Search Results - Than, Swe Swe

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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 by 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

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    DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers by Kuchenbaecker, Karoline, Pita, Guillermo, de la Hoya, Miguel, Martínez-Bouzas, Cristina, Soucy, Penny, Lee, Andrew, Olopade, Olufunmilayo I, Beattie, Mary S, Domchek, Susan M, Nathanson, Katherine, Rebbeck, Timothy R, Karlan, Beth Y, Lester, Jenny, Whittemore, Alice S, Daly, Mary B, Buys, Saundra S, Dorfling, Cecilia M, van Rensburg, Elizabeth J, Ding, Yuan Chun, Jønson, Lars, Ejlertsen, Bent, Gerdes, Anne-Marie, Infante, Mar, Moreno, Leticia Thais, Weitzel, Jeffrey N, Herzog, Josef, Volorio, Sara, Viel, Alessandra, Papi, Laura, Tibiletti, Maria Grazia, Yannoukakos, Drakoulis, Garber, Judy, Ellis, Steve, Platte, Radka, Fineberg, Elena, Evans, Gareth, 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, Rhiem, Kerstin, Engel, Christoph, Wang-Gohrke, Shan, Preisler-Adams, Sabine, Varon-Mateeva, Raymonda, Sinilnikova, Olga M, Damiola, Francesca, Claes, Kathleen, Piedmonte, Marion, Tucker, Kathy, Backes, Floor, Wakeley, Katie, Rookus, Matti A, van Os, Theo A M, de Lange, J L, Gómez Garcia, Encarna B, Hoogerbrugge, Nicoline, Collée, J Margriet, van Deurzen, Carolien H M, van der Luijt, Rob B, Olah, Edith, Lázaro, Conxi, Jakubowska, Anna, Cybulski, Cezary, Durda, Katarzyna, Jaworska-Bieniek, Katarzyna, Montagna, Marco, Tognazzo, Silvia, Teixeira, Manuel R, Olswold, Curtis, Guidugli, Lucia, Vijai, Joseph, Kauff, Noah, Fink-Retter, Anneliese, Singer, Christian F, Pfeiler, Georg, Tea, Muy-Kheng, Berger, Andreas, Greene, Mark H, Andrulis, Irene, Glendon, Gord, Toland, Amanda Ewart, Bojesen, Anders, Pedersen, Inge Sokilde, Sunde, Lone, Friedman, Eitan, Shimon, Shani Paluch, Antoniou, Antonis C

    Published in PLoS genetics
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    Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases by 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 by Blanco, Ignacio, Wang, Xianshu, Barrowdale, Daniel, de Garibay, Gorka Ruiz, Librado, Pablo, Sánchez-Gracia, Alejandro, Bonifaci, Núria, McGuffog, Lesley, Berenguer, Antoni, Català, Isabel, Feliubadaló, Lidia, Tornero, Eva, Benítez, Javier, Osorio, Ana, Ramón y Cajal, Teresa, Nevanlinna, Heli, Aittomäki, Kristiina, Lester, Jenny, Greene, Mark H, Andrulis, Irene L, Domchek, Susan M, Nathanson, Katherine L, Lubinski, Jan, Claes, Kathleen, Caldés, Trinidad, Cook, Margaret, Pichert, Gabriella, Chu, Carol, Dorkins, Huw, Teixeira, Manuel R, Seynaeve, Caroline, Ligtenberg, Marjolijn J L, Wijnen, Juul T, Rookus, Matti A, Blok, Marinus J, van den Ouweland, Ans M W, Nerenstone, Stacy R, Bae-Jump, Victoria L, Ratner, Elena S, Schmutzler, Rita K, Wappenschmidt, Barbara, Rhiem, Kerstin, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Niederacher, Dieter, Sutter, Christian, Wang-Gohrke, Shan, Steinemann, Doris, Kast, Karin, Varon-Mateeva, Raymonda, Thomassen, Mads, Foretova, Lenka, Peterlongo, Paolo, Bernard, Loris, Peissel, Bernard, Scuvera, Giulietta, Manoukian, Siranoush, Radice, Paolo, Montagna, Marco, Agata, Simona, Maugard, Christine, Fink-Retter, Anneliese, Rappaport, Christine, Pfeiler, Georg, John, Esther M, Miron, Alex, Terry, Mary Beth, Chung, Wendy K, Daly, Mary B, Janavicius, Ramunas, van Rensburg, Elisabeth J, Garber, Judy, Olah, Edith, Narod, Steven A, Rennert, Gad, Paluch, Shani Shimon, Laitman, Yael, Loman, Niklas, Imyanitov, Evgeny N, Hamann, Ute, Spurdle, Amanda B, Herzog, Josef, Gorrini, Chiara, Sayols, Sergi, Heyn, Holger, Barjhoux, Laure, Fassy-Colcombet, Marion, de Pauw, Antoine, Ferrer, Sandra Fert, Bignon, Yves-Jean, Damiola, Francesca, Mazoyer, Sylvie, Sinilnikova, Olga M, Robson, Mark, Lee, Adam, Lindor, Noralane, Offit, Kenneth, Antoniou, Antonis C, Pujana, Miguel Angel

