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Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. / Ramus, Susan J; Kartsonaki, Christiana; Gayther, Simon A; Pharoah, Paul D P; Sinilnikova, Olga M; Beesley, Jonathan; Chen, Xiaoqing; McGuffog, Lesley; Healey, Sue; Couch, Fergus J; Wang, Xianshu; Fredericksen, Zachary; Peterlongo, Paolo; Manoukian, Siranoush; Peissel, Bernard; Zaffaroni, Daniela; Roversi, Gaia; Barile, Monica; Viel, Alessandra; Allavena, Anna; Ottini, Laura; Papi, Laura; Gismondi, Viviana; Capra, Fabio; Radice, Paolo; Greene, Mark H; Mai, Phuong L; Andrulis, Irene L; Glendon, Gord; Ozcelik, Hilmi; Thomassen, Mads; Gerdes, Anne-Marie; Kruse, Torben A; Cruger, Dorthe; Jensen, Uffe Birk; Caligo, Maria Adelaide; Olsson, Håkan; Kristoffersson, Ulf; Lindblom, Annika; Arver, Brita; Karlsson, Per W.; Stenmark Askmalm, Marie; Borg, Ake; Neuhausen, Susan L; Ding, Yuan Chun; Nathanson, Katherine L; Domchek, Susan M; Hansen, Thomas v O; Jønson, Lars; Ejlertsen, Bent; OCGN.
I:
National Cancer Institute. Journal (Print), Bind 103, Nr. 2, 2011, s. 105-16.
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Harvard
Ramus, SJ, Kartsonaki, C, Gayther, SA, Pharoah, PDP, Sinilnikova, OM, Beesley, J, Chen, X, McGuffog, L, Healey, S, Couch, FJ, 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, MH, Mai, PL, Andrulis, IL, Glendon, G, Ozcelik, H, Thomassen, M
, Gerdes, A-M, Kruse, TA, Cruger, D, Jensen, UB, Caligo, MA, Olsson, H, Kristoffersson, U, Lindblom, A, Arver, B, Karlsson, PW, Stenmark Askmalm, M, Borg, A, Neuhausen, SL, Ding, YC, Nathanson, KL, Domchek, SM
, Hansen, TVO, Jønson, L
, Ejlertsen, B & OCGN 2011, '
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers',
National Cancer Institute. Journal (Print), bind 103, nr. 2, s. 105-16.
https://doi.org/10.1093/jnci/djq494APA
Ramus, S. J., Kartsonaki, C., Gayther, S. A., Pharoah, P. D. P., Sinilnikova, O. M., Beesley, J., Chen, X., McGuffog, L., Healey, S., Couch, F. J., Wang, X., Fredericksen, Z., Peterlongo, P., Manoukian, S., Peissel, B., Zaffaroni, D., Roversi, G., Barile, M., Viel, A., ... OCGN (2011).
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers.
National Cancer Institute. Journal (Print),
103(2), 105-16.
https://doi.org/10.1093/jnci/djq494Vancouver
Ramus SJ, Kartsonaki C, Gayther SA, Pharoah PDP, Sinilnikova OM, Beesley J o.a.
Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers.
National Cancer Institute. Journal (Print). 2011;103(2):105-16.
https://doi.org/10.1093/jnci/djq494Author
Ramus, Susan J ; Kartsonaki, Christiana ; Gayther, Simon A ; Pharoah, Paul D P ; Sinilnikova, Olga M ; Beesley, Jonathan ; Chen, Xiaoqing ; McGuffog, Lesley ; Healey, Sue ; Couch, Fergus J ; Wang, Xianshu ; Fredericksen, Zachary ; Peterlongo, Paolo ; Manoukian, Siranoush ; Peissel, Bernard ; Zaffaroni, Daniela ; Roversi, Gaia ; Barile, Monica ; Viel, Alessandra ; Allavena, Anna ; Ottini, Laura ; Papi, Laura ; Gismondi, Viviana ; Capra, Fabio ; Radice, Paolo ; Greene, Mark H ; Mai, Phuong L ; Andrulis, Irene L ; Glendon, Gord ; Ozcelik, Hilmi ; Thomassen, Mads ; Gerdes, Anne-Marie ; Kruse, Torben A ; Cruger, Dorthe ; Jensen, Uffe Birk ; Caligo, Maria Adelaide ; Olsson, Håkan ; Kristoffersson, Ulf ; Lindblom, Annika ; Arver, Brita ; Karlsson, Per W. ; Stenmark Askmalm, Marie ; Borg, Ake ; Neuhausen, Susan L ; Ding, Yuan Chun ; Nathanson, Katherine L ; Domchek, Susan M ; Hansen, Thomas v O ; Jønson, Lars ; Ejlertsen, Bent ; OCGN. / Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. I: National Cancer Institute. Journal (Print). 2011 ; Bind 103, Nr. 2. s. 105-16.
