Genetics in Medicine, 22(10), 1653-1666. Lippincott Williams and Wilkins Genetics in Medicine Genetics in Medicine, 2020, 22 (10), pp.1653-1666. ⟨10.1038/s41436-020-0862-x⟩ Scientia Barnes, D R, Rookus, M A, McGuffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L L, Chung, W K, Claes, K B M, Colas, C, Collonge-Rame, M A, Cook, J, Daly, M B, Davidson, R, de la Hoya, M, de Putter, R, Delnatte, C, Devilee, P, Horvath, J, Nielsen, F C, Pedersen, I S, GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators, GENEPSO Investigators & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x Barnes, D R, Rookus, M A, Mcguffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L L, Chung, W K, Claes, K B M, Colas, C, Collonge-rame, M, Cook, J, Daly, M B, Davidson, R, De La Hoya, M, De Putter, R, Delnatte, C, Devilee, P, Ejlertsen, B, Gerdes, A, Nielsen, F C & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x Barnes, D R, Rookus, M A, McGuffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L L, Chung, W K, Claes, K B M, Colas, C, Collonge-Rame, M-A, Cook, J, Daly, M B, Davidson, R, de la Hoya, M, de Putter, R, Delnatte, C, Devilee, P, Diez, O, Ding, Y C & Pedersen, I S 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x Genetics in Medicine, 22(10), 1653-1666. Nature Publishing Group Genetics in Medicine, 22(10), 1653-1666. Lippincott Williams & Wilkins Genetics in Medicine, 22(10), 1653-1666. SPRINGERNATURE Genetics in Medicine, Nature Publishing Group, 2020, 22 (10), pp.1653-1666. ⟨10.1038/s41436-020-0862-x⟩ Barnes, D R, Rookus, M A, McGuffog, L, Leslie, G, Mooij, T M, Dennis, J, Mavaddat, N, Adlard, J, Ahmed, M, Aittomäki, K, Andrieu, N, Andrulis, I L, Arnold, N, Arun, B K, Azzollini, J, Balmaña, J, Barkardottir, R B, Barrowdale, D, Benitez, J, Berthet, P, Białkowska, K, Blanco, A M, Blok, M J, Bonanni, B, Boonen, S E, Borg, Å, Bozsik, A, Bradbury, A R, Brennan, P, Brewer, C, Brunet, J, Buys, S S, Caldés, T, Caligo, M A, Campbell, I, Christensen, L-L, Chung, W K, Claes, K B M, Colas, C, Collonge-Rame, M A, Cook, J, Daly, M B, Davidson, R, de la Hoya, M, de Putter, R, Gerdes, A M, Kruse, T A, Pedersen, I S, Rønlund, K, Thomassen, M, GEMO Study Collaborators, EMBRACE Collaborators, kConFab Investigators, HEBON Investigators, GENEPSO Investigators & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x Genetics in Medicine, 22, 1653-1666 GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators, GENEPSO Investigators & Consortium of Investigators of Modifiers of BRCA and BRCA2 2020, ' Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants ', Genetics in Medicine, vol. 22, no. 10, pp. 1653-1666 . https://doi.org/10.1038/s41436-020-0862-x Dipòsit Digital de la UB Universidad de Barcelona GENETICS IN MEDICINE Genetics in Medicine, 22, 10, pp. 1653-1666
