(Q37604068)

English

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 controls

scientific article published on 31 July 2013

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

21 August 2017

0 references

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 controls (English)

1 reference

Europe PubMed Central

21 August 2017

venous thromboembolism

1 reference

based on heuristic

inferred from title

Factor V Leiden

1 reference

based on heuristic

inferred from title

12

object named as

Mary Cushman

1 reference

Europe PubMed Central

21 August 2017

Véronique Ducros

21

object named as

Véronique Ducros

1 reference

Europe PubMed Central

21 August 2017

Andrzej Szczeklik

24

object named as

Andrzej Szczeklik

1 reference

Europe PubMed Central

21 August 2017

Nicola Nicolotti

object named as

Nicola Nicolotti

34

0 references

object named as

Silvana Penco

13

0 references

object named as

Donato Gemmati

17

0 references

object named as

Ida Martinelli

5

0 references

Martin den Heijer

object named as

Martin den Heijer

11

0 references

Valerio De Stefano

object named as

Valerio De Stefano

2

0 references

Aaron R. Folsom

8

object named as

Aaron R Folsom

1 reference

Europe PubMed Central

21 August 2017

Walter Ricciardi

36

object named as

Walter Ricciardi

1 reference

Europe PubMed Central

21 August 2017

7

object named as

Elena Rossi

1 reference

Europe PubMed Central

21 August 2017

35

object named as

Emma De Feo

1 reference

Europe PubMed Central

21 August 2017

Simone Benedetto

1

object named as

Benedetto Simone

1 reference

Europe PubMed Central

21 August 2017

Stefania Boccia

37

object named as

Stefania Boccia

1 reference

Europe PubMed Central

21 August 2017

author name string

Emanuele Leoncini

3

1 reference

Europe PubMed Central

21 August 2017

Jeppe Zacho

4

1 reference

Europe PubMed Central

21 August 2017

Joseph Emmerich

6

1 reference

Europe PubMed Central

21 August 2017

Wassim Y Almawi

9

1 reference

Europe PubMed Central

21 August 2017

Pierre Y Scarabin

10

1 reference

Europe PubMed Central

21 August 2017

Amparo Vaya

14

1 reference

Europe PubMed Central

21 August 2017

Pantep Angchaisuksiri

15

1 reference

Europe PubMed Central

21 August 2017

Gulfer Okumus

16

1 reference

Europe PubMed Central

21 August 2017

Simona Cima

18

1 reference

Europe PubMed Central

21 August 2017

Nejat Akar

19

1 reference

Europe PubMed Central

21 August 2017

Kivilcim I Oguzulgen

20

1 reference

Europe PubMed Central

21 August 2017

Christoph Lichy

22

1 reference

Europe PubMed Central

21 August 2017

Consuelo Fernandez-Miranda

23

1 reference

Europe PubMed Central

21 August 2017

José A Nieto

25

1 reference

Europe PubMed Central

21 August 2017

Jose Domingo Torres

26

1 reference

Europe PubMed Central

21 August 2017

Véronique Le Cam-Duchez

27

1 reference

Europe PubMed Central

21 August 2017

Petar Ivanov

28

1 reference

Europe PubMed Central

21 August 2017

Carlos Cantu-Brito

29

1 reference

Europe PubMed Central

21 August 2017

Veronika M Shmeleva

30

1 reference

Europe PubMed Central

21 August 2017

Mojka Stegnar

31

1 reference

Europe PubMed Central

21 August 2017

Dotun Ogunyemi

32

1 reference

Europe PubMed Central

21 August 2017

Suhair S Eid

33

1 reference

Europe PubMed Central

21 August 2017

publication date

31 July 2013

1 reference

Europe PubMed Central

21 August 2017

European Journal of Epidemiology

1 reference

Europe PubMed Central

21 August 2017

28

1 reference

Europe PubMed Central

21 August 2017

621-647

1 reference

Europe PubMed Central

21 August 2017

8

1 reference

Europe PubMed Central

21 August 2017

https://scigraph.springernature.com/pub.10.1007/s10654-013-9825-8

0 references

Recommendations from the EGAPP Working Group: routine testing for Factor V Leiden (R506Q) and prothrombin (20210G>A) mutations in adults with a history of idiopathic venous thromboembolism and their adult family members

