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

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

    Research output: Contribution to journalArticlepeer-review

    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 ODushlaine 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. © 2011 Macmillan Publishers Limited All rights reserved.
    Original languageEnglish
    Pages (from-to)1082-1089
    Number of pages7
    JournalEuropean Journal of Human Genetics
    Volume19
    Issue number10
    DOIs
    Publication statusPublished - Oct 2011

    Keywords

    • autism
    • family-based association test
    • gene ontology
    • genome-wide association analysis
    • pathway analysis

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