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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|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Heart, Lung, Blood and Sleep Disorders
Last data update: Jun 21, 2024
. (Total: 64207 Documents since 2012)
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Stroke, Myocardial Infarction, and Pulmonary Embolism after Bivalent Booster.
Marie-Joelle Jabagi et al. N Engl J Med 2023 388(15) 1431-1432
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Vaccination status and long COVID symptoms in patients discharged from hospital.
Teresa Cristina D C Nascimento et al. Scientific reports 2023 13(1) 2481
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Epidemiology and prevention of venous thromboembolism.
Lutsey Pamela L et al. Nature reviews. Cardiology 2022
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Myocardial Infarction, Stroke, and Pulmonary Embolism After BNT162b2 mRNA COVID-19 Vaccine in People Aged 75 Years or Older
MJ Jabagi et al, JAMA,November 22,2021
Safety of the BNT162b2 mRNA Covid-19 Vaccine in a Nationwide Setting.
Barda Noam et al. The New England journal of medicine 2021
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Natural history of patients with venous thromboembolism and hereditary hemorrhagic telangiectasia. Findings from the RIETE registry.
Riera-Mestre Antoni et al. Orphanet journal of rare diseases 2019 14(1) 196
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New Precision Medicine Treatment Could Benefit Many Men with Treatment-Resistant Metastatic Prostate Cancer
by Andrea K. Miyahira, Prostate Cancer Foundation, October 1, 2019
Venous Thromboembolism (Blood Clots) and Cancer
CDC, October 2019
Thrombin generation profile in non-thrombotic factor V Leiden carriers.
Billoir Paul et al. Journal of thrombosis and thrombolysis 2019 Apr 47(3) 473-477
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CLINGEN Actionability Report for Factor V Leiden, Homozygous (also includes compound heterozygous FVL + prothrombin G20210A) - F5
ClinGen Actionability Working Group
CLINGEN Actionability Report for Thrombophilia due to protein S deficiency - PROS1
ClinGen Actionability Working Group
CLINGEN Actionability Report for Factor V Leiden, Heterozygous - F5
ClinGen Actionability Working Group
CLINGEN Actionability Report for Thrombophilia due to protein C deficiency - PROC
ClinGen Actionability Working Group
Pathophysiology, diagnosis and management of peripartum cardiomyopathy: a position statement from the Heart Failure Association of the European Society of Cardiology Study Group on peripartum cardiomyopathy.
Bauersachs Johann et al. European journal of heart failure 2019 Jun
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Clinical Outcomes Associated With Sickle Cell Trait: A Systematic Review.
Naik Rakhi P, et al. Annals of internal medicine 2018 11 0. (9) 619-627
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Systematic review study supports that sickle cell trait increases risk for some health conditions- More research needed to clarify all health outcomes associated with SCT
J Mjoseth, NHGRI, October 30, 2018
Utilizing Whole-Exome Sequencing to Characterize the Phenotypic Variability of Sickle Cell Disease.
Alsultan Abdulrahman et al. Genetic testing and molecular biomarkers 2018 Sep
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Cost Effectiveness of Genotype-Guided Warfarin Dosing in Patients with Mechanical Heart Valve Replacement Under the Fee-for-Service System.
Kim Dong-Jin et al. Applied health economics and health policy 2017 Oct 15(5) 657-667
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The impact of real-world cardiovascular-related pharmacogenetic testing in an insured population.
Billings Jennifer et al. International journal of clinical practice 2018 May e13088
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Laboratory Testing for Activated Protein C Resistance (APCR).
Mohammed Soma et al. Methods in molecular biology (Clifton, N.J.) 2017 1646137-143
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Personal Stories of People Living with Deep Vein Thrombosis and Pulmonary Embolism
Are you at risk for clots?
A family history of blood clots can increase a person?s risk.
Hereditary Thrombophilia in Trauma Patients with Venous Thromboembolism: Is Routine Screening Necessary?
Cannon Kathleen A et al. The journal of trauma and acute care surgery 2017 Nov
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Impact of ABCB1 and CYP2D6 polymorphisms on tamoxifen treatment outcomes and adverse events in breast cancer patients.
Argalacsova Sona et al. Journal of B.U.ON. : official journal of the Balkan Union of Oncology 22(5) 1217-1226
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Family history of venous thromboembolism (VTE) and risk of recurrent hospitalization for VTE: a nationwide family study in Sweden.
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Page last reviewed:
Feb 1, 2024
Page last updated:
Jun 21, 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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