Works by Colas, Chrystelle

Results: 36
    1

    High prevalence of constitutional BRCA1 epimutation in patients with early-onset triple-negative breast cancer.

    Published in:
    Clinical Epigenetics, 2025, v. 17, n. 1, p. 1, doi. 10.1186/s13148-025-01885-1
    By:
    • Schwartz, Mathias;
    • Ibadioune, Sabrina;
    • Delhomelle, Hélène;
    • Barraud, Solenn;
    • Caputo, Sandrine M.;
    • Trabelsi-Grati, Olfa;
    • Villy, Marie-Charlotte;
    • Laugé, Anthony;
    • Tang, Roseline;
    • Rouleau, Etienne;
    • Mouret-Fourme, Emmanuelle;
    • Stoppa-Lyonnet, Dominique;
    • Pasmant, Éric;
    • Golmard, Lisa;
    • Colas, Chrystelle;
    • Bièche, Ivan
    Publication type:
    Article
    2

    Leiden open variation database of the MUTYH gene.

    Published in:
    2010
    By:
    • Out, Astrid A.;
    • Tops, Carli M.J.;
    • Nielsen, Maartje;
    • Weiss, Marjan M.;
    • van Minderhout, Ivonne J.H.M.;
    • Fokkema, Ivo F.A.C.;
    • Buisine, Marie-Pierre;
    • Claes, Kathleen;
    • Colas, Chrystelle;
    • Fodde, Riccardo;
    • Fostira, Florentia;
    • Franken, Patrick F.;
    • Gaustadnes, Mette;
    • Heinimann, Karl;
    • Hodgson, Shirley V.;
    • Hogervorst, Frans B.L.;
    • Holinski-Feder, Elke;
    • Lagerstedt-Robinson, Kristina;
    • Olschwang, Sylviane;
    • Ans M.W., van den Ouweland
    Publication type:
    Other
    3

    Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants.

    Published in:
    NPJ Precision Oncology, 2024, v. 8, n. 1, p. 1, doi. 10.1038/s41698-024-00603-z
    By:
    • Gallon, Richard;
    • Brekelmans, Carlijn;
    • Martin, Marie;
    • Bours, Vincent;
    • Schamschula, Esther;
    • Amberger, Albert;
    • Muleris, Martine;
    • Colas, Chrystelle;
    • Dekervel, Jeroen;
    • De Hertogh, Gert;
    • Coupier, Jérôme;
    • Colleye, Orphal;
    • Sepulchre, Edith;
    • Burn, John;
    • Brems, Hilde;
    • Legius, Eric;
    • Wimmer, Katharina
    Publication type:
    Article
    4

    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
    5

    First report of medulloblastoma in a patient with MUTYH‐associated polyposis.

    Published in:
    Neuropathology & Applied Neurobiology, 2023, v. 49, n. 4, p. 1, doi. 10.1111/nan.12929
    By:
    • Villy, Marie‐Charlotte;
    • Warcoin, Mathilde;
    • Filser, Mathilde;
    • Buecher, Bruno;
    • Golmard, Lisa;
    • Suybeng, Voreak;
    • Schwartz, Mathias;
    • Bieche, Ivan;
    • Vacher, Sophie;
    • Laurence, Valérie;
    • Bourdeaut, Franck;
    • Bernier, Michèle;
    • Gutman, Tom;
    • Stoppa‐Lyonnet, Dominique;
    • Masliah‐Planchon, Julien;
    • Colas, Chrystelle
    Publication type:
    Article
    6

    Glioma oncogenesis in the Constitutional mismatch repair deficiency (CMMRD) syndrome.

    Published in:
    Neuro-Oncology Advances, 2024, v. 6, n. 1, p. 1, doi. 10.1093/noajnl/vdae120
    By:
    • Guerrini-Rousseau, Lea;
    • Merlevede, Jane;
    • Denizeau, Philippe;
    • Andreiuolo, Felipe;
    • Varlet, Pascale;
    • Puget, Stéphanie;
    • Beccaria, Kevin;
    • Blauwblomme, Thomas;
    • Cabaret, Odile;
    • Hamzaoui, Nadim;
    • Bourdeaut, Franck;
    • Faure-Conter, Cécile;
    • Muleris, Martine;
    • Colas, Chrystelle;
    • Beaumais, Tiphaine Adam de;
    • Castel, David;
    • Rouleau, Etienne;
    • Brugières, Laurence;
    • Grill, Jacques;
    • Debily, Marie-Anne
    Publication type:
    Article
    7

    Germline MBD4 Mutations and Predisposition to Uveal Melanoma.

