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

A.C. Antoniou; C. Kartsonaki; O.M. Sinilnikova; P. Soucy; L. McGuffog; S. Healey; A. Lee; P. Peterlongo; S. Manoukian; B. Peissel; D. Zaffaroni; E. Cattaneo; M. Barile; V. Pensotti; B. Pasini; R. Dolcetti; G. Giannini; A.L. Putignano; L. Varesco; P. Radice; P.L. Mai; M.H. Greene; I.L. Andrulis; G. Glendon; H. Ozcelik; M. Thomassen; A.M. Gerdes; T.A. Kruse; U.B. Jensen; D.G. Cruger; M.A. Caligo; Y. Laitman; R. Milgrom; B. Kaufman; S. Paluch-Shimon; E. Friedman; N. Loman; K. Harbst; A. Lindblom; B. Arver; H. Ehrencrona; B. Melin; K.L. Nathanson; S.M. Domchek; T. Rebbeck; A. Jakubowska; J. Lubinski; J. Gronwald; T. Huzarski; T. Byrski; C. Cybulski; B. Gorski; A. Osorio; T.R.Y. Cajal; F. Fostira; R. Andres; J. Benitez; U. Hamann; FB Hogervorst; M.A. Rookus; M.J. Hooning; M.R. Nelen; R.B. van der Luijt; T.A.M. van Os; C.J. van Asperen; P. Devilee; E.J. Meijers-Heijboer; E.B.G. Garcia; S. Peock; M. Cook; D. Frost; R. Platte; J. Leyland; D.G. Evans; F. Lalloo; R. Eeles; L. Izatt; J. Adlard; R. Davidson; D. Eccles; K.R. Ong; J. Cook; F. Douglas; J. Paterson; M.J. Kennedy; Z. Miedzybrodzka; A. Godwin; D. Stoppa-Lyonnet; B. Buecher; M. Belotti; C. Tirapo; S. Mazoyer; L. Barjhoux; C. Lasset; D. Leroux; L. Faivre; M. Bronner; F. Prieur; C. Nogues; G. Chenevix-Trench

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

A.C. Antoniou, C. Kartsonaki, O.M. Sinilnikova, P. Soucy, L. McGuffog, S. Healey, A. Lee, P. Peterlongo, S. Manoukian, B. Peissel, D. Zaffaroni, E. Cattaneo, M. Barile, V. Pensotti, B. Pasini, R. Dolcetti, G. Giannini, A.L. Putignano, L. Varesco, P. RadiceP.L. Mai, M.H. Greene, I.L. Andrulis, G. Glendon, H. Ozcelik, M. Thomassen, A.M. Gerdes, T.A. Kruse, U.B. Jensen, D.G. Cruger, M.A. Caligo, Y. Laitman, R. Milgrom, B. Kaufman, S. Paluch-Shimon, E. Friedman, N. Loman, K. Harbst, A. Lindblom, B. Arver, H. Ehrencrona, B. Melin, K.L. Nathanson, S.M. Domchek, T. Rebbeck, A. Jakubowska, J. Lubinski, J. Gronwald, T. Huzarski, T. Byrski, C. Cybulski, B. Gorski, A. Osorio, T.R.Y. Cajal, F. Fostira, R. Andres, J. Benitez, U. Hamann, FB Hogervorst, M.A. Rookus, M.J. Hooning, M.R. Nelen, R.B. van der Luijt, T.A.M. van Os, C.J. van Asperen, P. Devilee, E.J. Meijers-Heijboer, E.B.G. Garcia, S. Peock, M. Cook, D. Frost, R. Platte, J. Leyland, D.G. Evans, F. Lalloo, R. Eeles, L. Izatt, J. Adlard, R. Davidson, D. Eccles, K.R. Ong, J. Cook, F. Douglas, J. Paterson, M.J. Kennedy, Z. Miedzybrodzka, A. Godwin, D. Stoppa-Lyonnet, B. Buecher, M. Belotti, C. Tirapo, S. Mazoyer, L. Barjhoux, C. Lasset, D. Leroux, L. Faivre, M. Bronner, F. Prieur, C. Nogues, G. Chenevix-Trench

