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Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers von 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.
Veröffentlicht in Human molecular genetics
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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 von Dunning, Alison M, Kuchenbaecker, Karoline B, Pooley, Karen A, Dicks, Ed, Sinnott-Armstrong, Nicholas A, Lee, Jason S, Jarosz, Monika, Drury, Suzie, Bolla, Manjeet K, Dennis, Joe, Wang, Qin, Schmidt, Marjanka K, Muir, Kenneth, Dos-Santos-Silva, Isabel, Sawyer, Elinor J, Burwinkel, Barbara, Marme, Frederik, Guénel, Pascal, Perez, Jose IA, Arndt, Volker, Brenner, Hermann, Meindl, Alfons, Schmutzler, Rita K, Hamann, Ute, Bogdanova, Natasha, Lindblom, Annika, Tseng, Chiu-Chen, Lambrechts, Diether, Wildiers, Hans, Chang-Claude, Jenny, Rudolph, Anja, Olson, Janet E, Milne, Roger L, Goldberg, Mark S, Yip, Cheng Har, Pylkäs, Katri, Figueroa, Jonine, Shu, Xiao-Ou, Cox, Angela, Ghoussaini, Maya, Perkins, Barbara J, Lee, Soo Chin, Hartman, Mikael, Torres, Diana, Jakubowska, Anna, Lubinski, Jan, Brennan, Paul, Wu, Pei-Ei, Healey, Sue, Terry, Mary Beth, Goldgar, David E, Janavicius, Ramunas, Tihomirova, Laima, Tung, Nadine, van Rensburg, Elizabeth J, Neuhausen, Susan L, Hansen, Thomas VO, Osorio, Ana, Benitez, Javier, Bonanni, Bernardo, Peissel, Bernard, Ottini, Laura, Konstantopoulou, Irene, Apostolou, Paraskevi, Garber, Judy, EMBRACE, Izatt, Louise, Ellis, Steve, Niederacher, Dieter, Sagne, Charlotte, GEMO Study Collaborators, Sinilnikova, Olga M, Mazoyer, Sylvie, de la Hoya, Miguel, Hooning, Maartje J, Rookus, Matti A, Pujana, Miquel Angel, Huzarski, Tomasz, Laframboise, Rachel, Soucy, Penny, kConFab Investigators, Rappaport, Christine, Phelan, Catherine M, Greene, Mark H, Piedmonte, Marion, Bojesen, Anders, Rantala, Johanna, Olopade, Olufunmilayo I, Ganz, Patricia A, Nussbaum, Robert L, Gayther, Simon A, Nathanson, Katherine L, Woolcott, Christy, Scott, Christopher, Stone, Jennifer, Helland, Åslaug, Dowsett, Mitch, García-Closas, Montserrat, Vachon, Celine, Easton, Douglas F
Veröffentlicht in Nature genetics
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Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers von ENGEL, Christoph, VERSMOLD, Beatrix, GARETH EVANS, D, EELES, Rosalind, PATERSON, Joan, BREWER, Carole, MCGUFFOG, Lesley, ANTONIOU, Antonis C, STOPPA-LYONNET, Dominique, SINILNIKOVA, Olga M, BARJHOUX, Laure, FRENAY, Marc, WAPPENSCHMIDT, Barbara, MICHEL, Cécile, LEROUX, Dominique, DREYFUS, Helene, TOULAS, Christine, GLADIEFF, Laurence, UHRHAMMER, Nancy, BIGNON, Yves-Jean, MEINDL, Alfons, ARNOLD, Norbert, VARON-MATEEVA, Raymonda, SIMARD, Jacques, NIEDERACHER, Dieter, PREISLER-ADAMS, Sabine, KAST, Karin, DEISSLER, Helmut, SUTTER, Christian, GADZICKI, Dorothea, CHENEVIX-TRENCH, Georgia, SPURDLE, Amanda