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pro vyhledávání: '"van der Luijt, R. B."'
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Gaudet, Mia M., Kuchenbaecker, Karoline B., Vijai, Joseph, Klein, Robert J., Kirchhoff, Tomas, McGuffog, Lesley, Barrowdale, Daniel, Dunning, Alison M., Lee, Andrew, Dennis, Joe, Healey, Sue, Dicks, Ed, Soucy, Penny, Sinilnikova, Olga M., Pankratz, Vernon S., Wang, Xianshu, Eldridge, Ronald C., Tessier, Daniel C., Vincent, Daniel, Bacot, Francois, Hogervorst, Frans B.L., Peock, Susan, Stoppa-Lyonnet, Dominique, Coulet, Florence, Colas, Chrystelle, Soubrier, Florent, Peterlongo, Paolo, Schmutzler, Rita K., Nathanson, Katherine L., Piedmonte, Marion, Singer, Christian F., Thomassen, Mads, Sokolowska, Johanna, Bronner, Myriam, Hansen, Thomas V.O., Neuhausen, Susan L., Blanco, Ignacio, Greene, Mark H., Garber, Judith, Weitzel, Jeffrey N., Andrulis, Irene L., Goldgar, David E., D'Andrea, Emma, Caldes, Trinidad, Nevanlinna, Heli, Osorio, Ana, van Rensburg, Elizabeth J., Arason, Adalgeir, Rennert, Gad, van den Ouweland, Ans M.W., van der Hout, Annemarie H., Kets, Carolien M., Aalfs, Cora M., Wijnen, Juul T., Ausems, Margreet G.E.M., Frost, Debra, Ellis, Steve, Fineberg, Elena, Platte, Radka, Evans, D. Gareth, Jacobs, Chris, Adlard, Julian, Tischkowitz, Marc, Porteous, Mary, Damiola, Francesca, Golmard, Lisa, Barjhoux, Laure, Longy, Michel, Belotti, Muriel, Ferrer, Sandra Fert, Mazoyer, Sylvie, Spurdle, Amanda B., Manoukian, Siranoush, Barile, Monica, Genuardi, Maurizio, Arnold, Norbert, Meindl, Alfons, Sutter, Christian, Wappenschmidt, Barbara, Domchek, Susan M., Pfeiler, Georg, Friedman, Eitan, Jensen, Uffe Birk, Robson, Mark, Shah, Sohela, Lazaro, Conxi, Mai, Phuong L., Benitez, Javier, Southey, Melissa C., Schmidt, M. K., Fasching, Peter A., Peto, Julian, Humphreys, Manjeet K., Wang, Qin, Michailidou, Kyriaki, Sawyer, Elinor J., Burwinkel, Barbara, Guénel, Pascal, Bojesen, Stig E., Milne, Roger L., Brenner, Hermann, Lochmann, Magdalena, Brauch, Hiltrud, Ko, Yon Dschun, Baisch, Christian, Fischer, Hand Peter, Bruening, Thomas, Pesch, Beate, Rabstein, Sylvia, Spickenheuer, Anne, Aittomäki, Kristiina, Dörk, Thilo, Margolin, Sara, Mannermaa, Arto, Lambrechts, Diether, Chang-Claude, Jenny, Radice, Paolo, Giles, Graham G., Haiman, Christopher A., Winqvist, Robert, Devillee, Peter, García-Closas, Montserrat, Schoof, Nils, Hooning, M. J., Cox, Angela, Pharoah, Paul D.P., Jakubowska, Anna, Orr, Nick, González-Neira, Anna, Pita, Guillermo, Alonso, M. Rosario, Hall, Per, Couch, Fergus J., Simard, Jacques, Altshuler, David, Easton, Douglas F., Chenevix-Trench, Georgia, Antoniou, Antonis C., Offit, Kenneth, Rookus, M. A., van Leeuwen, F. E., Verhoef, S., de Lange, J. L., Collée, J. M., Seynaeve, C., van Deurzen, C. H.M., van Asperen, C. J., Tollenaar, R. A., Devilee, P., van Cronenburg, T. C.T.E.F., Mensenkamp, A. R., van der Luijt, R. B., van Os, T. A.M., Gille, J. J.P., Waisfisz, Q., Meijers-Heijboer, H. E.J., Gómez-Garcia, E. B., Blok, M. J., Oosterwijk, J. C., Mourits, M. J., de Bock, G. H., Vasen, H. F., Miedzybrodzka, Zosia, Gregory, Helen, Morrison, Patrick, Jeffers, Lisa, Cole, Trevor, Ong, Kai ren, Hoffman, Jonathan, Donaldson, Alan, James, Margaret, Paterson, Joan, Taylor, Amy, Murray, Alexandra, Rogers, Mark T., McCann, Emma, Kennedy, M. John, Barton, David, Drummond, Sarah, Brewer, Carole, Kivuva, Emma, Searle, Anne, Goodman, Selina, Hill, Kathryn, Davidson, Rosemarie, Murday, Victoria, Bradshaw, Nicola, Snadden, Lesley, Longmuir, Mark, Watt, Catherine, Gibson, Sarah, Haque, Eshika, Tobias, Ed, Duncan, Alexis, Izatt, Louise, Langman, Caroline, Brady, Angela, Dorkins, Huw, Melville, Athalie, Randhawa, Kashmir, Barwell, Julian, Serra-Feliu, Gemma, Ellis, Ian, Houghton, Catherine, Lalloo, Fiona, Taylor, Jane, Side, Lucy, Male, Alison, Berlin, Cheryl, Eason, Jacqueline, Douglas, Fiona, Claber, Oonagh, Collier, Rebecca, Jobson, Irene, Walker, Lisa, McLeod, Diane, Durell, Sarah, Stayner, Barbara, Eeles, Rosalind A., Shanley, Susan, Rahman, Nazneen, Houlston, Richard, Bancroft, Elizabeth, Page, Elizabeth, Ardern-Jones, Audrey, Kohut, Kelly, Wiggins, Jennifer, Castro, Elena, Killick, Emma, Martin, Sue, Rea, Gillian, Kulkarni, Anjana, Cook, Jackie, Quarrell, Oliver, Bardsley, Cathryn, Hodgson, Shirley, Goff, Sheila, Brice, Glen, Winchester, Lizzie, Eddy, Charlotte, Tripathi, Vishakha, Attard, Virginia, Lehmann, Anna, Eccles, Diana, Lucassen, Anneke, Crawford, Gillian, McBride, Donna, Smalley, Sarah, Sinilnikova, Olga, Verny-Pierre, Carole, Giraud, Sophie, Léone, Mélanie, Gauthier-Villars, Marion, Buecher, Bruno, Houdayer, Claude, Moncoutier, Virginie, Tirapo, Carole, de Pauw, Antoine, Bressac-de-Paillerets, Brigitte, Caron, Olivier, Bignon, Yves Jean, Uhrhammer, Nancy, Lasset, Christine, Bonadona, Valérie, Handallou, Sandrine, Hardouin, Agnés, Berthet, Pascaline, Sobol, Hagay, Bourdon, Violaine, Noguchi, Tetsuro, Remenieras, Audrey, Coupier, Isabelle, Pujol, Pascal, Peyrat, Jean Philippe, Fournier, Joëlle, Révillion, Françoise, Vennin, Philippe, Adenis, Claude, Rouleau, Etienne, Lidereau, Rosette, Demange, Liliane, Nogues, Catherine, Muller, Danièle, Fricker, Jean Pierre, Barouk-Simonet, Emmanuelle, Bonnet, Françoise, Bubien, Virginie, Sevenet, Nicolas, Toulas, Christine, Guimbaud, Rosine, Gladieff, Laurence, Feillel, Viviane, Dreyfus, Hélène, Rebischung, Christine, Peysselon, Magalie, Coron, Fanny, Faivre, Laurence, Prieur, Fabienne, Lebrun, Marine, Kientz, Caroline, Frénay, Marc, Vénat-Bouvet, Laurence, Delnatte, Capucine, Mortemousque, Isabelle, Lynch, Henry T., Snyder, Carrie L.
