Breast cancer risk after salpingo-oophorectomy in healthy BRCA1/2 mutation carriers: revisiting the evidence for risk reduction by Heemskerk-Gerritsen, B A M, Seynaeve, C, van Asperen, C J, Ausems, M G E M, Collée, J M, van Doorn, H C, Gomez Garcia, E B, Kets, C M, van Leeuwen, F E, Meijers-Heijboer, H E J, Mourits, M J E, van Os, T A M, Vasen, H F A, Verhoef, S, Rookus, M A, Hooning, M J

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Improved overall survival after contralateral risk‐reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: A prospective analysis by Heemskerk‐Gerritsen, Bernadette A.M., Rookus, Matti A., Aalfs, Cora M., Ausems, Margreet G.E.M., Collée, Johanna M., Jansen, Liesbeth, Kets, C. Marleen, Keymeulen, Kristien B.M.I., Koppert, Linetta B., Meijers‐Heijboer, Hanne E.J., Mooij, Thea M., Tollenaar, Rob A.E.M., Vasen, Hans F.A., HEBON, Hooning, Maartje J., Seynaeve, Caroline

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Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) by MAVADDAT, Nasim, BARROWDALE, Daniel, MULLIGAN, Anna Marie, COUCH, Fergus J, ENGEL, Christoph, MCGUFFOG, Lesley, HEALER, Sue, SINILNIKOVA, Olga M, SOUTHEY, Melissa C, TERRY, Mary Beth, GOLDGAR, David, O'MALLEY, Frances, ANDRULIS, Irene L, JOHN, Esther M, JANAVICIUS, Ramunas, TIHOMIROVA, Laima, HANSEN, Thomas V. O, NIELSEN, Finn C, OSORIO, Ana, STAVROPOULOU, Alexandra, BENITEZ, Javier, MANOUKIAN, Siranoush, PEISSEL, Bernard, DOMCHEK, Susan M, BARILE, Monica, VOLORIO, Sara, PASIN, Barbara, DOLCETTI, Riccardo, PUTIGNANO, Anna Laura, OTTINI, Laura, RADICE, Paolo, HAMANN, Ute, RASHID, Muhammad U, HOGERVORST, Frans B, ECCLES, Diana, KRIEGE, Mieke, VAN DER LUIJT, Rob B, HEBON, PEOCK, Susan, FROST, Debra, GARETH EVANS, D, BREWER, Carole, WALKER, Lisa, ROGERS, Mark T, SIDE, Lucy E, NEVANLINNA, Heli, HOUGHTON, Catherine, EMBRACE, WEAVER, Joellen, GODWIN, Andrew K, SCHMUTZLER, Rita K, WAPPENSCHMIDT, Barbara, MEINDL, Alfons, KAST, Karin, RAMUS, Susan J, SPURDLE, Amanda, ROBSON, Mark, SHERMAN, Mark

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Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers by Mavaddat, Nasim, Antoniou, Antonis C, Mooij, Thea M, Hooning, Maartje J, Heemskerk-Gerritsen, Bernadette A, Noguès, Catherine, Gauthier-Villars, Marion, Caron, Olivier, Gesta, Paul, Pujol, Pascal, Lortholary, Alain, Barrowdale, Daniel, Frost, Debra, Evans, D Gareth, Izatt, Louise, Adlard, Julian, Eeles, Ros, Brewer, Carole, Tischkowitz, Marc, Henderson, Alex, Cook, Jackie, Eccles, Diana, van Engelen, Klaartje, Mourits, Marian J E, Ausems, Margreet G E M, Koppert, Linetta B, Hopper, John L, John, Esther M, Chung, Wendy K, Andrulis, Irene L, Daly, Mary B, Buys, Saundra S, Benitez, Javier, Caldes, Trinidad, Jakubowska, Anna, Simard, Jacques, Singer, Christian F, Tan, Yen, Olah, Edith, Navratilova, Marie, Foretova, Lenka, Gerdes, Anne-Marie, Roos-Blom, Marie-José, Van Leeuwen, Flora E, Arver, Brita, Olsson, Håkan, Schmutzler, Rita K, Engel, Christoph, Kast, Karin, Phillips, Kelly-Anne, Terry, Mary Beth, Milne, Roger L, Goldgar, David E, Rookus, Matti A, Andrieu, Nadine, Easton, Douglas F

