SORA

Advancing, promoting and sharing knowledge of health through excellence in teaching, clinical practice and research into the prevention and treatment of illness

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

Full text not available from this repository.
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
Related URLs:
Dates:
DateEvent
1 January 2011Published
Web of Science ID: WOS:000286472800008
Download EPMC Full text (PDF)
Download EPMC Full text (HTML)
URI: https://openaccess.sgul.ac.uk/id/eprint/26
Publisher's version: https://doi.org/10.1093/jnci/djq494

Actions (login required)

Edit Item Edit Item