Publikováno v:
Plos Genetics, 9, 3, pp. e1003173
Plos Genetics, 9, e1003173
Gaudet, M M, Kuchenbaecker, K B, Vijai, J, Klein, R J, Kirchhoff, T, McGuffog, L, Barrowdale, D, Dunning, A M, Lee, A R, Dennis, J, Healey, S, Dicks, E, Soucy, P, Sinilnikova, O M, Pankratz, V S, Wang, X, Eldridge, R C, Tessier, D C, Vincent, D, Bacot, F, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Peterlongo, P, Schmutzler, R K, Nathanson, K L, Piedmonte, M, Singer, C F, Thomassen, M, Hansen, T V O, Neuhausen, S L, Blanco, I, Greene, M H, Garber, J, Weitzel, J N, Andrulis, I L, Goldgar, D E, D'Andrea, E, Caldes, T, Nevanlinna, H, Osorio, A, van Rensburg, E J, Arason, A, Rennert, G, van den Ouweland, A M W, van der Hout, A H, Kets, C M, Aalfs, C M, Wijnen, J T, Ausems, M G E M & kConFab Investigators 2013, ' Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk ', P L o S Genetics, vol. 9, no. 3, e1003173 . https://doi.org/10.1371/journal.pgen.1003173
Dipòsit Digital de la UB
Universidad de Barcelona
Gaudet, M M, Kuchenbaecker, K B, Vijai, J, Klein, R J, Kirchhoff, T, McGuffog, L, Barrowdale, D, Dunning, A M, Lee, A R, Dennis, J, Healey, S, Dicks, E, Soucy, P, Sinilnikova, O M, Pankratz, V S, Wang, X, Eldridge, R C, Tessier, D C, Vincent, D, Bacot, F, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Peterlongo, P, Schmutzler, R K, Nathanson, K L, Piedmonte, M, Singer, C F, Thomassen, M, Hansen, T V O, Neuhausen, S L, Blanco, I, Greene, M H, Garber, J, Weitzel, J N, Andrulis, I L, Goldgar, D E, D'Andrea, E, Caldes, T, Nevanlinna, H, Osorio, A, van Rensburg, E J, Arason, A, Rennert, G, van den Ouweland, A M W, van der Hout, A H, Kets, C M, Aalfs, C M, Wijnen, J T, Jensen, U B & KConFab Investigators 2013, ' Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk ', PLoS genetics, vol. 9, no. 3, pp. e1003173 . https://doi.org/10.1371/journal.pgen.1003173
Gaudet, M M, Kuchenbaecker, K B, Vijai, J, Klein, R J, Kirchhoff, T, McGuffog, L, Barrowdale, D, Dunning, A M, Lee, A, Dennis, J, Healey, S, Dicks, E, Soucy, P, Sinilnikova, O M, Pankratz, V S, Wang, X, Eldridge, R C, Tessier, D C, Vincent, D, Bacot, F, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Coulet, F, Colas, C, Soubrier, F, Peterlongo, P, Schmutzler, R K, Nathanson, K L, Piedmonte, M, Singer, C F, Thomassen, M, Sokolowska, J, Bronner, M, Hansen, T V O, Neuhausen, S L, Blanco, I, Greene, M H, Garber, J, Weitzel, J N, Andrulis, I L, Goldgar, D E, D'Andrea, E, Caldes, T, Nevanlinna, H, Osorio, A, van Rensburg, E J, Arason, A, Rennert, G, van den Ouweland, A M W, van der Hout, A H, Kets, C M, Aalfs, C M, Wijnen, J T, Ausems, M G E M, Frost, D, Ellis, S, Fineberg, E, Platte, R, Evans, D G, Jacobs, C, Adlard, J, Tischkowitz, M, Porteous, M, Damiola, F, Golmard, L, Barjhoux, L, Longy, M, Belotti, M, Ferrer, S F, Mazoyer, S, Spurdle, A B, Manoukian, S, Barile, M, Genuardi, M, Arnold, N, Meindl, A, Sutter, C, Wappenschmidt, B, Domchek, S M, Pfeiler, G, Friedman, E, Jensen, U B, Robson, M, Shah, S, Lazaro, C, Mai, P L, Benitez, J, Southey, M C, Schmidt, M K, Fasching, P A, Peto, J, Humphreys, M K, Wang, Q, Michailidou, K, Sawyer, E J, Burwinkel, B, Guénel, P, Bojesen, S E, Milne, R L, Brenner, H, Lochmann, M, Brauch, H, Ko, Y D, Baisch, C, Fischer, H P, Bruening, T, Pesch, B, Rabstein, S, Spickenheuer, A, Aittomäki, K, Dörk, T, Margolin, S, Mannermaa, A, Lambrechts, D, Chang-Claude, J, Radice, P, Giles, G G, Haiman, C A, Winqvist, R, Devillee, P, García-Closas, M, Schoof, N, Hooning, M J, Cox, A, Pharoah, P D P, Jakubowska, A, Orr, N, González-Neira, A, Pita, G, Alonso, M R, Hall, P, Couch, F J, Simard, J, Altshuler, D, Easton, D F, Chenevix-Trench, G, Antoniou, A C, Offit, K, Rookus, M A, van Leeuwen, F E, Verhoef, S, de Lange, J L, Collée, J M, Seynaeve, C, van Deurzen, C H M, van Asperen, C J, Tollenaar, R A, Devilee, P, van Cronenburg, T C T E F, Mensenkamp, A R, van der Luijt, R B, van Os, T A M, Gille, J J P, Waisfisz, Q, Meijers-Heijboer, H E J, Gómez-Garcia, E B, Blok, M J, Oosterwijk, J C, Mourits, M J, de Bock, G H, Vasen, H F, Miedzybrodzka, Z, Gregory, H, Morrison, P, Jeffers, L, Cole, T, Ong, K R, Hoffman, J, Donaldson, A, James, M, Paterson, J, Taylor, A, Murray, A, Rogers, M T, McCann, E, Kennedy, M J, Barton, D, Porteous, M, Drummond, S, Brewer, C, Kivuva, E, Searle, A, Goodman, S, Hill, K, Davidson, R, Murday, V, Bradshaw, N, Snadden, L, Longmuir, M, Watt, C, Gibson, S, Haque, E, Tobias, E, Duncan, A, Izatt, L, Langman, C, Brady, A, Dorkins, H, Melville, A, Randhawa, K, Barwell, J, Serra-Feliu, G, Ellis, I, Houghton, C, Lalloo, F, Taylor, J, Side, L, Male, A, Berlin, C, Eason, J, Douglas, F, Claber, O, Collier, R, Jobson, I, Walker, L, McLeod, D, Durell, S, Stayner, B, Eeles, R A, Shanley, S, Rahman, N, Houlston, R, Bancroft, E, Page, E, Ardern-Jones, A, Kohut, K, Wiggins, J, Castro, E, Killick, E, Martin, S, Rea, G, Kulkarni, A, Cook, J, Quarrell, O, Bardsley, C, Hodgson, S, Goff, S, Brice, G, Winchester, L, Eddy, C, Tripathi, V, Attard, V, Lehmann, A, Eccles, D, Lucassen, A, Crawford, G, McBride, D, Smalley, S, Sinilnikova, O, Verny-Pierre, C, Giraud, S, Léone, M, Gauthier-Villars, M, Buecher, B, Houdayer, C, Moncoutier, V, Tirapo, C, de Pauw, A, Bressac-de-Paillerets, B, Caron, O, Bignon, Y J, Uhrhammer, N, Lasset, C, Bonadona, V, Handallou, S, Hardouin, A, Berthet, P, Sobol, H, Bourdon, V, Noguchi, T, Remenieras, A, Coupier, I, Pujol, P, Peyrat, J P, Fournier, J, Révillion, F, Vennin, P, Adenis, C, Rouleau, E, Lidereau, R, Demange, L, Nogues, C, Muller, D, Fricker, J P, Barouk-Simonet, E, Bonnet, F, Bubien, V, Sevenet, N, Toulas, C, Guimbaud, R, Gladieff, L, Feillel, V, Dreyfus, H, Rebischung, C, Peysselon, M, Coron, F, Faivre, L, Prieur, F, Lebrun, M, Kientz, C, Frénay, M, Vénat-Bouvet, L, Delnatte, C, Mortemousque, I, Lynch, H T, Snyder, C L, EMBRACE, HEBON, GENICA Network, GEMO Study, KConFab Investigators & Ontario Cancer Genetics Network 2013, ' Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk ', PLoS Genetics, vol. 9, no. 3, e1003173 . https://doi.org/10.1371/journal.pgen.1003173
PLoS Genetics; Vol 9
PLoS Genetics, 9(3)
Recercat. Dipósit de la Recerca de Catalunya
instname
PLoS Genetics (print), 9(3). Public Library of Science
PLoS Genetics
PLoS genetics, 9(3). Public Library of Science
PLoS Genetics, 9(3):e1003173. Public Library of Science
PLoS genetics, 9(3). PUBLIC LIBRARY SCIENCE
PLoS Genetics, Vol 9, Iss 3, p e1003173 (2013)
Plos Genetics, 9, e1003173
Gaudet, M M, Kuchenbaecker, K B, Vijai, J, Klein, R J, Kirchhoff, T, McGuffog, L, Barrowdale, D, Dunning, A M, Lee, A R, Dennis, J, Healey, S, Dicks, E, Soucy, P, Sinilnikova, O M, Pankratz, V S, Wang, X, Eldridge, R C, Tessier, D C, Vincent, D, Bacot, F, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Peterlongo, P, Schmutzler, R K, Nathanson, K L, Piedmonte, M, Singer, C F, Thomassen, M, Hansen, T V O, Neuhausen, S L, Blanco, I, Greene, M H, Garber, J, Weitzel, J N, Andrulis, I L, Goldgar, D E, D'Andrea, E, Caldes, T, Nevanlinna, H, Osorio, A, van Rensburg, E J, Arason, A, Rennert, G, van den Ouweland, A M W, van der Hout, A H, Kets, C M, Aalfs, C M, Wijnen, J T, Ausems, M G E M & kConFab Investigators 2013, ' Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk ', P L o S Genetics, vol. 9, no. 3, e1003173 . https://doi.org/10.1371/journal.pgen.1003173
Dipòsit Digital de la UB
Universidad de Barcelona
Gaudet, M M, Kuchenbaecker, K B, Vijai, J, Klein, R J, Kirchhoff, T, McGuffog, L, Barrowdale, D, Dunning, A M, Lee, A R, Dennis, J, Healey, S, Dicks, E, Soucy, P, Sinilnikova, O M, Pankratz, V S, Wang, X, Eldridge, R C, Tessier, D C, Vincent, D, Bacot, F, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Peterlongo, P, Schmutzler, R K, Nathanson, K L, Piedmonte, M, Singer, C F, Thomassen, M, Hansen, T V O, Neuhausen, S L, Blanco, I, Greene, M H, Garber, J, Weitzel, J N, Andrulis, I L, Goldgar, D E, D'Andrea, E, Caldes, T, Nevanlinna, H, Osorio, A, van Rensburg, E J, Arason, A, Rennert, G, van den Ouweland, A M W, van der Hout, A H, Kets, C M, Aalfs, C M, Wijnen, J T, Jensen, U B & KConFab Investigators 2013, ' Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk ', PLoS genetics, vol. 9, no. 3, pp. e1003173 . https://doi.org/10.1371/journal.pgen.1003173
Gaudet, M M, Kuchenbaecker, K B, Vijai, J, Klein, R J, Kirchhoff, T, McGuffog, L, Barrowdale, D, Dunning, A M, Lee, A, Dennis, J, Healey, S, Dicks, E, Soucy, P, Sinilnikova, O M, Pankratz, V S, Wang, X, Eldridge, R C, Tessier, D C, Vincent, D, Bacot, F, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Coulet, F, Colas, C, Soubrier, F, Peterlongo, P, Schmutzler, R K, Nathanson, K L, Piedmonte, M, Singer, C F, Thomassen, M, Sokolowska, J, Bronner, M, Hansen, T V O, Neuhausen, S L, Blanco, I, Greene, M H, Garber, J, Weitzel, J N, Andrulis, I L, Goldgar, D E, D'Andrea, E, Caldes, T, Nevanlinna, H, Osorio, A, van Rensburg, E J, Arason, A, Rennert, G, van den Ouweland, A M W, van der Hout, A H, Kets, C M, Aalfs, C M, Wijnen, J T, Ausems, M G E M, Frost, D, Ellis, S, Fineberg, E, Platte, R, Evans, D G, Jacobs, C, Adlard, J, Tischkowitz, M, Porteous, M, Damiola, F, Golmard, L, Barjhoux, L, Longy, M, Belotti, M, Ferrer, S F, Mazoyer, S, Spurdle, A B, Manoukian, S, Barile, M, Genuardi, M, Arnold, N, Meindl, A, Sutter, C, Wappenschmidt, B, Domchek, S M, Pfeiler, G, Friedman, E, Jensen, U B, Robson, M, Shah, S, Lazaro, C, Mai, P L, Benitez, J, Southey, M C, Schmidt, M K, Fasching, P A, Peto, J, Humphreys, M K, Wang, Q, Michailidou, K, Sawyer, E J, Burwinkel, B, Guénel, P, Bojesen, S E, Milne, R L, Brenner, H, Lochmann, M, Brauch, H, Ko, Y D, Baisch, C, Fischer, H P, Bruening, T, Pesch, B, Rabstein, S, Spickenheuer, A, Aittomäki, K, Dörk, T, Margolin, S, Mannermaa, A, Lambrechts, D, Chang-Claude, J, Radice, P, Giles, G