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Academic Journal

Applying High-Resolution Variant Classification to Cardiac Arrhythmogenic Gene Testing in a Demographically Diverse Cohort of Sudden Unexplained Deaths.

  • Authors : Lin Y; From the Laboratory Division, Molecular Genetics Laboratory, New York City Office of Chief Medical Examiner (Y.L., N.W., D.W., B.Z., L.S.E., S.Y.U., R.B., B.A.S., Y.T.); Departments of Pediatrics, Biochemistry and Molecular Pharmacology, and Physiology and Neuroscience, NYU School of Medicine (W.C.)

Subjects: Genetic Testing* ; Genetic Variation*; Arrhythmias, Cardiac/Arrhythmias, Cardiac/Arrhythmias, Cardiac/*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

Genetic Testing in Pediatric Left Ventricular Noncompaction.

  • Authors : Miller EM; From the Division of Cardiology (E.M.M., R.B.H., R.C., A.L., A.P., A.R.S.) and Division of Biostatistics and Epidemiology (R.F.I.), Cincinnati Children's Hospital Medical Center, OH; and Department of Pediatrics and Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis (S.M.W.). .

Subjects: Genetic Testing*; Isolated Noncompaction of the Ventricular Myocardium/Isolated Noncompaction of the Ventricular Myocardium/Isolated Noncompaction of the Ventricular Myocardium/*diagnosis ; Isolated Noncompaction of the Ventricular Myocardium/Isolated Noncompaction of the Ventricular Myocardium/Isolated Noncompaction of the Ventricular Myocardium/*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

Genomic Triangulation and Coverage Analysis in Whole-Exome Sequencing-Based Molecular Autopsies.

  • Authors : Shanks GW; From the Department of Molecular Pharmacology and Experimental Therapeutics (G.W.S., D.J.T., M.J.A.), Windland Smith Rice Sudden Death Genomics Laboratory (G.W.S., D.J.T., M.J.A.), Mayo Clinic Graduate School of Biomedical Sciences (G.W.S., D.J.T., M.J.A.), Division of Heart Rhythm Services, Department of Cardiovascular Diseases (D.J.T., M.J.A.), Department of Biomedical Statistics and Informatics (S.N., J.M.E.), and Division of Pediatric Cardiology, Department of Pediatric and Adolescent Medicine (M.J.A.), Mayo Clinic, Rochester, MN.; Tester DJ

Subjects: Death, Sudden, Cardiac* ; Exome* ; Genome, Human*

  • 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

α-Galactosidase A Genotype N215S Induces a Specific Cardiac Variant of Fabry Disease.

  • Authors : Oder D; From the Department of Internal Medicine I and Comprehensive Heart Failure Center (CHFC) (D.O., D.L., K.H., T.S., J.M., K.L., G.E., C.W., P.N.), Fabry Center for Interdisciplinary Therapy (FAZIT) (D.O., D.L., K.H., N.Ü., T.S., J.M., C.S., G.E., C.W., P.N.), and Department of Neurology (N.Ü., C.S.), University Hospital Würzburg, Germany; West German Heart and Vascular Center Essen, University Hospital Essen, Germany (K.L.)

Subjects: Genotype* ; Mutation, Missense*; Cardiomyopathy, Hypertrophic, Familial/Cardiomyopathy, Hypertrophic, Familial/Cardiomyopathy, Hypertrophic, Familial/*genetics Fabry Disease, Cardiac Variant

  • 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

Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular Noncompaction.

Subjects: Genetic Association Studies*; Ventricular Dysfunction, Left/Ventricular Dysfunction, Left/Ventricular Dysfunction, Left/*diagnosis; Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/Adaptor Proteins, Signal Transducing/genetics

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Aug; Vol. 10 (4).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Clinical Characteristics and Long-Term Outcome of Hypertrophic Cardiomyopathy in Individuals With a MYBPC3 (Myosin-Binding Protein C) Founder Mutation.

  • Authors : van Velzen HG; From the Department of Cardiology, Thoraxcenter (H.G.v.V., A.F.L.S., M.M.), Department of Clinical Genetics (R.A.O., M.A.v.S.), and Department of Pediatrics (I.M.E.F.-M.), Erasmus Medical Center, Rotterdam, The Netherlands; Department of Physiology, Institute for Cardiovascular Research, VU University Medical Center, Amsterdam, The Netherlands (J.v.d.V.)

Subjects: Cardiomyopathy, Hypertrophic/Cardiomyopathy, Hypertrophic/Cardiomyopathy, Hypertrophic/*genetics ; Carrier Proteins/Carrier Proteins/Carrier Proteins/*genetics; Adolescent

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Aug; Vol. 10 (4).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Fabry Disease in Families With Hypertrophic Cardiomyopathy: Clinical Manifestations in the Classic and Later-Onset Phenotypes.

  • Authors : Adalsteinsdottir B; From the Faculty of Medicine, University of Iceland, Reykjavik, Iceland (B.A., R.P., R.A., G.T.G.); Division of Cardiology (B.A., R.D.), Department of Genetics (R.A.), Division of Nephrology (R.P.), and Department of Radiology (M.G.), Landspitali-The National University Hospital of Iceland, Reykjavik, Iceland

Subjects: Cardiomyopathy, Hypertrophic/Cardiomyopathy, Hypertrophic/Cardiomyopathy, Hypertrophic/*diagnosis ; Fabry Disease/Fabry Disease/Fabry Disease/*diagnosis; Adolescent

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Aug; Vol. 10 (4).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Prediction of Adulthood Obesity Using Genetic and Childhood Clinical Risk Factors in the Cardiovascular Risk in Young Finns Study.

  • Authors : Seyednasrollah F; From the Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, Finland (F.S., J.M., L.L.E.); Department of Mathematics and Statistics (F.S.), Research Centre of Applied and Preventive Cardiovascular Medicine (N.P., O.T.R.), and Department of Medicine (M.J., J.V.), University of Turku, Finland

Subjects: Obesity/Obesity/Obesity/*etiology; Adolescent ; Adult

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Jun; Vol. 10 (3).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Prediction of Adult Dyslipidemia Using Genetic and Childhood Clinical Risk Factors: The Cardiovascular Risk in Young Finns Study.

Subjects: Dyslipidemias/Dyslipidemias/Dyslipidemias/*etiology; Adolescent ; Adult

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Jun; Vol. 10 (3).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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Academic Journal

Associations of Age and Sex With Marfan Phenotype: The National Heart, Lung, and Blood Institute GenTAC (Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions) Registry.

Subjects: Registries*; Marfan Syndrome/Marfan Syndrome/Marfan Syndrome/*diagnosis; Adolescent

  • Source: Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2017 Jun; Vol. 10 (3).Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101489144 Publication Model: Print Cited Medium: Internet

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