Last Posted: Mar 30, 2023
- Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population.
Helkkula Pyry, et al. Communications biology 2023 0 (1) 71
- Risk Factors for Superficial Thrombophlebitis: A Retrospective Case Control Study.
Schamroth Pravda Miri, et al. The Israel Medical Association journal : IMAJ 2022 0 (12) 847-850
- Chronic venous insufficiency, cardiovascular disease, and mortality: a population study.
Prochaska Jürgen H, et al. European heart journal 2021 0 (40) 4157-4165
- [Frequency and risk factors for thromboembolic complications in patients with inflammatory bowel diseases].
Lishchinskaya A A, et al. Terapevticheskii arkhiv 2022 0 (2) 172-179
- Factor V Leiden mutation and high FVIII are associated with an increased risk of VTE in women with breast cancer during adjuvant tamoxifen - results from a prospective, single center, case control study.
Kovac Mirjana, et al. European journal of internal medicine 2015 0 (1) 63-7
- Varicose Veins and Risk of Venous Thromboembolic Diseases: A Two-Sample-Based Mendelian Randomization Study.
Li Ruihao, et al. Frontiers in cardiovascular medicine 2022 0 849027
- A genome-wide association study for varicose veins.
Lee Meng-Lin, et al. Phlebology 2022 1 2683555211069248
- Cardiometabolic, Lifestyle, and Nutritional Factors in Relation to Varicose Veins: A Mendelian Randomization Study.
Yuan Shuai, et al. Journal of the American Heart Association 2021 10 e022286
- Association of varicose veins with rare protein-truncating variants in PIEZO1 identified by exome sequencing of a large clinical population.
Smelser Diane T, et al. Journal of vascular surgery. Venous and lymphatic disorders 2021 8
- Investigation of association between genetic polymorphisms of MMP2, MMP8, MMP9 and TIMP2 and development of varicose veins in the Slovak Population - pilot study.
Mazuchová J, et al. Physiological research 2021 1 (Suppl 3) S443-S454
- Sex-Specific Genetically Predicted Iron Status in relation to 12 Vascular Diseases: A Mendelian Randomization Study in the UK Biobank.
Yang Fangkun et al. BioMed research international 2020 20206246041
- Exome sequencing and characterization of 49,960 individuals in the UK Biobank.
Van Hout Cristopher V et al. Nature 2020 Oct
- The Causal Effects of Blood Iron and Copper on Lipid Metabolism Diseases: Evidence from Phenome-Wide Mendelian Randomization Study.
Zhou Jingqi et al. Nutrients 2020 Oct 12(10)
- A variant of the castor zinc finger 1 (CASZ1) gene is differentially associated with the clinical classification of chronic venous disease.
Jones Gregory T, et al. Scientific reports 2019 9 (1) 14011
- Varicose veins of lower extremities: Insights from the first large-scale genetic study.
Shadrina Alexandra S, et al. PLoS genetics 2019 4 (4) e1008110
- Polymorphisms in inflammation-related genes and the risk of primary varicose veins in ethnic Russians.
Shadrina Alexandra, et al. Immunologic research 2018 0 (1) 141-150
- Incidence of the MTHFR polymorphisms in patients with varicose veins.
Ekim M, et al. Hippokratia 0 0 (4) 175-179
- Correction to: Polymorphisms of genes involved in inflammation and blood vessel development influence the risk of varicose veins.
Shadrina A, et al. Clinical genetics 2018 11 (5) 491
- The Effect of PAI-1 Gene Variants and PAI-1 Plasma Levels on Development of Thrombophilia in Patients With Klinefelter Syndrome.
Erkal Burcin, et al. American journal of men's health 2018 0 (6) 2152-2156
- Clinical and Genetic Determinants of Varicose Veins.
Fukaya Eri, et al. Circulation 2018 12 (25) 2869-2880
HLBS-PopOmics is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to Heart and Vascular Diseases(H), Lung Diseases(L), Blood Diseases(B), and Sleep Disorders(S)...more
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Mensah GA, Yu W, Barfield WL, Clyne M, Engelgau MM, Khoury MJ. HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders. Genet Med. 2018 Sep 10. doi: 10.1038/s41436-018-0118-1
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
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