Clinical genetics

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

Original language	Undefined/Unknown
Pages (from-to)	3304-3321
Journal	Human Molecular Genetics
Volume	20
Issue number	16
DOIs	https://doi.org/10.1093/hmg/ddr226
Publication status	Published - 2011

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10.1093/hmg/ddr226

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Antoniou, A. C., Kartsonaki, C., Sinilnikova, O. M., Soucy, P., McGuffog, L., Healey, S., ... Chenevix-Trench, G. (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(16), 3304-3321. https://doi.org/10.1093/hmg/ddr226

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. ; Radice, P. ; Mai, P.L. ; Greene, M.H. ; Andrulis, I.L. ; Glendon, G. ; Ozcelik, H. ; Thomassen, M. ; Gerdes, A.M. ; Kruse, T.A. ; Jensen, U.B. ; Cruger, D.G. ; Caligo, M.A. ; Laitman, Y. ; Milgrom, R. ; Kaufman, B. ; Paluch-Shimon, S. ; Friedman, E. ; Loman, N. ; Harbst, K. ; Lindblom, A. ; Arver, B. ; Ehrencrona, H. ; Melin, B. ; Nathanson, K.L. ; Domchek, S.M. ; Rebbeck, T. ; Jakubowska, A. ; Lubinski, J. ; Gronwald, J. ; Huzarski, T. ; Byrski, T. ; Cybulski, C. ; Gorski, B. ; Osorio, A. ; Cajal, T.R.Y. ; Fostira, F. ; Andres, R. ; Benitez, J. ; Hamann, U. ; Hogervorst, FB ; Rookus, M.A. ; Hooning, M.J. ; Nelen, M.R. ; van der Luijt, R.B. ; van Os, T.A.M. ; van Asperen, C.J. ; Devilee, P. ; Meijers-Heijboer, E.J. ; Garcia, E.B.G. ; Peock, S. ; Cook, M. ; Frost, D. ; Platte, R. ; Leyland, J. ; Evans, D.G. ; Lalloo, F. ; Eeles, R. ; Izatt, L. ; Adlard, J. ; Davidson, R. ; Eccles, D. ; Ong, K.R. ; Cook, J. ; Douglas, F. ; Paterson, J. ; Kennedy, M.J. ; Miedzybrodzka, Z. ; Godwin, A. ; Stoppa-Lyonnet, D. ; Buecher, B. ; Belotti, M. ; Tirapo, C. ; Mazoyer, S. ; Barjhoux, L. ; Lasset, C. ; Leroux, D. ; Faivre, L. ; Bronner, M. ; Prieur, F. ; Nogues, C. ; Chenevix-Trench, G. / Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers. In: Human Molecular Genetics. 2011 ; Vol. 20, No. 16. pp. 3304-3321.

