Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.

@article{Morrison2010GenomicVA,
  title={Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.},
  author={Alanna C. Morrison and Janine F. Felix and L. Adrienne Cupples and Nicole L. Glazer and Laura R. Loehr and Abbas Dehghan and Serkalem Demissie and Joshua C Bis and Wayne D. Rosamond and Yurii S. Aulchenko and Ying A Wang and Talin Haritunians and Aaron R Folsom and Fernando Rivadeneira and Emelia J Benjamin and Thomas S. Lumley and David Couper and Bruno Hch Stricker and Christopher J. O'Donnell and Kenneth M Rice and Patricia Pat-Yue Chang and Albert Hofman and Daniel L{\'e}vy and Jerome I Rotter and Ervin R. Fox and Andr{\'e} G. Uitterlinden and Thomas J. Wang and Bruce M. Psaty and James T. Willerson and Cornelia M van Duijn and Eric Boerwinkle and Jacqueline C. M. Witteman and Ramachandran S. Vasan and Nicholas L. Smith},
  journal={Circulation. Cardiovascular genetics},
  year={2010},
  volume={3 3},
  pages={248-55}
}
BACKGROUND Prognosis and survival are significant concerns for individuals with heart failure (HF). To better understand the pathophysiology of HF prognosis, the association between 2,366,858 single-nucleotide polymorphisms (SNPs) and all-cause mortality was evaluated among individuals with incident HF from 4 community-based prospective cohorts: the Atherosclerosis Risk in Communities Study, the Cardiovascular Health Study, the Framingham Heart Study, and the Rotterdam Study. METHODS AND… CONTINUE READING

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