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Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
Authors :
Ramus, S Kartsonaki, C Gayther, S Pharoah, P Sinilnikova, O Beesley, J Chen, X Mcguffog, L Healey, S Couch, F 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, M Mai, P Andrulis, I Glendon, G Ozcelik, H Thomassen, M Gerdes, A Kruse, T Cruger, D Jensen, U Caligo, M Olsson, H Kristoffersson, U Lindblom, A Arver, B Karlsson, P Stenmark Askmalm, M Borg, A Neuhausen, S Ding, Y Nathanson, K Domchek, S Jakubowska, A Lubiński, J Huzarski, T Byrski, T Gronwald, J Górski, B Cybulski, C Dębniak, T Osorio, A Durán, M Tejada, M Benítez, J Hamann, U Rookus, M Verhoef, S Tilanus Linthorst, M Vreeswijk, M Bodmer, D Ausems, M van Os, T Asperen, C Blok, M Meijers Heijboer, H Peock, S Cook, M Oliver, C Frost, D Dunning, A Evans, D Eeles, R Pichert, G Cole, T Hodgson, S Brewer, C Morrison, P Porteous, M Kennedy, M Rogers, M Side, L 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, Y Prieur, F Collonge Rame, M Venat Bouvet, L Fert Ferrer, S Miron, A Buys, S Hopper, J Daly, M John, E Terry, M Goldgar, D Hansen, T Jønson, L Ejlertsen, B Agnarsson, B Offit, K Kirchhoff, T Vijai, J Dutra Clarke, A Przybylo, J Montagna, M Casella, C Imyanitov, E Janavicius, R Blanco, I Lázaro, C Moysich, K Karlan, B Gross, J Beattie, M 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 Spurdle, A Holland, H Chenevix Trench, G Easton, D Antoniou, A Ramus, SJ Gayther, SA Pharoah, PDP Sinilnikova, OM McGuffog, L Couch, FJ Greene, MH Mai, PL Andrulis, IL Kruse, TA Jensen, UB Caligo, MA Neuhausen, SL Ding, YC Nathanson, KL Domchek, SM Rookus, MA Tilanus Linthorst, MA Vreeswijk, MP Ausems, MGEM van Os, TA Asperen, CJ Blok, MJ Meijers Heijboer, HEJ Dunning, AM Evans, DG Morrison, PJ Kennedy, MJ Rogers, MT Side, LE Buys, SS Hopper, JL Daly, MB John, EM Terry, MB Hansen, TvO Agnarsson, BA Dutra Clarke, AVC Przybylo, JA Imyanitov, EN Moysich, KB Karlan, BY Beattie, MS Spurdle, AB Easton, DF Antoniou, AC ROVERSI, GAIA Ramus, S Kartsonaki, C Gayther, S Pharoah, P Sinilnikova, O Beesley, J Chen, X Mcguffog, L Healey, S Couch, F 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, M Mai, P Andrulis, I Glendon, G Ozcelik, H Thomassen, M Gerdes, A Kruse, T Cruger, D Jensen, U Caligo, M Olsson, H Kristoffersson, U Lindblom, A Arver, B Karlsson, P Stenmark Askmalm, M Borg, A Neuhausen, S Ding, Y Nathanson, K Domchek, S Jakubowska, A Lubiński, J Huzarski, T Byrski, T Gronwald, J Górski, B Cybulski, C Dębniak, T Osorio, A Durán, M Tejada, M Benítez, J Hamann, U Rookus, M Verhoef, S Tilanus Linthorst, M Vreeswijk, M Bodmer, D Ausems, M van Os, T Asperen, C Blok, M Meijers Heijboer, H Peock, S Cook, M Oliver, C Frost, D Dunning, A Evans, D Eeles, R Pichert, G Cole, T Hodgson, S Brewer, C Morrison, P Porteous, M Kennedy, M Rogers, M Side, L 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, Y Prieur, F Collonge Rame, M Venat Bouvet, L Fert Ferrer, S Miron, A Buys, S Hopper, J Daly, M John, E Terry, M Goldgar, D Hansen, T Jønson, L Ejlertsen, B Agnarsson, B Offit, K Kirchhoff, T Vijai, J Dutra Clarke, A Przybylo, J Montagna, M Casella, C Imyanitov, E Janavicius, R Blanco, I Lázaro, C Moysich, K Karlan, B Gross, J Beattie, M 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 Spurdle, A Holland, H Chenevix Trench, G Easton, D Antoniou, A Ramus, SJ Gayther, SA Pharoah, PDP Sinilnikova, OM McGuffog, L Couch, FJ Greene, MH Mai, PL Andrulis, IL Kruse, TA Jensen, UB Caligo, MA Neuhausen, SL Ding, YC Nathanson, KL Domchek, SM Rookus, MA Tilanus Linthorst, MA Vreeswijk, MP Ausems, MGEM van Os, TA Asperen, CJ Blok, MJ Meijers Heijboer, HEJ Dunning, AM Evans, DG Morrison, PJ Kennedy, MJ Rogers, MT Side, LE Buys, SS Hopper, JL Daly, MB John, EM Terry, MB Hansen, TvO Agnarsson, BA Dutra Clarke, AVC Przybylo, JA Imyanitov, EN Moysich, KB Karlan, BY Beattie, MS Spurdle, AB Easton, DF Antoniou, AC ROVERSI, GAIA
Publication Year :
2011
Abstract
Germline mutations in the BRCA1 and BRCA2 genes are associated with increased risks of breast and ovarian cancers. Although several common variants have been associated with breast cancer susceptibility in mutation carriers, none have been associated with ovarian cancer susceptibility. A genome-wide association study recently identified an association between the rare allele of the single-nucleotide polymorphism (SNP) rs3814113 (ie, the C allele) at 9p22.2 and decreased risk of ovarian cancer for women in the general population. We evaluated the association of this SNP with ovarian cancer risk among BRCA1 or BRCA2 mutation carriers by use of data from the Consortium of Investigators of Modifiers of BRCA1/2.
Details
Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1346404947
Document Type :
Electronic Resource