9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response (Q39048288)

8 September 2017

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

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8 September 2017

coronary artery disease

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9

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8 September 2017

1

Olivier Harismendy

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8 September 2017

Dimple Notani

2

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8 September 2017

Xiaoyuan Song

3

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8 September 2017

Nazli G Rahim

4

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8 September 2017

Bogdan Tanasa

5

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8 September 2017

Nathaniel Heintzman

6

1 reference

8 September 2017

Bing Ren

7

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8 September 2017

Xiang-Dong Fu

8

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8 September 2017

Michael G Rosenfeld

10

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8 September 2017

Kelly A Frazer

11

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8 September 2017

language of work or name

English

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publication date

1 February 2011

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8 September 2017

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8 September 2017

470

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8 September 2017

7333

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8 September 2017

264-268

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https://scigraph.springernature.com/pub.10.1038/nature09753

8 September 2017

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cites work

Molecular interplay of the noncoding RNA ANRIL and methylated histone H3 lysine 27 by polycomb CBX7 in transcriptional silencing of INK4a

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8q24 prostate, breast, and colon cancer risk loci show tissue-specific long-range interaction with MYC.

9 September 2017

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

A common variant at 9p21 is associated with sudden and arrhythmic cardiac death

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Comprehensive mapping of long-range interactions reveals folding principles of the human genome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

INK4/ARF transcript expression is associated with chromosome 9p21 variants linked to atherosclerosis

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Histone modifications at human enhancers reflect global cell-type-specific gene expression

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Candidate gene polymorphisms and the 9p21 locus in acute coronary syndromes

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

FoxA1 translates epigenetic signatures into enhancer-driven lineage-specific transcription

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

A second generation human haplotype map of over 3.1 million SNPs

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Genomewide association analysis of coronary artery disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

A common allele on chromosome 9 associated with coronary heart disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

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

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

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.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Analysis of the vertebrate insulator protein CTCF-binding sites in the human genome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Sensitive ChIP-DSL technology reveals an extensive estrogen receptor alpha-binding program on human gene promoters.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Interchromosomal interactions and olfactory receptor choice

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Signal transducer and activator of transcription 1 activation in endothelial cells is a negative regulator of angiogenesis

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Latent membrane protein 1 regulates STAT1 through NF-kappaB-dependent interferon secretion in Epstein-Barr virus-immortalized B cells

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

The ENCODE (ENCyclopedia Of DNA Elements) Project

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Capturing chromosome conformation

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

Atherosclerosis is an inflammatory disease

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3079517

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

9 September 2017

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

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/10.1038%2FNATURE09753

Rapid evolution of noncoding RNAs: lack of conservation does not mean lack of function

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

Characterization of the genomic Xist locus in rodents reveals conservation of overall gene structure and tandem repeats but rapid evolution of unique sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

Epigenetic silencing of tumour suppressor gene p15 by its antisense RNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

A comparison of bayesian methods for haplotype reconstruction from population genotype data

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

ChIP-chip: data, model, and analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

Model-based analysis of two-color arrays (MA2C).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

The protein CTCF is required for the enhancer blocking activity of vertebrate insulators

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

A Gibbs sampling method to detect overrepresented motifs in the upstream regions of coexpressed genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

Systems biology approaches identify ATF3 as a negative regulator of Toll-like receptor 4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

Formaldehyde-mediated DNA-protein crosslinking: a probe for in vivo chromatin structures

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE09753

21 January 2018

Identifiers

DOI

10.1038/NATURE09753

1 reference

Dimensions Publication ID

8 September 2017

0 references

1 reference

8 September 2017

1 reference