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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)
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Last data update: May 18, 2024
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Ethical use of artificial intelligence to prevent sudden cardiac death: an interview study of patient perspectives.
Menno T Maris et al. BMC Med Ethics 2024 25(1) 42
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Genetic Characterization of Dilated Cardiomyopathy in Romanian Adult Patients.
Oana Raluca Voinescu et al. Int J Mol Sci 2024 25(5)
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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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Patients With Hypertrophic Cardiomyopathy and Normal Genetic Investigations Have Few Affected Relatives.
Søren K Nielsen et al. J Am Coll Cardiol 2023 82(18) 1751-1761
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Sarcomeric gene variants among Indians with hypertrophic cardiomyopathy: A scoping review.
Linda Koshy et al. Indian J Med Res 2023 158(2) 119-135
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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
Patient-reported outcome measures on mental health and psychosocial factors in patients with Brugada syndrome.
Stefaan Six et al. Europace 2023 25(9)
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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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Ethnic and racial differences in Asian populations with ion channelopathies associated with sudden cardiac death.
Sahil Zaveri et al. Front Cardiovasc Med 2023 101253479
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Legal aspects of genetic testing in the evaluation of ventricular tachycardias.
Regina Duryagina et al. Herzschrittmacherther Elektrophysiol 2023
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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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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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[Association between clinical phenotypes of hypertrophic cardiomyopathy and Ca gene variation gene variation].
J Zhao et al. Zhonghua Xin Xue Guan Bing Za Zhi 2023 51(5) 497-503
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A systematic literature review of economic evaluations and cost-of-illness studies of inherited cardiomyopathies.
Isabell Wiethoff et al. Neth Heart J 2023
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Post-mortem genetic testing in sudden cardiac death and genetic screening of relatives at risk: lessons learned from a Czech pilot multidisciplinary study.
Pavel Votýpka et al. Int J Legal Med 2023
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CineECG analysis provides new insights into Familial ST-segment Depression Syndrome.
Rasmus Frosted et al. Europace 2023
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Addressing the underdiagnosis of familial hypercholesterolemia: A mixed methods study exploring the knowledge and practice behaviors of cardiology healthcare providers.
Isha Kalia et al. J Clin Transl Sci 2023 7(1) e92
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2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death.
Katja Zeppenfeld et al. Eur Heart J 2022 43(40) 3997-4126
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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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Novel filamin C (FLNC) variant causes a severe form of familial mixed hypertrophic-restrictive cardiomyopathy.
Nathalie Gaudreault et al. American journal of medical genetics. Part A 2023
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Global research trends of hypertrophic cardiomyopathy from 2000 to 2022: Insights from bibliometric analysis.
Xifeng Zheng et al. Frontiers in cardiovascular medicine 2023 101039098
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Sudden cardiac death in the young: An update for NPs.
Julianne Doucette et al. The Nurse practitioner 2023 48(3) 21-28
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Sudden arrhythmic death and cardiomyopathy are important causes of sudden cardiac death in the UK: results from a national coronial autopsy database.
Mary N Sheppard et al. Histopathology 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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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 characterization of juvenile sudden cardiac arrest and death in Tuscany: The ToRSADE registry.
Girolami Francesca et al. Frontiers in cardiovascular medicine 2023 91080608
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Topic: Hypertrophic Cardiomyopathy: Current Treatment and Future Options.
Sebastian Sneha Annie et al. Current problems in cardiology 2022 101552
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Characterisation and long-term follow-up of children with Brugada syndrome: experience from a tertiary paediatric referral centre.
Fernandes Sara I L et al. Cardiology in the young 2022 1-6
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Familial Hypercholesterolemia and Its Current Diagnostics and Treatment Possibilities: A Literature Analysis.
Zubieliene Kristina et al. Medicina (Kaunas, Lithuania) 2022 58(11)
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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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Page last reviewed:
Feb 1, 2024
Page last updated:
May 18, 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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