檢索結果 - Sandra Fert‐Ferrer
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Overexpression of CEBPA resulting from the translocation t(14;19)(q32;q13) of human precursor B acute lymphoblastic leukemia 由 Élise Chapiro, Lisa J. Russell, I. Radford-Weiss, Christian Bastard, M Lessard, Stéphanie Struski, Hélène Cavé, Sandra Fert‐Ferrer, Carole Barin, Odile Maarek, Véronique Della-Valle, Jonathan C. Strefford, Roland Berger, Christine J. Harrison, Olivier Bernard, Florence Nguyen‐Khac
出版 2006Artigo -
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Genetic characterization of B-cell prolymphocytic leukemia: a prognostic model involving MYC and TP53 由 Élise Chapiro, Élodie Pramil, M’Boyba Diop, Damien Roos‐Weil, Clémentine Dillard, Clémentine Gabillaud, Karim Maloum, Catherine Settegrana, Lucile Baseggio, Jean‐François Lesesve, Mélanie Yon, Ludovic Jondreville, Claude Lesty, Frédéric Davi, Magali Le Garff‐Tavernier, Nathalie Droin, Philippe Dessen, Caroline Algrin, Véronique Leblond, Jean Gabarre, Simon Bouzy, Virginie Éclache, Baptiste Gaillard, Evelyne Callet‐Bauchu, Marc Müller, Christine Lefebvre, Nathalie Nadal, Antoine Ittel, Stéphanie Struski, Marie‐Agnès Collonge‐Rame, Benoît Quilichini, Sandra Fert‐Ferrer, Nathalie Auger, Isabelle Radford‐Weiss, Lena Wagner, Sebastian Scheinost, Thorsten Zenz, Santos A. Susín, Olivier Bernard, Florence Nguyen‐Khac
出版 2019Artigo -
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Screening Mammography and Breast Cancer: Variation in Risk with Rare Deleterious or Predicted Deleterious Variants in DNA Repair Genes 由 Maximiliano Ribeiro Guerra, Marie‐Gabrielle Dondon, Séverine Eon‐Marchais, Dorothée Le Gal, Juana Beauvallet, Noura Mebirouk, Muriel Belotti, Eve Cavaciuti, Claude Adenis-Lavignasse, Séverine Audebert‐Bellanger, Pascaline Berthet, Valérie Bonadona, Bruno Buecher, Olivier Caron, Mathias Cavaillé, Jean Chiésa, Chrystelle Colas, Isabelle Coupier, Capucine Delnatte, Hélène Dreyfus, Anne Fajac, Sandra Fert‐Ferrer, Jean‐Pierre Fricker, Marion Gauthier‐Villars, Paul Gesta, Sophie Giraud, Laurence Gladieff, Christine Lasset, S. Lejeune-Dumoulin, Jean–Marc Limacher, Michel Longy, Alain Lortholary, Élisabeth Luporsi, Christine M. Maugard, Isabelle Mortemousque, Sophie Nambot, Catherine Noguès, Pascal Pujol, Laurence Venat‐Bouvet, Florent Soubrier, Julie Tinat, A. Tardivon, Fabienne Lesueur, Dominique Stoppa‐Lyonnet, Nadine Andrieu
出版 2025Artigo -
4
Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation 由 Maximiliano Ribeiro Guerra, Juliette Coignard, Séverine Eon‐Marchais, Marie‐Gabrielle Dondon, Dorothée Le Gal, Juana Beauvallet, Noura Mebirouk, Muriel Belotti, Olivier Caron, Marion Gauthier‐Villars, Isabelle Coupier, Bruno Buecher, Alain Lortholary, Jean‐Pierre Fricker, Paul Gesta, Catherine Noguès, Laurence Faivre, Pascaline Berthet, Élisabeth Luporsi, Capucine Delnatte, Valérie