Zobrazeno 71 - 80
of 179
pro vyhledávání: '"Orland Diez"'
Autor:
Marco Montagna, Bruno Buecher, Goska Leslie, Daniel Barrowdale, Anita Bane, Louise Izatt, Eitan Friedman, Yosr Hamdi, Kenneth Offit, Klaartje van Engelen, Soo Hwang Teo, Frans B. L. Hogervorst, Conxi Lázaro, Sylvie Mazoyer, Diana Eccles, Yuan Chun Ding, Laura Papi, Georgia Chenevix-Trench, Katarzyna Kaczmarek, Laima Tihomirova, Jacek Gronwald, Jocelyne Chiquette, Patricia A. Ganz, Thomas P. Slavin, Kathleen Claes, Paolo Radice, Elizabeth J. van Rensburg, Adalgeir Arason, Lenka Foretova, Milena Mariani, Johanna Rantala, Pascaline Berthet, Evgeny N. Imyanitov, Claudine Isaacs, Esther M. John, Maite Laurent, Irene L. Andrulis, Juul T. Wijnen, Paolo Peterlongo, Susan M. Domchek, Banu Arun, Amanda E. Toland, Anna Marie Mulligan, Penny Soucy, Kristiina Aittomäki, Orland Diez, Heli Nevanlinna, Anne-Marie Gerdes, Austin Miller, Olufunmilayo I. Olopade, Raymonda Varon-Mateeva, Alfons Meindl, Cecilia M. Dorfling, Niklas Loman, Paul A. James, Susan L. Neuhausen, Muy Kheng Tea, Inge Søkilde Pedersen, Arnaud Droit, D. Gareth Evans, Mark E. Robson, Jennifer T. Loud, Jan C. Oosterwijk, Judy Garber, Douglas F. Easton, Jacques Simard, Mark H. Greene, Pamela S. Ganschow, Edith Olah, Audrey Lemaçon, Norbert Arnold, Catherine M. Phelan, Gad Rennert, Judy Kirk, Johanna Sokolowska, Tomi Pastinen, Robert L. Nussbaum, Simon A. Gayther, Karoline B. Kuchenbaeker, Mads Thomassen, Ros Eeles, Riccardo Dolcetti, Hanne Meijers-Heijboer, Marc Tischkowitz, George Fountzilas, Laure Barjhoux, Kristie Bobolis, Christoph Engel, Bernardo Bonanni, Sue K. Park, Beth Y. Karlan, Nicolas Sevenet, Bent Ejlertsen, Wendy K. Chung, Timothy R. Rebbeck, Amanda B. Spurdle, Peter J. Hulick, Mary B. Daly, Yen Y. Tan, Annelie Liljegren, Carolien M. Kets, Miguel de la Hoya, Gord Glendon, Mieke Kriege, Rita K. Schmutzler, Manuel R. Teixeira, Christine Rappaport-Fuerhauser, Pedro Pérez Segura, William D. Foulkes, Rosemarie Davidson, Steven N. Hart, Javier Benitez, Jenny Lester, Melissa C. Southey, Ramunas Janavicius, Uffe Birk Jensen, Zakaria Einbeigi, Christian F. Singer, Jacopo Azzollini, Alex Teulé, David E. Goldgar, Ans M.W. van den Ouweland, Anna Jakubowska, Angela R. Bradbury, Dominique Stoppa-Lyonnet, Carole Brewer, Zsofia K. Stadler, Nadine Tung, Eric Hahnen, Vijai Joseph, Grzegorz Sukiennicki, Siranoush Manoukian, Debra Frost, Maria A. Caligo, Andrew K. Godwin, Christian Sutter, Bernard Peissel, Andrea L. Richardson, Kim De Leeneer, Antonis C. Antoniou, Florentia Fostira, Lesley McGuffog, Matti A. Rookus, Mary Beth Terry, Saundra S. Buys, Fabienne Lesueur, Gustavo C. Rodriguez, Julian Adlard, Barbara Wappenschmidt, Marinus J. Blok, Yael Laitman, Rob B. van der Luijt, Thomas Hansen, Francesca Damiola, Katherine L. Nathanson, Silje Nord, Kai Ren Ong, Ana Osorio, Katie Snape, Fergus J. Couch, John L. Hays, Walter Just, Ute Hamann, Silvia Tognazzo, Payal D. Shah, Valérie Bonadona, Ida Marie Heeholm Sonderstrup, Lídia Feliubadaló
Publikováno v:
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Breast Cancer Research and Treatment, 161(1), 117-134. Springer, Cham
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, De la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadalo, L, Foretova, L, Fostira, F, Pedersen, I S & EMBRACE 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2
Breast Cancer Research and Treatment, 161(1), 117-134. Springer New York
Breast Cancer Research and Treatment, 161, 1, pp. 117-134
Breast Cancer Research and Treatment, 161, 117-134
Hamdi, Y; Soucy, P; Kuchenbaeker, KB; Pastinen, T; Droit, A; Lemacon, A; et al.(2017). 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. BREAST CANCER RESEARCH AND TREATMENT, 161(1), 117-134. doi: 10.1007/s10549-016-4018-2. UCLA: Retrieved from: http://www.escholarship.org/uc/item/03k1w9cm
Breast Cancer Research and Treatment, 161(1), 117-134
Breast Cancer Research and Treatment, 161(1), 117. Springer New York
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, De la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadalo, L, Foretova, L, Jensen, U B, Pedersen, I S & EMBRACE 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117–134 . https://doi.org/10.1007/s10549-016-4018-2
Breast cancer research and treatment, 161(1), 117-134. Springer New York
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Azzollini, J, Arun, B K, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K A, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, de la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, EMBRACE, Engel, C, Gareth Evans, D, Feliubadaló, L, Foretova, L, Fostira, F, Gerdes, A-M, Easton, D F, Antoniou, A C & Simard, J 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2
kConFab Investigators, HEBON, GEMO Study Collaborators & EMBRACE 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2
BREAST CANCER RESEARCH AND TREATMENT
Repisalud
Instituto de Salud Carlos III (ISCIII)
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, De la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadalo, L, Meijers-Heijboer, H E J, Oosterwijk, J C, van Engelen, K, EMBRACE, GEMO Study Collaborators, HEBON & KConFab Investigators 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2
Breast Cancer Research and Treatment
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benítez, J, Berthet, P, Blok, M J, Bobolis, K A, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, de la Hoya, M, De Leeneer, K, Díez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadaló, L, Foretova, L, Gerdes, A-M, Thomassen, M & EMBRACE 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2
Breast Cancer Research and Treatment, 161(1), 117-134. SPRINGER
Consejería de Sanidad de la Comunidad de Madrid
Breast Cancer Research and Treatment, 161(1), 117-134. Springer, Cham
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, De la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadalo, L, Foretova, L, Fostira, F, Pedersen, I S & EMBRACE 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2
Breast Cancer Research and Treatment, 161(1), 117-134. Springer New York
Breast Cancer Research and Treatment, 161, 1, pp. 117-134
Breast Cancer Research and Treatment, 161, 117-134
Hamdi, Y; Soucy, P; Kuchenbaeker, KB; Pastinen, T; Droit, A; Lemacon, A; et al.(2017). 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. BREAST CANCER RESEARCH AND TREATMENT, 161(1), 117-134. doi: 10.1007/s10549-016-4018-2. UCLA: Retrieved from: http://www.escholarship.org/uc/item/03k1w9cm
Breast Cancer Research and Treatment, 161(1), 117-134
Breast Cancer Research and Treatment, 161(1), 117. Springer New York
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, De la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadalo, L, Foretova, L, Jensen, U B, Pedersen, I S & EMBRACE 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117–134 . https://doi.org/10.1007/s10549-016-4018-2
Breast cancer research and treatment, 161(1), 117-134. Springer New York
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Azzollini, J, Arun, B K, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K A, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, de la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, EMBRACE, Engel, C, Gareth Evans, D, Feliubadaló, L, Foretova, L, Fostira, F, Gerdes, A-M, Easton, D F, Antoniou, A C & Simard, J 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2
kConFab Investigators, HEBON, GEMO Study Collaborators & EMBRACE 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2
BREAST CANCER RESEARCH AND TREATMENT
Repisalud
Instituto de Salud Carlos III (ISCIII)
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benitez, J, Berthet, P, Blok, M J, Bobolis, K, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, De la Hoya, M, De Leeneer, K, Diez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadalo, L, Meijers-Heijboer, H E J, Oosterwijk, J C, van Engelen, K, EMBRACE, GEMO Study Collaborators, HEBON & KConFab Investigators 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2
Breast Cancer Research and Treatment
Hamdi, Y, Soucy, P, Kuchenbaeker, K B, Pastinen, T, Droit, A, Lemaçon, A, Adlard, J, Aittomäki, K, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Azzollini, J, Bane, A, Barjhoux, L, Barrowdale, D, Benítez, J, Berthet, P, Blok, M J, Bobolis, K A, Bonadona, V, Bonanni, B, Bradbury, A R, Brewer, C, Buecher, B, Buys, S, Caligo, M A, Chiquette, J, Chung, W K, Claes, K B M, Daly, M B, Damiola, F, Davidson, R, de la Hoya, M, De Leeneer, K, Díez, O, Ding, Y C, Dolcetti, R, Domchek, S M, Dorfling, C M, Eccles, D, Eeles, R, Einbeigi, Z, Ejlertsen, B, Engel, C, Gareth Evans, D, Feliubadaló, L, Foretova, L, Gerdes, A-M, Thomassen, M & EMBRACE 2017, ' 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 ', Breast Cancer Research and Treatment, vol. 161, no. 1, pp. 117-134 . https://doi.org/10.1007/s10549-016-4018-2
Breast Cancer Research and Treatment, 161(1), 117-134. SPRINGER
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 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba8cf2d9bb045cb1dbafc6fe95cfcd7b
https://hdl.handle.net/20.500.12530/33541
https://hdl.handle.net/20.500.12530/33541
Autor:
Orland Diez, Katherine A. Hoadley, Judith Balmaña, Cristina Cruz, Charles M. Perou, Aleix Prat
Publikováno v:
Breast Cancer Research and Treatment
BRCA1-mutated breast cancer is associated with basal-like disease; however, it is currently unclear if the presence of a BRCA1 mutation depicts a different entity within this subgroup. In this study, we compared the molecular features among basal-lik
Autor:
Anna Tenés, Eva Esteban-Cardeñosa, Orland Diez, Teresa Ramón y Cajal, Sandra Bonache, Judith Balmaña, Ana Vega, Kira Yanowsky, Alicia Barroso, Marta Santamariña, Gemma Montalban, Trinidad Caldés, Eduardo Díaz-Rubio, Gorka Ruiz de Garibay, Mar Infante, Ana Osorio, Ana Blanco, Javier Benitez, Miguel de la Hoya, Sara Gutiérrez-Enríquez, Mónica Cornet, Neus Gadea, Adriana Lasa
Publikováno v:
International Journal of Cancer. 134:2088-2097
RAD51D mutations have been recently identified in breast (BC) and ovarian cancer (OC) families. Although an etiological role in OC appears to be present, the association of RAD51D mutations and BC risk is more unclear. We aimed to determine the preva
Autor:
Eva Esteban-Cardeñosa, Cristina Miner, Eva María Sánchez-Tapia, Mar Infante, Mercedes Durán, Lídia Feliubadaló, María García-González, Ana Osorio, Orland Diez, Beatriz Díez-Gómez, Cristina Martínez-Bouzas, Miguel de la Hoya, Alberto Acedo, Alicia Barroso, Rogelio González-Sarmiento, Adriana Lasa, Eladio Velasco, Javier Godino, Enrique Lastra, Alexandre Teulé
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
CARCINOGENESIS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
CARCINOGENESIS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Supplementary Tables S1–S3 and figures S1 and S2 can be found at: http://carcin.oxfordjournals.org/.-- et al.
