(Q34404142)

2 August 2017

title

The chromosome 9p21 risk locus is associated with angiographic severity and progression of coronary artery disease (English)

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2 August 2017

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coronary artery disease

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7

Anna Helgadottir

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2 August 2017

10

Kari Stefansson

1 reference

2 August 2017

9

Jeffrey R Gulcher

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2 August 2017

12

Viola Vaccarino

1 reference

2 August 2017

14

Arshed A Quyyumi

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2 August 2017

1

Riyaz S Patel

1 reference

2 August 2017

Shaoyong Su

2

1 reference

2 August 2017

Ian J Neeland

3

1 reference

2 August 2017

Ayushi Ahuja

4

1 reference

2 August 2017

Emir Veledar

5

1 reference

2 August 2017

Jinying Zhao

6

1 reference

2 August 2017

Hilma Holm

8

1 reference

2 August 2017

Salina Waddy

11

1 reference

2 August 2017

A Maziar Zafari

13

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2 August 2017

publication date

20 August 2010

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2 August 2017

published in

European Heart Journal

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2 August 2017

volume

31

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2 August 2017

issue

24

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2 August 2017

page(s)

3017-3023

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Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice

2 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

Association between 9p21 genomic markers and heart disease: a meta-analysis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

Susceptibility loci for intracranial aneurysm in European and Japanese populations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective 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=3001587

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=3001587

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=3001587

Arterial stiffness: a new surrogate end point for cardiovascular 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=3001587

Future use of genomics in 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=3001587

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=3001587

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=3001587

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=3001587

A novel endonuclease IV post-PCR genotyping system

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

Coronary angiography and intravascular ultrasound

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

Compensatory enlargement of human atherosclerotic coronary arteries

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

A new method of scoring coronary angiograms to reflect extent of coronary atherosclerosis and improve correlation with major risk factors

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

ANRIL expression is associated with atherosclerosis risk at 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=3001587

Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

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

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

Distinct Heritable Patterns of Angiographic Coronary Artery Disease in Families With Myocardial Infarction

9 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3001587

A reporting system on patients evaluated for coronary artery disease. Report of the Ad Hoc Committee for Grading of Coronary Artery Disease, Council on Cardiovascular Surgery, American Heart Association

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20729229

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20729229

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20729229

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/EURHEARTJ/EHQ272

1 reference

2 August 2017

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2 August 2017

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