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Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. / Gaudet, Mia M; Kirchhoff, Tomas; Green, Todd; Vijai, Joseph; Korn, Joshua M; Guiducci, Candace; Segrè, Ayellet V; McGee, Kate; McGuffog, Lesley; Kartsonaki, Christiana; Morrison, Jonathan; Healey, Sue; Sinilnikova, Olga M; Stoppa-Lyonnet, Dominique; Mazoyer, Sylvie; Gauthier-Villars, Marion; Sobol, Hagay; Longy, Michel; Frenay, Marc; GEMO Study Collaborators; Hogervorst, Frans B L; Rookus, Matti A; Collée, J Margriet; Hoogerbrugge, Nicoline; van Roozendaal, Kees E P; Piedmonte, Marion; Rubinstein, Wendy; Nerenstone, Stacy; Van Le, Linda; Blank, Stephanie V; Caldés, Trinidad; de la Hoya, Miguel; Nevanlinna, Heli; Aittomäki, Kristiina; Lazaro, Conxi; Blanco, Ignacio; Arason, Adalgeir; Johannsson, Oskar T; Barkardottir, Rosa B; Devilee, Peter; Olopade, Olofunmilayo I; Neuhausen, Susan L; Wang, Xianshu; Fredericksen, Zachary S; Peterlongo, Paolo; Manoukian, Siranoush; Barile, Monica; Viel, Alessandra; Overeem Hansen, Thomas V; Nielsen, Finn C; HEBON Study Collaborators.
I:
P L o S Genetics, Bind 6, Nr. 10, 01.10.2010, s. e1001183.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
Gaudet, MM, Kirchhoff, T, Green, T, Vijai, J, Korn, JM, Guiducci, C, Segrè, AV, McGee, K, McGuffog, L, Kartsonaki, C, Morrison, J, Healey, S, Sinilnikova, OM, Stoppa-Lyonnet, D, Mazoyer, S, Gauthier-Villars, M, Sobol, H, Longy, M, Frenay, M, GEMO Study Collaborators, Hogervorst, FBL, Rookus, MA, Collée, JM, Hoogerbrugge, N, van Roozendaal, KEP, Piedmonte, M, Rubinstein, W, Nerenstone, S, Van Le, L, Blank, SV, Caldés, T, de la Hoya, M, Nevanlinna, H, Aittomäki, K, Lazaro, C, Blanco, I, Arason, A, Johannsson, OT, Barkardottir, RB, Devilee, P, Olopade, OI, Neuhausen, SL, Wang, X, Fredericksen, ZS, Peterlongo, P, Manoukian, S, Barile, M, Viel, A
, Overeem Hansen, TV, Nielsen, FC & HEBON Study Collaborators 2010, '
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer',
P L o S Genetics, bind 6, nr. 10, s. e1001183.
https://doi.org/10.1371/journal.pgen.1001183APA
Gaudet, M. M., Kirchhoff, T., Green, T., Vijai, J., Korn, J. M., Guiducci, C., Segrè, A. V., McGee, K., McGuffog, L., Kartsonaki, C., Morrison, J., Healey, S., Sinilnikova, O. M., Stoppa-Lyonnet, D., Mazoyer, S., Gauthier-Villars, M., Sobol, H., Longy, M., Frenay, M., ... HEBON Study Collaborators (2010).
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.
P L o S Genetics,
6(10), e1001183.
https://doi.org/10.1371/journal.pgen.1001183Vancouver
Gaudet MM, Kirchhoff T, Green T, Vijai J, Korn JM, Guiducci C o.a.
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.
P L o S Genetics. 2010 okt. 1;6(10):e1001183.
https://doi.org/10.1371/journal.pgen.1001183Author
Gaudet, Mia M ; Kirchhoff, Tomas ; Green, Todd ; Vijai, Joseph ; Korn, Joshua M ; Guiducci, Candace ; Segrè, Ayellet V ; McGee, Kate ; McGuffog, Lesley ; Kartsonaki, Christiana ; Morrison, Jonathan ; Healey, Sue ; Sinilnikova, Olga M ; Stoppa-Lyonnet, Dominique ; Mazoyer, Sylvie ; Gauthier-Villars, Marion ; Sobol, Hagay ; Longy, Michel ; Frenay, Marc ; GEMO Study Collaborators ; Hogervorst, Frans B L ; Rookus, Matti A ; Collée, J Margriet ; Hoogerbrugge, Nicoline ; van Roozendaal, Kees E P ; Piedmonte, Marion ; Rubinstein, Wendy ; Nerenstone, Stacy ; Van Le, Linda ; Blank, Stephanie V ; Caldés, Trinidad ; de la Hoya, Miguel ; Nevanlinna, Heli ; Aittomäki, Kristiina ; Lazaro, Conxi ; Blanco, Ignacio ; Arason, Adalgeir ; Johannsson, Oskar T ; Barkardottir, Rosa B ; Devilee, Peter ; Olopade, Olofunmilayo I ; Neuhausen, Susan L ; Wang, Xianshu ; Fredericksen, Zachary S ; Peterlongo, Paolo ; Manoukian, Siranoush ; Barile, Monica ; Viel, Alessandra ; Overeem Hansen, Thomas V ; Nielsen, Finn C ; HEBON Study Collaborators. / Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. I: P L o S Genetics. 2010 ; Bind 6, Nr. 10. s. e1001183.
