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Circulation: Genomic and Precision Medicine

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Mechanisms

  • Collections >
  • Basic, Translational, and Clinical Research >
  • Mechanisms
  • You have accessRestricted access
    Who’s Who of Pulmonary HypertensionRedefining Classification to Advance Precision Care
    Meghan M. Cirulis and John J. Ryan
    Circ Genom Precis Med. 2018;11:e002116, originally published April 9, 2018
    https://doi.org/10.1161/CIRCGEN.118.002116
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  • You have accessRestricted access
    Functionally Conserved Noncoding Regulators of Cardiomyocyte Proliferation and Regeneration in Mouse and Human
    Martyna Adamowicz, Claire C. Morgan, Bernhard J. Haubner, Michela Noseda, Melissa J. Collins, Marta Abreu Paiva, Prashant K. Srivastava, Pascal Gellert, Bonnie Razzaghi, Peter O’Gara, Priyanka Raina, Laurence Game, Leonardo Bottolo, Michael D. Schneider, Sian E. Harding, Josef Penninger and Timothy J. Aitman
    Circ Genom Precis Med. 2018;11:e001805, originally published February 1, 2018
    https://doi.org/10.1161/CIRCGEN.117.001805
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    Modifying Mendel ReduxUnbiased Approaches Can Find Modifiers
    Kim L. McBride and Stephanie M. Ware
    Circulation: Genomic and Precision Medicine. 2017;10:e001891, originally published October 12, 2017
    https://doi.org/10.1161/CIRCGENETICS.117.001891
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    Connecting the Dots in Atrial Fibrillation
    Sylvia T. Nurnberg
    Circulation: Genomic and Precision Medicine. 2017;10:e001908, originally published September 28, 2017
    https://doi.org/10.1161/CIRCGENETICS.117.001908
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    Previously Unreported in Women Galactosidase Alpha Pro409Ser Variant Is Associated With Fabry Disease
    Sushil Allen Luis, Joseph J. Maleszewski, Phillip M. Young, Hartzell V. Schaff and Naveen L. Pereira
    Circulation: Genomic and Precision Medicine. 2017;10:e001661, originally published August 2, 2017
    https://doi.org/10.1161/CIRCGENETICS.116.001661
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    Functional Validation of a Common Nonsynonymous Coding Variant in ZC3HC1 Associated With Protection From Coronary Artery DiseaseCLINICAL PERSPECTIVE
    Tara Linseman, Sébastien Soubeyrand, Amy Martinuk, Majid Nikpay, Paulina Lau and Ruth McPherson
    Circulation: Genomic and Precision Medicine. 2017;10:e001498, originally published January 23, 2017
    https://doi.org/10.1161/CIRCGENETICS.116.001498
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    Letter by Amin et al Regarding Article, “Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3′ Untranslated Region of KCNQ1?”
    Ahmad S. Amin, Yigal M. Pinto, Michael J. Ackerman and Arthur A.M. Wilde
    Circulation: Genomic and Precision Medicine. 2016;9:580, originally published December 20, 2016
    https://doi.org/10.1161/CIRCGENETICS.116.001629
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    Sucrose Nonfermenting-Related Kinase Enzyme–Mediated Rho-Associated Kinase Signaling is Responsible for Cardiac FunctionCLINICAL PERSPECTIVE
    Stephanie M. Cossette, Vijesh J. Bhute, Xiaoping Bao, Leanne M. Harmann, Mark A. Horswill, Indranil Sinha, Adam Gastonguay, Shabnam Pooya, Michelle Bordas, Suresh N. Kumar, Shama P. Mirza, Sean P. Palecek, Jennifer L. Strande and Ramani Ramchandran
    Circulation: Genomic and Precision Medicine. 2016;9:474-486, originally published October 25, 2016
    https://doi.org/10.1161/CIRCGENETICS.116.001515
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    Genetic Modifiers for the Long-QT SyndromeClinical PerspectiveHow Important Is the Role of Variants in the 3′ Untranslated Region of KCNQ1?
    Lia Crotti, Annukka M. Lahtinen, Carla Spazzolini, Elisa Mastantuono, Maria Cristina Monti, Caterina Morassutto, Gianfranco Parati, Marshall Heradien, Althea Goosen, Peter Lichtner, Thomas Meitinger, Paul A. Brink, Kimmo Kontula, Heikki Swan and Peter J. Schwartz
    Circulation: Genomic and Precision Medicine. 2016;9:330-339, originally published August 16, 2016
    https://doi.org/10.1161/CIRCGENETICS.116.001419
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    Exome Sequencing Identified a Splice Site Mutation in FHL1 that Causes Uruguay Syndrome, an X-Linked Disorder With Skeletal Muscle Hypertrophy and Premature Cardiac DeathCLINICAL PERSPECTIVE
    Yuan Xue, Benedikt Schoser, Aliz R. Rao, Roberto Quadrelli, Alicia Vaglio, Verena Rupp, Christine Beichler, Stanley F. Nelson, Gudrun Schapacher-Tilp, Christian Windpassinger and William R. Wilcox
    Circulation: Genomic and Precision Medicine. 2016;9:130-135, originally published March 1, 2016
    https://doi.org/10.1161/CIRCGENETICS.115.001193
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Current Issue

Circulation: Genomic and Precision Medicine: 11 (4)
Circ Genom Precis Med
April 2018, Volume 11, Issue 4
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