    Published in:
    2021
    By:
    • Derrien, Anne-Céline;
    • Rodrigues, Manuel;
    • Eeckhoutte, Alexandre;
    • Dayot, Stéphane;
    • Houy, Alexandre;
    • Mobuchon, Lenha;
    • Gardrat, Sophie;
    • Lequin, Delphine;
    • Ballet, Stelly;
    • Pierron, Gaëlle;
    • Alsafadi, Samar;
    • Mariani, Odette;
    • El-Marjou, Ahmed;
    • Matet, Alexandre;
    • Colas, Chrystelle;
    • Cassoux, Nathalie;
    • Stern, Marc-Henri
    Publication type:
    journal article
    8

    The Balance Between Cytotoxic T-cell Lymphocytes and Immune Checkpoint Expression in the Prognosis of Colon Tumors.

    Published in:
    2018
    By:
    • Marisa, Laetitia;
    • Svrcek, Magali;
    • Collura, Ada;
    • Becht, Etienne;
    • Cervera, Pascale;
    • Wanherdrick, Kristell;
    • Buhard, Olivier;
    • Goloudina, Anastasia;
    • Jonchère, Vincent;
    • Selves, Janick;
    • Milano, Gerard;
    • Guenot, Dominique;
    • Cohen, Romain;
    • Colas, Chrystelle;
    • Laurent-Puig, Pierre;
    • Olschwang, Sylviane;
    • Lefévre, Jérémie H.;
    • Parc, Yann;
    • Ghiringhelli, François;
    • de Reynies, Aurélien
    Publication type:
    journal article
    9

    No Overt Clinical Immunodeficiency Despite Immune Biological Abnormalities in Patients With Constitutional Mismatch Repair Deficiency.

    Published in:
    Frontiers in Immunology, 2018, p. N.PAG, doi. 10.3389/fimmu.2018.01506
    By:
    • Tesch, Victoria K.;
    • IJspeert, Hanna;
    • Raicht, Andrea;
    • Rueda, Daniel;
    • Dominguez-Pinilla, Nerea;
    • Allende, Luis M.;
    • Colas, Chrystelle;
    • Rosenbaum, Thorsten;
    • Ilencikova, Denisa;
    • Baris, Hagit N.;
    • Nathrath, Michaela H. M.;
    • Suerink, Manon;
    • Januszkiewicz-Lewandowska, Danuta;
    • Ragab, Iman;
    • Azizi, Amedeo A.;
    • Wenzel, Soeren S.;
    • Zschocke, Johannes;
    • Schwinger, Wolfgang;
    • Kloor, Matthias;
    • Blattmann, Claudia
    Publication type:
    Article
    10
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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
    13

    Hereditary cancer predispositions: Comparison of multigene panel sequencing on fresh‐frozen breast/ovarian tumor versus blood.

    Published in:
    Clinical Genetics, 2023, v. 104, n. 1, p. 107, doi. 10.1111/cge.14327
    By:
    • Schwartz, Mathias;
    • Moncoutier, Virginie;
    • Peytral, Adrien;
    • Le Gall, Jessica;
    • Suybeng, Voreak;
    • Pagès, Mélanie;
    • Masliah‐Planchon, Julien;
    • Trabelsi‐Grati, Olfa;
    • Melaabi, Samia;
    • Callens, Céline;
    • Bièche, Ivan;
    • Delhomelle, Hélène;
    • De Pauw, Antoine;
    • Saule, Claire;
    • Mouret‐Fourme, Emmanuelle;
    • Gauthier‐Villars, Marion;
    • Buecher, Bruno;
    • Colas, Chrystelle;
    • Stoppa‐Lyonnet, Dominique;
    • Golmard, Lisa
    Publication type:
    Article
    14

    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
    15

    The mechanisms underlying MMR deficiency in immunodeficiency-related non-Hodgkin lymphomas are different from those in other sporadic microsatellite instable neoplasms.

    Published in:
    International Journal of Cancer, 2009, v. 125, n. 10, p. 2360, doi. 10.1002/ijc.24681
    By:
    • Borie, Claire;
    • Colas, Chrystelle;
    • Dartigues, Peggy;
    • Lazure, Thierry;
    • Rince, Patricia;
    • Buhard, Olivier;
    • Folliot, Patrick;
    • Chalastanis, Alexandra;
    • Muleris, Martine;
    • Hamelin, Richard;
    • Mercier, Dominique;
    • Oliveira, Carla;
    • Seruca, Raquel;
    • Chadburn, Amy;
    • Leblond, Véronique;
    • Barete, Stéphane;
    • Gaïdano, Gianluca;
    • Martin, Antoine;
    • Gaulard, Philippe;
    • Fléjou1, Jean-François
    Publication type:
    Article
    16
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    19

    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
    20
    21

    Comprehensive analysis of constitutional mismatch repair deficiency‐associated non‐Hodgkin lymphomas in a global cohort.

