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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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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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Evaluating thromboprophylaxis in the sickle cell disease population: Navigating the evidence gap.
Jennifer Davila et al. Br J Haematol 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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Lipoprotein(a), platelet function and cardiovascular disease.
Harpreet S Bhatia et al. Nat Rev Cardiol 2023
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Genomic science of risk prediction for venous thromboembolic disease: convenient clarification or compounding complexity.
Jihee Han et al. J Thromb Haemost 2023
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Acute Myocardial Infarction in Patients with Hereditary Thrombophilia-A Focus on Factor V Leiden and Prothrombin G20210A.
Minerva Codruta Badescu et al. Life (Basel) 2023 13(6)
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Thrombophilia Testing - a Systematic Review.
Lars Asmis et al. Clin Lab 2023 69(4)
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Assessing the performance of genetic risk score for stratifying risk of post-sepsis cardiovascular complications.
Brian McElligott et al. Frontiers in cardiovascular medicine 2023 101076745
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Identifying individuals at extreme risk of venous thromboembolism using polygenic risk scores.
Michael Chong et al. Nature genetics 2023 55(3) 358-360
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A practical guideline of genomics-driven drug discovery in the era of global biobank meta-analysis.
Shinichi Namba et al. Cell genomics 2023 2(10) 100190
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Impact of SERPINC1 mutation on thrombotic phenotype in children with congenital antithrombin deficiency - first analysis of the International Society on Thrombosis and Haemostasis (ISTH) Pediatric Antithrombin Deficiency Database and Biorepository.
Riten Kumar et al. Journal of thrombosis and haemostasis : JTH 2023
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The risk of major bleeding in patients with factor V Leiden or prothrombin G20210A gene mutation while on extended anticoagulant treatment for venous thromboembolism.
Lucia Caiano et al. Journal of thrombosis and haemostasis : JTH 2023
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Prediction of venous thromboembolism incidence in the general adult population using two published genetic risk scores.
Aaron R Folsom et al. PloS one 2023 18(1) e0280657
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Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism.
Ghouse Jonas et al. Nature genetics 2023
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Thromboembolic Disease in Haemophilic Patients Undergoing Major Orthopaedic Surgery: Is Thromboprophylaxis Mandatory?
Badulescu Oana Viola et al. Diagnostics (Basel, Switzerland) 2023 13(1)
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Association of Supernumerary Sex Chromosome Aneuploidies With Venous Thromboembolism.
Berry Alexander S F et al. JAMA 2023 329(3) 235-243
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Genome-Wide Association Study Identifies Copy Number Variants Associated with Warfarin Dose Response and Risk of Venous Thromboembolism in African Americans.
Zhang Honghong et al. Clinical pharmacology and therapeutics 2022
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A review of laboratory considerations in thrombophilia testing.
Ong Jeremy et al. Pathology 2022
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Epidemiology and prevention of venous thromboembolism.
Lutsey Pamela L et al. Nature reviews. Cardiology 2022
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Clinical and Genetic Risk Factors for Acute Incident Venous Thromboembolism in Ambulatory Patients With COVID-19
J Xie et al, JAMA Internal Medicine, August 18, 2022
Hereditary Thrombophilia Testing Among Hospitalized Patients: Is It Warranted?
Abughanimeh Omar K et al. Cureus 2022 14(5) e24855
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Shared genetic etiology and causality between COVID-19 and venous thromboembolism: evidence from genome-wide cross trait analysis and bi-directional Mendelian randomization study
X Huang et al, MEDRXIV, May 27, 2022
Shared genetic etiology and causality between COVID-19 and venous thromboembolism: evidence from genome-wide cross trait analysis and bi-directional Mendelian randomization study
X Huang et al, MEDRXIV, May 21, 2022
Whole exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Pankratz Nathan et al. Human molecular genetics 2022
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Genetic risk and incident venous thromboembolism in middle-aged and older adults following 1 Covid-19 vaccination
J Xie et al, MEDRXIV, April 18, 2022
Venous Thromboembolism in Ambulatory Covid-19 patients: Clinical and Genetic Determinants
J Xie et al, MEDRXIV, March 22, 2022
Oral postmenopausal hormone therapy and genetic risk on venous thromboembolism: gene-hormone interaction results from a large prospective cohort study.
Kim Jihye et al. Menopause (New York, N.Y.) 2022
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The utility of hereditary thrombophilia testing among patients with unprovoked venous thromboembolism.
Olivo Freites Cristina et al. International journal of laboratory hematology 2021
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The Angiotensin Converting Enzyme Deletion/Deletion Genotype Is a Risk Factor for Severe COVID-19: Implication and Utility for Patients Admitted to Emergency Department.
Annunziata Anna et al. Medicina (Kaunas, Lithuania) 2021 57(8)
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Venous thromboembolism incidence in cancer patients with germline BRCA mutations.
Muñoz A J et al. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2021
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Manifestations of HbSE sickle cell disease: a systematic review.
Khamees Ibrahim et al. Journal of translational medicine 2021 19(1) 262
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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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