(Q36843011)

16 August 2017

1 reference

title

Molecular genetics of myocardial infarction (English)

1 reference

16 August 2017

1 reference

myocardial infarction

1 reference

Yoshiji Yamada

1

1 reference

16 August 2017

Sahoko Ichihara

series ordinal

2

1 reference

16 August 2017

Tamotsu Nishida

series ordinal

3

1 reference

16 August 2017

1 January 2008

1 reference

16 August 2017

1 reference

16 August 2017

2

1 reference

16 August 2017

1-2

1 reference

16 August 2017

7-22

1 reference

Collaborative pooled analysis of data on C-reactive protein gene variants and coronary disease: judging causality by Mendelian randomisation

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

How to interpret a genome-wide association study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A comparison of bare-metal and drug-eluting stents for off-label indications

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

C-reactive protein (CRP) gene polymorphisms, CRP levels, and risk of incident coronary heart disease in two nested case-control studies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Genetic risk for myocardial infarction determined by polymorphisms of candidate genes in a Japanese population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Future use of genomics in coronary artery disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A second generation human haplotype map of over 3.1 million SNPs

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Mechanisms of disease: The genetic basis of coronary heart disease.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Genomewide association analysis of coronary artery disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Relevance of genetics and genomics for prevention and treatment of cardiovascular disease: a scientific statement from the American Heart Association Council on Epidemiology and Prevention, the Stroke Council, and the Functional Genomics and Transla

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A common allele on chromosome 9 associated with coronary heart disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Heart disease and stroke statistics--2007 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Increased risk of acute myocardial infarction and elevated levels of C-reactive protein in carriers of the Thr-87 variant of the ATP receptor P2Y11

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Identification of genetic factors and development of genetic risk diagnosis systems for cardiovascular diseases and stroke

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Genetic susceptibility to myocardial infarction and coronary artery disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Inflammatory gene polymorphisms and risk of postoperative myocardial infarction after cardiac surgery

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

The thrombospondin-1 N700S polymorphism is associated with early myocardial infarction without altering von Willebrand factor multimer size

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Meta-analysis of MTHFR 677C->T polymorphism and coronary heart disease: does totality of evidence support causal role for homocysteine and preventive potential of folate?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Identification of four gene variants associated with myocardial infarction

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

CCL2 polymorphisms are associated with serum monocyte chemoattractant protein-1 levels and myocardial infarction in the Framingham Heart Study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

VEGF polymorphisms and severity of atherosclerosis.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

What can mendelian randomisation tell us about modifiable behavioural and environmental exposures?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Association between the gene encoding 5-lipoxygenase-activating protein and stroke replicated in a Scottish population

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Finishing the euchromatic sequence of the human genome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Meta-analysis: apolipoprotein E genotypes and risk for coronary heart disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

APOA5 gene variants, lipoprotein particle distribution, and progression of coronary heart disease: results from the LOCAT study

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Arachidonate 5-lipoxygenase promoter genotype, dietary arachidonic acid, and atherosclerosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease?*

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Alanine for proline substitution in the peroxisome proliferator-activated receptor gamma-2 (PPARG2) gene and the risk of incident myocardial infarction

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Association of polymorphism in glutamate-cysteine ligase catalytic subunit gene with coronary vasomotor dysfunction and myocardial infarction

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Expanding expression of the 5-lipoxygenase pathway within the arterial wall during human atherogenesis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Genetic epidemiological studies of coronary heart disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Polymorphism in the 5'-flanking region of human glutamate-cysteine ligase modifier subunit gene is associated with myocardial infarction

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Apolipoprotein E polymorphism and cardiovascular disease: a HuGE review

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Identification of the G994--> T missense in exon 9 of the plasma platelet-activating factor acetylhydrolase gene as an independent risk factor for coronary artery disease in Japanese men.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Polymorphism of the NADH/NADPH oxidase p22 phox gene in patients with coronary artery disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Common mutation in methylenetetrahydrofolate reductase. Correlation with homocysteine metabolism and late-onset vascular disease.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Common sequence variants of lipoprotein lipase: standardized studies of in vitro expression and catalytic function