BRCA2-c.2808_2811del (3036delACAA) is one of the most reported germline mutations in non-Ashkenazi breast cancer patients. We investi
BRCA2-c.2808_2811del (3036delACAA) is one of the most reported germline mutations in non-Ashkenazi breast cancer patients. We investi
Autor:
Miriam Masas, Miguel de la Hoya, Sara Gutiérrez-Enríquez, Sandra Bonache, Judith Balmaña, Anna Tenés, Orland Diez
Publikováno v:
Journal of Cancer Research and Clinical Oncology. 139:529-532
About 5-10 % of breast cancer is due to inherited disease predisposition. Currently known susceptibility genes such as BRCA1 and BRCA2 explain less than 25 % of familial aggregation of breast cancer, which suggests the involvement of additional genet
Autor:
Agustin Barnadas, Harry Ostrer, Søren M. Bentzen, David Azria, Rebecca Elliott, C.A. Koch, John Yarnold, Petra Seibold, M. Molla, Christian Nicolaj Andreassen, Laura Fachal, Ana Vega, David P. Dearnaley, Emma Hall, Barry S. Rosenstein, Sarah L. Kerns, Michael Blackshaw, Piet Ost, Matthew Parliament, Marie Overgaard, Jamie A. Cesaretti, Catharine M L West, Teresa Ramón y Cajal, Michael Sia, Charlotte E. Coles, Orland Diez, Dirk De Ruysscher, Matthew R. Sydes, Jenny Chang-Claude, Antonio Gómez-Caamaño, Jan Alsner, Christopher J. Talbot, Maria J. Fuentes-Raspall, Odilia Popanda, Gillian C. Barnett, Jens Overgaard, Neil G. Burnet, Hubert Thierens, Leila Dorling, Sara Gutiérrez-Enríquez, R. Paul Symonds, Danny Vesprini, Alison M. Dunning, Kim De Ruyck
Publikováno v:
Radiotherapy and Oncology, 121(3), 431-439. Elsevier Ireland Ltd
Radiotherapy and Oncology
Radiotherapy and Oncology, Elsevier, 2016, 121 (3), pp.431-439. ⟨10.1016/j.radonc.2016.06.017⟩
RADIOTHERAPY AND ONCOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Andreassen, C N, Rosenstein, B S, Kerns, S L, Ostrer, H, De Ruysscher, D, Cesaretti, J A, Barnett, G C, Dunning, A M, Dorling, L, West, C M L, Burnet, N G, Elliott, R, Coles, C, Hall, E, Fachal, L, Vega, A, Gómez-Caamaño, A, Talbot, C J, Symonds, R P, De Ruyck, K, Thierens, H, Ost, P, Chang-Claude, J, Seibold, P, Popanda, O, Overgaard, M, Dearnaley, D, Sydes, M R, Azria, D, Koch, C A, Parliament, M, Blackshaw, M, Sia, M, Fuentes-Raspall, M J, Ramon Y Cajal, T, Barnadas, A, Vesprini, D, Gutiérrez-Enríquez, S, Mollà, M, Díez, O, Yarnold, J R, Overgaard, J, Bentzen, S M, Alsner, J & International Radiogenomics Consortium (RgC) 2016, ' Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients ', Radiotherapy and Oncology, vol. 121, no. 3, pp. 431-439 . https://doi.org/10.1016/j.radonc.2016.06.017
Andreassen, C N, Rosenstein, B S, Kerns, S L, Ostrer, H, De Ruysscher, D, Cesaretti, J A, Barnett, G C, Dunning, A M, Dorling, L, West, C M L, Burnet, N G, Elliott, R, Coles, C, Hall, E, Fachal, L, Vega, A, Gómez-Caamaño, A, Talbot, C J, Symonds, R P, De Ruyck, K, Thierens, H, Ost, P, Chang-Claude, J, Seibold, P, Popanda, O, Overgaard, M, Dearnaley, D, Sydes, M R, Azria, D, Koch, C A, Parliament, M, Blackshaw, M, Sia, M, Fuentes-Raspall, M J, Ramon Y Cajal, T, Barnadas, A, Vesprini, D, Gutiérrez-Enríquez, S, Mollà, M, Díez, O, Yarnold, J R, Overgaard, J, Bentzen, S M, Alsner, J & International Radiogenomics Consortium (RgC) 2016, ' Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients ', Radiotherapy & Oncology . https://doi.org/10.1016/j.radonc.2016.06.017
Radiotherapy and Oncology
Radiotherapy and Oncology, Elsevier, 2016, 121 (3), pp.431-439. ⟨10.1016/j.radonc.2016.06.017⟩
RADIOTHERAPY AND ONCOLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Andreassen, C N, Rosenstein, B S, Kerns, S L, Ostrer, H, De Ruysscher, D, Cesaretti, J A, Barnett, G C, Dunning, A M, Dorling, L, West, C M L, Burnet, N G, Elliott, R, Coles, C, Hall, E, Fachal, L, Vega, A, Gómez-Caamaño, A, Talbot, C J, Symonds, R P, De Ruyck, K, Thierens, H, Ost, P, Chang-Claude, J, Seibold, P, Popanda, O, Overgaard, M, Dearnaley, D, Sydes, M R, Azria, D, Koch, C A, Parliament, M, Blackshaw, M, Sia, M, Fuentes-Raspall, M J, Ramon Y Cajal, T, Barnadas, A, Vesprini, D, Gutiérrez-Enríquez, S, Mollà, M, Díez, O, Yarnold, J R, Overgaard, J, Bentzen, S M, Alsner, J & International Radiogenomics Consortium (RgC) 2016, ' Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients ', Radiotherapy and Oncology, vol. 121, no. 3, pp. 431-439 . https://doi.org/10.1016/j.radonc.2016.06.017
Andreassen, C N, Rosenstein, B S, Kerns, S L, Ostrer, H, De Ruysscher, D, Cesaretti, J A, Barnett, G C, Dunning, A M, Dorling, L, West, C M L, Burnet, N G, Elliott, R, Coles, C, Hall, E, Fachal, L, Vega, A, Gómez-Caamaño, A, Talbot, C J, Symonds, R P, De Ruyck, K, Thierens, H, Ost, P, Chang-Claude, J, Seibold, P, Popanda, O, Overgaard, M, Dearnaley, D, Sydes, M R, Azria, D, Koch, C A, Parliament, M, Blackshaw, M, Sia, M, Fuentes-Raspall, M J, Ramon Y Cajal, T, Barnadas, A, Vesprini, D, Gutiérrez-Enríquez, S, Mollà, M, Díez, O, Yarnold, J R, Overgaard, J, Bentzen, S M, Alsner, J & International Radiogenomics Consortium (RgC) 2016, ' Individual patient data meta-analysis shows a significant association between the ATM rs1801516 SNP and toxicity after radiotherapy in 5456 breast and prostate cancer patients ', Radiotherapy & Oncology . https://doi.org/10.1016/j.radonc.2016.06.017
Purpose: Several small studies have indicated that the ATM rsl 801516 SNP is associated with risk of normal tissue toxicity after radiotherapy. However, the findings have not been consistent. In order to test this SNP in a well-powered study, an indi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed3c24daed41f38a52930d0eada05be2
https://europepmc.org/articles/PMC5559879/
https://europepmc.org/articles/PMC5559879/
Autor:
Kenneth Offit, Hoda Anton-Culver, Ans M.W. van den Ouweland, Siranoush Manoukian, Christine L. Clarke, Kyriaki Michailidou, Antonis C. Antoniou, Maria Kabisch, Isabel dos-Santos-Silva, Douglas F. Easton, Curtis Olswold, Graham G. Giles, Tien Yin Wong, Ursula Eilber, Mads Thomassen, Christopher A. Haiman, Alice J. Sigurdson, Lothar Haeberle, Florence Menegaux, Ana Osorio, Marco Montagna, Katarzyna Jaworska-Bieniek, Eitan Friedman, Simon S. Cross, Daniel Barrowdale, Elinor J. Sawyer, Adam N. Freeman, Caroline Seynaeve, Min Hyuk Lee, Arnaud Droit, Per Hall, Minouk J. Schoemaker, Trinidad Caldés, Peter Hillemanns, Frederik Marmé, Jenny Lester, Michele M. Doody, Bernard Peissel, Peter Kraft, Elza Khusnutdinova, Anna H. Wu, Stéphanie Peeters, Georg Pfeiler, Pascal Guénel, Hidemi Ito, Xingyi Guo, Antoinette Hollestelle, Heli Nevanlinna, Kathleen Claes, Ylva Paulsson-Karlsson, Cecilia M. Dorfling, Roger L. Milne, Daehee Kang, Judith S. Brand, Diether Lambrechts, Olufunmilayo I. Olopade, Simona Agata, Saundra S. Buys, Muhammad Usman Rashid, Fabienne Lesueur, Alicia Beeghly-Fadiel, Peter Devilee, Manjeet K. Bolla, Natalia Antonenkova, Irene Konstantopoulou, Claudine Isaacs, Anja Rudolph, Carl Blomqvist, Tjoung Won Park-Simon, Judy Garber, Csilla Szabo, Francois Bacot, Arto Mannermaa, Yu-Tang Gao, Stig E. Bojesen, Susan L. Neuhausen, Marina Bermisheva, Qiuyin Cai, Zakaria Einbeigi, Christian F. Singer, Qin Wang, Kerstin Rhiem, Sofia Khan, Fiona Lalloo, Robert L. Nussbaum, Thilo Dörk, William J. Blot, Sylvie Mazoyer, Julia A. Knight, Katherine L. Nathanson, Clare Turnbull, Nazneen Rahman, Anne Lise Børresen-Dale, Chuen Neng Lee, Annegien Broeks, Martha J. Shrubsole, Ava Kwong, Jirong Long, Ian G. Campbell, Sara Margolin, Fergus J. Couch, Laima Tihomirova, Mary Beth Terry, Jenny Chang-Claude, Alice S. Whittemore, Joseph Vijai, Alfons