Literature DB >> 21522181

Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders.

Richard J L Anney1, Elaine M Kenny, Colm O'Dushlaine, Brian L Yaspan, Elena Parkhomenka, Joseph D Buxbaum, James Sutcliffe, Michael Gill, Louise Gallagher, Joseph D Buxbaum, James Sutcliffe, Michael Gill, Louise Gallagher.   

Abstract

Recent genome-wide association studies (GWAS) have implicated a range of genes from discrete biological pathways in the aetiology of autism. However, despite the strong influence of genetic factors, association studies have yet to identify statistically robust, replicated major effect genes or SNPs. We apply the principle of the SNP ratio test methodology described by O'Dushlaine et al to over 2100 families from the Autism Genome Project (AGP). Using a two-stage design we examine association enrichment in 5955 unique gene-ontology classifications across four groupings based on two phenotypic and two ancestral classifications. Based on estimates from simulation we identify excess of association enrichment across all analyses. We observe enrichment in association for sets of genes involved in diverse biological processes, including pyruvate metabolism, transcription factor activation, cell-signalling and cell-cycle regulation. Both genes and processes that show enrichment have previously been examined in autistic disorders and offer biologically plausibility to these findings.

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Year:  2011        PMID: 21522181      PMCID: PMC3190264          DOI: 10.1038/ejhg.2011.75

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  30 in total

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6.  A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.

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  15 in total

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Authors:  Barbara Ruggeri; Ugis Sarkans; Gunter Schumann; Antonio M Persico
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2.  A review of the evidence for the canonical Wnt pathway in autism spectrum disorders.

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3.  Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci.

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4.  Di-(2-ethylhexyl) phthalate and autism spectrum disorders.

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5.  Mapk/Erk activation in an animal model of social deficits shows a possible link to autism.

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6.  Pathway-PDT: a flexible pathway analysis tool for nuclear families.

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7.  Comparative RNA editing in autistic and neurotypical cerebella.

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8.  Individual common variants exert weak effects on the risk for autism spectrum disorders.

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Journal:  Hum Mol Genet       Date:  2012-07-26       Impact factor: 6.150

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

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10.  Enrichment of elevated plasma F2t-isoprostane levels in individuals with autism who are stratified by presence of gastrointestinal dysfunction.

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