Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Bruce Poppe"'
Publikováno v:
Acta Neurologica Belgica. 121:191-197
Fabry disease (FD) is a X-linked multi-systemic metabolic disorder with mainly renal, cardiac and neurological dysfunction. The neuropsychological impact is still unclear, with previous study results ranging from disturbance of speed of information p
Autor:
Johan Saenen, Frederic Van Heuverswyn, Rik Willems, Jan De Keyser, Antoine Bondue, Bruce Poppe, Stefaan Van de Walle, Hans Vandekerckhove, Carlo de Asmundis, Wim Terryn, Dimitri Hemelsoet, Pascal Godart, Hedwig Stepman, Christoph Kampmann
Publikováno v:
Circulation
Autor:
Pascal Guénel, John J. Spinelli, Hoda Anton-Culver, Veli-Matti Kosma, Beth Y. Karlan, Antonis C. Antoniou, Brian D. Carter, Drakoulis Yannoukakos, Orland Diez, Montserrat Garcia-Closas, Uffe Birk Jensen, Susan M. Gapstur, Christine L. Clarke, Florentia Fostira, Trinidad Caldés, Wei Zheng, Diana Eccles, Don M. Conroy, Kristan J. Aronson, Sara Margolin, Thomas U. Ahearn, Hedy S. Rennert, Evgeny N. Imyanitov, Rulla M. Tamimi, Mary Beth Terry, Jenny Chang-Claude, Per Hall, Daniel R. Barnes, Alex Teulé, D. Gareth Evans, Åke Borg, Frans B. L. Hogervorst, Yon-Dschun Ko, Celine M. Vachon, Graham G. Giles, Simona Agata, Gad Rennert, Yuan Chun Ding, J. Margriet Collée, Alison M. Dunning, Regina M. Santella, Banu Arun, William J. Tapper, Melissa C. Southey, Finn Cilius Nielsen, Michael T. Parsons, Marjanka K. Schmidt, Alfons Meindl, Vassilios Georgoulias, Simon A. Gayther, Debra Frost, Noura Mebirouk, Hebon Investigators, Austin Miller, Sue K. Park, Anthony J Swerdlow, Emmanouil Saloustros, Isabel dos-Santos-Silva, Laura Ottini, Jack A. Taylor, Siranoush Manoukian, Maria A. Caligo, Douglas F. Easton, Christoph Engel, Antoinette Hollestelle, Ana Vega, Muriel A. Adank, Mia M. Gaudet, Heko Becher, Lothar Haeberle, Priyanka Sharma, Katherine L. Nathanson, Mads Thomassen, Miriam Dwek, Manuela Gago-Dominguez, Hiltrud Brauch, Kamila Czene, Peter A. Fasching, Peter J. Hulick, David E. Goldgar, Lesley McGuffog, Anna Jakubowska, Paul D.P. Pharoah, Adrià López-Fernández, Bruce Poppe, Volker Arndt, Georgia Chenevix-Trench, Tjoung-Won Park-Simon, Jennifer Stone, Wendy K. Chung, Joseph Vijai, Qin Wang, Penny Soucy, Miquel Angel Pujana, Diether Lambrechts, Vanesa García-Barberán, Andrea Gehrig, Anna González-Neira, Thérèse Truong, Jenny Lester, Wei He, Dale P. Sandler, Rita K. Schmutzler, Julian Peto, A. Heather Eliassen, Paolo Radice, Yael Laitman, Johanna Rantala, Kelly-Anne Phillips, Amanda E. Toland, Bernardo Bonanni, Muhammad Usman Rashid, Heli Nevanlinna, John L. Hopper, Kevin Punie, kConFab Investigators, Thilo Dörk, Judy Garber, Alison H. Trainer, Irene L. Andrulis, Jeffrey N. Weitzel, Michael Jones, Caroline Baynes, David J. Hunter, Mark S. Goldberg, Kristiina Aittomäki, Barbara Burwinkel, Jonathan Beesley, Maria Rossing, Norbert Arnold, Kathleen Claes, Renske Keeman, Esther M. John, John W.M. Martens, Katie