Rare germline copy number variants (CNVs) and breast cancer risk
- Creator: 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
- Resource Type: journal article
- Date: 2022
Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition
- Creator: 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,
- Resource Type: journal article
- Date: 2015