    Published in PloS one
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    Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers by Soucy, Penny, Chen, Xiaoqing, McGuffog, Lesley, Lee, Andrew, Barrowdale, Daniel, Healey, Sue, Sinilnikova, Olga M, Caligo, Maria A, Loman, Niklas, Harbst, Katja, Lindblom, Annika, Nathanson, Kate, Domchek, Susan, Rebbeck, Tim, Durda, Katarzyna, Osorio, Ana, Durán, Mercedes, Benítez, Javier, Hamann, Ute, van Os, Theo A, Verhoef, Senno, Ligtenberg, Marjolijn J, Ausems, Margreet G E M, Oosterwijk, Jan C, Frost, Debra, Ellis, Steve D, Platte, Radka, Evans, D Gareth, Jacobs, Chris, Eeles, Ros, Adlard, Julian, Paterson, Joan, Douglas, Fiona, Brewer, Carole, Hodgson, Shirley, Morrison, Patrick J, Donaldson, Alan, Godwin, Andrew K, Bove, Betsy, Stoppa-Lyonnet, Dominique, Buecher, Bruno, de Pauw, Antoine, Mazoyer, Sylvie, Calender, Alain, Léoné, Mélanie, Bressac-de Paillerets, Brigitte, Ferrer, Sandra U, Buys, Saundra, Daly, Mary, Miron, Alexander, Terry, Mary U, Singer, Christian F, Tea, Muy-Kheng, Kaulich, Daphne U, Barkardottir, Rosa B, Gaudet, Mia, Joseph, Vijai, Dutra-Clarke, Ana, Offit, Kenneth, Kirk, Judy, Fiorica, James, Oliani, Cristina, Imyanitov, Evgeny, Isaacs, Claudine, Blanco, Ignacio, Teulé, Alex, Valle, J Del, Gayther, Simon A, Olah, Edith, Ganz, Patricia A, Beattie, Mary S, Dorfling, Cecelia M, Wappenschmidt, Barbara, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Niederacher, Dieter, Gadzicki, Dorothea, Varon-Mateeva, Raymonda, Deissler, Helmut, Kast, Karin, Fiebig, Britta, Caldes, Trinidad, de la Hoya, Miguel, Nevanlinna, Heli, Fredericksen, Zachary, Pankratz, Vernon S, Lindor, Noralane M, Manoukian, Siranoush, Bonanni, Bernardo, Bernard, Loris, Dolcetti, Riccardo, Papi, Laura, Ottini, Laura, Mulligan, Anna U, Gerdes, Anne-Marie, Jensen, Uffe B, Skytte, Anne-Bine, Chenevix-Trench, Georgia, Simard, Jacques

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    Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk by Couch, Fergus J, Soucy, Penny, Dicks, Ed, Sinilnikova, Olga M, Bacot, François, Vincent, Daniel, Hogervorst, Frans B L, Peock, Susan, Radice, Paolo, Singer, Christian F, Friedman, Eitan, Hansen, Thomas V O, Neuhausen, Susan L, Blanco, Ignacio, Greene, Mark H, Karlan, Beth Y, Montagna, Marco, Godwin, Andrew K, Caldes, Trinidad, van Rensburg, Elizabeth J, Olopade, Olufunmilayo I, Southey, Melissa C, Kwong, Ava, Diez, Orland, Rennert, Gad, Seynaeve, Caroline, Rookus, Matti A, Verhoef, Senno, Wijnen, Juul T, Frost, Debra, Fineberg, Elena, Eccles, Diana M, Douglas, Fiona, Morrison, Patrick J, Rogers, Mark T, Gregory, Helen, McCann, Emma, Murray, Alex, Calender, Alain, Berthet, Pascaline, Lasset, Christine, Rouleau, Etienne, Damiola, Francesca, Sobol, Hagay, Gauthier-Villars, Marion, Lubinski, Jan, Jaworska, Katarzyna, Spurdle, Amanda B, Bonanni, Bernardo, Ottini, Laura, Papi, Laura, Volorio, Sara, Pensotti, Valeria, Arnold, Norbert, Gehrig, Andrea, Kast, Karin, Meindl, Alfons, Ditsch, Nina, Plendl, Hansjoerg, Varon-Mateeva, Raymonda, Weber, Bernhard H F, Arver, Brita, Rosenquist, Richard, Cohn, David E, Small, Laurie, Friedlander, Michael, Fink-Retter, Anneliese, Rappaport, Christine, Gschwantler-Kaulich, Daphne, Pfeiler, Georg, Lindor, Noralane M, Kaufman, Bella, Gerdes, Anne-Marie, Moeller, Sanne Traasdahl, Kruse, Torben A, Robson, Mark, Mulligan, Anna Marie, Andersen, Mette K, Steele, Linda, Foretova, Lenka, Lazaro, Conxi, Brunet, Joan, Pujana, Miquel Angel, Mai, Phuong L, Loud, Jennifer T, Lester, Jenny, Sand, Sharon R, Agata, Simona, Weaver, Joellen, Stavropoulou, Alexandra V, Muranen, Taru A, Duran, Mercedes, Lasa, Adriana, Miron, Alexander, Chan, Salina B, Lejbkowicz, Flavio, Wang, Chen, Pastinen, Tomi, Easton, Douglas F, Antoniou, Antonis C

    Published in PLoS genetics
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