M. O'Brien, Paolo Peterlongo, Mark H. Greene, Tracy A. O'Mara, Saundra S. Buys, Craig Luccarini, Atocha Romero, Paul A. James, Siddhartha Yadav, Zoe Steinsnyder, Diana Torres, Rudolf Kaaks, Camilla Wendt, Fabienne Lesueur, Ana Osorio, Olufunmilayo I. Olopade, Christopher A. Haiman, Agnes Jager, Tricia Lindstrom, Peter Devilee, Kristin K. Zorn, Loic Le Marchand, Darling J. Horcasitas, Michael Lush, Mark E. Robson, Jennifer T. Loud, Roger L. Milne, Lin Fritschi, Johanna I. Kiiski, Eric Hahnen, Jacques Simard, Annelie Augustinsson, Stig E. Bojesen, Kenneth Offit, Nadine Andrieu, Xiaohong R. Yang, Pooja Middha Kapoor, Joe Dennis, Beth N. Peshkin, Nadege Presneau, Darcy L. Thull, Fergus J. Couch, Gunnar Schmidt, Ute Hamann, Susan M. Domchek, Henrik Flyger, Mary B. Daly, Håkan Olsson, Clarice R. Weinberg, Niclas Håkansson, Elza Khusnutdinova, Inge Søkilde Pedersen, Manjeet K. Bolla, Steven N. Hart, Carl Blomqvist, Janet E. Olson, Maren T. Scheuner, Barbara Wappenschmidt, Marc Tischkowitz, Dominique Stoppa-Lyonnet, Nadine Tung, Stephen J. Chanock, Leslie Bernstein, Mikael Eriksson, José A. García-Sáenz, Jonathan Tyrer, Jose E. Castelao, Peter Kraft, Goska Leslie, Arto Mannermaa, Christopher G. Scott, Jacopo Azzollini, Eitan Friedman, Allison W. Kurian, Katarzyna Białkowska, Argyrios Ziogas, Hermann Brenner, Andrew K. Godwin, Patricia Harrington, Juliette Coignard, Daniele Campa, Susan L. Neuhausen, Marco Montagna, Marina Bermisheva, Alicja Wolk, Eric C. Polley, Abctb Investigators, Daniel Barrowdale
Publikováno v:
Nature Communications
Nat Commun
Nature Communications, Vol 12, Iss 1, Pp 1-2 (2021)
Nat Commun
Nature Communications, Vol 12, Iss 1, Pp 1-2 (2021)
Author(s): 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; Aittomaki, Kristiin
Association of Type and Location of BRCA1 and BRCA2 Mutations With Risk of Breast and Ovarian Cancer
Autor:
Caroline Seynaeve, Katja Harbst, Eric A. Ross, Nandita Mitra, Elisa Alducci, Marco Montagna, Janusz Menkiszak, Marion Gauthier-Villars, Javier Benitez, Carole Brewer, Etienne Rouleau, Inge Søkilde Pedersen, Orland Diez, Anya Kushnir, Antonis C. Antoniou, Christine Rappaport, Florentia Fostira, Maurizio Genuardi, Simona Agata, Mark H. Greene, Mary Beth Terry, Nicola Dikow, David E. Goldgar, Anna Jakubowska, Min Hyuk Lee, Sylvie Mazoyer, Diana Eccles, Shirley Hodgson, Anne-Marie Gerdes, Alexander Miron, Laima Tihomirova, Alan Donaldson, Adalgeir Arason, Rosalind A. Eeles, Fergus J. Couch, Hans Jörg Plendl, Francesca Vignolo-Lutati, Ute Hamann, Jackie Cook, Torben A Kruse, Shani Paluch-Shimon, Lisa Walker, Doris Steinemann, Dorothea Gadzicki, Juul T. Wijnen, Markus C. Fleisch, Kenneth Offit, Mary B. Daly, Jamal Zidan, Georgia Chenevix-Trench, Stephanie V. Blank, Marc Tischkowitz, Esther Darder, Annette Fontaine, Louise Izatt, Elżbieta Złowocka-Perłowska, Nadia Boutry-Kryza, Frans B. L. Hogervorst, Stefanie Engert, Danièle Muller, Susan M. Domchek, Phuong L. Mai, Senno Verhoef, Bernhard