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Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2 by Silvestri, Valentina, Barrowdale, Daniel, Mulligan, Anna Marie, Neuhausen, Susan L, Fox, Stephen, Karlan, Beth Y, Carter, Natalie J, Nathanson, Katherine L, Domchek, Susan M, Nussbaum, Robert L, Rantala, Johanna, Yoon, Sook-Yee, Caligo, Maria A, Spugnesi, Laura, Bojesen, Anders, Pedersen, Inge Sokilde, Jensen, Uffe Birk, Senter, Leigha, Andrulis, Irene L, Hulick, Peter J, Imyanitov, Evgeny N, Greene, Mark H, Mai, Phuong L, Rappaport-Fuerhauser, Christine, Kramer, Gero, Vijai, Joseph, Offit, Kenneth, Robson, Mark, Machackova, Eva, Foretova, Lenka, Navratilova, Marie, Vasickova, Petra, Hallberg, Emily, Ruddy, Kathryn J, Sharma, Priyanka, Teixeira, Manuel R, Pinto, Pedro, Arason, Adalgeir, Johannsson, Oskar Th, Barkardottir, Rosa B, Izquierdo, Angel, Pujana, Miguel Angel, Balmaña, Judith, Ivady, Gabriella, Papp, Janos, Olah, Edith, Kwong, Ava, Perez Segura, Pedro, Caldes, Trinidad, Van Maerken, Tom, Isaacs, Claudine, Elan, Camille, Lasset, Christine, Stoppa-Lyonnet, Dominique, Barjhoux, Laure, Belotti, Muriel, Gehrig, Andrea, Sutter, Christian, Hahnen, Eric, Kast, Karin, Wand, Dorothea, Godwin, Andrew K, Evans, D Gareth, Frost, Debra, Perkins, Jo, Adlard, Julian, Platte, Radka, Eeles, Ros, Ellis, Steve, Hamann, Ute, Fostira, Florentia, Fountzilas, George, Pasini, Barbara, Rizzolo, Piera, Cortesi, Laura, Papi, Laura, Varesco, Liliana, Zanna, Ines, Savarese, Antonella, Manoukian, Siranoush, Barile, Monica, Bonanni, Bernardo, Viel, Alessandra, Pensotti, Valeria, Tommasi, Stefania, Peterlongo, Paolo, Weitzel, Jeffrey N, Osorio, Ana, Benitez, Javier, McGuffog, Lesley, Gerdes, Anne-Marie, Ejlertsen, Bent, Hansen, Thomas V O, Ding, Yuan Chun, Goldgar, David E, Buys, Saundra S, Terry, Mary Beth, John, Esther M, Southey, Melissa, Antoniou, Antonis C

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Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus by Lawrenson, Kate, Kuchenbaeker, Karoline, Aittomäki, Kristiina, Arun, Banu K, Arver, Brita, Bandera, Elisa V, Barrowdale, Daniel, Benitez, Javier, Bjorge, Line, Bojesen, Anders, Bojesen, Stig E, Brauch, Hiltrud, Bruinsma, Fiona, Brunet, Joan, Buhari, Shaik Ahmad, Butzow, Ralf, Cai, Qiuyin, Campbell, Ian, Canniotto, Rikki, Choi, Ji-Yeob, Cox, Angela, Cybulski, Cezary, Daly, Mary B, Dansonka-Mieszkowska, Agnieszka, Dennis, Joe, Doherty, Jennifer A, Ehrencrona, Hans, Ellis, Steve, Engel, Christoph, Fasching, Peter A, Feliubadalo, Lidia, Fletcher, Olivia, Foulkes, William D, García-Closas, Montserrat, Gentry-Maharaj, Aleksandra, Giles, Graham G, Godwin, Andrew K, Goldberg, Mark S, Goldgar, David E, González-Neira, Anna, Goodman, Marc T, Gronwald, Jacek, Hallberg, Emily, Hansen, Thomas V O, Heitz, Florian, Høgdall, Claus K, Hopper, John L, Huzarski, Tomasz, Janavicius, Ramunas, Johnson, Nichola, Kabisch, Maria, Khan, Sofia, Kosma, Veli-Matti, Kristensen, Vessela, Kupryjanczyk, Jolanta, Kwong, Ava, Lester, Jenny, Lu, Karen, Margolin, Sara, Marme, Frederik, McLean, Catriona, Meindl, Alfons, Montagna, Marco, Moysich, Kirsten B, Ness, Roberta B, Nord, Silje, Olson, Janet E, Olswold, Curtis, O'Malley, David, Orr, Nick, Osorio, Ana, Pearce, Celeste L, Pejovic, Tanja, Pfeiler, Georg, Phelan, Catherine M, Poole, Elizabeth M, Radice, Paolo, Rantala, Johanna, Rashid, Muhammad Usman, Rossing, Mary Anne, Sangrajrang, Suleeporn, Sawyer, Elinor J, Seynaeve, Caroline, Sinilnikova, Olga M, Teixeira, Manuel R, Tseng, Chiu-Chen, Vanderstichele, Adriaan, Wang, Qin, Weitzel, Jeffrey N, Wentzensen, Nicolas, Whittemore, Alice S, Wildiers, Hans, Wu, Anna H, Yannoukakos, Drakoulis, Zheng, Wei, Simard, Jacques, Easton, Douglas F, Dunning, Alison M, Edwards, Stacey L, Antoniou, Antonis C