G, Haiman, C A, Winqvist, R, Devillee, P, García-Closas, M, Schoof, N, Hooning, M J, Cox, A, Pharoah, P D P, Jakubowska, A, Orr, N, González-Neira, A, Pita, G, Alonso, M R, Hall, P, Couch, F J, Simard, J, Altshuler, D, Easton, D F, Chenevix-Trench, G, Antoniou, A C, Offit, K, Rookus, M A, van Leeuwen, F E, Verhoef, S, de Lange, J L, Collée, J M, Seynaeve, C, van Deurzen, C H M, van Asperen, C J, Tollenaar, R A, Devilee, P, van Cronenburg, T C T E F, Mensenkamp, A R, van der Luijt, R B, van Os, T A M, Gille, J J P, Waisfisz, Q, Meijers-Heijboer, H E J, Gómez-Garcia, E B, Blok, M J, Oosterwijk, J C, Mourits, M J, de Bock, G H, Vasen, H F, Miedzybrodzka, Z, Gregory, H, Morrison, P, Jeffers, L, Cole, T, Ong, K R, Hoffman, J, Donaldson, A, James, M, Paterson, J, Taylor, A, Murray, A, Rogers, M T, McCann, E, Kennedy, M J, Barton, D, Porteous, M, Drummond, S, Brewer, C, Kivuva, E, Searle, A, Goodman, S, Hill, K, Davidson, R, Murday, V, Bradshaw, N, Snadden, L, Longmuir, M, Watt, C, Gibson, S, Haque, E, Tobias, E, Duncan, A, Izatt, L, Langman, C, Brady, A, Dorkins, H, Melville, A, Randhawa, K, Barwell, J, Serra-Feliu, G, Ellis, I, Houghton, C, Lalloo, F, Taylor, J, Side, L, Male, A, Berlin, C, Eason, J, Douglas, F, Claber, O, Collier, R, Jobson, I, Walker, L, McLeod, D, Durell, S, Stayner, B, Eeles, R A, Shanley, S, Rahman, N, Houlston, R, Bancroft, E, Page, E, Ardern-Jones, A, Kohut, K, Wiggins, J, Castro, E, Killick, E, Martin, S, Rea, G, Kulkarni, A, Cook, J, Quarrell, O, Bardsley, C, Hodgson, S, Goff, S, Brice, G, Winchester, L, Eddy, C, Tripathi, V, Attard, V, Lehmann, A, Eccles, D, Lucassen, A, Crawford, G, McBride, D, Smalley, S, Sinilnikova, O, Verny-Pierre, C, Giraud, S, Léone, M, Gauthier-Villars, M, Buecher, B, Houdayer, C, Moncoutier, V, Tirapo, C, de Pauw, A, Bressac-de-Paillerets, B, Caron, O, Bignon, Y J, Uhrhammer, N, Lasset, C, Bonadona, V, Handallou, S, Hardouin, A, Berthet, P, Sobol, H, Bourdon, V, Noguchi, T, Remenieras, A, Coupier, I, Pujol, P, Peyrat, J P, Fournier, J, Révillion, F, Vennin, P, Adenis, C, Rouleau, E, Lidereau, R, Demange, L, Nogues, C, Muller, D, Fricker, J P, Barouk-Simonet, E, Bonnet, F, Bubien, V, Sevenet, N, Toulas, C, Guimbaud, R, Gladieff, L, Feillel, V, Dreyfus, H, Rebischung, C, Peysselon, M, Coron, F, Faivre, L, Prieur, F, Lebrun, M, Kientz, C, Frénay, M, Vénat-Bouvet, L, Delnatte, C, Mortemousque, I, Lynch, H T, Snyder, C L, EMBRACE, HEBON, GENICA Network, GEMO Study, KConFab Investigators & Ontario Cancer Genetics Network 2013, ' Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk ', PLoS Genetics, vol. 9, no. 3, e1003173 . https://doi.org/10.1371/journal.pgen.1003173
PLoS Genetics; Vol 9
PLoS Genetics, 9(3)
Recercat. Dipósit de la Recerca de Catalunya
instname
PLoS Genetics (print), 9(3). Public Library of Science
PLoS Genetics
PLoS genetics, 9(3). Public Library of Science
PLoS Genetics, 9(3):e1003173. Public Library of Science
PLoS genetics, 9(3). PUBLIC LIBRARY SCIENCE
PLoS Genetics, Vol 9, Iss 3, p e1003173 (2013)
Contains fulltext : 118578.pdf (Publisher’s version ) (Open Access) Common genetic variants contribute to the observed variation in breast cancer risk for BRCA2 mutation carriers; those known to date have all been found through population-based gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be8bbb324fd27ffcb52b62a1a013638c
https://hdl.handle.net/2066/118578
https://hdl.handle.net/2066/118578
Autor:
Couch, Fergus J., Xianshu, Wang, Lesley, Mcguffog, Andrew, Lee, Curtis, Olswold, Kuchenbaecker, Karoline B., Penny, Soucy, Zachary, Fredericksen, Daniel, Barrowdale, Joe, Dennis, Gaudet, Mia M., Dicks, Ed, Matthew, Kosel, Sue, Healey, Sinilnikova, Olga M., Adam, Lee, François, Bacot, Daniel, Vincent, Hogervorst, Frans B. L., Susan, Peock, Dominique Stoppa Lyonnet, Anna, Jakubowska, Paolo, Radice, Rita Katharina Schmutzler, Domchek, S. M., Piedmonte, M., Singer, C. F., Friedman, E., Thomassen, M., Hansen, T. V. O., Neuhausen, S. L., Szabo, C. I., Blanco, I., Greene, M. H., Karlan, B. Y., Garber, J., Phelan, C. M., Weitzel, J. N., Montagna, M., Olah, E., Andrulis, I. L., Godwin, A. K., Yannoukakos, D., Goldgar, D. E., Caldes, T., Nevanlinna, H., Osorio, A., Terry, M. B., Daly, M. B., Van Rensburg, E. J., Hamann, U., Ramus, S. J., Ewart Toland, A., Caligo, M. A., Olopade, O. I., Tung, N., Claes, K., Beattie, M. S., Southey, M. C., Imyanitov, E. N., Tischkowitz, M., Janavicius, R., John, E. M., Kwong, A., Diez, O., Balmana, J., Barkardottir, R. B., Arun, B. K., Rennert, G., Teo, S. H., Ganz, P. A., Campbell, I., Van Der Hout, A. H., Van Deurzen, C. H. M., Seynaeve, C., Gomez Garcia, E. B., Van Leeuwen, F. E., Meijers Heijboer, H. E. J., Gille, J. J. P., Ausems, M. G. E. M., Blok, M. J., Ligtenberg, M. J. L., Rookus, M. A., Devilee, P., Verhoef, S., Van Os, T. A. M., Wijnen, J. T., Frost, D., Ellis, S., Fineberg, E., Platte, R., Evans, D. G., Izatt, L., Eeles, R. A., Adlard, J., Eccles, D. M., Cook, J., Brewer, C., Douglas, F., Hodgson, S., Morrison, P. J., Side, L. E., Donaldson, A., Houghton, C., Rogers, M. T., Dorkins, H., Eason, J., Gregory, H., Mccann, E., Murray, A., Calender, A., Hardouin, A., Berthet, P., Delnatte, C., Nogues, C., Lasset, C., Houdayer, C., Leroux, D., Rouleau, E., Prieur, F., Damiola, F., Sobol, H., Coupier, I., Venat Bouvet, L., Castera, L., Gauthier Villars, M., Leone, M., Pujol, P., Mazoyer, S., Bignon, Y. J., Zlowocka Perlowska, E., Gronwald, J., Lubinski, J., Durda, K., Jaworska, K., Huzarski, T., Spurdle, A. B., Viel, A., Peissel, B., Bonanni, B., Melloni, G., Ottini, Laura, Papi, L., Varesco, L., Tibiletti, M. G., Peterlongo, P., Volorio, S., Manoukian, S., Pensotti, V., Arnold, N., Engel, C., Deissler, H., Gadzicki, D., Gehrig, A., Kast, K., Rhiem, K., Meindl, A., Niederacher, D., Ditsch, N., Plendl, H., Preisler Adams, S., Engert, S., Sutter, C., Varon Mateeva, R., Wappenschmidt, B., Weber, B. H. F., Arver, B., Stenmark Askmalm, M., Loman, N., Rosenquist, R., Einbeigi, Z., Nathanson, K. L., Rebbeck, T. R., Blank, S. V., Cohn, D. E., Rodriguez, G. C., Small, L., Friedlander, M., Bae Jump, V. L., Fink Retter, A., Rappaport, C., Gschwantler Kaulich, D., Pfeiler, G., Tea, M. K., Lindor, N. M., Kaufman, B., Shimon Paluch, S., Laitman, Y., Skytte, A. B., Gerdes, A. M., Pedersen, I. S., Moeller, S. T., Kruse, T. A., Jensen, U. B., Vijai, J., Sarrel, K., Robson, M., Kauff, N., Mulligan, A. M., Glendon, G., Ozcelik, H., Ejlertsen, B., Nielsen, F. C., Jonson, L., Andersen, M. K., Ding, Y. C., Steele, L., Foretova, L., Teule, A., Lazaro, C., Brunet, J., Pujana, M. A., Mai, P. L., Loud, J. T., Walsh, C., Lester, J., Orsulic, S., Narod, S. A., Herzog, J., Sand, S. R., Tognazzo, S., Agata, S., Vaszko, T., Weaver, J., Stavropoulou, A. V., Buys, S. S., Romero, A., De La Hoya, M., Aittomaki, K., Muranen, T. A., Duran, M., Chung, W. K., Lasa, A., Dorfling, C. M., Miron, A., Benitez, J., Senter, L., Huo, D., Chan, S. B., Sokolenko, A. P., Chiquette, J., Tihomirova, L., Friebel, T. M., Agnarsson, B. A., K. H., Lu, Lejbkowicz, F., James, P. A., Hall, P., Dunning, A. M., Tessier, D., Cunningham, J., Slager, S. L., Wang, C., Hart, S., Stevens, K., Simard, J., Pastinen, T., Pankratz, V. S., Offit, K., Easton, D. F., Chenevix Trench, G., Antoniou, A. C., Thorne, H., Niedermayr, E., Borg, A., Olsson, H., Jernstrom, H., Henriksson, K., Harbst, K., Soller, M., Kristoffersson, U., Ofverholm, A., Nordling, M., Karlsson, P., Von Wachenfeldt, A., Liljegren, A., Lindblom, A., Bustinza, G. B., Rantala, J., Melin, B., Ardnor, C. E., Emanuelsson, M., Ehrencrona, H., Pigg, M. H., Liedgren, S., Hogervorst, F. B. L., Schmidt, M. K., De Lange, J., Collee, J. M., Van Den Ouweland, A. M. W., Hooning, M. J., Van Asperen, C. J., Tollenaar, R. A., Van Cronenburg, T. C. T. E. F., Kets, C. M., Mensenkamp, A. R., Van Der Luijt, R. B., Aalfs, C. M., Waisfisz, Q., Oosterwijk, J. C., Van Der Hout, H., Mourits, M. J., De Bock, G. H., Peock, S., Miedzybrodzka, Z., Morrison, P., Jeffers, L., Cole, T., Ong, K. R., Hoffman, J., James, M., Paterson, J., Taylor, A., Kennedy, M. J., Barton, D., Porteous, M., Drummond, S., Kivuva, E., Searle, A., Goodman, S., Hill, K., Davidson, R., Murday, V., Bradshaw, N., Snadden, L., Longmuir, M., Watt, C., Gibson, S., Haque, E., Tobias, E., Duncan, A., Jacobs, C., Langman, C., Brady, A., Melville, A., Randhawa, K., Barwell, J., Serra Feliu, G., Ellis, I., Lalloo, F., Taylor, J., Side, L., Male, A., Berlin, C., Collier, R., Claber, O., Jobson, I., Walker, L., Mcleod, D., Halliday, D., Durell, S., Stayner, B., Shanley, S., Rahman, N., Houlston, R., Stormorken, A., Bancroft, E., Page, E., Ardern Jones, A., Kohut, K., Wiggins, J., Castro, E., Killick, E., Martin, S., Rea, G., Kulkarni, A., Quarrell, O., Bardsley, C., Goff, S., Brice, G., Winchester, L., Eddy, C., Tripathi, V., Attard, V., Lehmann, A., Eccles, D., Lucassen, A., Crawford, G., Mcbride, D., Smalley, S., Sinilnikova, O., Barjhoux, L., Verny Pierre, C., Giraud, S., Stoppa Lyonnet, D., Buecher, B., Moncoutier, V., Belotti, M., Tirapo, C., De Pauw, A., Bressac De Paillerets, B., Caron, O., Uhrhammer, N., Bonadona, V., Handallou, S., Bourdon, V., Noguchi, T., Remenieras, A., Eisinger, F., Peyrat, J. P., Fournier, J., Revillion, F., Vennin, P., Adenis, C., Lidereau, R., Demange, L., Muller, D., Fricker, J. P., Barouk Simonet, E., Bonnet, F., Bubien, V., Sevenet, N., Longy, M., Toulas, C., Guimbaud, R., Gladieff, L., Feillel, V., Dreyfus, H., Rebischung, C., Peysselon, M., Coron, F., Faivre, L., Lebrun, M., Kientz, C., Ferrer, S. F., Frenay, M., Mortemousque, I., Coulet, F., Colas, C., Soubrier, F., Sokolowska, J., Bronner, M., Lynch, H. T., Snyder, C. L., Angelakos, M., Maskiell, J., Dite, G.
