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| Issue Date | Title | Author(s) |
|---|---|---|
| 11-Nov-2016 | Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women | Rebbeck, Timothy R.; Friebel, Tara M.; Mitra, Nandita; Wan, Fei; Chen, Stephanie; Andrulis, Irene L.; Apostolou, Paraskevi; Arnold, Norbert; Arun, Banu K.; Barrowdale, Daniel; Benitez, Javier; Ramus, Susan J.; Berger, Raanan; Berthet, Pascaline; Borg, Åke; Buys, Saundra S.; Caldes, Trinidad; Carter, Jonathan; Chiquette, Jocelyne; Claes, Kathleen B. M.; Couch, Fergus J.; Cybulski, Cezary; Daly, Mary B.; Hoya, Miguel de la; Díez Gibert, Orland; Domchek, Susan M.; Nathanson, Katherine L.; Durda, Katarzyna; Ellis, Steve; Evans, D. Gareth; EMBRACE Collaborators; Foretova, Lenka; Friedman, Eitan; Frost, Debra; Ganz, Patricia A.; HEBON Investigators; Garber, Judy; Glendon, Gord; Godwin, Andrew K.; Greene, Mark H.; KConFab Investigators; Gronwald, Jacek; Hahnen, Eric; Hallberg, Emily; Hamann, Ute; Hansen, Thomas V. O.; Imyanitov, Evgeny N.; Isaacs, Claudine; Jakubowska, Anna; Janavicius, Ramunas; Jaworska-Bieniek, Katarzyna; John, Esther M.; Karlan, Beth Y.; Kaufman, Bella; Kwong, Ava; Laitman, Yael; Lasset, Christine; Lázaro García, Conxi; Lester, Jenny; Loman, Niklas; Lubinski, Jan; Manoukian, Siranoush; Mitchell, Gillian; Montagna, Marco; Neuhausen, Susan L.; Nevanlinna, Heli; Niederacher, Dieter; Nussbaum, Robert L.; Offit, Kenneth; Olah, Edith; Olopade, Olufunmilayo I.; Kyung Park, Sue; Piedmonte, Marion; Radice, Paolo; Rappaport-Fuerhauser, Christine; Rookus, Matti A.; Seynaeve, Caroline; Simard, Jacques; Singer, Christian F.; Soucy, Penny; Southey, Melissa C.; Stoppa-Lyonnet, Dominique; Sukiennicki, Grzegorz; Szabo, Csilla I.; Tancredi, Mariella; Teixeira, Manuel R.; Teo, Soo-Hwang; Terry, Mary Beth; Thomassen, Mads; Tihomirova, Laima; Tischkowitz, Marc; Ewart Toland, Amanda; Toloczko-Grabarek, Aleksandra; Tung, Nadine; Rensburg, Elizabeth J. van; Villano, Danylo J.; Wang-Gohrke, Shan; Wappenschmidt, Barbara; Weitzel, Jeffrey N.; Zidan, Jamal; Zorn, Kristin K.; McGuffog, Lesley; Easton, Douglas F.; Chenevix-Trench, Georgia; Antoniou, Antonis C. |
| 31-Dec-2014 | Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers | Lázaro García, Conxi; Blanco Guillermo, Ignacio; Teulé-Vega, Àlex; Menéndez Vilà, Mireia; Epidemiological study of BRCA1 & BRCA2 Mutation Carriers (EMBRACE); Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers (GEMO); Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON); KConFab Investigators |
| 21-Jun-2016 | Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus | Lázaro García, Conxi; Teulé-Vega, Àlex; Epidemiological study of BRCA1 & BRCA2 Mutation Carriers (EMBRACE); Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers (GEMO); Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON); KConFab Investigators; AOCS Investigators |
| 1-Feb-2017 | Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriers | Lázaro García, Conxi; BCFR Investigators; EMBRACE Collaborators; GEMO Study Collaborators; HEBON Investigators; KConFab Investigators |
| 1-Nov-2019 | The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer | Figlioli, Gisella; Lázaro García, Conxi; Pujana Genestar, M. Ángel; ABCTB Investigators; GEMO Study Collaborators; KConFab Investigators |
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