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Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers by Robson, Mark, Andrulis, Irene L, Spurdle, Amanda B, Schmidt, Marjanka K, Engel, Christoph, Wappenschmidt, Barbara, Southey, Melissa, Radice, Paolo, Lee, Andrew, Rebbeck, Timothy R, James, Paul, Lester, Jenny, Daly, Mary B, Goldgar, David E, Tihomirova, Laima, van Rensburg, Elizabeth J, v O Hansen, Thomas, Gerdes, Anne-Marie, Nielsen, Finn C, Hart, Steven, Slager, Susan, Benitez, Javier, Tafur, Isaac, Hander, Mary, Scuvera, Giulietta, Mariani, Paolo, Volorio, Sara, Varesco, Liliana, Papi, Laura, Tibiletti, Maria Grazia, Giannini, Giuseppe, Fostira, Florentia, Konstantopoulou, Irene, Garber, Judy, Brewer, Carole, Foo, Claire, Douglas, Fiona, Tischkowitz, Marc, Barwell, Julian, Ong, Kai-ren, Side, Lucy E, Rogers, Mark T, Morrison, Patrick J, Eeles, Ros, Hodgson, Shirley, Ellis, Steve, Godwin, Andrew K, Rhiem, Kerstin, Meindl, Alfons, Arnold, Norbert, Plendl, Hansjoerg, Niederacher, Dieter, Steinemann, Doris, Varon-Mateeva, Raymonda, Wang-Gohrke, Shan, Buecher, Bruno, Rouleau, Etienne, Damiola, Francesca, Faivre, Laurence, Longy, Michel, Sinilnikova, Olga M, Mazoyer, Sylvie, Caux-Moncoutier, Virginie, Isaacs, Claudine, Khan, Sofia, Meijers-Heijboer, Hanne E J, van der Hout, Annemarie H, Wijnen, Juul T, van Roozendaal, K E P, Mensenkamp, Arjen R, van der Luijt, Rob B, Teulé, Alex, Menendez, Mireia, Cybulski, Cezary, Gronwald, Jacek, Durda, Katarzyna, Arason, Adalgeir, Maugard, Christine, Montagna, Marco, Agata, Simona, Vijai, Joseph, Jacobs, Lauren, Fink-Retter, Anneliese, Rappaport, Christine, Kaulich, Daphne Gschwantler, Pfeiler, Georg, Tea, Muy-Kheng, Greene, Mark H, Imyanitov, Evgeny N, Toland, Amanda Ewart, Pedersen, Inge Sokilde, Berger, Raanan, Laitman, Yael, Rantala, Johanna, Arver, Brita, Loman, Niklas, Ehrencrona, Hans, Olopade, Olufunmilayo I, Easton, Douglas F, Offit, Kenneth

