Genome-Wide DNA Methylation Analysis Reveals Epigenetic Pattern of SH2B1 in Chinese Monozygotic Twins Discordant for Autism Spectrum Disorder

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A beta-mixture quantile normalization method for correcting probe design bias in Illumina Infinium 450 k DNA methylation data

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DNA methylation arrays as surrogate measures of cell mixture distribution

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Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother

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Prevalence of Autism Spectrum Disorders in a Total Population Sample

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Autism Spectrum Disorders and Epigenetics

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The conundrums of understanding genetic risks for autism spectrum disorders

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Global methylation profiling of lymphoblastoid cell lines reveals epigenetic contributions to autism spectrum disorders and a novel autism candidate gene, RORA, whose protein product is reduced in autistic brain

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Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity

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Association between Microdeletion and Microduplication at 16p11.2 and Autism

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