Treffer 1 - 20 von 22 für Suche 'Ahearn, Kathleen K.', Suchdauer: 1,42s Treffer weiter einschränken
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    A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (vol 12, 1078, 2021) von Coignard, Juliette, Lush, Michael, Beesley, Jonathan, O'Mara, Tracy A., Dennis, Joe, Tyrer, Jonathan P., Barnes, Daniel R., McGuffog, Lesley, Leslie, Goska, Bolla, Manjeet K., Adank, Muriel A., Agata, Simona, Ahearn, Thomas, Aittomaki, Kristiina, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arnold, Norbert, Aronson, Kristan J., Arun, Banu K., Augustinsson, Annelie, Azzollini, Jacopo, Barrowdale, Daniel, Baynes, Caroline, Becher, Heko, Bermisheva, Marina, Bernstein, Leslie, Bialkowska, Katarzyna, Blomqvist, Carl, Bojesen, Stig E., Bonanni, Bernardo, Borg, Ake, Brauch, Hiltrud, Brenner, Hermann, Burwinkel, Barbara, Buys, Saundra S., Caldes, Trinidad, Caligo, Maria A., Campa, Daniele, Carter, Brian D., Castelao, Jose E., Chang-Claude, Jenny, Chanock, Stephen J., Chung, Wendy K., Claes, Kathleen B. M., Clarke, Christine L., Collee, J. Margriet, Conroy, Don M., Czene, Kamila, Daly, Mary B., Devilee, Peter, Diez, Orland, Ding, Yuan Chun, Domchek, Susan M., Doerk, Thilo, dos-Santos-Silva, Isabel, Dunning, Alison M., Dwek, Miriam, Eccles, Diana M., Eliassen, A. Heather, Engel, Christoph, Eriksson, Mikael, Evans, D. Gareth, Fasching, Peter A., Flyger, Henrik, Fostira, Florentia, Friedman, Eitan, Fritschi, Lin, Frost, Debra, Gago-Dominguez, Manuela, Gapstur, Susan M., Garber, Judy, Garcia-Barberan, Vanesa, Garcia-Closas, Montserrat, Garcia-Saenz, Jose A., Gaudet, Mia M., Gayther, Simon A., Gehrig, Andrea, Georgoulias, Vassilios, Giles, Graham G., Godwin, Andrew K., Goldberg, Mark S., Goldgar, David E., Gonzalez-Neira, Anna, Greene, Mark H., Guenel, Pascal, Haeberle, Lothar, Hahnen, Eric, Haiman, Christopher A., Hakansson, Niclas, Hall, Per, Hamann, Ute, Harrington, Patricia A., Hart, Steven N., He, Wei, Hogervorst, Frans B. L., Hollestelle, Antoinette, Hopper, John L., Horcasitas, Darling J., Hulick, Peter J.

    Veröffentlicht in NATURE COMMUNICATIONS

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    A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Lush, Michael, Beesley, Jonathan, O'Mara, Tracy A, Dennis, Joe, Tyrer, Jonathan P, Barnes, Daniel R, McGuffog, Lesley, Leslie, Goska, Bolla, Manjeet K, Adank, Muriel A, Agata, Simona, Ahearn, Thomas, Aittomaeki, Kristiina, Andrulis, Irene L, Anton-Culver, Hoda, Arndt, Volker, Arnold, Norbert, Aronson, Kristan J, Arun, Banu K, Augustinsson, Annelie, Azzollini, Jacopo, Barrowdale, Daniel, Baynes, Caroline, Becher, Heko, Bermisheva, Marina, Bernstein, Leslie, Bialkowska, Katarzyna, Blomqvist, Carl, Bojesen, Stig E, Bonanni, Bernardo, Borg, Ake, Brauch, Hiltrud, Brenner, Hermann, Burwinkel, Barbara, Buys, Saundra S, Caldes, Trinidad, Caligo, Maria A, Campa, Daniele, Carter, Brian D, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Chung, Wendy K, Claes, Kathleen B.M, Clarke, Christine L, Collee, J. Margriet, Conroy, Don M, Czene, Kamila, Daly, Mary B, Devilee, Peter, Diez, Orland, Ding, Yuan Chun, Domchek, Susan M, Dork, Thilo, dos-Santos-Silva, Isabel, Dunning, Alison M, Dwek, Miriam, Eccles, Diana M, Eliassen, A. Heather, Engel, Christoph, Eriksson, Mikael, Evans, D. Gareth, Fasching, Peter A, Flyger, Henrik, Fostira, Florentia, Friedman, Eitan, Fritschi, Lin, Frost, Debra, Gago-Dominguez, Manuela, Gapstur, Susan M, Garber, Judy, Garcia-Barberan, Vanesa, Garcia-Closas, Montserrat, Garcia-Saenz, Jose A, Gaudet, Mia M, Gayther, Simon A, Gehrig, Andrea, Georgoulias, Vassilios, Giles, Graham G, Godwin, Andrew K, Goldberg, Mark S, Goldgar, David E, Gonzalez-Neira, Anna, Greene, Mark H, Guenel, Pascal, Haeberle, Lothar, Hahnen, Eric, Haiman, Christopher A, Hakansson, Niclas, Hall, Per, Hamann, Ute, Harrington, Patricia A, Hart, Steven N, He, Wei, Hogervorst, Frans B.L, Hollestelle, Antoinette, Hopper, John L, Horcasitas, Darling J, Hulick, Peter J