Bonadona, Christine M. Maugard, Pascal Pujol, Christine Lasset, Michel Longy, Yves‐Jean Bignon, Claude Adenis-Lavignasse, Laurence Venat‐Bouvet, Hélène Dreyfus, Laurence Gladieff, Isabelle Mortemousque, Séverine Audebert‐Bellanger, Florent Soubrier, Sophie Giraud, S. Lejeune-Dumoulin, Jean–Marc Limacher, Jean Chiésa, Anne Fajac, Anne Floquet, François Eisinger, Julie Tinat, Sandra Fert‐Ferrer, Chrystelle Colas, Thierry Frébourg, Francesca Damiola, Laure Barjhoux, Eve Cavaciuti, Sylvie Mazoyer, A. Tardivon, Fabienne Lesueur, Dominique Stoppa‐Lyonnet, Nadine Andrieu
出版 2021Artigo -
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Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing 由 Elodie Girard, Séverine Eon‐Marchais, Robert Olaso, Anne‐Laure Renault, Francesca Damiola, Marie‐Gabrielle Dondon, Laure Barjhoux, Didier Goidin, Vincent Meyer, Dorothée Le Gal, Juana Beauvallet, Noura Mebirouk, Christine Lonjou, Juliette Coignard, Morgane Marcou, Eve Cavaciuti, Céline Baulard, Marie‐Thérèse Bihoreau, Odile Cohen‐Haguenauer, Dominique Leroux, Clotilde Penet, Sandra Fert‐Ferrer, Chrystelle Colas, Thierry Frébourg, François Eisinger, Claude Adenis, Anne Fajac, Laurence Gladieff, Julie Tinat, Anne Floquet, Jean Chiésa, Sophie Giraud, Isabelle Mortemousque, Florent Soubrier, Séverine Audebert‐Bellanger, Jean‐marc Limacher, Christine Lasset, S. Lejeune-Dumoulin, Hélène Dreyfus, Yves‐Jean Bignon, Michel Longy, Pascal Pujol, Laurence Venat‐Bouvet, Valérie Bonadona, Pascaline Berthet, Élisabeth Luporsi, Christine M. Maugard, Catherine Noguès, Capucine Delnatte, Jean‐Pierre Fricker, Paul Gesta, Laurence Faivre, Alain Lortholary, Bruno Buecher, Olivier Caron, Marion Gauthier‐Villars, Isabelle Coupier, Nicolas Servant, Anne Boland, Sylvie Mazoyer, Jean‐François Deleuze, Dominique Stoppa‐Lyonnet, Nadine Andrieu, Fabienne Lesueur
出版 2018Artigo -
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Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus 由 Kate Lawrenson, Siddhartha Kar, Karen McCue, Karoline B. Kuchenbaeker, Kyriaki Michailidou, Jonathan P. Tyrer, Jonathan Beesley, Susan J. Ramus, Qiyuan Li, Melissa K. Delgado, Janet M. Lee, Kristiina Aittomäki, Irene L. Andrulis, Hoda Anton‐Culver, Volker Arndt, Banu K. Arun, Brita Arver, Elisa V. Bandera, Monica Barile, Rósa B. Barkardóttir, Daniel Barrowdale, Matthias W. Beckmann, Javier Benı́tez, Andrew Berchuck, Maria Bisogna, Line Bjørge, Carl Blomqvist, William J. Blot, Natalia Bogdanova, Anders Bojesen, Stig E. Bojesen, Manjeet K. Bolla, Bernardo Bonanni, Anne‐Lise Børresen‐Dale, Hiltrud Brauch, Paul Brennan, Hermann Brenner, Fiona Bruinsma, Joan Brunet, Shaik Ahmad Buhari, Barbara Burwinkel, Ralf Bützow, Saundra S. Buys, Qiuyin Cai, Trinidad Caldés, Ian Campbell, Rikki Canniotto, Jenny Chang‐Claude, Jocelyne Chiquette, Ji‐Yeob Choi, Kathleen Claes, Marie- Agnès Collonge-Rame, Alexandre