts with sensory experience to alter the early development of behavior and sensory coding in zebrafish.
Sex differences in brain development in fetuses and infants who are at low or high likelihood for autism.
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