H. F. Weber, Cecilia M. Dorfling, Kathleen Claes, Kristiina Aittomäki, Annemarie H. van der Hout, Sharon Sand, Olufunmilayo I. Olopade, Margreet G. E. M. Ausems, Aleksandra Tołoczko-Grabarek, Trevor Cole, Giulietta Scuvera, Ana Osorio, Niklas Loman, Timothy R. Rebbeck, Riccardo Dolcetti, Marit Beer, Harsh B. Pathak, Douglas F. Easton, Lone Sunde, Conxi Lázaro, Raanan Berger, Paolo Radice, Mads Thomassen, Ignacio Blanco, Joseph Vijai, Kristie Bobolis, János Papp, Jean-Pierre Fricker, Christine Walsh, Patricia A. Ganz, Marie Stenmark-Askmalm, Andrea Gehrig, Vernon S. Pankratz, Atocha Romero, Xianshu Wang, Loris Bernard, Viviana Gismondi, Mary Porteous, Muy-Kheng Tea, Karen H. Lu, Gustavo C. Rodriguez, Bernardo Bonanni, Christoph Mundhenke, Julian Adlard, Bent Ejlertsen, Dominique Stoppa-Lyonnet, Nadine Tung, Patrick J. Morrison, Dezheng Huo, Cezary Cybulski, Jack Basil, Georg Pfeiler, Daphne Gschwantler-Kaulich, Heli Nevanlinna, Anders Bojesen, Marion Piedmonte, Katherine L. Nathanson, Amanda E. Toland, Sung-Won Kim, Judy Garber, Amanda B. Spurdle, Noralane M. Lindor, Sanne Traasdahl Moeller, Hans Ehrencrona, Trinidad Caldés, Rosemarie Davidson, Karin Kast, Jenny Lester, Shan Wang-Gohrke, Norbert Arnold, Ana Peixoto, Christine Lasset, Andreas Berger, Olga M. Sinilnikova, Katie Wakely, Claude Houdayer, Mercedes Durán, Robert L. Nussbaum, Ramūnas Janavičius, Christina G. Selkirk, Paolo Aretini, Nina Ditsch, J. Margriet Collée, Rosa B. Barkardottir, Sue Healey, Tomasz Huzarski, Cora M. Aalfs, Gillian Mitchell, Peter J. Hulick, Encarna B. Gomez Garcia, Zakaria Einbeigi, Christian F. Singer, Leigha Senter, Yuan Chun Ding, Dieter Niederacher, Yael Laitman, Siranoush Manoukian, Christoph Engel, Anne De Paepe, Anneliese Fink-Retter, Irene L. Andrulis, Rachel Laframboise, Maria A. Caligo, Priyanka Sharma, Miguel de la Hoya, Teresa Ramón y Cajal, Bruce Poppe, Thomas Hansen, Francesca Damiola, Anne-Bine Skytte, Susan L. Neuhausen, Christian Sutter, Marie-Agnès Collonge-Rame, Johannes J. P. Gille, Barbara Pasini, Wendy K. Chung, Noah D. Kauff, M. John Kennedy, Diana Torres, Salina B. Chan, Mark E. Robson, Elizabeth J. van Rensburg, Eric Hahnen, Barbara Wappenschmidt, Grzegorz Sukiennicki, Esther M. John, Rohini Rau-Murthy, Alice S. Whittemore, Kunle Odunsi, Masoud Azodi, John F. Boggess, Sue K. Park, Rita K. Schmutzler, Muriel Belotti, Jeffrey N. Weitzel, Simon A. Gayther, Fei Wan, Andrew K. Godwin, Arjen R. Mensenkamp, Daniela Zaffaroni, Jacques Simard, Susan Peock, Soo Hwang Teo, Claus R. Bartram, Evgeny N. Imyanitov, Maria-Isabel Tejada, Giuseppe Giannini, Mónica Salinas, Banu Arun, Jan C. Oosterwijk, Jacek Gronwald, Alexandra Becker, Tara M. Friebel, Lenka Foretova, Catherine Noguès, Muhammad Usman Rashid, Valeria Pensotti, Antonella Savarese, Debra Frost, Beatrice Melin, Drakoulis Yannoukakos, Steve Ellis, Jean-Philippe Peyrat, Hagay Sobol, Kim De Leeneer, Radka Platte, Jan Lubinski, Javier Godino, Lesley McGuffog, Tomasz Byrski, Claudine Isaacs, Johanna Rantala, Kelly-Anne Phillips, Carolien M. Kets, Uffe Birk Jensen, Katarzyna Durda, Linda Steele, Beth Y. Karlan, Ava Kwong, Alfons Meindl, Lucia Guidugli, Raymonda Varon-Mateeva, D. Gareth Evans, Edith Olah, Isabelle Mortemousque, Manuel R. Teixeira, Joyce Seldon, Katarzyna Jaworska-Bieniek, Bernard Peissel, Saundra S. Buys, Peter Devilee, Kerstin Rhiem, Eitan Friedman
