(Q46467566)

English

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

scientific article published on 23 July 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

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 (English)

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

coronary artery disease

1 reference

based on heuristic

inferred from title

Jeanette Erdmann

3

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

Massimo Mangino

8

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

Andreas Ziegler

11

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

Patrick Linsel-Nitschke

6

object named as

Patrick Linsel-Nitschke

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

object named as

Mark Caulfield

12

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Martin D Tobin

15

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1

object named as

Nilesh J Samani

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

Heribert Schunkert

14

object named as

Heribert Schunkert

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

4

object named as

Anika Götz

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

Christian Hengstenberg

9

object named as

Christian Hengstenberg

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

author name string

Peter S Braund

2

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

Maciej Tomaszewski

5

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

Cother Hajat

7

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

Klaus Stark

10

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

Paul R Burton

13

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

publication date

23 July 2008

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

Journal of Molecular Medicine

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

86

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

11

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Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

1233-1241

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

https://scigraph.springernature.com/pub.10.1007/s00109-008-0387-2

0 references

Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study

1 reference

https://api.crossref.org/works/10.1007%2FS00109-008-0387-2

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic susceptibility to death from coronary heart disease in a study of twins

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lymphotoxin-α and galectin-2 SNPs are not associated with myocardial infarction in two different German populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SNPselector: a web tool for selecting SNPs for genetic association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common variants in genes underlying monogenic hypertension and hypotension and blood pressure in the general population

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lipoprotein lipase gene polymorphism, cholesterol subfractions and myocardial infarction in large samples of the general population

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SNP Function Portal: a web database for exploring the function implication of SNP alleles

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sortilin/neurotensin receptor-3 binds and mediates degradation of lipoprotein lipase

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Blood cholesterol and vascular mortality by age, sex, and blood pressure: a meta-analysis of individual data from 61 prospective studies with 55,000 vascular deaths

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mapping the genetic architecture of gene expression in human liver

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LDL-cholesterol concentrations: a genome-wide association study

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ssSNPer: identifying statistically similar SNPs to aid interpretation of genetic association studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common allele on chromosome 9 associated with coronary heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomewide association analysis of coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic susceptibility to coronary artery disease: from promise to progress.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new approach to modelling interactions between treatment and continuous covariates in clinical trials by using fractional polynomials

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Key concepts in genetic epidemiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Heart disease and stroke statistics--2007 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extending the simple linear regression model to account for correlated responses: an introduction to generalized estimating equations and multi-level mixed modelling.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18649068

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00109-008-0387-2

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

release_nzg4drkuezaa7cj6zpcse6obku

1 reference

https://api.fatcat.wiki/v0/release/nzg4drkuezaa7cj6zpcse6obku

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

22 December 2017

http://europepmc.org/abstract/MED/18649068

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