نتائج البحث - "van der Luijt, Rob"

1

دورية أكاديمية

Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry

المؤلفون: Dumont, Martine, Weber-Lassalle, Nana, Joly-Beauparlant, Charles, Ernst, Corinna, Droit, Arnaud, Feng, Bing-Jian, Dubois, Stéphane, Collin-Deschesnes, Annie-Claude, Soucy, Penny, Vallée, Maxime, Fournier, Frédéric, Lemaçon, Audrey, Adank, Muriel A., Allen, Jamie, Altmüller, Janine, Arnold, Norbert, Ausems, Margreet G. E. M., Berutti, Riccardo, Bolla, Manjeet K., Bull, Shelley, Carvalho, Sara, Cornelissen, Sten, Dufault, Michael R., Dunning, Alison M., Engel, Christoph, Gehrig, Andrea, Geurts-Giele, Willemina R. R., Gieger, Christian, Green, Jessica, Hackmann, Karl, Helmy, Mohamed, Hentschel, Julia, Hogervorst, Frans B. L., Hollestelle, Antoinette, Hooning, Maartje J., Horváth, Judit, Ikram, M. Arfan, Kaulfuß, Silke, Keeman, Renske, Kuang, Da, Luccarini, Craig, Maier, Wolfgang, Martens, John W. M., Niederacher, Dieter, Nürnberg, Peter, Ott, Claus-Eric, Peters, Annette, Pharoah, Paul D. P., Ramirez, Alfredo, Ramser, Juliane, Riedel-Heller, Steffi, Schmidt, Gunnar, Shah, Mitul, Scherer, Martin, Stäbler, Antje, Strom, Tim M., Sutter, Christian, Thiele, Holger, van Asperen, Christi J., van der Kolk, Lizet, van der Luijt, Rob B., Volk, Alexander E., Wagner, Michael, Waisfisz, Quinten, Wang, Qin, Wang-Gohrke, Shan, Weber, Bernhard H. F., Devilee, Peter, Tavtigian, Sean, Bader, Gary D., Meindl, Alfons, Goldgar, David E., Andrulis, Irene L., Schmutzler, Rita K., Easton, Douglas F., Schmidt, Marjanka K., Hahnen, Eric, Simard, Jacques

