Simons Simplex Collection

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.

Application of DSM-5 criteria for autism spectrum disorder to three samples of children with DSM-IV diagnoses of pervasive developmental disorders.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.

Using large clinical datasets to infer pathogenicity for rare copy number variants in autism cohorts.

Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autism.

Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion.

Patterns and predictors of anxiety among siblings of children with autism spectrum disorders.

Soy infant formula may be associated with autistic behaviors.

Face recognition deficits in autism spectrum disorders are both domain specific and process specific.

Using whole-exome sequencing to identify inherited causes of autism.

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