A Genome Wide Search for Genes Underlying the Developmental Origins of Health and Disease

  • Pennell, Craig (Chief Investigator)
  • Palmer, Lyle (Investigator 02)
  • Beilin, Lawrence (Investigator 03)
  • Newnham, John (Investigator 04)
  • Lye, Stephen (Investigator 05)
  • Smith, George Davey (Investigator 06)

Project Details

StatusFinished
Effective start/end date31/12/08 → 31/12/11

Funding

  • National Health & Medical Research Council NHMRC: A$989,500.00

Access Project

  • Dietary and supplemental intake of vitamins C and E is associated with altered DNA methylation in an epigenome-wide association study meta-analysis

    Keshawarz, A., Joehanes, R., Ma, J., Lee, G. Y., Costeira, R., Tsai, P. C., Masachs, O. M., Bell, J. T., Wilson, R., Thorand, B., Winkelmann, J., Peters, A., Linseisen, J., Waldenberger, M., Lehtimäki, T., Mishra, P. P., Kähönen, M., Raitakari, O., Helminen, M., Wang, C. A., & 14 othersMelton, P. E., Huang, R. C., Pennell, C. E., O'Sullivan, T. A., Ochoa-Rosales, C., Voortman, T., van Meurs, J. B. J., Young, K. L., Graff, M., Wang, Y., Kiel, D. P., Smith, C. E., Jacques, P. F. & Levy, D., 1 Dec 2023, In: Epigenetics. 18, 1, 1 p., 2211361.

    Research output: Contribution to journal › Article › peer-review

    Open Access

  • Language and reading impairments are associated with increased prevalence of non-right-handedness

    Abbondanza, F., Dale, P. S., Wang, C. A., Hayiou-Thomas, M. E., Toseeb, U., Koomar, T. S., Wigg, K. G., Feng, Y., Price, K. M., Kerr, E. N., Guger, S. L., Lovett, M. W., Strug, L. J., van Bergen, E., Dolan, C. V., Tomblin, J. B., Moll, K., Schulte-Körne, G., Neuhoff, N., Warnke, A., & 13 othersFisher, S. E., Barr, C. L., Michaelson, J. J., Boomsma, D. I., Snowling, M. J., Hulme, C., Whitehouse, A. J. O., Pennell, C. E., Newbury, D. F., Stein, J., Talcott, J. B., Bishop, D. V. M. & Paracchini, S., 1 Jul 2023, In: Child Development. 94, 4, p. 970-984 15 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    1 Citation (Web of Science)

  • A saturated map of common genetic variants associated with human height

    23andMe Research Team, VA Million Vet Program, DiscovEHR DiscovEHR MyCode Communi, eEMERGE Elect Med Records Genomics, LifeLines Cohort Study, PRACTICAL Consortium & Understanding Soc Sci Grp, 27 Oct 2022, In: Nature. 610, 7933, p. 704-712 9 p.

    Research output: Contribution to journal › Article › peer-review

    Open Access
    70 Citations (Scopus)
View all 11 research outputs