المساهمون: Dumont, Martine, 1Genomics Center, CHU de Québec-Université Laval Research Center, 2705 Laurier Boulevard, Quebec City, QC GIV 4G2, Canada, martine.dumont@crchudequebec.ulaval.ca (M.D.), charles.joly-beauparlant@crchudequebec.ulaval.ca (C.J.-B.), arnaud.droit@crchudequebec.ulaval.ca (A.D.), stephane.dubois@crchudequebec.ulaval.ca (S.D.), annie-c.c-deschesnes@crchudequebec.ulaval.ca (A.-C.C.-D.), penny.soucy@crchudequebec.ulaval.ca (P.S.), maxime.vallee@chu-lyon.fr (M.V.), frederic.fournier.4@ulaval.ca (F.F.), audrey@mims.ai (A.L.), Weber-Lassalle, Nana, 2Center for Familial Breast and Ovarian Cancer, Center for Integrated Oncology (CIO), Faculty of Medicine and University Hospital Cologne, University of Cologne, 50937 Cologne, Germany, nana.weber-lassalle@uk-koeln.de (N.W.-L.), corinna.ernst@uk-koeln.de (C.E.), rita.schmutzler@uk-koeln.de (R.K.S.), eric.hahnen@uk-koeln.de (E.H.), Joly-Beauparlant, Charles, Ernst, Corinna, Droit, Arnaud, Feng, Bing-Jian, 3Department of Dermatology, University of Utah, Salt Lake City, UT 84103, USA, bingjian.feng@hsc.utah.edu (B.-J.F.), david.goldgar@hsc.utah.edu (D.E.G.), Dubois, Stéphane, Collin-Deschesnes, Annie-Claude, Soucy, Penny, Vallée, Maxime, Fournier, Frédéric, Lemaçon, Audrey, Adank, Muriel A., 5Family Cancer Clinic, The Netherlands Cancer Institute—Antoni van Leeuwenhoek Hospital, 1066 Amsterdam, The Netherlands, m.adank@nki.nl (M.A.A.), f.hogervorst@nki.nl (F.B.L.H.), l.vd.kolk@nki.nl (L.v.d.K.), Allen, Jamie, 6Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge CB1 8RN, UK, jma@ebi.ac.uk (J.A.), mkh39@medschl.cam.ac.uk (M.K.B.), sc2017@medschl.cam.ac.uk (S.C.), paul.pharoah@medschl.cam.ac.uk (P.D.P.P.), qw232@medschl.cam.ac.uk (Q.W.), dfe20@medschl.cam.ac.uk (D.F.E.), Altmüller, Janine, 7Cologne Center for Genomics (CCG), Faculty of Medicine, University Hospital Cologne, University of Cologne, 50931 Cologne, Germany, janine.altmueller@mdc-berlin.de (J.A.), holger.thiele@uni-koeln.de (H.T.), Arnold, Norbert, 8Institute of Clinical Molecular Biology, Department of Gynaecology and Obstetrics, University Hospital of Schleswig-Holstein, Campus Kiel, Christian-Albrechts University Kiel, 24105 Kiel, Germany, norbert.arnold@uksh.de, Ausems, Margreet G. E. M., 9Division Laboratories, Pharmacy and Biomedical Genetics, Department of Genetics, University Medical Center Utrecht, 3584 Utrecht, The Netherlands, m.g.e.m.ausems@umcutrecht.nl, Berutti, Riccardo, 10Institute of Human Genetics, Technische Universität München, 81675 Munich, Germany, riccardo.berutti@helmholtz-muenchen.de (R.B.), tim.strom@tum.de (T.M.S.), Bolla, Manjeet K., Bull, Shelley, 11Lunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, ON M5G 1X5, Canada, bull@lunenfeld.ca (S.B.), jessica.green@sinaihealth.ca (J.G.), gary.bader@utoronto.ca (G.D.B.), andrulis@lunenfeld.ca (I.L.A.), Carvalho, Sara, Cornelissen, Sten, 13Division of Molecular Pathology, The Netherlands Cancer Institute—Antoni van Leeuwenhoek Hospital, 1066 Amsterdam, The Netherlands, s.cornelissen@nki.nl (S.C.), r.keeman@nki.nl (R.K.), mk.schmidt@nki.nl (M.K.S.), Dufault, Michael R., 14Precision Medicine and Computational Biology, Sanofi Genzyme, Cambridge, MA 02142, USA, michael.dufault@sanofi.com, Dunning, Alison M., 15Centre for Cancer Genetic Epidemiology, Department of Oncology, University of Cambridge, Cambridge CB1 8RN, UK, amd24@medschl.cam.ac.uk (A.M.D.), craig@srl.cam.ac.uk (C.L.), ms483@medschl.cam.ac.uk (M.S.), Engel, Christoph, 16Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, 04107 Leipzig, Germany, christoph.engel@imise.uni-leipzig.de, Gehrig, Andrea, 17Centre of Familial Breast and Ovarian Cancer, Department of Medical Genetics, Institute of Human Genetics, University of Würzburg, 97074 Würzburg, Germany, gehrig@biozentrum.uni-wuerzburg.de, Geurts-Giele, Willemina R. R., 18Department of Clinical Genetics, Erasmus University Medical Center, 3015 Rotterdam, The Netherlands, w.geurts-giele@erasmusmc.nl, Gieger, Christian, 19Institute of Epidemiology, Helmholtz Zentrum München, German Research Center for Environmental Health, 85764 Neuherberg, Germany, christian.gieger@helmholtz-muenchen.de (C.G.), peters@helmholtz-muenchen.de (A.P.), Green, Jessica, Hackmann, Karl, 22Institute for Clinical Genetics, Faculty of Medicine Carl Gustav Carus, Technische Universität Dresden, 01307 Dresden, Germany, karl.hackmann@uniklinikum-dresden.de, Helmy, Mohamed, 23The Donnelly Centre, University of Toronto, Toronto, ON M5S 3E1, Canada, mohamed_helmy@bii.a-star.edu.sg, Hentschel, Julia, 26Institute of Human Genetics, University Leipzig, 04103 Leipzig, Germany, julia.hentschel@medizin.uni-leipzig.de, Hogervorst, Frans B. L., Hollestelle, Antoinette, 27Department of Medical Oncology, Erasmus MC Cancer Institute, 3015 Rotterdam, The Netherlands, a.hollestelle@erasmusmc.nl (A.H.), m.hooning@erasmusmc.nl (M.J.H.), j.martens@erasmusmc.nl (J.W.M.M.), Hooning, Maartje J., Horváth, Judit, 28Institute of Human Genetics, University of Münster, 48149 Münster, Germany, judit.horvath@ukmuenster.de, Ikram, M. Arfan, 29Department of Epidemiology, Erasmus MC University Medical Center, 3015 Rotterdam, The Netherlands, m.a.ikram@erasmusmc.nl, Kaulfuß, Silke, 30Institute of Human Genetics, University Medical Center Göttingen, 37075 Göttingen, Germany, silke.kaulfuss@med.uni-goettingen.de, Keeman, Renske, Kuang, Da, 21Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada, kvn.kuang@mail.utoronto.ca, Luccarini, Craig, Maier, Wolfgang, 31German Center for Neurodegenerative Diseases (DZNE), Department of Neurodegenerative Diseases and Geriatric Psychiatry, Medical Faculty, University Hospital Bonn, 53127 Bonn, Germany, wolfgang.maier@ukb.uni-bonn.de, Martens, John W. M., Niederacher, Dieter, 32Department of Gynecology and Obstetrics, University Hospital Düsseldorf, Heinrich-Heine University Düsseldorf, 40225 Düsseldorf, Germany, niederac@med.uni-duesseldorf.de, Nürnberg, Peter, 33Center for Molecular Medicine Cologne (CMMC), Cologne Center for Genomics (CCG), Faculty of Medicine, University Hospital Cologne, University of Cologne, 50931 Cologne, Germany, nuernberg@uni-koeln.de, Ott, Claus-Eric, 34Institute of Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, 13353 Berlin, Germany, claus-eric.ott@charite.de, Peters, Annette, Pharoah, Paul D. P., Ramirez, Alfredo, 36Division for Neurogenetics and Molecular Psychiatry, Medical Faculty, University of Cologne, 50937 Cologne, Germany, alfredo.ramirez@uk-koeln.de, Ramser, Juliane, 37Division of Gynaecology and Obstetrics, Klinikum Rechts der Isar der Technischen Universität München, 81675 Munich, Germany, juliane.ramser@mri.tum.de (J.R.), alfons.meindl@gmx.de (A.M.), Riedel-Heller, Steffi, 38Institute of Social Medicine, Occupational Health and Public Health, Faculty of Medicine, University of Leipzig, 04103 Leipzig, Germany, steffi.riedel-heller@medizin.uni-leipzig.de, Schmidt, Gunnar, 39Institute of Human Genetics, Hannover Medical School, 30625 Hannover, Germany, schmidt.gunnar@mh-hannover.de, Shah, Mitul, Scherer, Martin, 40Department of Primary Medical Care, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany, m.scherer@uke.de, Stäbler, Antje, 41Institute of Medical Genetics and Applied Genomics, University of Tübingen, 72076 Tübingen, Germany, antje.staebler@med.uni-tuebingen.de, Strom, Tim M., Sutter, Christian, 42Institute of Human Genetics, University Hospital Heidelberg, 69120 Heidelberg, Germany, christian.sutter@med.uni-heidelberg.de, Thiele, Holger, van Asperen, Christi J., 43Department of Clinical Genetics, Leiden University Medical Center, 2333 Leiden, The Netherlands, c.j.van_asperen@lumc.nl (C.J.v.A.), r.b.van_der_luijt@lumc.nl (R.B.v.d.L.), van der Kolk, Lizet, van der Luijt, Rob B., Volk, Alexander E., 45Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany, a.volk@uke.de, Wagner, Michael, 46Department of Neurodegenerative Diseases and Geriatric Psychiatry, University Hospital Bonn, 53127 Bonn, Germany, michael.wagner@ukbonn.de, Waisfisz, Quinten, 47Department of Human Genetics, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 Amsterdam, The Netherlands, q.waisfisz@vumc.nl, Wang, Qin, Wang-Gohrke, Shan, 48Department of Gynaecology and Obstetrics, University of Ulm, 89081 Ulm, Germany, shan.wang-gohrke@uniklinik-ulm.de, Weber, Bernhard H. F., 49Institute of Human Genetics, Regensburg University, 93053 Regensburg, Germany, bweb@klinik.uni-regensburg.de, Devilee, Peter, 51Department of Pathology, Department of Human Genetics, Leiden University Medical Center, 2333 Leiden, The Netherlands, p.devilee@lumc.nl, Tavtigian, Sean, 4Huntsman Cancer Institute, University of Utah, Salt Lake City, UT 84112, USA, sean.tavtigian@hci.utah.edu, Bader, Gary D., Meindl, Alfons, Goldgar, David E., Andrulis, Irene L., Schmutzler, Rita K., Easton, Douglas F., Schmidt, Marjanka K., Hahnen, Eric, Simard, Jacques

