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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
. (Total: 63675 Documents since 2012)
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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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An extra X chromosome among adult women in the Million Veteran Program: A more benign perspective of trisomy X.
Shanlee M Davis et al. Am J Med Genet C Semin Med Genet 2024 e32083
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Cardiomyopathies in children and adolescents: aetiology, management, and outcomes in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Registry.
Juan Pablo Kaski et al. Eur Heart J 2024
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Genetic contributions to risk of adverse pregnancy outcomes.
Zachary H Hughes et al. Curr Cardiovasc Risk Rep 2024 17(11) 185-193
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Organ aging signatures in the plasma proteome track health and disease.
Hamilton Se-Hwee Oh et al. Nature 2023 624(7990) 164-172
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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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Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart Transplantation.
Yuri Kim et al. Circ Genom Precis Med 2023 e004062
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Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry.
Elizabeth Jordan et al. JAMA 2023 330(5) 432-441
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Association of Longer Leukocyte Telomere Length With Cardiac Size, Function, and Heart Failure
N Aung et al, JAMA Cardiology, July 26, 2023
Clinical Penetrance of the Transthyretin V122I Variant in Older Black Patients With Heart Failure: The SCAN-MP (Screening for Cardiac Amyloidosis With Nuclear Imaging in Minority Populations) Study.
Avni Madhani et al. J Am Heart Assoc 2023 e028973
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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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Genetic Evaluation and Screening in Cardiomyopathies: Opportunities and Challenges for Personalized Medicine.
Sahana Aiyer et al. J Pers Med 2023 13(6)
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Clinical Outcomes and Genetic Analyses of Restrictive Cardiomyopathy in Children.
Hidekazu Ishida et al. Circ Genom Precis Med 2023 e004054
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Mendelian randomization evidence for the causal effects of socio-economic inequality on human longevity among Europeans.
Chao-Jie Ye et al. Nat Hum Behav 2023
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Diagnostic and prognostic relevance of using large gene panels in the genetic testing of patients with dilated cardiomyopathy.
Sophie L V M Stroeks et al. Eur J Hum Genet 2023
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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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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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Risk stratification in transthyretin-related cardiac amyloidosis.
Riccardo Scirpa et al. Frontiers in cardiovascular medicine 2023 101151803
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A Novel Loss-of-function Mutation in MYBPC3 Causes Familial Hypertrophic Cardiomyopathy with Extreme Intrafamilial Phenotypic Heterogeneity.
Y Peng et al. Balkan journal of medical genetics : BJMG 2023 25(1) 71-78
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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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Validation of a Polygenic Score for Beta-Blocker Survival Benefit in Patients With Heart Failure Using the United Kingdom Biobank.
David E Lanfear et al. Circulation. Genomic and precision medicine 2023 e003835
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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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The role of aldehyde dehydrogenase 2 in cardiovascular disease.
Jian Zhang et al. Nature reviews. Cardiology 2023
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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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Familial Associations of Complete Atrioventricular Block: A National Family Study in Sweden.
Artur Fedorowski et al. Circulation. Genomic and precision medicine 2023 e003654
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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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Approaches to Genetic Screening in Cardiomyopathies: Practical Guidance for Clinicians.
Amy R Kontorovich et al. JACC. Heart failure 2023 11(2) 133-142
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Opportunistic Genetic Screening for Familial Hypercholesterolemia in Heart Transplant Patients.
María Salgado et al. Journal of clinical medicine 2023 12(3)
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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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Genetic causes of heart failure with preserved ejection fraction: emerging pharmacological treatments.
Olivotto Iacopo et al. European heart journal 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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