Publikováno v:
BASE-Bielefeld Academic Search Engine
Rebbeck, T R, Mitra, N, Wan, F, Sinilnikova, O M, Healey, S, McGuffog, L, Mazoyer, S, Chenevix-Trench, G, Easton, D F, Antoniou, A C, Nathanson, K L, Laitman, Y, Kushnir, A, Paluch-Shimon, S, Berger, R, Zidan, J, Friedman, E, Ehrencrona, H, Stenmark-Askmalm, M, Einbeigi, Z, Loman, N, Harbst, K, Rantala, J, Melin, B, Huo, D, Olopade, O I, Seldon, J, Ganz, P A, Nussbaum, R L, Chan, S B, Odunsi, K, Gayther, S A, Domchek, S M, Arun, B K, Lu, K H, Mitchell, G, Karlan, B Y, Walsh, C, Lester, J, Godwin, A K, Pathak, H, Ross, E, Gerdes, A-M, Hansen, T V O, Bojesen, A, Thomassen, M, Moeller, S T, Kruse, T A, Pedersen, I S, Skytte, A-B & CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', J A M A: The Journal of the American Medical Association, vol. 313, no. 13, pp. 1347-1361 . https://doi.org/10.1001/jama.2014.5985
JAMA-Journal of the American Medical Association, 313(13), 1347-1361. American Medical Association
JAMA-Journal of the American Medical Association, 313(13), 1347-1361. AMER MEDICAL ASSOC
Digital.CSIC. Repositorio Institucional del CSIC
instname
Jama : Journal of the American Medical Association, 313, 13, pp. 1347-61
JAMA, 313(13), 1347-1361. American Medical Association
Rebbeck, T R, Mitra, N, Wan, F, Sinilnikova, O M, Healey, S, McGuffog, L, Mazoyer, S, Chenevix-Trench, G, Easton, D F, Antoniou, A C, Nathanson, K L, Laitman, Y, Kushnir, A, Paluch-Shimon, S, Berger, R, Zidan, J, Friedman, E, Ehrencrona, H, Stenmark-Askmalm, M, Einbeigi, Z, Loman, N, Harbst, K, Rantala, J, Melin, B, Huo, D, Olopade, O I, Seldon, J, Ganz, P A, Nussbaum, R L, Chan, S B, Odunsi, K, Gayther, S A, Domchek, S M, Arun, B K, Lu, K H, Mitchell, G, Karlan, B Y, Walsh, C, Lester, J, Godwin, A K, Pathak, H, Ross, E, Daly, M B, Whittemore, A S, John, E M, Miron, A, Terry, M B, Chung, W K, Goldgar, D E, Pedersen, I S & CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', JAMA: The Journal of the American Medical Association, vol. 313, no. 13, pp. 1347-61 . https://doi.org/10.1001/jama.2014.5985
CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', JAMA, vol. 313, no. 13, pp. 1347-61 . https://doi.org/10.1001/jama.2014.5985
Jama : Journal of the American Medical Association, 313, 1347-61
