G20210A prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects (Q35581904)

9 August 2017

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G20210A prothrombin gene polymorphism and coronary ischaemic syndromes: a phenotype-specific meta-analysis of 12 034 subjects (English)

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9 August 2017

Burzotta F

1

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9 August 2017

Paciaroni K

2

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9 August 2017

De Stefano V

3

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9 August 2017

Crea F

4

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9 August 2017

Maseri A

5

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9 August 2017

Leone G

6

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9 August 2017

Andreotti F

7

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9 August 2017

language of work or name

English

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publication date

1 January 2004

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9 August 2017

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9 August 2017

volume

90

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9 August 2017

issue

1

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9 August 2017

page(s)

82-86

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Genetic variation in coagulation and fibrinolytic proteins and their relation with acute myocardial infarction: a systematic review

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

Correlation of polymorphisms to coagulation and biochemical risk factors for cardiovascular diseases

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

Meta-analysis for model-free methods

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

Association studies of genetic polymorphisms and complex disease

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

Myocardial infarction in young patients

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

The venous thrombosis risk factor 20210 A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

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.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

Increased prevalence of the G20210A prothrombin gene variant in acute coronary syndromes without metabolic or acquired risk factors or with limited extent of disease.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

Platelet glycoprotein receptor IIIa polymorphism PLA1/PLA2 and coronary risk: a meta-analysis.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

Coagulation factors II, V, VII, and X, prothrombin gene 20210G-->A transition, and factor V Leiden in coronary artery disease: high factor V clotting activity is an independent risk factor for myocardial infarction.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

Prevalence of the prothrombin 20210 G-to-A variant in blacks: infants, patients with venous thrombosis, patients with myocardial infarction, and control subjects

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

Genetic risk factors in acute coronary disease

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1768005

Polymorphisms in the genes for coagulation factors II, V, and VII in patients with ischemic heart disease

15 November 2018

1 reference

12 December 2020

Lack of association of the prothrombin gene variant G20210A with myocardial infarction in Caucasian males

1 reference

12 December 2020

From syndromes to specific disease mechanisms. The search for the causes of myocardial infarction

1 reference

12 December 2020

G20210A prothrombin gene polymorphism and extent of coronary disease

1 reference

12 December 2020

A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women

1 reference

12 December 2020

Increased prevalence of a polymorphism in the gene coding for human prothrombin in patients with coronary heart disease

1 reference

12 December 2020

Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A

1 reference

12 December 2020

Prevalence of the prothrombin gene variant 20210 G --> A among patients with myocardial infarction

1 reference

12 December 2020

Geographic distribution of the 20210 G to A prothrombin variant

1 reference

12 December 2020

The prothrombin 20210 G to A variation and thrombosis

1 reference

12 December 2020

No association between the 20210 G/A prothrombin gene mutation and premature coronary artery disease

1 reference

12 December 2020

The prevalence of the prothrombin 20210 G-->A mutation is not increased in angiographically confirmed coronary artery disease

1 reference

12 December 2020

G20210A mutation in prothrombin gene and risk of myocardial infarction, stroke, and venous thrombosis in a large cohort of US men

1 reference

12 December 2020

The factor II G20210A and factor V G1691A gene transitions and coronary heart disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Synergistic effects of prothrombotic polymorphisms and atherogenic factors on the risk of myocardial infarction in young males

1 reference

12 December 2020

Prothrombotic genetic risk factors in young survivors of myocardial infarction

1 reference

12 December 2020

The prothrombin 20210A allele and its association with myocardial infarction

1 reference

12 December 2020

The 20210 G-->A mutation in the 3'-untranslated region of the prothrombin gene and the risk for arterial thrombotic disease

1 reference

12 December 2020

Prevalence of factor V Leiden and prothrombin variant G20210A in patients age <50 years with no significant stenoses at angiography three to four weeks after myocardial infarction

1 reference

12 December 2020

Genetic variation in coagulation factors II, V, VII and fatal MI

1 reference

12 December 2020

Identifiers

DOI

10.1136/HEART.90.1.82

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9 August 2017

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9 August 2017

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