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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
Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Diabetes
Last data update: Apr 25, 2024
. (Total: 63675 Documents since 2012)
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Modification of coronary artery disease clinical risk factors by coronary artery disease polygenic risk score.
Buu Truong et al. Med 2024
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Familial aggregation and heritability of childhood-onset and adult-onset type 1 diabetes: a Swedish register-based cohort study.
Yuxia Wei et al. Lancet Diabetes Endocrinol 2024
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Burden of Mendelian disorders in a large Middle Eastern biobank.
Waleed Aamer et al. Genome Med 2024 16(1) 46
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A New Tool to Identify Pediatric Patients with Atypical Diabetes Associated with Gene Polymorphisms.
Sophie Welsch et al. Diabetes Metab J 2024
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Family Recall of and Response to Germline Pathologic Variants Found on Paired Tumor-Germline Sequencing in Pediatric Oncology.
Michelle F Jacobs et al. JCO Precis Oncol 2024 8e2300539
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Multi-ancestry polygenic mechanisms of type 2 diabetes
K Smith et al, Nature Medicine, March 6, 2024
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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Type 2 diabetes and its genetic susceptibility are associated with increased severity and mortality of COVID-19 in UK Biobank.
Aeyeon Lee et al. Commun Biol 2024 7(1) 122
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Precision prognostics for cardiovascular disease in Type 2 diabetes: a systematic review and meta-analysis
A Ahmad et al, Com Med January 22, 2024
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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Predictive improvement of adding Coronary Calcium Score and a Genetic Risk Score to a Traditional Risk Model for cardiovascular events prediction.
Margarida Temtem et al. Eur J Prev Cardiol 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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Mediating Factors in the Association of Maternal Educational Level With Pregnancy Outcomes: A Mendelian Randomization Study.
Tormod Rogne et al. JAMA Netw Open 2024 7(1) e2351166
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Implementing a Pharmacogenomic-driven Algorithm to Guide Antiplatelet Therapy among Caribbean Hispanics: A non-randomized prospective cohort study.
Héctor Nuñez-Medina et al. medRxiv 2023
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Increased FH-Risk-Score and Diabetes Are Cardiovascular Risk Equivalents in Heterozygous Familial Hypercholesterolemia.
Martine Paquette et al. Arterioscler Thromb Vasc Biol 2023
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What Is Prediabetes?
J Jin, JAMA Patient Corner, December 1, 2023
DNA Testing for Preventative Health: Do Outcomes Justify Continued Investment?
Jim Banks et al. IEEE Pulse 2023 14(4) 19-23
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Affected brother as the highest risk factor of type 1 diabetes development in children and adolescents: One center data before implementing type 1 diabetes national screening.
Anna Wedrychowicz et al. Adv Clin Exp Med 2023
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Including diverse populations enhances the discovery of type 2 diabetes loci
S Fatumo, Nat Rev Genetics, November 22, 2023
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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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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Digital lifestyle treatment improves long-term metabolic control in type 2 diabetes with different effects in pathophysiological and genetic subgroups.
Vishal A Salunkhe et al. NPJ Digit Med 2023 6(1) 199
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Identification of monogenic diabetes in an Australian cohort using the Exeter maturity-onset diabetes of the young (MODY) probability calculator and next-generation sequencing gene panel testing.
Sunita M C De Sousa et al. Acta Diabetol 2023
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Genetic Inhibition of APOL1 Pore-Forming Function Prevents APOL1-Mediated Kidney Disease.
Adriana M Hung et al. J Am Soc Nephrol 2023
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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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Precision medicine of obesity as an integral part of type 2 diabetes management – past, present, and future
L Szczerbinski et al. The Lancet Diabetes Endocr, October 4, 2023
Precision medicine for cardiometabolic disease: a framework for clinical translation
PW Franks et al, The Lancet Diabetes Endoc, October 4, 2023
Understanding diabetes heterogeneity: key steps towards precision medicine in diabetes
RD Leslie et al, The Lancet Diabetes and Endocrinology, October 4, 2023
Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine
DK Tobias et al, Nature Medicine, October 5, 2023
Participant characteristics in the prevention of gestational diabetes as evidence for precision medicine: a systematic review and meta-analysis
S Lim et al, Comm Medicine, October 5, 2023
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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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