Human Mutation Human Mutation, Wiley, 2018, 39 (5), pp.593-620. ⟨10.1002/humu.23406⟩ Dipòsit Digital de la UB Universidad de Barcelona Rebbeck, T R, Friebel, T M, Friedman, E, Hamann, U, Huo, D, Kwong, A, Olah, E, Olopade, O I, Solano, A R, Teo, S-H, Thomassen, M, Weitzel, J N, Chan, T L, Couch, F J, Goldgar, D E, Kruse, T A, Palmero, E I, Park, S K, Torres, D, van Rensburg, E J, McGuffog, L, Parsons, M T, Leslie, G, Aalfs, C M, Abugattas, J, Adlard, J, Agata, S, Aittomäki, K, Andrews, L, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Asseryanis, E, Auerbach, L, Azzollini, J, Balmaña, J, Barile, M, Barkardottir, R B, Barrowdale, D, Benitez, J, Berger, A, Berger, R, Blanco, A M, Blazer, K R, Blok, M J, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caldes, T, Caliebe, A, Caligo, M A, Campbell, I, Caputo, S M, Chiquette, J, Chung, W K, Claes, K B M, Collée, J M, Cook, J, Davidson, R, de la Hoya, M, De Leeneer, K, de Pauw, A, Delnatte, C, Diez, O, Ding, Y C, Ditsch, N, Domchek, S M, Dorfling, C M, Velazquez, C, Dworniczak, B, Eason, J, Easton, D F, Eeles, R, Ehrencrona, H, Ejlertsen, B, EMBRACE, Engel, C, Engert, S, Evans, D G, Faivre, L, Feliubadaló, L, Ferrer, S F, Foretova, L, Fowler, J, Frost, D, Galvão, H C R, Ganz, P A, Garber, J, Gauthier-Villars, M, Gehrig, A, GEMO Study Collaborators, Gerdes, A-M, Gesta, P, Giannini, G, Giraud, S, Glendon, G, Godwin, A K, Greene, M H, Gronwald, J, Gutierrez-Barrera, A, Hahnen, E, Hauke, J, HEBON, Henderson, A, Hentschel, J, Hogervorst, F B L, Honisch, E, Imyanitov, E N, Isaacs, C, Izatt, L, Izquierdo, A, Jakubowska, A, James, P, Janavicius, R, Jensen, U B, John, E M, Vijai, J, Kaczmarek, K, Karlan, B Y, Kast, K, KConFab Investigators, Kim, S-W, Konstantopoulou, I, Korach, J, Laitman, Y, Lasa, A, Lasset, C, Lázaro, C, Lee, A, Lee, M H, Lester, J, Lesueur, F, Liljegren, A, Lindor, N M, Longy, M, Loud, J T, Lu, K H, Lubinski, J, Machackova, E, Manoukian, S, Mari, V, Martínez-Bouzas, C, Matrai, Z, Mebirouk, N, Meijers-Heijboer, H E J, Meindl, A, Mensenkamp, A, Mickys, U, Miller, A, Montagna, M, Moysich, K B, Mulligan, A M, Musinsky, J, Neuhausen, S L, Nevanlinna, H, Ngeow, J, Nguyen, H P, Niederacher, D, Nielsen, H R, Nielsen, F C, Nussbaum, R L, Offit, K, Öfverholm, A, Ong, K-R, Osorio, A, Papi, L, Papp, J, Pasini, B, Pedersen, I S, Peixoto, A, Peruga, N, Peterlongo, P, Pohl, E, Pradhan, N, Prajzendanc, K, Prieur, F, Pujol, P, Radice, P, Ramus, S J, Rantala, J, Rashid, M U, Rhiem, K, Robson, M, Rodriguez, G C, Rogers, M T, Rudaitis, V, Schmidt, A Y, Schmutzler, R K, Senter, L, Shah, P D, Sharma, P, Side, L E, Simard, J, Singer, C F, Skytte, A-B, Slavin, T P, Snape, K, Sobol, H, Southey, M C, Steele, L, Steinemann, D, Sukiennicki, G, Sutter, C, Szabo, C I, Tan, Y Y, Teixeira, M R, Terry, M B, Teulé, A, Thomas, A, Thull, D L, Tischkowitz, M, Tognazzo, S, Toland, A E, Topka, S, Trainer, A H, Tung, N, van Asperen, C J, van der Hout, A H, van der Kolk, L E, van der Luijt, R B, Van Heetvelde, M, Varesco, L, Varon-Mateeva, R, Vega, A, Villarreal-Garza, C, von Wachenfeldt, A, Walker, L, Wang-Gohrke, S, Wappenschmidt, B, Weber, B H F, Yannoukakos, D, Yoon, S-Y, Zanzottera, C, Zidan, J, Zorn, K K, Selkirk, C G H, Hulick, P J, Chenevix-Trench, G, Spurdle, A B, Antoniou, A C & Nathanson, K L 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406 Jensen, U B 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. ' . https://doi.org/10.1002/humu.23406 