@article{1ea143fe5dc34e5fb6fc8286df4f28f6,

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

author = "A.C. Antoniou and C. Kartsonaki and O.M. Sinilnikova and P. Soucy and L. McGuffog and S. Healey and A. Lee and P. Peterlongo and S. Manoukian and B. Peissel and D. Zaffaroni and E. Cattaneo and M. Barile and V. Pensotti and B. Pasini and R. Dolcetti and G. Giannini and A.L. Putignano and L. Varesco and P. Radice and P.L. Mai and M.H. Greene and I.L. Andrulis and G. Glendon and H. Ozcelik and M. Thomassen and A.M. Gerdes and T.A. Kruse and U.B. Jensen and D.G. Cruger and M.A. Caligo and Y. Laitman and R. Milgrom and B. Kaufman and S. Paluch-Shimon and E. Friedman and N. Loman and K. Harbst and A. Lindblom and B. Arver and H. Ehrencrona and B. Melin and K.L. Nathanson and S.M. Domchek and T. Rebbeck and A. Jakubowska and J. Lubinski and J. Gronwald and T. Huzarski and T. Byrski and C. Cybulski and B. Gorski and A. Osorio and T.R.Y. Cajal and F. Fostira and R. Andres and J. Benitez and U. Hamann and FB Hogervorst and M.A. Rookus and M.J. Hooning and M.R. Nelen and {van der Luijt}, R.B. and {van Os}, T.A.M. and {van Asperen}, C.J. and P. Devilee and E.J. Meijers-Heijboer and E.B.G. Garcia and S. Peock and M. Cook and D. Frost and R. Platte and J. Leyland and D.G. Evans and F. Lalloo and R. Eeles and L. Izatt and J. Adlard and R. Davidson and D. Eccles and K.R. Ong and J. Cook and F. Douglas and J. Paterson and M.J. Kennedy and Z. Miedzybrodzka and A. Godwin and D. Stoppa-Lyonnet and B. Buecher and M. Belotti and C. Tirapo and S. Mazoyer and L. Barjhoux and C. Lasset and D. Leroux and L. Faivre and M. Bronner and F. Prieur and C. Nogues and G. Chenevix-Trench",

year = "2011",

doi = "10.1093/hmg/ddr226",

language = "Undefined/Unknown",

volume = "20",

pages = "3304--3321",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

number = "16",

}

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, AM, Kruse, TA, Jensen, UB, Cruger, 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, Huzarski, T, Byrski, T, Cybulski, C, Gorski, B, Osorio, A, Cajal, TRY, Fostira, F, Andres, R, Benitez, J, Hamann, U, Hogervorst, FB, Rookus, MA, Hooning, MJ, Nelen, MR, van der Luijt, RB, van Os, TAM, van Asperen, CJ, Devilee, P, Meijers-Heijboer, EJ, Garcia, EBG, Peock, S, Cook, M, Frost, D, Platte, R, Leyland, J, Evans, DG, Lalloo, F, Eeles, R, Izatt, L, Adlard, J, Davidson, R, Eccles, D, Ong, KR, Cook, J, Douglas, F, Paterson, J, Kennedy, MJ, Miedzybrodzka, Z, Godwin, A, Stoppa-Lyonnet, D, Buecher, B, Belotti, M, Tirapo, C, Mazoyer, S, Barjhoux, L, Lasset, C, Leroux, D, Faivre, L, Bronner, M, Prieur, F, Nogues, C & Chenevix-Trench, G 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, no. 16, pp. 3304-3321. https://doi.org/10.1093/hmg/ddr226

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers. / 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.; Radice, P.; Mai, P.L.; Greene, M.H.; Andrulis, I.L.; Glendon, G.; Ozcelik, H.; Thomassen, M.; Gerdes, A.M.; Kruse, T.A.; Jensen, U.B.; Cruger, D.G.; Caligo, M.A.; Laitman, Y.; Milgrom, R.; Kaufman, B.; Paluch-Shimon, S.; Friedman, E.; Loman, N.; Harbst, K.; Lindblom, A.; Arver, B.; Ehrencrona, H.; Melin, B.; Nathanson, K.L.; Domchek, S.M.; Rebbeck, T.; Jakubowska, A.; Lubinski, J.; Gronwald, J.; Huzarski, T.; Byrski, T.; Cybulski, C.; Gorski, B.; Osorio, A.; Cajal, T.R.Y.; Fostira, F.; Andres, R.; Benitez, J.; Hamann, U.; Hogervorst, FB; Rookus, M.A.; Hooning, M.J.; Nelen, M.R.; van der Luijt, R.B.; van Os, T.A.M.; van Asperen, C.J.; Devilee, P.; Meijers-Heijboer, E.J.; Garcia, E.B.G.; Peock, S.; Cook, M.; Frost, D.; Platte, R.; Leyland, J.; Evans, D.G.; Lalloo, F.; Eeles, R.; Izatt, L.; Adlard, J.; Davidson, R.; Eccles, D.; Ong, K.R.; Cook, J.; Douglas, F.; Paterson, J.; Kennedy, M.J.; Miedzybrodzka, Z.; Godwin, A.; Stoppa-Lyonnet, D.; Buecher, B.; Belotti, M.; Tirapo, C.; Mazoyer, S.; Barjhoux, L.; Lasset, C.; Leroux, D.; Faivre, L.; Bronner, M.; Prieur, F.; Nogues, C.; Chenevix-Trench, G.