Publikováno v:
Couch, F J, Wang, X S, McGuffog, L, Lee, A, Olswold, C, Kuchenbaecker, K B, Soucy, P, Fredericksen, Z, Barrowdale, D, Dennis, J, Gaudet, M M, Dicks, E, Kosel, M, Healey, S, Sinilnikova, O M, Bacot, F, Vincent, D, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Jakubowska, A, Radice, P, Schmutzler, R K, Domchek, S M, Piedmonte, M, Singer, C F, Friedman, E, Thomassen, M, Hansen, T V O, Neuhausen, S L, Szabo, C I, Blanco, I, Greene, M H, Karlan, B Y, Garber, J, Phelan, C M, Weitzel, J N, Montagna, M, Olah, E, Andrulis, I L, Godwin, A K, Yannoukakos, D, Goldgar, D E, Caldes, T, Nevanlinna, H, Osorio, A, Terry, M B, Daly, M B, van Rensburg, E J, Hamann, U, Ramus, S J, Toland, A E, Caligo, M A, Olopade, O I, Tung, N, Claes, K, Beattie, M S, Southey, M C, Imyanitov, E N, Tischkowitz, M, Janavicius, R, John, E M, Kwong, A, Diez, O, Balmana, J, Barkardottir, R B, Arun, B K, Rennert, G, Teo, S H, Ganz, P A, Campbell, I, van der Hout, A H, van Deurzen, C H M, Seynaeve, C, Garcia, E B G, van Leeuwen, F E, Meijers-Heijboer, H E J, Gille, J J P, Ausems, M G E M, Blok, M J, Ligtenberg, M J L, Rookus, M A, Devilee, P, Verhoef, S, van Os, T A M, Wijnen, J T, Frost, D, Ellis, S, Fineberg, E, Platte, R, Evans, D G, Izatt, L, Eeles, R A, Adlard, J, Eccles, D M, Cook, J, Brewer, C, Douglas, F & Hodgson, S 2013, ' Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk ', PLoS Genetics, vol. 9, no. 3, e1003212 . https://doi.org/10.1371/journal.pgen.1003212
Plos Genetics, 9
kConFab Investigators 2013, ' Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk ', P L o S Genetics, vol. 9, no. 3, e1003212., pp. 1-21 . https://doi.org/10.1371/journal.pgen.1003212
Plos Genetics, 9(3):1003212. Public Library of Science
Plos Genetics, 9, 3
PLoS Genetics
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
PLoS genetics, 9(3):e1003212. PUBLIC LIBRARY SCIENCE
PLoS Genetics; 9(3), no e1003212 (2013)
PLoS Genetics, 9(3)
PLoS Genetics, 2013, 9, pp.e1003212. ⟨10.1371/journal.pgen.1003212⟩
Digital.CSIC. Repositorio Institucional del CSIC
PLoS Genetics (print), 9(3). Public Library of Science
Couch, F J, Wang, X, McGuffog, L, Lee, A R, Olswold, C, Kuchenbaecker, K B, Soucy, P, Fredericksen, Z, Barrowdale, D, Dennis, J, Gaudet, M M, Dicks, E, Kosel, M, Healey, S, Sinilnikova, O M, Lee, A, Bacot, F, Vincent, D, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Jakubowska, A, Radice, P, Schmutzler, R K, Domchek, S M, Piedmonte, M, Singer, C F, Friedman, E, Thomassen, M, Hansen, T V O, Neuhausen, S L, Szabo, C I, Blanco, I, Greene, M H, Karlan, B Y, Garber, J, Phelan, C M, Weitzel, J N, Montagna, M, Olah, E, Andrulis, I L, Godwin, A K, Yannoukakos, D, Goldgar, D E, Caldes, T, Nevanlinna, H, Skytte, A-B, Gerdes, A-M, Moeller, S T, Kruse, T A & kConFab Investigators 2013, ' Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk ', P L o S Genetics, vol. 9, no. 3, pp. e1003212 . https://doi.org/10.1371/journal.pgen.1003212
PLOS GENETICS
PLoS Genetics, Vol 9, Iss 3, p e1003212 (2013)
Dipòsit Digital de la UB
Universidad de Barcelona
PLoS Genetics, 9(3):e1003212. Public Library of Science
Recercat. Dipósit de la Recerca de Catalunya
Couch, F J, Wang, X, McGuffog, L, Lee, A R, Olswold, C, Kuchenbaecker, K B, Soucy, P, Fredericksen, Z, Barrowdale, D, Dennis, J, Gaudet, M M, Dicks, E, Kosel, M, Healey, S, Sinilnikova, O M, Lee, A, Bacot, F, Vincent, D, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Jakubowska, A, Investigators, K, Radice, P, Schmutzler, R K, Domchek, S M, Piedmonte, M, Singer, C F, Friedman, E, Thomassen, M, Hansen, T V O, Neuhausen, S L, Szabo, C I, Blanco, I, Greene, M H, Karlan, B Y, Garber, J, Phelan, C M, Weitzel, J N, Montagna, M, Olah, E, Andrulis, I L, Godwin, A K, Yannoukakos, D, Goldgar, D E, Caldes, T, Nevanlinna, H, Osorio, A, Pedersen, I S, Jensen, U B, SWE-BRCA & Skytte, A-B S 2013, ' Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk ', PLoS genetics, vol. 9, no. 3, pp. e1003212 . https://doi.org/10.1371/journal.pgen.1003212
PLoS Genetics, Public Library of Science, 2013, 9, pp.e1003212. ⟨10.1371/journal.pgen.1003212⟩
PLoS Genetics; Vol 9
PLoS genetics, 9(3). Public Library of Science
Plos Genetics, 9(3). Public Library of Science
Plos Genetics, 9
kConFab Investigators 2013, ' Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk ', P L o S Genetics, vol. 9, no. 3, e1003212., pp. 1-21 . https://doi.org/10.1371/journal.pgen.1003212
Plos Genetics, 9(3):1003212. Public Library of Science
Plos Genetics, 9, 3
PLoS Genetics
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
PLoS genetics, 9(3):e1003212. PUBLIC LIBRARY SCIENCE
PLoS Genetics; 9(3), no e1003212 (2013)
PLoS Genetics, 9(3)
PLoS Genetics, 2013, 9, pp.e1003212. ⟨10.1371/journal.pgen.1003212⟩
Digital.CSIC. Repositorio Institucional del CSIC
PLoS Genetics (print), 9(3). Public Library of Science
Couch, F J, Wang, X, McGuffog, L, Lee, A R, Olswold, C, Kuchenbaecker, K B, Soucy, P, Fredericksen, Z, Barrowdale, D, Dennis, J, Gaudet, M M, Dicks, E, Kosel, M, Healey, S, Sinilnikova, O M, Lee, A, Bacot, F, Vincent, D, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Jakubowska, A, Radice, P, Schmutzler, R K, Domchek, S M, Piedmonte, M, Singer, C F, Friedman, E, Thomassen, M, Hansen, T V O, Neuhausen, S L, Szabo, C I, Blanco, I, Greene, M H, Karlan, B Y, Garber, J, Phelan, C M, Weitzel, J N, Montagna, M, Olah, E, Andrulis, I L, Godwin, A K, Yannoukakos, D, Goldgar, D E, Caldes, T, Nevanlinna, H, Skytte, A-B, Gerdes, A-M, Moeller, S T, Kruse, T A & kConFab Investigators 2013, ' Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk ', P L o S Genetics, vol. 9, no. 3, pp. e1003212 . https://doi.org/10.1371/journal.pgen.1003212
PLOS GENETICS
PLoS Genetics, Vol 9, Iss 3, p e1003212 (2013)
Dipòsit Digital de la UB
Universidad de Barcelona
PLoS Genetics, 9(3):e1003212. Public Library of Science
Recercat. Dipósit de la Recerca de Catalunya
Couch, F J, Wang, X, McGuffog, L, Lee, A R, Olswold, C, Kuchenbaecker, K B, Soucy, P, Fredericksen, Z, Barrowdale, D, Dennis, J, Gaudet, M M, Dicks, E, Kosel, M, Healey, S, Sinilnikova, O M, Lee, A, Bacot, F, Vincent, D, Hogervorst, F B L, Peock, S, Stoppa-Lyonnet, D, Jakubowska, A, Investigators, K, Radice, P, Schmutzler, R K, Domchek, S M, Piedmonte, M, Singer, C F, Friedman, E, Thomassen, M, Hansen, T V O, Neuhausen, S L, Szabo, C I, Blanco, I, Greene, M H, Karlan, B Y, Garber, J, Phelan, C M, Weitzel, J N, Montagna, M, Olah, E, Andrulis, I L, Godwin, A K, Yannoukakos, D, Goldgar, D E, Caldes, T, Nevanlinna, H, Osorio, A, Pedersen, I S, Jensen, U B, SWE-BRCA & Skytte, A-B S 2013, ' Genome-Wide Association Study in BRCA1 Mutation Carriers Identifies Novel Loci Associated with Breast and Ovarian Cancer Risk ', PLoS genetics, vol. 9, no. 3, pp. e1003212 . https://doi.org/10.1371/journal.pgen.1003212
PLoS Genetics, Public Library of Science, 2013, 9, pp.e1003212. ⟨10.1371/journal.pgen.1003212⟩
PLoS Genetics; Vol 9
PLoS genetics, 9(3). Public Library of Science
Plos Genetics, 9(3). Public Library of Science
This is an open-access article distributed under the terms of the Creative Commons Attribution License.-- CIMBA et al.