Human Mutation, 39, 5, pp. 593-620 Human Mutation, 39(5), 593-620. Wiley Human Mutation: Variation, Informatics and Disease, 39(5), 593-620 Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid Consejería de Sanidad de la Comunidad de Madrid Rebbeck, T R, Friebel, T M, Friedman, E, Hamann, U, Huo, D, Kwong, A, Olah, E, Olopade, O I, Solano, A R, Teo, S-H, Thomassen, M, Weitzel, J N, Chan, T L, Couch, F J, Goldgar, D E, Kruse, T A, Palmero, E I, Park, S K, Torres, D, van Rensburg, E J, McGuffog, L, Parsons, M T, Leslie, G, Aalfs, C M, Abugattas, J, Adlard, J, Agata, S, Aittomäki, K, Andrews, L, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Asseryanis, E, Auerbach, L, Azzollini, J, Balmaña, J, Barile, M, Barkardottir, R B, Barrowdale, D, Benitez, J, Berger, A, Berger, R, Blanco, A M, Blazer, K R, Blok, M J, Bonadona, V, Gerdes, A-M, Nielsen, H R, Skytte, A-B & EMBRACE 2018, ' Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406 HUMAN MUTATION r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau instname Human Mutation, 39, 593-620 Human Mutation, 39(5), 593-620. Wiley-Liss Inc. Digital.CSIC. Repositorio Institucional del CSIC EMBRACE, GEMO Study Collaborators, HEBON & KConFab Investigators 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406 EMBRACE 2018, ' Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations ', Human Mutation, vol. 39, no. 5, pp. 593-620 . https://doi.org/10.1002/humu.23406 Human mutation, 39(5), 593-620. Wiley-Liss Inc. The CIMBA Consortium & Evans, D G 2018, ' Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations ', Human Mutation . https://doi.org/10.1002/humu.23406 Rebbeck, TR; Friebel, TM; Friedman, E; Hamann, U; Huo, D; Kwong, A; et al.(2018). Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations. HUMAN MUTATION, 39(5), 593-620. doi: 10.1002/humu.23406. UCLA: Retrieved from: http://www.escholarship.org/uc/item/3q49q09h
Couch, F J, Kuchenbaecker, K B, Michailidou, K, Mendoza-Fandino, G A, Nord, S, Lilyquist, J, Olswold, C, Hallberg, E, Agata, S, Ahsan, H, Aittomäki, K, Ambrosone, C, Andrulis, I L, Anton-Culver, H, Arndt, V, Arun, B K, Arver, B, Barile, M, Barkardottir, R B, Barrowdale, D, Beckmann, L, Beckmann, M W, Benítez, J, Blank, S V, Blomqvist, C, Bogdanova, N V, Bojesen, S E, Bolla, M K, Bonanni, B, Brauch, H, Brenner, H, Burwinkel, B, Buys, S, Caldes, T, Caligo, M A, Canzian, F, Carpenter, J, Chang-Claude, J, Chanock, S J, Chung, W K, Claes, K B M, Cox, A, Cross, S S, Cunningham, J M, Czene, K, Daly, M B, Damiola, F, Darabi, H, de la Hoya, M, Devilee, P, Díez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Dos Santos Silva, I, Dumont, M, Dunning, A M, Eccles, D M, Ehrencrona, H, Ekici, A B, Eliassen, H, Ellis, S, Fasching, P A, Figueroa, J, Flesch-Janys, D, Försti, A, Fostira, F, Foulkes, W D, Friebel, T M, Friedman, E, Frost, D, Gabrielson, M, Gammon, M D, Ganz, P A, Gapstur, S M, Garber, J, Gaudet, M, Gayther, S A, Gerdes, A-M, Ghoussaini, M, Giles, G, Glendon, G, Godwin, A K, Goldberg, M S, Goldgar, D E, González-Neira, A, Greene, M H, Gronwald, J, Guénel, P, Gunter, M J, Haeberle, L, Haiman, C