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Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers

Ramus, SJ; Kartsonaki, C; Gayther, SA; Pharoah, PD; Sinilnikova, OM; Beesley, J; Chen, X; McGuffog, L; Healey, S; Couch, FJ; et al. Ramus, SJ; Kartsonaki, C; Gayther, SA; Pharoah, PD; Sinilnikova, OM; Beesley, J; Chen, X; McGuffog, L; Healey, S; Couch, FJ; Wang, X; Fredericksen, Z; Peterlongo, P; Manoukian, S; Peissel, B; Zaffaroni, D; Roversi, G; Barile, M; Viel, A; Allavena, A; Ottini, L; Papi, L; Gismondi, V; Capra, F; Radice, P; Greene, MH; Mai, PL; Andrulis, IL; Glendon, G; Ozcelik, H; OCGN, ; Thomassen, M; Gerdes, AM; Kruse, TA; Cruger, D; Jensen, UB; Caligo, MA; Olsson, H; Kristoffersson, U; Lindblom, A; Arver, B; Karlsson, P; Stenmark Askmalm, M; Borg, A; Neuhausen, SL; Ding, YC; Nathanson, KL; Domchek, SM; Jakubowska, A; Lubiński, J; Huzarski, T; Byrski, T; Gronwald, J; Górski, B; Cybulski, C; Dębniak, T; Osorio, A; Durán, M; Tejada, MI; Benítez, J; Hamann, U; Rookus, MA; Verhoef, S; Tilanus-Linthorst, MA; Vreeswijk, MP; Bodmer, D; Ausems, MG; van Os, TA; Asperen, CJ; Blok, MJ; Meijers-Heijboer, HE; HEBON, ; EMBRACE, ; Peock, S; Cook, M; Oliver, C; Frost, D; Dunning, AM; Evans, DG; Eeles, R; Pichert, G; Cole, T; Hodgson, S; Brewer, C; Morrison, PJ; Porteous, M; Kennedy, MJ; Rogers, MT; Side, LE; Donaldson, A; Gregory, H; Godwin, A; Stoppa-Lyonnet, D; Moncoutier, V; Castera, L; Mazoyer, S; Barjhoux, L; Bonadona, V; Leroux, D; Faivre, L; Lidereau, R; Nogues, C; Bignon, YJ; Prieur, F; Collonge-Rame, MA; Venat-Bouvet, L; Fert-Ferrer, S; GEMO Study Collaborators, ; Miron, A; Buys, SS; Hopper, JL; Daly, MB; John, EM; Terry, MB; Goldgar, D; BCFR, ; Hansen, TV; Jønson, L; Ejlertsen, B; Agnarsson, BA; Offit, K; Kirchhoff, T; Vijai, J; Dutra-Clarke, AV; Przybylo, JA; Montagna, M; Casella, C; Imyanitov, EN; Janavicius, R; Blanco, I; Lázaro, C; Moysich, KB; Karlan, BY; Gross, J; Beattie, MS; Schmutzler, R; Wappenschmidt, B; Meindl, A; Ruehl, I; Fiebig, B; Sutter, C; Arnold, N; Deissler, H; Varon-Mateeva, R; Kast, K; Niederacher, D; Gadzicki, D; Caldes, T; de la Hoya, M; Nevanlinna, H; Aittomäki, K; Simard, J; Soucy, P; kConFab Investigators, ; Spurdle, AB; Holland, H; Chenevix-Trench, G; Easton, DF; Antoniou, AC; Consortium of Investigators of Modifiers of BRCA1/2, (2011) Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 103 (2). ? - ? (12). ISSN 0027-8874 https://doi.org/10.1093/jnci/djq494
SGUL Authors: Hodgson, Shirley Victoria

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Item Type: Article
Additional Information: PubMed ID: 21169536
Keywords: Adult, Aged, Aged, 80 and over, Alleles, Chromosomes, Human, Pair 9, Female, Genes, BRCA1, Genes, BRCA2, Genotype, Germ-Line Mutation, Heterozygote, Humans, Likelihood Functions, Middle Aged, Odds Ratio, Ovarian Neoplasms, Polymorphism, Single Nucleotide, Retrospective Studies, Risk Factors, Science & Technology, Life Sciences & Biomedicine, Oncology, GENOME-WIDE ASSOCIATION, BREAST-CANCER, SUSCEPTIBILITY LOCI, GERMLINE MUTATIONS, ALLELES, IDENTIFICATION, BASONUCLIN-2, POPULATION, PROTEINS, FAMILIES
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cell Sciences (INCCCS)
Journal or Publication Title: JOURNAL OF THE NATIONAL CANCER INSTITUTE
ISSN: 0027-8874
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Dates:
DateEvent
1 January 2011Published
Web of Science ID: WOS:000286472800008
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URI: http://openaccess.sgul.ac.uk/id/eprint/26
Publisher's version: https://doi.org/10.1093/jnci/djq494

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