Bibtex
@article{b9d7cdd50ee942bcbcbd13128fbe502f,
title = "Common genetic variants and modification of penetrance of BRCA2-associated breast cancer",
abstract = "The considerable uncertainty regarding cancer risks associated with inherited mutations of BRCA2 is due to unknown factors. To investigate whether common genetic variants modify penetrance for BRCA2 mutation carriers, we undertook a two-staged genome-wide association study in BRCA2 mutation carriers. In stage 1 using the Affymetrix 6.0 platform, 592,163 filtered SNPs genotyped were available on 899 young (",
author = "Gaudet, {Mia M} and Tomas Kirchhoff and Todd Green and Joseph Vijai and Korn, {Joshua M} and Candace Guiducci and Segr{\`e}, {Ayellet V} and Kate McGee and Lesley McGuffog and Christiana Kartsonaki and Jonathan Morrison and Sue Healey and Sinilnikova, {Olga M} and Dominique Stoppa-Lyonnet and Sylvie Mazoyer and Marion Gauthier-Villars and Hagay Sobol and Michel Longy and Marc Frenay and {GEMO Study Collaborators} and Hogervorst, {Frans B L} and Rookus, {Matti A} and Coll{\'e}e, {J Margriet} and Nicoline Hoogerbrugge and {van Roozendaal}, {Kees E P} and Marion Piedmonte and Wendy Rubinstein and Stacy Nerenstone and {Van Le}, Linda and Blank, {Stephanie V} and Trinidad Cald{\'e}s and {de la Hoya}, Miguel and Heli Nevanlinna and Kristiina Aittom{\"a}ki and Conxi Lazaro and Ignacio Blanco and Adalgeir Arason and Johannsson, {Oskar T} and Barkardottir, {Rosa B} and Peter Devilee and Olopade, {Olofunmilayo I} and Neuhausen, {Susan L} and Xianshu Wang and Fredericksen, {Zachary S} and Paolo Peterlongo and Siranoush Manoukian and Monica Barile and Alessandra Viel and {Overeem Hansen}, {Thomas V} and Nielsen, {Finn C} and Nielsen, {Finn Cilius}",
year = "2010",
month = oct,
day = "1",
doi = "http://dx.doi.org/10.1371/journal.pgen.1001183",
language = "English",
volume = "6",
pages = "e1001183",
journal = "P L o S Genetics",
issn = "1553-7390",
publisher = "Public Library of Science",
number = "10",
}
RIS
TY - JOUR
T1 - Common genetic variants and modification of penetrance of BRCA2-associated breast cancer
AU - Gaudet, Mia M
AU - Kirchhoff, Tomas
AU - Green, Todd
AU - Vijai, Joseph
AU - Korn, Joshua M
AU - Guiducci, Candace
AU - Segrè, Ayellet V
AU - McGee, Kate
AU - McGuffog, Lesley
AU - Kartsonaki, Christiana
AU - Morrison, Jonathan
AU - Healey, Sue
AU - Sinilnikova, Olga M
AU - Stoppa-Lyonnet, Dominique
AU - Mazoyer, Sylvie
AU - Gauthier-Villars, Marion
AU - Sobol, Hagay
AU - Longy, Michel
AU - Frenay, Marc
AU - GEMO Study Collaborators, null
AU - Hogervorst, Frans B L
AU - Rookus, Matti A
AU - Collée, J Margriet
AU - Hoogerbrugge, Nicoline
AU - van Roozendaal, Kees E P
AU - Piedmonte, Marion
AU - Rubinstein, Wendy
AU - Nerenstone, Stacy
AU - Van Le, Linda
AU - Blank, Stephanie V
AU - Caldés, Trinidad
AU - de la Hoya, Miguel
AU - Nevanlinna, Heli
AU - Aittomäki, Kristiina
AU - Lazaro, Conxi
AU - Blanco, Ignacio
AU - Arason, Adalgeir
AU - Johannsson, Oskar T
AU - Barkardottir, Rosa B
AU - Devilee, Peter
AU - Olopade, Olofunmilayo I
AU - Neuhausen, Susan L
AU - Wang, Xianshu
AU - Fredericksen, Zachary S
AU - Peterlongo, Paolo
AU - Manoukian, Siranoush
AU - Barile, Monica
AU - Viel, Alessandra
AU - Overeem Hansen, Thomas V
AU - Nielsen, Finn C
AU - HEBON Study Collaborators
PY - 2010/10/1
Y1 - 2010/10/1
N2 - The considerable uncertainty regarding cancer risks associated with inherited mutations of BRCA2 is due to unknown factors. To investigate whether common genetic variants modify penetrance for BRCA2 mutation carriers, we undertook a two-staged genome-wide association study in BRCA2 mutation carriers. In stage 1 using the Affymetrix 6.0 platform, 592,163 filtered SNPs genotyped were available on 899 young (
AB - The considerable uncertainty regarding cancer risks associated with inherited mutations of BRCA2 is due to unknown factors. To investigate whether common genetic variants modify penetrance for BRCA2 mutation carriers, we undertook a two-staged genome-wide association study in BRCA2 mutation carriers. In stage 1 using the Affymetrix 6.0 platform, 592,163 filtered SNPs genotyped were available on 899 young (
U2 - http://dx.doi.org/10.1371/journal.pgen.1001183
DO - http://dx.doi.org/10.1371/journal.pgen.1001183
M3 - Journal article
VL - 6
SP - e1001183
JO - P L o S Genetics
JF - P L o S Genetics
SN - 1553-7390
IS - 10
ER -
