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Advancing precision oncology through systematic germline and tumor genetic analysis: The oncogenetic point of view on findings from a prospective multicenter clinical trial of 666 patients
Mazel, Benoit, Bertolone, Geoffrey, Baurand, Amandine, Cosset, Elodie, Sawka, Caroline, Robert, Marion, Gautier, Elodie, Lançon, Allan, Réda, Manon, Favier, Laure, Dérangère, Valentin, Richard, Corentin, Binquet, Christine, Boidot, Romain, Goussot, Vincent, Albuisson, Juliette, Ghiringhelli, François, Faivre, Laurence, Nambot, Sophie
Published in Cancer medicine (Malden, MA) (01.09.2023)
Published in Cancer medicine (Malden, MA) (01.09.2023)
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Journal Article
Prognosis of Adults With Isolated Left Ventricular Non-Compaction: Results of a Prospective Multicentric Study
Gerard, Hilla, Iline, Nicolas, Martel, Hélène, Nguyen, Karine, Richard, Pascale, Donal, Erwan, Eicher, Jean-Christophe, Huttin, Olivier, Selton-Suty, Christine, Raud-Raynier, Pascale, Jondeau, Guillaume, Mansencal, Nicolas, Sawka, Caroline, Ader, Flavie, Pruny, Jean-François, Casalta, Anne-Claire, Michel, Nicolas, Donghi, Valeria, Faivre, Laurence, Giorgi, Roch, Charron, Philippe, Habib, Gilbert
Published in Frontiers in cardiovascular medicine (02.05.2022)
Published in Frontiers in cardiovascular medicine (02.05.2022)
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Journal Article
Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction: Phenotype/Genotype of Noncompaction
Cambon-Viala, Marie, Gerard, Hilla, Nguyen, Karine, Richard, Pascale, Ader, Flavie, Pruny, Jean-François, Donal, Erwan, Eicher, Jean-Christophe, Huttin, Olivier, Selton-Suty, Christine, Raud-Raynier, Pascale, Jondeau, Guillaume, Mansencal, Nicolas, Sawka, Caroline, Casalta, Anne-Claire, Michel, Nicolas, Donghi, Valeria, Martel, Hélène, Faivre, Laurence, Charron, Philippe, Habib, Gilbert
Published in Journal of cardiac failure (01.06.2021)
Published in Journal of cardiac failure (01.06.2021)
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Journal Article
Cardiogenetics and uncertainty: Evaluation of professional vulnerability in France
Gaudillat, Lea, Patay, Lea, Sawka, Caroline, Baurand, Amandine, Nambot, Sophie, Level, Camille, Laurent, Gabriel, Eicher, Jean-Christophe, Bertaux, Geraldine, Eicher, Sylvie Falcon, Denis, Charlotte, Carvallo, Sarah, Cazeneuve, Cécile, Janin, Alexandre, Millat, Gilles, Peyron, Christine, Thauvin-Robinet, Christel, Charron, Philippe, Faivre, Laurence
Published in European journal of medical genetics (01.04.2025)
Published in European journal of medical genetics (01.04.2025)
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Journal Article
Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study)
Viora-Dupont, Eléonore, Robert, Françoise, Chassagne, Aline, Pélissier, Aurore, Staraci, Stéphanie, Sanlaville, Damien, Edery, Patrick, Lesca, Gaetan, Putoux, Audrey, Pons, Linda, Cadenes, Amandine, Baurand, Amandine, Sawka, Caroline, Bertolone, Geoffrey, Spetchian, Myrtille, Yousfi, Meriem, Salvi, Dominique, Gautier, Elodie, Vitobello, Antonio, Denommé-Pichon, Anne-Sophie, Bruel, Ange-Line, Tran Mau-Them, Frédéric, Faudet, Anne, Keren, Boris, Labalme, Audrey, Chatron, Nicolas, Abel, Carine, Dupuis-Girod, Sophie, Poisson, Alice, Buratti, Julien, Mignot, Cyril, Afenjar, Alexandra, Whalen, Sandra, Charles, Perrine, Heide, Solveig, Mouthon, Linda, Moutton, Sébastien, Sorlin, Arthur, Nambot, Sophie, Briffaut, Anne-Sophie, Asensio, Marie-Laure, Philippe, Christophe, Thauvin-Robinet, Christel, Héron, Delphine, Rossi, Massimiliano, Meunier-Bellard, Nicolas, Gargiulo, Marcela, Peyron, Christine, Binquet, Christine, Faivre, Laurence
