Field, J.H., Summerhayes, G.R., Luu, S., Coster, A.C.F., Ford, A., Mandui, Herman, Fullagar, R., Hayes, E., Leavesley, M., Lovave, M., and Kealhofer, L. (2020) Functional studies of flaked and ground stone artefacts reveal starchy tree nut and root exploitation in mid-Holocene highland New Guinea. The Holocene, 30 (9). pp. 1360-1374.

Gresle, Melissa M., Jordan, Margaret A., Stankovich, Jim, Spelman, Tim, Johnson, Laura J., Laverick, Louise, Hamlett, Alison, Smith, Letitia D., Jokubaitis, Vilija G., Baker, Josephine, Haartsen, Jodi, Taylor, Bruce, Charlesworth, Jac, Bahlo, Melanie, Speed, Terence P., Brown, Matthew A., Field, Judith, Baxter, Alan G., and Butzkueven, Helmut (2020) Multiple Sclerosis risk variants regulate gene expression in innate and adaptive immune cells. Life Science Alliance, 3 (7). e202000650.

Field, J., Fox, A., Jordan, M.A., Baxter, A.G., Spelman, T., Gresle, M., Butzkueven, H., Kilpatrick, T.J., and Rubio, J.P. (2017) Interleukin-2 receptor-α proximal promoter hypomethylation is associated with multiple sclerosis. Genes and Immunity, 18. pp. 59-66.

Binder, Michele D., Fox, Andrew D., Merlo, Daniel, Johnson, Laura J., Giuffrida, Lauren, Calvert, Sarah E., Akkermann, Rainer, Ma, Gerry Z.M., Perera, Ashwyn A., Gresle, Melissa M., Laverick, Louise, Foo, Grace, Fabis-Pedrini, Marzena J., Spelman, Timothy, Jordan, Margaret A., Baxter, Alan G., Foote, Simon, Butzkueven, Helmut, Kilpatrick, Trevor J., and Field, Judith (2016) Common and low Frequency variants in MERTK are independently associated with multiple sclerosis susceptibility with discordant association dependent upon HLA-DRB1*15:01 status. PLoS Genetics, 12 (3). e1005853. pp. 1-25.

Field, Judith, Merlo, Daniel, Johnson, Laura, Giuffrida, Lauren, Perera, Ashwyn D., Calvert, Sarah, Akkermann, Rainer, Ma, Gerry, ANZgene Consortium, , Gresle, Melissa, Laverick, Louise, Foo, Grace, Spelman, Tim, Jordan, Margaret, Baxter, Alan, Butzkueven, Helmut, Kilpatrick, Trevor, and Binder, Michele D. (2015) Low and moderate frequency variants in MERTK are independently associated with Multiple Sclerosis susceptibility with discordant association dependent upon HLA-DRB1*1501 status. Multiple Sclerosis Journal, 21 (14). p. 29.