Research Articles

Psychometric properties of the Simons Simplex Collection sleep interview.

Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.

Establishing cerebral organoids as models of human-specific brain evolution.

Using multiple measurements of tissue to estimate cell-type-specific gene expression via deconvolution.

Synthesis and evaluation of a new 18F-labeled radiotracer for studying the GABAB receptor in the mouse brain.

Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes.

Dendritic spines in early postnatal fragile X mice are insensitive to novel sensory experience.

Genome-wide CRISPR-Cas9 interrogation of splicing networks reveals a mechanism for recognition of autism-misregulated neuronal microexons.

Single-cell RNA sequencing of microglia throughout the mouse lifespan and in the injured brain reveals complex cell-state changes.