Damette, Emmanuelle Barouk-Simonet, Françoise Bonnet, Virginie Bubien, Nicolas Sévenet, Michel Longy, Pascaline Berthet, Dominique Vaur, Laurent Castéra, Sandra Fert Ferrer, Yves‐Jean Bignon, Nancy Uhrhammer, Fanny Coron, Laurence Faivre, Amandine Baurand, Caroline Jacquot, Geoffrey Bertolone, Sarab Lizard, Dominique Leroux, Hélène Dreyfus, Christine Rebischung, Magalie Peysselon, Jean‐Philippe Peyrat, Joëlle Fournier, Françoise Révillion, Claude Adenis, Laurence Venat‐Bouvet, Mélanie Léone, Nadia Boutry‐Kryza, Alain Calender, Sophie Giraud, Carole Verny-Pierre, Christine Lasset, Valérie Bonadona, Laure Barjhoux, Hagay Sobol, Violaine Bourdon, Tetsuro Noguchi, Audrey Remenieras, Isabelle Coupier, Pascal Pujol, Johanna Sokolowska, Myriam Bronner, Capucine Delnatte, Stéphane Bézieau, Véronique Mari, Marion Gauthier‐Villars, Bruno Buecher
出版 2016Artigo -
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Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers 由 Antonis C. Antoniou, Karoline Kuchenbaecker, Penny Soucy, Jonathan Beesley, Xiaohong Chen, Lesley McGuffog, Andrew Lee, Daniel Barrowdale, Sue Healey, Olga M. Sinilnikova, Maria A. Caligo, Niklas Loman, Katja Harbst, Annika Lindblom, Brita Arver, Richard Rosenquist, Per Karlsson, Katherine L. Nathanson, Susan M. Domchek, Tim Rebbeck, Anna Jakubowska, Jan Lubiński, Katarzyna Jaworska, Katarzyna Durda, Elżbieta Złowowcka-Perłowska, Ana Osório, M. Durán, Raquel Andrés, Javier Benı́tez, Ute Hamann, Frans B.L. Hogervorst, Theo A. van Os, Senno Verhoef, Hanne Meijers‐Heijboer, Juul Wijnen, E. Gómez, Marjolijn J. L. Ligtenberg, Mieke Kriege, J. Margriet Collée, Margreet G.E.M. Ausems, Jan C. Oosterwijk, Susan Peock, Debra Frost, Steve D. Ellis, Radka Platte, Elena Fineberg, D. Gareth Evans, Fiona Lalloo, Chris Jacobs, Rosalind A. Eeles, Julian Adlard, Rosemarie Davidson, Trevor Cole, Jackie Cook, Joan Paterson, Fiona Douglas, Carole Brewer, Shirley Hodgson, Patrick J. Morrison, Lisa Walker, Mark T. Rogers, Alan Donaldson, Huw Dorkins, Andrew K. Godwin, Betsy Bove, Dominique Stoppa‐Lyonnet, Claude Houdayer, Bruno Buecher, Antoine De Pauw, Sylvie Mazoyer, Alain Calender, Mélanie Léoné, Brigitte Bressac–de Paillerets, Olivier Caron, Hagay Sobol, Marc Frénay, Fabienne Prieur, Sandra Fert Ferrer, Isabelle Mortemousque, Saundra S. Buys, Mary B. Daly, Alexander Miron, Mary Beth Terry, John L. Hopper, Esther M. John, Melissa C. Southey, David E. Goldgar, Christian F. Singer, A. Fink-Retter, Muy‐Kheng Tea, Daphne Geschwantler Kaulich, Thomas van Overeem Hansen, Finn C. Nielsen, Rósa B. Barkardóttir, Mia M. Gaudet, Tomas Kirchhoff, Joseph Vijai, Ana Dutra-Clarke, Kenneth Offit, Marion Piedmonte
出版 2012Artigo -