B, XIAOQING CHEN, BEESLEY, Jonathan, EASTON, Douglas F, OLSSON, Håkan, KRISTOFFERSSON, Ulf, EHRENCRONA, Hans, LILJEGREN, Annelie, VAN DER LUIJT, Rob B, VAN OS, Theo A, VAN LEEUWEN, Flora E, DOMCHEK, Susan M, REBBECK, Timothy R, NATHANSON, Katherine L, PEOCK, Susan, OSORIO, Ana, RAMON Y CAJAL, Teresa, KONSTANTOPOULOU, Irene, BENITEZ, Javier, FRIEDMAN, Eitan, KAUFMAN, Bella, LAITMAN, Yael, MAI, Phuong L, GREENE, Mark H, NEVANLINNA, Heli, COOK, Margaret, OLIVER, Clare, FROST, Debra, MAYES, Rebecca
Veröffentlicht in Cancer epidemiology, biomarkers & prevention
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Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer von Gaudet, Mia M., Kirchhoff, Tomas, Green, Todd, Vijai, Joseph, Korn, Joshua M., Guiducci, Candace, Segrè, Ayellet V., McGee, Kate, McGuffog, Lesley, Kartsonaki, Christiana, Morrison, Jonathan, Healey, Sue, Sinilnikova, Olga M., Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Gauthier-Villars, Marion, Sobol, Hagay, Longy, Michel, Frenay, Marc, GEMO Study Collaborators, Frans B. L., Rookus, Matti A., Collée, J. Margriet, Hoogerbrugge, Nicoline, van Roozendaal, Kees E. P., Piedmonte, Marion, Rubinstein, Wendy, Nerenstone, Stacy, Van Le, Linda, Blank, Stephanie V., Caldés, Trinidad, de la Hoya, Miguel, Nevanlinna, Heli, Aittomäki, Kristiina, Lazaro, Conxi, Blanco, Ignacio, Arason, Adalgeir, Johannsson, Oskar T., Barkardottir, Rosa B., Devilee, Peter, Olopade, Olofunmilayo I., Neuhausen, Susan L., Wang, Xianshu, Fredericksen, Zachary S., Peterlongo, Paolo, Manoukian, Siranoush, Barile, Monica, Viel, Alessandra, Radice, Paolo, Phelan, Catherine M., Narod, Steven, Rennert, Gad, Lejbkowicz, Flavio, Flugelman, Anath, Andrulis, Irene L., Glendon, Gord, Ozcelik, Hilmi, Toland, Amanda E., Montagna, Marco, D'Andrea, Emma, Friedman, Eitan, Laitman, Yael, Borg, Ake, Beattie, Mary, Ramus, Susan J., Domchek, Susan M., Nathanson, Katherine L., Rebbeck, Tim, Spurdle, Amanda B., Chen, Xiaoqing, Holland, Helene, John, Esther M., Hopper, John L., Buys, Saundra S., Daly, Mary B., Southey, Melissa C., Terry, Mary Beth, Tung, Nadine, Overeem Hansen, Thomas V., Nielsen, Finn C., Greene, Mark H., Mai, Phuong L., Osorio, Ana, Durán, Mercedes, Andres, Raquel, Benítez, Javier, Weitzel, Jeffrey N., Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Platte, Radka, Evans, D. Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Walker, Lisa, Eason, Jacqueline, Barwell, Julian
Veröffentlicht in PLoS genetics
