Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing...
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3
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Author / Creator
Soucy, Penny , Pastinen, Tomi , Droit, Arnaud , Arason, Adalgeir , Arun, Banu K. , Azzollini, Jacopo , Bane, Anita , Barjhoux, Laure , Barrowdale, Daniel , Benitez, Javier , Berthet, Pascaline , Blok, Marinus J. , Bonanni, Bernardo , Bradbury, Angela R. , Buecher, Bruno , Buys, Saundra S. , Chiquette, Jocelyne , Chung, Wendy K. , Claes, Kathleen B. M. , Daly, Mary B. , Davidson, Rosemarie , De la Hoya, Miguel , De Leeneer, Kim , Dolcetti, Riccardo , Dorfling, Cecilia M. , Eccles, Diana , Einbeigi, Zakaria , Engel, Christoph , Feliubadalo, Lidia , Foretova, Lenka , Fostira, Florentia , Fountzilas, George , Friedman, Eitan , Frost, Debra , Ganschow, Pamela , Garber, Judy , Gayther, Simon A. , Greene, Mark H. , Gronwald, Jacek , Hamann, Ute , Hart, Steven , Imyanitov, Evgeny N. , Jakubowska, Anna , Janavicius, Ramunas , Jensen, Uffe Birk , John, Esther M. , Joseph, Vijai , Just, Walter , Karlan, Beth Y. , Kets, Carolien M. , Kirk, Judy , Kriege, Mieke , Laurent, Maïté , Lazaro, Conxi , Lester, Jenny , Liljegren, Annelie , Loud, Jennifer T. , Manoukian, Siranoush , Mariani, Milena , Meindl, Alfons , Montagna, Marco , Mulligan, Anna Marie , Neuhausen, Susan L. , Nevanlinna, Heli , Nussbaum, Robert L. , Olah, Edith , Olopade, Olufunmilayo I. , Ong, Kai-ren , Oosterwijk, Jan C. , Papi, Laura , Park, Sue Kyung , Pedersen, Inge Sokilde , Peterlongo, Paolo , Rantala, Johanna , Rappaport-Fuerhauser, Christine , Richardson, Andrea , Robson, Mark , Rookus, Matti A. , Shah, Payal D. , Slavin, Thomas P. , Sokolowska, Johanna , Spurdle, Amanda B. , Stadler, Zsofia , Tea, Muy-Kheng , Teulé, Alex , Terry, Mary Beth , Tihomirova, Laima , Tischkowitz, Marc , Tognazzo, Silvia , Toland, Amanda Ewart , Tung, Nadine , van den Ouweland, Ans M. W. , van der Luijt, Rob B. , van Engelen, Klaartje , Varon-Mateeva, Raymonda , Wijnen, Juul T. , Rebbeck, Timothy , Chenevix-Trench, Georgia , Nord, Silje , Easton, Douglas F. , KConFab Investigators , HEBON , EMBRACE , GEMO Study Collaborators , Faculty of Medicine , Department of Clinical Sciences, Lund , Medicinska fakulteten , Lund University , Bröstcancer-genetik , Institutionen för kliniska vetenskaper, Lund , Section I , Breastcancer-genetics , Lunds universitet and Sektion I
Publisher
New York: Springer US
Journal title
Language
English
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Publication information
Publisher
New York: Springer US
Subjects
More information
Scope and Contents
Contents
Purpose
Cis
-acting regulatory SNPs resulting in differential allelic expression (DAE) may, in part, explain the underlying phenotypic variation associated with many complex diseases. To investigate whether common variants associated with DAE were involved in breast cancer susceptibility among
BRCA1
and
BRCA2
mutation carriers, a...
Alternative Titles
Full title
Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3
Authors, Artists and Contributors
Author / Creator
Pastinen, Tomi
Droit, Arnaud
Arason, Adalgeir
Arun, Banu K.
Azzollini, Jacopo
Bane, Anita
Barjhoux, Laure
Barrowdale, Daniel
Benitez, Javier
Berthet, Pascaline
Blok, Marinus J.
Bonanni, Bernardo
Bradbury, Angela R.
Buecher, Bruno
Buys, Saundra S.
Chiquette, Jocelyne
Chung, Wendy K.
Claes, Kathleen B. M.
Daly, Mary B.
Davidson, Rosemarie
De la Hoya, Miguel
De Leeneer, Kim
Dolcetti, Riccardo
Dorfling, Cecilia M.
Eccles, Diana
Einbeigi, Zakaria
Engel, Christoph
Feliubadalo, Lidia
Foretova, Lenka
Fostira, Florentia
Fountzilas, George
Friedman, Eitan
Frost, Debra
Ganschow, Pamela
Garber, Judy
Gayther, Simon A.
Greene, Mark H.
Gronwald, Jacek
Hamann, Ute
Hart, Steven
Imyanitov, Evgeny N.
Jakubowska, Anna
Janavicius, Ramunas
Jensen, Uffe Birk
John, Esther M.
Joseph, Vijai
Just, Walter
Karlan, Beth Y.
Kets, Carolien M.
Kirk, Judy
Kriege, Mieke
Laurent, Maïté
Lazaro, Conxi
Lester, Jenny
Liljegren, Annelie
Loud, Jennifer T.
Manoukian, Siranoush
Mariani, Milena
Meindl, Alfons
Montagna, Marco
Mulligan, Anna Marie
Neuhausen, Susan L.
Nevanlinna, Heli
Nussbaum, Robert L.
Olah, Edith
Olopade, Olufunmilayo I.
Ong, Kai-ren
Oosterwijk, Jan C.
Papi, Laura
Park, Sue Kyung
Pedersen, Inge Sokilde
Peterlongo, Paolo
Rantala, Johanna
Rappaport-Fuerhauser, Christine
Richardson, Andrea
Robson, Mark
Rookus, Matti A.
Shah, Payal D.
Slavin, Thomas P.
Sokolowska, Johanna
Spurdle, Amanda B.
Stadler, Zsofia
Tea, Muy-Kheng
Teulé, Alex
Terry, Mary Beth
Tihomirova, Laima
Tischkowitz, Marc
Tognazzo, Silvia
Toland, Amanda Ewart
Tung, Nadine
van den Ouweland, Ans M. W.
van der Luijt, Rob B.
van Engelen, Klaartje
Varon-Mateeva, Raymonda
Wijnen, Juul T.
Rebbeck, Timothy
Chenevix-Trench, Georgia
Nord, Silje
Easton, Douglas F.
KConFab Investigators
HEBON
EMBRACE
GEMO Study Collaborators
Faculty of Medicine
Department of Clinical Sciences, Lund
Medicinska fakulteten
Lund University
Bröstcancer-genetik
Institutionen för kliniska vetenskaper, Lund
Section I
Breastcancer-genetics
Lunds universitet
Sektion I
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_swepub_primary_oai_swepub_ki_se_501410
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_swepub_ki_se_501410
Other Identifiers
ISSN
0167-6806,1573-7217
E-ISSN
1573-7217
DOI
10.1007/s10549-016-4018-2
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