Works by Florence, Coulet

Results: 45
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    Consistent Safety and Efficacy of Sotatercept for Pulmonary Arterial Hypertension in BMPR2 Mutation Carriers and Noncarriers: A Planned Analysis of a Phase II, Double-Blind, Placebo-controlled Clinical Trial (PULSAR).

    Published in:
    American Journal of Respiratory & Critical Care Medicine, 2025, v. 211, n. 6, p. 1028, doi. 10.1164/rccm.202409-1698OC
    By:
    • Montani, David;
    • McLaughlin, Vallerie V.;
    • Gibbs, J. Simon R.;
    • Gomberg-Maitland, Mardi;
    • Hoeper, Marius M.;
    • Preston, Ioana R.;
    • Souza, Rogerio;
    • Waxman, Aaron B.;
    • Escribano Subias, Pilar;
    • Feldman, Jeremy;
    • Meyer, Gisela M.;
    • Olsson, Karen M.;
    • Coulet, Florence;
    • Manimaran, Solaiappan;
    • Zhao, Yujie;
    • Lau, Anna;
    • de Oliveira Pena, Janethe;
    • Badesch, David B.;
    • Humbert, Marc
    Publication type:
    Article
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    BRCA Share: A Collection of Clinical BRCA Gene Variants.

    Published in:
    Human Mutation, 2016, v. 37, n. 12, p. 1318, doi. 10.1002/humu.23113
    By:
    • Béroud, Christophe;
    • Letovsky, Stanley I.;
    • Braastad, Corey D.;
    • Caputo, Sandrine M.;
    • Beaudoux, Olivia;
    • Bignon, Yves Jean;
    • Paillerets, Brigitte;
    • Bronner, Myriam;
    • Buell, Crystal M.;
    • Collod‐Béroud, Gwenaëlle;
    • Coulet, Florence;
    • Derive, Nicolas;
    • Divincenzo, Christina;
    • Elzinga, Christopher D.;
    • Garrec, Céline;
    • Houdayer, Claude;
    • Karbassi, Izabela;
    • Lizard, Sarab;
    • Love, Angela;
    • Muller, Danièle
    Publication type:
    Article
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    Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/ in vitro studies on BRCA1 and BRCA2 variants.

    Published in:
    Human Mutation, 2012, v. 33, n. 8, p. 1228, doi. 10.1002/humu.22101
    By:
    • Houdayer, Claude;
    • Caux-Moncoutier, Virginie;
    • Krieger, Sophie;
    • Barrois, Michel;
    • Bonnet, Françoise;
    • Bourdon, Violaine;
    • Bronner, Myriam;
    • Buisson, Monique;
    • Coulet, Florence;
    • Gaildrat, Pascaline;
    • Lefol, Cédrick;
    • Léone, Mélanie;
    • Mazoyer, Sylvie;
    • Muller, Danielle;
    • Remenieras, Audrey;
    • Révillion, Françoise;
    • Rouleau, Etienne;
    • Sokolowska, Joanna;
    • Vert, Jean-Philippe;
    • Lidereau, Rosette
    Publication type:
    Article
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    Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension.

    Published in:
    Human Mutation, 2011, v. 32, n. 12, p. 1385, doi. 10.1002/humu.21605
    By:
    • Nasim, Md. Talat;
    • Ogo, Takeshi;
    • Ahmed, Mohammad;
    • Randall, Rebecca;
    • Chowdhury, Hasnin M.;
    • Snape, Katie M.;
    • Bradshaw, Teisha Y.;
    • Southgate, Laura;
    • Lee, Grace J.;
    • Jackson, Ian;
    • Lord, Graham M.;
    • Gibbs, J. Simon R.;
    • Wilkins, Martin R.;
    • Ohta-Ogo, Keiko;
    • Nakamura, Kazufumi;
    • Girerd, Barbara;
    • Coulet, Florence;
    • Soubrier, Florent;
    • Humbert, Marc;
    • Morrell, Nicholas W.
    Publication type:
    Article
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    Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension.

