Arama Sonuçları - Isabelle Mortemousque
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1
Screening Mammography and Breast Cancer: Variation in Risk with Rare Deleterious or Predicted Deleterious Variants in DNA Repair Genes Yazar: 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
Baskı/Yayın Bilgisi 2025Artigo -
2
Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents Yazar: Sahra Bodo, Chrystelle Colas, Olivier Buhard, Ada Collura, Julie Tinat, Noémie Lavoine, Agathe Guilloux, Alexandra Chalastanis, Philippe Lafitte, Florence Coulet, Marie‐Pierre Buisine, Denisa Ilenčíková, Clara Ruíz-Ponte, Miriam Kinzel, S Grandjouan, Hilde Brems, Sophie Lejeune, Hélène Blanché, Qing Wang, Olivier Caron, Odile Cabaret, Magali Svrcek, Dominique Vidaud, Béatrice Parfait, Alain Verloès, Ulrich J. Knappe, Florent Soubrier, Isabelle Mortemousque, Alexander Leis, Jessie Auclair‐Perrossier, Thierry Frébourg, Jean–François Fléjou, Natacha Entz‐Werlé, Julie Leclerc, David Malka, Odile Cohen‐Haguenauer, Yael Goldberg, Anne‐Marie Gerdes, Faten Fedhila, Michèle Mathieu‐Dramard, Richard Hamelin, Wafaa Badre, Marion Gauthier‐Villars, Franck Bourdeaut, Eamonn Sheridan, Hans F. A. Vasen, Laurence Brugières, Katharina Wimmer, Martine Muleris, Alex Duval
Baskı/Yayın Bilgisi 2015Artigo -
3
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma Yazar: Betty Gardie, Audrey Remenieras, Darouna Kattygnarath, Johny Bombled, Sandrine-Hélène Lefèvre, Victoria Perrier-Trudova, Pierre Rustin, M. Barrois, Abdelhamid Slama, M.-F. Avril, D. Bessis, Olivier Caron, F. Caux, Patrick Collignon, I. Coupier, Catherine Cremin, Hélène Dollfus, Catherine Dugast, B. Escudier, Laurence Faivre, Michael Field, Brigitte Gilbert‐Dussardier, Nicolas Janin, Y. Leport, Dominique Leroux, Dan Lipsker, F. Malthieu, B. McGilliwray, Christine Maugard, A. Méjean, Isabelle Mortemousque, Ghislaine Plessis, Bruce Poppe, C. Pruvost‐Balland, S. Rooker, J. Roume, Nadem Soufir, M. Steinraths, Min Tan, Christine Théodore, L. Thomas, P. Vabres, E. Van Glabeke, Jean‐Baptiste Méric, Virginie Verkarre, Gilbert Lenoir, V. Joulin, Scott DeVeaux, Véronica Cusin, Jean Feunteun, Bin Tean Teh, Brigitte Bressac–de Paillerets, Richard J. Kahnoski
Baskı/Yayın Bilgisi 2011Artigo -
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 Yazar: 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
Baskı/Yayın Bilgisi 2021Artigo -
5
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing Yazar: 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
Baskı/Yayın Bilgisi 2018Artigo -
6
Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2mutation carriers Yazar: 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
Baskı/Yayın Bilgisi 2012Artigo -
7
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... Yazar: 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
Baskı/Yayın Bilgisi 2011Artigo
Arama Araçları:
İlgili Konular
Medicine
Biology
Gene
Genetics
Breast cancer
Cancer
Germline mutation
Internal medicine
Mutation
Oncology
DNA repair
Allele
BRCA2 Protein
Cancer research
DNA
DNA mismatch repair
Missense mutation
Surgical oncology
BRCA mutation
CHEK2
Cancer syndrome
Disease
Environmental health
Exome
Exome sequencing
Family history
Genetic counseling
Genetic predisposition
Germline
Gynecology