Meindl, Xiao-Ou Shu, Shan Wang-Gohrke, Wei Zheng, Beth Y. Karlan, Jacques Simard, Angela Cox, Shahana Ahmed, Polly A. Newcomb, Ritu Salani, Chen-Yang Shen, Adalgeir Arason, Sandrine Tchatchou, Ute Hamann, Elizabeth J. van Rensburg, Michael Jones, Mark H. Greene, Anthony J. Swerdlow, Senno Verhoef, Jonine Figueroa, Hermann Brenner, Volker Arndt, Charles Joly Beauparlant, Esther M. John, Nadege Presneau, Jingmei Li, Laura Papi, Marjanka K. Schmidt, Montserrat Garcia-Closas, Uffe Birk Jensen, Georgia Chenevix-Trench, Paolo Peterlongo, Penny Soucy, Thomas Brüning, Jaana M. Hartikainen, Siddhartha Kar, Ji Yeob Choi, Manuel R. Teixeira, Phuong L. Mai, Alex Teulé, Jyh Cherng Yu, Paul Brennan, Maya Ghoussaini, Edith Olah, Henrik Flyger, Michael Friedlander, Soo Hwang Teo, Frans B. L. Hogervorst, Kathleen M. Egan, David J. Hunter, Kristiina Aittomäki, Joe Dennis, Anna González-Neira, Mikael Hartman, Alison M. Dunning, Doris Steinemann, Debra Frost, Melissa C. Southey, Ramunas Janavicius, Evgeny N. Imyanitov, Catherine M. Phelan, Amanda E. Toland, Anna Marie Mulligan, David ven den Berg, Rita K. Schmutzler, Julian Peto, Irene L. Andrulis, Chenjie Zeng, Kenneth Muir, Peter Schürmann, Saila Kauppila, Banu Arun, Jane Carpenter, Jeffrey N. Weitzel, Yael Laitman, Susan M. Domchek, Robert Winqvist, Caroline Baynes, Brita Arver, Marc Tischkowitz, Kamila Czene, Keitaro Matsuo, Barbara Burwinkel, Miriam Dwek, Kim De Leeneer, David E. Goldgar, Anna Jakubowska, Paul D.P. Pharoah, Peter A. Fasching, Bernd Dworniczak, Susan J. Ramus, Lesley McGuffog, Andrea Gehrig, Michael J. Kerin, Thomas Hansen, Francesca Damiola, John L. Hopper, Loic Le Marchand, Peter J. Hulick, Annika Lindblom, Emily Hallberg, Miguel de la Hoya, Gaetana Gambino, Martine Dumont, Susan L. Slager, Bernardo Bonanni, Bent Ejlertsen, Norhashimah Hassan, Sue Healey, Orland Diez, Mary B. Daly, Carolyn B. Hendricks, Artitaya Lophatananon, Annelie Liljegren, Steven N. Hart, Jan Lubinski, Natalia Bogdanova, Drakoulis Yannoukakos, Steve Ellis, Silje Nord, Hiltrud Brauch, Gad Rennert, Conxi Lázaro, Daniel C. Tessier, Paolo Radice, Dominique Stoppa-Lyonnet, Nadine Tung, Andrew K. Godwin, Suleeporn Sangrajrang, Karoline Kuchenbaecker, Javier Benitez
Publikováno v:
BREAST CANCER RESEARCH
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Zeng, C, Guo, X, Long, J, Kuchenbaecker, K B, Droit, A, Michailidou, K, Ghoussaini, M, Kar, S, Freeman, A, Hopper, J L, Milne, R L, Bolla, M K, Wang, Q, Dennis, J, Agata, S, Ahmed, S, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Arason, A, Arndt, V, Arun, B K, Arver, B, Bacot, F, Barrowdale, D, Baynes, C, Beeghly-Fadiel, A, Benítez, J, Bermisheva, M, Blomqvist, C, Blot, W J, Bogdanova, N V, Bojesen, S E, Bonanni, B, Borresen-Dale, A-L, Brand, J S, Brauch, H, Brennan, P, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Buys, S, Cai, Q, Caldes, T, Campbell, I, Hansen, T V O, Shen, C-Y, Thomassen, M & EMBRACE 2016, ' Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus ', Breast Cancer Research (Online), vol. 18, 64 . https://doi.org/10.1186/s13058-016-0718-0
Zeng, C, Guo, X, Long, J, Kuchenbaecker, K B, Droit, A, Michailidou, K, Ghoussaini, M, Kar, S, Freeman, A, Hopper, J L, Milne, R L, Bolla, M K, Wang, Q, Dennis, J, Agata, S, Ahmed, S, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Arason, A, Arndt, V, Arun, B K, Arver, B, Bacot, F, Barrowdale, D, Baynes, C, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Blomqvist, C, Blot, W J, Bogdanova, N V, Bojesen, S E, Bonanni, B, Borresen-Dale, A L, Brand, J S, Brauch, H, Brennan, P, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Buys, S S, Cai, Q, Caldes, T, Campbell, I, Carpenter, J, Chang-Claude, J, Choi, J Y, Claes, K B M, Clarke, C, Cox, A, Cross, S S, Czene, K, Daly, M B, de la Hoya, M, De Leeneer, K, Devilee, P, Diez, O, Domchek, S M, Doody, M, Dorfling, C M, Dörk, T, dos-Santos-Silva, I, Dumont, M, Dwek, M, Dworniczak, B, Egan, K, Eilber, U, Einbeigi, Z, Ejlertsen, B, Ellis, S, Frost, D, Lalloo, F, Fasching, P A, Figueroa, J, Flyger, H, Friedlander, M, Friedman, E, Gambino, G, Gao, Y T, Garber, J, García-Closas, M, Gehrig, A, Damiola, F, Lesueur, F, Mazoyer, S, Stoppa-Lyonnet, D, Giles, G G, Godwin, A K, Goldgar, D E, González-Neira, A, Greene, M H, Guénel, P, Haeberle, L, Haiman, C A, Hallberg, E, Hamann, U, Hansen, T V O, Hart, S, Hartikainen, J M, Hartman, M, Hassan, N, Healey, S, Hogervorst, F B L, Verhoef, S, Hendricks, C B, Hillemanns, P, Hollestelle, A, Hulick, P J, Hunter, D J, Imyanitov, E N, Isaacs, C, Ito, H, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, Jensen, U B, John, E M, Joly Beauparlant, C, Jones, M, Kabisch, M, Kang, D, Karlan, B Y, Kauppila, S, Kerin, M J, Khan, S, Khusnutdinova, E, Knight, J A, Konstantopoulou, I, Kraft, P, Kwong, A, Laitman, Y, Lambrechts, D, Lazaro, C, Le Marchand, L, Lee, C N, Lee, M H, Lester, J, Li, J, Liljegren, A, Lindblom, A, Lophatananon, A, Lubinski, J, Mai, P L, Mannermaa, A, Manoukian, S, Margolin, S, Marme, F, Matsuo, K, McGuffog, L, Meindl, A, Menegaux, F, Montagna, M, Muir, K, Mulligan, A M, Nathanson, K L, Neuhausen, S L, Nevanlinna, H, Newcomb, P A, Nord, S, Nussbaum, R L, Offit, K, Olah, E, Olopade, O I, Olswold, C, Osorio, A, Papi, L, Park-Simon, T W, Paulsson-Karlsson, Y, Peeters, S, Peissel, B, Peterlongo, P, Peto, J, Pfeiler, G, Phelan, C M, Presneau, N, Radice, P, Rahman, N, Ramus, S J, Rashid, M U, Rennert, G, Rhiem, K, Rudolph, A, Salani, R, Sangrajrang, S, Sawyer, E J, Schmidt, M K, Schmutzler, R K, Schoemaker, M J, Schürmann, P, Seynaeve, C, Shen, C Y, Shrubsole, M J, Shu, X O, Sigurdson, A, Singer, C F, Slager, S, Soucy, P, Southey, M, Steinemann, D, Swerdlow, A, Szabo, C I, Tchatchou, S, Teixeira, M R, Teo, S H, Terry, M B, Tessier, D C, Teulé, A, Thomassen, M, Tihomirova, L, Tischkowitz, M, Toland, A E, Tung, N, Turnbull, C, van den Ouweland, A M W, van Rensburg, E J, ven den Berg, D, Vijai, J, Wang-Gohrke, S, Weitzel, J N, Whittemore, A S, Winqvist, R, Wong, T Y, Wu, A H, Yannoukakos, D, Yu, J C, Pharoah, P D P, Hall, P, Chenevix-Trench, G, Dunning, A M, Simard, J, Couch, F J, Antoniou, A C, Easton, D F & Zheng, W 2016, ' Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus ', Breast Cancer Research, vol. 18, no. 1, 64 . https://doi.org/10.1186/s13058-016-0718-0
Zeng, Chenjie; Guo, Xingyi; Long, Jirong; Kuchenbaecker, Karoline B; Droit, Arnaud; Michailidou, Kyriaki; et al.(2016). Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Breast Cancer Research, 18(1). doi: 10.1186/s13058-016-0718-0. UC Office of the President: California Breast Cancer Research Program. Retrieved from: http://www.escholarship.org/uc/item/6138g1mj
Zeng, C, Guo, X, Long, J, Kuchenbaecker, K B, Droit, A, Michailidou, K, Ghoussaini, M, Kar, S, Freeman, A, Hopper, J L, Milne, R L, Bolla, M K, Wang, Q, Dennis, J, Agata, S, Ahmed, S, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Arason, A, Arndt, V, Arun, B K, Arver, B, Bacot, F, Barrowdale, D, Baynes, C, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Blomqvist, C, Blot, W J, Bogdanova, N V, Bojesen, S E, Bonanni, B, Borresen-Dale, A-L, Brand, J S, Brauch, H, Brennan, P, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Buys, S S, Cai, Q, Caldes, T, Campbell, I, Carpenter, J & Chang-Claude, J & Figueroa, J 2016, ' Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus ', Breast Cancer Research, vol. 18, no. 1, pp. 64 . https://doi.org/10.1186/s13058-016-0718-0
Breast cancer research, 18(64). BioMed Central Ltd.
