Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers
- Peterlongo, P.
- Chang-Claude, J.
- Moysich, K.B.
- Rudolph, A.
- Schmutzler, R.K.
- Simard, J.
- Soucy, P.
- Eeles, R.A.
- Easton, D.F.
- Hamann, U.
- Wilkening, S.
- Chen, B.
- Rookus, M.A.
- Schmidt, M.K.
- Baan, F.H. van der
- Spurdle, A.B.
- Walker, L.C.
- Lose, F.
- Maia, A.T.
- Montagna, M.
- Matricardi, L.
- Lubinski, J.
- Jakubowska, A.
- Garcia, E.B.
- Olopade, O.I.
- Nussbaum, R.L.
- Nathanson, K.L.
- Domchek, S.M.
- Rebbeck, T.R.
- Arun, B.K.
- Karlan, B.Y.
- Orsulic, S.
- Lester, J.
- Chung, W.K.
- Miron, A.
- Southey, M.C.
- Goldgar, D.E.
- Buys, S.S.
- Janavicius, R.
- Dorfling, C.M.
- Rensburg, E.J. van
- Ding, Y.C.
- Neuhausen, S.L.
- Hansen, T.V.
- Gerdes, A.M.
- Ejlertsen, B.
- Jonson, L.
- Osorio, A.
- Martinez-Bouzas, C.
- Benitez, J.
- Conway, E.E.
- Blazer, K.R.
- Weitzel, J.N.
- Manoukian, S.
- Peissel, B.
- Zaffaroni, D.
- Scuvera, G.
- Barile, M.
- Ficarazzi, F.
- Mariette, F.
- Fortuzzi, S.
- Viel, A.
- Giannini, G.
- Papi, L.
- Martayan, A.
- Tibiletti, M.G.
- Radice, P.
- Vratimos, A.
- Fostira, F.
- Garber, J.E.
- Donaldson, A.
- Brewer, C.
- Foo, C.
- Evans, D.G.
- Frost, D.
- Eccles, D.
- Brady, A.
- Cook, J.
- Tischkowitz, M.
- Adlard, J.
- Barwell, J.
- Izatt, L.
- Side, L.E.
- Kennedy, M.J.
- Rogers, M.T.
- Porteous, M.E.
- Morrison, P.J.
- Platte, R.
- Davidson, R.
- Hodgson, S.V.
- Ellis, S.
- Cole, T.
- Godwin, A.K.
- Claes, K.
- Maerken, T. Van
- Meindl, A.
- Gehrig, A.
- Sutter, C.
- Engel, C.
- Hoogerbrugge, N.
- et al.
DOIAbstract
BACKGROUND: BRCA1 and BRCA2 mutation carriers are at substantially increased risk for developing breast and ovarian cancer. The incomplete penetrance coupled with the variable age at diagnosis in carriers of the same mutation suggests the existence of genetic and nongenetic modifying factors. In this study, we evaluated the putative role of variants in many candidate modifier genes. METHODS: Genotyping data from 15,252 BRCA1 and 8,211 BRCA2 mutation carriers, for known variants (n = 3,248) located within or around 445 candidate genes, were available through the iCOGS custom-designed array. Breast and ovarian cancer association analysis was performed within a retrospective cohort approach. RESULTS: The observed P values of association ranged...
Add to ORKG