Rebbeck, T R, Mitra, N, Wan, F, Sinilnikova, O M, Healey, S, McGuffog, L, Mazoyer, S, Chenevix-Trench, G, Easton, D F, Antoniou, A C, Nathanson, K L, Laitman, Y, Kushnir, A, Paluch-Shimon, S, Berger, R, Zidan, J, Friedman, E, Ehrencrona, H, Stenmark-Askmalm, M, Einbeigi, Z, Loman, N, Harbst, K, Rantala, J, Melin, B, Huo, D, Olopade, O I, Seldon, J, Ganz, P A, Nussbaum, R L, Chan, S B, Odunsi, K, Gayther, S A, Domchek, S M, Arun, B K, Lu, K H, Mitchell, G, Karlan, B Y, Walsh, C, Lester, J, Godwin, A K, Pathak, H, Ross, E, Daly, M B, Whittemore, A S, John, E M, Miron, A, Pedersen, I S, Skytte, A-B, Sunde, L, Jensen, U B & CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', JAMA: The Journal of the American Medical Association, vol. 313, no. 13, pp. 1347-61 . https://doi.org/10.1001/jama.2014.5985
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
JAMA, 313(13), 1347-61. American Medical Association
Rebbeck, T R, Mitra, N, Wan, F, Sinilnikova, O M, Healey, S, McGuffog, L, Mazoyer, S, Chenevix-Trench, G, Easton, D F, Antoniou, A C, Nathanson, K L, Laitman, Y, Kushnir, A, Paluch-Shimon, S, Berger, R, Zidan, J, Friedman, E, Ehrencrona, H, Stenmark-Askmalm, M, Einbeigi, Z, Loman, N, Harbst, K, Rantala, J, Melin, B, Huo, D, Olopade, O I, Seldon, J, Ganz, P A, Nussbaum, R L, Chan, S B, Odunsi, K, Gayther, S A, Domchek, S M, Arun, B K, Lu, K H, Mitchell, G, Karlan, B Y, Walsh, C, Lester, J, Godwin, A K, Pathak, H, Ross, E, Gerdes, A-M, Hansen, T V O, Bojesen, A, Thomassen, M, Moeller, S T, Kruse, T A, Pedersen, I S, Skytte, A-B & CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', J A M A: The Journal of the American Medical Association, vol. 313, no. 13, pp. 1347-1361 . https://doi.org/10.1001/jama.2014.5985
JAMA-Journal of the American Medical Association, 313(13), 1347-1361. American Medical Association
JAMA-Journal of the American Medical Association, 313(13), 1347-1361. AMER MEDICAL ASSOC
Digital.CSIC. Repositorio Institucional del CSIC
instname
Jama : Journal of the American Medical Association, 313, 13, pp. 1347-61
JAMA, 313(13), 1347-1361. American Medical Association
Rebbeck, T R, Mitra, N, Wan, F, Sinilnikova, O M, Healey, S, McGuffog, L, Mazoyer, S, Chenevix-Trench, G, Easton, D F, Antoniou, A C, Nathanson, K L, Laitman, Y, Kushnir, A, Paluch-Shimon, S, Berger, R, Zidan, J, Friedman, E, Ehrencrona, H, Stenmark-Askmalm, M, Einbeigi, Z, Loman, N, Harbst, K, Rantala, J, Melin, B, Huo, D, Olopade, O I, Seldon, J, Ganz, P A, Nussbaum, R L, Chan, S B, Odunsi, K, Gayther, S A, Domchek, S M, Arun, B K, Lu, K H, Mitchell, G, Karlan, B Y, Walsh, C, Lester, J, Godwin, A K, Pathak, H, Ross, E, Daly, M B, Whittemore, A S, John, E M, Miron, A, Terry, M B, Chung, W K, Goldgar, D E, Pedersen, I S & CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', JAMA: The Journal of the American Medical Association, vol. 313, no. 13, pp. 1347-61 . https://doi.org/10.1001/jama.2014.5985
CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', JAMA, vol. 313, no. 13, pp. 1347-61 . https://doi.org/10.1001/jama.2014.5985
Jama : Journal of the American Medical Association, 313, 1347-61