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Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers by Antoniou, Antonis C, Soucy, Penny, McGuffog, Lesley, Healey, Sue, Lee, Andrew, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Barile, Monica, Pasini, Barbara, Dolcetti, Riccardo, Giannini, Giuseppe, Varesco, Liliana, Radice, Paolo, Greene, Mark H., Glendon, Gord, Birk Jensen, Uffe, Crüger, Dorthe G., Caligo, Maria A., Laitman, Yael, Milgrom, Roni, Kaufman, Bella, Friedman, Eitan, Lindblom, Annika, Ehrencrona, Hans, Nathanson, Katherine L., Domchek, Susan M., Rebbeck, Timothy, Jakubowska, Ania, Gronwald, Jacek, Byrski, Tomasz, Cybulski, Cezary, Osorio, Ana, Ramón y Cajal, Teresa, Fostira, Florentia, Hogervorst, Frans B., Hooning, Maartje J., Meijers-Heijboer, Hanne E.J., Gómez Garcia, Encarna B., Peock, Susan, Platte, Radka, Lalloo, Fiona, Eeles, Ros, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-ren, Cook, Jackie, Douglas, Fiona, Paterson, Joan, John Kennedy, M., Miedzybrodzka, Zosia, Godwin, Andrew, Stoppa-Lyonnet, Dominique, Buecher, Bruno, Tirapo, Carole, Barjhoux, Laure, Faivre, Laurence, Nogues, Catherine, Rouleau, Etienne, Pujol, Pascal, Coupier, Isabelle, Frénay, Marc, Daly, Mary B., John, Esther M., Singer, Christian F., Catharina Dressler, Anne, Offit, Kenneth, Rodriguez, Gustavo, Small, Laurie, Boggess, John, Blank, Stephanie, Basil, Jack, Ewart Toland, Amanda, Montagna, Marco, Tognazzo, Silvia, Blanco, Ignacio, Pharoah, Paul D.P., Karlan, Beth Y., Walsh, Christine S., Olah, Edith, Teo, Soo-Hwang, Beattie, Mary S., van Rensburg, Elizabeth J., Sluiter, Michelle D., Diez, Orland, Engel, Christoph, Meindl, Alfons, Ruehl, Ina, Varon-Mateeva, Raymonda, Niederacher, Dieter, Arnold, Norbert, Gadzicki, Dorothea, Caldes, Trinidad, de la Hoya, Miguel, Chen, Xiaoqing, Spurdle, Amanda B., Fredericksen, Zachary, Couch, Fergus, Simard, Jacques

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Variation in mutation spectrum partly explains regional differences in the breast cancer risk of female BRCA mutation carriers in the Netherlands by Vos, Janet R, Teixeira, Natalia, van der Kolk, Dorina M, Mourits, Marian J E, Rookus, Matti A, van Leeuwen, Flora E, Collée, Margriet, van Asperen, Christi J, Mensenkamp, Arjen R, Ausems, Margreet G E M, van Os, Theo A M, Meijers-Heijboer, Hanne E J, Gómez-Garcia, Encarna B, Vasen, Hans F, Brohet, Richard M, van der Hout, Annemarie H, Jansen, Liesbeth, Oosterwijk, Jan C, de Bock, Geertruida H

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Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of B... by Mulligan, Anna Marie, Couch, Fergus J, Barrowdale, Daniel, Domchek, Susan M, Nevanlinna, Heli, Sherman, Mark, McGuffog, Lesley, Janavicius, Ramunas, Hansen, Thomas vO, Osorio, Ana, Durán, Mercedes, Godino, Javier, Pertesi, Maroulio, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Cattaneo, Elisa, Bonanni, Bernardo, Viel, Alessandra, Ottini, Laura, Bernard, Loris, Radice, Paolo, Wijnen, Juul, Kets, C Marleen, van Os, Theo, Rookus, Matti, Jones, J Louise, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Adlard, Julian, Donaldson, Alan, Dorkins, Huw, Eason, Jacqueline, Houghton, Catherine, Barwell, Julian, Side, Lucy E, Murray, Alex, Godwin, Andrew K, Rhiem, Kerstin, Meindl, Alfons, Ruehl, Ina, Niederacher, Dieter, Schoenbuchner, Ines, Heinritz, Wolfram, Schäfer, Dieter, Gevensleben, Heidrun, Mazoyer, Sylvie, Hardouin, Agnès, Muller, Danièle, Fricker, Jean-Pierre, Mortemousque, Isabelle, Pujol, Pascal, Lebrun, Marine, Kientz, Caroline, Longy, Michel, Sevenet, Nicolas, Isaacs, Claudine, Caldes, Trinidad, de la Hoya, Miguel, Blanco, Ignacio, Soucy, Penny, Tognazzo, Silvia, Fox, Stephen, Yan, Max, Rebbeck, Tim, Olopade, Olufunmilayo, Weitzel, Jeffrey N, Ganz, Patricia A, Tomlinson, Gail E, Wang, Xianshu, Fredericksen, Zachary, Szabo, Csilla, Offit, Kenneth, Kauff, Noah, Tea, Muy-Kheng, Fink-Retter, Anneliese, Greene, Mark H, Ozcelik, Hilmi, Glendon, Gordon, Toland, Amanda E, Thomassen, Mads, Kruse, Torben A, Caligo, Maria A, Arver, Brita, Stenmark-Askmalm, Marie, Karlsson, Per, Ding, Yuan Chun, Neuhausen, Susan L, Beattie, Mary, Nathanson, Katherine L, Gross, Jenny, Southey, Melissa C, Hopper, John L, Terry, Mary Beth, Chung, Wendy, Chenevix-Trench, Georgia, Andrulis, Irene L, Antoniou, Antonis C