العلاقة: https://resolver.sub.uni-goettingen.de/purl?gro-2/112620Test

الإتاحة: https://doi.org/10.3390/cancers14143363Test
https://resolver.sub.uni-goettingen.de/purl?gro-2/112620Test

View record in BASE

النص الكامل

2

دورية أكاديمية

Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent.

المؤلفون: Guo, Yan, Warren Andersen, Shaneda, Shu, Xiao-Ou, Michailidou, Kyriaki, Bolla, Manjeet K, Wang, Qin, Garcia-Closas, Montserrat, Milne, Roger L, Schmidt, Marjanka K, Chang-Claude, Jenny, Dunning, Allison, Bojesen, Stig E, Ahsan, Habibul, Aittomäki, Kristiina, Andrulis, Irene L, Anton-Culver, Hoda, Arndt, Volker, Beckmann, Matthias W, Beeghly-Fadiel, Alicia, Benitez, Javier, Bogdanova, Natalia V, Bonanni, Bernardo, Børresen-Dale, Anne-Lise, Brand, Judith, Brauch, Hiltrud, Brenner, Hermann, Brüning, Thomas, Burwinkel, Barbara, Casey, Graham, Chenevix-Trench, Georgia, Couch, Fergus J, Cox, Angela, Cross, Simon S, Czene, Kamila, Devilee, Peter, Dörk, Thilo, Dumont, Martine, Fasching, Peter A, Figueroa, Jonine, Flesch-Janys, Dieter, Fletcher, Olivia, Flyger, Henrik, Fostira, Florentia, Gammon, Marilie, Giles, Graham G, Guénel, Pascal, Haiman, Christopher A, Hamann, Ute, Hooning, Maartje J, Hopper, John L, Jakubowska, Anna, Jasmine, Farzana, Jenkins, Mark, John, Esther M, Johnson, Nichola, Jones, Michael E, Kabisch, Maria, Kibriya, Muhammad, Knight, Julia A, Koppert, Linetta B, Kosma, Veli-Matti, Kristensen, Vessela, Le Marchand, Loic, Lee, Eunjung, Li, Jingmei, Lindblom, Annika, Luben, Robert, Lubinski, Jan, Malone, Kathi E, Mannermaa, Arto, Margolin, Sara, Marme, Frederik, McLean, Catriona, Meijers-Heijboer, Hanne, Meindl, Alfons, Neuhausen, Susan L, Nevanlinna, Heli, Neven, Patrick, Olson, Janet E, Perez, Jose IA, Perkins, Barbara, Peterlongo, Paolo, Phillips, Kelly-Anne, Pylkäs, Katri, Rudolph, Anja, Santella, Regina, Sawyer, Elinor J, Schmutzler, Rita K, Seynaeve, Caroline, Shah, Mitul, Shrubsole, Martha J, Southey, Melissa C, Swerdlow, Anthony J, Toland, Amanda E, Tomlinson, Ian, Torres, Diana, Truong, Thérèse, Ursin, Giske, Van Der Luijt, Rob B, Verhoef, Senno

المصدر: PLoS medicine. 13(8)

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/58s1333xTest

View record in eScholarship

3

دورية أكاديمية

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry.

