GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers.
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| Title: | GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers. |
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| Authors: | Lesueur F; INSERM, U900, Institut Curie, PSL Research University, Mines ParisTech, Paris, France., Mebirouk N; INSERM, U900, Institut Curie, PSL Research University, Mines ParisTech, Paris, France., Jiao Y; Service de Génétique, Institut Curie, Paris, France., Barjhoux L; Biopathologie, Centre Léon Bérard, Lyon, France., Belotti M; Service de Génétique, Institut Curie, Paris, France., Laurent M; Service de Génétique, Institut Curie, Paris, France., Léone M; Hospices Civils de Lyon, Groupement Hospitalier EST, Bron, France., Houdayer C; Service de Génétique, Institut Curie, Paris, France., Bressac-de Paillerets B; Gustave Roussy, Université Paris-Saclay, Département de Biopathologie et INSERM U1186, Villejuif, France., Vaur D; Département de Biopathologie, Centre François Baclesse, Caen, France., Sobol H; Institut Paoli Calmette, Département d'Anticipation et de Suivi des Cancers, Oncogénétique, Faculté de Médecine, Université d'Aix-Marseille, Marseille, France., Noguès C; Institut Paoli Calmette, Département d'Anticipation et de Suivi des Cancers, Oncogénétique, Faculté de Médecine, Université d'Aix-Marseille, Marseille, France., Longy M; Biopathologie, Institut Bergonié, Bordeaux, France., Mortemousque I; Service de Génétique, Hôpital Bretonneau, Tours, France., Fert-Ferrer S; Service de Génétique, Centre Hospitalier de Chambéry, Chambéry, France., Mouret-Fourme E; Service de Génétique, Institut Curie, Paris, France., Pujol P; Service de Génétique Médicale et Oncogénétique, Hôpital Arnaud de Villeneuve, CHU Montpellier, INSERM 896, CRCM Val d'Aurelle, Montpellier, France., Venat-Bouvet L; Service d'Oncologie Médicale, Hôpital Universitaire Dupuytren, Limoges, France., Bignon YJ; Université Clermont Auvergne, INSERM, U1240, Centre Jean Perrin, Clermont-Ferrand, France., Leroux D; Département de Génétique, CHU de Grenoble, Hôpital Couple-Enfant, Grenoble, France., Coupier I; Service de Génétique Médicale et Oncogénétique, Hôpital Arnaud de Villeneuve, CHU Montpellier, INSERM 896, CRCM Val d'Aurelle, Montpellier, France., Berthet P; Département de Biopathologie, Centre François Baclesse, Caen, France., Mari V; Unité d'Oncogénétique, Centre Antoine Lacassagne, Nice, France., Delnatte C; Unité d'Oncogénétique, Centre René Gauducheau, Nantes, France., Gesta P; Service d'Oncogénétique Régional Poitou-Charentes, Niort, France., Collonge-Rame MA; Service Génétique et Biologie du Développement-Histologie, CHU Hôpital Saint-Jacques, Besançon, France., Giraud S; Hospices Civils de Lyon, Groupement Hospitalier EST, Bron, France., Bonadona V; Université Claude Bernard Lyon 1, Villeurbanne, France.; CNRS UMR 5558; Unité de Prévention et Epidémiologie Génétique, Centre Léon Bérard, Lyon, France., Baurand A; Institut GIMI, CHU de Dijon et Centre de Lutte contre le Cancer Georges François Leclerc, Dijon, France., Faivre L; Institut GIMI, CHU de Dijon et Centre de Lutte contre le Cancer Georges François Leclerc, Dijon, France., Buecher B; Service de Génétique, Institut Curie, Paris, France., Lasset C; Université Claude Bernard Lyon 1, Villeurbanne, France.; CNRS UMR 5558; Unité de Prévention et Epidémiologie Génétique, Centre Léon Bérard, Lyon, France., Gauthier-Villars M; Service de Génétique, Institut Curie, Paris, France., Damiola F; Biopathologie, Centre Léon Bérard, Lyon, France., Mazoyer S; INSERM, U1028, CNRS, UMR5292, Centre de Recherche en Neurosciences de Lyon, Lyon, France., Caputo SM; Service de Génétique, Institut Curie, Paris, France., Andrieu N; INSERM, U900, Institut Curie, PSL Research University, Mines ParisTech, Paris, France., Stoppa-Lyonnet D; Service de Génétique, Institut Curie, Paris, France.; INSERM, U830, Université Paris Descartes, Paris, France. |
