Jordan, Margaret A., Gresle, Melissa M., Gemiarto, Adrian T., Stanley, Dragana, Smith, Letitia D., Laverick, Louise, Spelman, Tim, Stankovich, Jim, Willson, Annie M.L., Dinh, Xuyen T., Johnson, Laura, Robertson, Kylie, Reid, Christopher A.R., Field, Judith, Butzkueven, Helmut, and Baxter, Alan G. (2024) Transcriptional network analysis of peripheral blood leukocyte subsets in multiple sclerosis identifies a pathogenic role for a cytotoxicity‐associated gene network in myeloid cells. Immunology & Cell Biology. (In Press)

Yeh, W., Gresle, M., Lea, R., Jokubaitis, J., van der Walt, A., Jordan, M., Baxter, A., Smith, L., and Butzkueven, H. (2021) Differentially regulated pathways by endogenous vitamin D in multiple sclerosis identified by transcriptomics of immune cell subsets. Multiple Sclerosis Journal, 27 (2S). P333. p. 343.

Field, Judith, Shahijanian, Fernando, Schibeci, Stephen, Australia and New Zealand MS Genetics Consortium, (ANZgene), Johnson, Laura, Gresle, Melissa, Laverick, Louise, Parnell, Grant, Stewart, Graeme, McKay, Fiona, Kilpatrick, Trevor, Butzkueven, Helmut, and Booth, David (2015) The MS risk allele of CD40 is associated with reduced cell-membrane bound expression in antigen presenting cells: implications for gene function. PLoS ONE, 10 (6). e0127080. pp. 1-14.

Gu, Ben J., Field, Judith, Dutertre, Sébastien, Ou, Amber, Kilpatrick, Trevor J., Lechner-Scott, Jeannette, Scott, Rodney, Lea, Rodney, Taylor, Bruce V., Stankovich, Jim, Butzkueven, Helmut, Gresle, Melissa, Laws, Simon M., Petrou, Steven, Hoffjan, Sabine, Akkad, Denis A., Graham, Colin A., Hawkins, Stanley, Bedri, Sahl Khalid, Glaser, Anna, Hillert, Jan, Matute, Carlos, Antiguedad, Alfredo, Wiley, James S., and ANZgene Consortium inlcuding Alan G. Baxter (2015) A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis. Human Molecular Genetics, 24 (19). pp. 5644-5654.

Gresle, Melissa M., Schulz, Katrin, Jonas, Anna, Perreau, Victoria M., Cipriani, Tania, Baxter, Alan G., Miranda-Hernandez, Socorro, Field, Judith, Jokubaitis, Vilija G., Cherny, Robert, Volitakis, Irene, David, Samuel, Kilpatrick, Trevor J., and Butzkueven, Helmut (2014) Ceruloplasmin gene-deficient mice with experimental autoimmune encephalomyelitis show attenuated early disease evolution. Journal of Neuroscience Research, 92 (6). pp. 732-742.

Shahijanian, Fernando, Parnell, Grant P., McKay, Fiona C., Gatt, Prudence N., Shojoei, Maryam, O'Connor, Kate S., Schibeci, Stephen D., Brilot, Fabienne, Liddle, Christopher, Batten, Marcel, Baxter, Alan, Kermode, Allan, Carrol, William, Butzkueven, Helmut, Vucic, Steve, Wiley, James, Field, Judith, Tajouri, Lotti, Griffiths, Lyn, Barnett, Michael, Scott, Rodney, Lechner-Scott, Jeannette, Moscato, Pablo, Broadley, Simon, Slee, Mark, Kilpatrick, Trevor, Taylor, Bruce, Charlesworth, Jac, Brown, Matt, Mason, Deborah, Graeme, Stewart J., and Booth, David R. (2014) The CYP27B1 variant associated with an increased risk of autoimmune disease is underexpressed in tolerizing dendritic cells. Human Molecular Genetics, 23 (6). pp. 1425-1434.

Jordan, Margaret A., Field, Judith, Butzkueven, Helmut, and Baxter, Alan G. (2014) Genetic predisposition, humans. In: Rose, Noel R., and Mackay, Ian R., (eds.) The Autoimmune Diseases. Elsevier, Boston, MA, USA, pp. 341-364.