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Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.18/311

Title: Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism
Authors: Vieland, V.J.
Hallmayer, J.
Huang, Y.
Pagnamenta, A.T.
Pinto, D.
Khan, H.
Monaco, A.P.
Paterson, A.D.
Scherer, S.W.
Sutcliffe, J.S.
Szatmari, P.
The Autism Genome Project (AGP)
Keywords: Autism
Linkage analysis
Genome-wide association
PPL
PPLD
IQ
Perturbações do Desenvolvimento Infantil e Saúde Mental
Issue Date: Jun-2011
Publisher: Springer
Citation: J Neurodev Disord. 2011 Jun;3(2):113-123. Epub 2011 Jan 19
Abstract: The Autism Genome Project has assembled two large datasets originally designed for linkage analysis and genome-wide association analysis, respectively: 1,069 multiplex families genotyped on the Affymetrix 10 K platform, and 1,129 autism trios genotyped on the Illumina 1 M platform. We set out to exploit this unique pair of resources by analyzing the combined data with a novel statistical method, based on the PPL statistical framework, simultaneously searching for linkage and association to loci involved in autism spectrum disorders (ASD). Our analysis also allowed for potential differences in genetic architecture for ASD in the presence or absence of lower IQ, an important clinical indicator of ASD subtypes. We found strong evidence of multiple linked loci; however, association evidence implicating specific genes was low even under the linkage peaks. Distinct loci were found in the lower IQ families, and these families showed stronger and more numerous linkage peaks, while the normal IQ group yielded the strongest association evidence. It appears that presence/absence of lower IQ (LIQ) demarcates more genetically homogeneous subgroups of ASD patients, with not just different sets of loci acting in the two groups, but possibly distinct genetic architecture between them, such that the LIQ group involves more major gene effects (amenable to linkage mapping), while the normal IQ group potentially involves more common alleles with lower penetrances. The possibility of distinct genetic architecture across subtypes of ASD has implications for further research and perhaps for research approaches to other complex disorders as well.
Description: Member of the Autism Genome Project Consortium: Astrid M. Vicente
Peer Reviewed: yes
URI: http://hdl.handle.net/10400.18/311
ISSN: 1866-1947
Publisher version: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3105232/?tool=pubmed
Appears in Collections:DPSPDNT - Artigos em revistas internacionais

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