Identifying Novel Susceptibility Loci for Osteoporosis Through Whole Genome Sequencing

  • Wilson, Scott (Chief Investigator)
  • Walsh, John (Chief Investigator)
  • Richards, Brent (Chief Investigator)
  • Price, Roger (Chief Investigator)
  • Spector, Timothy (Chief Investigator)
  • Dudbridge, Frank (Chief Investigator)
    StatusFinished
    Effective start/end date1/01/13 → 31/12/15
    Linkshttp://purl.org/au-research/grants/nhmrc/1048216

    Funding

    • National Health & Medical Research Council NHMRC
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    Research Output

    Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes

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    Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density

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    DNA methylation and the social gradient of osteoporotic fracture: A conceptual model

    Research output: Contribution to journal › Literature review

    Genetic regulatory mechanisms in human osteoclasts suggest a role for the STMP1 and DCSTAMP genes in Paget’s disease of bone

    Research output: Contribution to journal › Article

    Meta-analysis of genomewide association studies reveals genetic variants for hip bone geometry

    Research output: Contribution to journal › Article

    Datasets

    BUA GWAS gender-combined meta-analysis summary results

    Dataset