| Corporate Authors: | GEMO Study Collaborators |
| Source: | Frontiers in oncology [Front Oncol] 2018 Oct 31; Vol. 8, pp. 490. Date of Electronic Publication: 2018 Oct 31 (Print Publication: 2018). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation] Country of Publication: Switzerland NLM ID: 101568867 Publication Model: eCollection Cited Medium: Print ISSN: 2234-943X (Print) Linking ISSN: 2234943X NLM ISO Abbreviation: Front Oncol Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 30430080 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: GEMO, a National Resource to Study Genetic Modifiers of Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Pathogenic Variant Carriers. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Lesueur+F%22">Lesueur F</searchLink>; INSERM, U900, Institut Curie, PSL Research University, Mines ParisTech, Paris, France.<br /><searchLink fieldCode="AU" term="%22Mebirouk+N%22">Mebirouk N</searchLink>; INSERM, U900, Institut Curie, PSL Research University, Mines ParisTech, Paris, France.<br /><searchLink fieldCode="AU" term="%22Jiao+Y%22">Jiao Y</searchLink>; Service de Génétique, Institut Curie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Barjhoux+L%22">Barjhoux L</searchLink>; Biopathologie, Centre Léon Bérard, Lyon, France.<br /><searchLink fieldCode="AU" term="%22Belotti+M%22">Belotti M</searchLink>; Service de Génétique, Institut Curie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Laurent+M%22">Laurent M</searchLink>; Service de Génétique, Institut Curie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Léone+M%22">Léone M</searchLink>; Hospices Civils de Lyon, Groupement Hospitalier EST, Bron, France.<br /><searchLink fieldCode="AU" term="%22Houdayer+C%22">Houdayer C</searchLink>; Service de Génétique, Institut Curie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Bressac-de+Paillerets+B%22">Bressac-de Paillerets B</searchLink>; Gustave Roussy, Université Paris-Saclay, Département de Biopathologie et INSERM U1186, Villejuif, France.<br /><searchLink fieldCode="AU" term="%22Vaur+D%22">Vaur D</searchLink>; Département de Biopathologie, Centre François Baclesse, Caen, France.<br /><searchLink fieldCode="AU" term="%22Sobol+H%22">Sobol H</searchLink>; Institut Paoli Calmette, Département d'Anticipation et de Suivi des Cancers, Oncogénétique, Faculté de Médecine, Université d'Aix-Marseille, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Noguès+C%22">Noguès C</searchLink>; Institut Paoli Calmette, Département d'Anticipation et de Suivi des Cancers, Oncogénétique, Faculté de Médecine, Université d'Aix-Marseille, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Longy+M%22">Longy M</searchLink>; Biopathologie, Institut Bergonié, Bordeaux, France.<br /><searchLink fieldCode="AU" term="%22Mortemousque+I%22">Mortemousque I</searchLink>; Service de Génétique, Hôpital Bretonneau, Tours, France.<br /><searchLink fieldCode="AU" term="%22Fert-Ferrer+S%22">Fert-Ferrer S</searchLink>; Service de Génétique, Centre Hospitalier de Chambéry, Chambéry, France.<br /><searchLink fieldCode="AU" term="%22Mouret-Fourme+E%22">Mouret-Fourme E</searchLink>; Service de Génétique, Institut Curie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Pujol+P%22">Pujol P</searchLink>; Service de Génétique Médicale et Oncogénétique, Hôpital Arnaud de Villeneuve, CHU Montpellier, INSERM 896, CRCM Val d'Aurelle, Montpellier, France.<br /><searchLink fieldCode="AU" term="%22Venat-Bouvet+L%22">Venat-Bouvet L</searchLink>; Service d'Oncologie Médicale, Hôpital Universitaire Dupuytren, Limoges, France.<br /><searchLink fieldCode="AU" term="%22Bignon+YJ%22">Bignon YJ</searchLink>; Université Clermont Auvergne, INSERM, U1240, Centre Jean Perrin, Clermont-Ferrand, France.