Rebbeck, T R, Mitra, N, Wan, F, Sinilnikova, O M, Healey, S, McGuffog, L, Mazoyer, S, Chenevix-Trench, G, Easton, D F, Antoniou, A C, Nathanson, K L, Laitman, Y, Kushnir, A, Paluch-Shimon, S, Berger, R, Zidan, J, Friedman, E, Ehrencrona, H, Stenmark-Askmalm, M, Einbeigi, Z, Loman, N, Harbst, K, Rantala, J, Melin, B, Huo, D, Olopade, O I, Seldon, J, Ganz, P A, Nussbaum, R L, Chan, S B, Odunsi, K, Gayther, S A, Domchek, S M, Arun, B K, Lu, K H, Mitchell, G, Karlan, B Y, Walsh, C, Lester, J, Godwin, A K, Pathak, H, Ross, E, Daly, M B, Whittemore, A S, John, E M, Miron, A, Pedersen, I S, Skytte, A-B, Sunde, L, Jensen, U B & CIMBA Consortium 2015, ' Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer ', JAMA: The Journal of the American Medical Association, vol. 313, no. 13, pp. 1347-61 . https://doi.org/10.1001/jama.2014.5985
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
JAMA, 313(13), 1347-61. American Medical Association
CIMBA Consortium et al.
PMID: 25849179
[Importance]: Limited information about the relationship between specific mutations in BRCA1 or BRCA2 (BRCA1/2) and cancer risk exists. [Objective]: To identify mutation-specific cancer risks for carri
PMID: 25849179
[Importance]: Limited information about the relationship between specific mutations in BRCA1 or BRCA2 (BRCA1/2) and cancer risk exists. [Objective]: To identify mutation-specific cancer risks for carri
Autor:
Kuchenbaecker, Karoline B., Lesley, Mcguffog, Daniel, Barrowdale, Andrew, Lee, Penny, Soucy, Sue, Healey, Joe, Dennis, Michael, Lush, Mark, Robson, Spurdle, Amanda B., Ramus, Susan J., Nasim, Mavaddat, Mary Beth Terry, Neuhausen, Susan L., Ute, Hamann, Melissa, Southey, John, Esther M., Chung, Wendy K., Daly, Mary B., Buys, Saundra S., Goldgar, David E., Dorfling, Cecilia M., van Rensburg, Elizabeth J., Yuan Chun Ding, Bent, Ejlertsen, Anne-Marie, Gerdes, Hansen, Thomas V. O., Susan, Slager, Emily, Hallberg, Javier, Benitez, Ana, Osorio, Nancy, Cohen, William, Lawler, Weitzel, Jeffrey N., Paolo, Peterlongo, Valeria, Pensotti, Riccardo, Dolcetti, Monica, Barile, Bernardo, Bonanni, Jacopo, Azzollini, Siranoush, Manoukian, Bernard, Peissel, Paolo, Radice, Antonella, Savarese, Papi, Laura, Giannini, Giuseppe, Florentia, Fostira, Irene, Konstantopoulou, Julian, Adlard, Carole, Brewer, Jackie, Cook, Rosemarie, Davidson, Diana, Eccles, Ros, Eeles, Steve, Ellis, Embrace, Debra, Frost, Shirley, Hodgson, Louise, Izatt, Fiona, Lalloo, Kai-ren, Ong, Godwin, Andrew K., Norbert, Arnold, Bernd, Dworniczak, Christoph, Engel, Andrea, Gehrig, Eric, Hahnen, Jan, Hauke, Karin, Kast, Alfons, Meindl, Dieter, Niederacher, Rita Katharina Schmutzler, Raymonda, Varon-Mateeva, Shan, Wang-Gohrke, Barbara, Wappenschmidt, Laure, Barjhoux, Marie-Agne`s, Collonge-Rame, Camille, Elan, GEMO Study Collaborators, Lisa, Golmard, Emmanuelle, Barouk-Simonet, Fabienne, Lesueur, Sylvie, Mazoyer, Joanna, Sokolowska, Dominique Stoppa- Lyonnet, Claudine, Isaacs, Claes, Kathleen B. M., Bruce, Poppe, Miguel de la Hoya, Vanesa, Garcia-Barberan, Kristiina, Aittom€aki, Heli, Nevanlinna, Ausems, Margreet G. E. M., de Lange, J. L., Gomez Garcia, Encarna B., Hebon, Hogervorst, Frans