(Q34327167)

1 August 2017

Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke (English)

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1 August 2017

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coronary artery disease

1 reference

Robin Lemmens

1

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An Goris

object named as

An Goris

7

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Wim Robberecht

3

object named as

Wim Robberecht

1 reference

1 August 2017

Shérine Abboud

2

1 reference

1 August 2017

Luc Vanhees

4

1 reference

1 August 2017

Massimo Pandolfo

5

1 reference

1 August 2017

Vincent Thijs

6

1 reference

1 August 2017

25 March 2009

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European Journal of Human Genetics

1 August 2017

1 reference

1 August 2017

17

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1 August 2017

10

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1 August 2017

1287-1293

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https://scigraph.springernature.com/pub.10.1038/ejhg.2009.42

1 August 2017

0 references

cites work

Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Non-coding RNAs, epigenetics and complexity

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Breakthrough of the year. Human genetic variation

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Relative reduction of endothelial nitric-oxide synthase expression and transcription in atherosclerosis-prone regions of the mouse aorta and in an in vitro model of disturbed flow.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Proprotein convertase subtilisin/kexin type 9 (PCSK9) gene is a risk factor of large-vessel atherosclerosis stroke

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Genomewide association analysis of coronary artery disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Niaspan increases angiogenesis and improves functional recovery after stroke

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

A common allele on chromosome 9 associated with coronary heart disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Differences in vascular bed disease susceptibility reflect differences in gene expression response to atherogenic stimuli

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Arteriogenesis in peripheral arterial disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Endothelial cell diversity revealed by global expression profiling

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

Ischaemic stroke: one or several complex genetic disorders?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2986638

6 July 2018

The Genomics Gold Rush

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.42

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/10.1038%2FEJHG.2009.42

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/10.1038%2FEJHG.2009.42

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/10.1038%2FEJHG.2009.42

Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.42

A neurovascular niche for neurogenesis after stroke.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.42

Impact of inflammation on epigenetic DNA methylation - a novel risk factor for cardiovascular disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.42

Stroke--1989. Recommendations on stroke prevention, diagnosis, and therapy. Report of the WHO Task Force on Stroke and other Cerebrovascular Disorders

21 January 2018

1 reference

12 December 2020

The CAREGENE study: polymorphisms of the beta1-adrenoceptor gene and aerobic power in coronary artery disease

1 reference

12 December 2020

Two common gene variants on chromosome 9 and risk of atherothrombosis

1 reference

12 December 2020

Atherosclerosis, lipids, inflammation and epigenetics

1 reference

12 December 2020

Associations between single nucleotide polymorphisms on chromosome 9p21 and risk of coronary heart disease in Chinese Han population

1 reference

12 December 2020

A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease

1 reference

12 December 2020

Mechanisms of endothelial cell heterogeneity in health and disease

1 reference

12 December 2020

Effects of splinting on wrist contracture after stroke: a randomized controlled trial.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2009.42

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/EJHG.2009.42

1 reference

1 August 2017

1 reference

1 August 2017

1 reference