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  1. Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations.

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  2. Identification of moderate effect size genes in autism spectrum disorder through a novel gene pairing approach.

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  3. KnockoffTrio: A knockoff framework for the identification of putative causal variants in genome-wide association studies with trio design.

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  4. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.

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  5. Comorbidities in autism spectrum disorder and their etiologies.

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  6. How rare and common risk variation jointly affect liability for autism spectrum disorder.

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  7. Whole-genome and RNA sequencing reveal variation and transcriptomic coordination in the developing human prefrontal cortex.

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

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  9. Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism.

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  10. A genome-wide scan statistic framework for whole-genome sequence data analysis.

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  11. Recessive gene disruptions in autism spectrum disorder.

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

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

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  14. An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder.

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  15. Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

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  16. Integrated Bayesian analysis of rare exonic variants to identify risk genes for schizophrenia and neurodevelopmental disorders.

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  17. Autism spectrum disorder: Neuropathology and animal models.

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  18. Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.

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

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

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  21. Maturation of cortical circuits requires semaphorin 7A.

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

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  23. DAWN: A framework to identify autism genes and subnetworks using gene expression and genetics.

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  24. Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.

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

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  26. Rare complete knockouts in humans: Population distribution and significant role in autism spectrum disorders.

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  27. The autism sequencing consortium: Large-scale, high-throughput sequencing in autism spectrum disorders.

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  28. A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.

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  29. Analysis of a purported SHANK3 mutation in a boy with autism: clinical impact of rare variant research in neurodevelopmental disabilities.

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  30. Haploinsufficiency of the autism-associated SHANK3 gene leads to deficits in synaptic function, social interaction, and social communication.

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  31. High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.

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  32. Common genetic variants on 5p14.1 associate with autism spectrum disorders.

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