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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)
Heart, Lung, Blood and Sleep Disorders
Last data update: Apr 25, 2024
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Arrhythmia[original query]>>Original Studies[Product Type]
An Arrhythmia classification approach via deep learning using single-lead ECG without QRS wave detection.
Liong-Rung Liu et al. Heliyon 2024 10(5) e27200
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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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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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The frequency of gene variant reclassification and its impact on clinical management in the inherited arrhythmia clinic.
William J Young et al. Heart Rhythm 2024
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Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing.
Jodell E Linder et al. Am J Hum Genet 2023
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Artificial intelligence-enhanced 12-lead electrocardiography for identifying atrial fibrillation during sinus rhythm (AIAFib) trial: protocol for a multicenter retrospective study.
Yong-Soo Baek et al. Front Cardiovasc Med 2023 101258167
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Prediction model of atrial fibrillation recurrence after Cox-Maze IV procedure in patients with chronic valvular disease and atrial fibrillation based on machine learning algorithm.
Zenan Jiang et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban 2023 48(7) 995-1007
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Single-lead arrhythmia detection through machine learning: cross-sectional evaluation of a novel algorithm using real-world data.
Henry Mitchell et al. Open Heart 2023 10(2)
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Screening and clinical characteristics analysis of familial hypercholesterolemia in a tertiary public hospital.
Tianzhou Shen et al. Front Cardiovasc Med 2023 101237261
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hERG agonists pose challenges to web-based machine learning methods for prediction of drug-hERG channel interaction.
Aziza E L Harchi et al. J Pharmacol Toxicol Methods 2023 107293
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Genetic Susceptibility to Atrial Fibrillation Identified via Deep Learning of 12-Lead Electrocardiograms.
Xin Wang et al. Circ Genom Precis Med 2023 e003808
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Use of machine learning algorithms to predict life-threatening ventricular arrhythmia in sepsis.
Le Li et al. Eur Heart J Digit Health 2023 4(3) 245-253
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Sudden cardiac death in the young: A qualitative study of experiences of family members with cardiogenetic evaluation.
Lieke van den Heuvel et al. J Genet Couns 2023
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Generalizable calibrated machine learning models for real-time atrial fibrillation risk prediction in ICU patients.
Jarne Verhaeghe et al. Int J Med Inform 2023 175105086
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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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Evaluation of a deep Learning-enabled automated computational heart modeling workflow for personalized assessment of ventricular arrhythmias.
Eric Sung et al. J Physiol 2023
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A descriptive study of the clinical impacts on COVID-19 survivors using telemonitoring (The TeleCOVID Study).
Josephine Sau Fan Chow et al. Frontiers in medical technology 2023 51126258
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Preterm birth and maternal heart disease: A machine learning analysis using the Korean national health insurance database.
Jue Seong Lee et al. PloS one 2023 18(3) e0283959
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Performance Evaluation of Quantum-Based Machine Learning Algorithms for Cardiac Arrhythmia Classification.
Zeynep Ozpolat et al. Diagnostics (Basel, Switzerland) 2023 13(6)
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Does genetic testing offer utility as a supplement to traditional family health history intake for inherited disease risk?
Thomas May et al. Family practice 2023
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A novel artificial intelligence based algorithm to reduce wearable cardioverter-defibrillator alarms.
Jeffrey Arkles et al. Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2023
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An intelligent health monitoring and diagnosis system based on the internet of things and fuzzy logic for cardiac arrhythmia COVID-19 patients.
Muhammad Zia Rahman et al. Computers in biology and medicine 2023 154106583
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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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Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction.
Miyazawa Kazuo et al. Nature genetics 2023
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Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant.
Hoorntje Edgar T et al. Circulation. Genomic and precision medicine 2022 e003672
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Concealed Cardiomyopathy in Autopsy-Inconclusive Cases of Sudden Cardiac Death and Implications for Families.
Isbister Julia C et al. Journal of the American College of Cardiology 2022 80(22) 2057-2068
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Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel.
Chen Jia et al. Orphanet journal of rare diseases 2022 17(1) 394
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Device agnostic AI-based analysis of ambulatory ECG recordings.
Kennedy Alan et al. Journal of electrocardiology 2022 74154-157
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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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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 25, 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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