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Publication date
2017 May 01
Authors
Wild, PS Felix, JF Schillert, A Teumer, A Chen, MH Leening, MJG Volker, U Grossmann, V Brody, JA Irvin, MR Shah, SJ Pramana, S Lieb, W Schmidt, R Stanton, AV Malzahn, D Smith, AV Sundstrom, J Minelli, C Ruggiero, D Lyytikainen, LP Tiller, D Smith, JG Monnereau, C Di Tullio, MR Musani, SK Morrison, AC Pers, TH Morley, M Kleber, ME Aragam, J Benjamin, EJ Bis, JC Bisping, E Broeckel, U Cheng, S Deckers, JW Del Greco, MF Edelmann, F Fornage, M Franke, L Friedrich, N Harris, TB Hofer, E Hofman, A Huang, J Hughes, AD Kahonen, M Kruppa, J Lackner, KJ Lannfelt, L Laskowski, R Launer, LJ Leosdottir, M Lin, HH Lindgren, CM Loley, C MacRae, CA Mascalzoni, D Mayet, J Medenwald, D Morris, AP Muller, C Muller-Nurasyid, M Nappo, S Nilsson, PM Nuding, S Nutile, T Peters, A Pfeufer, A Pietzner, D Pramstaller, PP Raitakari, OT Rice, KM Rivadeneira, F Rotter, JI Ruohonen, ST Sacco, RL Samdarshi, TE Schmidt, H Sharp, ASP Shields, DC Sorice, R Sotoodehnia, N Stricker, BH Surendran, P Thom, S Toglhofer, AM Uitterlinden, AG Wachter, R Volzke, H Ziegler, A Munzel, T Marz, W Cappola, TP Hirschhorn, JN Mitchell, GF Smith, NL Fox, ER Dueker, ND Jaddoe, VWV Melander, O Russ, M Lehtimaki, T Ciullo, M Hicks, AA Lind, L Gudnason, V Pieske, B Barron, AJ Zweiker, R Schunkert, H Ingelsson, E Liu, K Arnett, DK Psaty, BM Blankenberg, S Larson, MG Felix, SB Franco, OH Zeller, T Vasan, RS Dorr, M
Group authors
KNHI Investigators CHARGE Heart Failure Consortium AortaGen Consortium
Pubmed ID
28394258
Journal
The Journal of clinical investigation
Doctype
Article
KI Connection
Låg
Mesh SV
Genetiska loci Genome-Wide Association Study Hjärtmuskel Hjärtsjukdomar Kvinnlig Manlig Människa Polymorfism, enkelnukleotid Ärftlig kvantitativ egenskap
Mesh EN
Genetic Loci Genome-Wide Association Study Heart Diseases Myocardium Polymorphism, Single Nucleotide Quantitative Trait, Heritable
First date
2017-05-14T10:51:40.693Z