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Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer von Kirchhoff, Tomas, Green, Todd, Vijai, Joseph, Korn, Joshua M, Guiducci, Candace, McGee, Kate, McGuffog, Lesley, Healey, Sue, Stoppa-Lyonnet, Dominique, Gauthier-Villars, Marion, Sobol, Hagay, Longy, Michel, GEMO Study Collaborators, Hogervorst, Frans BL, Collee, JMargriet, Hoogerbrugge, Nicoline, van Roozendaal, Kees EP, Piedmonte, Marion, Rubinstein, Wendy, Nerenstone, Stacy, Van Le, Linda, Blank, Stephanie V, Caldes, Trinidad, de la Hoya, Miguel, Nevanlinna, Heli, Aittomaeki, Kristiina, Blanco, Ignacio, Arason, Adalgeir, Johannsson, Oskar T, Barkardottir, Rosa B, Devilee, Peter, Olopade, Olofunmilayo I, Neuhausen, Susan L, Wang, Xianshu, Fredericksen, Zachary S, Manoukian, Siranoush, Barile, Monica, Viel, Alessandra, Radice, Paolo, Phelan, Catherine M, Narod, Steven, Lejbkowicz, Flavio, Flugelman, Anath, Andrulis, Irene L, Glendon, Gord, Ozcelik, Hilmi, Toland, Amanda E, Montagna, Marco, D'Andrea, Emma, Laitman, Yael, Ramus, Susan J, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Tim, Spurdle, Amanda B, Chen, Xiaoqing, Holland, Helene, John, Esther M, Hopper, John L, Buys, Saundra S, Daly, Mary B, Southey, Melissa C, Terry, Mary Beth, Tung, Nadine, Nielsen, Finn C, Greene, Mark I, Mai, Phuong L, Duran, Mercedes, Andres, Raquel, Benitez, Javier, Weitzel, Jeffrey N, Garber, Judy, Hamann, Ute, Peock, Susan, Cook, Margaret, Oliver, Clare, Frost, Debra, Platte, Radka, Evans, DGareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Walker, Lisa, Eason, Jacqueline, Barwell, Julian, Godwin, Andrew K, Schmutzler, Rita K, Wappenschmidt, Barbara, Engert, Stefanie, Arnold, Norbert, Gadzicki, Dorothea, Dean, Michael, Gold, Bert, Klein, Robert J, Couch, Fergus J, Chenevix-Trench, Georgia, Easton, Douglas F, Antoniou, Antonis C, Altshuler, David M, Offit, Kenneth
Veröffentlicht in PLoS genetics
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Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 von Dunning, Alison M, Kuchenbaecker, Karoline B, Pooley, Karen A, Dicks, Ed, Sinnott-Armstrong, Nicholas A, Lee, Jason S, Jarosz, Monika, Drury, Suzie, Bolla, Manjeet K, Dennis, Joe, Wang, Qin, Schmidt, Marjanka K, Muir, Kenneth, Dos-Santos-Silva, Isabel, Sawyer, Elinor J, Burwinkel, Barbara, Marme, Frederik, Guénel, Pascal, Perez, Jose IA, Arndt, Volker, Brenner, Hermann, Meindl, Alfons, Schmutzler, Rita K, Hamann, Ute, Bogdanova, Natasha, Lindblom, Annika, Tseng, Chiu-Chen, Lambrechts, Diether, Wildiers, Hans, Chang-Claude, Jenny, Rudolph, Anja, Olson, Janet E, Milne, Roger L, Goldberg, Mark S, Yip, Cheng Har, Pylkäs, Katri, Figueroa, Jonine, Shu, Xiao-Ou, Cox, Angela, Ghoussaini, Maya, Perkins, Barbara J, Lee, Soo Chin, Hartman, Mikael, Torres, Diana, Jakubowska, Anna, Lubinski, Jan, Brennan, Paul, Wu, Pei-Ei, Healey, Sue, Terry, Mary Beth, Goldgar, David E, Janavicius, Ramunas, Tihomirova, Laima, Tung, Nadine, van Rensburg, Elizabeth J, Neuhausen, Susan L, Hansen, Thomas VO, Osorio, Ana, Benitez, Javier, Bonanni, Bernardo, Peissel, Bernard, Ottini, Laura, Konstantopoulou, Irene, Apostolou, Paraskevi, Garber, Judy, EMBRACE, Izatt, Louise, Ellis, Steve, Niederacher, Dieter, Sagne, Charlotte, GEMO Study