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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: May 02, 2024
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Diagnostic yield from cardiac gene testing for inherited cardiac conditions and re-evaluation of pre-ACMG variants of uncertain significance.
Jane Murphy et al. Ir J Med Sci 2024
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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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"Inherited cardiovascular disease mindset" can identify concealed inherited conditions at cardio-oncology evaluation: An opportunistic screening.
Rebeca Lorca et al. Int J Cardiol 2024 131825
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Unraveling Complexities in Genetically Elusive Long QT Syndrome.
Babken Asatryan et al. Circ Arrhythm Electrophysiol 2024 e012356
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Assessment of Sudden Cardiac Death Risk in Pediatric Primary Electrical Disorders: A Comprehensive Overview.
Adelina Pupaza et al. Diagnostics (Basel) 2023 13(23)
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Real-world utilization of guideline-directed genetic testing in inherited cardiovascular diseases.
Mauro Longoni et al. Front Cardiovasc Med 2023 101272433
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Return-to-Play for Elite Athletes With Genetic Heart Diseases Predisposing to Sudden Cardiac Death.
Katherine A Martinez et al. J Am Coll Cardiol 2023 82(8) 661-670
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EMQN: Recommendations for genetic testing in inherited cardiomyopathies and arrhythmias.
Jesse B Hayesmoore et al. Eur J Hum Genet 2023
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The diagnostic value of electrocardiogram-based machine learning in long QT syndrome: a systematic review and meta-analysis.
Min-Juan Wu et al. Front Cardiovasc Med 2023 101172451
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Management of Inherited Arrhythmia Syndromes: A HiRO Consensus Handbook on Process of Care.
Mikyla L Janzen et al. CJC Open 2023 5(4) 268-284
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Spotlight on the 2022 ESC guideline management of ventricular arrhythmias and prevention of sudden cardiac death: 10 novel key aspects.
Hilke Könemann et al. Europace 2023
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Phenotypes of Overdiagnosed Long QT Syndrome.
Sahej Bains et al. Journal of the American College of Cardiology 2023 81(5) 477-486
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Systematic review of long QT syndrome identified during fetal life.
Chivers Sian et al. Heart rhythm 2022
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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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The Outcome of Long QT Syndrome, a Korean Single Center Study.
Ahn Kyung Jin et al. Korean circulation journal 2022 52(10) 771-781
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Genetic variants in Colombian patients with inherited cardiac conditions.
Rucinski Cynthia et al. Molecular genetics & genomic medicine 2022 e2046
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Prevalence and Phenotypic Burden of Monogenic Arrhythmias Using Integration of Electronic Health Records With Genetics.
Nafissi Navid A et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN121003675
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Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes.
Halford Jennifer L et al. Nature communications 2022 13(1) 5106
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Prolonged QT interval in athletes: Distinguishing between pathology and physiology.
Christou Georgios A et al. Cardiology 2022
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Utility of Provocative Testing in the Diagnosis and Genotyping of Congenital Long QT Syndrome: A Systematic Review and Meta-Analysis.
Yang Ying et al. Journal of the American Heart Association 2022 11(14) e025246
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Precision Therapy in Congenital Long QT Syndrome.
Neves Raquel et al. Trends in cardiovascular medicine 2022
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A calibrated functional patch-clamp assay to enhance clinical variant interpretation in KCNH2-related long QT syndrome.
Jiang Connie et al. American journal of human genetics 2022
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Pathogenicity Assignment of Variants in Genes Associated With Cardiac Channelopathies Evolve Toward Diagnostic Uncertainty.
Rosamilia Michael B et al. Circulation. Genomic and precision medicine 2022 101161CIRCGEN121003491
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Noncancer-related Secondary Findings in a Cohort of 231 Children With Cancer and Their Parents.
Wagener Rabea et al. Journal of pediatric hematology/oncology 2022
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Experiences of athletes with arrhythmogenic cardiac conditions in returning to play.
Shapero Kayle et al. Heart rhythm O2 2022 3(2) 133-140
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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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shRNAs Targeting a Common KCNQ1 Variant Could Alleviate Long-QT1 Disease Severity by Inhibiting a Mutant Allele.
Cócera-Ortega Lucía et al. International journal of molecular sciences 2022 23(7)
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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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Prevalence of Inherited Cardiac Conditions in Pediatric First-Degree Relatives of Patients with Idiopathic Ventricular Fibrillation.
Brunet-Garcia Laia et al. Pediatric cardiology 2022
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A Phenotype-Enhanced Variant Classification Framework to Decrease the Burden of Missense Variants of Uncertain Significance in Type 1 Long QT Syndrome.
Bains Sahej et al. Heart rhythm 2021
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 02, 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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