Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke (Q30436210)

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English	Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke	scientific article

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scholarly article

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Europe PubMed Central

PMC publication ID

19 August 2017

Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

atherosclerosis

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based on heuristic

inferred from title

Thomas Meitinger

7

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Europe PubMed Central

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19 August 2017

object named as

Steve Bevan

2

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Mary J MacLeod

14

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Heinz Erich Wichmann

8

object named as

Erich Wichmann

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19 August 2017

Martin Dichgans

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Martin Dichgans

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19 August 2017

Andreas Gschwendtner

1

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Andreas Gschwendtner

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19 August 2017

Jonathan Rosand

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Jonathan Rosand

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Europe PubMed Central

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19 August 2017

James F Meschia

15

object named as

James F Meschia

1 reference

Europe PubMed Central

19 August 2017

PMC publication ID

International Stroke Genetics Consortium

21

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International Stroke Genetics Consortium

1 reference

Europe PubMed Central

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19 August 2017

18

object named as

Hugh S Markus

1 reference

Europe PubMed Central

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19 August 2017

10

object named as

Karen Furie

1 reference

Europe PubMed Central

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19 August 2017

author name string

John W Cole

3

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19 August 2017

Anna Plourde

4

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Europe PubMed Central

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19 August 2017

Mar Matarin

5

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Europe PubMed Central

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19 August 2017

Helen Ross-Adams

6

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Europe PubMed Central

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19 August 2017

Stephen S Rich

12

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19 August 2017

Paul D Syme

13

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19 August 2017

Steve J Kittner

17

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19 August 2017

publication date

1 May 2009

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19 August 2017

Annals of Neurology

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19 August 2017

65

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19 August 2017

5

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Europe PubMed Central

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19 August 2017

531-539

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Europe PubMed Central

PMC publication ID

19 August 2017

Ankle brachial index combined with Framingham Risk Score to predict cardiovascular events and mortality: a meta-analysis

1 reference

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20 June 2018

Systematic review of reviews of risk factors for intracranial aneurysms

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20 June 2018

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20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

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

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20 June 2018

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

Genomewide association analysis of coronary artery disease

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

A common allele on chromosome 9 associated with coronary heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

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.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

Prediction of clinical cardiovascular events with carotid intima-media thickness: a systematic review and meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

Genetics of ischaemic stroke

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

The regulation of INK4/ARF in cancer and aging

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

The incidence of stroke after myocardial infarction: a meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

Risk Factors for Subarachnoid Hemorrhage: An Updated Systematic Review of Epidemiological Studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

Risk of myocardial infarction and vascular death after transient ischemic attack and ischemic stroke: a systematic review and meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

Atherosclerotic Vascular Disease Conference: Writing Group I: epidemiology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

Carotid-artery intima and media thickness as a risk factor for myocardial infarction and stroke in older adults. Cardiovascular Health Study Collaborative Research Group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

Mortality by cause for eight regions of the world: Global Burden of Disease Study

1 reference

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20 June 2018

p15INK4B is a potential effector of TGF-beta-induced cell cycle arrest

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20 June 2018

Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

Compensatory enlargement of human atherosclerotic coronary arteries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

20 June 2018

A meta-analysis of the association of the deletion allele of the angiotensin-converting enzyme gene with myocardial infarction

1 reference

https://api.crossref.org/works/10.1002%2FANA.21590

21 January 2018

Frequency and severity of asymptomatic coronary disease in patients with different causes of stroke.

1 reference

https://api.crossref.org/works/10.1002%2FANA.21590

21 January 2018

Coronary Artery Disease-Associated Locus on Chromosome 9p21 and Early Markers of Atherosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

26 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

26 November 2018

Heritability of ischaemic stroke in women compared with men: a genetic epidemiological study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

26 November 2018

Apoptosis of vascular smooth muscle cells induces features of plaque vulnerability in atherosclerosis.

1 reference

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26 November 2018

Smad expression in human atherosclerotic lesions: evidence for impaired TGF-beta/Smad signaling in smooth muscle cells of fibrofatty lesions

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26 November 2018

Coronary risk evaluation in patients with transient ischemic attack and ischemic stroke: a scientific statement for healthcare professionals from the Stroke Council and the Council on Clinical Cardiology of the American Heart Association/American St

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2702695

26 November 2018

Relationship between coronary artery remodeling and plaque vulnerability

1 reference

https://pubmed.ncbi.nlm.nih.gov/19475673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two common gene variants on chromosome 9 and risk of atherothrombosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19475673

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/ANA.21590

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

ResearchGate publication ID

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