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Effects of race and ethnicity on the incidence of venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Management of venous thromboembolism: a clinical practice guideline from the American College of Physicians and the American Academy of Family Physicians

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

The pathogenesis of venous thromboembolism: evidence for multiple interrelated causes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

A nonsense polymorphism in the protein Z-dependent protease inhibitor increases the risk for venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Does use of hormonal contraceptives among women with thrombogenic mutations increase their risk of venous thromboembolism? A systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Prothrombotic mutations, hormone therapy, and venous thromboembolism among postmenopausal women: impact of the route of estrogen administration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Marburg I polymorphism of factor VII-activating protease is associated with idiopathic venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Cardiology patient pages. Prothrombin 20210 mutation (factor II mutation).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Deep vein thrombosis and pulmonary embolism in two cohorts: the longitudinal investigation of thromboembolism etiology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

The epidemiology of venous thromboembolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Screening for inherited thrombophilia: indications and therapeutic implications.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Polymorphisms in the methylenetetrahydrofolate reductase gene: clinical consequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

A prospective study of venous thromboembolism in relation to factor V Leiden and related factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Methionine synthase A2756G and methylenetetrahydrofolate reductase A1298C polymorphisms are not risk factors for idiopathic venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Genetics University of Toronto Thrombophilia Study in Women (GUTTSI): genetic and other risk factors for venous thromboembolism in women

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Factor V G1691A and prothrombin G20210A in childhood spontaneous venous thrombosis--evidence of an age-dependent thrombotic onset in carriers of factor V G1691A and prothrombin G20210A mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Laboratory diagnosis of vitamin B12 and folate deficiency: a guide for the primary care physician

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Epidemiology of factor V Leiden: clinical implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

23 August 2017

Pregnancy-associated venous thromboembolism: prevention and treatment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

6 September 2017

Hormone therapies and venous thromboembolism: where are we now?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

6 September 2017

Distinct association of factor V-Leiden and prothrombin G20210A mutations with deep venous thrombosis in Tunisia and Lebanon

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

6 September 2017

Risk factors for deep vein thrombosis and pulmonary embolism: a population-based case-control study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

6 September 2017

Relation of three genetic traits to venous thrombosis in an African-American population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

6 September 2017

Gain-of-function gene mutations and venous thromboembolism: distinct roles in different clinical settings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

25 June 2018

Estrogen plus progestin and risk of venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

25 June 2018

Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

25 June 2018

The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

25 June 2018

The factor V gene A4070G mutation and the risk of venous thrombosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

25 June 2018

The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

25 June 2018

The VITA project: C677T mutation in the methylene-tetrahydrofolate reductase gene and risk of venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

25 June 2018

Parental history and venous thromboembolism: a nationwide study of age-specific and sex-specific familial risks in Sweden.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Major and potential prothrombotic genotypes in patients with venous thrombosis and in healthy subjects from Slovenia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Should plasma homocysteine be used as a biomarker of venous thromboembolism? A case-control study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

The risk of first venous thromboembolism during pregnancy and puerperium in double heterozygotes for factor V Leiden and prothrombin G20210A.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Impact of thrombophilic genetic factors on pulmonary embolism: early onset and recurrent incidences.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Hereditary thrombophilic risk factors and venous thromboembolism in Istanbul, Turkey: the role in different clinical manifestations of venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

No association between the common MTHFR 677C->T polymorphism and venous thrombosis: results from the MEGA study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

The FXIIIVal34Leu, common and risk factors of venous thrombosis in early middle-age Costa Rican patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Interrelation of hyperhomocysteinemia and inherited risk factors for venous thromboembolism. Results from the E.D.I.TH. study: a hospital-based case-control study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

