Publications by authors named "Audrey Remenieras"

14Publications

MUTYH-associated polyposis: Review and update of the French recommendations established in 2012 under the auspices of the National Cancer institute (INCa).

Authors:
Chrystelle Colas Valérie Bonadona Stéphanie Baert-Desurmont Delphine Bonnet Florence Coulet Marion Dhooge Jean-Christophe Saurin Audrey Remenieras Yves-Jean Bignon Olivier Caron Antoine De Pauw Marie-Pierre Buisine Bruno Buecher

Eur J Med Genet 2020 Dec 12;63(12):104078. Epub 2020 Oct 12.

Department of Genetics. Institut Curie. PSL Research University, Paris, France. Electronic address:

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December 2020

[MUTYH-associated polyposis: Review and update of the French recommendations established in 2012 under the auspices of the National Cancer Institute (INCa)].

Authors:
Marie-Pierre Buisine Valérie Bonadona Stéphanie Baert-Desurmont Delphine Bonnet Florence Coulet Marion Dhooge Jean-Christophe Saurin Audrey Remenieras Yves-Jean Bignon Olivier Caron Antoine De Pauw Chrystelle Colas Bruno Buecher

Bull Cancer 2020 May 1;107(5):586-600. Epub 2020 May 1.

PSL Research University, Institut Curie, département de génétique, 26, rue d'Ulm, 75248 Paris cedex 05, France. Electronic address:

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May 2020

Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.

Authors:
Corine Bertolotto Fabienne Lesueur Sandy Giuliano Thomas Strub Mahaut de Lichy Karine Bille Philippe Dessen Benoit d'Hayer Hamida Mohamdi Audrey Remenieras Eve Maubec Arnaud de la Fouchardière Vincent Molinié Pierre Vabres Stéphane Dalle Nicolas Poulalhon Tanguy Martin-Denavit Luc Thomas Pascale Andry-Benzaquen Nicolas Dupin Françoise Boitier Annick Rossi Jean-Luc Perrot Bruno Labeille Caroline Robert Bernard Escudier Olivier Caron Laurence Brugières Simon Saule Betty Gardie Sophie Gad Stéphane Richard Jérôme Couturier Bin Tean Teh Paola Ghiorzo Lorenza Pastorino Susana Puig Celia Badenas Hakan Olsson Christian Ingvar Etienne Rouleau Rosette Lidereau Philippe Bahadoran Philippe Vielh Eve Corda Hélène Blanché Diana Zelenika Pilar Galan Valérie Chaudru Gilbert M Lenoir Mark Lathrop Irwin Davidson Marie-Françoise Avril Florence Demenais Robert Ballotti Brigitte Bressac-de Paillerets

Nature 2016 Mar 2;531(7592):126. Epub 2015 Dec 2.

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March 2016

Hereditary diffuse gastric cancer syndrome: improved performances of the 2015 testing criteria for the identification of probands with a CDH1 germline mutation.

Authors:
Patrick R Benusiglio Chystelle Colas Etienne Rouleau Nancy Uhrhammer Pierre Romero Audrey Remenieras Jessica Moretta Qing Wang Antoine De Pauw Bruno Buecher Dominique Stoppa-Lyonnet Emmanuelle Mouret-Fourme Catherine Noguès Marina Di Maria Camille Tlemsani Mathilde Warcoin Sophie Grandjouan David Malka Olivier Caron Martine Blayau

J Med Genet 2015 Aug 29;52(8):563-5. Epub 2015 May 29.

Service de Génétique Moléculaire et Génomique, Centre Hospitalier Universitaire de Rennes, Rennes, France.

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August 2015

Genomic variations integrated database for MUTYH-associated adenomatous polyposis.

Authors:
Philippe Grandval Aurélie J Fabre Pascaline Gaildrat Stéphanie Baert-Desurmont Martine Blayau Marie-Pierre Buisine Florence Coulet Christine Maugard Stéphane Pinson Audrey Remenieras Etienne Rouleau Nancy Uhrhammer Christophe Beroud Sylviane Olschwang

J Med Genet 2015 Jan 3;52(1):25-7. Epub 2014 Nov 3.

INSERM UMR_S910, Marseille, France Departments of medical Genetics and Gastroenterology, AP-HM La Timone, Marseille, France Gastroenterology Department, European Hospital, Marseille, France Oncology Department, Clairval Hospital, Marseille, France The first two authors contributed equally to this work.

