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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: Apr 19, 2024
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Sudden death[original query]>>Original Studies[Product Type]
Deep Learning-Augmented ECG Analysis for Screening and Genotype Prediction of Congenital Long QT Syndrome.
River Jiang et al. JAMA Cardiol 2024
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An ECG-based artificial intelligence model for assessment of sudden cardiac death risk
L Holmstrom et al, Comm Med, February 2024
Postmortem Identification of Genetic Variations Associated with Sudden Unexpected Death in Young People.
Aya Miura et al. Int Heart J 2024 65(1) 55-62
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The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young.
Megan J Puckelwartz et al. Genome Med 2024 16(1) 13
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Familial risk of vasospastic angina: a nationwide family study in Sweden.
Fabrizio Ricci et al. Open Heart 2023 10(2)
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Incremental value of machine learning for risk prediction in tetralogy of Fallot.
Ayako Ishikita et al. Heart 2023
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The burden of splice-disrupting variants in inherited heart disease and unexplained sudden cardiac death
ES Singer et al, NPJ Genomic Medicine, October 11, 2023
Machine Learning for Prediction of Adverse Cardiovascular Events in Adults With Repaired Tetralogy of Fallot Using Clinical and Cardiovascular Magnetic Resonance Imaging Variables.
Ayako Ishikita et al. Circ Cardiovasc Imaging 2023 16(6) e015205
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Rare Genetic Variants Associated With Sudden Cardiac Arrest in the Young: A Prospective, Population-Based Study.
Lauri Holmstrom et al. Circ Genom Precis Med 2023 e004105
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Molecular Genetic Characterization of Sudden Deaths Due to Thoracic Aortic Dissection or Rupture.
Sarah Saxton et al. Cardiovasc Pathol 2023 107540
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Sudden death in ischemic heart disease: looking for new predictors: polygenic risk.
Alessandro Boccanelli et al. Eur Heart J Suppl 25(Suppl B) B31-B33
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The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young.
Megan J Puckelwartz et al. medRxiv 2023
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Predicting personal cardiovascular disease risk based on family health history: Development of expert-based family criteria for the general population.
Tetske Dijkstra et al. European journal of human genetics : EJHG 2023
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Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort.
Estefanía Martinez-Barrios et al. International journal of legal medicine 2023
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Family History of Sudden Cardiac Death in the Young and Inherited Arrhythmia Syndromes: Awareness and Attitudes of General Practitioners and Private Practice Cardiologists.
Flavia Piciacchia et al. Circulation. Genomic and precision medicine 2023
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Genetic screening of relatives of decedents experiencing sudden unexpected death: medical examiner's office referrals to a multi-disciplinary cardiogenetics program.
Siskind Tamar et al. Journal of community genetics 2022
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Polygenic Risk Score Predicts Sudden Death in Patients With Coronary Disease and Preserved Systolic Function.
Sandhu Roopinder K et al. Journal of the American College of Cardiology 2022 80(9) 873-883
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Hematological, Biochemical Properties, and Clinical Correlates of Hemoglobin S Variant Disorder: A New Insight Into Sickle Cell Trait.
Khaled Safaa A A et al. Journal of hematology 2022 11(3) 92-108
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Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric Cardiomyopathy.
Kurzlechner Leonie M et al. Journal of personalized medicine 2022 12(5)
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KCNH2 p.Gly262AlafsTer98: A New Threatening Variant Associated with Long QT Syndrome in a Spanish Cohort.
Lorca Rebeca et al. Life (Basel, Switzerland) 2022 12(4)
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Genetic Determinants of Sudden Unexpected Death in Pediatrics.
Koh Hyun Yong et al. Genetics in medicine : official journal of the American College of Medical Genetics 2022 24(4) 839-850
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Left Cardiac Sympathetic Denervation for Long QT Syndrome: 50 Years' Experience Provides Guidance for Management.
Dusi Veronica et al. JACC. Clinical electrophysiology 2022 8(3) 281-294
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Family Screening After Sudden Death in a Population-Based Study of Children.
Kannankeril Prince J et al. Pediatrics 2022
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Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Barc Julien et al. Nature genetics 2022
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Variant interpretation in molecular autopsy: a useful dilemma.
Scheiper-Welling Stefanie et al. International journal of legal medicine 2022
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De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca regulation.
Halvorsen Matthew et al. Proceedings of the National Academy of Sciences of the United States of America 2021 118(52)
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Disease Expression and Outcomes in Black and White Adults With Hypertrophic Cardiomyopathy.
Arabadjian Milla E et al. Journal of the American Heart Association 2021 e019978
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Genomic Autopsy of Sudden Deaths in Young Individuals.
Webster Gregory et al. JAMA cardiology 2021
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Genomic Autopsy of Sudden Deaths in Young Individuals
G Webster et al, JAMA Cardiology, August 13, 2021
Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot.
Reuter Miriam S et al. Circulation. Genomic and precision medicine 2021
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 19, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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