Research Articles

DNMT3A haploinsufficiency results in behavioral deficits and global epigenomic dysregulation shared across neurodevelopmental disorders.

SCN2A-developmental and epileptic encephalopathies: Challenges to trial-readiness for non-seizure outcomes.

Regional, layer, and cell-type-specific connectivity of the mouse default mode network.

Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse neocortex.

Sex-specific stress-related behavioral phenotypes and central amygdala dysfunction in a mouse model of 16p11.2 microdeletion.

Altered hippocampal-prefrontal communication during anxiety-related avoidance in mice deficient for the autism-associated gene Pogz.

Towards a data driven approach to screen for autism risk at 12 months of age.

16p11.2 microdeletion imparts transcriptional alterations in human iPSC-derived models of early neural development.

Reduced sensory habituation in autism and its correlation with behavioral measures.

Computation of the electroencephalogram (EEG) from network models of point neurons.