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January 2015

The UMD-APC database, a model of nation-wide knowledge base: update with data from 3,581 variations.

Authors:
Philippe Grandval Martine Blayau Marie-Pierre Buisine Florence Coulet Christine Maugard Stéphane Pinson Audrey Remenieras Julie Tinat Nancy Uhrhammer Christophe Béroud Sylviane Olschwang

Hum Mutat 2014 May 7;35(5):532-6. Epub 2014 Apr 7.

UMR_S910, INSERM, Marseille, France; AP-HM La Timone, Gastroenterology Department, Marseille, France.

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May 2014

High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age.

Authors:
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

J Clin Oncol 2012 Jun 16;30(17):2087-93. Epub 2012 Apr 16.

Institut Gustave Roussy, Villejuif, France.

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June 2012

Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants.

Authors:
Claude Houdayer Virginie Caux-Moncoutier Sophie Krieger Michel Barrois Françoise Bonnet Violaine Bourdon Myriam Bronner Monique Buisson Florence Coulet Pascaline Gaildrat Cédrick Lefol Mélanie Léone Sylvie Mazoyer Danielle Muller Audrey Remenieras Françoise Révillion Etienne Rouleau Joanna Sokolowska Jean-Philippe Vert Rosette Lidereau Florent Soubrier Hagay Sobol Nicolas Sevenet Brigitte Bressac-de Paillerets Agnès Hardouin Mario Tosi Olga M Sinilnikova Dominique Stoppa-Lyonnet

Hum Mutat 2012 Aug 11;33(8):1228-38. Epub 2012 May 11.

Service de Génétique, Institut Curie et Université Paris Descartes, Sorbonne Paris Cité, Paris, France.

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August 2012

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma.

Authors:
Corine Bertolotto Fabienne Lesueur Sandy Giuliano Thomas Strub Mahaut de Lichy Karine Bille Philippe Dessen Benoit d'Hayer Hamida Mohamdi Audrey Remenieras Eve Maubec Arnaud de la Fouchardière Vincent Molinié Pierre Vabres Stéphane Dalle Nicolas Poulalhon Tanguy Martin-Denavit Luc Thomas Pascale Andry-Benzaquen Nicolas Dupin Françoise Boitier Annick Rossi Jean-Luc Perrot Bruno Labeille Caroline Robert Bernard Escudier Olivier Caron Laurence Brugières Simon Saule Betty Gardie Sophie Gad Stéphane Richard Jérôme Couturier Bin Tean Teh Paola Ghiorzo Lorenza Pastorino Susana Puig Celia Badenas Hakan Olsson Christian Ingvar Etienne Rouleau Rosette Lidereau Philippe Bahadoran Philippe Vielh Eve Corda Hélène Blanché Diana Zelenika Pilar Galan François Aubin Bertrand Bachollet Céline Becuwe Pascaline Berthet Yves Jean Bignon Valérie Bonadona Jean-Louis Bonafe Marie-Noëlle Bonnet-Dupeyron Fréderic Cambazard Jacqueline Chevrant-Breton Isabelle Coupier Sophie Dalac Liliane Demange Michel d'Incan Catherine Dugast Laurence Faivre Lynda Vincent-Fétita Marion Gauthier-Villars Brigitte Gilbert Florent Grange Jean-Jacques Grob Philippe Humbert Nicolas Janin Pascal Joly Delphine Kerob Christine Lasset Dominique Leroux Julien Levang Jean-Marc Limacher Cristina Livideanu Michel Longy Alain Lortholary Dominique Stoppa-Lyonnet Sandrine Mansard Ludovic Mansuy Karine Marrou Christine Matéus Christine Maugard Nicolas Meyer Catherine Nogues Pierre Souteyrand Laurence Venat-Bouvet Hélène Zattara Valérie Chaudru Gilbert M Lenoir Mark Lathrop Irwin Davidson Marie-Françoise Avril Florence Demenais Robert Ballotti Brigitte Bressac-de Paillerets

Nature 2011 Oct 19;480(7375):94-8. Epub 2011 Oct 19.

1] INSERM, U895 (équipe 1), Equipe labélisée Ligue Contre le Cancer, C3M, 06204 Nice, France [2] Université of Nice Sophia-Antipolis, UFR Médecine, 06204 Nice, France [3] Centre Hospitalier Universitaire de Nice, Service de Dermatologie, 06204 Nice, France [4].

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October 2011

Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.

