H
Henrique Tenreiro
Researcher at Curie Institute
Publications - 6
Citations - 157
Henrique Tenreiro is an academic researcher from Curie Institute. The author has contributed to research in topics: Ovarian cancer & Mutation (genetic algorithm). The author has an hindex of 5, co-authored 6 publications receiving 123 citations.
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Journal ArticleDOI
Streamlined ion torrent PGM-based diagnostics: BRCA1 and BRCA2 genes as a model
Julien Tarabeux,Bruno Zeitouni,Virginie Moncoutier,Henrique Tenreiro,Khadija Abidallah,Séverine Lair,Patricia Legoix-Né,Quentin Leroy,Etienne Rouleau,Lisa Golmard,Emmanuel Barillot,Marc-Henri Stern,Thomas Rio-Frio,Dominique Stoppa-Lyonnet,Claude Houdayer +14 more
TL;DR: An Ion Torrent’s PGM-based routine diagnostic procedure for BRCA1/2 sequencing is developed, and the pipeline described can be adapted by any user of PGM for diagnostic purposes.
Journal ArticleDOI
Contribution of germline deleterious variants in the RAD51 paralogs to breast and ovarian cancers.
Lisa Golmard,Laurent Castera,Sophie Krieger,Sophie Krieger,Virginie Moncoutier,Khadija Abidallah,Henrique Tenreiro,Anthony Laugé,Julien Tarabeux,Gaël A. Millot,Gaël A. Millot,André Nicolas,Marick Laé,Caroline Abadie,Pascaline Berthet,Florence Polycarpe,Thierry Frebourg,Thierry Frebourg,Camille Elan,Antoine De Pauw,Marion Gauthier-Villars,Bruno Buecher,Marc-Henri Stern,Marc-Henri Stern,Dominique Stoppa-Lyonnet,Dominique Stoppa-Lyonnet,Dominique Vaur,Claude Houdayer,Claude Houdayer +28 more
TL;DR: This study is the first evaluation of the five RAD51 paralogs in breast and ovarian cancer predisposition and it demonstrates that deleterious variants can be present in breast cancer only cases.
Journal ArticleDOI
Breast and ovarian cancer predisposition due to de novo BRCA1 and BRCA2 mutations
Lisa Golmard,Capucine Delnatte,Anthony Laugé,Virginie Moncoutier,Cédrick Lefol,Khadija Abidallah,Henrique Tenreiro,F Copigny,M Giraudeau,Christophe Guy,Catherine Barbaroux,G Amorim,Adrien Briaux,V Guibert,Julien Tarabeux,Sandrine M. Caputo,Agnès Collet,Paul Gesta,O Ingster,M-H Stern,Etienne Rouleau,A. De Pauw,Marion Gauthier-Villars,Bruno Buecher,Stéphane Bézieau,Dominique Stoppa-Lyonnet,Dominique Stoppa-Lyonnet,Claude Houdayer,Claude Houdayer +28 more
TL;DR: Although rare, it may be useful to take the possibility of de novo BRCA1/2 mutation into account in genetic counseling of relatives and to improve the understanding of complex family histories of breast and ovarian cancers.
Journal ArticleDOI
ART-DeCo: easy tool for detection and characterization of cross-contamination of DNA samples in diagnostic next-generation sequencing analysis
Alice Fiévet,Alice Fiévet,Virginie Bernard,Henrique Tenreiro,Catherine Dehainault,Elodie Girard,Vivien Deshaies,Philippe Hupé,Olivier Delattre,Olivier Delattre,Marc-Henri Stern,Marc-Henri Stern,Dominique Stoppa-Lyonnet,Dominique Stoppa-Lyonnet,Dominique Stoppa-Lyonnet,Lisa Golmard,Claude Houdayer +16 more
TL;DR: ART-DeCo, a tool using the allelic ratio (AR) of the Single Nucleotide Polymorphisms sequenced with regions of interest, which can be implemented in any NGS workflow, from gene panel to genome-wide analyses, is developed.