BRCA1-associated breast and ovarian cancer risks can be modified by common genetic variants. To identify further cancer risk-m
BRCA1-associated breast and ovarian cancer risks can be modified by common genetic variants. To identify further cancer risk-m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::977d68472191e441a9af93425ef49847
https://research.vumc.nl/en/publications/bcc1545a-afb1-4d84-b0a1-4bfa08ea8a06
https://research.vumc.nl/en/publications/bcc1545a-afb1-4d84-b0a1-4bfa08ea8a06
Autor:
Eijkelenkamp, K., Kerstens, M. N., Links, T. P., van der Horst‐Schrivers, A. N. A., Olderode‐Berends, M. J. W., van der Luijt, R. B., Robledo, M., van Dooren, M., Feelders, R. A., de Vries, J.
Publikováno v:
Clinical Genetics; May2018, Vol. 93 Issue 5, p1049-1056, 9p, 3 Diagrams, 3 Charts, 1 Graph
Autor:
Ramus, Susan J., Antoniou, Antonis C., Kuchenbaecker, Karoline B., Penny, Soucy, Jonathan, Beesley, Xiaoqing, Chen, Lesley, Mcguffog, Sinilnikova, Olga M., Sue, Healey, Daniel, Barrowdale, Andrew, Lee, Mads, Thomassen, Anne Marie Gerdes, Kruse, Torben A., Uffe Birk Jensen, Anne Bine Skytte, Caligo, Maria A., Annelie, Liljegren, Annika, Lindblom, Hakan, Olsson, Ulf, Kristoffersson, Marie Stenmark Askmalm, Swe Brca Melin, B., Swe, Brca, Domchek, Susan M., Domchek, Sm, Nathanson, Katherine L., Rebbeck, Timothy R., Anna, Jakubowska, Jan, Lubinski, Katarzyna, Jaworska, Katarzyna, Durda, Elzbieta, Złowocka, Jacek, Gronwald, Tomasz, Huzarski, Tomasz, Byrski, Cezary, Cybulski, Aleksandra Toloczko Grabarek, Ana, Osorio, Javier, Benitez, Mercedes, Duran, Maria Isabel Tejada, Ute, Hamann, Matti, Rookus, Van Leeuwen, Flora E., Aalfs, Cora M., Meijers Heijboer, Hanne E. J., Van Asperen, Christi J., Van Roozendaal, K. E. P., Nicoline, Hoogerbrugge, Collee, Margriet J., Margriet Collee, J., Mieke, Kriege, Hebon Van Der Luijt, R. B., Embrace, Embrace, Hebon, Susan, Peock, Debra, Frost, Ellis, Steve D., Radka, Platte, Elena, Fineberg, Gareth Evans, D., Fiona, Lalloo, Chris, Jacobs, Ros, Eeles, Julian, Adlard, Rosemarie, Davidson, Diana, Eccles, Trevor, Cole, Jackie, Cook, Joan, Paterson, Fiona, Douglas, Carole, Brewer, Shirley, Hodgson, Morrison, Patrick J., Lisa, Walker, Porteous, Mary E., John Kennedy, M., Harsh, Pathak, Godwin, Andrew K., Dominique Stoppa Lyonnet, Virginie Caux Moncoutier, Antoine Pauw, D. E., De Pauw, A., Marion Gauthier Villars, Sylvie, Mazoyer, Melanie, Leone, Alain, Calender, Christine, Lasset, Valerie, Bonadona, Agnes, Hardouin, Pascaline, Berthet, Yves Jean Bignon, Nancy, Uhrhammer, Laurence, Faivre, Catherine, Loustalot, Gemo, Saundra, Buys, Mary, Daly, Buys, Daly, S., Alex, Miron, Beth, Terry M., Mary Beth Terry, Terry, M. B., Chung, Wendy K., Esther, John M., John, Em, Melissa, Southey, David, Goldgar, Singer, Christian F., Muy Kheng Tea, Georg, Pfeiler, Anneliese Fink Retter, Hansen, Thomas V. O., Hansen, Tv, Bent, Ejlertsen, Oskar Th Johannsson, Kenneth, Offit, Tomas, Kirchhoff, Gaudet, Mia M., Joseph, Vijai, Mark, Robson, Marion, Piedmonte, Kelly Anne Phillips, Linda Van Le, Hoffman, James S., Amanda Ewart Toland, Ewart Toland, A., Marco, Montagna, Silvia, Tognazzo, Evgeny, Imyanitov, Claudine, Isaacs, Issacs, C., Ramunas, Janavicius, Conxi, Lazaro, Ignacio, Blanco, Eva, Tornero, Matilde, Navarro, Moysich, Kirsten B., Karlan, Beth Y., Jenny, Gross, Edith, Olah, Tibor, Vaszko, Soo Hwang Teo, Ganz, Patricia A., Beattie, Mary S., Dorfling, Cecelia M., Van Rensburg, Elizabeth J., Orland, Diez, Ava, Kwong, Schmutzler, Rita K., Barbara, Wappenschmidt, Christoph, Engel, Alfons, Meindl, Nina, Ditsch, Norbert, Arnold, Simone, Heidemann, Dieter, Niederacher, Sabine Preisler Adams, Dorotehea, Gadzicki, Raymonda Varon Mateeva, Helmut, Deissler, Andrea, Gehrig, Christian, Sutter, Karin, Kast, Britta, Fiebig, Dieter, Schafer, Trinidad, Caldes, Miguel De La Hoya, Heli, Nevanlinna, Kristiina, Aittomaki, Marie, Plante, Kconfab Spurdle, A. B., Kconfab, Neuhausen, Susan L., Neuhausen, Sl, Yuan Chun Ding, Xianshu, Wang, Noralane, Lindor, Zachary, Fredericksen, Shane Pankratz, V., Paolo, Peterlongo, Siranoush, Manoukian, Bernard, Peissel, Daniela, Zaffaroni, Bernardo, Bonanni, Loris, Bernard, Riccardo, Dolcetti, Laura, Papi, Ottini, Laura, Paolo, Radice, Greene, Mark H., Mai, Phuong L., Andrulis, Irene L., Gord, Glendon, Ocgn Ozcelik, H., Ocgn, Pharoah, Paul D. P., Pharoah, Pd, Gayther, Simon A., Jacques, Simard, Easton, Douglas F., Couch, Fergus J., Georgia Chenevix Trench, Behalf Of The Consortium Of Investigators Of Modifiers Of Brca1/2, O. N.
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2012, 33, pp.690-702. ⟨10.1002/humu.22025⟩
Recercat. Dipósit de la Recerca de Catalunya
instname
Human mutation, 33(4), 690-702. Wiley-Liss Inc.
Human Mutation, 2012, 33, pp.690-702. ⟨10.1002/humu.22025⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Human Mutation; Vol 33
Human Mutation, 33, 690-702
Human Mutation, 33, 4, pp. 690-702
Ramus, S J, Antoniou, A C, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, McGuffog, L, Sinilnikova, O M, Healey, S, Barrowdale, D, Lee, A R, Thomassen, M, Gerdes, A-M A, Kruse, T A, Jensen, U B, Skytte, A-B S, Caligo, M A, Liljegren, A, Lindblom, A, Olsson, H, Kristoffersson, U, Stenmark-Askmalm, M, Melin, B, Domchek, S M, Nathanson, K L, Rebbeck, T R, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Złowocka, E, Gronwald, J, Huzarski, T, Byrski, T, Cybulski, C, Toloczko-Grabarek, A, Osorio, A, Benitez, J, Duran, M, Tejada, M-I, Hamann, U, Rookus, M, van Leeuwen, F E, Aalfs, C M, Meijers-Heijboer, H E J, van Asperen, C J, van Roozendaal, K E P, Hoogerbrugge, N, Collée, J M, Hansen, T V O & SWE-BRCA 2012, ' Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers ', Human Mutation, vol. 33, no. 4, pp. 690-702 . https://doi.org/10.1002/humu.22025
Human Mutation, 33(4), 690-702. Wiley
Ramus, S J, Antoniou, A C, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, McGuffog, L, Sinilnikova, O M, Healey, S, Barrowdale, D, Lee, A, Thomassen, M, Gerdes, A-M, Kruse, T A, Jensen, U B, Skytte, A-B, Caligo, M A, Liljegren, A, Lindblom, A, Olsson, H, Kristoffersson, U, Stenmark-Askmalm, M, Melin, B, Domchek, S M, Nathanson, K L, Rebbeck, T R, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Złowocka, E, Gronwald, J, Huzarski, T, Byrski, T, Cybulski, C, Toloczko-Grabarek, A, Osorio, A, Benitez, J, Duran, M, Tejada, M-I, Hamann, U, Rookus, M, van Leeuwen, F E, Aalfs, C M, Meijers-Heijboer, H E J, van Asperen, C J, van Roozendaal, K E P, Hoogerbrugge, N, Collée, J M, Kriege, M & SWE-BRCA 2012, ' Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers ', Human Mutation, vol. 33, no. 4, pp. 690-702 . https://doi.org/10.1002/humu.22025
Human Mutation, 33(4), 690-702
Human Mutation, 33(4), 690-702. Wiley-Liss Inc.
Human Mutation, Wiley, 2012, 33, pp.690-702. ⟨10.1002/humu.22025⟩
Recercat. Dipósit de la Recerca de Catalunya
instname
Human mutation, 33(4), 690-702. Wiley-Liss Inc.
Human Mutation, 2012, 33, pp.690-702. ⟨10.1002/humu.22025⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Human Mutation; Vol 33
Human Mutation, 33, 690-702
Human Mutation, 33, 4, pp. 690-702
Ramus, S J, Antoniou, A C, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, McGuffog, L, Sinilnikova, O M, Healey, S, Barrowdale, D, Lee, A R, Thomassen, M, Gerdes, A-M A, Kruse, T A, Jensen, U B, Skytte, A-B S, Caligo, M A, Liljegren, A, Lindblom, A, Olsson, H, Kristoffersson, U, Stenmark-Askmalm, M, Melin, B, Domchek, S M, Nathanson, K L, Rebbeck, T R, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Złowocka, E, Gronwald, J, Huzarski, T, Byrski, T, Cybulski, C, Toloczko-Grabarek, A, Osorio, A, Benitez, J, Duran, M, Tejada, M-I, Hamann, U, Rookus, M, van Leeuwen, F E, Aalfs, C M, Meijers-Heijboer, H E J, van Asperen, C J, van Roozendaal, K E P, Hoogerbrugge, N, Collée, J M, Hansen, T V O & SWE-BRCA 2012, ' Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers ', Human Mutation, vol. 33, no. 4, pp. 690-702 . https://doi.org/10.1002/humu.22025
Human Mutation, 33(4), 690-702. Wiley
Ramus, S J, Antoniou, A C, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, McGuffog, L, Sinilnikova, O M, Healey, S, Barrowdale, D, Lee, A, Thomassen, M, Gerdes, A-M, Kruse, T A, Jensen, U B, Skytte, A-B, Caligo, M A, Liljegren, A, Lindblom, A, Olsson, H, Kristoffersson, U, Stenmark-Askmalm, M, Melin, B, Domchek, S M, Nathanson, K L, Rebbeck, T R, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Złowocka, E, Gronwald, J, Huzarski, T, Byrski, T, Cybulski, C, Toloczko-Grabarek, A, Osorio, A, Benitez, J, Duran, M, Tejada, M-I, Hamann, U, Rookus, M, van Leeuwen, F E, Aalfs, C M, Meijers-Heijboer, H E J, van Asperen, C J, van Roozendaal, K E P, Hoogerbrugge, N, Collée, J M, Kriege, M & SWE-BRCA 2012, ' Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers ', Human Mutation, vol. 33, no. 4, pp. 690-702 . https://doi.org/10.1002/humu.22025
Human Mutation, 33(4), 690-702
Human Mutation, 33(4), 690-702. Wiley-Liss Inc.
