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QT Interval Determinant: Mutations, Rare Variants, or Single-Nucleotide Polymorphisms?

  • Authors : Aiba T; From the Division of Arrhythmia and Electrophysiology, Department of Cardiovascular Medicine (T.A.) and Department of Genomic Medicine, Research Institute (A.T.), National Cerebral and Cardiovascular Center, Suita, Japan. .; Takahashi A

Subjects: Long QT Syndrome* ; Polymorphism, Single Nucleotide*; Humans

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Oct; Vol. 10 (5).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Heritability of Atrial Fibrillation.

  • Authors : Weng LC; From the Program in Medical and Population Genetics, Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, MA (L.-C.W., S.H.C., D.K., J.G.S. P.-R.L., M.C., C.R., O.L.H., C.N.-C., S.K., P.T.E., S.A.L.); Department of Cardiology, Clinical Sciences, Lund University, Sweden (J.G.S.)

Subjects: Genome-Wide Association Study* ; Polymorphism, Single Nucleotide*; Atrial Fibrillation/Atrial Fibrillation/Atrial Fibrillation/*genetics

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Dec; Vol. 10 (6).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential.

  • Authors : Tucker NR; From the Cardiovascular Research Center (N.R.T., E.V.D., R.R.C., J.Y., W.J.H., H.S.J., V.A.P., L.-C.W., R.W.M., J.L.-M., S.A.L., D.J.M., P.T.E.) and Department of Surgery (G.V.), Massachusetts General Hospital, Boston; National Heart, Lung and Blood Institute's and Boston University's Framingham Heart, MA (H.L., E.J.B., K.L.L.)

Subjects: Atrial Fibrillation*/Atrial Fibrillation*/Atrial Fibrillation*/genetics ; Atrial Fibrillation*/Atrial Fibrillation*/Atrial Fibrillation*/metabolism ; Atrial Fibrillation*/Atrial Fibrillation*/Atrial Fibrillation*/physiopathology

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Oct; Vol. 10 (5).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Validation of Polygenic Scores for QT Interval in Clinical Populations.

  • Authors : Rosenberg MA; From the University of Colorado School of Medicine, Aurora (M.A.R.); Massachusetts General Hospital, Boston (S.A.L., G.K., V.M.C., P.H., P.T.E., R.H.P., C.N.-C.)

Subjects: Genome-Wide Association Study* ; Multifactorial Inheritance* ; Polymorphism, Single Nucleotide*

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Oct; Vol. 10 (5).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians.

  • Authors : Li C; From the Department of Epidemiology, Tulane University School of Public Health and Tropical Medicine, New Orleans, LA (C.L., J.H., J.Z., T.N.K.); Center for Genome Science, Korea National Institute of Health, Osong Health Technology Administration Complex, Chungcheongbuk-do, Korea (Y.K.K., J.L., S.H., B.-G.H., S.M., B.-J.K.)

Subjects: Genetic Loci* ; Genome-Wide Association Study* ; Phenotype*

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Apr; Vol. 10 (2), pp. e001527.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Functional Validation of a Common Nonsynonymous Coding Variant in ZC3HC1 Associated With Protection From Coronary Artery Disease.

  • Authors : Linseman T; From the Atherogenomics Laboratory, University of Ottawa Heart Institute, Canada.; Soubeyrand S

Subjects: Polymorphism, Single Nucleotide*; Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/*genetics ; Cell Cycle Proteins/Cell Cycle Proteins/Cell Cycle Proteins/*genetics

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Jan; Vol. 10 (1).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Genome-Wide Prioritization and Transcriptomics Reveal Novel Signatures Associated With Thiazide Diuretics Blood Pressure Response.

Subjects: Pharmacogenomic Variants* ; Polymorphism, Single Nucleotide* ; Transcriptome*

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Jan; Vol. 10 (1).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery Abnormalities.

Subjects: Polymorphism, Single Nucleotide*; Calcium Signaling/Calcium Signaling/Calcium Signaling/*genetics ; Coronary Aneurysm/Coronary Aneurysm/Coronary Aneurysm/*genetics

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2016 Dec; Vol. 9 (6), pp. 559-568. Date of Electronic Publication: 2016 Nov 21.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Comprehensive Analysis of Established Dyslipidemia-Associated Loci in the Diabetes Prevention Program.

  • Authors : Varga TV; Dept of Clinical Sciences, Genetic & Molecular Epidemiology Unit, Lund Univ, Malmö, Sweden.; Winters AH

Subjects: Genetic Loci* ; Polymorphism, Single Nucleotide* ; Risk Reduction Behavior*

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2016 Dec; Vol. 9 (6), pp. 495-503. Date of Electronic Publication: 2016 Oct 26.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Defining a Contemporary Ischemic Heart Disease Genetic Risk Profile Using Historical Data.

  • Authors : Mosley JD; From the Department of Medicine (J.D.M., S.L.v.D., Q.S.W., C.M.S., J.C.D., D.M.R.), Department of Pediatrics (S.L.v.D.), Vanderbilt Epidemiology Center (T.L.E.), Biomedical Informatics (L.B., J.C.D., D.M.R.), and Department of Pharmacology (D.M.R.), Vanderbilt University, Nashville, TN; Essentia Institute of Rural Health, Duluth, MN (C.A.M.)

Subjects: Polymorphism, Single Nucleotide*; Myocardial Ischemia/Myocardial Ischemia/Myocardial Ischemia/*genetics; Aged

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2016 Dec; Vol. 9 (6), pp. 521-530. Date of Electronic Publication: 2016 Oct 25.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print-Electronic Cited Medium:

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