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Lei, Jieping, Rudolph, Anja, Moysich, Kirsten B., Behrens, Sabine, Goode, Ellen L., Bolla, Manjeet K., Dennis, Joe, Dunning, Alison M., Easton, Douglas F., Wang, Qin, Benitez, Javier, Hopper, John L., Southey, Melissa C., Schmidt, Marjanka K., Broeks, Annegien, Fasching, Peter A., Haeberle, Lothar, Peto, Julian, dos-Santos-Silva, Isabel, Sawyer, Elinor J., Tomlinson, Ian, Burwinkel, Barbara, Marme, Frederik, Guenel, Pascal ORCID: 0000-0002-8359-518X, Truong, Therese, Bojesen, Stig E., Flyger, Henrik, Nielsen, Sune F., Nordestgaard, Borge G., Gonzalez-Neira, Anna
ORCID: 0000-0002-5421-2020, Menendez, Primitiva, Anton-Culver, Hoda, Neuhausen, Susan L., Brenner, Hermann
ORCID: 0000-0002-6129-1572, Arndt, Volker
ORCID: 0000-0001-9320-8684, Meindl, Alfons, Schmutzler, Rita K., Brauch, Hiltrud
ORCID: 0000-0001-7531-2736, Hamann, Ute, Nevanlinna, Heli, Fagerholm, Rainer, Doerk, Thilo, Bogdanova, Natalia V., Mannermaa, Arto, Hartikainen, Jaana M., Van Dijck, Laurien, Smeets, Ann, Flesch-Janys, Dieter, Eilber, Ursula, Radice, Paolo
ORCID: 0000-0001-6298-4111, Peterlongo, Paolo
ORCID: 0000-0001-6951-6855, Couch, Fergus J., Hallberg, Emily, Giles, Graham G., Milne, Roger L., Haiman, Christopher A., Schumacher, Fredrick
ORCID: 0000-0002-3073-7463, Simard, Jacques, Goldberg, Mark S., Kristensen, Vessela, Borresen-Dale, Anne-Lise, Zheng, Wei
ORCID: 0000-0003-1226-070X, Beeghly-Fadiel, Alicia, Winqvist, Robert, Grip, Mervi, Andrulis, Irene L., Glendon, Gord, Garcia-Closas, Montserrat, Figueroa, Jonine, Czene, Kamila, Brand, Judith S.
ORCID: 0000-0002-3720-1274, Darabi, Hatef, Eriksson, Mikael, Hall, Per, Li, Jingmei
ORCID: 0000-0001-8587-7511, Cox, Angela
ORCID: 0000-0002-5138-1099, Cross, Simon S., Pharoah, Paul D. P., Shah, Mitul, Kabisch, Maria, Torres, Diana, Jakubowska, Anna
ORCID: 0000-0002-5650-0501, Lubinski, Jan
ORCID: 0000-0003-2931-3003, Ademuyiwa, Foluso, Ambrosone, Christine B., Swerdlow, Anthony
ORCID: 0000-0001-5550-4159, Jones, Michael
ORCID: 0000-0001-7479-3451 and Chang-Claude, Jenny
(2016).
Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium.
Hum. Genet., 135 (1).
S. 137 - 155.
NEW YORK:
SPRINGER.
ISSN 1432-1203