Treffer 1 - 20 von 26 für Suche 'Bernardo, Stephanie N', Suchdauer: 2,02s Treffer weiter einschränken
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    Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk von Couch, Fergus J, Wang, Xianshu, McGuffog, Lesley, Lee, Andrew, Olswold, Curtis, Kuchenbaecker, Karoline B, Soucy, Penny, Fredericksen, Zachary, Barrowdale, Daniel, Dennis, Joe, Gaudet, Mia M, Dicks, Ed, Kosel, Matthew, Healey, Sue, Sinilnikova, Olga M, Lee, Adam, Bacot, François, Vincent, Daniel, Hogervorst, Frans B L, Peock, Susan, Stoppa-Lyonnet, Dominique, Jakubowska, Anna, Radice, Paolo, Schmutzler, Rita Katharina, Domchek, Susan M, Piedmonte, Marion, Singer, Christian F, Friedman, Eitan, Thomassen, Mads, Hansen, Thomas V O, Neuhausen, Susan L, Szabo, Csilla I, Blanco, Ignacio, Greene, Mark H, Karlan, Beth Y, Garber, Judy, Phelan, Catherine M, Weitzel, Jeffrey N, Montagna, Marco, Olah, Edith, Andrulis, Irene L, Godwin, Andrew K, Yannoukakos, Drakoulis, Goldgar, David E, Caldes, Trinidad, Nevanlinna, Heli, Osorio, Ana, Terry, Mary Beth, Daly, Mary B, van Rensburg, Elizabeth J, Hamann, Ute, Ramus, Susan J, Toland, Amanda Ewart, Caligo, Maria A, Olopade, Olufunmilayo I, Tung, Nadine, Claes, Kathleen, Beattie, Mary S, Southey, Melissa C, Imyanitov, Evgeny N, Tischkowitz, Marc, Janavicius, Ramunas, John, Esther M, Kwong, Ava, Diez, Orland, Balmaña, Judith, Barkardottir, Rosa B, Arun, Banu K, Rennert, Gad, Teo, Soo-Hwang, Ganz, Patricia A, Campbell, Ian, van der Hout, Annemarie H, van Deurzen, Carolien H M, Seynaeve, Caroline, Gómez Garcia, Encarna B, van Leeuwen, Flora E, Meijers-Heijboer, Hanne E J, Gille, Johannes J P, Ausems, Margreet G E M, Blok, Marinus J, Ligtenberg, Marjolijn J L, Rookus, Matti A, Devilee, Peter, Verhoef, Senno, van Os, Theo A M, Wijnen, Juul T, Frost, Debra, Ellis, Steve, Fineberg, Elena, Platte, Radka, Evans, D Gareth, Izatt, Louise, Eeles, Rosalind A, Adlard, Julian, Eccles, Diana M, Cook, Jackie, Brewer, Carole, Douglas, Fiona, Hodgson, Shirley

