Multigene panel testing for hereditary breast and ovarian cancer in the province of Ontario
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00432-020-03377-6.pdf
Reference25 articles.
1. Burke W, Laberge AM, Press N (2010) Debating clinical utility. Public Health Genomics 13(4):215–223. https://doi.org/10.1159/000279623
2. Buys SS, Sandbach JF, Gammon A, Patel G, Kidd J, Brown KL et al (2017) A study of over 35,000 women with breast cancer tested with a 25-gene panel of hereditary cancer genes. Cancer 123(10):1721–1730. https://doi.org/10.1002/cncr.30498
3. Cybulski C, Wokolorczyk D, Jakubowska A, Huzarski T, Byrski T, Gronwald J et al (2011) Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer. J Clin Oncol 29(28):3747–3752. https://doi.org/10.1200/jco.2010.34.0778
4. Dossa F, Cusimano MC, Sutradhar R, Metcalfe K, Little T, Lerner-Ellis J et al (2018) Real-world health services utilisation and outcomes after BRCA1 and BRCA2 testing in Ontario, Canada: the What Comes Next Cohort Study protocol. BMJ Open 8(9):e025317. https://doi.org/10.1136/bmjopen-2018-025317
5. Feliubadalo L, Lopez-Fernandez A, Pineda M, Diez O, Del Valle J, Gutierrez-Enriquez S et al (2019) Opportunistic testing of BRCA1, BRCA2 and mismatch repair genes improves the yield of phenotype driven hereditary cancer gene panels. Int J Cancer 145(10):2682–2691. https://doi.org/10.1002/ijc.32304
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