Treffer 1 - 20 von 1.640 für Suche 'SWE, Than', Suchdauer: 2,46s Treffer weiter einschränken
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    FANCM c.5791C>T nonsense mutation (rs144567652) induces exon skipping, affects DNA repair activity and is a familial breast cancer risk factor von Peterlongo, Paolo, Catucci, Irene, Colombo, Mara, Caleca, Laura, Mucaki, Eliseos, Bogliolo, Massimo, Marin, Maria, Damiola, Francesca, Bernard, Loris, Pensotti, Valeria, Volorio, Sara, Dall'Olio, Valentina, Meindl, Alfons, Bartram, Claus, Sutter, Christian, Surowy, Harald, Sornin, Valérie, Dondon, Marie-Gabrielle, Eon-Marchais, Séverine, Stoppa-Lyonnet, Dominique, Andrieu, Nadine, Sinilnikova, Olga M, Mitchell, Gillian, James, Paul A, Thompson, Ella, Marchetti, Marina, Verzeroli, Cristina, Tartari, Carmen, Capone, Gabriele Lorenzo, Putignano, Anna Laura, Genuardi, Maurizio, Medici, Veronica, Marchi, Isabella, Federico, Massimo, Tognazzo, Silvia, Matricardi, Laura, Agata, Simona, Dolcetti, Riccardo, Della Puppa, Lara, Cini, Giulia, Gismondi, Viviana, Viassolo, Valeria, Perfumo, Chiara, Mencarelli, Maria Antonietta, Baldassarri, Margherita, Peissel, Bernard, Roversi, Gaia, Silvestri, Valentina, Rizzolo, Piera, Spina, Francesca, Vivanet, Caterina, Tibiletti, Maria Grazia, Caligo, Maria Adelaide, Gambino, Gaetana, Tommasi, Stefania, Pilato, Brunella, Tondini, Carlo, Corna, Chiara, Bonanni, Bernardo, Barile, Monica, Osorio, Ana, Benitez, Javier, Balestrino, Luisa, Ottini, Laura, Manoukian, Siranoush, Pierotti, Marco A, Renieri, Alessandra, Varesco, Liliana, Couch, Fergus J, Wang, Xianshu, Devilee, Peter, Hilbers, Florentine S, van Asperen, Christi J, Viel, Alessandra, Montagna, Marco, Cortesi, Laura, Diez, Orland, Balmaña, Judith, Hauke, Jan, Schmutzler, Rita K, Papi, Laura, Pujana, Miguel Angel, Lázaro, Conxi, Falanga, Anna, Offit, Kenneth, Vijai, Joseph, Campbell, Ian, Burwinkel, Barbara, Kvist, Anders, Ehrencrona, Hans, Mazoyer, Sylvie, Pizzamiglio, Sara, Verderio, Paolo, Surralles, Jordi, Rogan, Peter K, Radice, Paolo

