Simons Simplex Collection

Using latent class analysis to identify treatment-use subgroups among parents of children with autism spectrum disorder.

Variations in genes related to sleep patterns in children with autism spectrum disorder.

Linking social motivation with social skill: The role of emotion dysregulation in autism spectrum disorder.

Outgroup machine learning approach identifies single nucleotide variants in noncoding DNA associated with autism spectrum disorder.

A reference haplotype panel for genome-wide imputation of short tandem repeats.

Predicting splicing from primary sequence with deep learning.

Psychometric properties of the Simons Simplex Collection sleep interview.

Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity.

Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder.

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