المؤلفون: Arndt, Volker, Beckmann, Matthias, Beeghly-Fadiel, Alicia, Benitez, Javier, Blomqvist, Carl, Bogdanova, Natalia, Børresen-Dale, Anne-Lise, Brand, Judith, Brauch, Hiltrud, Brenner, Hermann, Burwinkel, Barbara, Cai, Qiuyin, Casey, Graham, Chenevix-Trench, Georgia, Couch, Fergus, Cox, Angela, Cross, Simon, Czene, Kamila, Dörk, Thilo, Dumont, Martine, Fasching, Peter, Figueroa, Jonine, Flesch-Janys, Dieter, Fletcher, Olivia, Flyger, Henrik, Fostira, Florentia, Gammon, Marilie, Giles, Graham, Guénel, Pascal, Haiman, Christopher, Hamann, Ute, Harrington, Patricia, Hartman, Mikael, Hooning, Maartje, Hopper, John, Jakubowska, Anna, Jasmine, Farzana, John, Esther, Johnson, Nichola, Kabisch, Maria, Khan, Sofia, Kibriya, Muhammad, Knight, Julia, Kosma, Veli-Matti, Kriege, Mieke, Kristensen, Vessela, Le Marchand, Loic, Lee, Eunjung, Li, Jingmei, Lindblom, Annika, Lophatananon, Artitaya, Luben, Robert, Lubinski, Jan, Malone, Kathleen, Mannermaa, Arto, Manoukian, Siranoush, Margolin, Sara, Marme, Frederik, McLean, Catriona, Meijers-Heijboer, Hanne, Meindl, Alfons, Miao, Hui, Muir, Kenneth, Neuhausen, Susan, Nevanlinna, Heli, Neven, Patrick, Olson, Janet, Perkins, Barbara, Peterlongo, Paolo, Phillips, Kelly-Anne, Pylkäs, Katri, Rudolph, Anja, Santella, Regina, Sawyer, Elinor, Schmutzler, Rita, Schoemaker, Minouk, Shah, Mitul, Shrubsole, Martha, Southey, Melissa, Swerdlow, Anthony, Toland, Amanda, Tomlinson, Ian, Torres, Diana, Truong, Thérèse, Ursin, Giske, Van Der Luijt, Rob, Verhoef, Senno, Wang-Gohrke, Shan, Whittemore, Alice, Winqvist, Robert, Pilar Zamora, M, Zhao, Hui, Dunning, Alison, Simard, Jacques, Hall, Per, Kraft, Peter, Pharoah, Paul, Hunter, David, Easton, Douglas, Zheng, Wei

المصدر: Cancer Causes and Control. 27(5)

مصطلحات موضوعية: Breast cancer, Epidemiology, GWAS, Genetic susceptibility, Type 2 diabetes, Breast Neoplasms, Case-Control Studies, Diabetes Mellitus, Type 2, Ethnicity, Female, Genetic Predisposition to Disease, Genetic Variation, Humans, Middle Aged, Odds Ratio, Polymorphism, Single Nucleotide, Risk Factors, White People

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8r82n8wcTest

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4

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

المؤلفون: Hamdi, Yosr, Soucy, Penny, Kuchenbaeker, Karoline B., Pastinen, Tomi, Droit, Arnaud, Lemaçon, Audrey, Adlard, Julian, Aittomäki, Kristiina, Andrulis, Irene L., Arason, Adalgeir, Arnold, Norbert, Arun, Banu K., Azzollini, Jacopo, Bane, Anita, Barjhoux, Laure, Barrowdale, Daniel, Benitez, Javier, Berthet, Pascaline, Blok, Marinus J., Bobolis, Kristie, Bonadona, Valérie, Bonanni, Bernardo, Bradbury, Angela R., Brewer, Carole, Buecher, Bruno, Buys, Saundra S., Caligo, Maria A., Chiquette, Jocelyne, Chung, Wendy K., Claes, Kathleen B M, Daly, Mary B., Damiola, Francesca, Davidson, Rosemarie, de la Hoya, Miguel, de Leeneer, Kim, Diez, Orland, Ding, Yuan Chun, Dolcetti, Riccardo, Domchek, Susan M., Dorfling, Cecilia M., Eccles, Diana, Eeles, Ros, Einbeigi, Zakaria, Ejlertsen, Bent, EMBRACE, Engel, Christoph, Gareth Evans, D., Feliubadalo, Lidia, Foretova, Lenka, Fostira, Florentia, Foulkes, William D., Fountzilas, George, Friedman, Eitan, Frost, Debra, Ganschow, Pamela, Ganz, Patricia A., Garber, Judy, Gayther, Simon A., Gemo Study Collaborators, Study Collaborators, Gerdes, Anne Marie, Glendon, Gord, Godwin, Andrew K., Goldgar, David E., Greene, Mark H., Gronwald, Jacek, Hahnen, Eric, Hamann, Ute, Hansen, Thomas V O, Hart, Steven, Hays, John L., HEBON, Hogervorst, Frans B L, Hulick, Peter J., Imyanitov, Evgeny N., Isaacs, Claudine, Izatt, Louise, Jakubowska, Anna, James, Paul, Janavicius, Ramunas, Jensen, Uffe Birk, John, Esther M., Joseph, Vijai, Just, Walter, Kaczmarek, Katarzyna, Karlan, Beth Y., Kconfab Investigators, Investigators, Kets, Carolien M., Kirk, Judy, Kriege, Mieke, Laitman, Yael, Laurent, Maïté, Lazaro, Conxi, Leslie, Goska, Lester, Jenny, Lesueur, Fabienne, Liljegren, Annelie, Loman, Niklas, Loud, Jennifer T., Manoukian, Siranoush, Mariani, Milena, Mazoyer, Sylvie, McGuffog, Lesley, Meijers-Heijboer, Hanne E J, Meindl, Alfons, Miller, Austin, Montagna, Marco, Mulligan, Anna Marie, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, Nussbaum, Robert L., Olah, Edith, Olopade, Olufunmilayo I., Ong, Kai ren, Oosterwijk, Jan C., Osorio, Ana, Papi, Laura, Park, Sue Kyung, Pedersen, Inge Sokilde, Peissel, Bernard, Segura, Pedro Perez, Peterlongo, Paolo, Phelan, Catherine M., Radice, Paolo, Rantala, Johanna, Rappaport-Fuerhauser, Christine, Rennert, Gad, Richardson, Andrea, Robson, Mark, Rodriguez, Gustavo C., Rookus, Matti A., Schmutzler, Rita Katharina, Sevenet, Nicolas, Shah, Payal D., Singer, Christian F., Slavin, Thomas P., Snape, Katie, Sokolowska, Johanna, Sønderstrup, Ida Marie Heeholm, Southey, Melissa, Spurdle, Amanda B., Stadler, Zsofia, Stoppa-Lyonnet, Dominique, Sukiennicki, Grzegorz, Sutter, Christian, Tan, Yen, Tea, Muy Kheng, Teixeira, Manuel R., Teulé, Alex, Teo, Soo Hwang, Terry, Mary Beth, Thomassen, Mads, 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, van Rensburg, Elizabeth J., Varon-Mateeva, Raymonda, Wappenschmidt, Barbara, Wijnen, Juul T., Rebbeck, Timothy, Chenevix-Trench, Georgia, Offit, Kenneth, Couch, Fergus J., Nord, Silje, Easton, Douglas F., Antoniou, Antonis C., Simard, Jacques