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Preliminary report: genetic variation in the human stromelysin promoter is associated with progression of coronary atherosclerosis

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Role of the apolipoprotein E polymorphism in determining normal plasma lipid and lipoprotein variation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Dietary fat clearance in normal subjects is regulated by genetic variation in apolipoprotein E.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

The apolipoprotein E polymorphism: a comparison of allele frequencies and effects in nine populations

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Adiponectin I164T mutation is associated with the metabolic syndrome and coronary artery disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A common mutation in the methylenetetrahydrofolate reductase gene and risk of coronary heart disease: results among U.S. men.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

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

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Lipoprotein lipase gene polymorphisms: associations with myocardial infarction and lipoprotein levels, the ECTIM study. Etude Cas Témoin sur l'Infarctus du Myocarde.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Influences of common variants of apolipoprotein E on measures of lipid metabolism in a sample selected for health

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A comprehensive linkage analysis for myocardial infarction and its related risk factors

27 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Insight into the nature of the CRP-coronary event association using Mendelian randomization.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

A polymorphism in the cyclooxygenase 2 gene as an inherited protective factor against myocardial infarction and stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Novel platelet membrane glycoprotein VI dimorphism is a risk factor for myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Association of arginase 1 gene polymorphisms with the risk of myocardial infarction and common carotid intima media thickness

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

R643G polymorphism in PECAM-1 influences transendothelial migration of monocytes and is associated with progression of CHD and CHD events.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Homozygosity for the C-->T polymorphism at nucleotide 46 in the 5' untranslated region of the factor XII gene protects from development of acute coronary syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Association between the low activity genotype of catechol-O-methyltransferase and myocardial infarction in a hypertensive population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms, and B vitamins: the Atherosclerosis Risk in Communities (ARIC) study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Manganese superoxide dismutase polymorphism affects the oxidized low-density lipoprotein-induced apoptosis of macrophages and coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Serotonin transporter gene polymorphism and myocardial infarction: Etude Cas-Témoins de l'Infarctus du Myocarde (ECTIM).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Codon 54 polymorphism of the fatty acid binding protein (FABP) 2 gene is associated with increased cardiovascular risk in the dyslipidemic diabetic participants of the Veterans Affairs HDL intervention trial (VA-HIT).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Effects of a 5-lipoxygenase-activating protein inhibitor on biomarkers associated with risk of myocardial infarction: a randomized trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Lipoprotein lipase gene variation is associated with a paternal history of premature coronary artery disease and fasting and postprandial plasma triglycerides: the European Atherosclerosis Research Study (EARS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Candidate gene genotypes, along with conventional risk factor assessment, improve estimation of coronary heart disease risk in healthy UK men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Arg389Gly polymorphism of the human beta1-adrenergic receptor in patients with nonfatal acute myocardial infarction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Association of Gln222Arg polymorphism in the deoxyribonuclease I (DNase I) gene with myocardial infarction in Japanese patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Apolipoprotein E genotype and cardiovascular disease in the Framingham Heart Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Adverse associations between CX3CR1 polymorphisms and risk of cardiovascular or cerebrovascular disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

The microsomal triglyceride transfer protein gene-493T variant lowers cholesterol but increases the risk of coronary heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Severity of coronary artery stenosis is associated with a polymorphism in the CXCL16/SR-PSOX gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Identification of 5-lipoxygenase as a major gene contributing to atherosclerosis susceptibility in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Association of two silent polymorphisms of platelet glycoprotein Ia/IIa receptor with risk of myocardial infarction: a case-control study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Genetic variability in the extracellular matrix as a determinant of cardiovascular risk: association of type III collagen COL3A1 polymorphisms with coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

ApoC-III gene polymorphisms and risk of coronary artery disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Tissue factor promotor polymorphism -603 A/G is associated with myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Association between ADAMTS1 matrix metalloproteinase gene variation, coronary heart disease, and benefit of statin therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Protective effect of the KCNMB1 E65K genetic polymorphism against diastolic hypertension in aging women and its relevance to cardiovascular risk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Association between estrogen receptor alpha gene variation and cardiovascular disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Association of the missense Glu298Asp variant of the endothelial nitric oxide synthase gene with myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Specific haplotypes of the P-selectin gene are associated with myocardial infarction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