    Veröffentlicht in Human molecular genetics

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    DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers von Osorio, Ana, Milne, Roger L, Kuchenbaecker, Karoline, Vaclová, Tereza, Pita, Guillermo, Alonso, Rosario, Peterlongo, Paolo, Blanco, Ignacio, de la Hoya, Miguel, Duran, Mercedes, Díez, Orland, Ramón Y Cajal, Teresa, Konstantopoulou, Irene, Martínez-Bouzas, Cristina, Andrés Conejero, Raquel, Soucy, Penny, McGuffog, Lesley, Barrowdale, Daniel, Lee, Andrew, Arver, Brita, Rantala, Johanna, Loman, Niklas, Ehrencrona, Hans, Olopade, Olufunmilayo I, Beattie, Mary S, Domchek, Susan M, Nathanson, Katherine, Rebbeck, Timothy R, Arun, Banu K, Karlan, Beth Y, Walsh, Christine, Lester, Jenny, John, Esther M, Whittemore, Alice S, Daly, Mary B, Southey, Melissa, Hopper, John, Terry, Mary B, Buys, Saundra S, Janavicius, Ramunas, Dorfling, Cecilia M, van Rensburg, Elizabeth J, Steele, Linda, Neuhausen, Susan L, Ding, Yuan Chun, Hansen, Thomas V O, Jønson, Lars, Ejlertsen, Bent, Gerdes, Anne-Marie, Infante, Mar, Herráez, Belén, Moreno, Leticia Thais, Weitzel, Jeffrey N, Herzog, Josef, Weeman, Kisa, Manoukian, Siranoush, Peissel, Bernard, Zaffaroni, Daniela, Scuvera, Giulietta, Bonanni, Bernardo, Mariette, Frederique, Volorio, Sara, Viel, Alessandra, Varesco, Liliana, Papi, Laura, Ottini, Laura, Tibiletti, Maria Grazia, Radice, Paolo, Yannoukakos, Drakoulis, Garber, Judy, Ellis, Steve, Frost, Debra, Platte, Radka, Fineberg, Elena, Evans, Gareth, Lalloo, Fiona, Izatt, Louise, Eeles, Ros, Adlard, Julian, Davidson, Rosemarie, Cole, Trevor, Eccles, Diana, Cook, Jackie, Hodgson, Shirley, Brewer, Carole, Tischkowitz, Marc, Douglas, Fiona, Porteous, Mary, Side, Lucy, Walker, Lisa, Morrison, Patrick, Donaldson, Alan, Kennedy, John, Foo, Claire, Godwin, Andrew K, Schmutzler, Rita Katharina, Wappenschmidt, Barbara, Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons

    Veröffentlicht in PLoS genetics

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    Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer von Edwards, Stacey L, Lawrenson, Kate, Woods, Nicholas, French, Juliet D, Bolla, Manjeet K, Dennis, Joe, Vincent, Daniel, Rossing, Mary Anne, Doherty, Jennifer A, Larson, Melissa C, Fridley, Brooke L, Peto, Julian, Braaf, Linde M, Andrulis, Irene L, Moysich, Kirsten B, Brenner, Hermann, Brauch, Hiltrud, Hillemanns, Peter, Butzow, Ralf, Bogdanova, Natalia V, Pelttari, Liisa M, Heitz, Florian, Matsuo, Keitaro, du Bois, Andreas, Wu, Anna H, Harter, Philipp, Blot, William, Hosono, Satoyo, Hamann, Ute, Kjaer, Susanne Krüger, Shen, Chen-Yang, Brown, Judith, Luben, Robert, Flyger, Henrik, Vachon, Celine, Gibson, Lorna, Fletcher, Olivia, Poole, Elizabeth M, Tworoger, Shelley S, Bandera, Elisa V, Li, Jingmei, Wauters, Els, Kiemeney, Lambertus A, Hoatlin, Maureen, Zamora, M Pilar, Cook, Linda S, Brooks-Wilson, Angela, Cybulski, Cezary, Henderson, Brian E, Schumacher, Fredrick, Engelholm, Svend Aage, Gore, Martin, Tsimiklis, Helen, Martens, John W M, Flanagan, James M, Whittemore, Alice S, McGuire, Valerie, Gao, Yu-Tang, McLaughlin, John R, Beckmann, Matthias W, Peissel, Bernard, Ashworth, Alan, Ko, Yon-Dschun, Kupryjanczyk, Jolanta, Rzepecka, Iwona K, Hartikainen, Jaana M, Deming-Halverson, Sandra, Lophatananon, Artitaya, Iwata, Hiroji, McKay, James, Piedmonte, Marion, Neuhausen, Susan L, Szabo, Csilla I, Godwin, Andrew K, Campbell, Ian, Rookus, Matti A, Frost, Debra, Fineberg, Elena, Barwell, Julian, Davidson, Rosemarie, Buecher, Bruno, Faivre, Laurence, Caron, Olivier, Giraud, Sophie, Byrski, Tomasz, Bonanni, Bernardo, Giannini, Giuseppe, Dolcetti, Riccardo, Salani, Ritu, Kaulich, Daphne Gschwantler, Laitman, Yael, Jensen, Uffe Birk, Ejlertsen, Bent, Foretova, Lenka, Kuchenbaecker, Karoline B, Cunningham, Julie M, Monteiro, Alvaro N A, Gayther, Simon A, Berchuck, Andrew, Dunning, Alison M