[C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Factor V Leiden (G1691A) and prothrombin-G20210A alleles among patients with deep venous thrombosis and in the general population from Spain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Assessment of the role of genetic polymorphism in venous thrombosis through artificial neural networks.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Risk of cerebral venous thrombosis and novel gene polymorphisms of the coagulation and fibrinolytic systems.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Low levels of vitamin B12 and venous thromboembolic disease in elderly men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Effect of hyperhomocysteinemia and methylenetetrahydrofolate reductase 677C --> T mutation in venous thromboembolism risk of young adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Methylenetetrahydrofolate reductase polymorphism (C677T), hyperhomocysteinemia, and risk of ischemic cardiovascular disease and venous thromboembolism: prospective and case-control studies from the Copenhagen City Heart Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Hyperhomocysteinemia, low folate and vitamin B12 concentrations, and methylene tetrahydrofolate reductase mutation in cerebral venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Association of factor V deficiency with factor V HR2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Prevalence of hyperhomocysteinemia and the MTHFR C677T polymorphism in patients with arterial and venous thrombosis from North Western Russia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Venous thromboembolism, oral contraceptives and high prothrombin levels.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

The epidemiology of venous thromboembolism in Caucasians and African-Americans: the GATE Study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Hyperhomocysteinemia in cerebral vein thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Association between inherited thrombophilias, antiphospholipid antibodies, and lipoprotein A levels and venous thromboembolism in pregnancy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Genetic polymorphisms associated with acute pulmonary embolism and deep venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Coagulation factor V G allele and HR2 haplotype: factor V activity, activated protein C resistance and risk of venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

CBS 844ins68, MTHFR TT677 and EPCR 4031ins23 genotypes in patients with deep-vein thrombosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Lack of association between the C677T mutation in the 5,10-methylenetetrahydrofolate reductase gene and venous thromboembolism in Northwestern Greece

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Hyperhomocysteinemia and venous thromboembolism: a risk factor more prevalent in the elderly and in idiopathic cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Hyperhomocysteinemia increases the risk of venous thrombosis independent of the C677T mutation of the methylenetetrahydrofolate reductase gene in selected Brazilian patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Red blood cell methylfolate and plasma homocysteine as risk factors for venous thromboembolism: a matched case-control study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Major and potential prothrombotic genotypes in a cohort of patients with venous thromboembolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Comparative prevalence of antiphospholipid antibodies and thrombophilic genotypes in consecutive patients with venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Prevalence of factor V Leiden and prothrombin 20210 A variant in Bulgarian patients with pulmonary thromboembolism and deep venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism--pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study Group for Pooled-Analysis in Venous Thromboembolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Increased lipoprotein (a) levels as an independent risk factor for venous thromboembolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Contribution of the cystathionine beta-synthase gene (844ins68) polymorphism to the risk of early-onset venous and arterial occlusive disease and of fasting hyperhomocysteinemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Prevalence of methylenetetrahydrofolate reductase mutations in patients with venous thrombosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Thrombophilic predisposition in stroke and venous thromboembolism in Danish patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

A common polymorphism in the tumour necrosis factor-alpha gene associated with high TNF levels is not a risk factor for venous thromboembolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

The mutation G20210-->A in the prothrombin gene is a strong risk factor for pulmonary embolism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

The methylenetetrahydrofolate reductase TT677 genotype is associated with venous thrombosis independently of the coexistence of the FV Leiden and the prothrombin A20210 mutation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Plasma homocysteine as a risk factor for vascular disease. The European Concerted Action Project.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

1 September 2018

Familial risk of venous thromboembolism: a nationwide cohort study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3935237

3 December 2018

A prothrombin gene mutation is significantly associated with venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3'-untranslated region of the prothrombin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prothrombin G20210A, factor V Leiden, and factor XIII Val34Leu: common mutations of blood coagulation factors and deep vein thrombosis in Austria

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relative impact of risk factors for deep vein thrombosis and pulmonary embolism: a population-based study

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of factor V Leiden and prothrombin G20210A mutations in unselected patients with venous thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The deletion polymorphism in the angiotensin-converting enzyme gene is a moderate risk factor for venous thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase C677T genotype and venous thromboembolic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of plasminogen activator inhibitor-1 polymorphism, factor-V-Leiden, and prothrombin-20210 mutations in pulmonary thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The TFPI 536C-->T mutation is not associated with increased risk for venous or arterial thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ACE D/D genotype is protective against the development of idiopathic deep vein thrombosis and pulmonary embolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The value of family history as a risk indicator for venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mutation Ala677-->Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prothrombin 20210A allele and the factor V Leiden are associated with venous thrombosis but not with early coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of polymorphisms in the 5'-untranslated region of the TAFI gene: relationship with plasma TAFI levels and risk of venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The PlA1/A2 polymorphism of platelet glycoprotein IIIa is not associated with deep venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The angiotensin-converting-enzyme insertion/deletion polymorphism is not related to venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Geographic distribution of the 20210 G to A prothrombin variant