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Bias Explains Most of the Parent-of-Origin Effect on Breast Cancer Risk in BRCA1/2 Mutation Carriers by Vos, Janet R, Oosterwijk, Jan C, Aalfs, Cora M, Rookus, Matti A, Adank, Muriel A, van der Hout, Annemarie H, van Asperen, Christi J, Gómez Garcia, Encarna B, Mensenkamp, Arjen R, Jager, Agnes, Ausems, Margreet G E M, Mourits, Marian J, de Bock, Geertruida H

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Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers by Ramus, Susan J., Kuchenbaecker, Karoline B., Beesley, Jonathan, Healey, Sue, Thomassen, Mads, Jensen, Uffe Birk, Skytte, Anne-Bine, Lindblom, Annika, Olsson, Håkan, Melin, Beatrice, Domchek, Susan M., Nathanson, Katherine L., Jakubowska, Anna, Lubinski, Jan, Jaworska, Katarzyna, Durda, Katarzyna, Złowocka, Elżbieta, Gronwald, Jacek, Huzarski, Tomasz, Byrski, Tomasz, Benitez, Javier, Tejada, Maria-Isabel, Aalfs, Cora M., Meijers-Heijboer, Hanne E.J., van Asperen, Christi J., van Roozendaal, K.E.P., Collée, J. Margriet, van der Luijt, Rob B., Frost, Debra, Platte, Radka, Fineberg, Elena, Evans, D. Gareth, Lalloo, Fiona, Jacobs, Chris, Adlard, Julian, Davidson, Rosemarie, Cook, Jackie, Paterson, Joan, Morrison, Patrick J., Kennedy, M. John, Godwin, Andrew K., Caux-Moncoutier, Virginie, Gauthier-Villars, Marion, Mazoyer, Sylvie, Lasset, Christine, Hardouin, Agnès, Berthet, Pascaline, Faivre, Laurence, Buys, Saundra, Beth Terry, Mary, Chung, Wendy K., John, Esther M, Tea, Muy-Kheng, Pfeiler, Georg, Fink-Retter, Anneliese, Hansen, Thomas v. O., Ejlertsen, Bent, Offit, Kenneth, Gaudet, Mia M., Vijai, Joseph, Robson, Mark, Phillips, Kelly-Anne, Hoffman, James S, Montagna, Marco, Tognazzo, Silvia, Isaacs, Claudine, Janavicius, Ramunas, Blanco, Ignacio, Navarro, Matilde, Karlan, Beth Y., Olah, Edith, Vaszko, Tibor, Teo, Soo-Hwang, Ganz, Patricia A., Diez, Orland, Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Arnold, Norbert, Niederacher, Dieter, Deissler, Helmut, Fiebig, Britta, Nevanlinna, Heli, Aittomäki, Kristiina, Plante, Marie, Spurdle, Amanda B., Ding, Yuan Chun, Lindor, Noralane, Fredericksen, Zachary, Pankratz, V. Shane, Peissel, Bernard, Bernard, Loris, Dolcetti, Riccardo, Radice, Paolo, Greene, Mark H., Mai, Phuong L., Ozcelik, Hilmi, Couch, Fergus J., Chenevix-Trench, Georgia

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Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers by RAMUS, Susan J, KARTSONAKI, Christiana, XIANSHU WANG, FREDERICKSEN, Zachary, PETERLONGO, Paolo, MANOUKIAN, Siranoush, PEISSEL, Bernard, ZAFFARONI, Daniela, ROVERSI, Gaia, BARILE, Monica, VIEL, Alessandra, ALLAVENA, Anna, GAYTHER, Simon A, OTTINI, Laura, PAPI, Laura, GISMONDI, Viviana, CAPRA, Fabio, RADICE, Paolo, GREENE, Mark H, MAI, Phuong L, ANDRULIS, Irene L, GLENDON, Gord, OZCELIK, Hilmi, PHAROAH, Paul D. P, THOMASSEN, Mads, GERDES, Anne-Marie, KRUSE, Torben A, CRUGER, Dorthe, JENSEN, Uffe Birk, CALIGO, Maria Adelaide, OLSSON, Hakan, KRISTOFFERSSON, Ulf, LINDBLOM, Annika, ARVER, Brita, SINILNIKOVA, Olga M, KARLSSON, Per, ASKMALM, Marie Stenmark, BORG, Ake, NEUHAUSEN, Susan L, YUAN CHUN DING, NATHANSON, Katherine L, DOMCHEK, Susan M, JAKUBOWSKA, Anna, LUBINSKI, Jan, HUZARSKI, Tomasz, BEESLEY, Jonathan, BYRSKI, Tomasz, GRONWALD, Jacek, GORSKI, Bohdan, CYBULSKI, Cezary, DEBNIAK, Tadeusz, OSORIO, Ana, DURAN, Mercedes, TEJADA, Maria-Isabel, BENITEZ, Javier, HAMANN, Ute, XIAOQING CHEN, MCGUFFOG, Lesley, HEALEY, Sue, COUCH, Fergus J