    Published in:
    Nature Genetics, 2013, v. 45, n. 5, p. 518, doi. 10.1038/ng.2581
    By:
    • Germain, Marine;
    • Eyries, Mélanie;
    • Montani, David;
    • Poirier, Odette;
    • Girerd, Barbara;
    • Dorfmüller, Peter;
    • Coulet, Florence;
    • Nadaud, Sophie;
    • Maugenre, Svetlana;
    • Guignabert, Christophe;
    • Carpentier, Wassila;
    • Vonk-Noordegraaf, Anton;
    • Lévy, Marilyne;
    • Chaouat, Ari;
    • Lambert, Jean-Charles;
    • Bertrand, Marion;
    • Dupuy, Anne-Marie;
    • Letenneur, Luc;
    • Lathrop, Mark;
    • Amouyel, Philippe
    Publication type:
    Article
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    Clinical implications of CTNNA1 germline mutations in asymptomatic carriers.

    Published in:
    Gastric Cancer, 2019, v. 22, n. 4, p. 899, doi. 10.1007/s10120-018-00907-7
    By:
    • Benusiglio, Patrick R.;
    • Colas, Chrystelle;
    • Guillerm, Erell;
    • Canard, Axelle;
    • Delhomelle, Hélène;
    • Warcoin, Mathilde;
    • Bellanger, Jérôme;
    • Eyries, Mélanie;
    • Zizi, Mohamed;
    • Netter, Jeanne;
    • Soubrier, Florent;
    • Parc, Yann;
    • Mourregot, Anne;
    • Maran Gonzalez, Aurélie;
    • Cusin, Veronica;
    • Denis, Jérôme A.;
    • Coupier, Isabelle;
    • Svrcek, Magali;
    • Coulet, Florence
    Publication type:
    Article
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    Lung cancer is also a hereditary disease.

    Published in:
    European Respiratory Review, 2021, v. 30, n. 162, p. 1, doi. 10.1183/16000617.0045-2021
    By:
    • Benusiglio, Patrick R.;
    • Fallet, Vincent;
    • Sanchis-Borja, Mateo;
    • Coulet, Florence;
    • Cadranel, Jacques
    Publication type:
    Article
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    Cerebral dural arteriovenous fistulas in patients with PTEN‐related hamartoma tumor syndrome.

    Published in:
    Clinical Genetics, 2024, v. 106, n. 1, p. 90, doi. 10.1111/cge.14515
    By:
    • Gerasimenko, Anna;
    • Mignot, Cyril;
    • Naggara, Olivier;
    • Coulet, Florence;
    • Ekram, Samar;
    • Heide, Solveig;
    • Sorato, Clarisse;
    • Mazowiecki, Maxime;
    • Perrin, Laurence;
    • Colas, Chrystelle;
    • Cusin, Veronica;
    • Caux, Frédéric;
    • Dardenne, Antoine;
    • El Chehadeh, Salima;
    • Verloes, Alain;
    • Maurey, Hélène;
    • Afenjar, Alexandra;
    • Petit, Florence;
    • Barete, Stéphane;
    • Boespflug‐Tanguy, Odile
    Publication type:
    Article
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    Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium.

    Published in:
    Clinical Genetics, 2021, v. 99, n. 5, p. 662, doi. 10.1111/cge.13925
    By:
    • Boulouard, Flavie;
    • Kasper, Edwige;
    • Buisine, Marie‐Pierre;
    • Lienard, Gwendoline;
    • Vasseur, Stéphanie;
    • Manase, Sandrine;
    • Bahuau, Michel;
    • Barouk Simonet, Emmanuelle;
    • Bubien, Virginie;
    • Coulet, Florence;
    • Cusin, Véronica;
    • Dhooge, Marion;
    • Golmard, Lisa;
    • Goussot, Vincent;
    • Hamzaoui, Nadim;
    • Lacaze, Elodie;
    • Lejeune, Sophie;
    • Mauillon, Jacques;
    • Beaumont, Marie‐Pascale;
    • Pinson, Stéphane
    Publication type:
    Article
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    Familial pancreatic adenocarcinoma: A retrospective analysis of germline genetic testing in a French multicentre cohort.