    Published in:
    Pediatric Blood & Cancer, 2024, v. 71, n. 12, p. 1, doi. 10.1002/pbc.31302
    By:
    • Rigaud, Charlotte;
    • Forster, Victoria J.;
    • Al‐Tarrah, Hiba;
    • Attarbaschi, Andishe;
    • Bianchi, Vanessa;
    • Burke, Amos;
    • Burkhardt, Birgit;
    • Colas, Chrystelle;
    • Devalck, Christine;
    • Edwards, Melissa;
    • Elitzur, Sarah;
    • Garthe, Anne‐Kathrin;
    • Goldberg, Yael;
    • Guerrini‐Rousseau, Léa;
    • Horpaopan, Sukanya;
    • Januszkiewicz‐Lewandowska, Danuta;
    • Kabíčková, Edita;
    • Kratz, Christian P.;
    • Loeffen, Jan;
    • Pérez‐Alonso, Vanessa
    Publication type:
    Article
    22

    Screening Mammography and Breast Cancer: Variation in Risk with Rare Deleterious or Predicted Deleterious Variants in DNA Repair Genes.

    Published in:
    Cancers, 2025, v. 17, n. 7, p. 1062, doi. 10.3390/cancers17071062
    By:
    • Ribeiro-Guerra, Maximiliano;
    • Dondon, Marie-Gabrielle;
    • Eon-Marchais, Séverine;
    • Le Gal, Dorothée;
    • Beauvallet, Juana;
    • Mebirouk, Noura;
    • Belotti, Muriel;
    • Cavaciuti, Eve;
    • Adenis-Lavignasse, Claude;
    • Audebert-Bellanger, Séverine;
    • Berthet, Pascaline;
    • Bonadona, Valérie;
    • Buecher, Bruno;
    • Caron, Olivier;
    • Cavaille, Mathias;
    • Chiesa, Jean;
    • Colas, Chrystelle;
    • Coupier, Isabelle;
    • Delnatte, Capucine;
    • Dreyfus, Hélène
    Publication type:
    Article
    23

    Early Colorectal Cancers Provide New Evidence for a Lynch Syndrome-to-CMMRD Phenotypic Continuum.

    Published in:
    Cancers, 2019, v. 11, n. 8, p. 1081, doi. 10.3390/cancers11081081
    By:
    • Fernández-Rozadilla, Ceres;
    • Alvarez-Barona, Miriam;
    • Schamschula, Esther;
    • Bodo, Sahra;
    • Lopez-Novo, Anael;
    • Dacal, Andres;
    • Calviño-Costas, Consuelo;
    • Lancho, Angel;
    • Amigo, Jorge;
    • Bello, Xabier;
    • Cameselle-Teijeiro, Jose Manuel;
    • Carracedo, Angel;
    • Colas, Chrystelle;
    • Muleris, Martine;
    • Wimmer, Katharina;
    • Ruiz-Ponte, Clara
    Publication type:
    Article
    24

    Variation in breast cancer risk associated with factors related to pregnancies according to truncating mutation location, in the French National BRCA1 and BRCA2 mutations carrier cohort (GENEPSO).

    Published in:
    2012
    By:
    • Lecarpentier, Julie;
    • Noguès, Catherine;
    • Mouret-Fourme, Emmanuelle;
    • Gauthier-Villars, Marion;
    • Lasset, Christine;
    • Fricker, Jean-Pierre;
    • Caron, Olivier;
    • Stoppa-Lyonnet, Dominique;
    • Berthet, Pascaline;
    • Faivre, Laurence;
    • Bonadona, Valérie;
    • Buecher, Bruno;
    • Coupier, Isabelle;
    • Gladieff, Laurence;
    • Gesta, Paul;
    • Eisinger, François;
    • Frénay, Marc;
    • Luporsi, Elisabeth;
    • Lortholary, Alain;
    • Colas, Chrystelle
    Publication type:
    journal article
    25

    Identification of a germline deep intronic PTEN-deletion leading to exonization through whole genome and targeted RNA sequencing.