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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers 由 Antonis C. Antoniou, Olga M. Sinilnikova, Lesley McGuffog, Sue Healey, Heli Nevanlinna, Tuomas Heikkinen, Jacques Simard, Amanda B. Spurdle, Jonathan Beesley, Xiaohong Chen, Susan L. Neuhausen, Yuan Chun Ding, Fergus J. Couch, Xianshu Wang, Zachary Fredericksen, Paolo Peterlongo, Bernard Peissel, Bernardo Bonanni, Alessandra Viel, Loris Bernard, Paolo Radice, Csilla I. Szabo, Lenka Foretová, Michal Zikán, Kathleen Claes, Mark H. Greene, L. Phuong, Gad Rennert, Flavio Lejbkowicz, Irene L. Andrulis, Hilmi Özçelik, Gord Glendon, Anne‐Marie Gerdes, Mads Thomassen, Lone Sunde, Maria A. Caligo, Yael Laitman, Tair Kontorovich, Shimrit Cohen, Bella Kaufman, Efrat Dagan, Ruth Gershoni Baruch, Eitan Friedman, Katja Harbst, Gisela Barbany, Johanna Rantala, Hans Ehrencrona, Per Karlsson, Susan M. Domchek, Katherine L. Nathanson, Ana Osório, Ignacio Blanco, Adriana Lasa, Javier Benı́tez, Ute Hamann, Frans B.L. Hogervorst, Matti A. Rookus, J. Margriet Collée, Peter Devilee, Marjolijn J. L. Ligtenberg, Rob B. van der Luijt, Cora M. Aalfs, Quinten Waisfisz, Juul Wijnen, C. E. P. van Roozendaal, Susan Peock, Margaret Cook, Debra Frost, Clare Oliver, Radka Platte, D. Gareth Evans, Fiona Lalloo, Rosalind A. Eeles, Louise Izatt, Rosemarie Davidson, Carol Chu, Diana Eccles, Trevor Cole, Shirley Hodgson, Andrew K. Godwin, Dominique Stoppa‐Lyonnet, Bruno Buecher, Mélanie Léoné, Brigitte Bressac–de Paillerets, Audrey Remenieras, Olivier Caron, Gilbert Lenoir, Nicolas Sévenet, Michel Longy, Sandra Fert Ferrer, Fabienne Prieur, David E. Goldgar, Alexander Miron, Esther M. John, Saundra S. Buys, Mary B. Daly, John L. Hopper, Mary Beth Terry, Yosuf Yassin, Daphne Gschwantler‐Kaulich
出版 2009Artigo -
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Mutational spectrum in a worldwide study of 29,700 families with<i>BRCA1</i>or<i>BRCA2</i>mutations 由 Timothy R. Rebbeck, Tara M. Friebel, Eitan Friedman, Ute Hamann, Dezheng Huo, Ava Kwong, Edith Oláh, Olufunmilayo I. Olopade, Ángela R. Solano, Soo‐Hwang Teo, Mads Thomassen, Jeffrey N. Weitzel, TL Chan, Fergus J. Couch, David E. Goldgar, Torben A. Kruse, Edenir Inêz Palmero, Sue K. Park, Diana Torres, Elizabeth J. van Rensburg, Lesley McGuffog, Michael T. Parsons, Goska Leslie, Cora M. Aalfs, Julio E. Abugattas, Julian Adlard, Simona Agata, Kristiina Aittomäki, Lesley Andrews, Irene L. Andrulis, Aðalgeir Arason, Norbert Arnold, Banu Arun, Ella Asseryanis, Leo Auerbach, Jacopo Azzollini, Judith Balmañà, Monica Barile, Rósa B. Barkardóttir, Daniel Barrowdale, Javier Benı́tez, Andreas Berger, Raanan Berger, Amie Blanco, Kathleen R. Blazer, Marinus J. Blok, Valérie Bonadona, Bernardo Bonanni, Angela R. Bradbury, Carole Brewer, Bruno Buecher, Saundra S. Buys, Trinidad Caldés, Almuth Caliebe, Maria A. Caligo, Ian Campbell, Sandrine M. Caputo, Jocelyne Chiquette, Wendy K. Chung, Kathleen Claes, J. Margriet Collée, Jackie Cook, Rosemarie Davidson, Miguel de la Hoya, Kim