A, Hamann, U, Hansen, T V O, Hart, S, Healey, S, Heikkinen, T, Henderson, B E, Herzog, J, Hogervorst, F B L, Hollestelle, A, Hooning, M J, Hoover, R N, Hopper, J L, Humphreys, K, Hunter, D J, Huzarski, T, Imyanitov, E N, Isaacs, C, Jakubowska, A, James, P A, Janavicius, R, Jensen, U B, John, E M, Jones, M, Kabisch, M, Kar, S, Karlan, B Y, Khan, S, Khaw, K-T, Kibriya, M G, Knight, J A, Ko, Y-D, Konstantopoulou, I, Kosma, V-M, Kristensen, V, Kwong, A, Laitman, Y, Lambrechts, D, Lázaro, C, Lee, E, Le Marchand, L, Lester, J, Lindblom, A, Lindor, N, Lindstrom, S, Liu, J, Long, J, Lubinski, J, Mai, P L, Makalic, E, Malone, K E, Mannermaa, A, Manoukian, S, Margolin, S, Marme, F, Martens, J W M, McGuffog, L, Meindl, A, Miller, A, Milne, R L, Miron, P, Montagna, M, Mazoyer, S, Mulligan, A M, Muranen, T A, Nathanson, K L, Neuhausen, S L, Nevanlinna, H, Nordestgaard, B G, Nussbaum, R L, Offit, K, Olah, E, Olopade, O I, Olson, J E, Osorio, A, Park, S K, Peeters, P H M, Peissel, B, Peterlongo, P, Peto, J, Phelan, C M, Pilarski, R, Poppe, B, Pylkäs, K, Radice, P, Rahman, N, Rantala, J, Rappaport, C, Rennert, G, Richardson, A, Robson, M, Romieu, I, Rudolph, A, Rutgers, E J, Sánchez, M-J, Santella, R M, Sawyer, E J, Schmidt, D F, Schmidt, M K, Schmutzler, R K, Schumacher, F, Scott, R J, Senter, L, Sharma, P, Simard, J, Singer, C F, Sinilnikova, O M, Soucy, P, Southey, M, Steinemann, D, Stenmark Askmalm, M, Stoppa-Lyonnet, D, Swerdlow, A, Szabo, C I, Tamimi, R, Tapper, W, Teixeira, M R, Teo, S-H, Terry, M B, Thomassen, M, Thompson, D J, Tihomirova, L, Toland, A E, Tollenaar, R A E M, Tomlinson, I, Truong, T, Tsimiklis, H, Teulé, A, Tumino, R, Tung, N, Turnbull, C, Ursin, G, van Deurzen, C H M, van Rensburg, E J, Varon-Mateeva, R, Wang, Z, Wang-Gohrke, S, Weiderpass, E, Weitzel, J N, Whittemore, A S, Wildiers, H, Winqvist, R, Yang, X R, Yannoukakos, D, Yao, S, Zamora, M P, Zheng, W, Hall, P, Kraft, P, Vachon, C, Slager, S, Chenevix-Trench, G, Pharoah, P D P, Monteiro, A N A, Garcia-Closas, M, Easton, D F & Antoniou, A C 2016, ' Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer ', Nature Communications, vol. 7, 11375 . https://doi.org/10.1038/ncomms11375 Recercat. Dipósit de la Recerca de Catalunya instname Repisalud Instituto de Salud Carlos III (ISCIII) Dipòsit Digital de Documents de la UAB Universitat Autònoma de Barcelona Nature Communications Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid Consejería de Sanidad de la Comunidad de Madrid NATURE COMMUNICATIONS Nature Communications, 7 Tomlinson, I 2016, ' Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer ', Nature Communications, vol. 7, 11375 . https://doi.org/10.1038/ncomms11375 Nature Communications, Vol 7, Iss 1, Pp 1-13 (2016) Nature Communications [E], 7. Nature Publishing Group Couch, F J, Kuchenbaecker, K B, Michailidou, K, Mendoza-Fandino, G A, Nord, S, Lilyquist, J, Olswold, C, Hallberg, E, Agata, S, Ahsan, H, Aittomäki, K, Ambrosone, C, Andrulis, I L, Anton-Culver, H, Arndt, V, Arun, B K, Arver, B, Barile, M, Barkardottir, R B, Barrowdale, D, Beckmann, L, Beckmann, M W, Benitez, J, Blank, S V, Blomqvist, C, Bogdanova, N