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Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.18/247

Título: A genome-wide linkage and association scan reveals novel loci for autism
Autor: Weiss, L.A.
Arking, D.E.
Gene Discovery Project of Johns Hopkins
The Autism Consortium
Daly, M.J.
Chakravarti, A.
Palavras-chave: Perturbações do Desenvolvimento Infantil e Saúde Mental
Issue Date: 8-Oct-2009
Editora: Nature Publishing Group
Citação: Nature. 2009 Oct 8;461(7265):802-8
Resumo: Although autism is a highly heritable neurodevelopmental disorder, attempts to identify specific susceptibility genes have thus far met with limited success. Genome-wide association studies using half a million or more markers, particularly those with very large sample sizes achieved through meta-analysis, have shown great success in mapping genes for other complex genetic traits. Consequently, we initiated a linkage and association mapping study using half a million genome-wide single nucleotide polymorphisms (SNPs) in a common set of 1,031 multiplex autism families (1,553 affected offspring). We identified regions of suggestive and significant linkage on chromosomes 6q27 and 20p13, respectively. Initial analysis did not yield genome-wide significant associations; however, genotyping of top hits in additional families revealed an SNP on chromosome 5p15 (between SEMA5A and TAS2R1) that was significantly associated with autism (P = 2 x 10(-7)). We also demonstrated that expression of SEMA5A is reduced in brains from autistic patients, further implicating SEMA5A as an autism susceptibility gene. The linkage regions reported here provide targets for rare variation screening whereas the discovery of a single novel association demonstrates the action of common variants.
Descrição: Member of the Autism Genome Project Consortium: Astrid M. Vicente
Arbitragem científica: yes
URI: http://hdl.handle.net/10400.18/247
ISSN: 0028-0836
Versão do Editor: http://dx.doi.org/10.1038/nature08490
Appears in Collections:DPSPDNT - Artigos em revistas internacionais

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