Works matching AU Delnatte, Capucine


Results: 7
    1

    Mutation analysis of PALB2 gene in French breast cancer families.

    Published in:
    Breast Cancer Research & Treatment, 2015, v. 154, n. 3, p. 463, doi. 10.1007/s10549-015-3625-7
    By:
    • Damiola, Francesca;
    • Schultz, Inès;
    • Barjhoux, Laure;
    • Sornin, Valérie;
    • Dondon, Marie-Gabrielle;
    • Eon-Marchais, Séverine;
    • Marcou, Morgane;
    • Caron, Olivier;
    • Gauthier-Villars, Marion;
    • Pauw, Antoine;
    • Luporsi, Elisabeth;
    • Berthet, Pascaline;
    • Delnatte, Capucine;
    • Bonadona, Valérie;
    • Maugard, Christine;
    • Pujol, Pascal;
    • Lasset, Christine;
    • Longy, Michel;
    • Bignon, Yves-Jean;
    • Fricker, Jean-Pierre
    Publication type:
    Article
    2

    Gestational choriocarcinoma associated with a germline TP53 mutation.

    Published in:
    Familial Cancer, 2018, v. 17, n. 1, p. 113, doi. 10.1007/s10689-017-9996-7
    By:
    • Brehin, Anne-Claire;
    • Patrier-Sallebert, Sophie;
    • Bougeard, Gaëlle;
    • Side-Pfennig, Gwendoline;
    • Llamas Gutierrez, Francisco;
    • Lamy, Aude;
    • Colasse, Elodie;
    • Kandel-Aznar, Christine;
    • Delnatte, Capucine;
    • Vuillemin, Eric;
    • Sadot-Lebouvier, Sophie;
    • Odent, Sylvie;
    • Sabourin, Jean-Christophe;
    • Golfier, François;
    • Frebourg, Thierry
    Publication type:
    Article
    3

    Uptake of a randomized breast cancer prevention trial comparing letrozole to placebo in BRCA1/ 2 mutations carriers: the LIBER trial.

    Published in:
    Familial Cancer, 2012, v. 11, n. 1, p. 77, doi. 10.1007/s10689-011-9484-4
    By:
    • Pujol, Pascal;
    • Lasset, Christine;
    • Berthet, Pascaline;
    • Dugast, Catherine;
    • Delaloge, Suzette;
    • Fricker, Jean-Pierre;
    • Tennevet, Isabelle;
    • Chabbert-Buffet, Nathalie;
    • This, Pascale;
    • Baudry, Karen;
    • Lemonnier, Jerome;
    • Roca, Lise;
    • Mijonnet, Sylvie;
    • Gesta, Paul;
    • Chiesa, Jean;
    • Dreyfus, Helene;
    • Vennin, Philippe;
    • Delnatte, Capucine;
    • Bignon, Yves;
    • Lortholary, Alain
    Publication type:
    Article
    4

    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
    5

    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
    6

    Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation.

    Published in:
    2021
    By:
    • Ribeiro Guerra, Maximiliano;
    • Coignard, Juliette;
    • Eon-Marchais, Séverine;
    • Dondon, Marie-Gabrielle;
    • Le Gal, Dorothée;
    • Beauvallet, Juana;
    • Mebirouk, Noura;
    • Belotti, Muriel;
    • Caron, Olivier;
    • Gauthier-Villars, Marion;
    • Coupier, Isabelle;
    • Buecher, Bruno;
    • Lortholary, Alain;
    • Fricker, Jean-Pierre;
    • Gesta, Paul;
    • Noguès, Catherine;
    • Faivre, Laurence;
    • Berthet, Pascaline;
    • Luporsi, Elisabeth;
    • Delnatte, Capucine
    Publication type:
    journal article
    7

    Osteosarcoma without prior retinoblastoma related to RB1 low‐penetrance germline pathogenic variants: A novel type of RB1‐related hereditary predisposition syndrome?

    Published in:
    Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 12, p. N.PAG, doi. 10.1002/mgg3.913
    By:
    • Imbert‐Bouteille, Marion;
    • Gauthier‐Villars, Marion;
    • Leroux, Dominique;
    • Meunier, Isabelle;
    • Aerts, Isabelle;
    • Lumbroso‐Le Rouic, Livia;
    • Lejeune, Sophie;
    • Delnatte, Capucine;
    • Abadie, Caroline;
    • Pujol, Pascal;
    • Houdayer, Claude;
    • Corsini, Carole
    Publication type:
    Article