(Q52951935)

9 May 2018

title

Overestimation of genetic risks owing to small sample sizes in cardiovascular studies. (English)

1 reference

9 May 2018

1 reference

Morgan TM

1

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9 May 2018

Coffey CS

series ordinal

2

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9 May 2018

Krumholz HM

series ordinal

3

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9 May 2018

publication date

1 July 2003

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9 May 2018

published in

Clinical Genetics

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9 May 2018

volume

64

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9 May 2018

issue

1

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9 May 2018

page(s)

7-17

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9 May 2018

A meta-analysis of the association of the deletion allele of the angiotensin-converting enzyme gene with myocardial infarction

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ACE gene polymorphism as a risk factor for ischemic cerebrovascular disease

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Enhanced predictability of myocardial infarction in Japanese by combined genotype analysis

21 January 2018

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Deletion polymorphism of the angiotensin I-converting enzyme gene is associated with increased plasma angiotensin-converting enzyme activity but not with increased risk for myocardial infarction and coronary artery disease.

21 January 2018

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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).

21 January 2018

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Activated protein c resistance (APC) and inherited factor V (FV) mis‐sense mutation in patients with venous and arterial thrombosis in a haematology clinic

21 January 2018

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Increased risk for venous thrombosis in carriers of the prothrombin G-->A20210 gene variant.

21 January 2018

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ACE gene polymorphism in cardiovascular disease: meta-analyses of small and large studies in whites

21 January 2018

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Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators

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Plasma level and gene polymorphism of angiotensin-converting enzyme in relation to myocardial infarction

21 January 2018

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Lack of association between angiotensin-converting enzyme gene polymorphism and coronary heart disease in a Chinese population

21 January 2018

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Lack of association of angiotensin converting enzyme gene polymorphism or serum enzyme activity with coronary artery disease in Japanese subjects

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Gene Polymorphism but not Catalytic Activity of Angiotensin I–Converting Enzyme Is Associated With Coronary Artery Disease and Myocardial Infarction in Low-Risk Patients

21 January 2018

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The II genotype of the angiotensin-converting enzyme gene delays the onset of acute coronary syndromes

21 January 2018

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Angiotensin-converting enzyme gene polymorphism is associated with myocardial infarction but not with development of coronary stenosis

21 January 2018

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Association of ACE gene polymorphisms with coronary artery disease in a northern area of Japan

21 January 2018

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Genotype distribution of angiotensin-converting enzyme polymorphism in Australian healthy and coronary populations and relevance to myocardial infarction and coronary artery disease

21 January 2018

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Activated protein C resistance and factor V Leiden mutation are independent risk factors for venous thromboembolism

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Assessment of genetic markers for coronary thrombosis: promise and precaution

21 January 2018

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7 January 2021

Power and replication in case-control studies

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7 January 2021

Publication bias: a brief review for clinicians

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7 January 2021

Platelet glycoprotein polymorphisms as risk factors for thrombosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Activated protein C resistance due to a common factor V gene mutation is a major risk factor for venous thrombosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Linkage between inherited resistance to activated protein C and factor V gene mutation in venous thrombosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Associations between a polymorphism in the gene encoding glycoprotein IIIa and myocardial infarction or coronary artery disease

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https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Acute myocardial infarction in young adults: Prognostic role of angiotensin-converting enzyme, angiotensin II type I receptor, apolipoprotein E, endothelial constitutive nitric oxide synthase, and glycoprotein IIIa genetic polymorphisms at medium-ter

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Increased binding of fibrinogen to glycoprotein IIIa-proline33 (HPA-1b, PlA2, Zwb) positive platelets in patients with cardiovascular disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Polymorphisms of HPA-1 through 6 on platelet membrane glycoprotein receptors are not a genetic risk factor for myocardial infarction in the Japanese population

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

The relationship between polymorphisms in the endothelial cell nitric oxide synthase gene and the platelet GPIIIa gene with myocardial infarction and venous thromboembolism in African Americans

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Lipoprotein(a) and the significance of the association between platelet glycoprotein IIIa polymorphisms and the risk of premature myocardial infarction.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Genetic polymorphism of platelet glycoprotein IIIa in patients with acute myocardial infarction and acute ischaemic stroke