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of methylenetetrahydrofolate reductase 677 C-T, 1298 A-C, and 1317 T-C on factor V 1691 mutation in Turkish deep vein thrombosis patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphism of methylenetetrahydrofolate reductase and venous thromboembolism: a case-control study

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Leiden (R506Q) and risk of venous thromboembolism: a case-control study based on the Spanish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oral contraceptives, hormone replacement therapy, thrombophilias and risk of venous thromboembolism: a systematic review

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of Venous Thrombosis in Carriers of a Common Mutation in the Homocysteine Regulatory Enzyme Methylenetetrahydrofolate Reductase

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C677T mutation in the methylene tetrahydrofolate reductase gene as a risk factor for venous thrombotic disease in Austrian patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The PORtromb Project: prothrombin G20210A mutation and venous thromboembolism in young people

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor XIII Val34Leu polymorphism and risk of deep vein thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of the protein C promoter CG haplotype and the factor II G20210A mutation is a risk factor for cerebral venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of the C677T methylenetetra- hydrofolate reductase mutation in Thai patients with deep vein thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish population

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Leiden prevalence in venous thromboembolism patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allele 4G of gene PAI-1 associated with prothrombin mutation G20210A increases the risk for venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Homocysteine, 5,10-methylenetetrahydrofolate reductase and deep venous thrombosis. Survey of 120 patients in internal medicine]

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Low folate levels and thermolabile methylenetetrahydrofolate reductase as primary determinant of mild hyperhomocystinemia in normal and thromboembolic subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The risk of recurrent venous thromboembolism in carriers and non-carriers of the G1691A allele in the coagulation factor V gene and the G20210A allele in the prothrombin gene. DURAC Trial Study Group. Duration of Anticoagulation

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inherited Thrombophilic Risk Factors and Venous Thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Increased Factor V Leiden frequency is associated with venous thrombotic events among young Brazilian patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Definitions of infertility and recurrent pregnancy loss

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The C677T MTHFR variant and the risk of venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The factor V R2 allele: risk of venous thromboembolism, factor V levels and resistance to activated protein C

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in the TAFI gene and the risk of venous thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk of venous thromboembolism associated with the common hereditary haemochromatosis Hfe gene (C282Y) mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Update on factor V Leiden association with venous thromboembolism in the LITE Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second mutation in the methylenetetrahydrofolate reductase gene and the risk of venous thrombotic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prothrombin nt20210 A allele as a risk factor for venous thromboembolism: detection of heterozygous and homozygous carriers by alternative methods

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prothrombin G20210A gene mutation and further prothrombotic risk factors in childhood thrombophilia

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Turkish patients with thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Effect of the angiotensin-converting enzyme gene deletion polymorphism on the risk of venous thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Different circumstances of the first venous thromboembolism among younger or older heterozygous carriers of the G20210A polymorphism in the prothrombin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thermolabile methylenetetrahydrofolate reductase and factor V Leiden in the risk of deep-vein thrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comparison of polymorphism in the 3'-untranslated region of the prothrombin gene between Chinese and Caucasians in Australia

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence and association of the factor V Leiden and prothrombin G20210A in healthy subjects and patients with venous thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prevalence of factor V Leiden as a risk factor for venous thromboembolism in the population of North-Western Greece

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prothrombin G20210A mutation and oral contraceptive use increase upper-extremity deep vein thrombotic risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Factor V Leiden and factor V R2 allele: high-throughput analysis and association with venous thromboembolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/23900608

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10654-013-9825-8

1 reference

Europe PubMed Central

21 August 2017

1 reference

Europe PubMed Central

21 August 2017

1 reference

Europe PubMed Central

21 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q37604068&oldid=1754984543"