GENETIC EPIDEMIOLOGY Feng, H, Gusev, A, Pasaniuc, B, Wu, L, Long, J, Abu-full, Z, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antoniou, A C, Arason, A, Arndt, V, Aronson, K J, Arun, B K, Asseryanis, E, Auer, P L, Azzollini, J, Balmaña, J, Barkardottir, R B, Barnes, D R, Barrowdale, D, Beckmann, M W, Behrens, S, Benitez, J, Bermisheva, M, Białkowska, K, Blanco, A, Blomqvist, C, Boeckx, B, Bogdanova, N V, Bojesen, S E, Bolla, M K, Bonanni, B, Borg, A, Brauch, H, Brenner, H, Briceno, I, Broeks, A, Brüning, T, Burwinkel, B, Cai, Q, Caldés, T, Caligo, M A, Campbell, I, Canisius, S, Campa, D, Carter, B D, Carter, J, Skytte, A B, Thomassen, M, ABCTB Investigators, HEBON Investigators, BCFR Investigators, OCGN Investigators, GEMO Study Collaborators, EMBRACE Collaborators & GC-HBOC study Collaborators 2020, ' Transcriptome-wide association study of breast cancer risk by estrogen-receptor status ', Genetic Epidemiology, vol. 44, no. 5, pp. 442-468 . https://doi.org/10.1002/gepi.22288 Genetic Epidemiology, 44(5), 442-468. WILEY Dipòsit Digital de la UB Universidad de Barcelona Genetic Epidemiology Genetic Epidemiology, 44(5), 442-468. Wiley-Liss Inc. Genetic epidemiology Feng, H, Gusev, A, Pasaniuc, B, Wu, L, Long, J, Abu-full, Z, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antoniou, A C, Arason, A, Arndt, V, Aronson, K J, Arun, B K, Asseryanis, E, Auer, P L, Azzollini, J, Balmaña, J, Barkardottir, R B, Barnes, D R, Barrowdale, D, Beckmann, M W, Behrens, S, Benitez, J, Bermisheva, M, Białkowska, K, Blanco, A, Blomqvist, C, Boeckx, B, Bogdanova, N V, Bojesen, S E, Bolla, M K, Bonanni, B, Borg, A, Brauch, H, Brenner, H, Briceno, I, Broeks, A, Brüning, T, Burwinkel, B, Cai, Q, Caldés, T, Caligo, M A, Campbell, I, Canisius, S, GEMO Study Collaborators, EMBRACE Collaborators, GC-HBOC study Collaborators, ABCTB Investigators, HEBON Investigators, BCFR Investigators, OCGN Investigators & Skytte, A B 2020, ' Transcriptome-wide association study of breast cancer risk by estrogen-receptor status ', Genetic Epidemiology, vol. 44, no. 5, pp. 442-468 . https://doi.org/10.1002/gepi.22288 Scientia Feng, H, Gusev, A, Pasaniuc, B, Wu, L, Long, J, Abu-full, Z, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antoniou, A C, Arason, A, Arndt, V, Aronson, K J, Arun, B K, Asseryanis, E, Auer, P L, Azzollini, J, Balmaña, J, Barkardottir, R B, Barnes, D R, Barrowdale, D, Beckmann, M W, Behrens, S, Benitez, J, Bermisheva, M, Białkowska, K, Blanco, A, Blomqvist, C, Boeckx, B, Bogdanova, N V, Bojesen, S E, Bolla, M K, Bonanni, B, Borg, A, Brauch, H, Brenner, H, Briceno, I, Broeks, A, Brüning, T, Burwinkel, B, Cai, Q, Caldés, T, Caligo, M A, Campbell, I, Canisius, S, Christiansen, H, Ejlertsen, B, Flyger, H, Nielsen, F C, Wang, Q, ABCTB Investigators, HEBON Investigators, BCFR Investigators, OCGN Investigators, GEMO Study Collaborators, EMBRACE Collaborators & GC-HBOC Study Collaborators 2020, ' Transcriptome-wide association study of breast cancer risk by estrogen-receptor status ', Genetic Epidemiology, vol. 44, no. 5, pp. 442-468 . https://doi.org/10.1002/gepi.22288
Repisalud Instituto de Salud Carlos III (ISCIII) Nature Communications Nature Communications, 11(1):312. 