Project & related outputs

Davis, M.D.M., Grahame, J., van Hoffen, C., Roxburgh, N., Sargent, E., Gardiner, B, Hannan, K., Fitzgerald, L., Coman, C., Smith, A.J.K., Newman, C. (2026). Creating safer and more useful health data systems for sexuality and gender diverse people in Australia: Project report and recommendations, July 2026, Monash University, 36 pages, https://doi.org/10.26180/33044282

Davis, M.D.M., Grahame, J., Coman, C., Sargent, E. and Smith, A.K.J. (2026) Practitioner narratives on health data management for sexuality and gender diverse people: Benefits, drawbacks, data fixity, and the exposure/erasure duality in the clinical encounter, Health: Sage.https://journals.sagepub.com/doi/10.1177/13634593261472140

Davis, M. D. M. (2025). Data studies. In R. Cover, & C. E. Newman (Eds.), Elgar Encyclopedia of Queer Studies (1st ed., pp. 83-85). Edward Elgar Publishing. https://doi.org/10.4337/9781803922102.ch021

Holt, M., MacGibbon, J., Smith, A. K J., Broady, T. R., Davis, M.D.M. and Newman, C. (2023) Knowledge of Australia’s My Health Record and factors associated with opting out: results from a national survey of the Australian general population and communities affected by HIV and sexually transmissible infections, PLOS Digital Health. https://doi.org/10.1371/journal.pdig.0000200

Smith, A. K J., Davis, M. D. M., MacGibbon, J., Broady, T. R., Ellard, J., Rule, J., Cook, T., Duck-Chong, E., Holt, M., & Newman, C. E. (2023). Engaging stigmatised communities in Australia with digital health systems: towards data justice in public health. Sexuality Research & Social Policy. https://doi.org/10.1007/s13178-023-00791-6

Davis, M., Schermuly, A., Smith, A., Newman, C. (2022) Diversity via datafication? Digital patient records and citizenship for sexuality and gender diverse people. BioSocieties. https://doi.org/10.1057/s41292-022-00277-5

Newman, C., MacGibbon, J., Smith, A. K. J., Broady, T., Lupton, D., Davis, M., Bear, B., Bath, N., Comensoli, D., Cook, T., Duck-Chong, E., Ellard, J., Kim, J., Rule, J., & Holt, M. (2020). Why trust digital health? Understanding the perspectives of communities affected by BBVs and STIs in Australia. Sydney: UNSW Centre for Social Research in Health. http://doi.org/10.26190/5f6d72f17d2b5