V, Bojesen, S E, Bolla, M K, Bonanni, B, Brauch, H, Brenner, H, Burwinkel, B, Buys, S S, Caldes, T, Caligo, M A, Canzian, F, Carpenter, J, Chang-Claude, J, Chanock, S J, Chung, W K, Claes, K B M, Cox, A, Cross, S S, Cunningham, J M, Czene, K, Daly, M B, Damiola, F, Darabi, H, de la Hoya, M, Devilee, P, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Dos-Santos-Silva, I, Dumont, M, Dunning, A M, Eccles, D M, Ehrencrona, H, Ekici, A B, Eliassen, H, Ellis, S, Fasching, P A, Figueroa, J, Flesch-Janys, D, Försti, A, Fostira, F, Foulkes, W D, Friebel, T, Friedman, E, Frost, D, Gabrielson, M, Gammon, M D, Ganz, P A, Gapstur, S M, Garber, J, Gaudet, M M, Gayther, S A, Gerdes, A-M, Ghoussaini, M, Giles, G G, Glendon, G, Godwin, A K, Goldberg, M S, Goldgar, D E, González-Neira, A, Greene, M H, Gronwald, J, Guénel, P, Gunter, M, Haeberle, L, Haiman, C A, Hamann, U, Hansen, T V O, Hart, S, Healey, S, Heikkinen, T, Henderson, B E, Herzog, J, Hogervorst, F B L, Hollestelle, A, Hooning, M J, Hoover, R N, Hopper, J L, Humphreys, K, Hunter, D J, Huzarski, T, Imyanitov, E N, Isaacs, C, Jakubowska, A, James, P, Janavicius, R, Jensen, U B, John, E M, Jones, M, Kabisch, M, Kar, S, Karlan, B Y, Khan, S, Khaw, K-T, Kibriya, M G, Knight, J A, Ko, Y-D, Konstantopoulou, I, Kosma, V-M, Kristensen, V, Kwong, A, Laitman, Y, Lambrechts, D, Lazaro, C, Lee, E, Le Marchand, L, Lester, J, Lindblom, A, Lindor, N, Lindstrom, S, Liu, J, Long, J, Lubinski, J, Mai, P L, Makalic, E, Malone, K E, Mannermaa, A, Manoukian, S, Margolin, S, Marme, F, Martens, J W M, McGuffog, L, Meindl, A, Miller, A, Milne, R L, Miron, P, Montagna, M, Mazoyer, S, Mulligan, A M, Muranen, T A, Nathanson, K L, Neuhausen, S L, Nevanlinna, H, Nordestgaard, B G, Nussbaum, R L, Offit, K, Olah, E, Olopade, O I, Olson, J E, Osorio, A, Park, S K, Peeters, P H, Peissel, B, Peterlongo, P, Peto, J, Phelan, C M, Pilarski, R, Poppe, B, Pylkäs, K, Radice, P, Rahman, N, Rantala, J, Rappaport, C, Rennert, G, Richardson, A, Robson, M, Romieu, I, Rudolph, A, Rutgers, E J, Sanchez, M-J, Santella, R M, Sawyer, E J, Schmidt, D F, Schmidt, M K, Schmutzler, R K, Schumacher, F, Scott, R, Senter, L, Sharma, P, Simard, J, Singer, C F, Sinilnikova, O M, Soucy, P, Southey, M, Steinemann, D, Stenmark-Askmalm, M, Stoppa-Lyonnet, D, Swerdlow, A, Szabo, C I, Tamimi, R, Tapper, W, Teixeira, M R, Teo, S-H, Terry, M B, Thomassen, M, Thompson, D, Tihomirova, L, Toland, A E, Tollenaar, R A E M, Tomlinson, I, Truong, T, Tsimiklis, H, Teulé, A, Tumino, R, Tung, N, Turnbull, C, Ursin, G, van Deurzen, C H M, van Rensburg, E J, Varon-Mateeva, R, Wang, Z, Wang-Gohrke, S, Weiderpass, E, Weitzel, J N, Whittemore, A, Wildiers, H, Winqvist, R, Yang, X R, Yannoukakos, D, Yao, S, Zamora, M P, Zheng, W, Hall, P, Kraft, P, Vachon, C, Slager, S, Chenevix-Trench, G, Pharoah, P D P, Monteiro, A A N, García-Closas, M, Easton, D F & Antoniou, A C 2016, ' Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer ', Nature Communications, vol. 7, 11375 . https://doi.org/10.1038/ncomms11375 Nature Communications, 7:11375. 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