Preprints

Dissecting autism genetic risk using single-cell RNA-seq data.

The general impact of haploinsufficiency on brain connectivity underlies the pleiotropic effect of neuropsychiatric CNVs.

Natural selection influenced the genetic architecture of brain structure, behavioral and neuropsychiatric traits.

Genome-wide molecular effects of the neuropsychiatric 16p11 CNVs in an iPSC-to-iN neuronal model.

The oft-overlooked massively parallel reporter assay: Where, when, and which psychiatric genetic variants are functional?

Massively parallel disruption of enhancers active during human corticogenesis.

Towards neurosubtypes in autism.

G-graph: An interactive genomic graph viewer.

FMRP binding to a ranked subset of long genes is revealed by coupled CLIP and TRAP in specific neuronal cell types.

Shared risk alleles with discordant polygenic effects: Disentangling the genetic overlap between ASD and ADHD.