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 (Q37604068)

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scientific article published on 31 July 2013

Language	Label	Description	Also known as
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

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

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Europe PubMed Central

21 August 2017

Véronique Ducros

21

object named as

Véronique Ducros

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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

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object named as

Donato Gemmati

17

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object named as

Ida Martinelli

5

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Martin den Heijer

object named as

Martin den Heijer

11

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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

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7

object named as

Elena Rossi

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Europe PubMed Central

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35

object named as

Emma De Feo

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Europe PubMed Central

21 August 2017

Simone Benedetto

1

object named as

Benedetto Simone

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Stefania Boccia

37

object named as

Stefania Boccia

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21 August 2017

author name string

Emanuele Leoncini

3

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Europe PubMed Central

21 August 2017

Jeppe Zacho

4

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Europe PubMed Central

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Joseph Emmerich

6

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Europe PubMed Central

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Wassim Y Almawi

9

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Europe PubMed Central

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Pierre Y Scarabin

10

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Europe PubMed Central

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Amparo Vaya

14

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Europe PubMed Central

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Pantep Angchaisuksiri

15

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Europe PubMed Central

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Gulfer Okumus

16

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Europe PubMed Central

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Simona Cima

18

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Europe PubMed Central

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Nejat Akar

19

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Europe PubMed Central

21 August 2017

Kivilcim I Oguzulgen

20

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Europe PubMed Central

21 August 2017

Christoph Lichy

22

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Europe PubMed Central

21 August 2017

Consuelo Fernandez-Miranda

23

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21 August 2017

José A Nieto

25

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Europe PubMed Central

21 August 2017

Jose Domingo Torres

26

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Europe PubMed Central

21 August 2017

Véronique Le Cam-Duchez

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Europe PubMed Central

21 August 2017

Petar Ivanov

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Europe PubMed Central

21 August 2017

Carlos Cantu-Brito

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Veronika M Shmeleva

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Europe PubMed Central

21 August 2017

Mojka Stegnar

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21 August 2017

Dotun Ogunyemi

32

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Europe PubMed Central

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Suhair S Eid

33

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Europe PubMed Central

21 August 2017

publication date

31 July 2013

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Europe PubMed Central

21 August 2017

European Journal of Epidemiology

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Europe PubMed Central

21 August 2017

28

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Europe PubMed Central

21 August 2017

621-647

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Europe PubMed Central

21 August 2017

8

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Europe PubMed Central

21 August 2017

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

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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

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

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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

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Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism

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

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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

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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.

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Pregnancy-associated venous thromboembolism: prevention and treatment

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Hormone therapies and venous thromboembolism: where are we now?

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

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

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

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

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Estrogen plus progestin and risk of venous thrombosis

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

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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

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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

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

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[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]

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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)

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