In: Human Molecular Genetics, Vol. 20, No. 16, 2011, p. 3304-3321.

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

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, A.C.

AU - Kartsonaki, C.

AU - Sinilnikova, O.M.

AU - Soucy, P.

AU - McGuffog, L.

AU - Healey, S.

AU - Lee, A.

AU - Peterlongo, P.

AU - Manoukian, S.

AU - Peissel, B.

AU - Zaffaroni, D.

AU - Cattaneo, E.

AU - Barile, M.

AU - Pensotti, V.

AU - Pasini, B.

AU - Dolcetti, R.

AU - Giannini, G.

AU - Putignano, A.L.

AU - Varesco, L.

AU - Radice, P.

AU - Mai, P.L.

AU - Greene, M.H.

AU - Andrulis, I.L.

AU - Glendon, G.

AU - Ozcelik, H.

AU - Thomassen, M.

AU - Gerdes, A.M.

AU - Kruse, T.A.

AU - Jensen, U.B.

AU - Cruger, D.G.

AU - Caligo, M.A.

AU - Laitman, Y.

AU - Milgrom, R.

AU - Kaufman, B.

AU - Paluch-Shimon, S.

AU - Friedman, E.

AU - Loman, N.

AU - Harbst, K.

AU - Lindblom, A.

AU - Arver, B.

AU - Ehrencrona, H.

AU - Melin, B.

AU - Nathanson, K.L.

AU - Domchek, S.M.

AU - Rebbeck, T.

AU - Jakubowska, A.

AU - Lubinski, J.

AU - Gronwald, J.

AU - Huzarski, T.

AU - Byrski, T.

AU - Cybulski, C.

AU - Gorski, B.

AU - Osorio, A.

AU - Cajal, T.R.Y.

AU - Fostira, F.

AU - Andres, R.

AU - Benitez, J.

AU - Hamann, U.

AU - Hogervorst, FB

AU - Rookus, M.A.

AU - Hooning, M.J.

AU - Nelen, M.R.

AU - van der Luijt, R.B.

AU - van Os, T.A.M.

AU - van Asperen, C.J.

AU - Devilee, P.

AU - Meijers-Heijboer, E.J.

AU - Garcia, E.B.G.

AU - Peock, S.

AU - Cook, M.

AU - Frost, D.

AU - Platte, R.

AU - Leyland, J.

AU - Evans, D.G.

AU - Lalloo, F.

AU - Eeles, R.

AU - Izatt, L.

AU - Adlard, J.

AU - Davidson, R.

AU - Eccles, D.

AU - Ong, K.R.

AU - Cook, J.

AU - Douglas, F.

AU - Paterson, J.

AU - Kennedy, M.J.

AU - Miedzybrodzka, Z.

AU - Godwin, A.

AU - Stoppa-Lyonnet, D.

AU - Buecher, B.

AU - Belotti, M.

AU - Tirapo, C.

AU - Mazoyer, S.

AU - Barjhoux, L.

AU - Lasset, C.

AU - Leroux, D.

AU - Faivre, L.

AU - Bronner, M.

AU - Prieur, F.

AU - Nogues, C.

AU - Chenevix-Trench, G.

PY - 2011

Y1 - 2011

U2 - 10.1093/hmg/ddr226

DO - 10.1093/hmg/ddr226

M3 - Article

C2 - 21593217

VL - 20

SP - 3304

EP - 3321

JO - Human Molecular Genetics

JF - Human Molecular Genetics

SN - 0964-6906

IS - 16

ER -