| 2022-01-18 | Rare germline copy number variants (CNVs) and breast cancer risk. | Dennis, J; Tyrer, JP; Walker, LC; Michailidou, K; Dorling, L; Bolla, MK; Wang, Q; Ahearn, TU; Andrulis, IL; Anton-Culver, H; Antonenkova, NN; Arndt, V; Aronson, KJ; Freeman, LEB; Beckmann, MW; Behrens, S; Benitez, J; Bermisheva, M; Bogdanova, NV; Bojesen, SE; Brenner, H; Castelao, JE; Chang-Claude, J; Chenevix-Trench, G; Clarke, CL; NBCS Collaborators,; Collée, JM; CTS Consortium,; Couch, FJ; Cox, A; Cross, SS; Czene, K; Devilee, P; Dörk, T; Dossus, L; Eliassen, AH; Eriksson, M; Evans, DG; Fasching, PA; Figueroa, J; Fletcher, O; Flyger, H; Fritschi, L; Gabrielson, M; Gago-Dominguez, M; García-Closas, M; Giles, GG; González-Neira, A; Guénel, P; Hahnen, E; Haiman, CA; Hall, P; Hollestelle, A; Hoppe, R; Hopper, JL; Howell, A; ABCTB Investigators,; kConFab/AOCS Investigators,; Jager, A; Jakubowska, A; John, EM; Johnson, N; Jones, ME; Jung, A; Kaaks, R; Keeman, R; Khusnutdinova, E; Kitahara, CM; Ko, Y-D; Kosma, V-M; Koutros, S; Kraft, P; Kristensen, VN; Kubelka-Sabit, K; Kurian, AW; Lacey, JV; Lambrechts, D; Larson, NL; Linet, M; Ogrodniczak, A; Mannermaa, A; Manoukian, S; Margolin, S; Mavroudis, D; Milne, RL; Muranen, TA; Murphy, RA; Nevanlinna, H; Olson, JE; Olsson, H; Park-Simon, T-W; Perou, CM; Peterlongo, P; Plaseska-Karanfilska, D; Pylkäs, K; Rennert, G; Saloustros, E; Sandler, DP; Sawyer, EJ; Schmidt, MK; Schmutzler, RK; Shibli, R; Smeets, A; Soucy, P; Southey, MC; Swerdlow, AJ; Tamimi, RM; Taylor, JA; Teras, LR; Terry, MB; Tomlinson, I; Troester, MA; Truong, T; Vachon, CM; Wendt, C; Winqvist, R; Wolk, A; Yang, XR; Zheng, W; Ziogas, A; Simard, J; Dunning, AM; Pharoah, PDP; Easton, DF |
