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Public Health Genomics and Precision Health Knowledge Base (v9.0)
PHGKB
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Public Health Genomics Branch
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 03, 2024
. (Total: 63769 Documents since 2012)
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Genetic testing in cardiovascular disease.
Michael P Gray et al. Med J Aust 2024
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Genetic risk, adherence to healthy lifestyle and acute cardiovascular and thromboembolic complications following SARS-COV-2 infection.
Junqing Xie et al. Nat Commun 2023 14(1) 4659
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The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary care.
Jason L Vassy et al. Am J Hum Genet 2023 110(11) 1841-1852
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Familial hypercholesterolemia is related to cardiovascular disease, heart failure and atrial fibrillation. Results from a population-based study.
Hayato Tada et al. Eur J Clin Invest 2023 e14119
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Cost-Effectiveness Analysis of Pharmacogenomics (PGx)-Based Warfarin, Apixaban, and Rivaroxaban Versus Standard Warfarin for the Management of Atrial Fibrillation in Ontario, Canada.
Aneeka Hafeez et al. Pharmacoeconomics 2023
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Genetic risk factors for postoperative atrial fibrillation-a nationwide genome-wide association study (GWAS).
Mathias A Christensen et al. Front Cardiovasc Med 2023 101040757
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Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations.
Niall J Lennon et al. medRxiv 2023
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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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Genetic testing in monogenic early-onset atrial fibrillation.
Brandon Chalazan et al. Eur J Hum Genet 2023
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Common and rare variants associated with cardiometabolic traits across 98,622 whole-genome sequences in the All of Us research program.
Xin Wang et al. J Hum Genet
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Pompe disease ascertained through The Lantern Project, 2018-2021: Next-generation sequencing and enzymatic testing to overcome obstacles to diagnosis.
Lisa Sniderman King et al. Mol Genet Metab 139(1) 107565
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Generalizable and robust deep learning algorithm for atrial fibrillation diagnosis across geography, ages and sexes.
Shany Biton et al. NPJ digital medicine 2023 6(1) 44
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Association of accelerometer-derived circadian abnormalities and genetic risk with incidence of atrial fibrillation
L Yang et al, NPJ Digital Medicine, March 4, 2023
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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Investigating genes associated with heart failure, atrial fibrillation, and other cardiovascular diseases, and predicting disease using machine learning techniques for translational research and precision medicine.
Vignesh Venkat et al. Genomics 2023 110584
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Genetics of atrial fibrillation.
David S M Lee et al. Current opinion in cardiology 2023
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Association of Hypertensive Disorders of Pregnancy With Future Cardiovascular Disease.
Bilal Rayes et al. JAMA network open 2023 6(2) e230034
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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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Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction
K Miyazawa et al, Nature Genetics, January 19, 2023
Cardiomyopathy prevalence exceeds 30% in individuals with TTN variants and early atrial fibrillation.
Schiabor Barrett Kelly M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2023 100012
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Genomics and phenomics of body mass index reveals a complex disease network.
Huang Jie et al. Nature communications 2022 13(1) 7973
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Genome Reporting for Healthy Populations-Pipeline for Genomic Screening from the GENCOV COVID-19 Study.
Frangione Erika et al. Current protocols 2022 2(10) e534
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Transcriptomics-based network medicine approach identifies metformin as a repurposable drug for atrial fibrillation
JC Lal et al, Cell Reports Med, October 11, 2022
Identifying genetic variants associated with the ICD10 (International Classification of Diseases10)-based diagnosis of cerebrovascular disease using a large-scale biomedical database.
Alkhalfan Fahad et al. PloS one 2022 17(8) e0273217
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A polygenic risk score predicts atrial fibrillation in cardiovascular disease.
Marston Nicholas A et al. European heart journal 2022
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Joint Genetic Inhibition of PCSK9 and CETP and the Association With Coronary Artery Disease: A Factorial Mendelian Randomization Study.
Cupido Arjen J et al. JAMA cardiology 2022
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Polygenic Risk Scores for Cardiovascular Disease: A Scientific Statement From the American Heart Association.
O'Sullivan Jack W et al. Circulation 2022 101161CIR0000000000001077
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Incidence rates of dilated cardiomyopathy in adult first-degree relatives versus matched controls.
Andersson Charlotte et al. International journal of cardiology. Heart & vasculature 2022 41101065
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Arrhythmias as Presentation of Genetic Cardiomyopathy.
Lukas Laws J et al. Circulation research 2022 130(11) 1698-1722
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Rare and Common Genetic Variation Underlying the Risk of Hypertrophic Cardiomyopathy in a National Biobank.
Biddinger Kiran J et al. JAMA cardiology 2022
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 03, 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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