المصدر: Breast Cancer Research and Treatment. 161(1):117-134

مصطلحات موضوعية: BRCA1 and BRCA2 mutation carriers, Breast cancer, Cis-regulatory variants, Differential allelic expression, Genetic modifiers, Genetic susceptibility, Medicin och hälsovetenskap, Klinisk medicin, Cancer och onkologi, Medical and Health Sciences, Clinical Medicine, Cancer and Oncology

الوصول الحر: https://lup.lub.lu.se/record/de205e2a-c0eb-4400-a4ac-d4c9a2c26b2dTest
http://dx.doi.org/10.1007/s10549-016-4018-2Test

View record in SwePub

5

دورية أكاديمية

Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers.

المؤلفون: Blanco, Ignacio, Kuchenbaecker, Karoline, Cuadras, Daniel, Wang, Xianshu, Barrowdale, Daniel, de Garibay, Gorka, Librado, Pablo, Sánchez-Gracia, Alejandro, Rozas, Julio, Bonifaci, Núria, McGuffog, Lesley, Pankratz, Vernon, Islam, Abul, Mateo, Francesca, Berenguer, Antoni, Petit, Anna, Català, Isabel, Brunet, Joan, Feliubadaló, Lidia, Tornero, Eva, Benítez, Javier, Osorio, Ana, Ramón y Cajal, Teresa, Nevanlinna, Heli, Aittomäki, Kristiina, Arun, Banu, Toland, Amanda, Karlan, Beth, Walsh, Christine, Lester, Jenny, Greene, Mark, Mai, Phuong, Nussbaum, Robert, Andrulis, Irene, Domchek, Susan, Nathanson, Katherine, Rebbeck, Timothy, Barkardottir, Rosa, Jakubowska, Anna, Lubinski, Jan, Durda, Katarzyna, Jaworska-Bieniek, Katarzyna, Claes, Kathleen, Van Maerken, Tom, Díez, Orland, Hansen, Thomas, Jønson, Lars, Gerdes, Anne-Marie, Ejlertsen, Bent, de la Hoya, Miguel, Caldés, Trinidad, Dunning, Alison, Oliver, Clare, Fineberg, Elena, Cook, Margaret, Peock, Susan, McCann, Emma, Murray, Alex, Jacobs, Chris, Pichert, Gabriella, Lalloo, Fiona, Chu, Carol, Dorkins, Huw, Paterson, Joan, Ong, Kai-Ren, Teixeira, Manuel, Hogervorst, Frans, van der Hout, Annemarie, Seynaeve, Caroline, van der Luijt, Rob, Ligtenberg, Marjolijn, Devilee, Peter, Wijnen, Juul, Rookus, Matti, Meijers-Heijboer, Hanne, Blok, Marinus, van den Ouweland, Ans, Aalfs, Cora, Rodriguez, Gustavo, Phillips, Kelly-Anne, Piedmonte, Marion, Nerenstone, Stacy, Bae-Jump, Victoria, OMalley, David, Ratner, Elena, Schmutzler, Rita, Wappenschmidt, Barbara, Rhiem, Kerstin, Engel, Christoph, Meindl, Alfons, Ditsch, Nina, Arnold, Norbert, Plendl, Hansjoerg, Niederacher, Dieter, Sutter, Christian, Wang-Gohrke, Shan, Steinemann, Doris, Preisler-Adams, Sabine, Kast, Karin, Varon-Mateeva, Raymonda

المصدر: PLoS ONE. 10(4)

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/4m40d6jkTest
https://escholarship.org/content/qt4m40d6jk/qt4m40d6jk.pdfTest

