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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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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)
Heart, Lung, Blood and Sleep Disorders
Last data update: May 30, 2024
. (Total: 64035 Documents since 2012)
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Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study.
Mark Hofmeyer et al. Circulation 2023
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Association of Race With Disease Expression and Clinical Outcomes Among Patients With Hypertrophic Cardiomyopathy.
Eberly Lauren A, et al. JAMA cardiology 2019 12 0.
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Genetic Risk of Arrhythmic Phenotypes in Patients With Dilated Cardiomyopathy.
Gigli Marta, et al. Journal of the American College of Cardiology 2019 9 0. (11) 1480-1490
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Dilated Cardiomyopathy - From Epidemiologic to Genetic Phenotypes A Translational Review of Current Literature.
Reichart Daniel et al. Journal of internal medicine 2019 May
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Contemporary characteristics and outcomes of adults with familial dilated cardiomyopathy listed for heart transplantation.
Khayata Mohamed et al. World journal of cardiology 2019 Jan 11(1) 38-46
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Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations.
Domínguez Fernando et al. Journal of the American College of Cardiology 2018 Nov 72(20) 2471-2481
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Effect of CYP2C9 and VKORC1 Gene Variants on Warfarin Response in Patients with Continuous-Flow Left Ventricular Assist Devices.
Topkara Veli K et al. ASAIO journal (American Society for Artificial Internal Organs : 1992) 62(5) 558-64
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 30, 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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