    Veröffentlicht in NATURE COMMUNICATIONS

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    A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Lush, Michael, Beesley, Jonathan, Dennis, Joe, Tyrer, Jonathan P, McGuffog, Lesley, Adank, Muriel A, Ahearn, Thomas, Arun, Banu K, Baynes, Caroline, Białkowska, Katarzyna, Bojesen, Stig E, Brauch, Hiltrud, Burwinkel, Barbara, Buys, Saundra S, Caldés, Trinidad, Campa, Daniele, Chanock, Stephen J, EMBRACE Collaborators, Conroy, Don M, Daly, Mary B, Devilee, Peter, Dörk, Thilo, Eliassen, A Heather, Evans, D Gareth, Fostira, Florentia, Gago-Dominguez, Manuela, Gapstur, Susan M, Garcia-Barberan, Vanesa, García-Closas, Montserrat, Gaudet, Mia M, Gayther, Simon A, Gehrig, Andrea, Giles, Graham G, Godwin, Andrew K, Goldberg, Mark S, González-Neira, Anna, Greene, Mark H, Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A, Hamann, Ute, Harrington, Patricia A, He, Wei, Hollestelle, Antoinette, Horcasitas, Darling J, Hulick, Peter J, Hunter, David J, ABCTB Investigators, Jager, Agnes, James, Paul A, Jensen, Uffe Birk, Kaaks, Rudolf, Kiiski, Johanna I, Kosma, Veli-Matti, Kurian, Allison W, Laitman, Yael, Lambrechts, Diether, Le Marchand, Loic, Lester, Jenny, Lindstrom, Tricia, Luccarini, Craig, Mannermaa, Arto, Manoukian, Siranoush, Martens, John WM, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Nielsen, Finn C, O'Brien, Katie M, Olopade, Olufunmilayo I, Olson, Janet E, Ottini, Laura, Park-Simon, Tjoung-Won, Parsons, Michael T, Pedersen, Inge Sokilde, Poppe, Bruce, Presneau, Nadege, Punie, Kevin, Radice, Paolo, Rennert, Gad, Robson, Mark, Saloustros, Emmanouil, Scheuner, Maren T, Scott, Christopher, Stoppa-Lyonnet, Dominique, Swerdlow, Anthony, Thull, Darcy L, Tischkowitz, Marc, Vijai, Joseph, Wang, Qin, Wappenschmidt, Barbara, Yannoukakos, Drakoulis, Ziogas, Argyrios, Offit, Kenneth, Simard, Jacques, Easton, Douglas F, Antoniou, Antonis C

    Veröffentlicht in Nature communications

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    A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Lush, Michael, Beesley, Jonathan, Dennis, Joe, Tyrer, Jonathan P, McGuffog, Lesley, Adank, Muriel A, Ahearn, Thomas, Aittomaeki, Kristiina, Arun, Banu K, Baynes, Caroline, Bojesen, Stig E, Brauch, Hiltrud, Burwinkel, Barbara, Buys, Saundra S, Campa, Daniele, Chanock, Stephen J, Claes, Kathleen, Collee, J. Margriet, Daly, Mary B, Diez, Orland, Ding, Yuan Chun, dos-Santos-Silva, Isabel, Engel, Christoph, Eriksson, Mikael, Evans, D. Gareth, Fasching, Peter A, Flyger, Henrik, Friedman, Eitan, Fritschi, Lin, Frost, Debra, Gago-Dominguez, Manuela, Garber, Judy, Garcia-Saenz, Jose A, Gehrig, Andrea, Godwin, Andrew K, Goldgar, David E, Gonzalez-Neira, Anna, Greene, Mark H, Haeberle, Lothar, Haiman, Christopher A, Hogervorst, Frans B. L, Hollestelle, Antoinette, Hopper, John L, Imyanitov, Evgeny N, Jager, Agnes, John, Esther M, Kapoor, Pooja Middha, Karlan, Beth Y, Keeman, Renske, Kiiski, Johanna I, Ko, Yon-Dschun, Kosma, Veli-Matti, Kraft, Peter, Kurian, Allison W, Lambrechts, Diether, Lester, Jenny, Lindstrom, Tricia, Loud, Jennifer T, Manoukian, Siranoush, Mebirouk, Noura, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Nielsen, Finn C, O'Brien, Katie M, Olopade, Olufunmilayo I, Olson, Janet E, Olsson, Hakan, Osorio, Ana, Ottini, Laura, Pedersen, Inge Sokilde, Peto, Julian, Phillips, Kelly-Anne, Angel Pujana, Miquel, Punie, Kevin, Rennert, Gad, Robson, Mark, Sandler, Dale P, Scheuner, Maren T, Schmidt, Gunnar, Stoppa-Lyonnet, Dominique, Swerdlow, Anthony, Tamimi, Rulla M, Taylor, Jack A, Terry, Mary Beth, Tischkowitz, Marc, Truong, Therese, Vachon, Celine M, Vega, Ana, Vijai, Joseph, Wang, Qin, Yang, Xiaohong R, Ziogas, Argyrios, Zorn, Kristin K, Offit, Kenneth, Chenevix-Trench, Georgia, Andrieu, Nadine


