(Q34147477)

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Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--

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scholarly article

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Europe PubMed Central

31 July 2017

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Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey-- (English)

1 reference

Europe PubMed Central

31 July 2017

atherosclerosis

1 reference

based on heuristic

inferred from title

coronary artery disease

1 reference

based on heuristic

inferred from title

Leo-Pekka Lyytikäinen

3

1 reference

Europe PubMed Central

31 July 2017

Terho Lehtimäki

23

object named as

Terho Lehtimäki

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18

object named as

Samuli Ripatti

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21

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Mika Kähönen

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Nina Hutri-Kähönen

6

object named as

Nina Hutri-Kähönen

1 reference

Europe PubMed Central

31 July 2017

Ilkka Seppälä

2

object named as

Ilkka Seppälä

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20

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Jorma Viikari

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Europe PubMed Central

31 July 2017

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Markus Juonala

7

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16

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Antti Jula

1 reference

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31 July 2017

22

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Olli T Raitakari

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Europe PubMed Central

31 July 2017

15

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Tomi Laitinen

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Johannes Kettunen

17

object named as

Johannes Kettunen

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Europe PubMed Central

31 July 2017

4

object named as

Nina Mononen

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Europe PubMed Central

31 July 2017

Jussi A Hernesniemi

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object named as

Jussi A Hernesniemi

1 reference

Europe PubMed Central

31 July 2017

Leena Taittonen

8

object named as

Leena Taittonen

1 reference

Europe PubMed Central

31 July 2017

Ilkka Seppälä

2

object named as

Ilkka Seppälä

1 reference

Europe PubMed Central

31 July 2017

5

object named as

Niku Oksala

1 reference

Europe PubMed Central

31 July 2017

Reijo Laaksonen

19

object named as

Reijo Laaksonen

1 reference

Europe PubMed Central

31 July 2017

author name string

Erin N Smith

9

1 reference

Europe PubMed Central

31 July 2017

Nicholas J Schork

10

1 reference

Europe PubMed Central

31 July 2017

Wei Chen

11

1 reference

Europe PubMed Central

31 July 2017

Sathanur R Srinivasan

12

1 reference

Europe PubMed Central

31 July 2017

Gerald S Berenson

13

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31 July 2017

Sarah S Murray

14

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31 July 2017

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publication date

25 January 2012

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31 July 2017

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Europe PubMed Central

31 July 2017

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31 July 2017

e28931

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31 July 2017

1

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Europe PubMed Central

31 July 2017

copyright license

Creative Commons Attribution 4.0 International

25 January 2012

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April 2022 Public Data File from Crossref

copyright status

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Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque

1 reference

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

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A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses

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Genetic variants and their interactions in the prediction of increased pre-clinical carotid atherosclerosis: the cardiovascular risk in young Finns study

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Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study

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Extremes of unexplained variation as a phenotype: an efficient approach for genome-wide association studies of cardiovascular disease

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The value of carotid intima-media thickness for predicting cardiovascular risk

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Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk

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

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

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5 July 2018

Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective study

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5 July 2018

The search for new cardiovascular biomarkers

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Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes

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Genomewide association analysis of coronary artery disease

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

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A common allele on chromosome 9 associated with coronary heart disease

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5 July 2018

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

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5 July 2018

Prediction of clinical cardiovascular events with carotid intima-media thickness: a systematic review and meta-analysis

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Multiple biomarkers for the prediction of first major cardiovascular events and death

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Accuracy and impact of risk assessment in the primary prevention of cardiovascular disease: a systematic review

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Carotid intima-media thickening indicates a higher vascular risk across a wide age range: prospective data from the Carotid Atherosclerosis Progression Study (CAPS).

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

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12 December 2020

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10.1371/JOURNAL.PONE.0028931

1 reference

Europe PubMed Central

31 July 2017

2012PLoSO...728931H

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1 reference

Europe PubMed Central

31 July 2017

1 reference

Europe PubMed Central

31 July 2017

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