In-depth haplotype analysis of ABCA1 gene polymorphisms in relation to plasma ApoA1 levels and myocardial infarction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

A haplotype constituted of four MMP-2 promoter polymorphisms (-1575G/A, -1306C/T, -790T/G and -735C/T) is associated with coronary triple-vessel disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

A polymorphism in the promoter of the tumor necrosis factor-alpha gene (-308) is associated with coronary heart disease in type 2 diabetic patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Apolipoprotein E alleles, dyslipidemia, and coronary heart disease. The Framingham Offspring Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Genetic variants of the lipoprotein lipase gene and myocardial infarction in the Central Valley of Costa Rica.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Threonine for alanine substitution in the eotaxin (CCL11) gene and the risk of incident myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Assessment of genetic risk for myocardial infarction.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Polymorphisms of the interleukin-1beta gene affect the risk of myocardial infarction and ischemic stroke at young age and the response of mononuclear cells to stimulation in vitro

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

A promoter variant of the heme oxygenase-1 gene may reduce the incidence of ischemic heart disease in Japanese

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Thrombomodulin Ala455Val polymorphism and risk of coronary heart disease

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Lipoprotein lipase activity is decreased in a large cohort of patients with coronary artery disease and is associated with changes in lipids and lipoproteins.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Association of a common polymorphism in the factor XIII gene with myocardial infarction.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke

5 September 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Functional Polymorphism in the Regulatory Region of Gelatinase B Gene in Relation to Severity of Coronary Atherosclerosis

21 January 2018

3 references

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

21 January 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

20 October 2018

12 December 2020

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

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Association of hypo-responsive toll-like receptor 4 variants with risk of myocardial infarction*1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Lipoprotein Lipase Activity Is Associated With Severity of Angina Pectoris

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Independent association of an APOE gene promoter polymorphism with increased risk of myocardial infarction and decreased APOE plasma concentrations--the ECTIM Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Haplotype Effect of the Matrix Metalloproteinase-1 Gene on Risk of Myocardial Infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11568-008-9025-X

Polymorphisms in the thrombopoietin gene are associated with risk of myocardial infarction at a young age

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2518661

Methylenetetrahydrofolate reductase genotypes and early-onset coronary artery disease

20 October 2018

1 reference

12 December 2020

Low hepatic lipase activity is a novel risk factor for coronary artery disease

1 reference

12 December 2020

Association of polymorphisms of the apolipoprotein(a) gene with lipoprotein(a) levels and myocardial infarction

1 reference

12 December 2020

A common polymorphism in the annexin V Kozak sequence (-1C>T) increases translation efficiency and plasma levels of annexin V, and decreases the risk of myocardial infarction in young patients

1 reference

12 December 2020

Synergistic effect of cytochrome P450 epoxygenase CYP2J2*7 polymorphism with smoking on the onset of premature myocardial infarction

1 reference

12 December 2020

Beta fibrinogen gene polymorphisms are associated with plasma fibrinogen and coronary artery disease in patients with myocardial infarction. The ECTIM Study. Etude Cas-Temoins sur l'Infarctus du Myocarde

1 reference

12 December 2020

Association of a novel single nucleotide polymorphism of the prostacyclin synthase gene with myocardial infarction

1 reference

12 December 2020

Asp92Asn polymorphism in the myeloid IgA Fc receptor is associated with myocardial infarction in two disparate populations: CARE and WOSCOPS

1 reference

12 December 2020

Apolipoprotein E polymorphism and atherosclerosis

1 reference

12 December 2020

Plasma thrombin-activatable fibrinolysis inhibitor antigen concentration and genotype in relation to myocardial infarction in the north and south of Europe

1 reference

12 December 2020

Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation

1 reference

12 December 2020

Lipoprotein lipase mutations, plasma lipids and lipoproteins, and risk of ischemic heart disease. A meta-analysis

1 reference

12 December 2020

Association of gene polymorphisms with coronary artery disease in low- or high-risk subjects defined by conventional risk factors

