Autism BrainNet

The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.

Autism spectrum disorder: Neuropathology and animal models.

T-lymphocytes and cytotoxic astrocyte blebs correlate across autism brains.

Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue.

The microglial innate immune receptor TREM2 is required for synapse elimination and normal brain connectivity.

Autism-like phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing.

Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism.

Decreased parvalbumin mRNA levels in cerebellar Purkinje cells in autism.

Disruption of melatonin synthesis is associated with impaired 14-3-3 and miR-451 levels in patients with autism spectrum disorders.

Allele-specific expression in a family quartet with autism reveals mono-to-biallelic switch and novel transcriptional processes of autism susceptibility genes.