Cancer French Institute (2017) Cancer genetics national plan. http://www.e-cancer.fr/Professionnels-de-sante/L-organisation-de-l-offre-de-soins/Oncogenetique/Le-dispositif-national-d-oncogenetique. Accessed 26 Jan 2017
Müller D, Danner M, Rhiem K, Stollenwerk B, Engel C, Rasche L et al (2017) Cost-effectiveness of different strategies to prevent breast and ovarian cancer in German women with a BRCA 1 or 2 mutation. Eur J Health Econ. doi:10.1007/s1019801708875
PubMed
Article
Google Scholar
Nelson HD, Pappas M, Zakher B, Mitchell JP, Okinaka-Hu L, Fu R (2014) Risk assessment, genetic counseling, and genetic testing for BRCA-related cancer in women: a systematic review to update the U.S. Preventive Services Task Force recommendation. Ann Intern Med 160(4):255–266
Article
PubMed
Google Scholar
Cobain EF, Milliron KJ, Merajver SD (2016) Updates on breast cancer genetics: clinical implications of detecting syndromes of inherited increased susceptibility to breast cancer. Semin Oncol 43(5):528–535
Article
PubMed
Google Scholar
Madorsky-Feldman D, Sklair-Levy M, Perri T, Laitman Y, Paluch-Shimon S, Schmutzler R et al (2016) An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers. Breast Cancer Res Treat 157(2):319–327
Article
PubMed
PubMed Central
CAS
Google Scholar
Valachis A, Nearchou AD, Lind P (2014) Surgical management of breast cancer in BRCA-mutation carriers: a systematic review and meta-analysis. Breast Cancer Res Treat 144(3):443–455
Article
PubMed
CAS
Google Scholar
Bednar EM, Oakley HD, Sun CC, Burke CC, Munsell MF, Westin SN, Lu KH (2017) A universal genetic testing initiative for patients with high-grade, non-mucinous epithelial ovarian cancer and the implications for cancer treatment. Gynecol Oncol. doi:10.1016/jygyno201705037
PubMed
Article
PubMed Central
Google Scholar
Evans T, Matulonis U (2017) PARP inhibitors in ovarian cancer: evidence, experience and clinical potential. Ther Adv Med Oncol 9(4):253–267
Article
PubMed
PubMed Central
CAS
Google Scholar
Shugar AL, Quercia N, Trevors C, Rabideau MM, Ahmed S (2017) Risk for patient harm in Canadian genetic counseling practice: it’s time to consider regulation. J Genet Couns 26(1):93–104
Article
PubMed
Google Scholar
Cicero G, De Luca R, Dorangricchia P, Lo Coco G, Guarnaccia C, Fanale D et al (2017) Risk perception and psychological distress in genetic counselling for hereditary breast and/or ovarian cancer. J Genet Couns. doi:10.1007/s1089701700720
PubMed
Article
Google Scholar
Lumish HS, Steinfeld H, Koval C, Russo D, Levinson E, Wynn J et al (2017) Impact of panel gene testing for hereditary breast and ovarian cancer on patients. J Genet Couns. doi:10.1007/s108970170090y
Article
PubMed
Google Scholar
Antoniou AC, Pharoah PP, Smith P, Easton DF (2004) The BOADICEA model of genetic susceptibility to breast and ovarian cancer. Br J Cancer 91(8):1580–1590
Article
PubMed
PubMed Central
CAS
Google Scholar
Schwartz MD, Valdimarsdottir HB, Peshkin BN, Mandelblatt J, Nusbaum R, Huang AT et al (2014) Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer. J Clin Oncol 32(7):618–626
Article
PubMed
PubMed Central
Google Scholar
Sie AS, van Zelst-Stams WA, Spruijt L, Mensenkamp AR, Ligtenberg MJ, Brunner HG et al (2014) More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling. Fam Cancer 13(2):143–151
PubMed
Google Scholar
Kinney AY, Steffen LE, Brumbach BH, Kohlmann W, Du R, Lee JH et al (2016) Randomized noninferiority trial of telephone delivery of BRCA1/2 genetic counseling compared with in-person counseling: 1-year follow-up. J Clin Oncol 34(24):2914–2924
Article
PubMed
PubMed Central
Google Scholar
Høberg-Vetti H, Bjorvatn C, Fiane BE, Aas T, Woie K, Espelid H et al (2016) BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study. Eur J Hum Genet 24(6):881–888
Article
PubMed
CAS
Google Scholar
Sie AS, Spruijt L, van Zelst-Stams WA, Mensenkamp AR, Ligtenberg MJ, Brunner HG et al (2016) High satisfaction and low distress in breast cancer patients one year after BRCA-mutation testing without prior face-to-face genetic counseling. J Genet Couns 25(3):504–514
Article
PubMed
Google Scholar
Augestad MT, Høberg-Vetti H, Bjorvatn C, Sekse RJ (2017) Identifying needs: a qualitative study of women’s experiences regarding rapid genetic testing for hereditary breast and ovarian cancer in the DNA BONus Study. J Genet Couns 26(1):182–189
Article
PubMed
Google Scholar