Germline mutations in BRCA1 and BRCA2 are associated with increased risks of breast and ovarian cancer. A genome-wide association study (GWAS) identified six alleles associated with risk of ovarian cancer for women in the general population. We evalu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::886c548d4d0ecd806f9e2a03ffa5654c
https://hdl.handle.net/1887/97590
https://hdl.handle.net/1887/97590
Autor:
Cox, D. G., Simard, J., Sinnett, D., Hamdi, Y., Soucy, P., Ouimet, M., Barjhoux, L., Verny-Pierre, C., McGuffog, L., Healey, S., Szabo, C., Greene, M. H., Mai, P. L., Andrulis, I. L., Thomassen, M., Gerdes, A.-M., Caligo, M. A., Friedman, E., Laitman, Y., Kaufman, B., Paluch, S. S., Borg, A., Karlsson, P., Stenmark Askmalm, M., Barbany Bustinza, G., Nathanson, K. L., Domchek, S. M., Rebbeck, T. R., Benitez, J., Hamann, U., Rookus, M. A., van den Ouweland, A. M. W., Ausems, M. G. E. M., Aalfs, C. M., van Asperen, C. J., Devilee, P., Gille, H. J. J. P., Peock, S., Frost, D., Evans, D. G., Eeles, R., Izatt, L., Adlard, J., Paterson, J., Eason, J., Godwin, A. K., Remon, M.-A., Moncoutier, V., Gauthier-Villars, M., Lasset, C., Giraud, S., Hardouin, A., Berthet, P., Sobol, H., Eisinger, F., Bressac de Paillerets, B., Caron, O., Delnatte, C., Goldgar, D., Miron, A., Ozcelik, H., Buys, S., Southey, M. C., Terry, M. B., Singer, C. F., Dressler, A.-C., Tea, M.-K., Hansen, T. V. O., Johannsson, O., Piedmonte, M., Rodriguez, G. C., Basil, J. B., Blank, S., Toland, A. E., Montagna, M., Isaacs, C., Blanco, I., Gayther, S. A., Moysich, K. B., Schmutzler, R. K., Wappenschmidt, B., Engel, C., Meindl, A., Ditsch, N., Arnold, N., Niederacher, D., Sutter, C., Gadzicki, D., Fiebig, B., Caldes, T., Laframboise, R., Nevanlinna, H., Chen, X., Beesley, J., Spurdle, A. B., Neuhausen, S. L., Ding, Y. C., Couch, F. J., Wang, X., Peterlongo, P., Manoukian, S., Bernard, L., Radice, P., Easton, D. F., Chenevix-Trench, G., Antoniou, A. C., Stoppa-Lyonnet, D., Mazoyer, S., Sinilnikova, O. M., Dumont, M., Greene, M., Glendon, G., Selander, T., Weerasooriya, N., Nordling, M., Bergman, A., Einbeigi, Z., Stenmark-Askmalm, M., Liedgren, S., Loman, N., Olsson, H., Kristoffersson, U., Soller, M., Jernstrom, H., Harbst, K., Henriksson, K., Lindblom, A., Arver, B., von Wachenfeldt, A., Liljegren, A., Barbany-Bustinza, G., Rantala, J., Melin, B., Gronberg, H., Stattin, E.-L., Emanuelsson, M., Ehrencrona, H., Torres, D., Rashid, M. U., Seidel-Renkert, A., Hogervorst, F. B. L., Verhoef, S., Verheus, M., van't Veer, L. J., van Leeuwen, F. E., Collee, M., Jager, A., Hooning, M. J., Tilanus-Linthorst, M. M. A., Seynaeve, C., Wijnen, J. T., Vreeswijk, M. P., Tollenaar, R. A., Ligtenberg, M. J., Hoogerbrugge, N., Ausems, M. G., van der Luijt, R. B., van Os, T. A., Gille, J. J. P., Waisfisz, Q., Meijers-Heijboer, H. E. J., Gomez-Garcia, E. B., van Roozendaal, C. E., Blok, M. J., Caanen, B., Oosterwijk, J. C., van der Hout, A. H., Mourits, M. J., Vasen, H. F., Cook, M., Platte, R., Miedzybrodzka, Z., Gregory, H., Morrison, P., Jeffers, L., Cole, T., Ong, K.-r., Hoffman, J., Donaldson, A., James, M., Downing, S., Taylor, A., Murray, A., Rogers, M. T., McCann, E., Kennedy, M. J., Barton, D., Porteous, M., Drummond, S., Brewer, C., Kivuva, E., Searle, A., Goodman, S., Hill, K., Davidson, R., Murday, V., Bradshaw, N., Snadden, L., Longmuir, M., Watt, C., Gibson, S., Haque, E., Tobias, E., Duncan, A., Jacobs, C., Langman, C., Whaite, A., Dorkins, H., Barwell, J., Chu, C., Miller, J., Ellis, I., Houghton, C., Lalloo, F., Taylor, J., Side, L., Male, A., Berlin, C., Collier, R., Douglas, F., Claber, O., Jobson, I., Walker, L., McLeod, D., Halliday, D., Durell, S., Stayner, B., Shanley, S., Rahman, N., Houlston, R., Bancroft, E., D'Mello, L., Page, E., Ardern-Jones, A., Kohut, K., Wiggins, J., Castro, E., Mitra, A., Robertson, L., Cook, J., Quarrell, O., Bardsley, C., Hodgson, S., Goff, S., Brice, G., Winchester, L., Eddy, C., Tripathi, V., Attard, V., Eccles, D., Lucassen, A., Crawford, G., McBride, D., Smalley, S., Sinilnikova, O., Leone, M., Buecher, B., Houdayer, C., Belotti, M., Tirapo, C., de Pauw, A., Bressac-de-Paillerets, B., Remenieras, A., Byrde, V., Lenoir, G., Bignon, Y.-J., Uhrhammer, N., Bonadona, V., Bourdon, V., Noguchi, T., Coulet, F., Colas, C., Soubrier, F., Coupier, I., Pujol, P., Peyrat, J.-P., Fournier, J., Revillion, F., Vennin, P., Adenis, C., Rouleau, E., Lidereau, R., Demange, L., Nogues, C., Muller, D., Fricker, J.-P., Longy, M., Sevenet, N., Toulas, C., Guimbaud, R., Gladieff, L., Feillel, V., Leroux, D., Dreyfus, H., Rebischung, C., Coron, F., Faivre, L., Prieur, F., Lebrun, M., Ferrer, S. F., Frenay, M., Venat-Bouvet, L., Mortemousque, I., Lynch, H. T., Snyder, C. L., Ejlertsen, B., Andersen, M. K., Kjaergaard, S., Senter, L., Sweet, K., O'Connor, M., Craven, C., Pharoah, P., Ramus, S., Pye, C., Harrington, P., Wozniak, E., Varon-Mateeva, R., Kast, K., Preisler-Adams, S., Deissler, H., Schonbuchner, I., Heinritz, W., Schafer, D., Aittomaki, K., Blomqvist, C., Heikkinen, T., Erkkila, R. N. I., Thorne, H., Niedermayr, E., de la Hoya, M., Perez-Segura, P.
