Research Articles

The visual perception of human and animal motion in point-light displays.

Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+.

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities.

MET and autism susceptibility: family and case-control studies.

Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.

Partial reversal of Rett syndrome-like symptoms in MeCP2 mutant mice.

Intact rapid detection of fearful faces in the absence of the amygdala.

Ube3a is required for experience-dependent maturation of the neocortex.

A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum export.

Pharmacological inhibition of mTORC1 suppresses anatomical, cellular, and behavioral abnormalities in neural-specific PTEN knock-out mice.