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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: Mar 28, 2024
. (Total: 63390 Documents since 2012)
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Heart disease[original query]>>Original Studies[Product Type]
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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Automated valvular heart disease detection using heart sound with a deep learning algorithm.
Zihan Jiang et al. Int J Cardiol Heart Vasc 2024 51101368
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A machine learning-based risk score for prediction of infective endocarditis among patients with Staphylococcus aureus bacteraemia - The SABIER score.
Christopher Koon-Chi Lai et al. J Infect Dis 2024
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Machine learning based predictive model of Type 2 diabetes complications using Malaysian National Diabetes Registry: A study protocol.
Mohamad Zulfikrie Abas et al. J Public Health Res 2024 13(1) 22799036241231786
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A call for increased inclusivity and global representation in pharmacogenetic testing.
April Kennedy et al. NPJ Genom Med 2024 9(1) 13
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Coronary heart disease classification using deep learning approach with feature selection for improved accuracy.
Anandhavalli Muniasamy et al. Technol Health Care 2024
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Familial Hypercholesterolemia Variant and Cardiovascular Risk in Individuals With Elevated Cholesterol.
Yiyi Zhang et al. JAMA Cardiol 2024
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The Impact of Integration of a Genetic Clinic Into a Pediatric Cardiac Unit.
Ayman Elfky et al. Cureus 2024 15(12) e50941
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Machine learning-based prediction of composite risk of cardiovascular events in patients with stable angina pectoris combined with coronary heart disease: development and validation of a clinical prediction model for Chinese patients.
Zihan Wang et al. Front Pharmacol 2024 141334439
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Empowerment of genetic information by women at-risk of being carriers of Duchenne and Becker muscular dystrophies.
Alice Maria Luderitz Hoefel et al. J Community Genet 2024
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Application of machine learning algorithms to construct and validate a prediction model for coronary heart disease risk in patients with periodontitis: a population-based study.
Yicheng Wang et al. Front Cardiovasc Med 2023 101296405
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Family history, socioeconomic factors, comorbidities, health behaviors, and the risk of sudden cardiac arrest.
Eujene Jung et al. Sci Rep 2023 13(1) 21341
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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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Cat eye syndrome: Clinical, cytogenetics and familial findings in a large cohort of 43 patients highlighting the importance of congenital heart disease and inherited cases.
Guillaume Jedraszak et al. Am J Med Genet A 2023
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Stigma manifestations in cardiomyopathy care impact outcomes for black patients: a qualitative study.
Morgan Wolfgang et al. BMC Cardiovasc Disord 2023 23(1) 553
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Genetic counselors and congenital heart disease: Clinical roles, genetic testing practices, and perceived genetic testing utility.
Sara M Fitzgerald-Butt et al. J Genet Couns 2023
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Repurposing Normal Chromosomal Microarray Data to Harbor Genetic Insights into Congenital Heart Disease.
Nephi A Walton et al. Biology (Basel) 2023 12(10)
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Novel Finnish-enriched variants causing severe hypercholesterolemia and their clinical impact on coronary artery disease.
Nella Junna et al. Atherosclerosis 2023 117327
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Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot.
Drayton C Harvey et al. Front Cardiovasc Med 2023 101249605
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Genetic and Nongenetic Components of Stroke Family History: A Population Study of Adopted and Nonadopted Individuals.
Ernst Mayerhofer et al. J Am Heart Assoc 2023 12(20) e031566
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Deep Learning Algorithms to Detect Murmurs Associated With Structural Heart Disease.
John Prince et al. J Am Heart Assoc 2023 12(20) e030377
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Health status and comorbidities of adult patients with late-diagnosed phenylketonuria (PKU) born before the newborn screening in France - A nationwide study of health insurance claims data.
Claire Douillard et al. Mol Genet Metab 2023 140(3) 107704
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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
Prenatal diagnosis of hypoplastic left heart syndrome on ultrasound using artificial intelligence: How does performance compare to a current screening programme?
Thomas G Day et al. Prenat Diagn 2023
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A linear weighted combination of polygenic scores for a broad range of traits improves prediction of coronary heart disease.
Kristjan Norland et al. Eur J Hum Genet 2023
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Risk perception and intended behavior change after uninformative genetic results for adult-onset hereditary conditions in unselected patients.
Nandana D Rao et al. Eur J Hum Genet 2023
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Impact of providing genetics-based future cardiovascular risk on LDL-C in patients with familial hypercholesterolemia.
Akihiro Nomura et al. J Clin Lipidol 2023
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A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease.
Benjamin J Landis et al. J Am Heart Assoc 2023 e029340
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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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Refinement of the diagnostic approach for the identification of children and adolescents affected by familial hypercholesterolemia: Evidence from the LIPIGEN study.
Manuela Casula et al. Atherosclerosis 2023 117231
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Page last reviewed:
Feb 1, 2024
Page last updated:
Mar 28, 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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