Research Articles

Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes.

Hierarchical cortical transcriptome disorganization in autism.

Epidemiological and serological investigation into the role of gestational maternal influenza virus infection and autism spectrum disorders.

Shank is a dose-dependent regulator of Ca_v1 calcium current and CREB target expression.

Differing developmental trajectories in heart rate responses to speech stimuli in infants at high and low risk for autism spectrum disorder.

Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains.

Talking about death or suicide: Prevalence and clinical correlates in youth with autism spectrum disorder in the psychiatric inpatient setting.

A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly, epilepsy and autistic features.

Measuring shared variants in cohorts of discordant siblings with applications to autism.

Prenatal fever and autism risk.