Europe PubMed Central
Breast Cancer Research : BCR
Zeng, C, Guo, X, Long, J, Kuchenbaecker, K B, Droit, A, Michailidou, K, Ghoussaini, M, Kar, S, Freeman, A, Hopper, J L, Milne, R L, Bolla, M K, Wang, Q, Dennis, J, Agata, S, Ahmed, S, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Arason, A, Arndt, V, Arun, B K, Arver, B, Bacot, F, Barrowdale, D, Baynes, C, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Blomqvist, C, Blot, W J, Bogdanova, N V, Bojesen, S E, Bonanni, B, Borresen-Dale, A-L, Brand, J S, Brauch, H, Brennan, P, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Buys, S S, Clarke, C, Cross, S S, Egan, K, Hunter, D J, Teo, S H, Antoniou, A C 2016, ' Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus ', Breast Cancer Research, vol. 18, no. 1, pp. 64 . https://doi.org/10.1186/s13058-016-0718-0
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Breast Cancer Research, 18:64. BioMed Central Ltd.
Breast Cancer Research, 18
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
instname
Zeng, C, Guo, X, Long, J, Kuchenbaecker, K B, Droit, A, Michailidou, K, Ghoussaini, M, Kar, S, Freeman, A, Hopper, J L, Milne, R L, Bolla, M K, Wang, Q, Dennis, J, Agata, S, Ahmed, S, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Arason, A, Arndt, V, Arun, B K, Arver, B, Bacot, F, Barrowdale, D, Baynes, C, Beeghly-Fadiel, A, Benítez, J, Bermisheva, M, Blomqvist, C, Blot, W J, Bogdanova, N V, Bojesen, S E, Bonanni, B, Borresen-Dale, A-L, Brand, J S, Brauch, H, Brennan, P, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Buys, S, Cai, Q, Caldes, T, Campbell, I, Hansen, T V O, Shen, C-Y, Thomassen, M & EMBRACE 2016, ' Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus ', Breast Cancer Research (Online), vol. 18, 64 . https://doi.org/10.1186/s13058-016-0718-0
Zeng, C, Guo, X, Long, J, Kuchenbaecker, K B, Droit, A, Michailidou, K, Ghoussaini, M, Kar, S, Freeman, A, Hopper, J L, Milne, R L, Bolla, M K, Wang, Q, Dennis, J, Agata, S, Ahmed, S, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Arason, A, Arndt, V, Arun, B K, Arver, B, Bacot, F, Barrowdale, D, Baynes, C, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Blomqvist, C, Blot, W J, Bogdanova, N V, Bojesen, S E, Bonanni, B, Borresen-Dale, A L, Brand, J S, Brauch, H, Brennan, P, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Buys, S S, Cai, Q, Caldes, T, Campbell, I, Carpenter, J, Chang-Claude, J, Choi, J Y, Claes, K B M, Clarke, C, Cox, A, Cross, S S, Czene, K, Daly, M B, de la Hoya, M, De Leeneer, K, Devilee, P, Diez, O, Domchek, S M, Doody, M, Dorfling, C M, Dörk, T, dos-Santos-Silva, I, Dumont, M, Dwek, M, Dworniczak, B, Egan, K, Eilber, U, Einbeigi, Z, Ejlertsen, B, Ellis, S, Frost, D, Lalloo, F, Fasching, P A, Figueroa, J, Flyger, H, Friedlander, M, Friedman, E, Gambino, G, Gao, Y T, Garber, J, García-Closas, M, Gehrig, A, Damiola, F, Lesueur, F, Mazoyer, S, Stoppa-Lyonnet, D, Giles, G G, Godwin, A K, Goldgar, D E, González-Neira, A, Greene, M H, Guénel, P, Haeberle, L, Haiman, C A, Hallberg, E, Hamann, U, Hansen, T V O, Hart, S, Hartikainen, J M, Hartman, M, Hassan, N, Healey, S, Hogervorst, F B L, Verhoef, S, Hendricks, C B, Hillemanns, P, Hollestelle, A, Hulick, P J, Hunter, D J, Imyanitov, E N, Isaacs, C, Ito, H, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, Jensen, U B, John, E M, Joly Beauparlant, C, Jones, M, Kabisch, M, Kang, D, Karlan, B Y, Kauppila, S, Kerin, M J, Khan, S, Khusnutdinova, E, Knight, J A, Konstantopoulou, I, Kraft, P, Kwong, A, Laitman, Y, Lambrechts, D, Lazaro, C, Le Marchand, L, Lee, C N, Lee, M H, Lester, J, Li, J, Liljegren, A, Lindblom, A, Lophatananon, A, Lubinski, J, Mai, P L, Mannermaa, A, Manoukian, S, Margolin, S, Marme, F, Matsuo, K, McGuffog, L, Meindl, A, Menegaux, F, Montagna, M, Muir, K, Mulligan, A M, Nathanson, K L, Neuhausen, S L, Nevanlinna, H, Newcomb, P A, Nord, S, Nussbaum, R L, Offit, K, Olah, E, Olopade, O I, Olswold, C, Osorio, A, Papi, L, Park-Simon, T W, Paulsson-Karlsson, Y, Peeters, S, Peissel, B, Peterlongo, P, Peto, J, Pfeiler, G, Phelan, C M, Presneau, N, Radice, P, Rahman, N, Ramus, S J, Rashid, M U, Rennert, G, Rhiem, K, Rudolph, A, Salani, R, Sangrajrang, S, Sawyer, E J, Schmidt, M K, Schmutzler, R K, Schoemaker, M J, Schürmann, P, Seynaeve, C, Shen, C Y, Shrubsole, M J, Shu, X O, Sigurdson, A, Singer, C F, Slager, S, Soucy, P, Southey, M, Steinemann, D, Swerdlow, A, Szabo, C I, Tchatchou, S, Teixeira, M R, Teo, S H, Terry, M B, Tessier, D C, Teulé, A, Thomassen, M, Tihomirova, L, Tischkowitz, M, Toland, A E, Tung, N, Turnbull, C, van den Ouweland, A M W, van Rensburg, E J, ven den Berg, D, Vijai, J, Wang-Gohrke, S, Weitzel, J N, Whittemore, A S, Winqvist, R, Wong, T Y, Wu, A H, Yannoukakos, D, Yu, J C, Pharoah, P D P, Hall, P, Chenevix-Trench, G, Dunning, A M, Simard, J, Couch, F J, Antoniou, A C, Easton, D F & Zheng, W 2016, ' Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus ', Breast Cancer Research, vol. 18, no. 1, 64 . https://doi.org/10.1186/s13058-016-0718-0
Zeng, Chenjie; Guo, Xingyi; Long, Jirong; Kuchenbaecker, Karoline B; Droit, Arnaud; Michailidou, Kyriaki; et al.(2016). Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus. Breast Cancer Research, 18(1). doi: 10.1186/s13058-016-0718-0. UC Office of the President: California Breast Cancer Research Program. Retrieved from: http://www.escholarship.org/uc/item/6138g1mj
Zeng, C, Guo, X, Long, J, Kuchenbaecker, K B, Droit, A, Michailidou, K, Ghoussaini, M, Kar, S, Freeman, A, Hopper, J L, Milne, R L, Bolla, M K, Wang, Q, Dennis, J, Agata, S, Ahmed, S, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Arason, A, Arndt, V, Arun, B K, Arver, B, Bacot, F, Barrowdale, D, Baynes, C, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Blomqvist, C, Blot, W J, Bogdanova, N V, Bojesen, S E, Bonanni, B, Borresen-Dale, A-L, Brand, J S, Brauch, H, Brennan, P, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Buys, S S, Cai, Q, Caldes, T, Campbell, I, Carpenter, J & Chang-Claude, J & Figueroa, J 2016, ' Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus ', Breast Cancer Research, vol. 18, no. 1, pp. 64 . https://doi.org/10.1186/s13058-016-0718-0
Breast cancer research, 18(64). BioMed Central Ltd.