Bibtex
@article{e670c9b2565e40a5939d1e873a7d5e2c,
title = "Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers",
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.",
author = "Ramus, {Susan J} and Christiana Kartsonaki and Gayther, {Simon A} and Pharoah, {Paul D P} and Sinilnikova, {Olga M} and Jonathan Beesley and Xiaoqing Chen and Lesley McGuffog and Sue Healey and Couch, {Fergus J} and Xianshu Wang and Zachary Fredericksen and Paolo Peterlongo and Siranoush Manoukian and Bernard Peissel and Daniela Zaffaroni and Gaia Roversi and Monica Barile and Alessandra Viel and Anna Allavena and Laura Ottini and Laura Papi and Viviana Gismondi and Fabio Capra and Paolo Radice and Greene, {Mark H} and Mai, {Phuong L} and Andrulis, {Irene L} and Gord Glendon and Hilmi Ozcelik and Mads Thomassen and Anne-Marie Gerdes and Kruse, {Torben A} and Dorthe Cruger and Jensen, {Uffe Birk} and Caligo, {Maria Adelaide} and H{\aa}kan Olsson and Ulf Kristoffersson and Annika Lindblom and Brita Arver and Karlsson, {Per W.} and {Stenmark Askmalm}, Marie and Ake Borg and Neuhausen, {Susan L} and Ding, {Yuan Chun} and Nathanson, {Katherine L} and Domchek, {Susan M} and Hansen, {Thomas v O} and Lars J{\o}nson and Bent Ejlertsen and Gerdes, {Anne-Marie Ax{\o}}",
year = "2011",
doi = "http://dx.doi.org/10.1093/jnci/djq494",
language = "English",
volume = "103",
pages = "105--16",
journal = "National Cancer Institute. Journal (Print)",
issn = "0027-8874",
publisher = "Oxford University Press",
number = "2",
}
RIS
TY - JOUR
T1 - Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers
AU - Ramus, Susan J
AU - Kartsonaki, Christiana
AU - Gayther, Simon A
AU - Pharoah, Paul D P
AU - Sinilnikova, Olga M
AU - Beesley, Jonathan
AU - Chen, Xiaoqing
AU - McGuffog, Lesley
AU - Healey, Sue
AU - Couch, Fergus J
AU - Wang, Xianshu
AU - Fredericksen, Zachary
AU - Peterlongo, Paolo
AU - Manoukian, Siranoush
AU - Peissel, Bernard
AU - Zaffaroni, Daniela
AU - Roversi, Gaia
AU - Barile, Monica
AU - Viel, Alessandra
AU - Allavena, Anna
AU - Ottini, Laura
AU - Papi, Laura
AU - Gismondi, Viviana
AU - Capra, Fabio
AU - Radice, Paolo
AU - Greene, Mark H
AU - Mai, Phuong L
AU - Andrulis, Irene L
AU - Glendon, Gord
AU - Ozcelik, Hilmi
AU - Thomassen, Mads
AU - Gerdes, Anne-Marie
AU - Kruse, Torben A
AU - Cruger, Dorthe
AU - Jensen, Uffe Birk
AU - Caligo, Maria Adelaide
AU - Olsson, Håkan
AU - Kristoffersson, Ulf
AU - Lindblom, Annika
AU - Arver, Brita
AU - Karlsson, Per W.
AU - Stenmark Askmalm, Marie
AU - Borg, Ake
AU - Neuhausen, Susan L
AU - Ding, Yuan Chun
AU - Nathanson, Katherine L
AU - Domchek, Susan M
AU - Hansen, Thomas v O
AU - Jønson, Lars
AU - Ejlertsen, Bent
AU - OCGN
PY - 2011
Y1 - 2011
N2 - 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.
AB - 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.
U2 - http://dx.doi.org/10.1093/jnci/djq494
DO - http://dx.doi.org/10.1093/jnci/djq494
M3 - Journal article
VL - 103
SP - 105
EP - 116
JO - National Cancer Institute. Journal (Print)
JF - National Cancer Institute. Journal (Print)
SN - 0027-8874
IS - 2
ER -