Journal ArticleDOI
Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach
Sandrine M. Caputo,Lisa Golmard,Mélanie Léoné,Francesca Damiola,Marine Guillaud-Bataille,Françoise Revillion,Etienne Rouleau,Nicolas Derive,Adrien Buisson,Noémie Basset,Mathias Schwartz,Paul Vilquin,Celine Garrec,Maud Privat,Mathilde Gay-Bellile,Mathilde Gay-Bellile,Caroline Abadie,Khadija Abidallah,Fabrice Airaud,Anne-Sophie Allary,Emmanuelle Barouk-Simonet,Muriel Belotti,Charlotte Benigni,Patrick R. Benusiglio,Christelle Berthemin,Pascaline Berthet,Ophelie Bertrand,Stéphane Bézieau,Marie Bidart,Yves-Jean Bignon,Anne-Marie Birot,Maud Blanluet,Amelie Bloucard,J Bombled,Valérie Bonadona,Françoise Bonnet,Marie-Noëlle Bonnet-Dupeyron,Manon Boulaire,Flavie Boulouard,Ahmed Bouras,Violaine Bourdon,Afane Brahimi,Fanny Brayotel,Brigitte Bressac-de Paillerets,Noémie Bronnec,Virginie Bubien,Bruno Buecher,Odile Cabaret,Jennifer Carriere,Jean Chiesa,Stephanie Chieze-Valéro,Camille Cohen,Odile Cohen-Haguenauer,Chrystelle Colas,Marie-Agnès Collonge-Rame,Anne-Laure Conoy,Florence Coulet,Isabelle Coupier,Louise Crivelli,Veronica Cusin,Antoine De Pauw,Catherine Dehainault,Hélène Delhomelle,Capucine Delnatte,Sophie Demontety,Philippe Denizeau,Pierre Devulder,Helene Dreyfus,Catherine Dubois d’Enghein,Anaïs Dupré,Anne Durlach,Sophie Dussart,Anne Fajac,Samira Fekairi,Sandra Fert-Ferrer,Alice Fiévet,Robin Fouillet,Emmanuelle Mouret-Fourme,Marion Gauthier-Villars,Paul Gesta,Sophie Giraud,Laurence Gladieff,Veronica Goldbarg,Vincent Goussot,Virginie Guibert,Erell Guillerm,Christophe Guy,Agnès Hardouin,Céline Heude,Claude Houdayer,Olivier Ingster,Caroline Jacquot-Sawka,Natalie Jones,Sophie Krieger,Sofiane Lacoste,Hakima Lallaoui,Helene Larbre,Anthony Laugé,Gabrielle Le Guyadec,Marine Le Mentec,Caroline Lecerf,Jessica Le Gall,Bérengère Legendre,Clémentine Legrand,Angélina Legros,Sophie Lejeune,Rosette Lidereau,Norbert Lignon,Jean-Marc Limacher,Doriane Livon,Sarab Lizard,Michel Longy,Alain Lortholary,Pierre Macquere,Audrey Mailliez,Sarah Malsa,Henri Margot,Véronique Mari,Christine Maugard,Cindy Meira,Julie Menjard,Diane Molière,Virginie Moncoutier,Jessica Moretta-Serra,Etienne Muller,Zoe Nevière,Thien-vu Nguyen Minh Tuan,Tetsuro Noguchi,Catherine Noguès,Florine Oca,Cornel Popovici,Fabienne Prieur,Sabine Raad,Jean-Marc Rey,Agathe Ricou,Lucie Salle,Claire Saule,Nicolas Sevenet,Fatoumata Simaga,Hagay Sobol,Voreak Suybeng,Isabelle Tennevet,Henrique Tenreiro,Julie Tinat,Christine Toulas,Isabelle Turbiez,Nancy Uhrhammer,Nancy Uhrhammer,Pierre Vande Perre,Dominique Vaur,Laurence Venat,Nicolas Viellard,Marie-Charlotte Villy,Mathilde Warcoin,Alice Yvard,Helene Zattara,Olivier Caron,Christine Lasset,Audrey Remenieras,Nadia Boutry-Kryza,Laurent Castera,Dominique Stoppa-Lyonnet,Dominique Stoppa-Lyonnet +162 more
TL;DR: In this paper, the first results of the ongoing French national COVAR (cosegregation variant) study were reported, the aim of which is to classify BRCA1/2 VUSs.