Preprints

Phenotype and genetic analysis of data collected within the first year of NeuroDev.

Isoform-level transcriptome-wide association uncovers extensive novel genetic risk mechanisms for neuropsychiatric disorders in the human brain.

Polygenic architecture of rare coding variation across 400,000 exomes.

Human iPSC-derived neuron of 16p11.2 deletion reveals haplotype-specific expression of MAPK3 and its contribution to variable NDD phenotypes.

Integrative single-cell analysis of cardiogenesis identifies developmental trajectories and non-coding mutations in congenital heart disease.

Rare CNVs and phenome-wide profiling: A tale of brain-structural divergence and phenotypical convergence.

Physical and functional convergence of the autism risk genes Scn2a and Ank2 in neocortical pyramidal cell dendrites.

Combined omic analyses reveal novel loss-of-function NLGN3 variants in GnRH deficiency and autism.

Variation in glutamate and GABA genes and their association with brain structure and chemistry in autism.

Narrowband gamma oscillations propagate and synchronize throughout the mouse thalamocortical visual system.