Dennis, J, Tyrer, J P, Walker, L C, Michailidou, K, Dorling, L, Bolla, M K, Wang, Q, Ahearn, T U, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Arndt, V, Aronson, K J, Freeman, L E B, Beckmann, M W, Behrens, S, Benitez, J, Bermisheva, M, Bogdanova, N V, Bojesen, S E, Brenner, H, Castelao, J E, Chang-Claude, J, Chenevix-Trench, G, Clarke, C L, Collée, J M, Couch, F J, Cox, A, Cross, S S, Czene, K, Devilee, P, Dörk, T, Dossus, L, Eliassen, A H, Eriksson, M, Evans, D G, Fasching, P A, Figueroa, J, Fletcher, O, Flyger, H, Fritschi, L, Gabrielson, M, Gago-Dominguez, M, García-Closas, M, Giles, G G, González-Neira, A, Guénel, P, Hahnen, E, Haiman, C A, Hall, P, NBCS Collaborators, CTS Consortium, ABCTB Investigators & kConFab/AOCS Investigators 2022, ' Rare germline copy number variants (CNVs) and breast cancer risk ', Communications Biology, vol. 5, no. 1, pp. 65 . https://doi.org/10.1038/s42003-021-02990-6 Dennis, J, Tyrer, J P, Walker, L C, Michailidou, K, Dorling, L, Bolla, M K, Wang, Q, Ahearn, T U, Andrulis, I L, Anton-culver, H, Antonenkova, N N, Arndt, V, Aronson, K J, Freeman, L E B, Beckmann, M W, Behrens, S, Benitez, J, Bermisheva, M, Bogdanova, N V, Bojesen, S E, Brenner, H, Castelao, J E, Chang-claude, J, Chenevix-trench, G, Clarke, C L, Kristensen, V N, Sahlberg, K K, Børresen-dale, A, Gram, I T, Engebråten, O, Naume, B, Geisler, J, Alnæs, G I G, Collée, J M, Lacey, J, Martinez, E, Couch, F J, Cox, A, Cross, S S, Czene, K, Devilee, P, Dörk, T, Dossus, L, Eliassen, A H, Eriksson, M, Evans, D G, Fasching, P A, Figueroa, J, Fletcher, O, Flyger, H, Fritschi, L, Gabrielson, M, Gago-dominguez, M, García-closas, M, Giles, G G, González-neira, A, Guénel, P, Hahnen, E, Haiman, C A, Hall, P, Hollestelle, A, Hoppe, R, Hopper, J L, Howell, A, Clarke, C, Carpenter, J, Marsh, D, Scott, R, Baxter, R, Yip, D, Davis, A, Pathmanathan, N, Simpson, P, Graham, D, Sachchithananthan, M, Campbell, I, De Fazio, A, Fox, S, Kirk, J, Lindeman, G, Milne, R L, Southey, M C, Spurdle, A, Thorne, H, Jager, A, Jakubowska, A, John, E M, Johnson, N, Jones, M E, Jung, A, Kaaks, R, Keeman, R, Khusnutdinova, E, Kitahara, C M, Ko, Y, Kosma, V, Koutros, S, Kraft, P, Kristensen, V N, Kubelka-sabit, K, Kurian, A W, Lacey, J V, Lambrechts, D, Larson, N L, Linet, M, Ogrodniczak, A, Mannermaa, A, Manoukian, S, Margolin, S, Mavroudis, D, Milne, R L, Muranen, T A, Murphy, R A, Nevanlinna, H, Olson, J E, Olsson, H, Park-simon, T, Perou, C M, Peterlongo, P, Plaseska-karanfilska, D, Pylkäs, K, Rennert, G, Saloustros, E, Sandler, D P, Sawyer, E J, Schmidt, M K, Schmutzler, R K, Shibli, R, Smeets, A, Soucy, P, Southey, M C, Swerdlow, A J, Tamimi, R M, Taylor, J A, Teras, L R, Terry, M B, Tomlinson, I, Troester, M A, Truong, T, Vachon, C M, Wendt, C, Winqvist, R, Wolk, A, Yang, X R, Zheng, W, Ziogas, A, Simard, J, Dunning, A M, Pharoah, P D P & Easton, D F 2022, ' Rare germline copy number variants (CNVs) and breast cancer risk ', Communications biology, vol. 5, no. 1 . https://doi.org/10.1038/s42003-021-02990-6 Communications Biology, 5(1). NATURE PORTFOLIO Communications Biology, Vol 5, Iss 1, Pp 1-15 (2022) Communications Biology, 5(1):65. Springer Nature Communications Biology
Michailidou, K., J. Beesley, S. Lindstrom, S. Canisius, J. Dennis, M. Lush, M. J. Maranian, et al. 2015. “Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.” Nature genetics 47 (4): 373-380. doi:10.1038/ng.3242. http://dx.doi.org/10.1038/ng.3242.