Published in European journal of human genetics : EJHG (27.05.2024)
Published in European journal of human genetics : EJHG (27.05.2024)
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Journal Article
Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study)
Viora-Dupont, Eléonore, Robert, Françoise, Chassagne, Aline, Pélissier, Aurore, Staraci, Stéphanie, Sanlaville, Damien, Edery, Patrick, Lesca, Gaetan, Putoux, Audrey, Pons, Linda, Cadenes, Amandine, Baurand, Amandine, Sawka, Caroline, Bertolone, Geoffrey, Spetchian, Myrtille, Yousfi, Meriem, Salvi, Dominique, Gautier, Elodie, Vitobello, Antonio, Denommé-Pichon, Anne-Sophie, Bruel, Ange-Line, Tran Mau-Them, Frédéric, Faudet, Anne, Keren, Boris, Labalme, Audrey, Chatron, Nicolas, Abel, Carine, Dupuis-Girod, Sophie, Poisson, Alice, Buratti, Julien, Mignot, Cyril, Afenjar, Alexandra, Whalen, Sandra, Charles, Perrine, Heide, Solveig, Mouthon, Linda, Moutton, Sébastien, Sorlin, Arthur, Nambot, Sophie, Briffaut, Anne-Sophie, Asensio, Marie-Laure, Philippe, Christophe, Thauvin-Robinet, Christel, Héron, Delphine, Rossi, Massimiliano, Meunier-Bellard, Nicolas, Gargiulo, Marcela, Peyron, Christine, Binquet, Christine, Faivre, Laurence
Published in European journal of human genetics : EJHG (01.09.2024)
Published in European journal of human genetics : EJHG (01.09.2024)
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Journal Article
The “extreme phenotype approach” applied to male breast cancer allows the identification of rare variants of ATR as potential breast cancer susceptibility alleles
Chevarin, Martin, Alcantara, Diana, Albuisson, Juliette, Collonge-Rame, Marie-Agnès, Populaire, Céline, Selmani, Zohair, Baurand, Amandine, Sawka, Caroline, Bertolone, Geoffrey, Callier, Patrick, Duffourd, Yannis, Jonveaux, Philippe, Bignon, Yves-Jean, Coupier, Isabelle, Cornelis, François, Cordier, Christophe, Mozelle-Nivoix, Monique, Rivière, Jean-Baptiste, Kuentz, Paul, Thauvin, Christel, Boidot, Romain, Ghiringhelli, François, O'Driscoll, Marc, Faivre, Laurence, Nambot, Sophie
Published in Oncotarget (07.02.2023)
Published in Oncotarget (07.02.2023)
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Journal Article
Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction
Cambon-Viala, Marie, Gerard, Hilla, Nguyen, Karine, Richard, Pascale, Ader, Flavie, Pruny, Jean-François, Donal, Erwan, Eicher, Jean-Christophe, Huttin, Olivier, Selton-Suty, Christine, Raud-Raynier, Pascale, Jondeau, Guillaume, Mansencal, Nicolas, Sawka, Caroline, Casalta, Anne-Claire, Michel, Nicolas, Donghi, Valeria, Martel, Hélène, Faivre, Laurence, Charron, Philippe, Habib, Gilbert
Published in Journal of cardiac failure (01.06.2021)
Published in Journal of cardiac failure (01.06.2021)
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Journal Article
Phenotype/Genotype Relationship in Left Ventricular Noncompaction: Ion Channel Gene Mutations Are Associated With Preserved Left Ventricular Systolic Function and Biventricular Noncompaction
Cambon-Viala, Marie, Gerard, Hilla, Nguyen, Karine, Richard, Pascale, Ader, Flavie, Pruny, Jean-François, Donal, Erwan, Eicher, Jean-Christophe, Huttin, Olivier, Selton-Suty, Christine, Raud-Raynier, Pascale, Jondeau, Guillaume, Mansencal, Nicolas, Sawka, Caroline, Casalta, Anne-Claire, Michel, Nicolas, Donghi, Valeria, Martel, Hélène, Faivre, Laurence, Charron, Philippe, Habib, Gilbert