Europe PubMed Central
Breast Cancer Research : BCR
Zeng, C, Guo, X, Long, J, Kuchenbaecker, K B, Droit, A, Michailidou, K, Ghoussaini, M, Kar, S, Freeman, A, Hopper, J L, Milne, R L, Bolla, M K, Wang, Q, Dennis, J, Agata, S, Ahmed, S, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Arason, A, Arndt, V, Arun, B K, Arver, B, Bacot, F, Barrowdale, D, Baynes, C, Beeghly-Fadiel, A, Benitez, J, Bermisheva, M, Blomqvist, C, Blot, W J, Bogdanova, N V, Bojesen, S E, Bonanni, B, Borresen-Dale, A-L, Brand, J S, Brauch, H, Brennan, P, Brenner, H, Broeks, A, Brüning, T, Burwinkel, B, Buys, S S, Clarke, C, Cross, S S, Egan, K, Hunter, D J, Teo, S H, Antoniou, A C 2016, ' Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus ', Breast Cancer Research, vol. 18, no. 1, pp. 64 . https://doi.org/10.1186/s13058-016-0718-0
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Breast Cancer Research, 18:64. BioMed Central Ltd.
Breast Cancer Research, 18
Article
Background Multiple recent genome-wide association studies (GWAS) have identified a single nucleotide polymorphism (SNP), rs10771399, at 12p11 that is associated with breast cancer risk. Method We performed a fine-scale mapping study of
Background Multiple recent genome-wide association studies (GWAS) have identified a single nucleotide polymorphism (SNP), rs10771399, at 12p11 that is associated with breast cancer risk. Method We performed a fine-scale mapping study of
Autor:
Jirong Long, Simon S. Cross, Marc Tischkowitz, Beth Y. Karlan, Trinidad Caldés, Fergus J. Couch, Charlotte Sagne, Ute Hamann, Olga M. Sinilnikova, Maria Kabisch, Richard C Sallari, Gad Rennert, Daniel Barrowdale, Elinor J. Sawyer, Anthony J. Swerdlow, Jenny Lester, Åke Borg, Anders Bojesen, Rosa B. Barkardottir, Simon A. Gayther, Heli Nevanlinna, Judy Garber, Norbert Arnold, Vilde Drageset Haakensen, Vessela N. Kristensen, Christopher G. Scott, Daehee Kang, Gillian Mitchell, Eitan Friedman, Laura Ottini, Diether Lambrechts, Manjeet K. Bolla, Robert L. Nussbaum, Tomasz Huzarski, Dieter Niederacher, Angela Cox, Rachel Laframboise, Maartje J. Hooning, Volker Arndt, Penny Soucy, Marjanka K. Schmidt, William Blot, Soo Hwang Teo, Anne Lise Børresen-Dale, Maria A. Caligo, Ana Osorio, Orland Diez, Gertraud Maskarinec, Johanna Rantala, Kelly-Anne Phillips, Pascal Guénel, Hidemi Ito, Miquel Angel Pujana, Anna H. Wu, Christy G. Woolcott, Maya Ghoussaini, Hatef Darabi, Sander Canisius, Kay-Tee Khaw, Irene Konstantopoulou, Carl Blomqvist, Christine Rappaport, Joan Brunet, Hermann Brenner, Sylvie Mazoyer, Irene L. Andrulis, Nicholas A Sinnott-Armstrong, Javier Benitez, Claudine Isaacs, Mahdi Moradi Marjaneh, Joseph Vijai, Jennifer Stone, Qin Wang, Caroline Seynaeve, Patricia A. Ganz, Sara Margolin, Paolo Radice, Janet E. Olson, Soo-Chin Lee, Mark H. Greene, Laura Papi, Carmel Apicella, Ava Kwong, Mitul Shah, Matthias W. Beckmann, Yael Laitman, Hoda Anton-Culver, Ans M.W. van den Ouweland, Sue K. Park, Annegien Broeks, Georgia Chenevix-Trench, Jonathan Beesley, Nadja Bogdanova-Markov, Paolo Peterlongo, Paraskevi Apostolou, Bernardo Bonanni, Frederik Marmé, Veli-Matti Kosma, Alfons Meindl, Brian E. Henderson, Rulla M. Tamimi, Siranoush Manoukian, Bent Ejlertsen, Miroslav Kapuscinski, Juliet D. French, Mark E. Sherman, Ji Yeob Choi, Graham G. Giles, Stacey L. Edwards, Evgeny N. Imyanitov, Kamila Czene, Thomas Hansen, Nick Orr, Susanne Kaufmann, Lenka Foretova, Celine M. Vachon, Edith Olah, Anja Rudolph, Arto Mannermaa, Phuong L. Mai, Isabel dos-Santos-Silva, Haran Sivakumaran, Francesca Damiola, Christian F. Singer, Muhammad Usman Rashid, Ed Dicks, Mikael Hartman, Antonis C. Antoniou, Dominique Stoppa-Lyonnet, Douglas F. Easton, Alison M. Dunning, John L. Hopper, Nadine Tung, Annika Lindblom, Kristiina Aittomäki, Kenneth Muir, Sue Healey, Cheng Har Yip, Mads Thomassen, Melissa C. Southey, Ramunas Janavicius, Cecilia M. Dorfling, Christine B. Ambrosone, Siddhartha Kar, Mary B. Daly, Artitaya Lophatananon, Rachel Rando, Banu Arun, Christopher A. Haiman, Catherine M. Phelan, Margaret Hills, Manuel R. Teixeira, Diana Torres, Hans Wildiers, Andrew K. Godwin, Keith Humphreys, Katri Pylkäs, Monika Jarosz, Susan L. Neuhausen, Montserrat Garcia-Closas, Robert Winqvist, Joe Dennis, Sook-Yee Yoon, Wei Zheng, Mitch Dowsett, Gord Glendon, Natasha Bogdanova, Suleeporn Sangrajrang, Steve Ellis, Paul Brennan, Lee Eunjung, Keitaro Matsuo, Jacek Gronwald, David E. Goldgar, Debra Frost, Chiu-Chen Tseng, Henrik Flyger, Kristine M. Hillman, Susan M. Domchek, Elena Lopez-Knowles, Bernard Peissel, Anna von Wachenfeldt, Karoline Kuchenbaecker, Anna Jakubowska, Paul D.P. Pharoah, Jose Ignacio Arias Perez, Kim De Leeneer, Roger L. Milne, Peter A. Fasching, Louise Izatt, Saundra S. Buys, Lesley McGuffog, Elizabeth J. van Rensburg, Pei-Ei Wu, Peter Devilee, Åslaug Helland, Qiuyin Cai, Peter J. Hulick, Miguel de la Hoya, Esther M. John, Kerstin Rhiem, Jan Lubinski, Karen A. Pooley, Marion Piedmonte, Catherine S. Healey, Mark S. Goldberg, Xiao-Ou Shu, Antoinette Hollestelle, Mary Beth Terry, Jenny Chang-Claude, Silje Nord, Chen-Yang Shen, Hiltrud Brauch, Kathleen Claes, Jason Sang Hun Lee, Sofia Khan, Katherine L. Nathanson, Hans Ehrencrona, Olufunmilayo I. Olopade, Stig E. Bojesen, Matti A. Rookus, Andrew Lee, Rita K. Schmutzler, Julian Peto, Jeffrey N. Weitzel, Barbara Burwinkel, Arjen R. Mensenkamp, Jacques Simard, Yu-Tang Gao, Robert Luben, S. Drury, Thilo Dörk, Laima Tihomirova, Per Hall, Barbara Perkins, Simona Agata, Jonine D. Figueroa, Julia A. Knight, Kenneth Offit, Kyriaki Michailidou, Anna González-Neira, Ian Tomlinson, Thérèse Truong, Amanda E. Toland, Anna Marie Mulligan, Noralane M. Lindor, Deborah J. Thompson, Marco Montagna
Publikováno v:
Nature Genetics, 48(4), 374-386. Nature Publishing Group
Nature Genetics, 48(4), 374
Dunning, A M, Michailidou, K, Kuchenbaecker, K B, Thompson, D J, French, J D, Beesley, J, Healey, C S, Kar, S, Pooley, K A, Lopez-Knowles, E, Dicks, E, Barrowdale, D, Sinnott-Armstrong, N A, Sallari, R C, Hillman, K M, Kaufmann, S, Sivakumaran, H, Moradi Marjaneh, M, Lee, J S, Hills, M, Jarosz, M, Drury, S, Canisius, S, Bolla, M K, Dennis, J, Wang, Q, Hopper, J L, Southey, M C, Broeks, A, Schmidt, M K, Lophatananon, A, Muir, K, Beckmann, M W, Fasching, P A, Dos Santos Silva, I, Peto, J, Sawyer, E J, Tomlinson, I, Burwinkel, B, Marme, F, Guénel, P, Truong, T, Bojesen, S E, Flyger, H, González-Neira, A, Perez, J I A, Shen, C-Y, Hansen, T V O, Bojesen, A, Thomassen, M & EMBRACE 2016, ' Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 ', Nature Genetics, vol. 48, no. 4, pp. 374-386 . https://doi.org/10.1038/ng.3521
Nature Genetics, 48(4), 374-+. Nature Publishing Group
Recercat. Dipósit de la Recerca de Catalunya
instname
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Dipòsit Digital de la UB
Universidad de Barcelona
