Research Articles

Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy.

Pleiotropy between language impairment and broader behavioral disorders-an investigation of both common and rare genetic variants.

Prediction of autism spectrum disorder diagnosis using nonlinear measures of language-related EEG at 6 and 12 months.

Identification of disease-linked hyperactivating mutations in UBE3A through large-scale functional variant analysis.

Exploring the genetic overlap of suicide-related behaviors and substance use disorders.

MYT1L-associated neurodevelopmental disorder: Description of 40 new cases and literature review of clinical and molecular aspects.

S100B dysregulation during brain development affects synaptic SHANK protein networks via alteration of zinc homeostasis.

Creation and evaluation of full-text literature-derived, feature-weighted disease models of genetically determined developmental disorders.

Postmitotic accumulation of histone variant H3.3 in new cortical neurons establishes neuronal chromatin, transcriptome, and identity.

Using the Clinical Global Impression Scale to assess social communication change in minimally verbal children with autism spectrum disorder.