    Veröffentlicht in Nature genetics

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    Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases von Trynka, Gosia, Stahl, Eli, Neale, Benjamin M., Farh, Kai-How, Pers, Tune H., Albus, Margot, Cahn, Wiepke, Cai, Guiqing, Carr, Vaughan J., Carrera, Noa, Cheng, Wei, Cheung, Eric F.C., Cohen, David, Cormican, Paul, Craddock, Nick, Demontis, Ditte, Djurovic, Srdjan, Donohoe, Gary, Dudbridge, Frank, Durmishi, Naser, Eriksson, Johan, Farrell, Martilias S., Freimer, Nelson B., Fromer, Menachem, Godard, Stephanie, Goldstein, Jacqueline I., Grove, Jakob, Hartmann, Annette M., Henskens, Frans A., Herms, Stefan, Hirschhorn, Joel N., Hoffmann, Per, Hougaard, David M., Ikeda, Masashi, Julià, Antonio, Kelly, Brian J., Kennedy, James L., Kucinskas, Vaidutis, Kuzelova-Ptackova, Hana, Laurent, Claudine, Lee, S. Hong, Li, Tao, Lieberman, Jeffrey, Limborska, Svetlana, Loughland, Carmel M., Lnnqvist, Jouko, Marsal, Sara, McCarley, Robert W., Meijer, Carin J., Melegh, Bela, Melle, Ingrid, Milani, Lili, Mors, Ole, Myin-Germeys, Inez, Nikitina-Zake, Liene, O’Callaghan, Eadbhard, O’Dushlaine, Colm, O’Neill, F. Anthony, Oh, Sang-Yun, Pantelis, Christos, Parkhomenko, Elena, Perkins, Diana O., Powell, John, Quested, Digby, Salomaa, Veikko, Schubert, Christian R., Shi, Jianxin, Sigurdsson, Engilbert, Sim, Kang, Stogmann, Elisabeth, Strengman, Eric, Suvisaari, Jaana, Thirumalai, Srinivas, Veijola, Juha, Walsh, Dermot, Weiser, Mark, Witt, Stephanie H., Wong, Emily H.M., Wu, Jing Qin, Stefansson, Kari, Blackwood, Douglas H.R., Ehrenreich, Hannelore, Gurling, Hugh, Hultman, Christina M., Kirov, George, Malhotra, Anil K., McCarroll, Steven A., McQuillin, Andrew, Palotie, Aarno, Rietschel, Marcella, Sham, Pak C., O’Donovan, Michael C., Bergen, Sarah, Magnusson, Patrik K.E., Scolnick, Edward, Purcell, Shaun M., Pasaniuc, Bogdan, Sullivan, Patrick F., Raychaudhuri, Soumya, Price, Alkes L.


