Search Results - Virginie Caux‐Moncoutier

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  1. 1
    A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation

    A deep intronic mutation in the RB1 gene leads to intronic sequence exonisation by Catherine Dehainault, Dorothée Michaux, Sabine Pagès-Berhouet, Virginie Caux‐Moncoutier, François Doz, Laurence Desjardins, Jérôme Couturier, Philippe Parent, Dominique Stoppa‐Lyonnet, Marion Gauthier‐Villars, Claude Houdayer

    Published 2007
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  2. 2
    Evaluation of in silico splice tools for decision-making in molecular diagnosis

    Evaluation of in silico splice tools for decision-making in molecular diagnosis by Claude Houdayer, Catherine Dehainault, Christophe Mattler, Dorothée Michaux, Virginie Caux‐Moncoutier, Sabine Pagès-Berhouet, Catherine Dubois d’Enghien, Anthony Laugé, Laurent Castéra, Marion Gauthier‐Villars, Dominique Stoppa‐Lyonnet

    Published 2008
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  3. 3
    Comprehensive screening for constitutional <i>RB1</i> mutations by DHPLC and QMPSF

    Comprehensive screening for constitutional <i>RB1</i> mutations by DHPLC and QMPSF by Claude Houdayer, Marion Gauthier‐Villars, Anthony Laugé, Sabine Pagès-Berhouet, Catherine Dehainault, Virginie Caux‐Moncoutier, P. Karczynski, Mario Tosi, François Doz, Laurence Desjardins, J Couturier, Dominique Stoppa‐Lyonnet

    Published 2004
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  4. 4
    Germline mutation in the RAD51B gene confers predisposition to breast cancer

    Germline mutation in the RAD51B gene confers predisposition to breast cancer by Lisa Golmard, Virginie Caux‐Moncoutier, Grégoire Davy, Essam Al Ageeli, Brigitte Poirot, Carole Tirapo, Dorothée Michaux, Catherine Barbaroux, Catherine Dubois d’Enghien, Nicolás André, Laurent Castéra, Xavier Sastre‐Garau, Marc‐Henri Stern, Claude Houdayer, Dominique Stoppa‐Lyonnet

    Published 2013
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  5. 5
    Ploidy and Large-Scale Genomic Instability Consistently Identify Basal-like Breast Carcinomas with <i>BRCA1/2</i> Inactivation

    Ploidy and Large-Scale Genomic Instability Consistently Identify Basal-like Breast Carcinomas with <i>BRCA1/2</i> Inactivation by Tatiana Popova, Élodie Manié, Guillaume Rieunier, Virginie Caux‐Moncoutier, Carole Tirapo, Thierry Dubois, Olivier Delattre, Brigitte Sigal‐Zafrani, Marc A. Bollet, Michel Longy, Claude Houdayer, Xavier Sastre‐Garau, Anne Vincent‐Salomon, Dominique Stoppa‐Lyonnet, Marc‐Henri Stern

    Published 2012
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  6. 6
    Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer

    Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer by Grégoire Davy, Antoine Rousselin, Nicolas Goardon, Laurent Castéra, Valentin Harter, Angélina Legros, Etienne Müller, Robin Fouillet, Baptiste Brault, Anna Smirnova Henriques, Frédéric Lemoine, Pierre de la Grange, Marine Guillaud-Bataille, Virginie Caux‐Moncoutier, Claude Houdayer, Françoise Bonnet, Cécile Blanc‐Fournier, Pascaline Gaildrat, Thierry Frébourg, Alexandra Martins, Dominique Vaur, Sophie Krieger

    Published 2017
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  7. 7
    Assessment of branch point prediction tools to predict physiological branch points and their alteration by variants

    Assessment of branch point prediction tools to predict physiological branch points and their alteration by variants by Raphaël Leman, Hélène Tubeuf, Sabine Raad, Isabelle Tournier, Céline Derambure, Raphaël Lanos, Pascaline Gaildrat, G Castelain, Julie Hauchard, Audrey Killian, Stéphanie Baert‐Desurmont, Angélina Legros, Nicolas Goardon, Céline Quesnelle, Agathe Ricou, Laurent Castéra, Dominique Vaur, Gérald Le Gac, Chandran Ka, Yann Fichou, Françoise Bonnet‐Dorion, Nicolas Sévenet, Marine Guillaud-Bataille, Nadia Boutry‐Kryza, Inès Schultz, Virginie Caux‐Moncoutier, Maria Rossing, Logan C. Walker, Amanda B. Spurdle, Claude Houdayer, Alexandra Martins, Sophie Krieger

    Published 2020
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  8. 8
    Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort

    Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort by Raphaël Leman, Pascaline Gaildrat, Gérald Le Gac, Chandran Ka, Yann Fichou, Marie‐Pierre Audrézet, Virginie Caux‐Moncoutier, Sandrine M. Caputo, Nadia Boutry‐Kryza, Mélanie Léoné, Sylvie Mazoyer, Françoise Bonnet‐Dorion, Nicolas Sévenet, Marine Guillaud-Bataille, Étienne Rouleau, Brigitte Bressac–de Paillerets, Barbara Wappenschmidt, Maria Rossing, Danielle Muller, Violaine Bourdon, Françoise Révillon, Michael T. Parsons, Antoine Rousselin, Grégoire Davy, G Castelain, Laurent Castéra, Joanna Sokołowska, Florence Coulet, Capucine Delnatte, Claude Férec, Amanda B. Spurdle, Alexandra Martins, Sophie Krieger, Claude Houdayer

    Published 2018
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  9. 9
    Germline BAP1 Mutations Predispose to Renal Cell Carcinomas

    Germline BAP1 Mutations Predispose to Renal Cell Carcinomas by Tatiana Popova, Lucie Hebert, Virginie Jacquemin, Sophie Gad, Virginie Caux-Moncoutier, C. Dubois-d’Enghien, Bénédicte Richaudeau, Xavier Renaudin, Jason Sellers, Nicolás André, Xavier Sastre‐Garau, Laurence Desjardins, Gàbor Gyapay, Virginie Raynal, Olga M. Sinilnikova, Nadine Andrieu, Élodie Manié, Antoine De Pauw, Paul Gesta, Valérie Bonadona, Christine M. Maugard, Clotilde Penet, Marie‐Françoise Avril, Emmanuel Barillot, Odile Cabaret, Olivier Delattre, Richard J. Kahnoski, Olivier Caron, M. Benfodda, Hui-Han Hu, Nadem Soufir, Brigitte Bressac–de Paillerets, Dominique Stoppa-Lyonnet, Marc‐Henri Stern

    Published 2013
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  10. 10
    Large scale multifactorial likelihood quantitative analysis of <i>BRCA1</i> and <i>BRCA2</i> variants: An ENIGMA resource to support clinical variant classification

    Large scale multifactorial likelihood quantitative analysis of <i>BRCA1</i> and <i>BRCA2</i> variants: An ENIGMA resource to support clinical variant classification by Michael T. Parsons, Emma Tudini, Hongyan Li, Eric Hahnen, Barbara Wappenschmidt, Lídia Feliubadaló, Cora M. Aalfs, Simona Agata, Kristiina Aittomäki, Elisa Alducci, María Concepción Alonso‐Cerezo, Norbert Arnold, Bernd Auber, Rachel Austin, Jacopo Azzollini, Judith Balmañà, Elena Barbieri, Claus R. Bartram, Ana Blanco, Britta Blümcke, Sandra Bonache, Bernardo Bonanni, Åke Borg, Beatrice Bortesi, Joan Brunet, Carla Bruzzone, Karolin Bucksch, Giulia Cagnoli, Trinidad Caldés, Almuth Caliebe, Maria A. Caligo, Mariarosaria Calvello, Gabriele Lorenzo Capone, Sandrine M. Caputo, Ileana Carnevali, Estela Carrasco, Virginie Caux‐Moncoutier, Pietro Cavalli, Giulia Cini, Edward Clarke, Paola Concolino, Elisa J. Cops, Laura Cortesi, Fergus J. Couch, Esther Darder, Miguel de la Hoya, Michael Dean, Irmgard Debatin, Jesús Del Valle, Capucine Delnatte, Nicolas Derive, Orland Dı́ez, Nina Ditsch, Susan M. Domchek, Véronique Dutrannoy, Diana Eccles, Hans Ehrencrona, Ute Enders, D. Gareth Evans, Chantal Farra, Ulrike Faust, Ute Felbor, Irène Feroce, Miriam Fine, William D. Foulkes, Henrique C.R. Galvão, Gaetana Gambino, Andrea Gehrig, Francesca Gensini, Anne‐Marie Gerdes, Aldo Germani, J Giesecke, Viviana Gismondi, Carolina Gómez, E. Gómez, Sara González, Èlia Grau, Sabine Grill, Eva Groß, Aliana Guerrieri‐Gonzaga, Marine Guillaud‐Bataille, Sara Gutiérrez‐Enríquez, Thomas Haaf, Karl Hackmann, Thomas van Overeem Hansen, Marion Harris, Jan Hauke, T. Heinrich, Heide Hellebrand, Karen Herold, Ellen Honisch, Judit Horváth, Claude Houdayer, Verena Hübbel, Sílvia Iglesias, À. Izquierdo, Paul A. James, Linda A.M. Janssen, Udo Jeschke, Silke Kaulfuß

    Published 2019
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  11. 11
    Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

    Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of B... by Anna Marie Mulligan, Fergus J. Couch, Daniel Barrowdale, Susan M. Domchek, Diana Eccles, Heli Nevanlinna, Susan J. Ramus, Mark E. Robson, Mark E. Sherman, Amanda B. Spurdle, Barbara Wappenschmidt, Andrew Lee, Lesley McGuffog, Sue Healey, Olga M. Sinilnikova, Ramūnas Janavičius, Thomas van Overeem Hansen, Finn C. Nielsen, Bent Ejlertsen, Ana Osório, Iván Muñoz‐Repeto, M. Durán, Javier Godino, Maroulio Pertesi, Javier Benítez, Paolo Peterlongo, Siranoush Manoukian, Bernard Peissel, Daniela Zaffaroni, Elisa Cattaneo, Bernardo Bonanni, Alessandra Viel, Barbara Pasini, Laura Papi, Laura Ottini, Antonella Savarese, Loris Bernard, Paolo Radice, Ute Hamann, Martijn Verheus, Hanne Meijers‐Heijboer, Juul Wijnen, E. Gómez, Marcel Nelen, C. Marleen Kets, Caroline Seynaeve, Madeleine M.A. Tilanus‐Linthorst, Rob B. van der Luijt, Theo van Os, Matti A. Rookus, Debra Frost, J. Louise Jones, D. Gareth Evans, Fiona Lalloo, Rosalind A. Eeles, Louise Izatt, Julian Adlard, Rosemarie Davidson, Jackie Cook, Alan Donaldson, Huw Dorkins, Helen Gregory, Jacqueline Eason, Catherine Houghton, Julian Barwell, Lucy Side, Emma McCann, Alex Murray, Susan Peock, Andrew K. Godwin, Rita K. Schmutzler, Kerstin Rhiem, Christoph Engel, Alfons Meindl, I. Ruehl, Norbert Arnold, Dieter Niederacher, Christian Sutter, Helmut Deißler, Dorothea Gadzicki, Karin Kast, Sabine Preisler-Adams, Raymonda Varon-Mateeva, Ines Schoenbuchner, Britta Fiebig, Wolfram Heinritz, Dieter Schäfer, Heidrun Gevensleben, Virginie Caux‐Moncoutier, Marion Fassy-Colcombet, François Cornélis, Sylvie Mazoyer, Mélanie Léoné, Nadia Boutry‐Kryza, Agnès Hardouin, Pascaline Berthet, Danièle Muller, Jean‐Pierre Fricker, Isabelle Mortemousque, Pascal Pujol

    Published 2011
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  12. 12
    Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

    Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer by Roger L. Milne, Karoline Kuchenbaecker, Kyriaki Michailidou, Jonathan Beesley, Siddhartha Kar, Sara Lindström, Shirley Hui, Audrey Lemaçon, Penny Soucy, Joe Dennis, Xia Jiang, Asha Rostamianfar, Hilary K. Finucane, Manjeet K. Bolla, Lesley McGuffog, Qin Wang, Cora M. Aalfs, Marcia Adams, Julian Adlard, Simona Agata, Shahana Ahmed, Habibul Ahsan, Kristiina Aittomäki, Fares Al‐Ejeh, Jamie Allen, Christine B. Ambrosone, Christopher I. Amos, Irene L. Andrulis, Hoda Anton‐Culver, Natalia Antonenkova, Volker Arndt, Norbert Arnold, Kristan J. Aronson, Bernd Auber, Paul L. Auer, Margreet G.E.M. Ausems, Jacopo Azzollini, François Bacot, Judith Balmañà, Monica Barile, Laure Barjhoux, Rósa B. Barkardóttir, Myrto Barrdahl, Daniel R. Barnes, Daniel Barrowdale, Caroline Baynes, Matthias W. Beckmann, Javier Benı́tez, Marina Bermisheva, Leslie Bernstein, Yves‐Jean Bignon, Kathleen R. Blazer, Marinus J. Blok, Carl Blomqvist, William J. Blot, Kristie Bobolis, Bram Boeckx, Natalia Bogdanova, Anders Bojesen, Stig E. Bojesen, Bernardo Bonanni, Anne‐Lise Børresen‐Dale, Anikó Bozsik, Angela R. Bradbury, Judith S. Brand, Hiltrud Brauch, Hermann Brenner, Brigitte Bressac–de Paillerets, Carole Brewer, Louise A. Brinton, Per Broberg, Angela Brooks‐Wilson, Joan Brunet, Thomas Brüning, Barbara Burwinkel, Saundra S. Buys, Jinyoung Byun, Qiuyin Cai, Trinidad Caldés, Maria A. Caligo, Ian Campbell, Federico Canzian, Olivier Caron, Ángel Carracedo, Brian D. Carter, Jose E. Castelao, Laurent Castéra, Virginie Caux‐Moncoutier, Salina Chan, Jenny Chang‐Claude, Stephen J. Chanock, Xiaohong Chen, Ting‐Yuan David Cheng, Jocelyne Chiquette, Hans Christiansen, Kathleen Claes, Christine L. Clarke, Thomas Conner, Don Conroy, Jackie Cook

    Published 2017
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