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    Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses von Zhan, Haoyu, Ahearn, Thomas U, Lecarpentier, Julie, Barnes, Daniel, Beesley, Jonathan, Qi, Guanghao, Jiang, Xia, O'Mara, Tracy A, Zhao, Ni, Bolla, Manjeet K, Dunning, Alison M, Dennis, Joe, Wang, Qin, Abu Ful, Zumuruda, Aittomaki, Kristiina, Andrulis, Irene L, Anton-Culver, Hoda, Arndt, Volker, Aronson, Kristan J, Arun, Banu K, Auer, Paul L, Azzollini, Jacopo, Barrowdale, Daniel, Becher, Heiko, Beckmann, Matthias W, Behrens, Sabine, Benitez, Javier, Bermisheva, Marina, Bialkowska, Katarzyna, Blanco, Ana, Blomqvist, Carl, Bogdanova, Natalia, Bojesen, Stig E, Bonanni, Bernardo, Bondavalli, Davide, Borg, Ake, Brauch, Hiltrud, Brenner, Hermann, Briceno, Ignacio, Broeks, Annegien, Brucker, Sara Y, Bruening, Thomas, Burwinkel, Barbara, Buys, Saundra S, Byers, Helen, Caldes, Trinidad, Caligo, Maria A, Calvello, Mariarosaria, Campa, Daniele, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Christiaens, Melissa, Christiansen, Hans, Chung, Wendy K, Claes, Kathleen B.M, Clarke, Christine L, Cornelissen, Sten, Couch, Fergus J, Cox, Angela, Cross, Simon S, Czene, Kamila, Daly, Mary B, Devilee, Peter, Diez, Orland, Domchek, Susan M, Doerk, Thilo, Dwek, Miriam, Eccles, Diana M, Ekici, Arif B, Evans, D. Gareth, Fasching, Peter A, Figueroa, Jonine, Foretova, Lenka, Fostira, Florentia, Friedman, Eitan, Frost, Debra, Gago-Dominguez, Manuela, Gapstur, Susan M, Garber, Judy, Garcia-Saenz, Jose A, Gaudet, Mia M, Gayther, Simon A, Giles, Graham G, Godwin, Andrew K, Goldberg, Mark S, Goldgar, David E, Gonzalez-Neira, Anna, Greene, Mark H, Gronwald, Jacek, Guenel, Pascal, Haeberle, Lothar, Hahnen, Eric, Haiman, Christopher A, Hake, Christopher R, Hall, Per, Hamann, Ute, Harkness, Elaine F, Heemskerk-Gerritsen, Bernadette A.M, Hillemanns, Peter

    Veröffentlicht in NATURE GENETICS

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    The FANCM:p.Arg658 truncating variant is associated with risk of triple-negative breast cancer von Figlioli, Gisella, Bogliolo, Massimo, Catucci, Irene, Caleca, Laura, Viz Lasheras, Sandra, Pujol, Roser, Kiiski, Johanna, Muranen, Taru A, Barnes, Daniel R, Dennis, Joe, Michailidou, Kyriaki, Bolla, Manjeet K, Leslie, Goska, Aalfs, Cora M, Adank, Muriel A, Adlard, Julian, Agata, Simona, Cadoo, Karen, Agnarsson, Bjarni A, Ahearn, Thomas, Aittomaki, Kristiina, Ambrosone, Christine B, Andrews, Lesley, Anton-Culver, Hoda, Antonenkova, Natalia N, Arndt, Volker, Arnold, Norbert, Aronson, Kristan J, Arun, Banu K, Asseryanis, Ella, Auber, Bernd, Auvinen, Paivi, Azzollini, Jacopo, Balmana, Judith, Barkardottir, Rosa B, Barrowdale, Daniel, Barwell, Julian, Freeman, Laura E. Beane, Beauparlant, Charles Joly, Beckmann, Matthias W, Behrens, Sabine, Benitez, Javier, Berger, Raanan, Bermisheva, Marina, Blanco, Amie M, Blomqvist, Carl, Bogdanova, Natalia, Bojesen, Anders, Bojesen, Stig E, Bonanni, Bernardo, Borg, Ake, Brady, Angela F, Brauch, Hiltrud, Brenner, Hermann, Bruening, Thomas, Burwinkel, Barbara, Buys, Saundra S, Caldes, Trinidad, Caliebe, Almuth, Caligo, Maria A, Campa, Daniele, Campbell, Ian G, Canzian, Federico, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Claes, Kathleen B.M, Clarke, Christine L, Collavoli, Anita, Conner, Thomas A, Cox, David G, Cybulski, Cezary, Czene, Kamila, Daly, Mary B, de la Hoya, Miguel, Devilee, Peter, Diez, Orland, Ding, Yuan Chun, Dite, Gillian S, Ditsch, Nina, Domchek, Susan M, Dorfling, Cecilia M, dos-Santos-Silva, Isabel, Durda, Katarzyna, Dwek, Miriam, Eccles, Diana M, Ekici, Arif B, Eliassen, A. Heather, Ellberg, Carolina, Eriksson, Mikael, Evans, D. Gareth, Fasching, Peter A, Figueroa, Jonine, Flyger, Henrik, Foulkes, William D, Friebel, Tara M, Friedman, Eitan, Gabrielson, Marike, Gaddam, Pragna, Gago-Dominguez, Manuela

