Research Articles

Reduced conditioned fear response in mice that lack DLX1 and show subtype-specific loss of interneurons.

A truncating mutation of TRAPPC9 is associated with autosomal-recessive intellectual disability and postnatal microcephaly.

Haploinsufficiency for Pten and serotonin transporter cooperatively influences brain size and social behavior.

A 15q13.3 microdeletion segregating with autism.

Damage to association fiber tracts impairs recognition of the facial expression of emotion.

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.