Preprints

HAT: de novo variant calling for highly accurate short-read and long-read sequencing data.

Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations.

The neural bases of language processing during social and non-social contexts: A fNIRS study of autistic and neurotypical preschool-aged children.

Tunable, proteolytic dosage control of CRISPR-Cas systems enables precise gene therapy for dosage sensitive disorders.

Molecular and cellular dynamics of the developing human neocortex at single-cell resolution.

Phenotypical divergence between self-reported and clinically ascertained autism.

Polygenic and developmental profiles of autism differ by age at diagnosis.

Human-specific gene expansions contribute to brain evolution.

Early developmental origins of cortical disorders modeled in human neural stem cells.

Decomposition of phenotypic heterogeneity in autism reveals distinct and coherent genetic programs.