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  1. Polygenic and developmental profiles of autism differ by age at diagnosis.

    Publication

  2. Phenotypic and ancestry-related assortative mating in autism.

    Publication

  3. Phenotype and genetic analysis of data collected within the first year of NeuroDev.

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  4. Validity of the SNAP-IV for ADHD assessment in South African children with neurodevelopmental disorders.

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  5. Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p.

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  6. Developmental variability in autism across 17000 autistic individuals and 4000 siblings without an autism diagnosis: Comparisons by cohort, intellectual disability, genetic etiology, and age at diagnosis.

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  7. A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex.

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  8. Genetic correlates of phenotypic heterogeneity in autism.

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  9. Polygenic architecture of rare coding variation across 400,000 exomes.

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  10. The female protective effect against autism spectrum disorder.

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  11. Prevalence of returnable genetic results based on recognizable phenotypes among children with autism spectrum disorder.

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  12. Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants.

    Publication

  13. Paternal-age-related de novo mutations and risk for five disorders.

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  14. Identification of common genetic risk variants for autism spectrum disorder.

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  15. The NeuroDev study: Phenotypic and genetic characterization of neurodevelopmental disorders in Kenya and South Africa.

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  16. Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders.

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  17. Identification of developmental and behavioral markers associated with genetic abnormalities in autism spectrum disorder.

    Publication

  18. Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.

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  19. ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties.

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  20. Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.

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  21. Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci.

    Publication

  22. Autism spectrum disorder severity reflects the average contribution of de novo and familial influences.

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  23. A framework for the interpretation of de novo mutation in human disease.

    Publication