Resultats de la cerca - Audrey Remenieras
- Mostrar 1 - 6 resultats de 6
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1
High Frequency of Germline <i>SUFU</i> Mutations in Children With Desmoplastic/Nodular Medulloblastoma Younger Than 3 Years of Age per Laurence Brugières, Audrey Remenieras, Gaëlle Pierron, Pascale Varlet, Sébastien Forget, Véronique Byrde, Johny Bombled, Stéphanie Puget, Olivier Caron, Christelle Dufour, Olivier Delattre, Brigitte Bressac–de Paillerets, Jacques Grill
Publicat 2012Artigo -
2
High Frequency of <i>TP53</i> Mutation in <i>BRCA1</i> and Sporadic Basal-like Carcinomas but not in <i>BRCA1</i> Luminal Breast Tumors per Élodie Manié, Anne Vincent‐Salomon, Jacqueline Lehmann‐Che, Gaëlle Pierron, Elisabeth Turpin, Mathilde Warcoin, Nadège Gruel, Ingrid Lebigot, Xavier Sastre‐Garau, Rosette Lidereau, Audrey Remenieras, Jean Feunteun, Olivier Delattre, Hugues de Thé, Dominique Stoppa‐Lyonnet, Marc‐Henri Stern
Publicat 2009Artigo -
3
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma per 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
Publicat 2011Artigo -
4
Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast–ovarian cancer susceptibility locus per 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
Publicat 2016Artigo -
5
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor–negative breast cancer in the general population per Antonis C. Antoniou, Xianshu Wang, Zachary S Fredericksen, Lesley McGuffog, Robert F. Tarrell, Olga M. Sinilnikova, Sue Healey, Jonathan J. Morrison, Christiana Kartsonaki, Timothy G. Lesnick, Maya Ghoussaini, Daniel Barrowdale, Susan Peock, Margaret Cook, Clare Oliver, Debra Frost, Diana Eccles, D. Gareth Evans, Rosalind A. Eeles, Louise Izatt, Carol Chu, Fiona Douglas, J. Paterson, Dominique Stoppa-Lyonnet, Claude Houdayer, Sylvie Mazoyer, Sophie Giraud, Christine Lasset, Audrey Remenieras, Olivier Caron, Agnès Hardouin, Pascaline Berthet, Frans B.L. Hogervorst, Matti A. Rookus, Agnes Jager, Ans van den Ouweland, Nicoline Hoogerbrugge, Rob B. van der Luijt, Hanne Meijers‐Heijboer, E. Gómez, Peter Devilee, Maaike P.G. Vreeswijk, Jan Lubiński, Anna Jakubowska, Jacek Gronwald, Tomasz Huzarski, Tomasz Byrski, Bohdan Górski, Cezary Cybulski, Amanda B. Spurdle, Helene Holland, David E. Goldgar, Esther M. John, John L. Hopper, Melissa C. Southey, Saundra S. Buys, Mary B. Daly, Mary Beth Terry, Rita K. Schmutzler, Barbara Wappenschmidt, Christoph Engel, Alfons Meindl, Sabine Preisler‐Adams, Norbert Arnold, Dieter Niederacher, Christian Sutter, Susan M. Domchek, Katherine L. Nathanson, Timothy R. Rebbeck, Joanne L. Blum, Marion Piedmonte, Gustavo C. Rodriguez, Katie Wakeley, John F. Boggess, Jack Basil, Stephanie V. Blank, Eitan Friedman, Bella Kaufman, Yael Laitman, Roni Milgrom, Irene L. Andrulis, Gord Glendon, Hilmi Özçelik, Tomas Kirchhoff, Joseph Vijai, Mia M. Gaudet, David Altshuler, Candace Guiducci, Niklas Loman, Katja Harbst, Johanna Rantala, Hans Ehrencrona, Anne‐Marie Gerdes, Mads Thomassen, Lone Sunde, Paolo Peterlongo, Siranoush Manoukian, Bernardo Bonanni, Alessandra Viel, Paolo Radice
Publicat 2010Artigo -
6
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers per 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
Publicat 2009Artigo
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Matèries relacionades
Biology
Gene
Genetics
Medicine
Breast cancer
Cancer
Internal medicine
Cancer research
Mutation
Oncology
Allele
Case-control study
Environmental health
Genome-wide association study
Genotype
Germline
Germline mutation
Odds ratio
Pathology
Phenotype
Population
Single-nucleotide polymorphism
Bioinformatics
Cancer syndrome
Estrogen receptor
Genetic testing
Immunohistochemistry
Immunology
Leiomyoma
Leiomyomatosis