Publikováno v:
Human Molecular Genetics, 20(23), 4732-4747
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (23), pp.4732-47. ⟨10.1093/hmg/ddr388⟩
Human Molecular Genetics, 20(23), 4732-4747. Oxford University Press
Human Molecular Genetics, 20, 23, pp. 4732-47
Human Molecular Genetics, 20, 4732-47
Human molecular genetics, 20(23), 4732-4747. Oxford University Press
Cox, D G, Simard, J, Sinnett, D, Hamdi, Y, Soucy, P, Ouimet, M, Barjhoux, L, Verny-Pierre, C, McGuffog, L, Healey, S, Szabo, C, Greene, M H, Mai, P L, Andrulis, I L, Thomassen, M, Gerdes, A M, Caligo, M A, Friedman, E, Laitman, Y, Kaufman, B, Paluch, S S, Borg, A, Karlsson, P, Askmalm, M S, Bustinza, G B, Nathanson, K L, Domchek, S M, Rebbeck, T R, Benitez, J, Hamann, U, Rookus, M A, van den Ouweland, A M W, Ausems, M G E M, Aalfs, C M, van Asperen, C J, Devilee, P, Gille, J J P, Peock, S, Frost, D, Evans, D G, Eeles, R, Izatt, L, Adlard, J, Paterson, J, Eason, J, Godwin, A K, Remon, M A, Moncoutier, V, Gauthier-Villars, M, Lasset, C, Giraud, S, Hardouin, A, Berthet, P, Sobol, H, Eisinger, F, de Paillerets, B B, Caron, O, Delnatte, C, Goldgar, D, Miron, A, Ozcelik, H, Buys, S, Southey, M C, Terry, M B, Singer, C F, Dressler, A C, Tea, M K, Hansen, T V O, Johannsson, O, Piedmonte, M, Rodriguez, G C, Basil, J B, Blank, S, Toland, A E, Montagna, M, Isaacs, C, Blanco, I, Gayther, S A, Moysich, K B, Schmutzler, R K, Wappenschmidt, B, Engel, C, Meindl, A, Ditsch, N, Arnold, N, Niederacher, D, Sutter, C, Gadzicki, D, Fiebig, B, Caldes, T, Laframboise, R, Nevanlinna, H, Chen, X Q, Beesley, J, Spurdle, A B, Neuhausen, S L, Ding, Y C, Couch, F J & Wang, X S 2011, ' Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers ', Human Molecular Genetics, vol. 20, no. 23, pp. 4732-4747 . https://doi.org/10.1093/hmg/ddr388
Human Molecular Genetics; Vol 20
Human Molecular Genetics, 2011, 20 (23), pp.4732-47. ⟨10.1093/hmg/ddr388⟩
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (23), pp.4732-47. 〈10.1093/hmg/ddr388〉
Cox, D G, Simard, J, Sinnett, D, Hamdi, Y, Soucy, P, Ouimet, M, Barjhoux, L, Verny-Pierre, C, McGuffog, L, Healey, S, Szabo, C, Greene, M H, Mai, P L, Andrulis, I L, Thomassen, M, Gerdes, A-M, Caligo, M A, Friedman, E, Laitman, Y, Kaufman, B, Paluch, S S, Borg, A, Karlsson, P, Stenmark Askmalm, M, Barbany Bustinza, G, Nathanson, K L, Domchek, S M, Rebbeck, T R, Benítez, J, Hamann, U, Rookus, M A, van den Ouweland, A M W, Ausems, M G E M, Aalfs, C M, van Asperen, C J, Devilee, P, Gille, H J J P, Peock, S, Frost, D, Evans, D G, Eeles, R, Izatt, L, Adlard, J, Paterson, J, Eason, J, Godwin, A K, Remon, M-A, Moncoutier, V, Gauthier-Villars, M, Lasset, C & Ontario Cancer Genetics Network 2011, ' Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers ', Human Molecular Genetics, vol. 20, no. 23, pp. 4732-4747 . https://doi.org/10.1093/hmg/ddr388
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (23), pp.4732-47. ⟨10.1093/hmg/ddr388⟩
Human Molecular Genetics, 20(23), 4732-4747. Oxford University Press
Human Molecular Genetics, 20, 23, pp. 4732-47
Human Molecular Genetics, 20, 4732-47
Human molecular genetics, 20(23), 4732-4747. Oxford University Press
Cox, D G, Simard, J, Sinnett, D, Hamdi, Y, Soucy, P, Ouimet, M, Barjhoux, L, Verny-Pierre, C, McGuffog, L, Healey, S, Szabo, C, Greene, M H, Mai, P L, Andrulis, I L, Thomassen, M, Gerdes, A M, Caligo, M A, Friedman, E, Laitman, Y, Kaufman, B, Paluch, S S, Borg, A, Karlsson, P, Askmalm, M S, Bustinza, G B, Nathanson, K L, Domchek, S M, Rebbeck, T R, Benitez, J, Hamann, U, Rookus, M A, van den Ouweland, A M W, Ausems, M G E M, Aalfs, C M, van Asperen, C J, Devilee, P, Gille, J J P, Peock, S, Frost, D, Evans, D G, Eeles, R, Izatt, L, Adlard, J, Paterson, J, Eason, J, Godwin, A K, Remon, M A, Moncoutier, V, Gauthier-Villars, M, Lasset, C, Giraud, S, Hardouin, A, Berthet, P, Sobol, H, Eisinger, F, de Paillerets, B B, Caron, O, Delnatte, C, Goldgar, D, Miron, A, Ozcelik, H, Buys, S, Southey, M C, Terry, M B, Singer, C F, Dressler, A C, Tea, M K, Hansen, T V O, Johannsson, O, Piedmonte, M, Rodriguez, G C, Basil, J B, Blank, S, Toland, A E, Montagna, M, Isaacs, C, Blanco, I, Gayther, S A, Moysich, K B, Schmutzler, R K, Wappenschmidt, B, Engel, C, Meindl, A, Ditsch, N, Arnold, N, Niederacher, D, Sutter, C, Gadzicki, D, Fiebig, B, Caldes, T, Laframboise, R, Nevanlinna, H, Chen, X Q, Beesley, J, Spurdle, A B, Neuhausen, S L, Ding, Y C, Couch, F J & Wang, X S 2011, ' Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers ', Human Molecular Genetics, vol. 20, no. 23, pp. 4732-4747 . https://doi.org/10.1093/hmg/ddr388
Human Molecular Genetics; Vol 20
Human Molecular Genetics, 2011, 20 (23), pp.4732-47. ⟨10.1093/hmg/ddr388⟩
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (23), pp.4732-47. 〈10.1093/hmg/ddr388〉
Cox, D G, Simard, J, Sinnett, D, Hamdi, Y, Soucy, P, Ouimet, M, Barjhoux, L, Verny-Pierre, C, McGuffog, L, Healey, S, Szabo, C, Greene, M H, Mai, P L, Andrulis, I L, Thomassen, M, Gerdes, A-M, Caligo, M A, Friedman, E, Laitman, Y, Kaufman, B, Paluch, S S, Borg, A, Karlsson, P, Stenmark Askmalm, M, Barbany Bustinza, G, Nathanson, K L, Domchek, S M, Rebbeck, T R, Benítez, J, Hamann, U, Rookus, M A, van den Ouweland, A M W, Ausems, M G E M, Aalfs, C M, van Asperen, C J, Devilee, P, Gille, H J J P, Peock, S, Frost, D, Evans, D G, Eeles, R, Izatt, L, Adlard, J, Paterson, J, Eason, J, Godwin, A K, Remon, M-A, Moncoutier, V, Gauthier-Villars, M, Lasset, C & Ontario Cancer Genetics Network 2011, ' Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers ', Human Molecular Genetics, vol. 20, no. 23, pp. 4732-4747 . https://doi.org/10.1093/hmg/ddr388
Item does not contain fulltext Mutations in the BRCA1 gene substantially increase a woman's lifetime risk of breast cancer. However, there is great variation in this increase in risk with several genetic and non-genetic modifiers identified. The BRCA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::207eefc35a6fe3701311eaf6bee86cb8
http://hdl.handle.net/1887/88113
http://hdl.handle.net/1887/88113
Autor:
Antoniou, A. C., Kartsonaki, C., Sinilnikova, O. M., Soucy, P., Mcguffog, L., Healey, S., Lee, A., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Cattaneo, E., Barile, M., Pensotti, V., Pasini, B., Dolcetti, R., Giannini, Giuseppe, Laura Putignano, A., Varesco, L., Radice, P., Mai, P. L., Greene, M. H., Andrulis, I. L., Glendon, G., Ozcelik, H., Thomassen, M., Gerdes, A. M., Kruse, T. A., Jensen, U. B., Cruger, D. G., Caligo, M. A., Laitman, Y., Milgrom, R., Kaufman, B., Paluch Shimon, S., Friedman, E., Loman, N., Harbst, K., Lindblom, A., Arver, B., Ehrencrona, H., Melin, B., Nathanson, K. L., Domchek, S. M., Rebbeck, T., Jakubowska, A., Lubinski, J., Gronwald, J., Huzarski, T., Byrski, T., Cybulski, C., Gorski, B., Osorio, A., Cajal, T. R., Fostira, F., Andres, R., Benitez, J., Hamann, U., Hogervorst, F. B., Rookus, M. A., Hooning, M. J., Nelen, M. R., Van Der Luijt, R. B., Van Os, T. A. M., Van Asperen, C. J., Devilee, P., Meijers Heijboer, H. E. J., Garcia, E. B. G., Peock, S., Cook, M., Frost, D., Platte, R., Leyland, J., Evans, D. G., Lalloo, F., Eeles, R., Izatt, L., Adlard, J., Davidson, R., Eccles, D., Ong, K. R., Cook, J., Douglas, F., Paterson, J., John Kennedy, M., Miedzybrodzka, Z., Godwin, A., Stoppa Lyonnet, D., Buecher, B., Belotti, M., Tirapo, C., Mazoyer, S., Barjhoux, L., Lasset, C., Leroux, D., Faivre, L., Bronner, M., Prieur, F., Nogues, C., Rouleau, E., Pujol, P., Coupier, I., Frenay, M., Hopper, J. L., Daly, M. B., Terry, M. B., John, E. M., Buys, S. S., Yassin, Y., Miron, A., Goldgar, D., Singer, C. F., Tea, M. K., Pfeiler, G., Catharina Dressler, A., Hansen, T. V. O., Jonson, L., Ejlertsen, B., Barkardottir, R. B., Kirchhoff, T., Offit, K., Piedmonte, M., Rodriguez, G., Small, L., Boggess, J., Blank, S., Basil, J., Azodi, M., Toland, A. E., Montagna, M., Tognazzo, S., Agata, S., Imyanitov, E., Janavicius, R., Lazaro, C., Blanco, I., Pharoah, P. D. P., Sucheston, L., Karlan, B. Y., Walsh, C. S., Olah, E., Bozsik, A., Teo, S. H., Seldon, J. L., Beattie, M. S., Van Rensburg, E. J., Sluiter, M. D., Diez, O., Schmutzler, R. K., Wappenschmidt, B., Engel, C., Meindl, A., Ruehl, I., Varon Mateeva, R., Kast, K., Deissler, H., Niederacher, D., Arnold, N., Gadzicki, D., Schonbuchner, I., Caldes, T., De La Hoya, M., Nevanlinna, H., Aittomaki, K., Dumont, M., Chiquette, J., Tischkowitz, M., Chen, X. Q., Beesley, J., Spurdle, A. B., Neuhausen, S. L., Ding, Y. C., Fredericksen, Z., Wang, X., Pankratz, V. S., Couch, F., Simard, J., Easton, D. F., Chenevix Trench, G., Karlsson, P., Nordling, M., Bergman, A., Einbeigi, Z., Stenmark Askmalm, M., Liedgren, S., Borg, A., Olsson, H., Kristoffersson, U., Jernstrom, H., Henriksson, K., Von Wachenfeldt, A., Liljegren, A., Barbany Bustinza, G., Rantala, J., Gronberg, H., Stattin, E. L., Emanuelsson, M., Brandell, R. R., Dahl, N., Hogervorst, F. B. L., Verhoef, S., Verheus, M., Veer, L. V., Van Leeuwen, F. E., Collee, M., Van Den Ouweland, A. M. W., Jager, A., Tilanus Linthorst, M. M. A., Seynaeve, C., Wijnen, J. T., Vreeswijk, M. P., Tollenaar, R. A., Ligtenberg, M. J., Hoogerbrugge, N., Ausems, M. G., Aalfs, C. M., Van Os, T. A., Gille, J. J. P., Waisfisz, Q., Gomez Garcia, E. B., Van Roozendaal, C. E., Blok, M. J., Caanen, B., Oosterwijk, J. C., Van Der Hout, A. H., Mourits, M. J., Vasen, H. F., Gregory, H., Morrison, P., Jeffers, L., Cole, T., Mckeown, C., Hoffman, J., Donaldson, A., Downing, S., Taylor, A., Murray, A., Rogers, M. T., Mccann, E., Kennedy, M. J., Barton, D., Porteous, M., Drummond, S., Brewer, C., Kivuva, E., Searle, A., Goodman, S., Hill, K., Murday, V., Bradshaw, N., Snadden, L., Longmuir, M., Watt, C., Gibson, S., Haque, E., Tobias, E., Duncan, A., Jacobs, C., Langman, C., Whaite, A., Dorkins, H., Barwell, J., Chu, C., Miller, J., Ellis, I., Houghton, C., Taylor, J., Side, L., Male, A., Berlin, C., Eason, J., Collier, R., Claber, O., Jobson, I., Walker, L., Mcleod, D., Halliday, D., Durell, S., Stayner, B., Shanley, S., Rahman, N., Houlston, R., Bancroft, E., D'Mello, L., Page, E., Ardern Jones, A., Kohut, K., Wiggins, J., Castro, E., Mitra, A., Robertson, L., Quarrell, O., Bardsley, C., Hodgson, S., Goff, S., Brice, G., Winchester, L., Eddy, C., Tripathi, V., Attard, V., Lucassen, A., Crawford, G., Mcbride, D., Smalley, S.