    Veröffentlicht in NPJ BREAST CANCER

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    The FANCM:p.Arg658 truncating variant is associated with risk of triple-negative breast cancer von Catucci, Irene, Kiiski, Johanna I, Muranen, Taru A, Bolla, Manjeet K, Leslie, Goska, Adlard, Julian, Ahearn, Thomas, Andrews, Lesley, Arnold, Norbert, Asseryanis, Ella, Auber, Bernd, Blanco, Amie M, Bonanni, Bernardo, Brenner, Hermann, Campa, Daniele, Chanock, Stephen J, Claes, Kathleen, Clarke, Christine L, Cybulski, Cezary, Daly, Mary B, de la Hoya, Miguel, Durda, Katarzyna, Dwek, Miriam, Ekici, Arif B, Fasching, Peter A, Foulkes, William D, Friebel, Tara M, Gabrielson, Marike, Gaddam, Pragna, Gao, Chi, Gapstur, Susan M, Garber, Judy, Gayther, Simon A, Godwin, Andrew K, Goldgar, David E, Guénel, Pascal, Gutierrez-Barrera, Angelica M, Hall, Per, Harrington, Patricia A, Hollestelle, Antoinette, Hopper, John L, Hu, Chunling, Jakimovska, Milena, Janni, Wolfgang, John, Esther M, Jones, Michael E, Karlan, Beth Y, Kraft, Peter, Lambrechts, Diether, Lazaro, Conxi, Lester, Jenny, Loud, Jennifer T, Lubinski, Jan, Manoukian, Siranoush, Maurer, Tabea, Meindl, Alfons, Neuhausen, Susan L, Nielsen, Finn Cilius, Nikitina-Zake, Liene, Olah, Edith, Olsson, Håkan, Osorio, Ana, Peto, Julian, Rack, Brigitte, Rantala, Johanna, Rennert, Gad, Rookus, Matti A, Rossing, Maria, Ruebner, Matthias, Saloustros, Emmanouil, Sanden, Kristin, Santamariña, Marta, Schmutzler, Rita K, Schneider, Michael, Senter, Leigha, Singer, Christian F, Soucy, Penny, Spinelli, John J, Stoppa-Lyonnet, Dominique, Tapper, William J, Terry, Mary Beth, van Rensburg, Elizabeth J, van Veen, Elke M, Vega, Ana, Weitzel, Jeffrey N, Wolk, Alicja, Ziogas, Argyrios, Zorn, Kristin K, Dunning, Alison M, McGuffog, Lesley, Pharoah, Paul DP, Toland, Amanda E, Andrulis, Irene L, Ramus, Susan J, Swerdlow, Anthony J, Milne, Roger L, Dörk, Thilo, Easton, Douglas F, Hahnen, Eric, Surrallés, Jordi


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    Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Lush, Michael, Beesley, Jonathan, Dennis, Joe, Tyrer, Jonathan P, McGuffog, Lesley, Adank, Muriel A, Ahearn, Thomas, Arun, Banu K, Baynes, Caroline, Białkowska, Katarzyna, Bojesen, Stig E, Brauch, Hiltrud, Burwinkel, Barbara, Buys, Saundra S, Caldés, Trinidad, Campa, Daniele, Chanock, Stephen J, EMBRACE Collaborators, Conroy, Don M, Daly, Mary B, Devilee, Peter, Dörk, Thilo, Eliassen, A Heather, Evans, D Gareth, Fostira, Florentia, Gago-Dominguez, Manuela, Gapstur, Susan M, Garcia-Barberan, Vanesa, García-Closas, Montserrat, Gaudet, Mia M, Gayther, Simon A, Gehrig, Andrea, Giles, Graham G, Godwin, Andrew K, Goldberg, Mark S, González-Neira, Anna, Greene, Mark H, Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A, Hamann, Ute, Harrington, Patricia A, He, Wei, Hollestelle, Antoinette, Horcasitas, Darling J, Hulick, Peter J, Hunter, David J, ABCTB Investigators, Jager, Agnes, James, Paul A, Jensen, Uffe Birk, Kaaks, Rudolf, Kiiski, Johanna I, Kosma, Veli-Matti, Kurian, Allison W, Laitman, Yael, Lambrechts, Diether, Le Marchand, Loic, Lester, Jenny, Lindstrom, Tricia, Luccarini, Craig, Mannermaa, Arto, Manoukian, Siranoush, Martens, John WM, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Nielsen, Finn C, O'Brien, Katie M, Olopade, Olufunmilayo I, Olson, Janet E, Ottini, Laura, Park-Simon, Tjoung-Won, Parsons, Michael T, Pedersen, Inge Sokilde, Poppe, Bruce, Presneau, Nadege, Punie, Kevin, Radice, Paolo, Rennert, Gad, Robson, Mark, Saloustros, Emmanouil, Scheuner, Maren T, Scott, Christopher, Stoppa-Lyonnet, Dominique, Swerdlow, Anthony, Thull, Darcy L, Tischkowitz, Marc, Vijai, Joseph, Wang, Qin, Wappenschmidt, Barbara, Yannoukakos, Drakoulis, Ziogas, Argyrios, Offit, Kenneth, Simard, Jacques, Easton, Douglas F, Antoniou, Antonis C

