Preprints

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.

Brunner syndrome associated MAOA dysfunction in human dopaminergic neurons results in NMDAR hyperfunction and increased network activity.

Gamete simulation improves polygenic transmission disequilibrium analysis.

Distinct ensembles in the noradrenergic locus coeruleus evoke diverse cortical states.