Risk prediction of recurrent venous thromboembolism: a multiple genetic risk model

A Ahmad, K Sundquist, K Palmér, PJ Svensson… - Journal of Thrombosis …, 2019 - Springer
A single genetic biomarker is unable to accurately predict the risk for venous
thromboembolism (VTE) recurrence. We aimed to:(a) develop a multiple single nucleotide …

Genetic mutations in Turkish population with pulmonary embolism and deep venous thrombosis

E Kupeli, H Verdi, A Simsek, FB Atac… - Clinical and Applied …, 2011 - journals.sagepub.com
Venous thromboembolism (VTE) is a universal health hazard. Inherited and acquired risk
factors increase the risk of VTE. We evaluated the relationship between factor V (G1691A …

Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in …

Y Lu, Y Zhao, G Liu, X Wang, Z Liu, B Chen, R Hui - Thrombosis research, 2002 - Elsevier
A mutation in coagulant factor V gene, a substitution in the 3′ untranslated region of
prothrombin gene, and a variant in 5, 10-methylenetetrahydrofolate reductase (MTHFR) …

Genetic polymorphisms associated with acute pulmonary embolism and deep venous thrombosis

E Nizankowska-Mogilnicka, L Adamek… - European …, 2003 - Eur Respiratory Soc
Frequently an inherited predisposition to thrombosis remains clinically silent until an
additional environmental factor intervenes. The present study aimed to assess distribution of …

An evaluation of candidate genes of inflammation and thrombosis in relation to the risk of venous thromboembolism: the women's genome health study

RYL Zee, RJ Glynn, S Cheng, L Steiner… - Circulation …, 2009 - Am Heart Assoc
Background—Although pathways associated with hemostasis and thrombosis are well
documented to have an impact on venous thromboembolism (VTE), whether the …

Multilocus genetic risk scores for venous thromboembolism risk assessment

JM Soria, PE Morange, J Vila, JC Souto… - Journal of the …, 2014 - Am Heart Assoc
Background Genetics plays an important role in venous thromboembolism (VTE). Factor V
Leiden (FVL or rs6025) and prothrombin gene G20210A (PT or rs1799963) are the genetic …

Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels

G Antoni, T Oudot-Mellakh, A Dimitromanolakis… - BMC medical …, 2011 - Springer
Background Elevated levels of factor VIII (FVIII) and von Willebrand Factor (vWF) are well-
established risk factors for cardiovascular diseases, in particular venous thrombosis …

[HTML][HTML] Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes

HG de Haan, A van Hylckama Vlieg, LA Lotta… - Journal of Thrombosis …, 2018 - Elsevier
Essentials• Deep vein thrombosis (DVT) has a large unknown genetic component.• We
sequenced coding areas of 734 hemostasis‐related genes in 899 DVT patients and 599 …

Combined genetic mutations have remarkable effect on deep venous thrombosis and/or pulmonary embolism occurence

E Simsek, A Yesilyurt, F Pinarli, N Eyerci, AT Ulus - Gene, 2014 - Elsevier
Purpose Although deep vein thrombosis and thromboembolic diseases differ among various
races, they are still important in our day. The difficulties in treatment and following-up of …

Genetic association between plasminogen activator inhibitor‐1 rs1799889 polymorphism and venous thromboembolism: Evidence from a comprehensive meta …

G Huang, P Wang, T Li, X Deng - Clinical Cardiology, 2019 - Wiley Online Library
Background Association between plasminogen activator inhibitor‐1 (PAI‐1) rs1799889
polymorphism and venous thromboembolism (VTE) were explored by many previous …