Cullen, M. B. R., Meiser, B., Barlow-Stewart, K., Green, M., Appelbaum, P. S., Carr, V. J., Cairns, M. J., Lebowitz, M. S., & Kaur, R. (2022). Perceptions of causal attribution and attitudes to genetic testing among people with schizophrenia and their first-degree relatives. European Journal of Human Genetics, 30(10), 1147–1154. https://doi.org/10.1038/s41431-022-01116-8

Wynn, J., Milo Rasouly, H., Vasquez‐Loarte, T., Saami, A. M., Weiss, R., Ziniel, S. I., Appelbaum, P. S., Wright Clayton, E., Christensen, K. D., Fasel, D., Green, R. C., Hain, H. S., Harr, M., Hoell, C., Kullo, I. J., Leppig, K. A., Myers, M. F., Pacyna, J. E., Perez, E. F., … Holm, I. A. (2021). Do research participants share genomic screening results with family members? Journal of Genetic Counseling, 31(2), 447–458. Portico. https://doi.org/10.1002/jgc4.1511

Garofalo, D. C., Rosenblum, H. A., Zhang, Y., Chen, Y., Appelbaum, P. S., & Sabatello, M. (2022). Increasing inclusivity in precision medicine research: Views of deaf and hard of hearing individuals. Genetics in Medicine, 24(3), 712–721. https://doi.org/10.1016/j.gim.2021.11.015