<br /><searchLink fieldCode="AU" term="%22Leroux+D%22">Leroux D</searchLink>; Département de Génétique, CHU de Grenoble, Hôpital Couple-Enfant, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Coupier+I%22">Coupier I</searchLink>; Service de Génétique Médicale et Oncogénétique, Hôpital Arnaud de Villeneuve, CHU Montpellier, INSERM 896, CRCM Val d'Aurelle, Montpellier, France.<br /><searchLink fieldCode="AU" term="%22Berthet+P%22">Berthet P</searchLink>; Département de Biopathologie, Centre François Baclesse, Caen, France.<br /><searchLink fieldCode="AU" term="%22Mari+V%22">Mari V</searchLink>; Unité d'Oncogénétique, Centre Antoine Lacassagne, Nice, France.<br /><searchLink fieldCode="AU" term="%22Delnatte+C%22">Delnatte C</searchLink>; Unité d'Oncogénétique, Centre René Gauducheau, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Gesta+P%22">Gesta P</searchLink>; Service d'Oncogénétique Régional Poitou-Charentes, Niort, France.<br /><searchLink fieldCode="AU" term="%22Collonge-Rame+MA%22">Collonge-Rame MA</searchLink>; Service Génétique et Biologie du Développement-Histologie, CHU Hôpital Saint-Jacques, Besançon, France.<br /><searchLink fieldCode="AU" term="%22Giraud+S%22">Giraud S</searchLink>; Hospices Civils de Lyon, Groupement Hospitalier EST, Bron, France.<br /><searchLink fieldCode="AU" term="%22Bonadona+V%22">Bonadona V</searchLink>; Université Claude Bernard Lyon 1, Villeurbanne, France.; CNRS UMR 5558; Unité de Prévention et Epidémiologie Génétique, Centre Léon Bérard, Lyon, France.<br /><searchLink fieldCode="AU" term="%22Baurand+A%22">Baurand A</searchLink>; Institut GIMI, CHU de Dijon et Centre de Lutte contre le Cancer Georges François Leclerc, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Faivre+L%22">Faivre L</searchLink>; Institut GIMI, CHU de Dijon et Centre de Lutte contre le Cancer Georges François Leclerc, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Buecher+B%22">Buecher B</searchLink>; Service de Génétique, Institut Curie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Lasset+C%22">Lasset C</searchLink>; Université Claude Bernard Lyon 1, Villeurbanne, France.; CNRS UMR 5558; Unité de Prévention et Epidémiologie Génétique, Centre Léon Bérard, Lyon, France.<br /><searchLink fieldCode="AU" term="%22Gauthier-Villars+M%22">Gauthier-Villars M</searchLink>; Service de Génétique, Institut Curie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Damiola+F%22">Damiola F</searchLink>; Biopathologie, Centre Léon Bérard, Lyon, France.<br /><searchLink fieldCode="AU" term="%22Mazoyer+S%22">Mazoyer S</searchLink>; INSERM, U1028, CNRS, UMR5292, Centre de Recherche en Neurosciences de Lyon, Lyon, France.<br /><searchLink fieldCode="AU" term="%22Caputo+SM%22">Caputo SM</searchLink>; Service de Génétique, Institut Curie, Paris, France.<br /><searchLink fieldCode="AU" term="%22Andrieu+N%22">Andrieu N</searchLink>; INSERM, U900, Institut Curie, PSL Research University, Mines ParisTech, Paris, France.<br /><searchLink fieldCode="AU" term="%22Stoppa-Lyonnet+D%22">Stoppa-Lyonnet D</searchLink>; Service de Génétique, Institut Curie, Paris, France.; INSERM, U830, Université Paris Descartes, Paris, France. – Name: AuthorCorporate Label: Corporate Authors Group: Au Data: <searchLink fieldCode="CA" term="%22GEMO+Study+Collaborators%22">GEMO Study Collaborators</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101568867%22">Frontiers in oncology</searchLink> [Front Oncol] 2018 Oct 31; Vol. 8, pp. 490. <i>Date of Electronic Publication: </i>2018 Oct 31 (<i>Print Publication: </i>2018). – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Frontiers+Research+Foundation]%22">Frontiers Research Foundation] </searchLink><i>Country of Publication: </i>Switzerland <i>NLM ID: </i>101568867 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>2234-943X (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%222234943X%22">2234943X </searchLink><i>NLM ISO Abbreviation: </i>Front Oncol <i>Subsets: </i>PubMed not MEDLINE |
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