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Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study by JAKUBOWSKA, A, ROZKRUT, D, FLUGELMAN, A, ANDRULIS, I. L, GLENDON, G, OZCELIK, H, THOMASSEN, M, PALIGO, M, ARETINI, P, KANTALA, J, AROER, B, VON WACHENFELDT, A, ANTONIOU, A, LILJEGREN, A, LOMAN, N, HERBST, K, KRISTOFFERSSON, U, ROSENQUIST, R, KARLSSON, P, STENMARK-ASKMALM, M, MELIN, B, NATHANSON, K. L, DOMCHEK, S. M, HAMANN, U, BYRSKI, T, HUZARSKI, T, GRONWALD, J, MENKISZAK, J, CYBULSKI, C, SERRANO, P, OSORIO, A, CAJAL, T. R, TSITLAIDOU, M, BENITEZ, J, SCOTT, R. J, GILBERT, M, ROOKUS, M, AALFS, C. M, KLUIJT, I, BOESSENKOOL-PAPE, J. L, MEIJERS-HEIJBOER, H. E. J, OOSTERWIJK, J. C, ASPEREN, Cj Van, BLOK, M. J, NELEN, M. R, MCGUFFOG, L, VAN DEN OUWELAND, A. M. W, SEYNAEVE, C, VAN DER LUIJT, R. B, DEVILEE, P, EASTON, D. F, PEOCK, S, FROST, D, PLATTE, R, ELLIS, S. D, FINEBERG, E, HEALY, S, SINILNIKOVA, O. M, RENNERT, G, LEJBKOWICZ, F

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Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers by Cox, David G., Simard, Jacques, Hamdi, Yosr, Soucy, Penny, Ouimet, Manon, Barjhoux, Laure, Verny-Pierre, Carole, McGuffog, Lesley, Healey, Sue, Greene, Mark H., Mai, Phuong L., Thomassen, Mads, Gerdes, Anne-Marie, Caligo, Maria A., Friedman, Eitan, Laitman, Yael, Kaufman, Bella, Paluch, Shani S., Borg, Åke, Karlsson, Per, Stenmark Askmalm, Marie, Barbany Bustinza, Gisela, Nathanson, Katherine L., Domchek, Susan M., Rebbeck, Timothy R., Benítez, Javier, Hamann, Ute, Rookus, Matti A., van den Ouweland, Ans M.W., Ausems, Margreet G.E.M., Aalfs, Cora M., van Asperen, Christi J., Devilee, Peter, Gille, Hans J.J.P., Peock, Susan, Frost, Debra, Evans, D. Gareth, Eeles, Ros, Izatt, Louise, Adlard, Julian, Paterson, Joan, Eason, Jacqueline, Godwin, Andrew K., Moncoutier, Virginie, Gauthier-Villars, Marion, Lasset, Christine, Giraud, Sophie, Hardouin, Agnès, Berthet, Pascaline, Sobol, Hagay, Eisinger, François, Bressac de Paillerets, Brigitte, Caron, Olivier, Delnatte, Capucine, Goldgar, David, Ozcelik, Hilmi, Buys, Saundra, Southey, Melissa C., Terry, Mary Beth, Singer, Christian F., Dressler, Anne-Catharina, Tea, Muy-Kheng, Hansen, Thomas V.O., Johannsson, Oskar, Piedmonte, Marion, Rodriguez, Gustavo C., Basil, Jack B., Blank, Stephanie, Toland, Amanda E., Montagna, Marco, Isaacs, Claudine, Blanco, Ignacio, Gayther, Simon A., Moysich, Kirsten B., Schmutzler, Rita K., Wappenschmidt, Barbara, Engel, Christoph, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Gadzicki, Dorothea, Caldes, Trinidad, Laframboise, Rachel, Nevanlinna, Heli, Chen, Xiaoqing, Beesley, Jonathan, Neuhausen, Susan L., Ding, Yuan C., Couch, Fergus J., Wang, Xianshu, Peterlongo, Paolo, Manoukian, Siranoush, Bernard, Loris, Easton, Douglas F., Antoniou, Antonis C., Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Sinilnikova, Olga M.

