Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes.
Research Articles
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.
Spectrum or subtypes? A latent profile analysis of restricted and repetitive behaviours in autism.
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