Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci.
Research Articles
Symmetrical dose-dependent DNA-methylation profiles in children with deletion or duplication of 7q11.23.
Sex differences in structural organization of motor systems and their dissociable links with repetitive/restricted behaviors in children with autism.
In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9.
Maternal gesture use and language development in infant siblings of children with autism spectrum disorder.
Mutations in SPATA5 are associated with microcephaly, intellectual disability, seizures, and hearing loss.
Contribution of mGluR5 to pathophysiology in a mouse model of human chromosome 16p11.2 microdeletion.
Cognitive decline preceding the onset of psychosis in patients with 22q11.2 deletion syndrome.
Correspondence between resting-state activity and brain gene expression.
Atypical visual saliency in autism spectrum disorder quantified through model-based eye tracking.
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