View record in eScholarship

6

دورية أكاديمية

A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers

المؤلفون: Coignard, Juliette, Lush, Michael, Beesley, Jonathan, O’Mara, Tracy A., Dennis, Joe, Tyrer, Jonathan P., Barnes, Daniel R., McGuffog, Lesley, Leslie, Goska, Bolla, Manjeet K., Adank, Muriel A., Agata, Simona, Ahearn, Thomas, Aittomäki, Kristiina, Andrulis, Irene L., Anton-Culver, Hoda, Arndt, Volker, Arnold, Norbert, Aronson, Kristan J., Arun, Banu K., Augustinsson, Annelie, Azzollini, Jacopo, Barrowdale, Daniel, Baynes, Caroline, Becher, Heko, Bermisheva, Marina, Bernstein, Leslie, Białkowska, Katarzyna, Blomqvist, Carl, Bojesen, Stig E., Bonanni, Bernardo, Borg, Ake, Brauch, Hiltrud, Brenner, Hermann, Burwinkel, Barbara, Buys, Saundra S., Caldés, Trinidad, Caligo, Maria A., Campa, Daniele, Carter, Brian D., Castelao, Jose E., Chang-Claude, Jenny, Chanock, Stephen J., Chung, Wendy K., Claes, Kathleen B. M., Clarke, Christine L., Bertrand, Ophélie, Caputo, Sandrine, Dupré, Anaïs, le Mentec, Marine, Belotti, Muriel, Birot, Anne-Marie, Buecher, Bruno, Fourme, Emmanuelle, Gauthier-Villars, Marion, Golmard, Lisa, Houdayer, Claude, Moncoutier, Virginie, de Pauw, Antoine, Saule, Claire, Sinilnikova, Olga, Mazoyer, Sylvie, Damiola, Francesca, Barjhoux, Laure, Verny-Pierre, Carole, Léone, M. lanie, Boutry-Kryza, Nadia, Calender, Alain, Giraud, Sophie, Caron, Olivier, Guillaud-Bataille, Marine, Bressac-de-Paillerets, Brigitte, Bignon, Yves- Jean, Uhrhammer, Nancy, Lasset, Christine, Bonadona, Valérie, Berthet, Pascaline, Vaur, Dominique, Castera, Laurent, Noguchi, Tetsuro, Popovici, Cornel, Sobol, Hagay, Bourdon, Violaine, Remenieras, Audrey, Noguès, Catherine, Coupier, Isabelle, Pujol, Pascal, Dumont, Aurélie, Révillion, Françoise, Adenis, Claude, Muller, Danièle, Barouk-Simonet, Emmanuelle, Bonnet, Françoise, Bubien, Virginie, Sevenet, Nicolas, Longy, Michel, Toulas, Christine, Guimbaud, Rosine, Gladieff, Laurence, Feillel, Viviane, Leroux, Dominique, Dreyfus, H. lène, Rebischung, Christine, Peysselon, Magalie, Coron, Fanny, Faivre, Laurence, Baurand, Amandine, Jacquot, Caroline, Bertolone, Geoffrey, Lizard, Sarab, Prieur, Fabienne, Lebrun, Marine, Kientz, Caroline, Ferrer, Sandra Fert, Mari, V. ronique, Vénat-Bouvet, Laurence, Delnatte, Capucine, Bézieau, Stéphane, Mortemousque, Isabelle, Coulet, Florence, Colas, Chrystelle, Soubrier, Florent, Warcoin, Mathilde, Sokolowska, Johanna, Bronner, Myriam, Collonge-Rame, Marie-Agnès, Damette, Alexandre, Gesta, Paul, Lallaoui, Hakima, Chiesa, Jean, Molina-Gomes, Denise, Ingster, Olivier, Gregory, Helen, Miedzybrodzka, Zosia, Morrison, Patrick J., Ong, Kai-ren, Donaldson, Alan, Rogers, Mark T., Kennedy, M. John, Porteous, Mary E., Brewer, Carole, Davidson, Rosemarie, Izatt, Louise, Brady, Angela, Barwell, Julian, Adlard, Julian, Foo, Claire, Lalloo, Fiona, Side, Lucy E., Eason, Jacqueline, Henderson, Alex, Walker, Lisa, Eeles, Rosalind A., Cook, Jackie, Snape, Katie, Eccles, Diana, Murray, Alex, McCann, Emma, Collée, J. Margriet, Conroy, Don M., Czene, Kamila, Daly, Mary B., Devilee, Peter, Diez, Orland, Ding, Yuan Chun, Domchek, Susan M., Dörk, Thilo, dos-Santos-Silva, Isabel, Dunning, Alison M., Dwek, Miriam, Eccles, Diana M., Eliassen, A. Heather, Engel, Christoph, Eriksson, Mikael, Evans, D. Gareth, Fasching, Peter A., Flyger, Henrik, Fostira, Florentia, Friedman, Eitan, Fritschi, Lin, Frost, Debra, Gago-Dominguez, Manuela, Gapstur, Susan M., Garber, Judy, Garcia-Barberan, Vanesa, García-Closas, Montserrat, García-Sáenz, José A., Gaudet, Mia M., Gayther, Simon A., Gehrig, Andrea, Georgoulias, Vassilios, Giles, Graham G., Godwin, Andrew K., Goldberg, Mark S., Goldgar, David E., González-Neira, Anna, Greene, Mark H., Guénel, Pascal, Haeberle, Lothar, Hahnen, Eric, Haiman, Christopher A., Håkansson, Niclas, Hall, Per, Hamann, Ute, Harrington, Patricia A., Hart, Steven N., He, Wei, Hogervorst, Frans B. L., Hollestelle, Antoinette, Hopper, John L., Horcasitas, Darling J., Hulick, Peter J., Hunter, David J., Imyanitov, Evgeny N., Fox, Stephen, Campbell, Ian, Spurdle, Amanda, Webb, Penny, de Fazio, Anna, Tassell, Margaret, Kirk, Judy, Lindeman, Geoff, Price, Melanie, Southey, Melissa, Milne, Roger, Deb, Sid, Bowtell, David, van der Hout, Annemieke H., van den Ouweland, Ans M. W., Mensenkamp, Arjen R., van Deurzen, Carolien H. M., Kets, Carolien M., Seynaeve, Caroline, van Asperen, Christi J., Aalfs, Cora M., Gómez Garcia, Encarna B., van Leeuwen, Flora E., de Bock, G. H., Meijers-Heijboer, Hanne E. J., Obdeijn, Inge M., Gille, J. J. P., Oosterwijk, Jan C., Wijnen, Juul T., van der Kolk, Lizet E., Hooning, Maartje J., Ausems, Margreet G. E. M., Mourits, Marian J. E., Blok, Marinus J., Rookus, Matti A., van der Luijt, Rob B., van Cronenburg, T. C. T. E. F., van der Pol, Carmen C., Russell, Nicola S., Siesling, Sabine, Overbeek, Lucy, Wijnands, R., de Lange, Judith L., Clarke, Christine, Graham, Dinny, Sachchithananthan, Mythily, Marsh, Deborah, Scott, Rodney, Baxter, Robert, Yip, Desmond, Carpenter, Jane, Davis, Alison, Pathmanathan, Nirmala, Simpson, Peter, Jager, Agnes, Jakubowska, Anna, James, Paul A., Jensen, Uffe Birk, John, Esther M., Jones, Michael E., Kaaks, Rudolf, Kapoor, Pooja Middha, Karlan, Beth Y., Keeman, Renske, Khusnutdinova, Elza, Kiiski, Johanna I., Ko, Yon-Dschun, Kosma, Veli-Matti, Kraft, Peter, Kurian, Allison W., Laitman, Yael, Lambrechts, Diether, le Marchand, Loic, Lester, Jenny, Lesueur, Fabienne, Lindstrom, Tricia, Lopez-Fernández, Adria, Loud, Jennifer T., Luccarini, Craig, Mannermaa, Arto, Manoukian, Siranoush, Margolin, Sara, Martens, John W. M., Mebirouk, Noura, Meindl, Alfons, Miller, Austin, Milne, Roger L., Montagna, Marco, Nathanson, Katherine L., Neuhausen, Susan L., Nevanlinna, Heli, Nielsen, Finn C., O’Brien, Katie M., Olopade, Olufunmilayo I., Olson, Janet E., Olsson, H. kan, Osorio, Ana, Ottini, Laura, Park-Simon, Tjoung-Won, Parsons, Michael T., Pedersen, Inge Sokilde, Peshkin, Beth, Peterlongo, Paolo, Peto, Julian, Pharoah, Paul D. P., Phillips, Kelly-Anne, Polley, Eric C., Poppe, Bruce, Presneau, Nadege, Pujana, Miquel Angel, Punie, Kevin, Radice, Paolo, Rantala, Johanna, Rashid, Muhammad U., Rennert, Gad, Rennert, Hedy S., Robson, Mark, Romero, Atocha, Rossing, Maria, Saloustros, Emmanouil, Sandler, Dale P., Santella, Regina, Scheuner, Maren T., Schmidt, Marjanka K., Schmidt, Gunnar, Scott, Christopher, Sharma, Priyanka, Soucy, Penny, Southey, Melissa C., Spinelli, John J., Steinsnyder, Zoe, Stone, Jennifer, Stoppa-Lyonnet, Dominique, Swerdlow, Anthony, Tamimi, Rulla M., Tapper, William J., Taylor, Jack A., Terry, Mary Beth, Teulé, Alex, Thull, Darcy L., Tischkowitz, Marc, Toland, Amanda E., Torres, Diana, Trainer, Alison H., Truong, Thérèse, Tung, Nadine, Vachon, Celine M., Vega, Ana, Vijai, Joseph, Wang, Qin, Wappenschmidt, Barbara, Weinberg, Clarice R., Weitzel, Jeffrey N., Wendt, Camilla, Wolk, Alicja, Yadav, Siddhartha, Yang, Xiaohong R., Yannoukakos, Drakoulis, Zheng, Wei, Ziogas, Argyrios, Zorn, Kristin K., Park, Sue K., Thomassen, Mads, Offit, Kenneth, Schmutzler, Rita K., Couch, Fergus J., Simard, Jacques, Chenevix-Trench, Georgia, Easton, Douglas F., Andrieu, Nadine, Antoniou, Antonis C.

