Rare germline copy number variants (CNVs) and breast cancer risk

by ABCTB Investigators, Ahearn, T.U, Andrulis, I.L, Anton-Culver, H., Antonenkova, N.N, Arndt, V., Aronson, K.J, Beckmann, M.W, Behrens, S., Benitez, J., Bermisheva, M., Bogdanova, N.V, Bojesen, S.E, Bolla, M.K, 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, CTS Consortium, Czene, K., Dennis, J., Devilee, P., Dörk, T., Dorling, L., Dossus, L., Dunning, A.M, Easton, D.F, Eliassen, A.H, Eriksson, M., Evans, D.G, Fasching, P.A, Figueroa, J., Fletcher, O., Flyger, H., Freeman, L.E.B, 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., Jager, A., Jakubowska, A., John, E.M, Johnson, N., Jones, M.E, Jung, A., Kaaks, R., kConFab/AOCS Investigators, Keeman, R., Khusnutdinova, E., Kitahara, C.M, Ko, Y.-D, Kosma, V.-M, Koutros, S., Kraft, P., Kristensen, V.N, Kubelka-Sabit, K., Kurian, A.W, Lacey, J.V, Lambrechts, D., Larson, N.L, Linet, M., Mannermaa, A., Manoukian, S., Margolin, S., Mavroudis, D., Michailidou, K., Milne, R.L, Muranen, T.A, Murphy, R.A, NBCS Collaborators, Nevanlinna, H., Ogrodniczak, A., Olson, J.E, Olsson, H., Park-Simon, T.-W, Perou, C.M, Peterlongo, P., Pharoah, P.D.P, Plaseska-Karanfilska, D., Pylkäs, K., Rennert, G., Saloustros, E., Sandler, D.P, Sawyer, E.J, Schmidt, M.K, Schmutzler, R.K, Shibli, R., Simard, J., 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., Tyrer, J.P, Vachon, C.M, Walker, L.C, Wang, Q., Wendt, C., Winqvist, R., Wolk, A., Yang, X.R, Zheng, W., Ziogas, A.
Published 2022