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    Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers von Blanco, Ignacio, Kuchenbaecker, Karoline, Cuadras, Daniel, Wang, Xianshu, Barrowdale, Daniel, de Garibay, Gorka Ruiz, Librado, Pablo, Sánchez-Gracia, Alejandro, Rozas, Julio, Bonifaci, Núria, McGuffog, Lesley, Pankratz, Vernon S, Islam, Abul, Mateo, Francesca, Berenguer, Antoni, Petit, Anna, Català, Isabel, Brunet, Joan, Feliubadaló, Lidia, Tornero, Eva, Benítez, Javier, Osorio, Ana, Ramón y Cajal, Teresa, Nevanlinna, Heli, Aittomäki, Kristiina, Arun, Banu K, Toland, Amanda E, Karlan, Beth Y, Walsh, Christine, Lester, Jenny, Greene, Mark H, Mai, Phuong L, Nussbaum, Robert L, Andrulis, Irene L, Domchek, Susan M, Nathanson, Katherine L, Rebbeck, Timothy R, Barkardottir, Rosa B, Jakubowska, Anna, Lubinski, Jan, Durda, Katarzyna, Jaworska-Bieniek, Katarzyna, Claes, Kathleen, Van Maerken, Tom, Díez, Orland, Hansen, Thomas V, Jønson, Lars, Gerdes, Anne-Marie, Ejlertsen, Bent, de la Hoya, Miguel, Caldés, Trinidad, Dunning, Alison M, Oliver, Clare, Fineberg, Elena, Cook, Margaret, Peock, Susan, McCann, Emma, Murray, Alex, Jacobs, Chris, Pichert, Gabriella, Lalloo, Fiona, Chu, Carol, Dorkins, Huw, Paterson, Joan, Ong, Kai-Ren, Teixeira, Manuel R, Hogervorst, Frans B L, van der Hout, Annemarie H, Seynaeve, Caroline, van der Luijt, Rob B, Ligtenberg, Marjolijn J L, Devilee, Peter, Wijnen, Juul T, Rookus, Matti A, Meijers-Heijboer, Hanne E J, Blok, Marinus J, van den Ouweland, Ans M W, Aalfs, Cora M, Rodriguez, Gustavo C, Phillips, Kelly-Anne A, Piedmonte, Marion, Nerenstone, Stacy R, Bae-Jump, Victoria L, O'Malley, David M, Ratner, Elena S, Schmutzler, Rita K, Wappenschmidt, Barbara, Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Plendl, Hansjoerg J, Niederacher, Dieter, Sutter, Christian, Wang-Gohrke, Shan, Steinemann, Doris, Preisler-Adams, Sabine, Kast, Karin, Varon-Mateeva, Raymonda

    Veröffentlicht in PloS one

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    A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population von Healey, Sue, Loud, Jennifer T, dos Santos Silva, Isabel, Hakonarson, Hakon, Garber, Judy, Blank, Stephanie V, Huzarski, Tomasz, Godwin, Andrew K, Spurdle, Amanda B, Soucy, Penny, Izatt, Louise, Southey, Melissa, Blum, Joanne L, Cox, Angela, Buys, Saundra S, Fasching, Peter A, Laitman, Yael, Rantala, Johanna, Peto, Julian, Montagna, Marco, Flesch-Janys, Dieter, Offit, Kenneth, Peock, Susan, Manoukian, Siranoush, Neuhausen, Susan L, Weitzel, Jeffrey, Wappenschmidt, Barbara, Sutter, Christian, Osorio, Ana, Rookus, Matti A, Terry, Mary-Beth, Friedman, Eitan, Ghoussaini, Maya, Martin, Nicholas G, Giraud, Sophie, Devilee, Peter, Gayther, Simon A, Engel, Christoph, Tung, Nadine, Singer, Christian F, Simard, Jacques, Byrski, Tomasz, Peterlongo, Paolo, Cook, Margaret, Bonanni, Bernardo, Goldgar, David E, Frost, Debra, Easton, Douglas F, Hoogerbrugge, Nicoline, Meindl, Alfons, Diasio, Robert B, Sinilnikova, Olga M, Kartsonaki, Christiana, Antoniou, Antonis C, Stoppa-Lyonnet, Dominique, Rodriguez, Gustavo C, Nathanson, Katherine L, Gaudet, Mia M, Cross, Simon S, Cybulski, Cezary, Winqvist, Robert, Fountzilas, George, van den Ouweland, Ans, Hansen, Thomas V O, Beattie, Mary S, Nielsen, Finn C, Douglas, Fiona, Caldes, Trinidad, Hopper, John L, Hogervorst, Frans B L, Oliver, Clare, Gerty, Sue M, Yannoukakos, Drakoulis, Lambrechts, Diether, Caron, Olivier, Lee, Adam M, Hardouin, Agnès, Vachon, Celine, Chenevix-Trench, Georgia, Holland, Helene, Blanco, Ignacio, Beckmann, Matthias W, Paridaens, Robert, Barrowdale, Daniel, Piedmonte, Marion, Couch, Fergus J, Lasset, Christine, Górski, Bohdan, Domchek, Susan M, Loman, Niklas, Nevanlinna, Heli, Rebbeck, Timothy, Thomassen, Mads, Narod, Stephen, Eccles, Diana, Benitez, Javier, Arason, Adalgeir, Basil, Jack, Lazaro, Conxi, Phelan, Catherine

    Veröffentlicht in Nature genetics

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