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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: Apr 18, 2024
. (Total: 63623 Documents since 2012)
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Impact of Genetic Variations on Thromboembolic Risk in Saudis with Sickle Cell Disease.
Mohammad A Alshabeeb et al. Genes (Basel) 2023 14(10)
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Pharmacogenetic Sex-Specific Effects of Methotrexate Response in Patients with Rheumatoid Arthritis.
Francisco C Ceballos et al. Pharmaceutics 2023 15(6)
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Polygenic prediction of preeclampsia and gestational hypertension.
Michael C Honigberg et al. Nat Med 2023
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Interactions of SNPs in Folate Metabolism Related Genes on Prostate Cancer Aggressiveness in European Americans and African Americans.
Hui-Yi Lin et al. Cancers 2023 15(6)
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Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and gastric cancer susceptibility: an updated meta-analysis.
Yuwei Wang et al. Bioscience reports 2023
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The Roles of MTRR and MTHFR Gene Polymorphisms in Colorectal Cancer Survival.
Wang Yu et al. Nutrients 2022 14(21)
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Dutch pharmacogenetics working group guideline for the gene-drug interaction of ABCG2, HLA-B and Allopurinol, and MTHFR, folic acid and methotrexate.
van der Pol Karel H et al. European journal of human genetics : EJHG 2022
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Dutch pharmacogenetics working group guideline for the gene-drug interaction of ABCG2, HLA-B and Allopurinol, and MTHFR, folic acid and methotrexate
KH van der Pol et al, EJHG, September 2, 2022
Periconception Red Blood Cell Folate and Offspring Congenital Heart Disease : Nested Case-Control and Mendelian Randomization Studies.
Chen Hongyan et al. Annals of internal medicine 2022
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Association of Inherited Thrombophilia with Recurrent Pregnancy Loss in A Population of Lebanese Women: A Case Control Study.
Khalife Sara et al. International journal of fertility & sterility 2022 16(3) 247-251
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A call to action: MTHFR polymorphisms should not be a part of inherited thrombophilia testing.
Deloughery Thomas G et al. Research and practice in thrombosis and haemostasis 2022 6(4) e12739
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Polymorphisms and avascular necrosis in patients with sickle cell disease - A systematic review.
Leandro Márcio Passos et al. Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo 2022 40e2021013
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Methylenetetrahydrofolate Reductase Polymorphism (rs1801133) and the Risk of Hypertension among African Populations: A Narrative Synthesis of Literature.
Mabhida Sihle E et al. Genes 2022 13(4)
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Genetic Polymorphisms in a Familial Hypercholesterolemia Population from North-Eastern Europe.
Ma?taleru Alexandra et al. Journal of personalized medicine 2022 12(3)
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Use of a Consultation Service Following Pharmacogenomic Testing in Psychiatry.
Dowd Daniel et al. CNS spectrums 2021 26(2) 179-180
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Understanding Pregnancy Loss, Infertility, Birth Defects and the MTHFR gene: What Everyone Should Know
J Gunter, the Vajenda, March 27, 2021
Methylenetetrahydrofolate reductase gene polymorphism, global DNA methylation and blood pressure: a population based study from North India.
Yadav Suniti et al. BMC medical genomics 2021 14(1) 59
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Gene-Centric Database Reveals Environmental and Lifestyle Relationships for Potential Risk Modification and Prevention.
Martin Ron L et al. Lifestyle genomics 2021 Jan 1-7
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Pharmacogenetic aspects of methotrexate in a cohort of Colombian patients with rheumatoid arthritis.
Londono John et al. Biomedical reports 2020 Oct 13(4) 34
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Medical Decision Support to Reduce Unwarranted Methylene Tetrahydrofolate Reductase (MTHFR) Genetic Testing.
Parkhurst Emily et al. Journal of medical systems 2020 Jul 44(9) 152
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MTHFR Gene Polymorphisms Prevalence and Cardiovascular Risk Factors Involved in Cardioembolic Stroke Type and Severity.
Chita Dana Simona et al. Brain sciences 2020 Jul 10(8)
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Methylenetetrahydrofolate reductase polymorphisms and colorectal cancer prognosis: A meta-analysis.
Chen Xin-Lin et al. The journal of gene medicine 2019 21(9) e3114
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Addendum: ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing.
Bashford Michael T et al. Genetics in medicine : official journal of the American College of Medical Genetics 2020 Jun
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Clinical evaluation of germline polymorphisms associated with capecitabine toxicity in breast cancer: TBCRC-015.
O'Donnell Peter H et al. Breast cancer research and treatment 2020 May
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Genetic testing costs and compliance with clinical best practices.
Montanez Kathleen et al. Journal of genetic counseling 2020 May
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MTHFR Gene and Folic Acid
CDC, February 2020
Pharmacogenomics at the center of precision medicine: challenges and perspective in an era of Big Data.
Primorac Dragan et al. Pharmacogenomics 2020 Jan 21(2) 141-156
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Local Coverage Determination (LCD): Biomarkers Overview (L35062)
The U.S. Centers for Medicare & Medicaid Services
Hereditary thrombophilia genetic variants in recurrent pregnancy loss.
Ahangari Najmeh et al. Archives of gynecology and obstetrics 2019 Jul
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Comparison of Nutrigenomics Technology Interface Tools for Consumers and Health Professionals: A Sequential Explanatory Mixed Methods Investigation.
Araujo Almeida Vanessa et al. Journal of medical Internet research 2019 Jun 21(6) e12580
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Page last reviewed:
Feb 1, 2024
Page last updated:
Apr 18, 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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