Project outputs

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