11q13 is a susceptibility locus for hormone receptor positive breast cancer

D Lambrechts, T Truong, C Justenhoven, M K Humphreys, J Wang, J L Hopper, G S Dite, C Apicella, M K Schmidt, A Broeks, S Cornelissen, R van Hien, E Sawyer, I Tomlinson, M Kerin, N Miller, R L Milne, M P Zamora, J I Perez, J BenitezU Hamann, Y D Ko, T Bruning, J Chang-Claude, U Eilber, R Hein, S Nickels, D Flesch-Janys, S Wang-Gohrke, E M John, A Miron, R Winqvist, K Pylkas, A Jukkola-Vuorinen, M Grip, G Chenevix-Trench, J Beesley, X Chen, F Menegaux, E Cordina-Duverger, C Y Shen, J C Yu, P E Wu, M F Hou, I L Andrulis, T Selander, G Glendon, A M Mulligan, H Anton-Culver, A Ziogas, K R Muir, A Lophatananon, S Rattanamongkongul, P Puttawibul, M Jones, N Orr, A Ashworth, A Swerdlow, G Severi, L Baglietto, G Giles, M Southey, F Marme, A Schneeweiss, C Sohn, B Burwinkel, B T Yesilyurt, P Neven, R Paridaens, H Wildiers, H Brenner, H Muller, V Arndt, C Stegmaier, A Meindl, S Schott, C R Bartram, R K Schmutzler, A Cox, I W Brock, G Elliott, S S Cross, P A Fasching, R Schulz-Wendtland, A B Ekici, M W Beckmann, O Fletcher, N Johnson, S Silva Idos, J Peto, H Nevanlinna, T A Muranen, K Aittomaki, C Blomqvist, T Dork, P Schurmann, M Bremer, P Hillemanns, N V Bogdanova, N N Antonenkova, Y I Rogov, J H Karstens, E Khusnutdinova, M Bermisheva, D Prokofieva, S Gancev, A Jakubowska, J Lubinski, K Jaworska, K Durda, B G Nordestgaard, S E Bojesen, C Lanng, A Mannermaa, V Kataja, V M Kosma, J M Hartikainen, P Radice, P Peterlongo, S Manoukian, L Bernard, F J Couch, J E Olson, X Wang, Z Fredericksen, G G Alnaes, V Kristensen, A L Borresen-Dale, P Devilee, R A Tollenaar, C M Seynaeve, M J Hooning, M Garcia-Closas, S J Chanock, J Lissowska, M E Sherman, P Hall, J Liu, K Czene, D Kang, K Y Yoo, D Y Noh, A Lindblom, S Margolin, A M Dunning, P D Pharoah, D F Easton, P Guenel, H Brauch

    Research output: Contribution to journalArticlepeer-review

    Abstract

    A recent two-stage genome-wide association study (GWAS) identified five novel breast cancer susceptibility loci on chromosomes 9, 10, and 11. To provide more reliable estimates of the relative risk associated with these loci and investigate possible heterogeneity by subtype of breast cancer, we genotyped the variants rs2380205, rs1011970, rs704010, rs614367, and rs10995190 in 39 studies from the Breast Cancer Association Consortium (BCAC), involving 49,608 cases and 48,772 controls of predominantly European ancestry. Four of the variants showed clear evidence of association (P
    Original languageEnglish
    Pages (from-to)1123-32
    Number of pages1090
    JournalHum Mutat
    Volume33
    Issue number7
    DOIs
    Publication statusPublished - 2012

    Keywords

    • Breast Neoplasms/ genetics
    • Chromosomes, Human, Pair 11/ genetics
    • European Continental Ancestry Group
    • Female
    • Genetic Predisposition to Disease/genetics
    • Genome-Wide Association Study
    • Genotype
    • Humans
    • Polymorphism, Single Nucleotide/genetics
    • Receptors, Estrogen/ genetics
    • Receptors, Progesterone/ genetics
    • Risk Factors

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