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Rare germline copy number variants (CNVs) and breast cancer risk

- Dennis, Joe, Tyrer, Jonathan P., Antonenkova, Natalia N., Arndt, Volker, Aronson, Kristan J., Freeman, Laura E. Beane, Beckmann, Matthias W., Behrens, Sabine, Benitez, Javier, Bermisheva, Marina, Bogdanova, Natalia V., Bojesen, Stig E., Walker, Logan C., Brenner, Hermann, Scott, Rodney, .,, Michailidou, Kyriaki, Dorling, Leila, Bolla, Manjeet K., Wang, Qin, ..,, Ahearn, Thomas U., Andrulis, Irene L., Anton-Culver, Hoda

Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition

- Moir-Meyer, Gemma L., Pearson, John F., Pharoah, Paul D., Dunning, Alison M., Thompson, Deborah J., Easton, Douglas F., Spurdle, Amanda B., Walker, Logan C., Lose, Felicity, The Australian National Endometrial Cancer Study Group,, Scott, Rodney J., McEvoy, Mark, Attia, John, Holliday, Elizabeth G., The Hunter Community Study,, Studies of Epidemiology and Risk Factors in Cancer Heredity,

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