Research Articles

Genoppi is an open-source software for robust and standardized integration of proteomic and genetic data.

Increased variability but intact integration during visual navigation in autism spectrum disorder.

Is motor impairment in autism spectrum disorder distinct from developmental coordination disorder? A report from the SPARK study.

VariCarta: A comprehensive database of harmonized genomic variants found in autism spectrum disorder sequencing studies.

Loss of the neural-specific BAF subunit ACTL6B relieves repression of early response genes and causes recessive autism.

Large mosaic copy number variations confer autism risk.

Enhancing WNT signaling restores cortical neuronal spine maturation and synaptogenesis in Tbr1 mutants.

Social stimuli induce activation of oxytocin neurons within the paraventricular nucleus of the hypothalamus to promote social behavior in male mice.

Co-localization between sequence constraint and epigenomic information improves interpretation of whole-genome sequencing data.

Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex.