Browsing by Author KConFab Investigators

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Showing results 1 to 12 of 12
Issue DateTitleAuthor(s)
17-Feb-2021A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriersPujana Genestar, M. Ángel; Teulé-Vega, Àlex; GEMO Study Collaborators; EMBRACE Collaborators; KConFab Investigators; HEBON Investigators; ABCTB Investigators
31-Dec-2014Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriersLázaro 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
28-Jul-2021Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk ScoresBarnes, Daniel R.; Angel Pujana, Miquel; Teulé Vega, Àlex; Balmaña, Judith; GEMO Study Collaborators; EMBRACE Collaborators; KConFab Investigators; HEBON Investigators; Consortium Of Investigators Of Modifiers Of Brca1 And Brca2, The; Brunet, Joan; Darder, Esther; Valle Domínguez, Jesús del; Diez, Orland; Feliubadaló i Elorza, Maria Lídia; Izquierdo, Angel; Lázaro García, Conxi; López Fernández, Adrià
1-Feb-2017Evaluation of copy-number variants as modifiers of breast and ovarian cancer risk for BRCA1 pathogenic variant carriersLázaro García, Conxi; BCFR Investigators; EMBRACE Collaborators; GEMO Study Collaborators; HEBON Investigators; KConFab Investigators
27-Jul-2016Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation CarriersVigorito, Elena; Kuchenbaecker, Karoline B.; Beesley, Jonathan; Adlard, Julian; Agnarsson, Bjarni A.; Andrulis, Irene L.; Arun, Banu K.; Barjhoux, Laure; Belotti, Muriel; Benitez, Javier; Berger, Andreas; Kwong, Ava; Vijai, Joseph; Peissel, Bernard; Ong, Kai Ren; Karlan, Beth Y.; Kast, Karin; Pedersen, Inge Søkilde; Piedmonte, Marion; Laitman, Yael; Niederacher, Dieter; Szabo, Csilla I.; Osorio, Ana; Lubinski, Jan; Mai, Phuong L.; Terry, Mary Beth; Meindl, Alfons; Olah, Edith; KConFab Investigators; Tognazzo, Silvia; Park, Sue K.; Peterlongo, Paolo; Steinemann, Doris; Pujana Genestar, M. Ángel; Vratimos, Athanassios; Pfeiler, Georg; Radice, Paolo; Sutter, Christian; Rennert, Gad; Varesco, Liliana; Rodriguez, Gustavo C.; Weitzel, Jeffrey N.; Teixeira, Manuel R.; Pharoah, Paul D. P.; Rookus, Matti A.; Hamann, Ute; Ross, Eric A.; Couch, Fergus J.; Tihomirova, Laima; Varon-Mateeva, Raymonda; Schmutzler, Rita Katharina; Bojesen, Anders; Simard, Jacques; Singer, Christian F.; Lindor, Noralane; Brewer, Carole; Teo, Soo-Hwang; Slavin, Thomas P.; Soucy, Penny; McGuffog, Lesley; Southey, Melissa C.; Stoppa-Lyonnet, Dominique; Sukiennicki, Grzegorz; Offit, Kenneth; Bonanni, Bernardo; Tea, Muy-Kheng; Kirk, Judy; Eccles, Diana; Ramus, Susan J.; Thomassen, Mads; Tibiletti, Maria Grazia; Goldgar, David E.; van Rensburg, Elizabeth J.; Toland, Amanda Ewart; Greene, Mark H.; Friedman, Eitan; Chenevix-Trench, Georgia; Caldes, Trinidad; Godwin, Andrew K.; Antoniou, Antonis C.; Fostira, Florentia; Caligo, Maria A.; Campbell, Ian; Ganz, Patricia A.; Frost, Debra; Chan, Salina B.; Garcia Barberan, Vanesa; Claes, Kathleen B. M.; Ejlertsen, Bent; Foulkes, William D.; Giraud, Sophie; Cohn, David E.; Healey, Sue; Cook, Jackie; Hogervorst, Frans B. L.; Easton, Douglas F.; Daly, Mary B.; Damiola, Francesca; Davidson, Rosemarie; Gaddam, Pragna; Dumont, Martine; Pauw, Antoine de; Ellis, Steve; Delnatte, Capucine; Gauthier-Villars, Marion; Díez Gibert, Orland; Domchek, Susan M.; Durda, Katarzyna; Hodgson, Shirley; Dworniczak, Bernd; Edwinsdotter Ardnor, Christina; Gehrig, Andrea; Eeles, Rosalind A.; Liljegren, Annelie; Evans, D. Gareth; Feliubadaló i Elorza, Maria Lídia; Garber, Judy; Mazoyer, Sylvie; Gerdes, Anne-Marie; Hake, Christopher R.; Houdayer, Claude; Nathanson, Katherine L.; Hansen, Thomas V. O.; Hulick, Peter J.; Khan, Sofia; Imyanitov, Evgeny N.; Mensenkamp, Arjen R.; Isaacs, Claudine; Neuhausen, Susan L.; Lester, Jenny; Izatt, Louise; Olopade, Olufunmilayo I.; Izquierdo i Font, Àngel Xavier; Paulsson-Karlsson, Ylva; Manoukian, Siranoush; Montagna, Marco; Jacobs, Lauren; Phelan, Catherine M.; Jakubowska, Anna; Janavicius, Ramunas; Poppe, Bruce; Lesueur, Fabienne; Jaworska-Bieniek, Katarzyna; Jensen, Uffe Birk; Nevanlinna, Heli; John, Esther M.
1-Sep-2016Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locusFeliubadaló i Elorza, Maria Lídia; Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers (GEMO); Epidemiological study of BRCA1 & BRCA2 Mutation Carriers (EMBRACE); Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON); KConFab Investigators; Australian Ovarian Cancer Study Group
21-Jun-2016Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locusLázaro 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
11-Nov-2016Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 womenRebbeck, 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.
9-Feb-2016Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2Pujana Genestar, M. Ángel; KConFab Investigators; Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON); Epidemiological study of BRCA1 & BRCA2 Mutation Carriers (EMBRACE)
1-Oct-2020Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variantsBrunet, Joan; Izquierdo i Font, Àngel Xavier; Lázaro García, Conxi; Pujana Genestar, M. Ángel; GEMO Study Collaborators; EMBRACE Collaborators; KConFab Investigators; HEBON Investigators; GENEPSO Investigators
1-Nov-2019The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancerFiglioli, Gisella; Lázaro García, Conxi; Pujana Genestar, M. Ángel; ABCTB Investigators; GEMO Study Collaborators; KConFab Investigators
20-Oct-2009The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriersSinilnikova, Olga M.; Antoniou, Antonis C.; Simard, Jacques; Healey, Sue; Léoné, Mélanie; Sinnett, Daniel; Spurdle, Amanda B.; Beesley, Jonathan; Chen, Xieng; KConFab Investigators; Greene, Mark H.; Loud, Jennifer T.; Lejbkowicz, Flavio; Rennert, Gad; Dishon, Sara; Andrulis, Irene L.; OCGN; Domchek, Susan M.; Nathanson, Katherine L.; Manoukian, Siranoush; Radice, Paolo; Konstantopoulou, Irene; Blanco Guillermo, Ignacio; Laborde, Adriana Lasa; Durán, Mercedes; Osorio, Ana; Benitez, Javier; Hamann, Ute; Hogervorst, Frans B. L.; Van Os, Theo A.; Gille, Hans J.P.; HEBON Investigators; Peock, Susan; Cook, Margaret; Luccarini, Craig; Evans, D. Gareth; Lalloo, Fiona; Eeles, Rosalind A.; Pichert, Gabriella; Davidson, Rosemarie