(Q35609476)

9 August 2017

title

The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 region (English)

1 reference

9 August 2017

main subject

coronary artery disease

1 reference

Jennifer A Smith

2

0 references

Myriam Fornage

4

object named as

Myriam Fornage

1 reference

9 August 2017

8

Sharon L R Kardia

1 reference

9 August 2017

5

Patricia A Peyser

1 reference

9 August 2017

Wei Zhao

1

1 reference

9 August 2017

Guangmei Mao

3

1 reference

9 August 2017

Yan V Sun

6

1 reference

9 August 2017

Stephen T Turner

7

1 reference

9 August 2017

language of work or name

1 reference

10 May 2015

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9 August 2017

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9 August 2017

volume

8

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9 August 2017

page(s)

21

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Creative Commons Attribution 4.0 International

9 August 2017

copyright license

start time

10 May 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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12 July 2018

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9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response

12 July 2018

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Common genetic variants on chromosome 9p21 are associated with myocardial infarction and type 2 diabetes in an Italian population

12 July 2018

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Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL Expression

12 July 2018

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The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people

12 July 2018

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Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants

12 July 2018

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

12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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12 July 2018

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

12 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4432789

Genomewide association analysis of coronary artery disease

12 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4432789

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12 July 2018

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

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4432789

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.

12 July 2018

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Gene-expression variation within and among human populations

12 July 2018

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Roles of ATP binding cassette transporters A1 and G1, scavenger receptor BI and membrane lipid domains in cholesterol export from macrophages

12 July 2018

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Tumor-associated alterations in caspase-14 expression in epithelial malignancies

12 July 2018

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Genetic variation in ABC transporter A1 contributes to HDL cholesterol in the general population

12 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4432789

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

12 July 2018

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Leukocyte ABCA1 controls susceptibility to atherosclerosis and macrophage recruitment into tissues.

12 July 2018

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12 July 2018

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Genetic epidemiology of coronary artery disease

12 July 2018

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12 July 2018

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High density lipoprotein as a protective factor against coronary heart disease. The Framingham Study

12 July 2018

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Increased risk of coronary artery disease in Caucasians with extremely low HDL cholesterol due to mutations in ABCA1, APOA1, and LCAT.

12 July 2018

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ANRIL expression is associated with atherosclerosis risk at chromosome 9p21.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4432789

The activity of class I, II, III and IV of alcohol dehydrogenase (ADH) isoenzymes and aldehyde dehydrogenase (ALDH) in the wall of abdominal aortic aneurysms

25 September 2018

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4432789

Tagging single nucleotide polymorphisms in cell cycle control genes and susceptibility to invasive epithelial ovarian cancer.

25 September 2018

1 reference

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Macrophage ATP-binding cassette transporter A1 overexpression inhibits atherosclerotic lesion progression in low-density lipoprotein receptor knockout mice

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4432789

Contribution of dihydro-beta-erythroidine sensitive nicotinic acetylcholine receptors in the ventral tegmental area to cocaine-induced behavioral sensitization in rats

25 September 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4432789

Acute ethanol administration oxidatively damages and depletes mitochondrial dna in mouse liver, brain, heart, and skeletal muscles: protective effects of antioxidants.

25 September 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4432789

Executive Summary: Heart Disease and Stroke Statistics—2014 Update

25 September 2018

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Genetic variants at the 9p21 locus contribute to atherosclerosis through modulation of ANRIL and CDKN2A/B

21 January 2018

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https://api.crossref.org/works/10.1186%2FS12920-015-0094-0

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

21 January 2018

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12 December 2020

Association between the coronary artery disease risk locus on chromosome 9p21.3 and abdominal aortic aneurysm

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12 December 2020

Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study

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12 December 2020

The chromosome 9p21 region and myocardial infarction in a European population

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12 December 2020

Associations between two common polymorphisms in the ABCA1 gene and subclinical atherosclerosis: Multi-Ethnic Study of Atherosclerosis (MESA)

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12 December 2020

The impact of severe LDL receptor mutations on SREBP-pathway regulation in homozygous familial hypercholesterolemia (FH)

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12 December 2020

Familial aggregation of hypertension treatment and control in the Genetic Epidemiology Network of Arteriopathy (GENOA) study

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12 December 2020

10.1186/S12920-015-0094-0

Identifiers

DOI

1 reference

Dimensions Publication ID

9 August 2017

0 references

1 reference

9 August 2017

1 reference