(Q34133152)

31 July 2017

title

Additive effect of multiple genetic variants on the risk of coronary artery disease (English)

1 reference

31 July 2017

Additive Effects of Multiple Genetic Variants on the Risk of Coronary Artery Disease (English)

0 references

main subject

coronary artery disease

1 reference

6

Jaume Marrugat

1 reference

31 July 2017

Carla Lluís-Ganella

1

1 reference

31 July 2017

Gavin Lucas

2

1 reference

31 July 2017

Isaac Subirana

3

1 reference

31 July 2017

Mariano Sentí

4

1 reference

31 July 2017

Jordi Jimenez-Conde

5

1 reference

31 July 2017

Marta Tomás

7

1 reference

31 July 2017

Roberto Elosua

8

1 reference

31 July 2017

language of work or name

1 reference

1 August 2010

1 reference

Revista Española de Cardiología

31 July 2017

January 2010

0 references

published in

1 reference

31 July 2017

volume

63

1 reference

31 July 2017

issue

8

1 reference

31 July 2017

page(s)

925-933

1 reference

New susceptibility locus for coronary artery disease on chromosome 3q22.3.

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

A common allele on chromosome 9 associated with coronary heart disease

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Genomewide association analysis of coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

The search for new cardiovascular biomarkers

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

An adaptation of the Framingham coronary heart disease risk function to European Mediterranean areas

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Criteria for evaluation of novel markers of cardiovascular risk: a scientific statement from the American Heart Association

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Cohort profile: 1958 British birth cohort (National Child Development Study).

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

SNPassoc: an R package to perform whole genome association studies

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Genome-wide association study identifies eight loci associated with blood pressure

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Joint effects of common genetic variants on the risk for type 2 diabetes in U.S. men and women of European ancestry

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Estimación del riesgo coronario en España mediante la ecuación de Framingham calibrada

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Impact of adding a single allele in the 9p21 locus to traditional risk factors on reclassification of coronary heart disease risk and implications for lipid-modifying therapy in the Atherosclerosis Risk in Communities study

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Cardiovascular disease risk prediction with and without knowledge of genetic variation at chromosome 9p21.3.

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men.

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Prediction of Coronary Heart Disease Risk using a Genetic Risk Score: The Atherosclerosis Risk in Communities Study

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Polymorphisms associated with cholesterol and risk of cardiovascular events

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

Association between a literature-based genetic risk score and cardiovascular events in women

1 reference

https://api.crossref.org/works/10.1016%2FS1885-5857%2810%2970186-9

7 January 2021

10.1016/S1885-5857(10)70186-9

Identifiers

DOI

0 references

1 reference