Literature DB >> 17520691

Decomposing the autism phenotype into familial dimensions.

Peter Szatmari1, Chantal Mérette, Claudia Emond, Lonnie Zwaigenbaum, Marshall B Jones, Michel Maziade, Marc-Andre Roy, Roberta Palmour.   

Abstract

The objective of this article is to decompose the level of functioning phenotype in autism to see if it can be conceptualized as two simpler, but still familial, dimensional phenotypes of language and non-verbal IQ. We assembled 80 sibpairs with either autism, Asperger syndrome or atypical autism. To see whether the familial correlation on language scores was accounted for by the familial correlation on non-verbal IQ, residual language scores were calculated for each member of the sibpair based on a multiple regression equation using their IQ score as an explanatory or independent variable and controlling for the age and gender of the affected individual. These residual scores were then used to calculate intraclass correlations between affected sibs. This process was repeated using IQ as the dependent variable and language as a covariate. Within affected individuals there was a strong relation between non-verbal IQ (as measured by the Leiter performance scale) and language (as measured by the Vineland Communication Scale). In addition, there was familial correlation between sibs on both measures. Evidence of familial aggregation on both non-verbal IQ and language remained even after partialling out the effect of the covariates by regression analysis and by generalized estimating equation. These findings suggest that non-verbal IQ and language in PDD may arise from independent genetic mechanisms. The implications of this finding for linkage analysis and for identifying genetically informative phenotypes are discussed. (c) 2007 Wiley-Liss, Inc.

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Year:  2008        PMID: 17520691     DOI: 10.1002/ajmg.b.30561

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  11 in total

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Journal:  Neurotoxicology       Date:  2009-07-09       Impact factor: 4.294

3.  PDD symptoms in ADHD, an independent familial trait?

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Journal:  J Abnorm Child Psychol       Date:  2009-04

4.  Eighteen-year-old man with autism, obsessive compulsive disorder and a SHANK2 variant presents with severe anorexia that responds to high-dose fluoxetine.

Authors:  Zhen A Lu; Weiyi Mu; Lauren M Osborne; Zachary A Cordner
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5.  Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism.

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6.  Infant siblings and the investigation of autism risk factors.

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7.  Genome-wide linkage analyses of quantitative and categorical autism subphenotypes.

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Journal:  Biol Psychiatry       Date:  2008-07-16       Impact factor: 13.382

8.  A molecular genetic study of autism and related phenotypes in extended pedigrees.

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9.  The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.

Authors:  A K Merikangas; R Segurado; E A Heron; R J L Anney; A D Paterson; E H Cook; D Pinto; S W Scherer; P Szatmari; M Gill; A P Corvin; L Gallagher
Journal:  Mol Psychiatry       Date:  2014-11-25       Impact factor: 15.992

10.  Language delay aggregates in toddler siblings of children with autism spectrum disorder.

Authors:  N Marrus; L P Hall; S J Paterson; J T Elison; J J Wolff; M R Swanson; J Parish-Morris; A T Eggebrecht; J R Pruett; H C Hazlett; L Zwaigenbaum; S Dager; A M Estes; R T Schultz; K N Botteron; J Piven; J N Constantino
Journal:  J Neurodev Disord       Date:  2018-10-22       Impact factor: 4.025

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