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NATURE PUBLISHING GROUP Escala-garcia, M, Abraham, J, Andrulis, I L, Anton-culver, H, Arndt, V, Ashworth, A, Auer, P L, Auvinen, P, Beckmann, M W, Beesley, J, Behrens, S, Benitez, J, Bermisheva, M, Blomqvist, C, Blot, W, Bogdanova, N V, Bojesen, S E, Bolla, M K, Børresen-dale, A, Brauch, H, Brenner, H, Brucker, S Y, Burwinkel, B, Caldas, C, Canzian, F, Chang-claude, J, Chanock, S J, Chin, S, Clarke, C L, Couch, F J, Cox, A, Cross, S S, Czene, K, Daly, M B, Dennis, J, Devilee, P, Dunn, J A, Dunning, A M, Dwek, M, Earl, H M, Eccles, D M, Eliassen, A H, Ellberg, C, Evans, D G, Fasching, P A, Figueroa, J, Flyger, H, Gago-dominguez, M, Gapstur, S M, García-closas, M, García-sáenz, J A, Gaudet, M M, George, A, Giles, G G, Goldgar, D E, González-neira, A, Grip, M, Guénel, P, Guo, Q, Haiman, C A, Håkansson, N, Hamann, U, Harrington, P A, Hiller, L, Hooning, M J, Hopper, J L, Howell, A, Huang, C, Huang, G, Hunter, D J, Jakubowska, A, John, E M, Kaaks, R, Kapoor, P M, Keeman, R, Kitahara, C M, Koppert, L B, Kraft, P, Kristensen, V N, Lambrechts, D, Le Marchand, L, Lejbkowicz, F, Lindblom, A, Lubiński, J, Mannermaa, A, Manoochehri, M, Manoukian, S, Margolin, S, Martinez, M E, Maurer, T, Mavroudis, D, Meindl, A, Milne, R L, Mulligan, A M, Neuhausen, S L, Nevanlinna, H, Newman, W G, Olshan, A F, Olson, J E, Olsson, H, Orr, N, Peterlongo, P, Petridis, C, Prentice, R L, Presneau, N, Punie, K, Ramachandran, D, Rennert, G, Romero, A, Sachchithananthan, M, Saloustros, E, Sawyer, E J, Schmutzler, R K, Schwentner, L, Scott, C, Simard, J, Sohn, C, Southey, M C, Swerdlow, A J, Tamimi, R M, Tapper, W J, Teixeira, M R, Terry, M B, Thorne, H, Tollenaar, R A E M, Tomlinson, I, Troester, M A, Truong, T, Turnbull, C, Vachon, C M, Van Der Kolk, L E, Wang, Q, Winqvist, R, Wolk, A, Yang, X R, Ziogas, A, Pharoah, P D P, Hall, P, Wessels, L F A, Chenevix-trench, G, Bader, G D, Dörk, T, Easton, D F, Canisius, S & Schmidt, M K 2020, ' A network analysis to identify mediators of germline-driven differences in breast cancer prognosis ', Nature Communications, vol. 11, no. 1 . https://doi.org/10.1038/s41467-019-14100-6
Journal of Medical Genetics, 53(12), 800-811. BMJ Publishing Group Southey, M C, Goldgar, D E, Winqvist, R, Pylkäs, K, Couch, F, Tischkowitz, M, Foulkes, W D, Dennis, J, Michailidou, K, van Rensburg, E J, Heikkinen, T, Nevanlinna, H, Hopper, J L, Dörk, T, Claes, K B, Reis-Filho, J, Teo, Z L, Radice, P, Catucci, I, Peterlongo, P, Tsimiklis, H, Odefrey, F A, Dowty, J G, Schmidt, M K, Broeks, A, Hogervorst, F B, Verhoef, S, Carpenter, J, Clarke, C, Scott, R J, Fasching, P A, Haeberle, L, Ekici, A B, Beckmann, M W, Peto, J, Dos-Santos-Silva, I, Fletcher, O, Johnson, N, Bolla, M K, Sawyer, E J, Tomlinson, I, Kerin, M J, Miller, N, Marme, F, Bojesen, S, Nordestgaard, B G, Kjaer, S K, Høgdall, E, Høgdall, C K, Engelholm, S A & Australian Ovarian Cancer Study Group 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk : data from COGS ', Journal of Medical Genetics, vol. 53, no. 12, pp. 800-811 . https://doi.org/10.1136/jmedgenet-2016-103839 Journal of Medical Genetics, 53(12), 800-811 Southey, M C, Goldgar, D E, Winqvist, R, Pylkäs, K, Couch, F, Tischkowitz, M, Foulkes, W D, Dennis, J, Michailidou, K, van Rensburg, E J, Heikkinen, T, Nevanlinna, H, Hopper, J L, Dörk, T, Claes, K B, Reis-Filho, J, Teo, Z L, Radice, P, Catucci, I, Peterlongo, P, Tsimiklis, H, Odefrey, F A, Dowty, J G, Schmidt, M K, Broeks, A, Hogervorst, F B, Verhoef, S, Carpenter, J, Clarke, C, Scott, R J, Fasching, P A, Haeberle, L, Ekici, A B, Beckmann, M W, Peto, J, Dos-Santos-Silva, I, Fletcher, O, Johnson, N, Bolla, M K, Sawyer, E J, Tomlinson, I, Kerin, M J, Miller, N, Marme, F, Burwinkel, B, Yang, R, Guénel, P, Truong, T, Menegaux, F, Muir, K & Australian Ovarian Cancer Study Group 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk : data from COGS ', Journal of Medical Genetics, vol. 53, no. 12, pp. 800-811 . https://doi.org/10.1136/jmedgenet-2016-103839 Southey, M C, Goldgar, D, Winqvist, R, et al. & Donovan, J 2016, ' PALB2, CHEK2 and ATM rare variants and cancer risk : data from COGS ', Journal of Medical Genetics, vol. 53, no. 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