B. L., Kets, Carolien M., Meijers-Heijboer, Hanne E. J., Oosterwijk, Jan C., Rookus, Matti A., van Asperen, Christi J., van den Ouweland, Ans M. W., van Doorn, Helena C., van Os, Theo A. M., Ava, Kwong, Edith, Olah, Orland, Diez, Joan, Brunet, Conxi, Lazaro, Alex, Teule´, Jacek, Gronwald, Anna, Jakubowska, Katarzyna, Kaczmarek, Jan, Lubinski, Grzegorz, Sukiennicki, Barkardottir, Rosa B., Jocelyne, Chiquette, Simona, Agata, Marco, Montagna, Teixeira, Manuel R., Kconfab, Investigators, Sue Kyung Park, Curtis, Olswold, Marc, Tischkowitz, Lenka, Foretova, Pragna, Gaddam, Joseph, Vijai, Georg, Pfeiler, Christine, Rappaport-Fuerhauser, Singer, Christian F., Tea, Muy-Kheng M., Greene, Mark H., Loud, Jennifer T., Gad, Rennert, Imyanitov, Evgeny N., Hulick, Peter J., Hays, John L., Marion, Piedmonte, Rodriguez, Gustavo C., Julie, Martyn, Gord, Glendon, Anna Marie Mulligan, Andrulis, Irene L., Amanda Ewart Toland, Uffe Birk Jensen, Kruse, Torben A., Inge Sokilde Pedersen, Mads, Thomassen, Caligo, Maria A., Soo-Hwang, Teo, Raanan, Berger, Eitan, Friedman, Yael, Laitman, Brita, Arver, Ake, Borg, Hans, Ehrencrona, Johanna, Rantala, Olopade, Olufunmilayo I., Ganz, Patricia A., Nussbaum, Robert L., Bradbury, Angela R., Domchek, Susan M., Nathanson, Katherine L., Arun, Banu K., Paul, James, Karlan, Beth Y., Jenny, Lester, Jacques, Simard, Pharoah, Paul D. P., Kenneth, Offit, Couch, Fergus J., Georgia, Chenevix-Trench, Easton, Douglas F., Antoniou, Antonis C.
Publikováno v:
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE
JNCI Journal of the National Cancer Institute
JNCI Journal of the National Cancer Institute
Background: Genome-wide association studies (GWAS) have identified 94 common single-nucleotide polymorphisms (SNPs) associated with breast cancer (BC) risk and 18 associated with ovarian cancer (OC) risk. Several of these are also associated with ris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4109753b16c39f5db17b458d2200be26
https://biblio.ugent.be/publication/8525301
https://biblio.ugent.be/publication/8525301
Autor:
Tuomas Heikkinen, Clare Turnbull, Penelope Miron, Deepak Subramanian, Florentia Fostira, Geoffrey J. Lindeman, Jeffrey N. Weitzel, Susan L. Neuhausen, Daniel Barrowdale, William D. Foulkes, Heli Nevanlinna, Sheila Seal, Katri Pylkäs, Paolo Radice, Andy C. H. Lee, Melissa C. Southey, Sofia Khan, Antonis C. Antoniou, Zhi Ling Teo, Carlo Tondini, Robert Winqvist, Marc Tischkowitz, Paolo Peterlongo, Jonathan Roberts, Douglas F. Easton, David E. Goldgar, Bruce Poppe, Nazneen Rahman, Patrick Concannon, Susan M. Domchek, Amanda E. Toland, Silvia Casadei, Paul A. James, Kristiina Aittomäki, Anne Kallioniemi, Drakoulis Yannoukakos, Mary Claire King, Irene L. Andrulis, Kim De Leeneer, Siranoush Manoukian, John L. Hopper, Jonine L. Bernstein, Fergus J. Couch, Eva Tomiak, Arto Mannermaa, Saundra S. Buys, Jukka S. Moilanen, Kathleen Claes
Publikováno v:
Scopus-Elsevier