    Published in:
    Familial Cancer, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s10689-025-00445-z
    By:
    • Boedec, Morgane;
    • Aucouturier, Camille;
    • Cavaillé, Mathias;
    • Leman, Raphaël;
    • Castéra, Laurent;
    • Delhomelle, Hélène;
    • Uhrhammer, Nancy;
    • Bernard, Virginie;
    • Giraud, Sophie;
    • Lasseaux, Eulalie;
    • Jones, Natalie;
    • Bidart, Marie;
    • Boutry-Kryza, Nadia;
    • Noguès, Catherine;
    • Colas, Chrystelle;
    • Maugard, Christine;
    • Krieger, Sophie;
    • Bouras, Ahmed
    Publication type:
    Article
    26

    Report of the sixth meeting of the European Consortium 'Care for CMMRD' (C<sub>4</sub>CMMRD), Paris, France, November 16th 2022.

    Published in:
    Familial Cancer, 2024, v. 23, n. 4, p. 447, doi. 10.1007/s10689-024-00403-1
    By:
    • Guerrini-Rousseau, Léa;
    • Gallon, Richard;
    • Pineda, Marta;
    • Brugières, Laurence;
    • Baert-Desurmont, Stéphanie;
    • Corsini, Carole;
    • Dangouloff-Ros, Volodia;
    • Gorris, Mark A. J.;
    • Haberler, Christine;
    • Hoarau, Pauline;
    • Jongmans, Marjolijn C.;
    • Kloor, Matthias;
    • Loeffen, Jan;
    • Rigaud, Charlotte;
    • Robbe, Julie;
    • Vibert, Roseline;
    • Weijers, Dilys;
    • Wimmer, Katharina;
    • Colas, Chrystelle
    Publication type:
    Article
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    Cancer risk and genotype-phenotype correlations in PTEN hamartoma tumor syndrome.

    Published in:
    Familial Cancer, 2014, v. 13, n. 1, p. 57, doi. 10.1007/s10689-013-9674-3
    By:
    • Nieuwenhuis, Marry;
    • Kets, C.;
    • Murphy-Ryan, Maureen;
    • Yntema, Helger;
    • Evans, D.;
    • Colas, Chrystelle;
    • Møller, Pal;
    • Hes, Frederik;
    • Hodgson, Shirley;
    • Olderode-Berends, Maran;
    • Aretz, Stefan;
    • Heinimann, Karl;
    • Gómez García, Encarna;
    • Douglas, Fiona;
    • Spigelman, Allan;
    • Timshel, Susanne;
    • Lindor, Noralane;
    • Vasen, Hans
    Publication type:
    Article
    30
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    33

    Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome.

    Published in:
    JAMA: Journal of the American Medical Association, 2011, v. 305, n. 22, p. 2304, doi. 10.1001/jama.2011.743
    By:
    • Bonadona, Valérie;
    • Bonaïti, Bernard;
    • Olschwng, Sylviane;
    • Grandjouan, Sophie;
    • Huiart, Laetitia;
    • Longy, Michel;
    • Guimbaud, Rosine;
    • Buecher, Bruno;
    • Bignon, Yves-Jean;
    • Caron, Olivier;
    • Colas, Chrystelle;
    • Noguès, Catherine;
    • Lejeune-Dumoulin, Sophie;
    • Olivier-Faivre, Laurence;
    • Polycarpe-Osaer, Florence;
    • Tan Dat Nguyen;
    • Desseigne, Françoise;
    • Saurin, Jean-Christophe;
    • Berthet, Pascaline;
    • Leroux, Dominique
    Publication type:
    Article
    34
    35

    Genetic counselling legislation and practice in cancer in EU Member States.

    Published in:
    European Journal of Public Health, 2024, v. 34, n. 4, p. 666, doi. 10.1093/eurpub/ckae093
    By:
    • McCrary, J Matt;
    • Valckenborgh, Els Van;
    • Poirel, Hélène A;
    • Putter, Robin de;
    • Rooij, Jeroen van;
    • Horgan, Denis;
    • Dierks, Marie-Luise;
    • Antonova, Olga;
    • Brunet, Joan;
    • Chirita-Emandi, Adela;
    • Colas, Chrystelle;
    • Dalmas, Miriam;
    • Ehrencrona, Hans;
    • Grima, Claire;
    • Janavičius, Ramūnas;
    • Klink, Barbara;
    • Koczok, Katalin;
    • Krajc, Mateja;
    • Lace, Baiba;
    • Leitsalu, Liis
    Publication type:
    Article
    36

    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