Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

Antonis C. Antoniou; Christiana Kartsonaki; Olga M. Sinilnikova; Penny Soucy; Lesley McGuffog; Sue Healey; Andrew Lee; Paolo Peterlongo; Siranoush Manoukian; Bernard Peissel; Daniela Zaffaroni; Elisa Cattaneo; Monica Barile; Valeria Pensotti; Barbara Pasini; Riccardo Dolcetti; Giuseppe Giannini; Anna Laura Putignano; Liliana Varesco; Paolo Radice; Phuong L. Mai; Mark H. Greene; Irene L. Andrulis; Gord Glendon; Hilmi Ozcelik; Mads Thomassen; Anne-Marie Gerdes; Torben A. Kruse; Uffe Birk Jensen; Dorthe G. Crueger; Maria A. Caligo; Yael Laitman; Roni Milgrom; Bella Kaufman; Shani Paluch-Shimon; Eitan Friedman; Niklas Loman; Katja Harbst; Annika Lindblom; Brita Arver; Hans Ehrencrona; Beatrice Melin; Katherine L. Nathanson; Susan M. Domchek; Timothy Rebbeck; Ania Jakubowska; Jan Lubinski; Jacek Gronwald; Heli Nevanlinna; Kristiina Aittomäki; CEMO Study Collaborators, EMBRACE, Breast Canc Family Registry, HEBON, kConFab Investigators, CIMBA, SWE-BRCA

doi:10.1093/hmg/ddr226

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

Antonis C. Antoniou, Christiana Kartsonaki, Olga M. Sinilnikova, Penny Soucy, Lesley McGuffog, Sue Healey, Andrew Lee, Paolo Peterlongo, Siranoush Manoukian, Bernard Peissel, Daniela Zaffaroni, Elisa Cattaneo, Monica Barile, Valeria Pensotti, Barbara Pasini, Riccardo Dolcetti, Giuseppe Giannini, Anna Laura Putignano, Liliana Varesco, Paolo RadicePhuong L. Mai, Mark H. Greene, Irene L. Andrulis, Gord Glendon, Hilmi Ozcelik, Mads Thomassen, Anne-Marie Gerdes, Torben A. Kruse, Uffe Birk Jensen, Dorthe G. Crueger, Maria A. Caligo, Yael Laitman, Roni Milgrom, Bella Kaufman, Shani Paluch-Shimon, Eitan Friedman, Niklas Loman, Katja Harbst, Annika Lindblom, Brita Arver, Hans Ehrencrona, Beatrice Melin, Katherine L. Nathanson, Susan M. Domchek, Timothy Rebbeck, Ania Jakubowska, Jan Lubinski, Jacek Gronwald, Heli Nevanlinna, Kristiina Aittomäki, CEMO Study Collaborators, EMBRACE, Breast Canc Family Registry, HEBON, kConFab Investigators, CIMBA, SWE-BRCA

Research output: Contribution to journal › Article › Scientific › peer-review

Original language	English
Journal	Human Molecular Genetics
Volume	20
Pages (from-to)	3304-3321
Number of pages	18
ISSN	0964-6906
DOIs	https://doi.org/10.1093/hmg/ddr226
Publication status	Published - 2011
MoE publication type	A1 Journal article-refereed

Fields of Science

GENOME-WIDE ASSOCIATION
ESTROGEN-RECEPTOR
CONFER SUSCEPTIBILITY
GENETIC MODIFIERS
VARIANTS
LOCUS
POPULATION
2Q35
3123 Gynaecology and paediatrics

Access to Document

10.1093/hmg/ddr226

Cite this

Antoniou, A. C., Kartsonaki, C., Sinilnikova, O. M., Soucy, P., McGuffog, L., Healey, S., Lee, A., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Cattaneo, E., Barile, M., Pensotti, V., Pasini, B., Dolcetti, R., Giannini, G., Putignano, A. L., Varesco, L., ... CEMO Study Collaborators, EMBRACE, Breast Canc Family Registry, HEBON, kConFab Investigators, CIMBA, SWE-BRCA (2011). Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers. Human Molecular Genetics, 20, 3304-3321. https://doi.org/10.1093/hmg/ddr226

@article{30b6450c312a4e6b9dd17f97ffe2c76d,

title = "Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers",

keywords = "GENOME-WIDE ASSOCIATION, ESTROGEN-RECEPTOR, CONFER SUSCEPTIBILITY, GENETIC MODIFIERS, VARIANTS, LOCUS, POPULATION, 2Q35, 3123 Gynaecology and paediatrics",

