Synthesis and evaluation of a new 18F-labeled radiotracer for studying the GABAB receptor in the mouse brain.
Research Articles
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.
Integrative functional genomic analysis of human brain development and neuropsychiatric risks.
Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder.
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.
m6A facilitates hippocampus-dependent learning and memory through YTHDF1.
Language delay aggregates in toddler siblings of children with autism spectrum disorder.
- Previous Page
- Viewing
- Next Page