Genetics

Quantitative fate mapping: Reconstructing progenitor field dynamics via retrospective lineage barcoding.

Potential role for immune-related genes in autism spectrum disorders: Evidence from genome-wide association meta-analysis of autistic traits.

Integrative analyses of de novo mutations provide deeper biological insights into autism spectrum disorder.

Estimating the prevalence and genetic risk mechanisms of ARFID in a large autism cohort.

Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency.

Precise genome editing across kingdoms of life using retron-derived DNA.

Environmental carcinogens disproportionally mutate genes implicated in neurodevelopmental disorders.

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.

PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans.

Phenotypic subtyping and re-analysis of existing methylation data from autistic probands in simplex families reveal ASD subtype-associated differentially methylated genes and biological functions.

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