(Q37241472)

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Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits

scientific article published on 24 March 2016

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits (English)

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

atherosclerosis

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

genetic variation

1 reference

based on heuristic

inferred from title

8

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Europe PubMed Central

PMC publication ID

19 August 2017

Hugh Christian Watkins

9

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Heribert Schunkert

10

object named as

Heribert Schunkert

0 references

Jeanette Erdmann

7

object named as

Jeanette Erdmann

0 references

Nathan O Stitziel

object named as

Nathan O Stitziel

2

0 references

object named as

Wei Zhao

3

0 references

Muredach P. Reilly

object named as

Muredach P Reilly

14

0 references

11

object named as

Nilesh J Samani

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Danish Saleheen

12

object named as

Danish Saleheen

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Sekar Kathiresan

13

object named as

Sekar Kathiresan

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

author name string

Jessica R Golbus

1

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Chenyi Xue

4

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Europe PubMed Central

PMC publication ID

19 August 2017

Martin Farrall

5

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Ruth McPherson

6

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

CARDIoGRAMplusC4D, Myocardial Infarction Genetics (MIGen), Exome Sequencing Project and Early-Onset Myocardial Infarction (ESP EOMI), and the Pakistan Risk of Myocardial Infarction Study (PROMIS) Consortia*

15

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

publication date

24 March 2016

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Circulation: Cardiovascular Genetics

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

9

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Europe PubMed Central

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19 August 2017

3

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Europe PubMed Central

PMC publication ID

19 August 2017

250-258

1 reference

Europe PubMed Central

PMC publication ID

19 August 2017

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Serum Fractalkine (CX3CL1) and Cardiovascular Outcomes and Diabetes: Findings From the Chronic Renal Insufficiency Cohort (CRIC) Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Genomic responses in mouse models poorly mimic human inflammatory diseases

1 reference

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6 September 2017

Large-scale association analysis identifies new risk loci for coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

An integrated map of genetic variation from 1,092 human genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

1 reference

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6 September 2017

Evolution and functional impact of rare coding variation from deep sequencing of human exomes

1 reference

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6 September 2017

Predicting the functional impact of protein mutations: application to cancer genomics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Fractalkine is a novel human adipochemokine associated with type 2 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Integrative genomics viewer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Chemokine receptor CCR5: from AIDS to atherosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

1 reference

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6 September 2017

Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

1 reference

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6 September 2017

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways

1 reference

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6 September 2017

Biological, clinical and population relevance of 95 loci for blood lipids

1 reference

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6 September 2017

MutationTaster evaluates disease-causing potential of sequence alterations

1 reference

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6 September 2017

A method and server for predicting damaging missense mutations

1 reference

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6 September 2017

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Identification of deleterious mutations within three human genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Gene profiling of human adipose tissue during evoked inflammation in vivo

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

Genetic diversity of CX3CR1 gene and coronary artery disease: new insights through a meta-analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

The Pakistan Risk of Myocardial Infarction Study: a resource for the study of genetic, lifestyle and other determinants of myocardial infarction in South Asia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

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6 September 2017

The many roles of chemokines and chemokine receptors in inflammation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

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

1 reference

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6 September 2017

CCR2 modulates inflammatory and metabolic effects of high-fat feeding

1 reference

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6 September 2017

Haploview: analysis and visualization of LD and haplotype maps

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6 September 2017

Of mice and not men: differences between mouse and human immunology

1 reference

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6 September 2017

Chemokine receptor mutant CX3CR1-M280 has impaired adhesive function and correlates with protection from cardiovascular disease in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

6 September 2017

MCP-1 deficiency reduces susceptibility to atherosclerosis in mice that overexpress human apolipoprotein B.

1 reference

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6 September 2017

Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models

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26 June 2018

Genetic variants of the monocyte chemoattractant protein-1 gene and its receptor CCR2 and risk of coronary artery disease: a meta-analysis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

3 September 2018

Genetic determinants of major blood lipids in Pakistanis compared with Europeans.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

3 September 2018

Adverse associations between CX3CR1 polymorphisms and risk of cardiovascular or cerebrovascular disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

3 September 2018

Decreased atherosclerotic lesion formation in CX3CR1/apolipoprotein E double knockout mice.

1 reference

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3 September 2018

Val64Ile polymorphism in the C-C chemokine receptor 2 is associated with reduced coronary artery calcification

1 reference

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3 September 2018

Association between polymorphism in the chemokine receptor CX3CR1 and coronary vascular endothelial dysfunction and atherosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5015681

3 September 2018

Combined Inhibition of CCL2, CX3CR1, and CCR5 Abrogates Ly6C hi and Ly6C lo Monocytosis and Almost Abolishes Atherosclerosis in Hypercholesterolemic Mice

1 reference

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4 December 2018

Impact of MCP-1 and CCR-2 gene polymorphisms on coronary artery disease susceptibility

1 reference

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12 December 2020

based on heuristic

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T-cell accumulation and regulated on activation, normal T cell expressed and secreted upregulation in adipose tissue in obesity

1 reference

https://pubmed.ncbi.nlm.nih.gov/27013693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of polymorphisms in the chemokine receptor CX3CR1 gene with coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/27013693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Involvement of polymorphisms in the chemokine system in the susceptibility for coronary artery disease (CAD). Coincidence of elevated Lp(a) and MCP-1 -2518 G/G genotype in CAD patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/27013693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic variation at the chemokine receptors CCR5/CCR2 in myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/27013693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of common polymorphisms in the fractalkine receptor (CX3CR1) with obesity

1 reference

https://pubmed.ncbi.nlm.nih.gov/27013693

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1161/CIRCGENETICS.115.001374

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

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