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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers.

Antoniou, AC; Kuchenbaecker, KB; Soucy, P; Beesley, J; Chen, X; McGuffog, L; Lee, A; Barrowdale, D; Healey, S; Sinilnikova, OM; et al. Antoniou, AC; Kuchenbaecker, KB; Soucy, P; Beesley, J; Chen, X; McGuffog, L; Lee, A; Barrowdale, D; Healey, S; Sinilnikova, OM; Caligo, MA; Loman, N; Harbst, K; Lindblom, A; Arver, B; Rosenquist, R; Karlsson, P; Nathanson, K; Domchek, S; Rebbeck, T; Jakubowska, A; Lubinski, J; Jaworska, K; Durda, K; Złowowcka-Perłowska, E; Osorio, A; Durán, M; Andrés, R; Benítez, J; Hamann, U; Hogervorst, FB; van Os, TA; Verhoef, S; Meijers-Heijboer, HE; Wijnen, J; Gómez Garcia, EB; Ligtenberg, MJ; Kriege, M; Collée, JM; Ausems, MG; Oosterwijk, JC; Peock, S; Frost, D; Ellis, SD; Platte, R; Fineberg, E; Evans, DG; Lalloo, F; Jacobs, C; Eeles, R; Adlard, J; Davidson, R; Cole, T; Cook, J; Paterson, J; Douglas, F; Brewer, C; Hodgson, S; Morrison, PJ; Walker, L; Rogers, MT; Donaldson, A; Dorkins, H; Godwin, AK; Bove, B; Stoppa-Lyonnet, D; Houdayer, C; Buecher, B; de Pauw, A; Mazoyer, S; Calender, A; Léoné, M; Bressac-de Paillerets, B; Caron, O; Sobol, H; Frenay, M; Prieur, F; Ferrer, SU; Mortemousque, I; Buys, S; Daly, M; Miron, A; Terry, MU; Hopper, JL; John, EM; Southey, M; Goldgar, D; Singer, CF; Fink-Retter, A; Tea, MK; Kaulich, DU; Hansen, TV; Nielsen, FC; Barkardottir, RB; Gaudet, M; Kirchhoff, T; Joseph, V; Dutra-Clarke, A; Offit, K; Piedmonte, M; Kirk, J; Cohn, D; Hurteau, J; Byron, J; Fiorica, J; Toland, AE; Montagna, M; Oliani, C; Imyanitov, E; Isaacs, C; Tihomirova, L; Blanco, I; Lazaro, C; Teulé, A; Valle, JD; Gayther, SA; Odunsi, K; Gross, J; Karlan, BY; Olah, E; Teo, SH; Ganz, PA; Beattie, MS; Dorfling, CM; van Rensburg, EU; Diez, O; Kwong, A; Schmutzler, RK; Wappenschmidt, B; Engel, C; Meindl, A; Ditsch, N; Arnold, N; Heidemann, S; Niederacher, D; Preisler-Adams, S; Gadzicki, D; Varon-Mateeva, R; Deissler, H; Gehrig, A; Sutter, C; Kast, K; Fiebig, B; Schäfer, D; Caldes, T; de la Hoya, M; Nevanlinna, H; Muranen, TA; Lespérance, B; Spurdle, AB; Neuhausen, SL; Ding, YC; Wang, X; Fredericksen, Z; Pankratz, VS; Lindor, NM; Peterlongo, P; Manoukian, S; Peissel, B; Zaffaroni, D; Bonanni, B; Bernard, L; Dolcetti, R; Papi, L; Ottini, L; Radice, P; Greene, MH; Loud, JT; Andrulis, IL; Ozcelik, H; Mulligan, AU; Glendon, G; Thomassen, M; Gerdes, AM; Jensen, UB; Skytte, AB; Kruse, TA; Chenevix-Trench, G; Couch, FJ; Simard, J; Easton, DF; CIMBA, SWE-BRCA; HEBON; EMBRACE; GEMO Collaborators Study; kConFab Investigators (2012) Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. Breast Cancer Res, 14 (1). R33 - ?. https://doi.org/10.1186/bcr3121

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Abstract

Several common alleles have been shown to be associated with breast and/or ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. Recent genome-wide association studies of breast cancer have identified eight additional breast cancer susceptibility loci: rs1011970 (9p21, CDKN2A/B), rs10995190 (ZNF365), rs704010 (ZMIZ1), rs2380205 (10p15), rs614367 (11q13), rs1292011 (12q24), rs10771399 (12p11 near PTHLH) and rs865686 (9q31.2).

Item Type: Article
Additional Information: PMCID: PMC3496151
Keywords: Adult, Aged, BRCA1 Protein, BRCA2 Protein, Chromosomes, Human, Pair 12, Chromosomes, Human, Pair 9, DNA-Binding Proteins, Female, Genetic Association Studies, Hereditary Breast and Ovarian Cancer Syndrome, Heterozygote, Humans, Middle Aged, Polymorphism, Single Nucleotide, Risk Factors, Transcription Factors
Journal or Publication Title: Breast Cancer Res
Dates:
DateEvent
2012Published
PubMed ID: 22348646
Web of Science ID: 22348646
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URI: http://sgultest.da.ulcc.ac.uk/id/eprint/100528
Publisher's version: https://doi.org/10.1186/bcr3121

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