المصدر: Coignard , J , Lush , M , Beesley , J , O’Mara , T A , Dennis , J , Tyrer , J P , Barnes , D R , McGuffog , L , Leslie , G , Bolla , M K , Adank , M A , Agata , S , Ahearn , T , Aittomäki , K , Andrulis , I L , Anton-Culver , H , Arndt , V , Arnold , N , Aronson , K J , Arun , B K , Augustinsson , A , Azzollini , J , Barrowdale , D ....

العلاقة: https://research.vumc.nl/en/publications/80074eac-e8e7-449d-97da-618112e6bae7Test

الإتاحة: https://doi.org/10.1038/s41467-020-20496-3Test
https://research.vumc.nl/en/publications/80074eac-e8e7-449d-97da-618112e6bae7Test
http://www.scopus.com/inward/record.url?scp=85101270098&partnerID=8YFLogxKTest

View record in BASE

7

دورية أكاديمية

Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiences

المؤلفون: Velthuizen, Mary E., van der Luijt, Rob B., de Vries, Beja J., Koudijs, Marco J., Bleiker, Eveline M.A., Ausems, Margreet G.E.M.

المساهمون: Genetica, Genetica Sectie Genoomdiagnostiek, Cancer, Genetica Klinische Genetica

مصطلحات موضوعية: Breast cancer risk, CHEK2 c.1100del pathogenic variant, Recontacting, Uptake testing, Oncology, Genetics(clinical)