Authors:
Betty Gardie Audrey Remenieras Darouna Kattygnarath Johny Bombled Sandrine Lefèvre Victoria Perrier-Trudova Pierre Rustin Michel Barrois Abdelhamid Slama Marie-Françoise Avril Didier Bessis Olivier Caron Frédéric Caux Patrick Collignon Isabelle Coupier Carol Cremin Hélène Dollfus Catherine Dugast Bernard Escudier Laurence Faivre Michel Field Brigitte Gilbert-Dussardier Nicolas Janin Yves Leport Dominique Leroux Dan Lipsker Félicia Malthieu Barbara McGilliwray Christine Maugard Arnaud Méjean Isabelle Mortemousque Ghislaine Plessis Bruce Poppe Christelle Pruvost-Balland Serena Rooker Joelle Roume Nadem Soufir Michelle Steinraths Min-Han Tan Christine Théodore Luc Thomas Pierre Vabres Emmanuel Van Glabeke Jean-Baptiste Meric Virginie Verkarre Gilbert Lenoir Virginie Joulin Sophie Deveaux Veronica Cusin Jean Feunteun Bin Tean Teh Brigitte Bressac-de Paillerets Stéphane Richard

J Med Genet 2011 Apr 12;48(4):226-34. Epub 2011 Mar 12.

Génétique Oncologique EPHE, INSERM U753, Institut de cancérologie Gustave Roussy Villejuif, Faculté de Médecine Paris-Sud, 63 avenue du Général Leclerc, 94276 Le Kremlin-Bicêtre, France.

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April 2011

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.

Authors:
Antonis C Antoniou Xianshu Wang Zachary S Fredericksen Lesley McGuffog Robert Tarrell Olga M Sinilnikova Sue Healey Jonathan Morrison Christiana Kartsonaki Timothy Lesnick Maya Ghoussaini Daniel Barrowdale Susan Peock Margaret Cook Clare Oliver Debra Frost Diana Eccles D Gareth Evans Ros Eeles Louise Izatt Carol Chu Fiona Douglas Joan 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 Encarna B Gómez García Peter Devilee Maaike P G Vreeswijk Jan Lubinski 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 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 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 Ozcelik 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 Trinidad Caldes Miguel de la Hoya Christian F Singer Anneliese Fink-Retter Mark H Greene Phuong L Mai Jennifer T Loud Lucia Guidugli Noralane M Lindor Thomas V O Hansen Finn C Nielsen Ignacio Blanco Conxi Lazaro Judy Garber Susan J Ramus Simon A Gayther Catherine Phelan Stephen Narod Csilla I Szabo Javier Benitez Ana Osorio Heli Nevanlinna Tuomas Heikkinen Maria A Caligo Mary S Beattie Ute Hamann Andrew K Godwin Marco Montagna Cinzia Casella Susan L Neuhausen Beth Y Karlan Nadine Tung Amanda E Toland Jeffrey Weitzel Olofunmilayo Olopade Jacques Simard Penny Soucy Wendy S Rubinstein Adalgeir Arason Gad Rennert Nicholas G Martin Grant W Montgomery Jenny Chang-Claude Dieter Flesch-Janys Hiltrud Brauch Gianluca Severi Laura Baglietto Angela Cox Simon S Cross Penelope Miron Sue M Gerty William Tapper Drakoulis Yannoukakos George Fountzilas Peter A Fasching Matthias W Beckmann Isabel Dos Santos Silva Julian Peto Diether Lambrechts Robert Paridaens Thomas Rüdiger Asta Försti Robert Winqvist Katri Pylkäs Robert B Diasio Adam M Lee Jeanette Eckel-Passow Celine Vachon Fiona Blows Kristy Driver Alison Dunning Paul P D Pharoah Kenneth Offit V Shane Pankratz Hakon Hakonarson Georgia Chenevix-Trench Douglas F Easton Fergus J Couch

Nat Genet 2010 Oct 19;42(10):885-92. Epub 2010 Sep 19.

Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.

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October 2010

International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation.