    Published in:
    Clinical Genetics, 2019, v. 96, n. 6, p. 579, doi. 10.1111/cge.13629
    By:
    • Schwartz, Mathias;
    • Korenbaum, Clement;
    • Benfoda, Meriem;
    • Mary, Mickael;
    • Colas, Chrystelle;
    • Coulet, Florence;
    • Parrin, Melissa;
    • Jonveaux, Philippe;
    • Ingster, Olivier;
    • Granier, Sandra;
    • De Mestier, Louis;
    • Cros, Jerome;
    • Riffault, Angelique;
    • Muller, Marie;
    • Levy, Philippe;
    • Rebours, Vinciane;
    • Greenhalf, William;
    • Soufir, Nadem;
    • Hammel, Pascal
    Publication type:
    Article
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    La polypose associée à MUTYH  : synthèse des données disponibles en 2020 et actualisation des recommandations françaises établies en 2012 sous l'égide de l'Institut National du Cancer (INCa).

    Published in:
    Hépato-Gastro & Oncologie Digestive, 2020, v. 27, n. 4, p. 396, doi. 10.1684/hpg.2020.1944
    By:
    • Buisine, Marie-Pierre;
    • Bonnet, Delphine;
    • Bonadona, Valérie;
    • Coulet, Florence;
    • Baert-Desurmont, Stéphanie;
    • Dhooge, Marion;
    • Saurin, Jean-Christophe;
    • Remenieras, Audrey;
    • Bignon, Yves-Jean;
    • Caron, Olivier;
    • De Pauw, Antoine;
    • Colas, Chrystelle;
    • Buecher, Bruno
    Publication type:
    Article
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    Soft tissue angiomatosis: another PIK3CA‐related disorder.

    Published in:
    Histopathology, 2020, v. 76, n. 4, p. 540, doi. 10.1111/his.14021
    By:
    • Boccara, Olivia;
    • Galmiche‐Rolland, Louise;
    • Dadone‐Montaudié, Bérengère;
    • Ariche‐Maman, Sonia;
    • Coulet, Florence;
    • Eyries, Mélanie;
    • Pannier, Stéphanie;
    • Soupre, Véronique;
    • Molina, Thierry;
    • Pedeutour, Florence;
    • Fraitag, Sylvie
    Publication type:
    Article
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    5′ Region Large Genomic Rearrangements in the BRCA1 Gene in French Families: Identification of a Tandem Triplication and Nine Distinct Deletions with Five Recurrent Breakpoints.

    Published in:
    Cancers, 2021, v. 13, n. 13, p. 3171, doi. 10.3390/cancers13133171
    By:
    • Caputo, Sandrine M.;
    • Telly, Dominique;
    • Briaux, Adrien;
    • Sesen, Julie;
    • Ceppi, Maurizio;
    • Bonnet, Françoise;
    • Bourdon, Violaine;
    • Coulet, Florence;
    • Castera, Laurent;
    • Delnatte, Capucine;
    • Hardouin, Agnès;
    • Mazoyer, Sylvie;
    • Schultz, Inès;
    • Sevenet, Nicolas;
    • Uhrhammer, Nancy;
    • Bonnet, Céline;
    • Tilkin-Mariamé, Anne-Françoise;
    • Houdayer, Claude;
    • Moncoutier, Virginie;
    • Andrieu, Catherine
    Publication type:
    Article
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    Interprétation des résultats issus du séquençage à haut débit pour les maladies génétiques: Mise en place d'une homogénéisation nationale en France.