    Veröffentlicht in PLoS genetics

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    Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer von Couch, Fergus J., Mendoza-Fandino, Gustavo A., Nord, Silje, Hallberg, Emily, Agata, Simona, Ahsan, Habibul, Aittomäki, Kristiina, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arver, Brita, Barile, Monica, Benitez, Javier, Blank, Stephanie V., Blomqvist, Carl, Bonanni, Bernardo, Brauch, Hiltrud, Brenner, Hermann, Burwinkel, Barbara, Caligo, Maria A., Claes, Kathleen B. M., Cross, Simon S., Darabi, Hatef, de la Hoya, Miguel, Devilee, Peter, Dolcetti, Riccardo, Dorfling, Cecilia M., Försti, Asta, Foulkes, William D., Friebel, Tara, Gabrielson, Marike, Garber, Judy, Gaudet, Mia M., Gerdes, Anne-Marie, Ghoussaini, Maya, Goldgar, David E., Haeberle, Lothar, Hart, Steven, Healey, Sue, Herzog, Josef, Hogervorst, Frans B. L., Hopper, John L., Huzarski, Tomasz, Jakubowska, Anna, Janavicius, Ramunas, Jones, Michael, Kar, Siddhartha, Karlan, Beth Y., Knight, Julia A., Ko, Yon-Dschun, Konstantopoulou, Irene, Kwong, Ava, Liu, Jianjun, Manoukian, Siranoush, Margolin, Sara, Marme, Frederik, Miller, Austin, Montagna, Marco, Mulligan, Anna M., Nathanson, Katherine L., Olson, Janet E., Osorio, Ana, Park, Sue K., Peto, Julian, Pilarski, Robert, Poppe, Bruce, Rappaport, Christine, Rennert, Gad, Richardson, Andrea, Robson, Mark, Romieu, Isabelle, Rutgers, Emiel J., Sanchez, Maria-Jose, Sawyer, Elinor J., Schmidt, Marjanka K., Schmutzler, Rita K., Scott, Rodney, Senter, Leigha, Simard, Jacques, Sinilnikova, Olga M., Szabo, Csilla I., Tapper, William, Teixeira, Manuel R., Thomassen, Mads, Thompson, Deborah, Truong, Thérèse, Tsimiklis, Helen, Turnbull, Clare, Ursin, Giski, Weitzel, Jeffrey N., Whittemore, Alice, Wildiers, Hans, Yang, Xiaohong R., Zheng, Wei, Hall, Per, Kraft, Peter, Vachon, Celine, Slager, Susan, Monteiro, Alvaro A. N., Easton, Douglas F.

    Veröffentlicht in NATURE COMMUNICATIONS

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    Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers von Antoniou, Antonis C., Sinilnikova, Olga M., McGuffog, Lesley, Healey, Sue, Nevanlinna, Heli, Chen, Xiaoqing, Neuhausen, Susan L., Ding, Yuan C., Couch, Fergus J., Wang, Xianshu, Fredericksen, Zachary, Peterlongo, Paolo, Peissel, Bernard, Viel, Alessandra, Radice, Paolo, Szabo, Csilla I., Foretova, Lenka, Zikan, Michal, Claes, Kathleen, Greene, Mark H., Mai, Phuong L., Ozcelik, Hilmi, Thomassen, Mads, Sunde, Lone, Caligo, Maria A., Laitman, Yael, Kontorovich, Tair, Kaufman, Bella, Dagan, Efrat, Baruch, Ruth Gershoni, Harbst, Katja, Barbany-Bustinza, Gisela, Rantala, Johanna, Domchek, Susan M., Nathanson, Katherine L., Osorio, Ana, Blanco, Ignacio, Lasa, Adriana, Hamann, Ute, Rookus, Matti A., Collee, J. Margriet, Devilee, Peter, van der Luijt, Rob B., Waisfisz, Quinten, Wijnen, Juul, van Roozendaal, Cornelis E.P., Peock, Susan, Cook, Margaret, Frost, Debra, Oliver, Clare, Platte, Radka, Evans, D. Gareth, Eeles, Rosalind, Izatt, Louise, Eccles, Diana, Cole, Trevor, Hodgson, Shirley, Buecher, Bruno, Léoné, Mélanie, Remenieras, Audrey, Caron, Olivier, Lenoir, Gilbert M., Sevenet, Nicolas, Longy, Michel, Ferrer, Sandra Fert, Prieur, Fabienne, Goldgar, David, Miron, Alexander, John, Esther M., Daly, Mary B., Hopper, John L., Gschwantler-Kaulich, Daphne, Staudigl, Christine, Hansen, Thomas v. O., Barkardottir, Rosa Bjork, Kirchhoff, Tomas, Pal, Prodipto, Kosarin, Kristi, Offit, Kenneth, Piedmonte, Marion, Rodriguez, Gustavo C., Wakeley, Katie, Boggess, John F., Schwartz, Peter E., Montagna, Marco, Imyanitov, Evgeny N., Allavena, Anna, Schmutzler, Rita K., Versmold, Beatrix, Engel, Christoph, Ditsch, Nina, Niederacher, Dieter, Deißler, Helmut, Fiebig, Britta, Suttner, Christian, Schönbuchner, Ines, Gadzicki, Dorothea, Caldes, Trinidad, Pooley, Karen A., Chenevix-Trench, Georgia

    Veröffentlicht in Human molecular genetics

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