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Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers by Im, Kate M., Kirchhoff, Tomas, Wang, Xianshu, Green, Todd, Chow, Clement Y., Korn, Joshua, Gaudet, Mia M., Fredericksen, Zachary, Shane Pankratz, V., Guiducci, Candace, Crenshaw, Andrew, McGuffog, Lesley, Kartsonaki, Christiana, Morrison, Jonathan, Healey, Sue, Sinilnikova, Olga M., Mai, Phuong L., Greene, Mark H., Piedmonte, Marion, Rubinstein, Wendy S., Hogervorst, Frans B., Rookus, Matti A., Collée, J. Margriet, Hoogerbrugge, Nicoline, Meijers-Heijboer, Hanne E. J., Van Roozendaal, Cees E., Perez-Segura, Pedro, Jakubowska, Anna, Huzarski, Tomasz, Blecharz, Paweł, Nevanlinna, Heli, Aittomäki, Kristiina, Lazaro, Conxi, Blanco, Ignacio, Barkardottir, Rosa B., D’Andrea, Emma, Devilee, Peter, Olopade, Olufunmilayo I., Peissel, Bernard, Bonanni, Bernardo, Peterlongo, Paolo, Singer, Christian F., Rennert, Gad, Lejbkowicz, Flavio, Andrulis, Irene L., Ozcelik, Hilmi, Toland, Amanda Ewart, Caligo, Maria Adelaide, Beattie, Mary S., Chan, Salina, Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Timothy R., Phelan, Catherine, Narod, Steven, John, Esther M., Hopper, John L., Buys, Saundra S., Southey, Melissa C., Terry, Mary-Beth, Tung, Nadine, Hansen, Thomas v. O., Benitez, Javier, Weitzel, Jeffrey N., Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare T., Frost, Debra, Eeles, Ros, Izatt, Louise, Paterson, Joan, Brewer, Carole, Hodgson, Shirley, Porteous, Mary, Walker, Lisa, Rogers, Mark T., Side, Lucy E., Godwin, Andrew K., Wappenschmidt, Barbara, Laitman, Yael, Deissler, Helmut, Varon-Mateeva, Raymonda, Preisler-Adams, Sabine, Kast, Karin, Venat-Bouvet, Laurence, Stoppa-Lyonnet, Dominique, Chenevix-Trench, Georgia, Easton, Douglas F., Klein, Robert J., Daly, Mark J., Friedman, Eitan, Dean, Michael, Clark, Andrew G., Altshuler, David M., Antoniou, Antonis C., Couch, Fergus J., Offit, Kenneth, Gold, Bert

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Germline BRCA -Associated Endometrial Carcinoma Is a Distinct Clinicopathologic Entity by de Jonge, Marthe M, Ritterhouse, Lauren L, de Kroon, Cornelis D, Vreeswijk, Maaike P G, Segal, Jeremy P, Puranik, Rutika, Hollema, Harry, Rookus, Matti A, van Asperen, Christi J, van Leeuwen, Flora E, Smit, Vincent T H B M, Howitt, Brooke E, Bosse, Tjalling

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Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2 by OSORIO, A, MILNE, R. L, KONSTANTOPOULOU, I, HOGERVORST, F. B, VERHOEF, S, VAN DOOREN, M. F, JAGER, A, AUSEMS, Mgem, AALFS, C. M, VAN ASPEREN, C. J, VREESWIJK, M, WAISFISZ, Q, ALONSO, R, VAN ROOZENDAAL, C. E, LIGTENBERG, M. J, HEBON, EMBRACE, EASTON, D. F, PEOCK, S, COOK, M, OLIVER, C. T, FROST, D, CURZON, B, PITA, G, EVANS, D. G, LALLOO, F, EELES, R, IZATT, L, DAVIDSON, R, ADLARD, J, ECCLES, D, ONG, K-R, DOUGLAS, F, DOWNING, S, PETERLONGO, P, BREWER, C, WALKER, L, NEVANLINNA, H, AITTOMAKI, K, COUCH, F. J, FREDERICKSEN, Z, LINDOR, N. M, GODWIN, A, ISAACS, C, CALIGO, M. A, TEULE, A, LOMAN, N, JERNSTRÖM, H, BARBANY-BUSTINZA, G, LILJEGREN, A, EHRENCRONA, H, STENMARK-ASKMALM, M, FELIUBADALO, L, MANOUKIAN, S, PEISSEL, B, ZAFFARONI, D, NATHANSON, K. L, DOMCHEK, S. M, REBBECK, T, LASA, A