Collaborators, Sinilnikova, Olga M, Mazoyer, Sylvie, de la Hoya, Miguel, Hooning, Maartje J, Rookus, Matti A, Pujana, Miquel Angel, Huzarski, Tomasz, Laframboise, Rachel, Soucy, Penny, kConFab Investigators, Rappaport, Christine, Phelan, Catherine M, Greene, Mark H, Piedmonte, Marion, Bojesen, Anders, Rantala, Johanna, Olopade, Olufunmilayo I, Ganz, Patricia A, Nussbaum, Robert L, Gayther, Simon A, Nathanson, Katherine L, Woolcott, Christy, Scott, Christopher, Stone, Jennifer, Helland, Åslaug, Dowsett, Mitch, García-Closas, Montserrat, Vachon, Celine, Easton, Douglas F
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Exploring the link between MORF4L1 and risk of breast cancer von Martrat, Griselda, Maxwell, Christopher A, Tominaga, Emiko, Bogliolo, Massimo, Lazaro, Conxi, Brunet, Joan, Aguilar, Helena, Fernández-Rodríguez, Juana, Seal, Sheila, Renwick, Anthony, Schindler, Detlev, Ramírez de Haro, Ma. José, Castellà, Maria, Hernández Viedma, Gonzalo, Easton, Douglas F, Cook, Margaret, Platte, Radka, Eeles, Rosalind, Izatt, Louise, Chu, Carol, Davids, Rosemarie, Ong, Kai-Ren, Douglas, Fiona, Hodgson, Shirley, Brewer, Carole, Morrison, Patrick J, Porteous, Mary, Peterlongo, Paolo, Manoukian, Siranoush, Peissel, Bernard, Roversi, Gaia, Viel, Alessandra, Pasini, Barbara, Ottini, Laura, Putignano, Anna Laura, Savarese, Antonella, Bernard, Loris, Radice, Paolo, Healey, Sue, Spurdle, Amanda, Chen, Xiaoqing, Beesley, Jonathan, Rookus, Matti A, Vreeswijk, Maaike P, Bodmer, Danielle, Ausems, Margreet G. E. M, van Os, Theo A, Blok, Marinus J, Hogervorst, Frans B. L, Goldgar, David E, Buys, Saundra, John, Esther M, Miron, Alexander, Southey, Melissa, Daly, Mary B, Harbst, Katja, Borg, Åke, Rantala, Johanna, Barbany-Bustinza, Gisela, Kaufman, Bella, Milgrom, Roni, Friedman, Eitan, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Timothy R, Johannsson, Oskar, Couch, Fergus J, Wang, Xianshu, Fredericksen, Zachary, Cuadras, Daniel, Morros, Rosa, Depping, Reinhard, Caldes, Trinidad, Osorio, Ana, Heikkinen, Tuomas, Surrallés i Calonge, Jordi, Pujana, Miguel Angel, Tominaga, Kaoru, Cerón, Julián, Fert Ferrer, Sandra, Collonge-Rame, Marie-Agnès, Mortemousque, Isabelle, Chenevix-Trench, Georgia, Pereira-Smith, Olivia M, Hamann, Ute, Caligo, Maria, Godwin, Andrew K, Imyanitov, Evgeny N, Janavicius, Ramunas, Sinilnikova, Olga M, Stoppa-Lyonnet, Dominique, Mazoyer, Sylvie, Castera, Laurent, De Pauw, Antoine, Peyrat, Jean-Philippe, Vennin, Philippe, The Netherlands Cancer Institute. Hereditary Breast and Ovarian Cancer Group (HEBON), University of Utah School of Medicine. Breast Cancer Family Registry (Salt Lake City, Estats Units d'Amèrica), Lund University. Swedish Breast Cancer Study (Lund, Suècia), Fédération Nationale des Centres de Lutte Contre le Cancer. Groupe Génétique et Cancer (Lyon, França)
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