Differential DNA methylation of steatosis and non-alcoholic fatty liver disease in adolescence

- Melton, Phillip E., Burton, M. A., Craig, J. M., Olynyk, J. K., Holbrook, J. D., Pennell, C. E., Oddy, W. H., Moses, E. K., Adams, L. A., Huang, R. C., Lillycrop, K. A., Godfrey, K. M., Rauschert, S., Anderson, D., Burdge, G. C., Mori, T. A., Beilin, L. J., Ayonrinde, O. T.

Brain iron accumulation affects myelin-related molecular systems implicated in a rare neurogenetic disease family with neuropsychiatric features

- Heidari, M., Johnstone, D. M., Olynyk, J. K., Trinder, D., Milward, E. A., Bassett, B., Graham, R. M., Chua, A. C. G., House, M. J., Collingwood, J. F., Bettencourt, C., Houlden, H., Ryten, M.

Brain transcriptome perturbations in the transferrin receptor 2 mutant mouse support the case for brain changes in iron loading disorders, including effects relating to long-term depression and long-term potentiation

- Acikyol, B., Graham, R. M., Trinder, D., House, M. J., Olynyk, J. K., Scott, R. J., Milward, E. A., Johnstone, D. M.

The C282Y polymorphism of the hereditary hemochromatosis gene is associated with increased sex hormone-binding globulin and normal testosterone levels in men

- Yeap, B. B., Beilin, J., Shi, Z., Knuiman, M. W., Olynyk, J. K., Chubb, S. A. P., Bruce, D. G., Milward, E. A.

Serum testosterone levels correlate with haemoglobin in middle-aged and older men

- Yeap, B. B., Beilin, J., Shi, Z., Knuiman, M. W., Olynyk, J. K., Bruce, D. G., Milward, E. A.

Hereditary haemochromatosis: to screen or not to screen? (editorial)

- Olynyk, J. K., Trinder, D., Milward, Adrienne Elizabeth