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Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Barc, Julien; Tadros, Rafik; Glinge, Charlotte; Chiang, David Y; Jouni, Mariam; Simonet, Floriane; Jurgens, Sean J; Baudic, Manon; Nicastro, Michele; Potet, Franck; Offerhaus, Joost A; Walsh, Roddy; Choi, Seung Hoan; Verkerk, Arie O; Mizusawa, Yuka; Anys, Soraya; Minois, Damien; Arnaud, Marine; Duchateau, Josselin; Wijeyeratne, Yanushi D; Muir, Alison; Papadakis, Michael; Castelletti, Silvia; Torchio, Margherita; Ortuño, Cristina Gil; Lacunza, Javier; Giachino, Daniela F; Cerrato, Natascia; Martins, Raphaël P; Campuzano, Oscar; Van Dooren, Sonia; Thollet, Aurélie; Kyndt, Florence; Mazzanti, Andrea; Clémenty, Nicolas; Bisson, Arnaud; Corveleyn, Anniek; Stallmeyer, Birgit; Dittmann, Sven; Saenen, Johan; Noël, Antoine; Honarbakhsh, Shohreh; Rudic, Boris; Marzak, Halim; Rowe, Matthew K; Federspiel, Claire; Le Page, Sophie; Placide, Leslie; Milhem, Antoine; Barajas-Martinez, Hector.
Afiliación
  • Barc J; Université de Nantes, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France. julien.barc@univ-nantes.fr.
  • Tadros R; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart: ERN GUARD-Heart, . julien.barc@univ-nantes.fr.
  • Glinge C; Department of Clinical and Experimental Cardiology, Heart Centre, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Chiang DY; Department of Medicine, Cardiovascular Genetics Center, Montreal Heart Institute and Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
  • Jouni M; Department of Clinical and Experimental Cardiology, Heart Centre, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Simonet F; The Department of Cardiology, The Heart Centre, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
  • Jurgens SJ; Medicine, Cardiovascular Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • Baudic M; Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Nicastro M; Université de Nantes, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.
  • Potet F; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Offerhaus JA; Université de Nantes, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.
  • Walsh R; Department of Clinical and Experimental Cardiology, Heart Centre, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Choi SH; Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Verkerk AO; Department of Clinical and Experimental Cardiology, Heart Centre, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Mizusawa Y; Department of Clinical and Experimental Cardiology, Heart Centre, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Anys S; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Minois D; Department of Clinical and Experimental Cardiology, Heart Centre, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Arnaud M; Department of Medical Biology, University of Amsterdam, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
  • Duchateau J; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart: ERN GUARD-Heart.
  • Wijeyeratne YD; Department of Clinical and Experimental Cardiology, Heart Centre, Amsterdam Cardiovascular Sciences, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
  • Muir A; Université de Nantes, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.
  • Papadakis M; Université de Nantes, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.
  • Castelletti S; Université de Nantes, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.
  • Torchio M; IHU Liryc, Electrophysiology and Heart Modeling Institute, fondation Bordeaux Université, Pessac-Bordeaux, France.
  • Ortuño CG; Université Bordeaux, Centre de recherche Cardio-Thoracique de Bordeaux, Bordeaux, France.
  • Lacunza J; INSERM, Centre de recherche Cardio-Thoracique de Bordeaux, Bordeaux, France.
  • Giachino DF; Electrophysiology and Ablation Unit, Bordeaux University Hospital (CHU), Pessac, France.
  • Cerrato N; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart: ERN GUARD-Heart.
  • Martins RP; Molecular and Clinical Sciences Research Institute, St. George's, University of London, London, UK.
  • Campuzano O; Cardiology Clinical Academic Group, St. George's University Hospitals' NHS Foundation Trust, London, UK.
  • Van Dooren S; Cardiology, Belfast Health and Social Care Trust and Queen's University Belfast, Belfast, UK.
  • Thollet A; Molecular and Clinical Sciences Research Institute, St. George's, University of London, London, UK.
  • Kyndt F; Cardiology Clinical Academic Group, St. George's University Hospitals' NHS Foundation Trust, London, UK.
  • Mazzanti A; Center for Cardiac Arrhythmias of Genetic Origin, Istituto Auxologico Italiano IRCCS, Milan, Italy.
  • Clémenty N; Laboratory of Cardiovascular Genetics, Istituto Auxologico Italiano IRCCS, Cusano Milanino, Italy.
  • Bisson A; Cardiogenetic, Unidad de Cardiopatías Familiares, Instituto Murciano de Investigación Biosanitaria, Universidad de Murcia, Murcia, Spain.
  • Corveleyn A; Cardiology, Unidad de Cardiopatías Familiares, Hospital Universitario Virgen de la Arrixaca, Universidad de Murcia, Murcia, Spain.
  • Stallmeyer B; Clinical and Biological Sciences, Medical Genetics, University of Torino, Orbassano, Italy.
  • Dittmann S; Medical Genetics, San Luigi Gonzaga University Hospital, Orbassano, Italy.
  • Saenen J; Medical Sciences, Cardiology, University of Torino, Torino, Italy.
  • Noël A; Cardiologie et Maladies vasculaires, Université Rennes1 - CHU Rennes, Rennes, France.
  • Honarbakhsh S; Cardiovascular Genetics Center, University of Girona-IDIBGI, Girona, Spain.
  • Rudic B; Medical Science Department, University of Girona, Girona, Spain.
  • Marzak H; Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV), Madrid, Spain.
  • Rowe MK; Biochemistry and Molecular Genetics Department, Hospital Clinic, University of Barcelona-IDIBAPS, Barcelona, Spain.
  • Federspiel C; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart: ERN GUARD-Heart.
  • Le Page S; Centre for Medical Genetics, research group Reproduction and Genetics, research cluster Reproduction, Genetics and Regenerative Medicine, Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Brussels, Belgium.
  • Placide L; Université de Nantes, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.
  • Milhem A; Université de Nantes, CHU Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.
  • Barajas-Martinez H; European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart: ERN GUARD-Heart.
Nat Genet ; 54(3): 232-239, 2022 03.
Article en En | MEDLINE | ID: mdl-35210625
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_cardiovascular_diseases Asunto principal: Síndrome de Brugada Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Adult / Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Francia
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_cardiovascular_diseases Asunto principal: Síndrome de Brugada Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Adult / Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Francia