MTHFR C677T (rs1801133) genetic polymorphism is associated with development risk of essential hypertension in the Turkish population
Open Access
- 17 January 2022
- journal article
- research article
- Published by Springer Science and Business Media LLC in Egyptian Journal of Medical Human Genetics
- Vol. 23 (1), 1-8
- https://doi.org/10.1186/s43042-022-00221-z
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
- Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controlsEuropean Journal of Epidemiology, 2013
- Genetic association studies in pre-eclampsia: systematic meta-analyses and field synopsisInternational Journal of Epidemiology, 2012
- Association of Methylenetetrahydrofolate Reductase Gene 677C>T Polymorphism with Hypertension in Older Women in a Population of Buenos Aires CityClinical and Experimental Hypertension, 2012
- Gene panels to help identify subgroups at high and low risk of coronary heart disease among those randomized to antihypertensive treatmentPharmacogenetics and Genomics, 2012
- Combined Effect of Factor V Leiden,MTHFR, and Angiotensin-Converting Enzyme (Insertion/Deletion) Gene Mutations in Hypertensive Adult Individuals: A Population-Based Study from Sivas and Canakkale, TurkeyGenetic Testing and Molecular Biomarkers, 2011
- Riboflavin lowers blood pressure in cardiovascular disease patients homozygous for the 677C→T polymorphism in MTHFRJournal of Hypertension, 2010
- Frequency of Thrombophilia-Related Genetic Variations in Patients with Idiopathic Pulmonary Embolism in an Urban Emergency DepartmentClinical Chemistry, 2006
- Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wideJournal of Medical Genetics, 2003
- The risk of venous thromboembolism in family members with mutations in the genes of factor V or prothrombin or bothBritish Journal of Haematology, 2000
- Prothrombin G20210A Mutation: Is It Associated with Pre-Eclampsia?Gynecologic and Obstetric Investigation, 2000