Preprints

Microglia complement signaling promotes neuronal elimination and normal brain functional connectivity.

fmr1 mutation interacts with sensory experience to alter the early development of behavior and sensory coding in zebrafish.

Sex differences in brain development in fetuses and infants who are at low or high likelihood for autism.

Whole-genome analysis of de novo and polymorphic retrotransposon insertions in autism spectrum disorder.

NeuroSCORE: A genome-wide omics-based model to identify candidate disease genes of the central nervous system.

SFARI genes and where to find them; classification modelling to identify genes associated with autism spectrum disorder from RNA-seq data.

Effects of early geometric confinement on the transcriptomic profile of human cerebral organoids.

Identifying cell type specific driver genes in autism-associated copy number loci from cerebral organoids.

Developmental loss of ErbB4 in PV interneurons disrupts state-dependent cortical circuit dynamics.

A configurable model of the synaptic proteome reveals the molecular mechanisms of disease co-morbidity.