1. Acheson, L. S., Wiesner, G. L., Zyzanski, S. J., Goodwin, M. A., & Stange, K. C. (2000). Family history-taking in community family practice: implications for genetic screening. Genetics in Medicine, 2, 180–185.
2. Acheson, L. S., Zyzanski, S. J., Stange, K. C., Deptowicz, A., & Wiesner, G. L. (2006). Validation of a self-administered, computerized tool for collecting and displaying the family history of cancer. Journal of Clinical Oncology, 34, 5395–5402.
3. Andermann, A. A. J., Austoker, J., Watson, E. K., Lucassen, A. M., & MacKay, J. (2002). Development and evaluation of a general information leaflet for women with a family history of breast cancer. Journal of Cancer Education, 17, 155–160.
4. Antoniou, A., Pharoah, D. P., Narod, S., Risch, H. A., Egfjord, J. E., & Hopper, J. L., et al. (2003). Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: A combined analysis of 22 studies. American Journal of Human Genetics, 72, 1117–1130.
5. Baty, B. J., Kinney, A. Y., & Ellis, S. M. (2003). Developing culturally sensitive cancer genetics communication aids for African Americans. American Journal of Human Genetics, 118A, 146–155.