Large scale association analysis of novel genetic loci for coronary artery disease (Q35859799)

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scientific article published on 22 January 2009

Large Scale Association Analysis of Novel Genetic Loci for Coronary Artery Disease

Language	Label	Description	Also known as
English	Large scale association analysis of novel genetic loci for coronary artery disease	scientific article published on 22 January 2009	Large Scale Association Analysis of Novel Genetic Loci for Coronary Artery Disease

Statements

scholarly article

1 reference

Europe PubMed Central

10 August 2017

Large scale association analysis of novel genetic loci for coronary artery disease (English)

1 reference

Europe PubMed Central

10 August 2017

coronary artery disease

1 reference

based on heuristic

inferred from title

object named as

K Kuulasmaa

6

0 references

object named as

N Soranzo

9

0 references

object named as

P Deloukas

3

0 references

Andreas Ziegler

object named as

A Ziegler

12

0 references

Heribert Schunkert

8

object named as

H Schunkert

1 reference

Europe PubMed Central

10 August 2017

1 reference

ORCID Public Data File 2021

author name string

Coronary Artery Disease Consortium

1

1 reference

Europe PubMed Central

10 August 2017

N J Samani

2

1 reference

Europe PubMed Central

10 August 2017

J Erdmann

4

1 reference

Europe PubMed Central

10 August 2017

C Hengstenberg

5

1 reference

Europe PubMed Central

10 August 2017

R McGinnis

7

1 reference

Europe PubMed Central

10 August 2017

J Thompson

10

1 reference

Europe PubMed Central

10 August 2017

L Tiret

11

1 reference

Europe PubMed Central

10 August 2017

language of work or name

0 references

publication date

22 January 2009

1 reference

Europe PubMed Central

10 August 2017

Arteriosclerosis, Thrombosis, and Vascular Biology

1 reference

Europe PubMed Central

10 August 2017

29

1 reference

Europe PubMed Central

10 August 2017

5

1 reference

Europe PubMed Central

10 August 2017

774-780

1 reference

Europe PubMed Central

10 August 2017

The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 2018

Assessing the combined impact of 18 common genetic variants of modest effect sizes 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=3315048

11 July 2018

Mapping the genetic architecture of gene expression in human liver

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 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=3315048

11 July 2018

LDL-cholesterol concentrations: a genome-wide association study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 2018

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 2018

Newly identified loci that influence lipid concentrations and risk 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=3315048

11 July 2018

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 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=3315048

11 July 2018

Migration of endothelial progenitor cells mediated by stromal cell-derived factor-1alpha/CXCR4 via PI3K/Akt/eNOS signal transduction pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 2018

Genomewide association 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=3315048

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 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=3315048

11 July 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=3315048

11 July 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=3315048

11 July 2018

Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 2018

Effect of stromal-cell-derived factor 1 on stem-cell homing and tissue regeneration in ischaemic cardiomyopathy.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 2018

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 2018

Expression, function and clinical relevance of MIA (melanoma inhibitory activity).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

11 July 2018

The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3315048

24 September 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=3315048

14 November 2018

Serum lipid precursors of coronary heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19164808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of several hundred genetic polymorphisms may improve assessment of the individual genetic burden for coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19164808

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1161/ATVBAHA.108.181388

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

1 reference

Europe PubMed Central

10 August 2017

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