(Q37441260)

20 August 2017

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title

Creating a genetic risk score for coronary artery disease (English)

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20 August 2017

Sonny Dandona

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20 August 2017

Robert Roberts

series ordinal

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20 August 2017

publication date

1 May 2009

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Current Atherosclerosis Reports

20 August 2017

published in

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20 August 2017

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20 August 2017

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20 August 2017

page(s)

175-181

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Lack of MEF2A mutations in coronary artery disease

20 August 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11883-009-0028-4

The matrix metalloproteinase-3 (MMP-3) 5A/6A promoter polymorphism is not associated with ischaemic heart disease: analysis employing a family based approach.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11883-009-0028-4

Association between C1019T polymorphism of connexin37 and acute myocardial infarction: a study in patients from Sicily.

21 January 2018

1 reference

12 December 2020

Genetics of premature myocardial infarction

1 reference

12 December 2020

Association of the Trp719Arg polymorphism in kinesin-like protein 6 with myocardial infarction and coronary heart disease in 2 prospective trials: the CARE and WOSCOPS trials.

1 reference

12 December 2020

The molecular mechanism for the genetic disorder familial defective apolipoprotein B100.

1 reference

12 December 2020

Lack of support for association between common variation in TNFSF4 and myocardial infarction in a German population

1 reference

12 December 2020

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

12 December 2020

A common variant on chromosome 9p21 affects the risk of myocardial infarction

1 reference

12 December 2020

A kinesin family member 6 variant is associated with coronary heart disease in the Women's Health Study

1 reference

12 December 2020

Thrombospondin-4 A387P polymorphism is not associated with coronary artery disease and myocardial infarction in the Chinese Han population

1 reference

12 December 2020

Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study

1 reference

12 December 2020

Do allelic variants of the connexin37 1019 gene polymorphism differentially predict for coronary artery disease and myocardial infarction?

1 reference

12 December 2020

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction

1 reference

12 December 2020

Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease

1 reference

12 December 2020

Robust association of the APOE ?4 allele with premature myocardial infarction especially in patients without hypercholesterolaemia: the Aachen study

1 reference

12 December 2020

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

1 reference

12 December 2020

Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction

1 reference

12 December 2020

A common allele on chromosome 9 associated with coronary heart disease

1 reference

12 December 2020

Relationship of the CAG repeat polymorphism of the MEF2A gene and coronary artery disease in a Chinese population

1 reference

12 December 2020

Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men.

1 reference

12 December 2020

Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease

1 reference

12 December 2020

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

1 reference

12 December 2020

Genomewide association analysis of coronary artery disease

1 reference

12 December 2020

Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease

1 reference

12 December 2020

Autosomal recessive hypercholesterolemia

1 reference

12 December 2020

Mutation of MEF2A in an inherited disorder with features of coronary artery disease

1 reference

12 December 2020

Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations

1 reference

12 December 2020

Genetically elevated C-reactive protein and ischemic vascular disease

1 reference

12 December 2020

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

1 reference

12 December 2020

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction

1 reference

12 December 2020

Multiple less common genetic variants explain the association of the cholesteryl ester transfer protein gene with coronary artery disease

1 reference

12 December 2020

Positional identification of TNFSF4, encoding OX40 ligand, as a gene that influences atherosclerosis susceptibility

1 reference

12 December 2020

Prediction of the risk of myocardial infarction from polymorphisms in candidate genes

1 reference

12 December 2020

Seven haemostatic gene polymorphisms in coronary disease: meta-analysis of 66,155 cases and 91,307 controls.

1 reference

12 December 2020

Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients

1 reference

12 December 2020

Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction

1 reference

12 December 2020

Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study

1 reference

12 December 2020

Polymorphism in KIF6 gene and benefit from statins after acute coronary syndromes: results from the PROVE IT-TIMI 22 study.

1 reference

12 December 2020

Familial hypercholesterolemia: defective binding of lipoproteins to cultured fibroblasts associated with impaired regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity

1 reference

12 December 2020

10.1007/S11883-009-0028-4

Identifiers

DOI

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20 August 2017

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