Published in Journal of cardiac failure (01.06.2021)
Published in Journal of cardiac failure (01.06.2021)
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Journal Article
Patient satisfaction, experience and preferences in the implementation of genetics teleconsultations in the North-eastern region of France
Lançon, Allan, Beaudouin, Amandine, Lambert, Laetitia, Baurand, Amandine, Petit, Estelle, Schaefer, Elise, Poirsier, Céline, Piard, Juliette, Patay, Léa, Garde, Aurore, Bournez, Marie, Bertolone, Geoffrey, Kastner, Claire, Tempé, Laurine, El Chehadeh, Salima, Spodenkiewick, Marta, Lissy, Lola, Doco-Fenzy, Martine, Cabrol, Christelle, Trouvé, Chloé, Brischoux, Elise Boucher, Cloteau, Mélanie, Burtin, Alexia, Renaud, Mathilde, Riviere, Axelle, Thomas, Quentin, De Souza, Clément Simao, Sawka, Caroline, Racine, Caroline, Robert, Marion, Gautier, Elodie, Delanne, Julian, Bertaut, Aurélie, Thauvin-Robinet, Christel, Faivre, Laurence, Nambot, Sophie
Published in European journal of medical genetics (01.10.2023)
Published in European journal of medical genetics (01.10.2023)
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Journal Article
A new hybrid record linkage process to make epidemiological databases interoperable: application to the GEMO and GENEPSO studies involving BRCA1 and BRCA2 mutation carriers
Jiao, Yue, Lesueur, Fabienne, Azencott, Chloé-Agathe, Laurent, Maïté, Mebirouk, Noura, Laborde, Lilian, Beauvallet, Juana, Dondon, Marie-Gabrielle, Eon-Marchais, Séverine, Laugé, Anthony, Noguès, Catherine C., Andrieu, Nadine, Stoppa-Lyonnet, Dominique, Caputo, Sandrine M, Boutry-Kryza, Nadia, Calender, Alain, Giraud, Sophie, Léone, Mélanie, Bressac- de Paillerets, Brigitte, Caron, Olivier, Guillaud-Bataille, Marine, Bignon, Yves-Jean, Uhrhammer, Nancy, Bonadona, Valérie, Lasset, Christine, Berthet, Pascaline, Castera, Laurent, Vaur, Dominique, Bourdon, Violaine, Noguchi, Tetsuro, Popovici, Cornel, Remenieras, Audrey, Sobol, Hagay, Coupier, Isabelle, Harmand, Pierre-Olivier, Pujol, Pascal, Vilquin, Paul, Dumont, Aurélie, Révillion, Françoise, Muller, Danièle, Barouk-Simonet, Emmanuelle, Bonnet, Françoise, Bubien, Virginie, Longy, Michel, Sevenet, Nicolas, Gladieff, Laurence, Guimbaud, Rosine, Feillel, Viviane, Toulas, Christine, Dreyfus, Hélène, Leroux, Dominique, Peysselon, Magalie, Rebischung, Christine, Baurand, Amandine, Bertolone, Geoffrey, Coron, Fanny, Faivre, Laurence, Goussot, Vincent, Jacquot, Caroline, Sawka, Caroline, Kientz, Caroline, Lebrun, Marine, Prieur, Fabienne, Fert-Ferrer, Sandra, Mari, Véronique, Venat-Bouvet, Laurence, Bézieau, Stéphane, Delnatte, Capucine, Mortemousque, Isabelle, Coulet, Florence, Soubrier, Florent, Warcoin, Mathilde, Bronner, Myriam, Lizard, Sarab, Sokolowska, Johanna, Collonge-Rame, Marie-Agnès, Damette, Alexandre, Gesta, Paul, Lallaoui, Hakima, Chiesa, Jean, Molina-Gomes, Denise, Ingster, Olivier, Manouvrier-Hanu, Sylvie, Lejeune, Sophie, Pontois, Pauline, Lyonnet, Dominique Stoppa, Gauthier-Villars, Marion, Buecher, Bruno, Mouret-Fourme, Emmanuelle, Fricker, Jean-Pierre, Luporsi, Elisabeth, Frenay, Marc, Eisinger, Francois, Moretta, Jessica, Dugast, Catherine, Colas, Chrystelle, Lortholary, Alain, Vennin, Philippe, Adenis, Claude, Nguyen, Tan Dat
Published in BMC medical research methodology (29.07.2021)
Published in BMC medical research methodology (29.07.2021)
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Journal Article