    Veröffentlicht in Nat Commun
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  12. 12

    A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Lush, Michael, Beesley, Jonathan, Dennis, Joe, Tyrer, Jonathan P, McGuffog, Lesley, Adank, Muriel A, Ahearn, Thomas, Arun, Banu K, Baynes, Caroline, Białkowska, Katarzyna, Bojesen, Stig E, Brauch, Hiltrud, Burwinkel, Barbara, Buys, Saundra S, Caldés, Trinidad, Campa, Daniele, Chanock, Stephen J, EMBRACE Collaborators, Conroy, Don M, Daly, Mary B, Devilee, Peter, Dörk, Thilo, Eliassen, A Heather, Evans, D Gareth, Fostira, Florentia, Gago-Dominguez, Manuela, Gapstur, Susan M, Garcia-Barberan, Vanesa, García-Closas, Montserrat, Gaudet, Mia M, Gayther, Simon A, Gehrig, Andrea, Giles, Graham G, Godwin, Andrew K, Goldberg, Mark S, González-Neira, Anna, Greene, Mark H, Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A, Hamann, Ute, Harrington, Patricia A, He, Wei, Hollestelle, Antoinette, Horcasitas, Darling J, Hulick, Peter J, Hunter, David J, ABCTB Investigators, Jager, Agnes, James, Paul A, Jensen, Uffe Birk, Kaaks, Rudolf, Kiiski, Johanna I, Kosma, Veli-Matti, Kurian, Allison W, Laitman, Yael, Lambrechts, Diether, Le Marchand, Loic, Lester, Jenny, Lindstrom, Tricia, Luccarini, Craig, Mannermaa, Arto, Manoukian, Siranoush, Martens, John WM, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Nielsen, Finn C, O'Brien, Katie M, Olopade, Olufunmilayo I, Olson, Janet E, Ottini, Laura, Park-Simon, Tjoung-Won, Parsons, Michael T, Pedersen, Inge Sokilde, Poppe, Bruce, Presneau, Nadege, Punie, Kevin, Radice, Paolo, Rennert, Gad, Robson, Mark, Saloustros, Emmanouil, Scheuner, Maren T, Scott, Christopher, Stoppa-Lyonnet, Dominique, Swerdlow, Anthony, Thull, Darcy L, Tischkowitz, Marc, Vijai, Joseph, Wang, Qin, Wappenschmidt, Barbara, Yannoukakos, Drakoulis, Ziogas, Argyrios, Offit, Kenneth, Simard, Jacques, Easton, Douglas F, Antoniou, Antonis C

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  13. 13

    The FANCM:p.Arg658 truncating variant is associated with risk of triple-negative breast cancer von Catucci, Irene, Kiiski, Johanna I, Muranen, Taru A, Bolla, Manjeet K, Leslie, Goska, Adank, Muriel A, Asseryanis, Ella, Auber, Bernd, Barkardottir, Rosa B, Beckmann, Matthias W, Behrens, Sabine, Benitez, Javier, Bogdanova, Natalia V, Bojesen, Anders, Borg, Ake, Brauch, Hiltrud, Caldés, Trinidad, Campbell, Ian G, Canzian, Federico, Castelao, Jose E, Cox, David G, de la Hoya, Miguel, Devilee, Peter, Diez, Orland, Dos-Santos-Silva, Isabel, Durda, Katarzyna, Dwek, Miriam, Eccles, Diana M, Ekici, Arif B, Eriksson, Mikael, Evans, D Gareth, Fasching, Peter A, Flyger, Henrik, Gabrielson, Marike, Gaddam, Pragna, Gago-Dominguez, Manuela, Gao, Chi, García-Closas, Montserrat, Gayther, Simon A, Glendon, Gord, Goldberg, Mark S, Goldgar, David E, Haeberle, Lothar, Haiman, Christopher A, Håkansson, Niclas, Hamann, Ute, Hein, Alexander, Heyworth, Jane, Howell, Anthony, Hulick, Peter J, Hunter, David J, Imyanitov, Evgeny N, KConFab, Isaacs, Claudine, Kaaks, Rudolf, Karlan, Beth Y, Khusnutdinova, Elza, Koutros, Stella, Lu, Karen H, Luben, Robert N, Mannermaa, Arto, Manoochehri, Mehdi, Martens, John WM, Mebirouk, Noura, Menon, Usha, Miller, Austin, Nguyen-Dumont, Tu, Olson, Janet E, Peissel, Bernard, Peixoto, Ana, Pujana, Miquel Angel, Punie, Kevin, Lejbkowicz, Flavio, Shu, Xiao-Ou, Simard, Jacques, Singer, Christian F, Sohn, Christof, Steele, Linda, Thompson, Jennifer, Thull, Darcy L, Tischkowitz, Marc, Tollenaar, Rob AEM, Torres, Diana, Troester, Melissa A, Vachon, Celine M, Viel, Alessandra, Wappenschmidt, Barbara, Wieme, Greet, Yang, Xiaohong R, Zheng, Wei, Lush, Michael, Parsons, Michael T, Pharoah, Paul DP, Fostira, Florentia, Swerdlow, Anthony J, Chung, Wendy K, Chenevix-Trench, Georgia, Radice, Paolo, Nevanlinna, Heli, Peterlongo, Paolo

    Veröffentlicht in npj Breast Cancer
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  14. 14

    The FANCM :p.Arg658 truncating variant is associated with risk of triple-negative breast cancer von Catucci, Irene, Kiiski, Johanna I, Muranen, Taru A, Bolla, Manjeet K, Leslie, Goska, Adlard, Julian, Ahearn, Thomas, Andrews, Lesley, Arnold, Norbert, Asseryanis, Ella, Auber, Bernd, Blanco, Amie M, Bonanni, Bernardo, Brenner, Hermann, Buys, Saundra, Campa, Daniele, Chanock, Stephen J, Claes, Kathleen, Clarke, Christine L, Cybulski, Cezary, Daly, Mary B, Durda, Katarzyna, Dwek, Miriam, Ekici, Arif B, Fasching, Peter A, Friebel, Tara M, Gabrielson, Marike, Gaddam, Pragna, Gao, Chi, Gapstur, Susan M, Garber, Judy, Gayther, Simon A, Godwin, Andrew K, Goldgar, David E, Guénel, Pascal, Gutierrez-Barrera, Angelica M, Hall, Per, Harrington, Patricia A, Heyworth, Jane, Hollestelle, Antoinette, Hopper, John L, Hu, Chunling, Jakimovska, Milena, Janni, Wolfgang, John, Esther M, Jones, Michael E, Karlan, Beth Y, Kraft, Peter, Lambrechts, Diether, Lazaro, Conxi, Lester, Jenny, Loud, Jennifer T, Lubinski, Jan, Manoukian, Siranoush, Martens, John W. M, Maurer, Tabea, Meindl, Alfons, Neuhausen, Susan L, Nielsen, Finn Cilius, Nikitina-Zake, Liene, Olah, Edith, Olsson, Håkan, Osorio, Ana, Peto, Julian, Rack, Brigitte, Rantala, Johanna, Rennert, Gad, Rookus, Matti A, Rossing, Maria, Ruebner, Matthias, Saloustros, Emmanouil, Sanden, Kristin, Santamariña, Marta, Schmutzler, Rita K, Schneider, Michael, Senter, Leigha, Singer, Christian F, Soucy, Penny, Spinelli, John J, Stoppa-Lyonnet, Dominique, Tapper, William J, Terry, Mary Beth, van Rensburg, Elizabeth J, van Veen, Elke M, Vega, Ana, Weitzel, Jeffrey N, Wolk, Alicja, Ziogas, Argyrios, Zorn, Kristin K, Dunning, Alison M, McGuffog, Lesley, Toland, Amanda E, Andrulis, Irene L, Ramus, Susan J, Swerdlow, Anthony J, Milne, Roger L, Dörk, Thilo, Easton, Douglas F, Hahnen, Eric, Surrallés i Calonge, Jordi

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    The FANCM:p.Arg658 truncating variant is associated with risk of triple-negative breast cancer von Catucci, Irene, Kiiski, Johanna I, Muranen, Taru A, Bolla, Manjeet K, Leslie, Goska, Adank, Muriel A, Asseryanis, Ella, Auber, Bernd, Barkardottir, Rosa B, Beckmann, Matthias W, Behrens, Sabine, Benitez, Javier, Bogdanova, Natalia V, Bojesen, Anders, Borg, Ake, Brauch, Hiltrud, Caldés, Trinidad, Campbell, Ian G, Canzian, Federico, Castelao, Jose E, Cox, David G, de la Hoya, Miguel, Devilee, Peter, Diez, Orland, Dos-Santos-Silva, Isabel, Durda, Katarzyna, Dwek, Miriam, Eccles, Diana M, Ekici, Arif B, Eriksson, Mikael, Evans, D Gareth, Fasching, Peter A, Flyger, Henrik, Gabrielson, Marike, Gaddam, Pragna, Gago-Dominguez, Manuela, Gao, Chi, García-Closas, Montserrat, Gayther, Simon A, Glendon, Gord, Goldberg, Mark S, Goldgar, David E, Haeberle, Lothar, Haiman, Christopher A, Håkansson, Niclas, Hamann, Ute, Hein, Alexander, Heyworth, Jane, Howell, Anthony, Hulick, Peter J, Hunter, David J, Imyanitov, Evgeny N, KConFab, Isaacs, Claudine, Kaaks, Rudolf, Karlan, Beth Y, Khusnutdinova, Elza, Koutros, Stella, Lu, Karen H, Luben, Robert N, Mannermaa, Arto, Manoochehri, Mehdi, Martens, John WM, Mebirouk, Noura, Menon, Usha, Miller, Austin, Nguyen-Dumont, Tu, Olson, Janet E, Peissel, Bernard, Peixoto, Ana, Pujana, Miquel Angel, Punie, Kevin, Lejbkowicz, Flavio, Shu, Xiao-Ou, Simard, Jacques, Singer, Christian F, Sohn, Christof, Steele, Linda, Thompson, Jennifer, Thull, Darcy L, Tischkowitz, Marc, Tollenaar, Rob AEM, Torres, Diana, Troester, Melissa A, Vachon, Celine M, Viel, Alessandra, Wappenschmidt, Barbara, Wieme, Greet, Yang, Xiaohong R, Zheng, Wei, Lush, Michael, Parsons, Michael T, Pharoah, Paul DP, Fostira, Florentia, Swerdlow, Anthony J, Chung, Wendy K, Chenevix-Trench, Georgia, Radice, Paolo, Nevanlinna, Heli, Peterlongo, Paolo

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    The FANCM :p.Arg658 truncating variant is associated with risk of triple-negative breast cancer von Catucci, Irene, Kiiski, Johanna I, Muranen, Taru A, Bolla, Manjeet K, Leslie, Goska, Adlard, Julian, Ahearn, Thomas, Andrews, Lesley, Arnold, Norbert, Asseryanis, Ella, Auber, Bernd, Blanco, Amie M, Bonanni, Bernardo, Brenner, Hermann, Buys, Saundra, Campa, Daniele, Chanock, Stephen J, Claes, Kathleen, Clarke, Christine L, Cybulski, Cezary, Daly, Mary B, Durda, Katarzyna, Dwek, Miriam, Ekici, Arif B, Fasching, Peter A, Foulkes, William D, Friebel, Tara M, Gabrielson, Marike, Gaddam, Pragna, Gao, Chi, Gapstur, Susan M, Garber, Judy, Gayther, Simon A, Godwin, Andrew K, Goldgar, David E, Guénel, Pascal, Gutierrez-Barrera, Angelica M, Hall, Per, Harrington, Patricia A, Hollestelle, Antoinette, Hopper, John L, Hu, Chunling, Jakimovska, Milena, Janni, Wolfgang, John, Esther M, Jones, Michael E, Karlan, Beth Y, Kraft, Peter, Lambrechts, Diether, Lazaro, Conxi, Lester, Jenny, Loud, Jennifer T, Lubinski, Jan, Manoukian, Siranoush, Martens, John W. M, Maurer, Tabea, Meindl, Alfons, Neuhausen, Susan L, Nielsen, Finn Cilius, Nikitina-Zake, Liene, Olah, Edith, Olsson, Håkan, Osorio, Ana, Peto, Julian, Rack, Brigitte, Rantala, Johanna, Rennert, Gad, Rookus, Matti A, Rossing, Maria, Ruebner, Matthias, Saloustros, Emmanouil, Sanden, Kristin, Santamariña, Marta, Schmutzler, Rita K, Schneider, Michael, Senter, Leigha, Singer, Christian F, Soucy, Penny, Spinelli, John J, Stoppa-Lyonnet, Dominique, Tapper, William J, Terry, Mary Beth, van Rensburg, Elizabeth J, van Veen, Elke M, Vega, Ana, Weitzel, Jeffrey N, Wolk, Alicja, Ziogas, Argyrios, Zorn, Kristin K, Dunning, Alison M, McGuffog, Lesley, Toland, Amanda E, Andrulis, Irene L, Ramus, Susan J, Swerdlow, Anthony J, Milne, Roger L, Dörk, Thilo, Easton, Douglas F, Hahnen, Eric, Surrallés i Calonge, Jordi

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    A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers (vol 12, 1078, 2021) von Coignard, Juliette, Lush, Michael, Beesley, Jonathan, O'Mara, Tracy A, Dennis, Joe, Tyrer, Jonathan P, Barnes, Daniel R, McGuffog, Lesley, Leslie, Goska, Bolla, Manjeet K, Adank, Muriel A, Agata, Simona, Ahearn, Thomas, Aittomaki, Kristiina, Andrulis, Irene L, Anton-Culver, Hoda, Arndt, Volker, Arnold, Norbert, Aronson, Kristan J, Arun, Banu K, Augustinsson, Annelie, Azzollini, Jacopo, Barrowdale, Daniel, Baynes, Caroline, Becher, Heko, Bermisheva, Marina, Bernstein, Leslie, Bialkowska, Katarzyna, Blomqvist, Carl, Bojesen, Stig E, Bonanni, Bernardo, Borg, Ake, Brauch, Hiltrud, Brenner, Hermann, Burwinkel, Barbara, Buys, Saundra S, Caldes, Trinidad, Caligo, Maria A, Campa, Daniele, Carter, Brian D, Castelao, Jose E, Chang-Claude, Jenny, Chanock, Stephen J, Chung, Wendy K, Claes, Kathleen B.M, Clarke, Christine L, Collee, J. Margriet, Conroy, Don M, Czene, Kamila, Daly, Mary B, Devilee, Peter, Diez, Orland, Ding, Yuan Chun, Domchek, Susan M, Doerk, Thilo, dos-Santos-Silva, Isabel, Dunning, Alison M, Dwek, Miriam, Eccles, Diana M, Eliassen, A. Heather, Engel, Christoph, Eriksson, Mikael, Evans, D. Gareth, Fasching, Peter A, Flyger, Henrik, Fostira, Florentia, Friedman, Eitan, Fritschi, Lin, Frost, Debra, Gago-Dominguez, Manuela, Gapstur, Susan M, Garber, Judy, Garcia-Barberan, Vanesa, Garcia-Closas, Montserrat, Garcia-Saenz, Jose A, Gaudet, Mia M, Gayther, Simon A, Gehrig, Andrea, Georgoulias, Vassilios, Giles, Graham G, Godwin, Andrew K, Goldberg, Mark S, Goldgar, David E, Gonzalez-Neira, Anna, Greene, Mark H, Guenel, Pascal, Haeberle, Lothar, Hahnen, Eric, Haiman, Christopher A, Hakansson, Niclas, Hall, Per, Hamann, Ute, Harrington, Patricia A, Hart, Steven N, He, Wei, Hogervorst, Frans B.L, Hollestelle, Antoinette, Hopper, John L, Horcasitas, Darling J, Hulick, Peter J

    Veröffentlicht in NATURE COMMUNICATIONS

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    Author Correction: A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers von Coignard, Juliette, Lush, Michael, Beesley, Jonathan, Dennis, Joe, Tyrer, Jonathan P, McGuffog, Lesley, Adank, Muriel A, Ahearn, Thomas, Arun, Banu K, Baynes, Caroline, Białkowska, Katarzyna, Bojesen, Stig E, Brauch, Hiltrud, Burwinkel, Barbara, Buys, Saundra S, Caldés, Trinidad, Campa, Daniele, Chanock, Stephen J, EMBRACE Collaborators, Conroy, Don M, Daly, Mary B, Devilee, Peter, Dörk, Thilo, Eliassen, A Heather, Evans, D Gareth, Fostira, Florentia, Gago-Dominguez, Manuela, Gapstur, Susan M, Garcia-Barberan, Vanesa, García-Closas, Montserrat, Gaudet, Mia M, Gayther, Simon A, Gehrig, Andrea, Giles, Graham G, Godwin, Andrew K, Goldberg, Mark S, González-Neira, Anna, Greene, Mark H, Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A, Hamann, Ute, Harrington, Patricia A, He, Wei, Hollestelle, Antoinette, Horcasitas, Darling J, Hulick, Peter J, Hunter, David J, ABCTB Investigators, Jager, Agnes, James, Paul A, Jensen, Uffe Birk, Kaaks, Rudolf, Kiiski, Johanna I, Kosma, Veli-Matti, Kurian, Allison W, Laitman, Yael, Lambrechts, Diether, Le Marchand, Loic, Lester, Jenny, Lindstrom, Tricia, Luccarini, Craig, Mannermaa, Arto, Manoukian, Siranoush, Martens, John WM, Meindl, Alfons, Montagna, Marco, Nathanson, Katherine L, Neuhausen, Susan L, Nevanlinna, Heli, Nielsen, Finn C, O'Brien, Katie M, Olopade, Olufunmilayo I, Olson, Janet E, Ottini, Laura, Park-Simon, Tjoung-Won, Parsons, Michael T, Pedersen, Inge Sokilde, Poppe, Bruce, Presneau, Nadege, Punie, Kevin, Radice, Paolo, Rennert, Gad, Robson, Mark, Saloustros, Emmanouil, Scheuner, Maren T, Scott, Christopher, Stoppa-Lyonnet, Dominique, Swerdlow, Anthony, Thull, Darcy L, Tischkowitz, Marc, Vijai, Joseph, Wang, Qin, Wappenschmidt, Barbara, Yannoukakos, Drakoulis, Ziogas, Argyrios, Offit, Kenneth, Simard, Jacques, Easton, Douglas F, Antoniou, Antonis C

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