1. Rothemund Y, Paepke S, Flor H. Perception of risk, anxiety, and health behaviors in women at high risk for breast cancer. Int J Behav Med. 2001. 8:230–239.
Article
2. Anderson G, Jun M, Choi K. Breast cancer screening for Korean women must consider traditional risks as well as two genetic risk factors: genetic polymorphisms and inheritable gene mutations. Cancer Nurs. 2007. 30:213–222.
Article
3. Han SA, Park SK, Ahn SH, Lee MH, Noh DY, Kim LS, et al. Korean Breast Cancer Study Group. The Korean Hereditary Breast Cancer (KOHBRA) study: protocols and interim report. Clin Oncol (R Coll Radiol). 2011. 23:434–441.
Article
4. Lee EH, Park SK, Park B, Kim SW, Lee MH, Ahn SH, et al. KOHBRA Research Group. Korean Breast Cancer Society. Effect of BRCA1/2 mutation on short-term and long-term breast cancer survival: a systematic review and meta-analysis. Breast Cancer Res Treat. 2010. 122:11–25.
Article
5. Ahn SH, Son BH, Yoon KS, Noh DY, Han WS, Kim SW, et al. BRCA1 and BRCA2 germline mutations in Korean breast cancer patients at high-risk of carrying mutations. Cancer Lett. 2007. 245:90–95.
Article
6. Crotser CB, Dickerson SS. Women receiving news of a family BRCA1/2 mutation:messages of fear and empowerment. J Nurs Scholarsh. 2010. 42:367–378.
Article
7. Vos J, Jansen AM, Menko F, van Asperen CJ, Stiggelbout AM, Tibben A. Family communication matters: the impact of telling relatives about unclassified variants and uninformative DNA-test results. Genet Med. 2011. 13:333–341.
Article
8. Welkenhuysen M, Evers-Kiebooms G, d'Ydewalle G. The language of uncertainty in genetic risk communication: Framing verbal versus numerical information. Patient Educ Couns. 2001. 43:179–187.
Article
9. Jun MH, Choi KS, Ahn SH, Gu BK. Experiences of high-risk breast cancer women undertaking genetic test. J Korean Oncol Nurs. 2005. 5:146–169.
10. Ropper J, Shapira J. Ethnography in nursing research. 2000. London: Sage Publication.
11. Agar M. The professional stranger. 1980. Orlando, FL: Academic Press.
12. Park TH. The influences of familism on interpersonal trust in South Korea. Korean Public Adm Rev. 2004. 9:121–135.
13. DudokdeWit AC, Tibben A, Frets PG, Meijers-Heijboer EJ, Devilee P, Klikin JGM, et al. BRCA1 in the family: a case description of the psychological implications. Am J Med Genet. 1997. 71:63–71.
Article
14. Marteau T, Richards M. The troubled helix: Social and psychological implications of the new human genetics. 1996. Cambridge: Cambridge Univ..
15. Claes E, Evers-Kiebooms G, Boogacrts A, Decruyenacre M, Denayer L, Legius E. Communication with close and distant relatives in the context of genetic testing for hereditary breast and ovarian cancer in cancer patients. Am J Med Genet. 2003. 116A:11–19.
Article
16. Kenen R, Arden-Jones A, Eeles R. Health women form suspected hereditary breast and ovarian cancer families: The significant others in their lives. Eur J Cancer Care (Engl). 2004. 13:169–179.
Article
17. Gu BK. Comparison of Knowledge According to the Risk of Hereditary Breast Cancer [dissertation]. 2007. Seoul: Ehwa Univ..
18. Friesen P, Pepler C, Hunter P. Interactive family learning following a cancer diagnosis. Oncol Nurs Forum. 2002. 29:981–987.
Article
19. Powe BD, Finnie R. Cancer fatalism. Cancer Nurs. 2003. 26:454–465.
Article
20. Chapman E. Ethical dilemmas in testing for late-onset conditions: Reactions to testing and perceived impact on other family members. J Genet Couns. 2002. 11:351–367.
Article
21. Doukas DJ, Berg JW. The family covenant and genetic testing. Am J Bioeth. 2001. 1:3–10.
Article
22. Loewy R. Families, communities, and making medical decisions. J Clin Ethics. 1991. 2:150–153.
23. Douglas HA, Hamilton RJ, Grubs RE. The effect of BRCA gene testing on family relationships: a thematic analysis of qualitative interviews. J Genet Couns. 2009. 18:418–435.
Article
24. Ersig AL, Hadley DW, Koehly LM. Understanding patterns of health communication in families at risk for hereditary nonpolyposis colorectal cancer: examining the effect of conclusive versus indeterminate genetic test results. Health Commun. 2011. 26:587–594.
Article
25. Hall MA, Rich SS. Patients' fear of genetic discrimination by health insurance: The impact of legal protections. Genet Med. 2000. 2:214–221.
Article
26. Hall M, Rich S. Laws restricting health insurers' use of genetic information: Impact on genetic discrimination. Am J Med Genet. 2000. 66:293–307.
Article
27. Hurst M, Lieber C, Lewis LJ, Grob R. Family stories: narrative genetics and conceptions of heritability in pregnant women. J Midwifery Womens Health. 2011. 56:26–32.
Article
28. Boylan M. Autonomy: the delicate balance: genetic testing. Camb Q Healthc Ethics. 2002. 11:246–256.