    Published in:
    Médecine Sciences, 2024, v. 40, n. 10, p. 767, doi. 10.1051/medsci/2024104
    By:
    • Gorokhova, Svetlana;
    • Rouzier, Cécile;
    • Acquaviva-Bourdain, Cécile;
    • Baert-Desurmont, Stéphanie;
    • Caputo, Sandrine;
    • Chatron, Nicolas;
    • Coulet, Florence;
    • Doco-Fenzy, Martine;
    • Keren, Boris;
    • Le Marechal, Cédric;
    • Nicolas, Gaël;
    • Procaccio, Vincent;
    • Richard, Pascale;
    • Romanet, Pauline;
    • Snanoudj, Sarah;
    • Muller, Jean;
    • Krahn, Martin;
    • Saugier-Veber, Pascale
    Publication type:
    Article
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    AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.

    Published in:
    Genes, Chromosomes & Cancer, 2023, v. 62, n. 4, p. 210, doi. 10.1002/gcc.23112
    By:
    • Leclerc, Julie;
    • Beaumont, Marie;
    • Vibert, Roseline;
    • Pinson, Stéphane;
    • Vermaut, Catherine;
    • Flament, Cathy;
    • Lovecchio, Tonio;
    • Delattre, Lucie;
    • Demay, Christophe;
    • Coulet, Florence;
    • Guillerm, Erell;
    • Hamzaoui, Nadim;
    • Benusiglio, Patrick R.;
    • Brahimi, Afane;
    • Cornelis, François;
    • Delhomelle, Hélène;
    • Fert‐Ferrer, Sandra;
    • Fournier, Benjamin P. J.;
    • Hovnanian, Alain;
    • Legrand, Clémentine
    Publication type:
    Article
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    Identification in Daily Practice of Patients With Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer): Revised Bethesda Guidelines-Based Approach Versus Molecular Screening.

    Published in:
    American Journal of Gastroenterology (Springer Nature), 2008, v. 103, n. 11, p. 2825, doi. 10.1111/j.1572-0241.2008.02084.x
    By:
    • Julié, Catherine;
    • Trésallet, Christophe;
    • Brouquet, Antoine;
    • Vallot, Céline;
    • Zimmermann, Ute;
    • Mitry, Emmanuel;
    • Radvanyi, François;
    • Rouleau, Etienne;
    • Lidereau, Rosette;
    • Coulet, Florence;
    • Olschwang, Sylviane;
    • Frébourg, Thierry;
    • Rougier, Philippe;
    • Nordlinger, Bernard;
    • Laurent-Puig, Pierre;
    • Penna, Christophe;
    • Boileau, Catherine;
    • Franc, Brigitte;
    • Muti, Christine;
    • Hofmann-Radvanyi, Hélène
    Publication type:
    Article
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    Genetic and Acquired Thrombotic Factors in Chronic Hepatitis C.

    Published in:
    American Journal of Gastroenterology (Springer Nature), 2004, v. 99, n. 3, p. 527, doi. 10.1111/j.1572-0241.2004.04092.x
    By:
    • Poujol-Robert, Armelle;
    • Rosmorduc, Olivier;
    • Serfaty, Lawrence;
    • Coulet, Florence;
    • Poupon, Raoul;
    • Robert, Annie
    Publication type:
    Article
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    Screening for Lynch Syndrome in Colorectal Cancer: Are We Doing Enough?

    Published in:
    Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2012, v. 19, n. 3, p. 809, doi. 10.1245/s10434-011-2014-7
    By:
    • Canard, Guillaume;
    • Lefevre, Jeremie;
    • Colas, Chrystelle;
    • Coulet, Florence;
    • Svrcek, Magali;
    • Lascols, Olivier;
    • Hamelin, Richard;
    • Shields, Conor;
    • Duval, Alex;
    • Fléjou, Jean-Francois;
    • Soubrier, Florent;
    • Tiret, Emmanuel;
    • Parc, Yann
    Publication type:
    Article
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