(Q37138039)

18 August 2017

1 reference

title

Identifying the susceptibility genes for coronary artery disease: from hyperbole through doubt to cautious optimism (English)

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18 August 2017

coronary artery disease

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2

P Eriksson

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18 August 2017

1

A Hamsten

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PubMed ID

18410597

18 August 2017

language of work or name

English

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publication date

1 May 2008

1 reference

Journal of Internal Medicine

18 August 2017

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18 August 2017

263

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18 August 2017

5

1 reference

18 August 2017

538-552

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Inflammation, atherosclerosis, and coronary artery disease

18 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Shattuck lecture--medical and societal consequences of the Human Genome Project.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

A common allele on chromosome 9 associated with coronary heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Genomewide association analysis of coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

A common genetic variant is associated with adult and childhood obesity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Parental cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults: a prospective study of parents and offspring

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Familial hypercholesterolemia and coronary heart disease: a HuGE association review

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

On the allelic spectrum of human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

The allelic structure of common disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Genome-wide association studies: theoretical and practical concerns

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Replication validity of genetic association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Genetic associations in large versus small studies: an empirical assessment

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

The future of genetic studies of complex human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Association study designs for complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Shaking the tree: mapping complex disease genes with linkage disequilibrium

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

The complex interplay among factors that influence allelic association.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Statistical significance for genomewide studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Coronary plaque erosion without rupture into a lipid core. A frequent cause of coronary thrombosis in sudden coronary death

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Genetic variation in alcohol dehydrogenase and the beneficial effect of moderate alcohol consumption on myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Finishing the euchromatic sequence of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

A haplotype map of the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

A second generation human haplotype map of over 3.1 million SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

The International HapMap Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

High-resolution haplotype structure in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

The structure of haplotype blocks in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Whole-genome patterns of common DNA variation in three human populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

A genome-wide scalable SNP genotyping assay using microarray technology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Whole-genome genotyping with the single-base extension assay

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Detection of large-scale variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Large-scale copy number polymorphism in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Global variation in copy number in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Relative impact of nucleotide and copy number variation on gene expression phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Genetic basis of atherosclerosis: part I: new genes and pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Genetic basis of atherosclerosis: part II: clinical implications

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Complex trait locus linkage mapping in atherosclerosis: time to take a step back before moving forward?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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/10.1111%2FJ.1365-2796.2008.01958.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/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.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/10.1111%2FJ.1365-2796.2008.01958.X

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/10.1111%2FJ.1365-2796.2008.01958.X

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/10.1111%2FJ.1365-2796.2008.01958.X

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/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Power to detect risk alleles using genome-wide tag SNP panels

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Genome-wide strategies for detecting multiple loci that influence complex diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.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/10.1111%2FJ.1365-2796.2008.01958.X

A genome-wide association study identifies novel risk loci for type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Dual role of matrix metalloproteinases (matrixins) in intimal thickening and atherosclerotic plaque rupture

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Abdominal aortic aneurysm expansion: risk factors and time intervals for surveillance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Initial sequencing and comparative analysis of the mouse genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Using mice to dissect genetic factors in atherosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

The mouse as a model for human biology: a resource guide for complex trait analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Insights from human/mouse genome comparisons

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Identifying novel genes for atherosclerosis through mouse-human comparative genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Genome-wide search for new genes controlling plasma lipid concentrations in mice and humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.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/10.1111%2FJ.1365-2796.2008.01958.X

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/10.1111%2FJ.1365-2796.2008.01958.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/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

The immune response in atherosclerosis: a double-edged sword

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

CD14 and toll-like receptor 4: a link between infection and acute coronary events?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Association of the Toll-like receptor 4 gene Asp299Gly polymorphism with acute coronary events.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.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/10.1111%2FJ.1365-2796.2008.01958.X

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/10.1111%2FJ.1365-2796.2008.01958.X

OX40: targeted immunotherapy--implications for tempering autoimmunity and enhancing vaccines

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

A large-scale genetic association study confirms IL12B and leads to the identification of IL23R as psoriasis-risk genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

An integrative genomics approach to infer causal associations between gene expression and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Cis-acting regulatory variation in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

In vivo characterization of regulatory polymorphisms by allele-specific quantification of RNA polymerase loading

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Allele-specific MMP-3 transcription under in vivo conditions

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Human evidence that the apolipoprotein a-II gene is implicated in visceral fat accumulation and metabolism of triglyceride-rich lipoproteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Progression of coronary atherosclerosis is associated with a common genetic variant of the human stromelysin-1 promoter which results in reduced gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Identification of novel, functional genetic variants in the human matrix metalloproteinase-2 gene: role of Sp1 in allele-specific transcriptional regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

A common functional polymorphism (C-->A substitution at position -863) in the promoter region of the tumour necrosis factor-alpha (TNF-alpha) gene associated with reduced circulating levels of TNF-alpha

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Unlocking the potential of the human genome with RNA interference

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Silence from within: endogenous siRNAs and miRNAs.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

GENE SEQUENCING: The Race for the $1000 Genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

21 January 2018

The year of sequencing.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Primer: Sequencing--the next generation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Genetic testing for cardiovascular disease susceptibility: a useful clinical management tool or possible misinformation?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

UK Biobank: from concept to reality

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Identification of pathways for atherosclerosis in mice: integration of quantitative trait locus analysis and global gene expression data

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

A genome-wide association study of global gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

Population genomics of human gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.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/10.1111%2FJ.1365-2796.2008.01958.X

Allelic Variation in Human Gene Expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.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/10.1111%2FJ.1365-2796.2008.01958.X

Human Evidence That the Cystatin C Gene Is Implicated in Focal Progression of Coronary Artery Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

What makes a good genetic association study?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

The case for a US prospective cohort study of genes and environment

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2796.2008.01958.X

10.1111/J.1365-2796.2008.01958.X

21 January 2018

Identifiers

DOI

1 reference

18 August 2017

1 reference

PubMed ID

18410597