author = "Antoniou, {Antonis C.} and Christiana Kartsonaki and Sinilnikova, {Olga M.} and Penny Soucy and Lesley McGuffog and Sue Healey and Andrew Lee and Paolo Peterlongo and Siranoush Manoukian and Bernard Peissel and Daniela Zaffaroni and Elisa Cattaneo and Monica Barile and Valeria Pensotti and Barbara Pasini and Riccardo Dolcetti and Giuseppe Giannini and Putignano, {Anna Laura} and Liliana Varesco and Paolo Radice and Mai, {Phuong L.} and Greene, {Mark H.} and Andrulis, {Irene L.} and Gord Glendon and Hilmi Ozcelik and Mads Thomassen and Anne-Marie Gerdes and Kruse, {Torben A.} and Jensen, {Uffe Birk} and Crueger, {Dorthe G.} and Caligo, {Maria A.} and Yael Laitman and Roni Milgrom and Bella Kaufman and Shani Paluch-Shimon and Eitan Friedman and Niklas Loman and Katja Harbst and Annika Lindblom and Brita Arver and Hans Ehrencrona and Beatrice Melin and Nathanson, {Katherine L.} and Domchek, {Susan M.} and Timothy Rebbeck and Ania Jakubowska and Jan Lubinski and Jacek Gronwald and Heli Nevanlinna and Kristiina Aittom{\"a}ki and {CEMO Study Collaborators, EMBRACE, Breast Canc Family Registry, HEBON, kConFab Investigators, CIMBA, SWE-BRCA}",

year = "2011",

doi = "10.1093/hmg/ddr226",

language = "English",

volume = "20",

pages = "3304--3321",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

}

Antoniou, AC, Kartsonaki, C, Sinilnikova, OM, Soucy, P, McGuffog, L, Healey, S, Lee, A, Peterlongo, P, Manoukian, S, Peissel, B, Zaffaroni, D, Cattaneo, E, Barile, M, Pensotti, V, Pasini, B, Dolcetti, R, Giannini, G, Putignano, AL, Varesco, L, Radice, P, Mai, PL, Greene, MH, Andrulis, IL, Glendon, G, Ozcelik, H, Thomassen, M, Gerdes, A-M, Kruse, TA, Jensen, UB, Crueger, DG, Caligo, MA, Laitman, Y, Milgrom, R, Kaufman, B, Paluch-Shimon, S, Friedman, E, Loman, N, Harbst, K, Lindblom, A, Arver, B, Ehrencrona, H, Melin, B, Nathanson, KL, Domchek, SM, Rebbeck, T, Jakubowska, A, Lubinski, J, Gronwald, J, Nevanlinna, H , Aittomäki, K & CEMO Study Collaborators, EMBRACE, Breast Canc Family Registry, HEBON, kConFab Investigators, CIMBA, SWE-BRCA 2011, 'Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers', Human Molecular Genetics, vol. 20, pp. 3304-3321. https://doi.org/10.1093/hmg/ddr226

TY - JOUR

T1 - Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

AU - Antoniou, Antonis C.

AU - Kartsonaki, Christiana

AU - Sinilnikova, Olga M.

AU - Soucy, Penny

AU - McGuffog, Lesley

AU - Healey, Sue

AU - Lee, Andrew

AU - Peterlongo, Paolo

AU - Manoukian, Siranoush

AU - Peissel, Bernard

AU - Zaffaroni, Daniela

AU - Cattaneo, Elisa

AU - Barile, Monica

AU - Pensotti, Valeria

AU - Pasini, Barbara

AU - Dolcetti, Riccardo

AU - Giannini, Giuseppe

AU - Putignano, Anna Laura

AU - Varesco, Liliana

AU - Radice, Paolo

AU - Mai, Phuong L.

AU - Greene, Mark H.

AU - Andrulis, Irene L.

AU - Glendon, Gord

AU - Ozcelik, Hilmi

AU - Thomassen, Mads

AU - Gerdes, Anne-Marie

AU - Kruse, Torben A.

AU - Jensen, Uffe Birk

AU - Crueger, Dorthe G.

AU - Caligo, Maria A.

AU - Laitman, Yael

AU - Milgrom, Roni

AU - Kaufman, Bella

AU - Paluch-Shimon, Shani

AU - Friedman, Eitan

AU - Loman, Niklas

AU - Harbst, Katja

AU - Lindblom, Annika

AU - Arver, Brita

AU - Ehrencrona, Hans

AU - Melin, Beatrice

AU - Nathanson, Katherine L.

AU - Domchek, Susan M.

AU - Rebbeck, Timothy

AU - Jakubowska, Ania

AU - Lubinski, Jan

AU - Gronwald, Jacek

AU - Nevanlinna, Heli

AU - Aittomäki, Kristiina

AU - CEMO Study Collaborators, EMBRACE, Breast Canc Family Registry, HEBON, kConFab Investigators, CIMBA, SWE-BRCA

PY - 2011

Y1 - 2011

KW - GENOME-WIDE ASSOCIATION

KW - ESTROGEN-RECEPTOR

KW - CONFER SUSCEPTIBILITY

KW - GENETIC MODIFIERS

KW - VARIANTS

KW - LOCUS

KW - POPULATION

KW - 2Q35

KW - 3123 Gynaecology and paediatrics

U2 - 10.1093/hmg/ddr226

DO - 10.1093/hmg/ddr226

M3 - Article

SN - 0964-6906

VL - 20

SP - 3304

EP - 3321

JO - Human Molecular Genetics

JF - Human Molecular Genetics

ER -