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

PIa1/a2 polymorphism of glycoprotein IIIa and risk of coronary artery disease and restenosis following coronary angioplasty

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Platelet glycoprotein IIIa PlA polymorphism and myocardial infarction

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Glycoprotein IIIa PlA1/A2 polymorphism and sudden cardiac death

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Platelet glycoprotein IIIa gene polymorphism and myocardial infarction

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Array-based multiplex analysis of candidate genes reveals two independent and additive genetic risk factors for myocardial infarction in the Finnish population

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

PIA1/A2 polymorphism of platelet glycoprotein IIIa and risks of myocardial infarction, stroke, and venous thrombosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Glycoprotein IIIa polymorphism and risk of myocardial infarction.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Lack of relationship between the P1A1/P1A2 polymorphism of platelet glycoprotein IIIa and premature myocardial infarction

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Platelet glycoprotein IIb/IIIa genetic polymorphism is associated with plasma fibrinogen levels in myocardial infarction patients. The REGICOR Investigators.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

A polymorphism of a platelet glycoprotein receptor as an inherited risk factor for coronary thrombosis.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Deletion polymorphism at the angiotensin-converting enzyme gene in Turkish patients with coronary artery disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Angiotensin-converting enzyme genotypes and risk for myocardial infarction in women.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Angiotensin converting enzyme gene deletion allele is independently and strongly associated with coronary atherosclerosis and myocardial infarction

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Angiotensin-converting enzyme gene polymorphism is not associated with coronary atherosclerosis and myocardial infarction in a sample of Italian patients

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Association of genetic polymorphisms in the ACE, ApoE, and TGF beta genes with early onset ischemic heart disease.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Atherogenic, hemostatic, and other potential risk markers in subjects with previous isolated myocardial infarction compared with long-standing uncomplicated stable angina.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Insertion/deletion (I/D) polymorphism at the locus for angiotensin I-converting enzyme and myocardial infarction

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Deletion polymorphism in the gene for angiotensin-converting enzyme is a potent risk factor for myocardial infarction

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Angiotensin I-converting enzyme gene polymorphism in a low-risk European population for coronary artery disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

A deletion polymorphism in the angiotensin converting enzyme gene is not associated with coronary heart disease in an Austrian population

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

ACE I/D gene polymorphism: presence of the ACE D allele increases the risk of coronary artery disease in younger individuals

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Association of angiotensinogen gene T235 variant with increased risk of coronary heart disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Angiotensin II type-I receptor and ACE polymorphisms and risk of myocardial infarction in men and women

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Angiotensinogen and angiotensin-I converting enzyme gene polymorphisms and the risk of coronary artery disease in Chinese

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

A prospective evaluation of an angiotensin-converting-enzyme gene polymorphism and the risk of ischemic heart disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Associations between candidate loci angiotensin-converting enzyme and angiotensinogen with coronary heart disease and myocardial infarction: the NHLBI Family Heart Study

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Angiotensin-converting enzyme and apolipoproteins genes polymorphism in coronary artery disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Significance of angiotensin I-converting enzyme and angiotensin II type 1 receptor gene polymorphisms as risk factors for coronary heart disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Insertion/deletion polymorphism of the angiotensin I-converting enzyme gene is associated with coronary artery plaque calcification as assessed by intravascular ultrasound

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

An angiotensin-converting enzyme gene variant is associated with acute myocardial infarction in women but not in men.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Angiotensin-I-converting enzyme DD genotype is a risk factor of coronary artery disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

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://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Factor V Leiden prevalence in venous thromboembolism patients

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Inherited Thrombophilic Risk Factors and Venous Thromboembolism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

The factor VR506Q mutation causing APC resistance is highly prevalent amongst unselected outpatients with clinically suspected deep venous thrombosis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Factor V Leiden paradox: risk of deep-vein thrombosis but not of pulmonary embolism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Publication bias in meta-analysis: its causes and consequences

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

Meta-analysis of multiple outcomes by regression with random effects.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

The continuing unethical conduct of underpowered clinical trials.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00088.X

7 January 2021

10.1034/J.1399-0004.2003.00088.X

Identifiers

DOI

1 reference

9 May 2018

1 reference

9 May 2018