وصف الملف: application/pdf

العلاقة: https://dspace.library.uu.nl/handle/1874/444982Test

الإتاحة: https://dspace.library.uu.nl/handle/1874/444982Test

View record in BASE

النص الكامل

8

دورية أكاديمية

The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant

المؤلفون: Lakeman, Inge, van den Broek, Alexandra, Vos, Juliën, Barnes, Daniel, Adlard, Julian, Andrulis, Irene, Arason, Adalgeir, Arnold, Norbert, Arun, Banu, Balmaña, Judith, Barrowdale, Daniel, Benitez, Javier, Borg, Ake, Caldés, Trinidad, Caligo, Maria, Chung, Wendy, Claes, Kathleen, Collée, J Margriet, Couch, Fergus, Daly, Mary, Dennis, Joe, Dhawan, Mallika, Domchek, Susan, Eeles, Ros, Engel, Christoph, Evans, D Gareth, Feliubadaló, Lidia, Foretova, Lenka, Friedman, Eitan, Frost, Debra, Ganz, Patricia, Garber, Judy, Gayther, Simon, Gerdes, Anne-Marie, Godwin, Andrew, Goldgar, David, Hahnen, Eric, Hake, Christopher, Hamann, Ute, Hogervorst, Frans, Hooning, Maartje, Hopper, John, Hulick, Peter, Imyanitov, Evgeny, Isaacs, Claudine, Izatt, Louise, Jakubowska, Anna, James, Paul, Janavicius, Ramunas, Jensen, Uffe Birk, Jiao, Yue, John, Esther, Joseph, Vijai, Karlan, Beth, Kets, Carolien, Konstantopoulou, Irene, Kwong, Ava, Legrand, Clémentine, Leslie, Goska, Lesueur, Fabienne, Loud, Jennifer, Lubiński, Jan, Manoukian, Siranoush, Mcguffog, Lesley, Miller, Austin, Gomes, Denise Molina, Montagna, Marco, Mouret-Fourme, Emmanuelle, Nathanson, Katherine, Neuhausen, Susan, Nevanlinna, Heli, Yie, Joanne Ngeow Yuen, Olah, Edith, Olopade, Olufunmilayo, Park, Sue, Parsons, Michael, Peterlongo, Paolo, Piedmonte, Marion, Radice, Paolo, Rantala, Johanna, Rennert, Gad, Risch, Harvey, Schmutzler, Rita, Sharma, Priyanka, Simard, Jacques, Singer, Christian, Stadler, Zsofia, Stoppa-Lyonnet, Dominique, Sutter, Christian, Tan, Yen Yen, Teixeira, Manuel, Teo, Soo Hwang, Teulé, Alex, Thomassen, Mads, Thull, Darcy, Tischkowitz, Marc, Toland, Amanda, Tung, Nadine, van Rensburg, Elizabeth, Vega, Ana, Wappenschmidt, Barbara, Devilee, Peter, van Asperen, Christi, Bernstein, Jonine, Offit, Kenneth, Easton, Douglas, Rookus, Matti, Chenevix-Trench, Georgia, Antoniou, Antonis, Robson, Mark, Schmidt, Marjanka, Claes, Kathleen B.M., Barouk-Simonet, Emmanuelle, Belotti, Muriel, Berthet, Pascaline, Bignon, Yves-Jean, Bonadona, Valérie, Bressac-de Paillerets, Brigitte, Buecher, Bruno, Caputo, Sandrine, Caron, Olivier, Castera, Laurent, Caux-Moncoutier, Virginie, Colas, Chrystelle, Collonge-Rame, Marie-Agnès, Coupier, Isabelle, de Pauw, Antoine, Delnatte, Capucine, Elan, Camille, Faivre, Laurence, Ferrer, Sandra Fert, Gauthier-Villars, Marion, Gesta, Paul, Giraud, Sophie, Golmard, Lisa, Houdayer, Claude, Lasset, Christine, Laurent, Maïté, Leroux, Dominique, Longy, Michel, Mari, Véronique, Mazoyer, Sylvie, Mebirouk, Noura, Mortemousque, Isabelle, Prieur, Fabienne, Pujol, Pascal, Saule, Claire, Schuster, Helene, Sevenet, Nicolas, Sobol, Hagay, Sokolowska, Johanna, Venat-Bouvet, Laurence, Ahmed, Munaza, Barwell, Julian, Brady, Angela, Brennan, Paul, Brewer, Carole, Cook, Jackie, Davidson, Rosemarie, Donaldson, Alan, Dunning, Alison, Eason, Jacqueline, Eccles, Diana, Gregory, Helen, Hanson, Helen, Harrington, Patricia, Henderson, Alex, Hodgson, Shirley, Kennedy, M. John, Lalloo, Fiona, Miller, Clare, Morrison, Patrick, Ong, Kai-Ren, O’shaughnessy-Kirwan, Aoife, Perkins, Jo, Porteous, Mary, Rogers, Mark, Side, Lucy, Snape, Katie, Walker, Lisa, Glendon, Gord, Mulligan, Anna Marie, Aalfs, Cora, Adank, Muriel, Ausems, Margreet G.E.M., Blok, Marinus, Gómez Garcia, Encarna, Heemskerk-Gerritsen, Bernadette A.M., Hollestelle, Antoinette, Jager, Agnes, Koppert, Linetta, Koudijs, Marco, Kriege, Mieke, Meijers-Heijboer, Hanne E.J., Mensenkamp, Arjen, Mooij, Thea, Oosterwijk, Jan, van den Ouweland, Ans M.W., van Der Baan, Frederieke, van Der Hout, Annemieke, van Der Kolk, Lizet, van Der Luijt, Rob, van Deurzen, Carolien H.M., van Doorn, Helena, van Engelen, Klaartje, van Hest, Liselotte, van Os, Theo A.M., Verhoef, Senno, Vogel, Maartje, Wijnen, Juul, Beesley, Jonathan, Fox, Stephen, Holland, Helene, Phillips, Kelly-Anne, Spurdle, Amanda

المساهمون: Chapel Allerton Hospital, University of Leeds, Departments of Molecular Genetics and Laboratory Medicine and Pathobiology, University of Toronto-Cancer Care Ontario, Reykjavík University, Division of Oncology, Department of Gynaecology and Obstetrics, University Hospital Schleswig–Holstein, The University of Texas M.D. Anderson Cancer Center Houston, Unitat d'Alt Risc i Prevenció del Càncer, Vall d'Hebron University Hospital Barcelona, University of Cambridge UK (CAM), Group of Human Genetics, Human Cancer Genetics Programme, Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), ISCIII, Department of Oncology, Clinical Sciences, Skåne University Hospital-Skane University Hospital Lund, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos Madrid, Spain (IdISSC), Section of Genetic Oncology, University of Pisa - Università di Pisa, Columbia University New York, Ghent University Hospital, Department of Clinical Genetics, Erasmus University Medical Center Rotterdam (Erasmus MC)-Family Cancer Clinic, Department of Laboratory Medicine and Pathology, Mayo Clinic, Division of Population Science, Fox Chase Cancer Center, Institut Curie Paris, Mines Paris - PSL (École nationale supérieure des mines de Paris), Université Paris Sciences et Lettres (PSL), Centre Hospitalier Universitaire CHU Grenoble (CHUGA), CHI Poissy-Saint-Germain, Unité de génétique et biologie des cancers (U830), Institut Curie Paris -Institut National de la Santé et de la Recherche Médicale (INSERM), Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier), Maladies infectieuses et vecteurs : écologie, génétique, évolution et contrôle (MIVEGEC), Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD France-Sud )

المصدر: ISSN: 1098-3600.

مصطلحات موضوعية: MESH: Adult, MESH: BRCA1 Protein, MESH: Risk Factors, MESH: BRCA2 Protein, MESH: Breast Neoplasms, MESH: Female, MESH: Genetic Predisposition to Disease, MESH: Heterozygote, MESH: Humans, MESH: Mutation, MESH: Retrospective Studies, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics