Treffer 1 - 15 von 15 für Suche 'GILES, FREDERIK P', Suchdauer: 1,44s Treffer weiter einschränken
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    Genetic modifiers of CHEK21100delC-associated breast cancer risk von Muranen, Taru A., Greco, Dario, Blomqvist, Carl, Aittomäki, Kristiina, Khan, Sofia, Hogervorst, Frans, Verhoef, Senno, Pharoah, Paul D.P., Dunning, Alison M., Shah, Mitul, Luben, Robert, Bojesen, Stig E., Nordestgaard, Børge G., Schoemaker, Minouk, Swerdlow, Anthony, García-Closas, Montserrat, Figueroa, Jonine, Dörk, Thilo, Bogdanova, Natalia V., Hall, Per, Li, Jingmei, Khusnutdinova, Elza, Bermisheva, Marina, Kristensen, Vessela, Borresen-Dale, Anne-Lise, Investigators, NBCS, Peto, Julian, dos Santos Silva, Isabel, Couch, Fergus J., Olson, Janet E., Hillemans, Peter, Park-Simon, Tjoung-Won, Brauch, Hiltrud, Hamann, Ute, Burwinkel, Barbara, Marme, Frederik, Meindl, Alfons, Schmutzler, Rita K., Cox, Angela, Cross, Simon S., Sawyer, Elinor J., Tomlinson, Ian, Lambrechts, Diether, Moisse, Matthieu, Lindblom, Annika, Margolin, Sara, Hollestelle, Antoinette, Martens, John W.M., Fasching, Peter A., Beckmann, Matthias W., Andrulis, Irene L., Knight, Julia A., Investigators, kConFab/AOCS, Anton-Culver, Hoda, Ziogas, Argyrios, Giles, Graham G., Milne, Roger L., Brenner, Hermann, Arndt, Volker, Mannermaa, Arto, Kosma, Veli-Matti, Chang-Claude, Jenny, Rudolph, Anja, Devilee, Peter, Seynaeve, Caroline, Hopper, John L., Southey, Melissa C., John, Esther M., Whittemore, Alice S., Bolla, Manjeet K., Wang, Qin, Michailidou, Kyriaki, Dennis, Joe, Easton, Douglas F., Schmidt, Marjanka K., Nevanlinna, Heli

    Veröffentlicht in Genetics in medicine

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    Genome-wide association analysis identifies three new breast cancer susceptibility loci von Fletcher, Olivia, Turnbull, Clare, Dicks, Ed, Dennis, Joe, Luccarini, Craig, Baynes, Caroline, Driver, Kristy, Orr, Nicholas, dos Santos Silva, Isabel, Uitterlinden, Andre G, Rivadeneira, Fernando, Hall, Per, Czene, Kamila, Aittomäki, Kristiina, Meindl, Alfons, Lichtner, Peter, Nickels, Stefan, Flesch-Janys, Dieter, Tsimiklis, Helen, Schmidt, Daniel, Bui, Minh, Apicella, Carmel, Park, Daniel J, Chanock, Stephen J, Verhoef, Senno, Hogervorst, Frans B L, Fasching, Peter A, Beckmann, Matthias W, Ekici, Arif B, Tomlinson, Ian, Kerin, Michael, Sohn, Christof, Burwinkel, Barbara, Guénel, Pascal, Truong, Thérèse, Menegaux, Florence, Nordestgaard, Børge G, Flyger, Henrik, Milne, Roger L, Alonso, M Rosario, Benítez, Javier, Anton-Culver, Hoda, Ziogas, Argyrios, Brenner, Hermann, Stegmaier, Christa, Brauch, Hiltrud, Brüning, Thomas, Eilber, Ursula, Bremer, Michael, Hillemanns, Peter, Antonenkova, Natalia N, Rogov, Yuri I, Karstens, Johann H, Bermisheva, Marina, Khusnutdinova, Elza, Lindblom, Annika, Margolin, Sara, Mannermaa, Arto, Hartikainen, Jaana M, Floris, Giuseppe, Fortuzzi, Stefano, Peterlongo, Paolo, Couch, Fergus J, Stevens, Kristen, Giles, Graham G, Baglietto, Laura, Severi, Gianluca, Alnæs, Grethe Grenaker, Kristensen, Vessela, Børrensen-Dale, Anne-Lise, John, Esther M, Miron, Alexander, Andrulis, Irene L, Devilee, Peter, Seynaeve, Caroline, Figueroa, Jonine D, Garcia-Closas, Montserrat, Brinton, Louise, Hooning, Maartje J, van den Ouweland, Ans M W, Reed, Malcolm W R, Shah, Mitul, Jakubowska, Ania, Lubinski, Jan, Durda, Katarzyna, Jones, Michael, Schoemaker, Minouk, Swerdlow, Anthony, Beesley, Jonathan, Chen, Xiaoqing, Lophatananon, Artitaya, Rattanamongkongul, Suthee, Noh, Dong-Young, Velentzis, Louiza, Tapper, Will J, Gerty, Susan M, Graham, Nikki J, Ponder, Bruce A J, Dunning, Alison M, Peto, Julian

    Veröffentlicht in Nature genetics

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    BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer von Shimelis, Hermela, Mesman, Romy L S, Von Nicolai, Catharina, Ehlen, Asa, Guidugli, Lucia, Martin, Charlotte, Calléja, Fabienne M G R, Meeks, Huong, Hallberg, Emily, Hinton, Jamie, Lilyquist, Jenna, Hu, Chunling, Aalfs, Cora M, Aittomäki, Kristiina, Andrulis, Irene, Anton-Culver, Hoda, Arndt, Volker, Beckmann, Matthias W, Benitez, Javier, Bogdanova, Natalia V, Bojesen, Stig E, Bolla, Manjeet K, Borresen-Dale, Anne-Lise, Brauch, Hiltrud, Brennan, Paul, Brenner, Hermann, Broeks, Annegien, Brouwers, Barbara, Brüning, Thomas, Burwinkel, Barbara, Chang-Claude, Jenny, Chenevix-Trench, Georgia, Cheng, Ching-Yu, Choi, Ji-Yeob, Collée, J Margriet, Cox, Angela, Cross, Simon S, Czene, Kamila, Darabi, Hatef, Dennis, Joe, Dörk, Thilo, Dos-Santos-Silva, Isabel, Dunning, Alison M, Fasching, Peter A, Figueroa, Jonine, Flyger, Henrik, García-Closas, Montserrat, Giles, Graham G, Glendon, Gord, Guénel, Pascal, Haiman, Christopher A, Hall, Per, Hamann, Ute, Hartman, Mikael, Hogervorst, Frans B, Hollestelle, Antoinette, Hopper, John L, Ito, Hidemi, Jakubowska, Anna, Kang, Daehee, Kosma, Veli-Matti, Kristensen, Vessela, Lai, Kah-Nyin, Lambrechts, Diether, Marchand, Loic Le, Li, Jingmei, Lindblom, Annika, Lophatananon, Artitaya, Lubinski, Jan, Machackova, Eva, Mannermaa, Arto, Margolin, Sara, Marme, Frederik, Matsuo, Keitaro, Miao, Hui, Michailidou, Kyriaki, Milne, Roger L, Muir, Kenneth, Neuhausen, Susan L, Nevanlinna, Heli, Olson, Janet E, Olswold, Curtis, Oosterwijk, Jan J C, Osorio, Ana, Peterlongo, Paolo, Peto, Julian, Pharoah, Paul D P, Pylkäs, Katri, Radice, Paolo, Rashid, Muhammad Usman, Rhenius, Valerie, Rudolph, Anja, Sangrajrang, Suleeporn, Sawyer, Elinor J, Schmidt, Marjanka K, Schoemaker, Minouk J, Seynaeve, Caroline, Shah, Mitul, Shen, Chen-Yang, Shrubsole, Martha

    Veröffentlicht in Cancer research (Chicago, Ill.)

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    Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21 von Hamdi, Yosr, Soucy, Penny, Adoue, Véronique, Michailidou, Kyriaki, Canisius, Sander, Lemaçon, Audrey, Droit, Arnaud, Andrulis, Irene L, Anton-Culver, Hoda, Arndt, Volker, Baynes, Caroline, Blomqvist, Carl, Bogdanova, Natalia V, Bojesen, Stig E, Bolla, Manjeet K, Bonanni, Bernardo, Borresen-Dale, Anne-Lise, Brand, Judith S, Brauch, Hiltrud, Brenner, Hermann, Broeks, Annegien, Burwinkel, Barbara, Chang-Claude, Jenny, Couch, Fergus J, Cox, Angela, Cross, Simon S, Czene, Kamila, Darabi, Hatef, Dennis, Joe, Devilee, Peter, Dörk, Thilo, Dos-Santos-Silva, Isabel, Eriksson, Mikael, Fasching, Peter A, Figueroa, Jonine, Flyger, Henrik, García-Closas, Montserrat, Giles, Graham G, Goldberg, Mark S, González-Neira, Anna, Grenaker-Alnæs, Grethe, Guénel, Pascal, Haeberle, Lothar, Haiman, Christopher A, Hamann, Ute, Hallberg, Emily, Hooning, Maartje J, Hopper, John L, Jakubowska, Anna, Jones, Michael, Kabisch, Maria, Kataja, Vesa, Lambrechts, Diether, Le Marchand, Loic, Lindblom, Annika, Lubinski, Jan, Mannermaa, Arto, Maranian, Mel, Margolin, Sara, Marme, Frederik, Milne, Roger L, Neuhausen, Susan L, Nevanlinna, Heli, Neven, Patrick, Olswold, Curtis, Peto, Julian, Plaseska-Karanfilska, Dijana, Pylkäs, Katri, Radice, Paolo, Rudolph, Anja, Sawyer, Elinor J, Schmidt, Marjanka K, Shu, Xiao-Ou, Southey, Melissa C, Swerdlow, Anthony, Tollenaar, Rob A E M, Tomlinson, Ian, Torres, Diana, Truong, Thérèse, Vachon, Celine, Van Den Ouweland, Ans M W, Wang, Qin, Winqvist, Robert, Zheng, Wei, Benitez, Javier, Chenevix-Trench, Georgia, Dunning, Alison M, Pharoah, Paul D P, Kristensen, Vessela, Hall, Per, Easton, Douglas F, Pastinen, Tomi, Nord, Silje, Simard, Jacques

    Veröffentlicht in ONCOTARGET

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    Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression von Darabi, Hatef, McCue, Karen, Beesley, Jonathan, Michailidou, Kyriaki, Nord, Silje, Kar, Siddhartha, Humphreys, Keith, Bolla, Manjeet K., Dennis, Joe, Canisius, Sander, Apicella, Carmel, Hopper, John L., Southey, Melissa C., Stone, Jennifer, Broeks, Annegien, Schmidt, Marjanka K., Lophatananon, Artitaya, Muir, Kenneth, Fasching, Peter A., Heusinger, Katharina, dos-Santos-Silva, Isabel, Peto, Julian, Tomlinson, Ian, Sawyer, Elinor J., Burwinkel, Barbara, Truong, Thérèse, González-Neira, Anna, Anton-Culver, Hoda, Neuhausen, Susan L., Arndt, Volker, Brenner, Hermann, Engel, Christoph, Meindl, Alfons, Schmutzler, Rita K., Brauch, Hiltrud, Hamann, Ute, Chang-Claude, Jenny, Nevanlinna, Heli, Ito, Hidemi, Dörk, Thilo, Lindblom, Annika, Margolin, Sara, Kosma, Veli-Matti, Mannermaa, Arto, Tseng, Chiu-chen, Floris, Giuseppe, Peterlongo, Paolo, Radice, Paolo, Couch, Fergus J., Vachon, Celine, McLean, Catriona, Milne, Roger L., Dugué, Pierre-Antoine, Haiman, Christopher A., Maskarinec, Gertraud, Woolcott, Christy, Henderson, Brian E., Goldberg, Mark S., Teo, Soo H., Mariapun, Shivaani, Helland, Åslaug, Haakensen, Vilde, Beeghly-Fadiel, Alicia, Tamimi, Rulla, Jukkola-Vuorinen, Arja, Winqvist, Robert, Andrulis, Irene L., Knight, Julia A., Devilee, Peter, Tollenaar, Robert A.E.M., Figueroa, Jonine, García-Closas, Montserrat, Czene, Kamila, Hooning, Maartje J., Tilanus-Linthorst, Madeleine, Gao, Yu-Tang, Shu, Xiao-Ou, Cox, Angela, Luben, Robert, Choi, Ji-Yeob, Kang, Daehee, Hartman, Mikael, Lim, Wei Yen, Kabisch, Maria, Torres, Diana, Jakubowska, Anna, McKay, James, Sangrajrang, Suleeporn, Toland, Amanda E., Yannoukakos, Drakoulis, Shen, Chen-Yang, Yu, Jyh-Cherng, Ziogas, Argyrios, Schoemaker, Minouk J., Swerdlow, Anthony, Borresen-Dale, Anne-Lise, French, Juliet D., Edwards, Stacey L., Easton, Douglas F., Hall, Per


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    Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2 von Orr, N., Dudbridge, F., Dryden, N., Maguire, S., Novo, D., Perrakis, E., Johnson, N., Ghoussaini, M., Hopper, J. L., Southey, M. C., Apicella, C., Stone, J., Schmidt, M. K., Broeks, A., Van't Veer, L. J., Hogervorst, F. B., Fasching, P. A., Haeberle, L., Ekici, A. B., Beckmann, M. W., Gibson, L., Aitken, Z., Warren, H., Sawyer, E., Tomlinson, I., Kerin, M. J., Miller, N., Burwinkel, B., Marme, F., Schneeweiss, A., Sohn, C., Guenel, P., Truong, T., Cordina-Duverger, E., Sanchez, M., Bojesen, S. E., Nordestgaard, B. G., Nielsen, S. F., Flyger, H., Benitez, J., Zamora, M. P., Arias Perez, J. I., Menendez, P., Anton-Culver, H., Neuhausen, S. L., Brenner, H., Dieffenbach, A. K., Arndt, V., Stegmaier, C., Hamann, U., Brauch, H., Justenhoven, C., Bruning, T., Ko, Y.-D., Nevanlinna, H., Aittomaki, K., Blomqvist, C., Khan, S., Bogdanova, N., Dork, T., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V.-M., Hartikainen, J. M., Chenevix-Trench, G., Beesley, J., Lambrechts, D., Moisse, M., Floris, G., Beuselinck, B., Chang-Claude, J., Rudolph, A., Seibold, P., Flesch-Janys, D., Radice, P., Peterlongo, P., Peissel, B., Pensotti, V., Couch, F. J., Olson, J. E., Slettedahl, S., Vachon, C., Giles, G. G., Milne, R. L., McLean, C., Haiman, C. A., Henderson, B. E., Schumacher, F., Le Marchand, L., Simard, J., Goldberg, M. S., Labreche, F., Dumont, M., Kristensen, V., Alnaes, G. G., Nord, S., Borresen-Dale, A.-L., Zheng, W.

    Veröffentlicht in Human molecular genetics

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