Authors:
Ana Peixoto Catarina Santos Manuela Pinheiro Pedro Pinto Maria José Soares Patrícia Rocha Leonor Gusmão António Amorim Annemarie van der Hout Anne-Marie Gerdes Mads Thomassen Torben A Kruse Dorthe Cruger Lone Sunde Yves-Jean Bignon Nancy Uhrhammer Lucie Cornil Etienne Rouleau Rosette Lidereau Drakoulis Yannoukakos Maroulio Pertesi Steven Narod Robert Royer Maurício M Costa Conxi Lazaro Lidia Feliubadaló Begoña Graña Ignacio Blanco Miguel de la Hoya Trinidad Caldés Philippe Maillet Gaelle Benais-Pont Bruno Pardo Yael Laitman Eitan Friedman Eladio A Velasco Mercedes Durán Maria-Dolores Miramar Ana Rodriguez Valle María-Teresa Calvo Ana Vega Ana Blanco Orland Diez Sara Gutiérrez-Enríquez Judith Balmaña Teresa Ramon y Cajal Carmen Alonso Montserrat Baiget William Foulkes Marc Tischkowitz Rachel Kyle Nelly Sabbaghian Patricia Ashton-Prolla Ingrid P Ewald Thangarajan Rajkumar Luisa Mota-Vieira Giuseppe Giannini Alberto Gulino Maria I Achatz Dirce M Carraro Brigitte Bressac de Paillerets Audrey Remenieras Cindy Benson Silvia Casadei Mary-Claire King Erik Teugels Manuel R Teixeira

Breast Cancer Res Treat 2011 Jun 22;127(3):671-9. Epub 2010 Jul 22.

Department of Genetics, Portuguese Oncology Institute, Rua Dr. António Bernardino de Almeida, Porto 4200-072, Portugal.

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June 2011

Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.

Authors:
Antonis C Antoniou Olga M Sinilnikova Lesley McGuffog Sue Healey Heli Nevanlinna Tuomas Heikkinen Jacques Simard Amanda B Spurdle Jonathan Beesley Xiaoqing Chen Susan L Neuhausen Yuan C Ding Fergus J Couch Xianshu Wang Zachary Fredericksen Paolo Peterlongo Bernard Peissel Bernardo Bonanni Alessandra Viel Loris Bernard Paolo Radice Csilla I Szabo Lenka Foretova Michal Zikan Kathleen Claes Mark H Greene Phuong L Mai Gad Rennert Flavio Lejbkowicz Irene L Andrulis Hilmi Ozcelik 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-Bustinza Johanna Rantala Hans Ehrencrona Per Karlsson Susan M Domchek Katherine L Nathanson Ana Osorio Ignacio Blanco Adriana Lasa Javier Benítez Ute Hamann Frans B L Hogervorst Matti A Rookus J Margriet Collee Peter Devilee Marjolijn J Ligtenberg Rob B van der Luijt Cora M Aalfs Quinten Waisfisz Juul Wijnen Cornelis E P van Roozendaal Susan Peock Margaret Cook Debra Frost Clare Oliver Radka Platte D Gareth Evans Fiona Lalloo Rosalind 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 M Lenoir Nicolas Sevenet Michel Longy Sandra Fert Ferrer Fabienne Prieur David Goldgar Alexander Miron Esther M John Saundra S Buys Mary B Daly John L Hopper Mary Beth Terry Yosuf Yassin Christian Singer Daphne Gschwantler-Kaulich Christine Staudigl Thomas v O Hansen Rosa Bjork Barkardottir Tomas Kirchhoff Prodipto Pal Kristi Kosarin Kenneth Offit Marion Piedmonte Gustavo C Rodriguez Katie Wakeley John F Boggess Jack Basil Peter E Schwartz Stephanie V Blank Amanda E Toland Marco Montagna Cinzia Casella Evgeny N Imyanitov Anna Allavena Rita K Schmutzler Beatrix Versmold Christoph Engel Alfons Meindl Nina Ditsch Norbert Arnold Dieter Niederacher Helmut Deissler Britta Fiebig Christian Suttner Ines Schönbuchner Dorothea Gadzicki Trinidad Caldes Miguel de la Hoya Karen A Pooley Douglas F Easton Georgia Chenevix-Trench

Hum Mol Genet 2009 Nov 5;18(22):4442-56. Epub 2009 Aug 5.

Department of Public Health and Primary Care, Cancer Research UK Genetic Epidemiology Unit, University of Cambridge, Cambridge, UK.

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November 2009

High frequency of TP53 mutation in BRCA1 and sporadic basal-like carcinomas but not in BRCA1 luminal breast tumors.

Authors:
Elodie Manié Anne Vincent-Salomon Jacqueline Lehmann-Che Gaelle 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

Cancer Res 2009 Jan;69(2):663-71

Institut Curie, Centre de Recherche, Paris, France.

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January 2009