De Leeneer, Antoine De Pauw, Capucine Delnatte, Orland Dı́ez, Yuan Chun Ding, Nina Ditsch, Susan M. Domchek, Cecilia M. Dorfling, Carolina Velázquez, Bernd Dworniczak, Jacqueline Eason, Douglas F. Easton, Rosalind A. Eeles, Hans Ehrencrona, Bent Ejlertsen, Christoph Engel, Stefanie Engert, D. Gareth Evans, Laurence Faivre, Lídia Feliubadaló, Sandra Fert Ferrer, Lenka Foretová, Jeffrey M. Fowler, Debra Frost, Henrique C.R. Galvão, Patricia A. Ganz, Judy E. Garber, Marion Gauthier‐Villars, Andrea Gehrig, Anne‐Marie Gerdes, Paul Gesta, Giuseppe Giannini, Sophie Giraud, Gord Glendon, Andrew K. Godwin, Mark H. Greene
出版 2018Artigo -
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Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk 由 Mia M. Gaudet, Karoline Kuchenbaecker, Joseph Vijai, Robert J. Klein, Tomas Kirchhoff, Lesley McGuffog, Daniel Barrowdale, Alison M. Dunning, Andrew Lee, Joe Dennis, Sue Healey, Ed Dicks, Penny Soucy, Olga M. Sinilnikova, V. Shane Pankratz, Xianshu Wang, Ronald C. Eldridge, Daniel C. Tessier, Daniel Vincent, François Bacot, Frans B.L. Hogervorst, Susan Peock, Dominique Stoppa‐Lyonnet, Paolo Peterlongo, Rita K. Schmutzler, Katherine L. Nathanson, Marion Piedmonte, Christian F. Singer, Mads Thomassen, Thomas van Overeem Hansen, Susan L. Neuhausen, Ignacio Blanco, Mark H. Greene, Judith Garber, Jeffrey N. Weitzel, Irene L. Andrulis, David E. Goldgar, Emma D’Andrea, Trinidad Caldés, Heli Nevanlinna, Ana Osório, Elizabeth J. van Rensburg, Aðalgeir Arason, Gad Rennert, Ans M.W. van den Ouweland, Annemarie H. van der Hout, Carolien M. Kets, Cora M. Aalfs, Juul Wijnen, Margreet G.E.M. Ausems, Debra Frost, Ian O. Ellis, Elena Fineberg, Radka Platte, D. Gareth Evans, Chris Jacobs, Julian Adlard, Marc Tischkowitz, Mary Porteous, Francesca Damiola, Lisa Golmard, Laure Barjhoux, Michel Longy, Muriel Belotti, Sandra Fert Ferrer, Sylvie Mazoyer, Amanda B. Spurdle, Siranoush Manoukian, Monica Barile, Maurizio Genuardi, Norbert Arnold, Thomas Ind, Christian Sutter, Barbara Wappenschmidt, Susan M. Domchek, Georg Pfeiler, Eitan Friedman, Uffe Birk Jensen, Mark E. Robson, Sohela Shah, Conxi Lázaro, L. Phuong, Javier Benı́tez, Melissa C. Southey, Marjanka K. Schmidt, Peter A. Fasching, Julian Peto, Manjeet K. Humphreys, Qin Wang, Kyriaki Michailidou, Elinor J. Sawyer, Barbara Burwinkel, Pascal Guénel, Stig E. Bojesen, Roger L. Milne, Hermann Brenner, Magdalena Lochmann, Kristiina Aittomäki, Thilo Dörk, Sara Margolin
出版 2013Artigo
相關主題
Biology
Genetics
Gene
Breast cancer
Cancer
Medicine
Germline mutation
Mutation
Oncology
Allele
Internal medicine
Population
BRCA2 Protein
Cancer research
DNA repair
Environmental health
Genotype
Leukemia
Locus (genetics)
Allele frequency
Antibody
BRCA mutation
Bioinformatics
Botany
CEBPA
CHEK2
Case-control study
Chromosomal translocation
Chronic lymphocytic leukemia
Computational biology