{"id":"W2151566815","doi":"10.1038/ng1985","title":"Mapping autism risk loci using genetic linkage and chromosomal rearrangements","year":2007,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Autism Spectrum Disorder Research","field":"Neuroscience","cited_by":1416,"is_retracted":false,"has_abstract":false,"ca_institutions":"McGill University; Centre for Addiction and Mental Health; Montreal Children's Hospital; Izaak Walton Killam Health Centre; Hospital for Sick Children; McMaster University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Center for Research Resources; National Institute of Child Health and Human Development; National Institute of Neurological Disorders and Stroke; Canadian Institutes of Health Research; University of California, San Francisco; Assistance publique-Hôpitaux de Paris; Fondation pour la Recherche Médicale; National Institute of Mental Health; Hospital for Sick Children; Centre National de la Recherche Scientifique; Sundhed og Sygdom, Det Frie Forskningsråd; Fondation de France; Deutsche Forschungsgemeinschaft; Ontario Genomics Institute; Orange; Institut National de la Santé et de la Recherche Médicale; University of South Carolina; National Institutes of Health; Ontario Genomics; Genome Canada; Medical Research Council; Howard Hughes Medical Institute; Autism Speaks; University of Miami; Wellcome Trust; Vanderbilt University","keywords":"Biology; Genetics; Copy-number variation; Autism; Genetic architecture; Linkage (software); Heritability of autism; Genetic linkage; SNP; Chromosome; Gene; Candidate gene; Synaptogenesis; Genetic variation; Single-nucleotide polymorphism; Quantitative trait locus; Genome; Phenotype; Genotype; Neuroscience","routes":{"ca_aff":true,"ca_fund":true,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null}