1 reference

12 December 2020

Interleukin-6 gene polymorphisms and susceptibility to myocardial infarction: the ECTIM study. Etude Cas-Témoin de l'Infarctus du Myocarde

1 reference

12 December 2020

Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease

1 reference

12 December 2020

Ser447stop mutation in lipoprotein lipase is associated with elevated HDL cholesterol levels in normolipidemic males

1 reference

12 December 2020

Interaction of the ACE D allele and the GNB3 825T allele in myocardial infarction

1 reference

12 December 2020

Apolipoprotein epsilon 4 homozygosity in young men with coronary heart disease

1 reference

12 December 2020

Association of polymorphisms in the CRP gene with circulating C-reactive protein levels and cardiovascular events

1 reference

12 December 2020

Tissue-type plasminogen activator -7,351C/T enhancer polymorphism is associated with a first myocardial infarction

1 reference

12 December 2020

Myocardial infarction in young women in relation to plasma total homocysteine, folate, and a common variant in the methylenetetrahydrofolate reductase gene

1 reference

12 December 2020

Association of the ScaI atrial natriuretic peptide gene polymorphism with nonfatal myocardial infarction and extent of coronary artery disease

1 reference

12 December 2020

The Role of a Common Variant of the Cholesteryl Ester Transfer Protein Gene in the Progression of Coronary Atherosclerosis

1 reference

12 December 2020

Association of a T29-->C polymorphism of the transforming growth factor-beta1 gene with genetic susceptibility to myocardial infarction in Japanese

1 reference

12 December 2020

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

1 reference

12 December 2020

The E27 beta2-adrenergic receptor polymorphism reduces the risk of myocardial infarction in dyslipidemic young males

1 reference

12 December 2020

Apolipoprotein B-gene DNA polymorphisms associated with myocardial infarction

1 reference

12 December 2020

Coronary artery disease and polymorphisms in a receptor mediating shear stress-dependent platelet activation

1 reference

12 December 2020

Chemokine receptor (CCR2) genotype is associated with myocardial infarction and heart failure in patients under 65 years of age

1 reference

12 December 2020

Genetic variation at the chemokine receptors CCR5/CCR2 in myocardial infarction

1 reference

12 December 2020

E-selectin polymorphism associated with myocardial infarction causes enhanced leukocyte-endothelial interactions under flow conditions

1 reference

12 December 2020

Apolipoprotein E polymorphism in the Finnish population: gene frequencies and relation to lipoprotein concentrations

1 reference

12 December 2020

Polymorphisms in the Coagulation Factor VII Gene and the Risk of Myocardial Infarction

1 reference

12 December 2020

Genetic variant showing a positive interaction with beta-blocking agents with a beneficial influence on lipoprotein lipase activity, HDL cholesterol, and triglyceride levels in coronary artery disease patients. The Ser447-stop substitution in the li

1 reference

12 December 2020

Synergistic effects of angiotensin-converting enzyme and angiotensin-II type 1 receptor gene polymorphisms on risk of myocardial infarction

1 reference

12 December 2020

Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians

1 reference

12 December 2020

VKORC1 haplotypes are associated with arterial vascular diseases (stroke, coronary heart disease, and aortic dissection)

1 reference

12 December 2020

C(-260)-->T polymorphism in the promoter of the CD14 monocyte receptor gene as a risk factor for myocardial infarction

1 reference

12 December 2020

Effects of gender and menopausal status on the association of apolipoprotein E phenotype with plasma lipoprotein levels. Results from the Framingham Offspring Study

1 reference

12 December 2020

The K121Q Polymorphism of the ENPP1/PC-1 Gene Is Associated With Insulin Resistance/Atherogenic Phenotypes, Including Earlier Onset of Type 2 Diabetes and Myocardial Infarction

1 reference

12 December 2020

Alanine to serine polymorphism at position 986 of the calcium-sensing receptor associated with coronary heart disease, myocardial infarction, all-cause, and cardiovascular mortality

1 reference

12 December 2020

10.1007/S11568-008-9025-X

Identifiers

DOI

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

18704761

1 reference