Germline loss-of-function mutations in PALB2 are known to confer a predisposition to breast cancer. However, the lifetime risk of breast cancer that is conferred by such mutations remains unknown.We analyzed the risk of breast cancer among 362 member
Autor:
Tasha Wainstein, Ans Baeyens, Ilse Coene, Flavia Zita Francies, Anne Vral, Brecht Crombez, Bruce Poppe, A. Cairns, Jacobus Slabbert, K De Leeneer, T. Van Maerken, Kathleen Claes, Amanda Krause, Sarah Nietz, Robyn Kerr, H. Cubasch, Marshall Murdoch
Publikováno v:
BMC Cancer
Background Current knowledge of the aetiology of hereditary breast cancer in the four main South African population groups (black, coloured, Indian and white) is limited. Risk assessments in the black, coloured and Indian population groups are challe
Autor:
C. Charrin, Anne Hagemeijer, Carole Barin, M J Mozzicconacci, Barbara Cauwelier, Christine Lefebvre, Bruno Verhasselt, Isabelle Luquet, M.J. Gregoire, Philippe Jonveaux, Hélène Cavé, Barbara De Moerloose, Christine Terré, Kim De Keersmaecker, Anne De Paepe, G Plessis, F Sigaux, Nicole Dastugue, Bruce Poppe, Michel Lessard, B Laurence, Laurent Mauvieux, Hélène Antoine-Poirel, Marina Lafage-Pochitaloff, Francine Mugneret, Emmanuelle Clappier, J van den Akker, J Soulier, C Graux, Yves Benoit, Jan Cools, Carine Gervais, Franki Speleman, Pascale Cornillet-Lefebvre, Marie-Pierre Pages, C Chalas, Dominique Leroux, N. Van Roy, Christine Perot, Pierre Heimann, Roland Berger
Publikováno v:
Leukemia
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (1), pp.121-8. ⟨10.1038/sj.leu.2404410⟩
Leukemia, 2007, 21 (1), pp.121-8. ⟨10.1038/sj.leu.2404410⟩
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (1), pp.121-8. <10.1038/sj.leu.2404410>
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (1), pp.121-8. ⟨10.1038/sj.leu.2404410⟩
Leukemia, 2007, 21 (1), pp.121-8. ⟨10.1038/sj.leu.2404410⟩
Leukemia, Nature Publishing Group: Open Access Hybrid Model Option B, 2007, 21 (1), pp.121-8. <10.1038/sj.leu.2404410>
International audience; Recently, we and others described a new chromosomal rearrangement, that is, inv(7)(p15q34) and t(7;7)(p15;q34) involving the T-cell receptor beta (TCRbeta) (7q34) and the HOXA gene locus (7p15) in 5% of T-cell acute lymphoblas
Autor:
Barbara Cauwelier, A. De Paepe, Anne Hagemeijer, Nicole Dastugue, Christian Herens, Bruce Poppe, Franki Speleman, Jan Cools
Publikováno v:
Leukemia. 20:1238-1244
Chromosomal aberrations of T-cell receptor (TCR) gene loci often involve the TCRalphadelta (14q11) locus and affect various known T-cell oncogenes. A systematic fluorescent in situ hybridization (FISH) screening for the detection of chromosomal aberr
BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families
Publikováno v:
British Journal of Cancer
Worldwide variation in the distribution of BRCA1 and BRCA2 mutations is well recognised, and for the Belgian population no comprehensive studies about BRCA1/2 mutation spectra or frequencies have been published. We screened the complete coding region