Simons Simplex Collection

Genome-wide detection of tandem DNA repeats that are expanded in autism.

DAS-II cognitive profiles are not diagnostically meaningful for autism: A ROC analysis.

Leveraging large genomic datasets to illuminate the pathobiology of autism spectrum disorders.

Gene discoveries in autism are biased towards comorbidity with intellectual disability.

Autism and attention-deficit/hyperactivity disorders and symptoms in children with neurofibromatosis type 1.

A structural variation reference for medical and population genetics.

Does the factor structure of IQ differ between the differential ability scales (DAS-II) normative sample and autistic children?

Large mosaic copy number variations confer autism risk.

Co-localization between sequence constraint and epigenomic information improves interpretation of whole-genome sequencing data.

A computational tool (H-MAGMA) for improved prediction of brain-disorder risk genes by incorporating brain chromatin interaction profiles.

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