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Association of PHB 1630 C andgt; T and MTHFR 677 C andgt; T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study by Jakubowska, A, Rozkrut, D, Antoniou, A, McGuffog, L, Healy, S, Sinilnikova, O M, Rennert, G, Lejbkowicz, F, Flugelman, A, Andrulis, I L, Glendon, G, Ozcelik, H, Thomassen, M, Paligo, M, Aretini, P, Kantala, J, Aroer, B, Von Wachenfeldt, A, Liljegren, A, Loman, N, Herbst, K, Kristoffersson, U, Rosenquist, R, Karlsson, P, Stenmark-Askmalm, Marie, Melin, B, Nathanson, K L, Domchek, S M, Byrski, T, Gronwald, J, Menkiszak, J, Serrano, P, Osorio, A, Cajal, T R, Tsitlaidou, M, Benitez, J, Gilbert, M, Rookus, M, Kluijt, I, Boessenkool-Pape, J L, Meijers-Heijboer, H E J, C Oosterwijk, J, J van Asperen, C, J Blok, M, R Nelen, M, M W van den Ouweland, A, Seynaeve, C, B van der Luijt, R, Devilee, P, F Easton, D, Peock, S, Frost, D, D Ellis, S, Fineberg, E, G Evans, D, Eeles, R, Jacobs, C, Adlard, J, Davidson, R, Eccles, D, Cole, T, Cook, J, Godwin, A, Bove, B, Stoppa-Lyonnet, D, Belotti, M, Mazoyer, S, Barjhoux, L, Boutry-Kryza, N, Pujol, P, Peyrat, J-P, Vennin, P, Muller, D, Fricker, J-P, Venat-Bouvet, L, Johannsson, OTh, Isaacs, C, Schmutzler, R, Wappenschmidt, B, Arnold, N, Varon-Mateeva, R, Niederacher, D, Sutter, C, Preisler-Adams, S, Simard, J, Soucy, P, Durocher, F, Beesley, J, Chen, X, Couch, F, Wang, X, Fredericksen, Z, S Pankratz, V, Peterlongo, P, Bonanni, B, Fortuzzi, S, Peissel, B, Szabo, C, L Mai, P, T Loud, J

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Association of PHB 1630 C > T and MTHFR 677 C > T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study by Jakubowska, A., Rozkrut, D., Antoniou, A., Hamann, U., Scott, R. J., McGuffog, L., Sinilnikova, O. M., Rennert, G., Lejbkowicz, F., Flugelman, A., Andrulis, I. L., Glendon, G., Ozcelik, H., Thomassen, M., Kantala, J., Aroer, B., Von Wachenfeldt, A., Liljegren, A., Loman, N., Kristoffersson, U., Rosenquist, R., Karlsson, P., Stenmark-Askmalm, M., Nathanson, K. L., Domchek, S. M., Byrski, T., Gronwald, J., Cybulski, C., Serrano, P., Osorio, A., Cajal, T. R., Tsitlaidou, M., Benitez, J., Gilbert, M., Rookus, M., Aalfs, C. M., Kluijt, I., Boessenkool-Pape, J. L., Oosterwijk, J. C., van Asperen, C. J., Blok, M. J., Nelen, M. R., van den Ouweland, A. M. W., van der Luijt, R. B., Devilee, P., Easton, D. F., Peock, S., Frost, D., Platte, R., Ellis, S. D., Fineberg, E., Evans, D. G., Lalloo, F., Eeles, R., Jacobs, C., Cole, T., Cook, J., Godwin, A., Bove, B., Stoppa-Lyonnet, D., Caux-Moncoutier, V., Belotti, M., Tirapo, C., Mazoyer, S., Barjhoux, L., Boutry-Kryza, N., Pujol, P., Vennin, P., Muller, D., Fricker, J-P, Venat-Bouvet, L., Johannsson, OTh, Isaacs, C., Schmutzler, R., Wappenschmidt, B., Meindl, A., Arnold, N., Varon-Mateeva, R., Niederacher, D., Sutter, C., Deissler, H., Preisler-Adams, S., Simard, J., Soucy, P., Durocher, F., Chenevix-Trench, G., Beesley, J., Chen, X., Rebbeck, T., Couch, F., Wang, X., Lindor, N., Pankratz, V. S., Peterlongo, P., Bonanni, B., Fortuzzi, S., Peissel, B., Mai, P. L., Loud, J. T., Lubinski, J.

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