References
- Bau, D.T., et al., 2007. DNA double-strand break repair capacity and risk of breast cancer. Carcinogenesis, 28, 1726–1730.
- Berwick, M. and Vineis, P. 2000. Markers of DNA repair and susceptibility to cancer in humans: an epidemiologic review. Journal of the National Cancer Institute, 92, 874–897.
- Bolognesi, C., et al. 2014. Clinical application of micronucleus test: a case-control study on the prediction of breast cancer risk/susceptibility. PLoS One, 9, e112354.
- Easton, D.F., et al. 2015. Gene-panel sequencing and the prediction of breast-cancer risk. The New England Journal of Medicine, 372, 2243–2257.
- Kappil, M., et al. 2016. Mismatch repair polymorphisms as markers of breast cancer prevalence in the breast cancer family registry. Anticancer Research, 36, 4437–4441.
- Leroy, T., et al. 1996. Evaluation of three methods for the detection of DNA single-strand breaks in human lymphocytes: alkaline elution, nick translation, and single-cell gel electrophoresis. Journal of Toxicology and Environmental Health, 47, 409–422.
- Mordukhovich, I., et al. 2016. Polymorphisms in DNA repair genes, traffic-related polycyclic aromatic hydrocarbon exposure and breast cancer incidence. International Journal of Cancer, 139, 310–321.
- Moreno-Villanueva, M., et al. 2011. The automated FADU-assay, a potential high-throughput in vitro method for early screening of DNA breakage. ALTEX, 28, 295–303.
- Paz-Elizur, T., Brenner, D.E., and Livneh, Z. 2005. Interrogating DNA repair in cancer risk assessment. Cancer Epidemiology, Biomarkers & Prevention, 14, 1585–1587.
- Rajeswari, N., et al. 2000. Risk assessment in first degree female relatives of breast cancer patients using the alkaline Comet assay. Carcinogenesis, 21, 557–561.
- Smith, T.R., et al. 2003. DNA damage and breast cancer risk. Carcinogenesis, 24, 883–889.