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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
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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Carpal Tunnel Syndrome and Transthyretin Amyloidosis in the All of Us Research Program.
Naman S Shetty et al. Mayo Clin Proc 2024
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Cardiovascular Risk Factors Among First-Degree Relatives of Patients with Premature Cardiovascular Disease in Malta. Baseline Findings from the CRISO Project.
Justin Lee Mifsud et al. Vasc Health Risk Manag 2024 20167-176
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Understanding what drives genetic study participation: Perspectives of patients, carers, and relatives.
Emilia M Swietlik et al. Pulm Circ 2024 14(1) e12346
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RNA Injection Every 6 Months to Improve Adherence and Lower Blood Pressure in Patients With Hypertension.
Ernesto L Schiffrin et al. JAMA 2024
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Measuring Costs of Cardiovascular Disease Prevention for Patients with Familial Hypercholesterolemia in Administrative Claims Data.
Lauren E Passero et al. High Blood Press Cardiovasc Prev 2024
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Familial Hypercholesterolemia in the Elderly: An Analysis of Clinical Profile and Atherosclerotic Cardiovascular Disease Burden from the Hellas-FH Registry.
Christina Antza et al. Biomedicines 2024 12(1)
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Assessment of ethnic inequalities in diagnostic coding of familial hypercholesterolaemia (FH): A cross-sectional database study in Lambeth, South London.
Mariam Molokhia et al. Atherosclerosis 2023 388117353
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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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[Genetic counselling and testing in pulmonary arterial hypertension - A consensus statement on behalf of the International Consortium for Genetic Studies in PAH - French version].
D Montani et al. Rev Mal Respir 2023
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A retrospective study of people with familial hypercholesterolaemia in a Belgian lipid clinic.
V Ide et al. Acta Cardiol 2023 1-10
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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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Frequency of adding salt to foods, genetic susceptibility, and incident type 2 diabetes: a prospective cohort study.
Yimin Zhao et al. J Clin Endocrinol Metab 2023
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Kidney Biopsy Utility: Patient and Clinician Perspectives from the Kidney Precision Medicine Project.
Lauren Bernard et al. Kidney Med 2023 5(10) 100707
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Yield of genetic evaluation in non-syndromic pediatric moyamoya patients.
Anna L Slingerland et al. Childs Nerv Syst 2023
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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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Primary aldosteronism: molecular medicine meets public health.
Elena A B Azizan et al. Nat Rev Nephrol 2023
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Determinants of lipid-lowering medication prescribing in a multi-ethnic adult population diagnosed with familial hypercholesterolaemia in South London.
Aya Ayoub et al. Br J Gen Pract 2023 73(suppl 1)
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No association between genetic markers and hypertension control in multiple cross-sectional studies.
Valeriya Chekanova et al. Sci Rep 2023 13(1) 11811
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Silencing Angiotensinogen in Hypertension.
Rhian M Touyz et al. N Engl J Med 2023 389(3) 278-281
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Zilebesiran, an RNA Interference Therapeutic Agent for Hypertension.
Akshay S Desai et al. N Engl J Med 2023 389(3) 228-238
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The cascade screening in heritable forms of pulmonary arterial hypertension.
Nidhy P Varghese et al. Pulm Circ 2023 13(3) e12259
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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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Health status and comorbidities of adult patients with phenylketonuria (PKU) in France with a focus on early-diagnosed patients - A nationwide study of health insurance claims data.
Sybil Charrière et al. Mol Genet Metab 2023 139(3) 107625
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Cost-Effectiveness Analysis of Personalized Hypertension Prevention
ST Wang, J Per Med, June 15, 2023
Current chemoprevention approaches in Lynch syndrome and Familial adenomatous polyposis: a global clinical practice survey.
Kathryn A Mraz et al. Front Oncol 2023 131141810
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Evaluating the clinical effectiveness of the NHS Health Check programme: a prospective analysis in the Genetics and Vascular Health Check (GENVASC) study.
Radoslaw Debiec et al. BMJ Open 2023 13(5) e068025
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Polygenic prediction of preeclampsia and gestational hypertension.
Michael C Honigberg et al. Nat Med 2023
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Genetic and Clinical Factors Underlying a Self-Reported Family History of Heart Disease.
Amanda Jowell et al. European journal of preventive cardiology 2023
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Obstetrical, perinatal and genetic outcomes associated with non-reportable prenatal cell free DNA screening results.
Mary E Norton et al. American journal of obstetrics and gynecology 2023
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Pharmacogenetic association of the NR1H3 promoter variant with antihypertensive response among patients with hypertension: A longitudinal study.
Yu Chen et al. Frontiers in pharmacology 2023 141083134
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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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