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Circulation: Genomic and Precision Medicine

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Heart Failure

  • Collections >
  • Heart Failure and Cardiac Disease >
  • Heart Failure
  • You have accessRestricted access
    Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human Subjects
    Ray Hu, Michael P. Morley, Jeffrey Brandimarto, Nathan R. Tucker, Victoria A. Parsons, Sihai D. Zhao, Benjamin Meder, Hugo A. Katus, Frank Rühle, Monika Stoll, Eric Villard, François Cambien, Honghuang Lin, Nicholas L. Smith, Janine F. Felix, Ramachandran S. Vasan, Pim van der Harst, Christopher Newton-Cheh, Jin Li, Cecilia E. Kim, Hakon Hakonarson, Sridhar Hannenhalli, Euan A. Ashley, Christine S. Moravec, W.H. Wilson Tang, Marjorie Maillet, Jeffery D. Molkentin, Patrick T. Ellinor, Kenneth B. Margulies and Thomas P Cappola
    Circ Genom Precis Med. 2018;11:e001901, originally published March 14, 2018
    https://doi.org/10.1161/CIRCGEN.117.001901
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  • You have accessRestricted access
    Revealing Pathways of Cardiac Regeneration
    Vinícius Bassaneze and Richard T. Lee
    Circ Genom Precis Med. 2018;11:e002053, originally published February 1, 2018
    https://doi.org/10.1161/CIRCGEN.117.002053
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  • You have accessRestricted access
    Chemotherapy-Related Cardiac DysfunctionA Systematic Review of Genetic Variants Modulating Individual Risk
    Marijke Linschoten, Arco J. Teske, Maarten J. Cramer, Elsken van der Wall and Folkert W. Asselbergs
    Circ Genom Precis Med. 2018;11:e001753, originally published January 10, 2018
    https://doi.org/10.1161/CIRCGEN.117.001753
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    MYH7 Rare Variant in a Family With Double-Chambered Left Ventricle
    Jing Wang, Xin Zhang, Xi Wang, Chuchu Wang, Fangyun Wang and Binbin Wang
    Circulation: Genomic and Precision Medicine. 2017;10:e001729, originally published December 13, 2017
    https://doi.org/10.1161/CIRCGENETICS.117.001729
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    Familial Ebstein AnomalyCLINICAL PERSPECTIVEWhole Exome Sequencing Identifies Novel Phenotype Associated With FLNA
    Catherine L. Mercer, Gaia Andreoletti, Aisling Carroll, Anthony P. Salmon, I. Karen Temple and Sarah Ennis
    Circulation: Genomic and Precision Medicine. 2017;10:e001683, originally published December 13, 2017
    https://doi.org/10.1161/CIRCGENETICS.116.001683
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    Gene-Based Risk Stratification for Cardiac Disorders in LMNA Mutation CarriersCLINICAL PERSPECTIVE
    Suguru Nishiuchi, Takeru Makiyama, Takeshi Aiba, Kenzaburo Nakajima, Sayako Hirose, Hirohiko Kohjitani, Yuta Yamamoto, Takeshi Harita, Mamoru Hayano, Yimin Wuriyanghai, Jiarong Chen, Kenichi Sasaki, Nobue Yagihara, Taisuke Ishikawa, Kenji Onoue, Nobuyuki Murakoshi, Ichiro Watanabe, Kimie Ohkubo, Hiroshi Watanabe, Seiko Ohno, Takahiro Doi, Satoshi Shizuta, Tohru Minamino, Yoshihiko Saito, Yasushi Oginosawa, Akihiko Nogami, Kazutaka Aonuma, Kengo Kusano, Naomasa Makita, Wataru Shimizu, Minoru Horie and Takeshi Kimura
    Circulation: Genomic and Precision Medicine. 2017;10:e001603, originally published December 13, 2017
    https://doi.org/10.1161/CIRCGENETICS.116.001603
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  • You have accessRestricted access
    FLNC (Filamin-C)A New(er) Player in the Field of Genetic Cardiomyopathies
    Andreas Brodehl, Anna Gaertner-Rommel and Hendrik Milting
    Circulation: Genomic and Precision Medicine. 2017;10:e001959, originally published December 6, 2017
    https://doi.org/10.1161/CIRCGENETICS.117.001959
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    Cardiovascular Risk and Matrix Metalloproteinase PolymorphismsNot Just a Simple Substitution
    Francis G. Spinale and Ashley A. Sapp
    Circulation: Genomic and Precision Medicine. 2017;10:e001958, originally published December 6, 2017
    https://doi.org/10.1161/CIRCGENETICS.117.001958
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    Reduced Cardiac Calcineurin Expression Mimics Long-Term Hypoxia-Induced Heart Defects in DrosophilaCLINICAL PERSPECTIVE
    Rachel Zarndt, Stanley M. Walls, Karen Ocorr and Rolf Bodmer
    Circulation: Genomic and Precision Medicine. 2017;10:e001706, originally published October 6, 2017
    https://doi.org/10.1161/CIRCGENETICS.117.001706
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  • You have accessRestricted access
    LMNA Mutations Associated With Mild and Late-Onset PhenotypeThe Case of the Dutch Founder Mutation p.(Arg331Gln)
    Eloisa Arbustini, Valentina Favalli and Nupoor Narula
    Circulation: Genomic and Precision Medicine. 2017;10:e001816, originally published August 8, 2017
    https://doi.org/10.1161/CIRCGENETICS.117.001816
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Current Issue

Circulation: Genomic and Precision Medicine: 11 (4)
Circ Genom Precis Med
April 2018, Volume 11, Issue 4
  • Table of Contents
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Related Collections

  • Cardiomyopathy (128)
  • Cardiorenal Syndrome (9)
  • Chronic Ischemic Heart Disease (25)
  • Congenital Heart Disease (82)
  • Heart Failure (78)
  • Hypertrophy (39)
  • Infectious Endocarditis (2)
  • Inflammatory Heart Disease (1)
  • Metabolic Syndrome (5)
  • Myocardial Infarction (92)
  • Remodeling (19)
  • Valvular Heart Disease (14)
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