Dunning, A M, Michailidou, K, Kuchenbaecker, K B, Thompson, D, French, J D, Beesley, J, Healey, C S, Kar, S, Pooley, K A, Lopez-Knowles, E, Dicks, E, Barrowdale, D, Sinnott-Armstrong, N A, Sallari, R C, Hillman, K M, Kaufmann, S, Sivakumaran, H, Moradi Marjaneh, M, Lee, J S, Hills, M, Jarosz, M, Drury, S, Canisius, S, Bolla, M K, Dennis, J, Wang, Q, Hopper, J L, Southey, M C, Broeks, A, Schmidt, M K, Lophatananon, A, Muir, K, Beckmann, M W, Fasching, P A, Dos-Santos-Silva, I, Peto, J, Sawyer, E J, Tomlinson, I, Burwinkel, B, Marme, F, Guénel, P, Truong, T, Bojesen, S E, Flyger, H, González-Neira, A & Perez, J I A & Anton-Culver, H & Eunjung, L & Arndt, V & Figueroa, J 2016, ' Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 ', Nature Genetics, vol. 48, no. 4, pp. 374-386 . https://doi.org/10.1038/ng.3521
Nature Genetics, 48, 374-86
Nature Genetics, 48, 4, pp. 374-86
Nature Genetics, 48(4), 374
Dunning, A M, Michailidou, K, Kuchenbaecker, K B, Thompson, D J, French, J D, Beesley, J, Healey, C S, Kar, S, Pooley, K A, Lopez-Knowles, E, Dicks, E, Barrowdale, D, Sinnott-Armstrong, N A, Sallari, R C, Hillman, K M, Kaufmann, S, Sivakumaran, H, Moradi Marjaneh, M, Lee, J S, Hills, M, Jarosz, M, Drury, S, Canisius, S, Bolla, M K, Dennis, J, Wang, Q, Hopper, J L, Southey, M C, Broeks, A, Schmidt, M K, Lophatananon, A, Muir, K, Beckmann, M W, Fasching, P A, Dos Santos Silva, I, Peto, J, Sawyer, E J, Tomlinson, I, Burwinkel, B, Marme, F, Guénel, P, Truong, T, Bojesen, S E, Flyger, H, González-Neira, A, Perez, J I A, Shen, C-Y, Hansen, T V O, Bojesen, A, Thomassen, M & EMBRACE 2016, ' Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 ', Nature Genetics, vol. 48, no. 4, pp. 374-386 . https://doi.org/10.1038/ng.3521
Nature Genetics, 48(4), 374-+. Nature Publishing Group
Recercat. Dipósit de la Recerca de Catalunya
instname
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Dipòsit Digital de la UB
Universidad de Barcelona
Dunning, A M, Michailidou, K, Kuchenbaecker, K B, Thompson, D, French, J D, Beesley, J, Healey, C S, Kar, S, Pooley, K A, Lopez-Knowles, E, Dicks, E, Barrowdale, D, Sinnott-Armstrong, N A, Sallari, R C, Hillman, K M, Kaufmann, S, Sivakumaran, H, Moradi Marjaneh, M, Lee, J S, Hills, M, Jarosz, M, Drury, S, Canisius, S, Bolla, M K, Dennis, J, Wang, Q, Hopper, J L, Southey, M C, Broeks, A, Schmidt, M K, Lophatananon, A, Muir, K, Beckmann, M W, Fasching, P A, Dos-Santos-Silva, I, Peto, J, Sawyer, E J, Tomlinson, I, Burwinkel, B, Marme, F, Guénel, P, Truong, T, Bojesen, S E, Flyger, H, González-Neira, A & Perez, J I A & Anton-Culver, H & Eunjung, L & Arndt, V & Figueroa, J 2016, ' Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170 ', Nature Genetics, vol. 48, no. 4, pp. 374-386 . https://doi.org/10.1038/ng.3521
Nature Genetics, 48, 374-86
Nature Genetics, 48, 4, pp. 374-86
To access publisher's full text version of this article click on the hyperlink at the bottom of the page We analyzed 3,872 common genetic variants across the ESR1 locus (encoding estrogen receptor α) in 118,816 subjects from three international cons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9243da2133c0ff63e63cff70cb87aac9
https://hdl.handle.net/1887/113197
https://hdl.handle.net/1887/113197
Autor:
Kenneth Offit, D. Gareth Evans, Dominique Stoppa-Lyonnet, Edith Olah, Nadine Tung, Andrew K. Godwin, Irene L. Andrulis, Jeffrey N. Weitzel, Eitan Friedman, Gord Glendon, Mary B. Daly, Kathleen Claes, Laima Tihomirova, Bella Kaufman, kConFab Investigators, Aleksandra Tołoczko-Grabarek, Katarzyna Jaworska-Bieniek, Fergus J. Couch, Jonathan Carter, Ute Hamann, Embrace, Emily Hallberg, Olufunmilayo I. Olopade, Niklas Loman, Claudine Isaacs, Raanan Berger, Caroline Seynaeve, Patricia A. Ganz, Trinidad Caldés, Jenny Lester, Steve Ellis, Fei Wan, Stephanie Chen, Cezary Cybulski, Saundra S. Buys, Åke Borg, Jamal Zidan, Matti A. Rookus, Javier Benitez, Csilla Szabo, Gillian Mitchell, Douglas F. Easton, Jocelyne Chiquette, Katherine L. Nathanson, Mary Beth Terry, Kristin K. Zorn, Danylo Villano, Mads Thomassen, Nandita Mitra, Mariella Tancredi, Conxi Lázaro, Hebon, Jacek Gronwald, Paolo Radice, Katarzyna Durda, Pascaline Berthet, Shan Wang-Gohrke, Orland Diez, Siranoush Manoukian, Amanda E. Toland, Ava Kwong, Barbara Wappenschmidt, Tara M. Friebel, Lenka Foretova, Beth Y. Karlan, Marco Montagna, Yael Laitman, Georgia Chenevix-Trench, Antonis C. Antoniou, Paraskevi Apostolou, Susan J. Ramus, Jacques Simard, Daniel Barrowdale, Timothy R. Rebbeck, Thomas Hansen, Jan Lubinski, Manuel R. Teixeira, Eric Hahnen, Grzegorz Sukiennicki, Christine Lasset, Sue K. Park, Christian F. Singer, Debra Frost, Elizabeth J. van Rensburg, Esther M. John, Susan L. Neuhausen, Lesley McGuffog, Dieter Niederacher, Penny Soucy, Heli Nevanlinna, Judy Garber, Norbert Arnold, Robert L. Nussbaum, Susan M. Domchek, Melissa C. Southey, Ramunas Janavicius, Mark H. Greene, Anna Jakubowska, Marc Tischkowitz, Christine Rappaport-Fuerhauser, Marion Piedmonte, Miguel de la Hoya, Soo Hwang Teo, Evgeny N. Imyanitov, Banu Arun
Publikováno v:
Dipòsit Digital de la UB
Universidad de Barcelona
Rebbeck, T R, Friebel, T M, Mitra, N, Wan, F, Chen, S, Andrulis, I L, Apostolou, P, Arnold, N, Arun, B K, Barrowdale, D, Benitez, J, Berger, R, Berthet, P, Borg, A, Buys, S S, Caldes, T, Carter, J, Chiquette, J, Claes, K B M, Couch, F J, Cybulski, C, Daly, M B, de la Hoya, M, Diez, O, Domchek, S M, Nathanson, K L, Durda, K, Ellis, S, Evans, D G, Foretova, L, Friedman, E, Frost, D, Ganz, P A, Garber, J, Glendon, G, Godwin, A K, Greene, M H, Gronwald, J, Hahnen, E, Hallberg, E, Hamann, U, Hansen, T V O, Imyanitov, E N, Isaacs, C, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, John, E M, Karlan, B Y, Kaufman, B & EMBRACE 2016, ' Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women ', Breast Cancer Research, vol. 18, no. 1, pp. 112 . https://doi.org/10.1186/s13058-016-0768-3
Rebbeck, TR; Friebel, TM; Mitra, N; Wan, F; Chen, S; Andrulis, IL; et al.(2016). Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women. BREAST CANCER RESEARCH, 18, 112. doi: 10.1186/s13058-016-0768-3. UCLA: Retrieved from: http://www.escholarship.org/uc/item/3g65b9w7
Breast Cancer Research, 18:112. BioMed Central Ltd.
Rebbeck, T R, Friebel, T M, Mitra, N, Wan, F, Chen, S, Andrulis, I L, Apostolou, P, Arnold, N, Arun, B K, Barrowdale, D, Benítez, J, Berger, R, Berthet, P, Borg, A, Buys, S, Caldes, T, Carter, J, Chiquette, J, Claes, K B M, Couch, F J, Cybulski, C, Daly, M B, de la Hoya, M, Díez, O, Domchek, S M, Nathanson, K L, Durda, K, Ellis, S, Evans, D G, Foretova, L, Friedman, E, Frost, D, Ganz, P A, Garber, J, Glendon, G, Godwin, A K, Greene, M H, Gronwald, J, Hahnen, E, Hallberg, E, Hamann, U, Imyanitov, E N, Isaacs, C, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, John, E M, Karlan, B Y, Kaufman, B, Thomassen, M & EMBRACE 2016, ' Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women ', Breast Cancer Research (Online), vol. 18, 112 . https://doi.org/10.1186/s13058-016-0768-3
Breast cancer research, 18(112):112. BioMed Central Ltd.
