Genetics

Unlocking epigenetic codes in neurogenesis.

De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder.

CRISPR-CAS9 knockin mice for genome editing and cancer modeling.

16p11.2 600 kb duplications confer risk for typical and atypical rolandic epilepsy.

The role of de novo mutations in the genetics of autism spectrum disorders.

The genetic landscape of autism spectrum disorders.

Genes for endosomal NHE6 and NHE9 are misregulated in autism brains.

Decoding neural transcriptomes and epigenomes via high-throughput sequencing.

A genotype-first approach to defining the subtypes of a complex disease.

Facilitated sequence counting and assembly by template mutagenesis.

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