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Functional impact of global rare copy number variation in autism spectrum disorders
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Prevalence of sensory impairments, physical and intellectual disabilities, and mental health in children and young people with self/proxy-reported autism: Observational study of a whole country population
Individual common variants exert weak effects on the risk for autism spectrum disorders
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Charles XII seems to have fulfilled all the criteria of Asperger syndrome
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
'Theory of mind' in the brain. Evidence from a PET scan study of Asperger syndrome
A genome-wide scan for common alleles affecting risk for autism