BREAST CANCER RESEARCH
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Recercat. Dipósit de la Recerca de Catalunya
instname
Breast Cancer Research : BCR
Universidad de Barcelona
Rebbeck, T R, Friebel, T M, Mitra, N, Wan, F, Chen, S, Andrulis, I L, Apostolou, P, Arnold, N, Arun, B K, Barrowdale, D, Benitez, J, Berger, R, Berthet, P, Borg, A, Buys, S S, Caldes, T, Carter, J, Chiquette, J, Claes, K B M, Couch, F J, Cybulski, C, Daly, M B, de la Hoya, M, Diez, O, Domchek, S M, Nathanson, K L, Durda, K, Ellis, S, Evans, D G, Foretova, L, Friedman, E, Frost, D, Ganz, P A, Garber, J, Glendon, G, Godwin, A K, Greene, M H, Gronwald, J, Hahnen, E, Hallberg, E, Hamann, U, Hansen, T V O, Imyanitov, E N, Isaacs, C, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, John, E M, Karlan, B Y, Kaufman, B & EMBRACE 2016, ' Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women ', Breast Cancer Research, vol. 18, no. 1, pp. 112 . https://doi.org/10.1186/s13058-016-0768-3
Rebbeck, TR; Friebel, TM; Mitra, N; Wan, F; Chen, S; Andrulis, IL; et al.(2016). Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women. BREAST CANCER RESEARCH, 18, 112. doi: 10.1186/s13058-016-0768-3. UCLA: Retrieved from: http://www.escholarship.org/uc/item/3g65b9w7
Breast Cancer Research, 18:112. BioMed Central Ltd.
Rebbeck, T R, Friebel, T M, Mitra, N, Wan, F, Chen, S, Andrulis, I L, Apostolou, P, Arnold, N, Arun, B K, Barrowdale, D, Benítez, J, Berger, R, Berthet, P, Borg, A, Buys, S, Caldes, T, Carter, J, Chiquette, J, Claes, K B M, Couch, F J, Cybulski, C, Daly, M B, de la Hoya, M, Díez, O, Domchek, S M, Nathanson, K L, Durda, K, Ellis, S, Evans, D G, Foretova, L, Friedman, E, Frost, D, Ganz, P A, Garber, J, Glendon, G, Godwin, A K, Greene, M H, Gronwald, J, Hahnen, E, Hallberg, E, Hamann, U, Imyanitov, E N, Isaacs, C, Jakubowska, A, Janavicius, R, Jaworska-Bieniek, K, John, E M, Karlan, B Y, Kaufman, B, Thomassen, M & EMBRACE 2016, ' Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women ', Breast Cancer Research (Online), vol. 18, 112 . https://doi.org/10.1186/s13058-016-0768-3
Breast cancer research, 18(112):112. BioMed Central Ltd.
BREAST CANCER RESEARCH
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Recercat. Dipósit de la Recerca de Catalunya
instname
Breast Cancer Research : BCR
BACKGROUND: Most BRCA1 or BRCA2 mutation carriers have inherited a single (heterozygous) mutation. Transheterozygotes (TH) who have inherited deleterious mutations in both BRCA1 and BRCA2 are rare, and the consequences of transheterozygosity are poor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::610313d92aeb738e2f59d8063f79e750
http://hdl.handle.net/2445/125360
http://hdl.handle.net/2445/125360
Autor:
Agnieszka Dansonka-Mieszkowska, Angela Brooks-Wilson, Ingo B. Runnebaum, Kenneth Offit, Melissa C. Southey, Ramunas Janavicius, Finn Cilius Nielsen, Christine Maugard, Marco Montagna, Annette Fontaine, Janusz Menkiszak, Robert Winqvist, Pascal Guénel, Rosalind Glasspool, Usha Menon, Daniel Barrowdale, Elinor J. Sawyer, Anna Jakubowska, Paul D.P. Pharoah, Martha J. Shrubsole, Lambertus A. Kiemeney, Camilla Krakstad, Dong Liang, Minouk J. Schoemaker, Judith S. Brand, Joseph Vijai, Marc T. Goodman, Thomas A. Sellers, David Van Den Berg, Celeste Leigh Pearce, Alice S. Whittemore, Irene L. Andrulis, Radka Platte, Kunle Odunsi, Orland Diez, Estrid Høgdall, Brooke L. Fridley, C. J. van Asperen, Mary Anne Rossing, Vessela N. Kristensen, Jonathan Tyrer, Tara M. Friebel, Douglas F. Easton, Per Hall, Mads Thomassen, Christine Walsh, Thilo Dörk, Louise A. Brinton, Keith Humphreys, Douglas A. Levine, Allison F. Vitonis, Anna H. Wu, Hermann Brenner, Maria Bisogna, Joellen M. Schildkraut, Maria A. Caligo, Jonine D. Figueroa, Lynne R. Wilkens, Grace Friel, Michael G. Schrauder, Evgeny N. Imyanitov, Sune F. Nielsen, Sylvie Mazoyer, Diana Eccles, Andrew Berchuck, Sara Margolin, Mitul Shah, Matthias W. Beckmann, Elizabeth M. Poole, Gad Rennert, Arif B. Ekici, Elisa Alducci, Bjarni A. Agnarsson, Linda S. Cook, Javier Benitez, Paolo Peterlongo, Natalia Antonenkova, Annika Lindblom, Patrick Neven, Julia A. Knight, Alan Ashworth, Matti A. Rookus, Frans B. L. Hogervorst, Daniela Zaffaroni, Banu Arun, Sue Healey, Robert P. Edwards, Susanne K. Kjaer, Laura J. van't Veer, John W.M. Martens, Christa Stegmaier, Claudine Isaacs, Daniel W. Cramer, Lars Beckmann, Liisa M. Pelttari, Dieter Flesch-Janys, Irene Orlow, Atocha Romero, Diana Torres, Marjanka K. Schmidt, Simon S. Cross, Alison M. Dunning, Rosemary L. Balleine, Sandra L. Halverson, Benoit Beuselinck, Melissa C. Larson, Senno Verhoef, Jirong Long, Angela Cox, Maartje J. Hooning, Bruce Poppe, Katarzyna Jaworska, Jolanta Kupryjanczyk, Nicolas Wentzensen, Gustavo C. Rodriguez, Tanja Pejovic, Roberta B. Ness, James Paul, Dominique Stoppa-Lyonnet, Nadine Tung, Gianluca Severi, Malcolm C. Pike, Hoda Anton-Culver, Ans M.W. van den Ouweland, Mark E. Robson, Roger L. Milne, Jan C. Oosterwijk, Laima Tihomirova, Helen Tsimiklis, Pierre Laurent-Puig, Florian Heitz, Beth Y. Karlan, Ian Tomlinson, Thérèse Truong, Bernardo Bonanni, Frederik Marmé, Qin Wang, Conxi Lázaro, Volker Arndt, Antoinette Hollestelle, Jacek Gronwald, M. Pilar Zamora, Barbara Wappenschmidt, Maren Weischer, Veli-Matti Kosma, Giulietta Scuvera, Jenny Lester, Andreas Berger, Stephen J. Chanock, Line Bjørge, Anthony J. Swerdlow, Andrew K. Godwin, Mervi Grip, Amanda E. Toland, Anna Marie Mulligan, Noralane M. Lindor, Paolo Radice, Bent Ejlertsen, Frederieke H. van der Baan, Lothar Haeberle, Valerie McGuire, Kamila Czene, Rob A. E. M. Tollenaar, Maria Soller, Katherine L. Nathanson, Sandrina Lambrechts, Susan J. Ramus, Anja Rudolph, Penny Soucy, Caroline Weltens, Hiltrud Brauch, Olivia Fletcher, Sara H. Olson, Yael Laitman, Marion Piedmonte, Arto Mannermaa, Agnieszka Budzilowska, Olga M. Sinilnikova, Christian F. Singer, Cezary Cybulski, Weiva Sieh, Ed Dicks, Elizabeth J. van Rensburg, Isabel dos Santos Silva, Hans Ehrencrona, Timothy R. Rebbeck, Jaana M. Hartikainen, Sandra Orsulic, Jingmei Li, Carmel Apicella, Anna deFazio, Ian G. Campbell, Ignace Vergote, Rita K. Schmutzler, Fredrick R. Schumacher, Julian Peto, Nadeem Siddiqui, Brian E. Henderson, Starr R. Guzman, Maria Kabisch, John L. Hopper, Arto Leminen, Jeffrey N. Weitzel, Honglin Song, J. Margriet Collée, Ingvild L. Tangen, Børge G. Nordestgaard, Antonis C. Antoniou, Lara Sucheston, Helena C. van Doorn, Lídia Feliubadaló, Leon F.A.G. Massuger, Iain A. McNeish, Nichola Johnson, Simon A. Gayther, Jennifer A. Doherty, Anders Bojesen, Gord Glendon, Yukie Bean, Celine M. Vachon, Barbara Burwinkel, Edith Olah, Shan Wang-Gohrke, Brita Arver, Marc Tischkowitz, Arja Jukkola-Vuorinen, Martin Gore, Vesa Kataja, Nicola Miller, Pamela J. Thompson, Malcolm W.R. Reed, Michelle A.T. Hildebrandt, Ritu Salani, Janet E. Olson, Catriona McLean, Cecilia M. Dorfling, Georgia Chenevix-Trench, Frederique Mariette, Laura Ottini, Fergus J. Couch, Linda E. Kelemen, Nhu D. Le, Michael J. Kerin, Claus Høgdall, Miguel de la Hoya, Jonathan Carter, Mercedes Durán, Inge Søkilde Pedersen, Julie M. Cunningham, Manjeet K. Bolla, Galina Lurie, Loic Le Marchand, Ute Hamann, Muy-Kheng Tea, Karoline Kuchenbaecker, Irene Konstantopoulou, Thomas Hansen, Francesca Damiola, Stefano Fortuzzi, Shelley S. Tworoger, Mikael Eriksson, Carl Blomqvist, Joan Brunet, Allan Jensen, Karen Lu, Elisa