Publikováno v:
Antoniou, A C, Kartsonaki, C, Sinilnikova, O M, Soucy, P, McGuffog, L, Healey, S, Lee, A, Peterlongo, P, Manoukian, S, Peissel, B, Zaffaroni, D, Cattaneo, E, Barile, M, Pensotti, V, Pasini, B, Dolcetti, R, Giannini, G, Putignano, A L, Varesco, L, Radice, P, Mai, P L, Greene, M H, Andrulis, I L, Glendon, G, Ozcelik, H, Thomassen, M, Gerdes, A-M, Kruse, T A, Jensen, U B, Crüger, D G, Caligo, M A, Laitman, Y, Milgrom, R, Kaufman, B, Paluch-Shimon, S, Friedman, E, Loman, N, Harbst, K, Lindblom, A, Arver, B, Ehrencrona, H, Melin, B, Nathanson, K L, Domchek, S M, Rebbeck, T, Jakubowska, A, Lubinski, J, Gronwald, J, Huzarski, T, Byrski, T & SWE-BRCA 2011, ' Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers ', Human Molecular Genetics, vol. 20, no. 16, pp. 3304-21 . https://doi.org/10.1093/hmg/ddr226
Human Molecular Genetics, 20(16), 3304-3321
Human Molecular Genetics, 20(16), 3304-3321. Oxford University Press
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (16), pp.3304-21. 〈10.1093/hmg/ddr226〉
Antoniou, A C, Kartsonaki, C, Sinilnikova, O M, Soucy, P, McGuffog, L, Healey, S, Lee, A, Peterlongo, P, Manoukian, S, Peissel, B, Zaffaroni, D, Cattaneo, E, Barile, M, Pensotti, V, Pasini, B, Dolcetti, R, Giannini, G, Putignano, A L, Varesco, L, Radice, P, Mai, P L, Greene, M H, Andrulis, I L, Glendon, G, Ozcelik, H, Thomassen, M, Gerdes, A M, Kruse, T A, Jensen, U B, Cruger, D G, Caligo, M A, Laitman, Y, Milgrom, R, Kaufman, B, Paluch-Shimon, S, Friedman, E, Loman, N, Harbst, K, Lindblom, A, Arver, B, Ehrencrona, H, Melin, B, Nathanson, K L, Domchek, S M, Rebbeck, T, Jakubowska, A, Lubinski, J, Gronwald, J, Huzarski, T, Byrski, T, Cybulski, C, Gorski, B, Osorio, A, Cajal, T R Y, Fostira, F, Andres, R, Benitez, J, Hamann, U, Hogervorst, FB, Rookus, M A, Hooning, M J, Nelen, M R, van der Luijt, R B, van Os, T A M, van Asperen, C J, Devilee, P, Meijers-Heijboer, E J, Garcia, E B G, Peock, S, Cook, M, Frost, D, Platte, R, Leyland, J, Evans, D G, Lalloo, F, Eeles, R, Izatt, L, Adlard, J, Davidson, R, Eccles, D, Ong, K R, Cook, J, Douglas, F, Paterson, J, Kennedy, M J, Miedzybrodzka, Z, Godwin, A, Stoppa-Lyonnet, D, Buecher, B, Belotti, M, Tirapo, C, Mazoyer, S, Barjhoux, L, Lasset, C, Leroux, D, Faivre, L, Bronner, M, Prieur, F, Nogues, C & Chenevix-Trench, G 2011, ' Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers ', Human Molecular Genetics, vol. 20, no. 16, pp. 3304-3321 . https://doi.org/10.1093/hmg/ddr226
Human Molecular Genetics, 20, 3304-21
Human Molecular Genetics, 2011, 20 (16), pp.3304-21. ⟨10.1093/hmg/ddr226⟩
HUMAN MOLECULAR GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (16), pp.3304-21. ⟨10.1093/hmg/ddr226⟩
Human Molecular Genetics, 20, 16, pp. 3304-21
Antoniou, A C, Kartsonaki, C, Sinilnikova, O M, Soucy, P, McGuffog, L, Healey, S, Lee, A R, Peterlongo, P, Manoukian, S, Peissel, B, Zaffaroni, D, Cattaneo, E, Barile, M, Pensotti, V, Pasini, B, Dolcetti, R, Giannini, G, Putignano, A L, Varesco, L, Radice, P, Mai, P L, Greene, M H, Andrulis, I L, Glendon, G, Ozcelik, H, Thomassen, M, Gerdes, A-M A, Kruse, T A, Jensen, U B, Crüger, D G, Caligo, M A, Laitman, Y, Milgrom, R, Kaufman, B, Paluch-Shimon, S, Friedman, E, Loman, N, Harbst, K, Lindblom, A, Arver, B, Ehrencrona, H, Melin, B, Nathanson, K L, Domchek, S M, Rebbeck, T, Jakubowska, A, Lubinski, J, Gronwald, J, Huzarski, T, Byrski, T & SWE-BRCA 2011, ' Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers ', Human Molecular Genetics, vol. 20, no. 16, pp. 3304-21 . https://doi.org/10.1093/hmg/ddr226
Human molecular genetics, 20(16), 3304-3321. Oxford University Press
Human Molecular Genetics; Vol 20
Human Molecular Genetics, 20(16), 3304-3321
Human Molecular Genetics, 20(16), 3304-3321. Oxford University Press
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (16), pp.3304-21. 〈10.1093/hmg/ddr226〉
Antoniou, A C, Kartsonaki, C, Sinilnikova, O M, Soucy, P, McGuffog, L, Healey, S, Lee, A, Peterlongo, P, Manoukian, S, Peissel, B, Zaffaroni, D, Cattaneo, E, Barile, M, Pensotti, V, Pasini, B, Dolcetti, R, Giannini, G, Putignano, A L, Varesco, L, Radice, P, Mai, P L, Greene, M H, Andrulis, I L, Glendon, G, Ozcelik, H, Thomassen, M, Gerdes, A M, Kruse, T A, Jensen, U B, Cruger, D G, Caligo, M A, Laitman, Y, Milgrom, R, Kaufman, B, Paluch-Shimon, S, Friedman, E, Loman, N, Harbst, K, Lindblom, A, Arver, B, Ehrencrona, H, Melin, B, Nathanson, K L, Domchek, S M, Rebbeck, T, Jakubowska, A, Lubinski, J, Gronwald, J, Huzarski, T, Byrski, T, Cybulski, C, Gorski, B, Osorio, A, Cajal, T R Y, Fostira, F, Andres, R, Benitez, J, Hamann, U, Hogervorst, FB, Rookus, M A, Hooning, M J, Nelen, M R, van der Luijt, R B, van Os, T A M, van Asperen, C J, Devilee, P, Meijers-Heijboer, E J, Garcia, E B G, Peock, S, Cook, M, Frost, D, Platte, R, Leyland, J, Evans, D G, Lalloo, F, Eeles, R, Izatt, L, Adlard, J, Davidson, R, Eccles, D, Ong, K R, Cook, J, Douglas, F, Paterson, J, Kennedy, M J, Miedzybrodzka, Z, Godwin, A, Stoppa-Lyonnet, D, Buecher, B, Belotti, M, Tirapo, C, Mazoyer, S, Barjhoux, L, Lasset, C, Leroux, D, Faivre, L, Bronner, M, Prieur, F, Nogues, C & Chenevix-Trench, G 2011, ' Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers ', Human Molecular Genetics, vol. 20, no. 16, pp. 3304-3321 . https://doi.org/10.1093/hmg/ddr226
Human Molecular Genetics, 20, 3304-21
Human Molecular Genetics, 2011, 20 (16), pp.3304-21. ⟨10.1093/hmg/ddr226⟩
HUMAN MOLECULAR GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Human Molecular Genetics, Oxford University Press (OUP), 2011, 20 (16), pp.3304-21. ⟨10.1093/hmg/ddr226⟩
Human Molecular Genetics, 20, 16, pp. 3304-21
Antoniou, A C, Kartsonaki, C, Sinilnikova, O M, Soucy, P, McGuffog, L, Healey, S, Lee, A R, Peterlongo, P, Manoukian, S, Peissel, B, Zaffaroni, D, Cattaneo, E, Barile, M, Pensotti, V, Pasini, B, Dolcetti, R, Giannini, G, Putignano, A L, Varesco, L, Radice, P, Mai, P L, Greene, M H, Andrulis, I L, Glendon, G, Ozcelik, H, Thomassen, M, Gerdes, A-M A, Kruse, T A, Jensen, U B, Crüger, D G, Caligo, M A, Laitman, Y, Milgrom, R, Kaufman, B, Paluch-Shimon, S, Friedman, E, Loman, N, Harbst, K, Lindblom, A, Arver, B, Ehrencrona, H, Melin, B, Nathanson, K L, Domchek, S M, Rebbeck, T, Jakubowska, A, Lubinski, J, Gronwald, J, Huzarski, T, Byrski, T & SWE-BRCA 2011, ' Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers ', Human Molecular Genetics, vol. 20, no. 16, pp. 3304-21 . https://doi.org/10.1093/hmg/ddr226
Human molecular genetics, 20(16), 3304-3321. Oxford University Press
Human Molecular Genetics; Vol 20
Item does not contain fulltext Two single nucleotide polymorphisms (SNPs) at 6q25.1, near the ESR1 gene, have been implicated in the susceptibility to breast cancer for Asian (rs2046210) and European women (rs9397435). A genome-wide association study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa62c8d58971fcfcc12e6e4779410b3c
https://portal.findresearcher.sdu.dk/da/publications/04dc1a26-2ca0-466d-b794-0d33ad844578
https://portal.findresearcher.sdu.dk/da/publications/04dc1a26-2ca0-466d-b794-0d33ad844578
Autor:
Hes, F. J., Van der Luijt, R. B., Janssen, A. L.W., Zewald, R. A., De Jong, G. J., Lenders, J. W., Links, T. P., Luyten, G. P.M., Sijmons, R. H., Eussen, H. J., Halley, D. J.J., Lips, C. J.M., Pearson, P. L., van den Ouweland, A. M.W., Majoor-Krakauer, D. F.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::7461b503fd4d15c3be65ee85e2496836
https://biblio.vub.ac.be/vubir/(52e7ad94-a4c1-4844-ab22-b2edbba91763).html
https://biblio.vub.ac.be/vubir/(52e7ad94-a4c1-4844-ab22-b2edbba91763).html
Publikováno v:
Dreijerink, K M A, Roijers, J F M, Van Der Luijt, R B, Höppener, J W M & Lips, C J M 2000, ' Multipele endocriene neoplasie type I : Recente ontwikkelingen en richtlijnen voor DNA-diagnostiek en periodiek klinisch onderzoek ', Nederlands Tijdschrift voor Geneeskunde, vol. 144, no. 51, pp. 2445-2449 .
Multiple endocrine neoplasia type I (MEN-I) is an autosomal dominantly inherited disorder, characterised by the occurrence of multiple tumours, particularly in the parathyroid glands, the pancreatic islets, the pituitary gland, the adrenal glands, as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10172::792e4ded7a04f89af18b440ecae8b4d7
https://research.vumc.nl/en/publications/92f054cc-042c-4d36-8c4a-390d15f37d3c
https://research.vumc.nl/en/publications/92f054cc-042c-4d36-8c4a-390d15f37d3c