Genetic susceptibility to myocardial infarction and coronary artery disease (Q36599259)

15 August 2017

1 reference

title

Genetic susceptibility to myocardial infarction and coronary artery disease (English)

1 reference

15 August 2017

main subject

myocardial infarction

1 reference

1

1 reference

15 August 2017

Jonathan Smith

2

1 reference

15 August 2017

Edward F Plow

series ordinal

3

1 reference

15 August 2017

Qing K Wang

series ordinal

4

1 reference

15 August 2017

language of work or name

1 reference

1 October 2006

1 reference

15 August 2017

published in

Human Molecular Genetics

1 reference

15 August 2017

volume

15 Spec No 2

1 reference

15 August 2017

page(s)

R117-23

1 reference

Complement factor H polymorphism in age-related macular degeneration

15 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Complement factor H polymorphism and age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Complement factor H variant increases the risk of age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

New genes in inflammatory bowel disease: lessons for complex diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Alternative projections of mortality and disability by cause 1990-2020: Global Burden of Disease Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

ALOX5AP gene and the PDE4D gene in a central European population of stroke patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Transcription factor MEF2A mutations in patients with coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Lack of MEF2A mutations in coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Identification of four gene variants associated with myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Cholesterol, racial variation and targeted medicines

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Biomedicine. Lowering LDL--not only how low, but how long?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Mechanism and effect of thrombospondin-4 polymorphisms on neutrophil function

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Using mice to dissect genetic factors in atherosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Loss of SR-BI expression leads to the early onset of occlusive atherosclerotic coronary artery disease, spontaneous myocardial infarctions, severe cardiac dysfunction, and premature death in apolipoprotein E-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Diet-induced occlusive coronary atherosclerosis, myocardial infarction, cardiac dysfunction, and premature death in scavenger receptor class B type I-deficient, hypomorphic apolipoprotein ER61 mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Simon Dack Lecture. The genomic basis of myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

The genetics of heart attack

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

Genetic susceptibility to coronary artery disease: from promise to progress.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDL183

21 January 2018

Identifiers

DOI

10.1093/HMG/DDL183

1 reference

15 August 2017

1 reference