V. Bandera, Anne M. van Altena, Anne-Marie Gerdes, Lene Lundvall, Susan L. Neuhausen, Wei Zheng, Ana Osorio, Fiona Bruinsma, Hannah P. Yang, Graham G. Giles, Christoph Engel, Nick Orr, Harvey A. Risch, Jan Lubinski, Jacoba P. Knol-Bout, Phuong L. Mai, Martine Dumont, Xifeng Wu, Christof Sohn, Noah D. Kauff, Kristiina Aittomäki, Natalia Bogdanova, Alexander Hein, Francesmary Modugno, Heli Nevanlinna, Helga B. Salvesen, Adriana Lasa, Daphne Gschwantler Kaulich, Dominiek Smeets, Jenny Permuth-Wey, Josef Herzog, Catherine M. Phelan, Clareann H. Bunker, Steve Ellis, Christopher A. Haiman, Jolanta Lissowska, Judy Garber, Joanna Plisiecka-Halasa, Robert A. Vierkant, Steven A. Narod, Mark H. Greene, Florence Menegaux, Norbert Arnold, Primitiva Menéndez, Robert L. Nussbaum, Katja K.H. Aben, Andreas Schneeweiss, Katri Pylkäs, Els Van Nieuwenhuysen, Tomasz Huzarski, Joe Dennis, Susan M. Domchek, Andreas du Bois, Aleksandra Gentry-Maharaj, Florentia Fostira, Mary Beth Terry, Jenny Chang-Claude, Eitan Friedman, Argyrios Ziogas, Hatef Darabi, Kathleen Claes, Ellen L. Goode, Olufunmilayo I. Olopade, Stig E. Bojesen, Jo Perkins, Raanan Berger, Sharon E. Johnatty, Taru A. Muranen, Montserrat Garcia-Closas, Uffe Birk Jensen, Thomas Brüning, Heiko Müller, Debra Frost, Peter A. Fasching, Lesley McGuffog, Diether Lambrechts, Kelly-Anne Phillips, Caroline M. Seynaeve, Kathryn L. Terry, Ira Schwaab, Ralf Bützow, Manuel R. Teixeira, Joseph H. Rothstein, Bernard Peissel, Anna von Wachenfeldt, Saundra S. Buys, Peter Devilee, Alfons Meindl, Laura Baglietto, Kirsten B. Moysich, Arjen R. Mensenkamp, Philipp Harter, Jacques Simard
Publikováno v:
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Gynecologic Oncology, 141, 386-401
Gynecologic Oncology, 141(2), 386-401. Academic Press
Ovarian Cancer Association Consortium, Breast Cancer Association Consortium, and Consortium of Modifiers of BRCA1 and BRCA2, Australian Ovarian Cancer Study Group, Breast Cancer Family Register, EMBRACE, GEMO Study Collaborators, GENICA Network, HEBON, kConFab Investigators & SWE-BRCA 2016, ' No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer ', Gynecologic Oncology, vol. 141, no. 2, pp. 386-401 . https://doi.org/10.1016/j.ygyno.2015.04.034
Hollestelle, A, van der Baan, F H, Berchuck, A, Johnatty, S E, Aben, K K, Agnarsson, B A, Aittomäki, K, Alducci, E, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Antoniou, A C, Apicella, C, Arndt, V, Arnold, N, Arun, B K, Arver, B, Ashworth, A, Baglietto, L, Balleine, R, Bandera, E V, Barrowdale, D, Bean, Y T, Beckmann, L, Beckmann, M W, Benitez, J, Berger, A, Berger, R, Beuselinck, B, Bisogna, M, Bjorge, L, Blomqvist, C, Bogdanova, N V, Bojesen, A, Bojesen, S E, Bolla, M K, Bonanni, B, Brand, J S, Brauch, H, Brenner, H, Brinton, L, Brooks-Wilson, A, Bruinsma, F, Brunet, J, Brüning, T, Budzilowska, A, Bunker, C H, Burwinkel, B, Butzow, R, Jensen, U B & Ovarian Cancer Association Consortium, Breast Cancer Association Consortium, and Consortium of Modifiers of BRCA1 and BRCA2 2015, ' No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer ', Gynecologic Oncology . https://doi.org/10.1016/j.ygyno.2015.04.034
Gynecologic Oncology, 141(2), 386-401
Hollestelle, A, van der Baan, F H, Berchuck, A, Johnatty, S E, Aben, K K, Agnarsson, B A, Aittomäki, K, Alducci, E, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Antoniou, A C, Apicella, C, Arndt, V, Arnold, N, Arun, B K, Arver, B, Ashworth, A, Baglietto, L, Balleine, R, Bandera, E V, Barrowdale, D, Bean, Y T, Beckmann, L, Beckmann, M W, Benitez, J, Berger, A, Berger, R, Beuselinck, B, Bisogna, M, Bjorge, L, Blomqvist, C, Bogdanova, N V, Bojesen, A, Bojesen, S E, Bolla, M K, Bonanni, B, Brand, J S, Brauch, H, Brenner, H, Brinton, L, Brooks-Wilson, A, Bruinsma, F, Brunet, J, Brüning, T, Budzilowska, A, Bunker, C H, Burwinkel, B, Butzow, R, Pedersen, I S & Ovarian Cancer Association Consortium, Breast Cancer Association Consortium, and Consortium of Modifiers of BRCA1 and BRCA2 2016, ' No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer ', Gynecologic Oncology, vol. 141, no. 2, pp. 386-401 . https://doi.org/10.1016/j.ygyno.2015.04.034
Gynecologic Oncology, 141, 2, pp. 386-401
Digital.CSIC. Repositorio Institucional del CSIC
instname
Consejería de Sanidad de la Comunidad de Madrid
Gynecologic Oncology, 141, 386-401
Gynecologic Oncology, 141(2), 386-401. Academic Press
Ovarian Cancer Association Consortium, Breast Cancer Association Consortium, and Consortium of Modifiers of BRCA1 and BRCA2, Australian Ovarian Cancer Study Group, Breast Cancer Family Register, EMBRACE, GEMO Study Collaborators, GENICA Network, HEBON, kConFab Investigators & SWE-BRCA 2016, ' No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer ', Gynecologic Oncology, vol. 141, no. 2, pp. 386-401 . https://doi.org/10.1016/j.ygyno.2015.04.034
Hollestelle, A, van der Baan, F H, Berchuck, A, Johnatty, S E, Aben, K K, Agnarsson, B A, Aittomäki, K, Alducci, E, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Antoniou, A C, Apicella, C, Arndt, V, Arnold, N, Arun, B K, Arver, B, Ashworth, A, Baglietto, L, Balleine, R, Bandera, E V, Barrowdale, D, Bean, Y T, Beckmann, L, Beckmann, M W, Benitez, J, Berger, A, Berger, R, Beuselinck, B, Bisogna, M, Bjorge, L, Blomqvist, C, Bogdanova, N V, Bojesen, A, Bojesen, S E, Bolla, M K, Bonanni, B, Brand, J S, Brauch, H, Brenner, H, Brinton, L, Brooks-Wilson, A, Bruinsma, F, Brunet, J, Brüning, T, Budzilowska, A, Bunker, C H, Burwinkel, B, Butzow, R, Jensen, U B & Ovarian Cancer Association Consortium, Breast Cancer Association Consortium, and Consortium of Modifiers of BRCA1 and BRCA2 2015, ' No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer ', Gynecologic Oncology . https://doi.org/10.1016/j.ygyno.2015.04.034
Gynecologic Oncology, 141(2), 386-401
Hollestelle, A, van der Baan, F H, Berchuck, A, Johnatty, S E, Aben, K K, Agnarsson, B A, Aittomäki, K, Alducci, E, Andrulis, I L, Anton-Culver, H, Antonenkova, N N, Antoniou, A C, Apicella, C, Arndt, V, Arnold, N, Arun, B K, Arver, B, Ashworth, A, Baglietto, L, Balleine, R, Bandera, E V, Barrowdale, D, Bean, Y T, Beckmann, L, Beckmann, M W, Benitez, J, Berger, A, Berger, R, Beuselinck, B, Bisogna, M, Bjorge, L, Blomqvist, C, Bogdanova, N V, Bojesen, A, Bojesen, S E, Bolla, M K, Bonanni, B, Brand, J S, Brauch, H, Brenner, H, Brinton, L, Brooks-Wilson, A, Bruinsma, F, Brunet, J, Brüning, T, Budzilowska, A, Bunker, C H, Burwinkel, B, Butzow, R, Pedersen, I S & Ovarian Cancer Association Consortium, Breast Cancer Association Consortium, and Consortium of Modifiers of BRCA1 and BRCA2 2016, ' No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer ', Gynecologic Oncology, vol. 141, no. 2, pp. 386-401 . https://doi.org/10.1016/j.ygyno.2015.04.034
Gynecologic Oncology, 141, 2, pp. 386-401
Digital.CSIC. Repositorio Institucional del CSIC
instname
Ovarian Cancer Association Consortium, Breast Cancer Association Consortium, and Consortium of Modifiers of BRCA1 and BRCA2: et al.
[Objective]: Clinical genetic testing is commercially available for rs61764370, an inherited variant residing in
[Objective]: Clinical genetic testing is commercially available for rs61764370, an inherited variant residing in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d41cdfb01971a707db6a3e157e2635a6
https://hdl.handle.net/20.500.12530/28922
https://hdl.handle.net/20.500.12530/28922