(Q33717049)

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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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scholarly article

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Europe PubMed Central

PubMed publication ID

28 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

atherosclerosis

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based on heuristic

inferred from title

Leo-Pekka Lyytikäinen

11

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Europe PubMed Central

PubMed publication ID

28 July 2017

Terho Lehtimäki

2

object named as

Terho Lehtimäki

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6

object named as

Mika Kähönen

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Nina Hutri-Kähönen

14

object named as

Nina Hutri-Kähönen

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Europe PubMed Central

PubMed publication ID

28 July 2017

object named as

Laura L Elo

3

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Tero Aittokallio

object named as

Tero Aittokallio

19

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object named as

Markus Juonala

7

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18

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Olli T Raitakari

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

17

object named as

Jorma S A Viikari

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

10

object named as

Tomi Laitinen

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

4

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Nina Mononen

1 reference

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PubMed publication ID

28 July 2017

Jussi A Hernesniemi

9

object named as

Jussi A Hernesniemi

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Leena Taittonen

15

object named as

Leena Taittonen

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

author name string

Sebastian Okser

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Nina Peltonen

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Yue-Mei Fan

8

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Riikka Rontu

12

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Carita Eklund

13

1 reference

Europe PubMed Central

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28 July 2017

Mikko Hurme

16

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

publication date

30 September 2010

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Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

6

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Europe PubMed Central

PubMed publication ID

28 July 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

e1001146

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Europe PubMed Central

PubMed publication ID

28 July 2017

copyright license

Creative Commons Attribution 4.0 International

30 September 2010

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April 2022 Public Data File from Crossref

copyright status

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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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Bioinformatics challenges for genome-wide association studies

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Common disorders are quantitative traits

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Human genetic variation and its contribution to complex traits

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Comparison of classification methods for detecting associations between SNPs and chick mortality

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Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers

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Usefulness of genetic polymorphisms and conventional risk factors to predict coronary heart disease in patients with familial hypercholesterolemia

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

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Progress and challenges in genome-wide association studies in humans

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Personal genomes: The case of the missing heritability

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21 June 2018

Gender differences in genetic risk profiles for cardiovascular disease

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21 June 2018

Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: a HuGE association review and meta-analysis

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21 June 2018

Epistasis--the essential role of gene interactions in the structure and evolution of genetic systems

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21 June 2018

Analysis of 17,576 potentially functional SNPs in three case-control studies of myocardial infarction

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Simultaneous analysis of all SNPs in genome-wide and re-sequencing association studies

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Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest).

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

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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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21 June 2018

A common allele on chromosome 9 associated with coronary heart disease

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21 June 2018

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

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21 June 2018

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

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21 June 2018

A tutorial on statistical methods for population association studies

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21 June 2018

Regulation of vascular calcification by osteoclast regulatory factors RANKL and osteoprotegerin

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Limitations of the odds ratio in gauging the performance of a diagnostic, prognostic, or screening marker

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Intima-media thickness: a tool for atherosclerosis imaging and event prediction

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Selection bias in gene extraction on the basis of microarray gene-expression data

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New tools for coronary risk assessment: what are their advantages and limitations?

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Carotid-artery intima and media thickness as a risk factor for myocardial infarction and stroke in older adults. Cardiovascular Health Study Collaborative Research Group

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osteoprotegerin-deficient mice develop early onset osteoporosis and arterial calcification

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Conventional cardiovascular risk factors and metabolic syndrome in predicting carotid intima-media thickness progression in young adults: the cardiovascular risk in young Finns study.

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Genetic variation at the 9p21 locus predicts angiographic coronary artery disease prevalence but not extent and has clinical utility.

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Childhood cardiovascular risk factors and carotid vascular changes in adulthood: the Bogalusa Heart Study

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Value of genetic profiling for the prediction of coronary heart disease

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Common disorders are quantitative traits

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Cohort Profile: The Cardiovascular Risk in Young Finns Study

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Statistical power of association using the extreme discordant phenotype design

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Allelic discrimination using fluorogenic probes and the 5' nuclease assay

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Machine learning classification procedure for selecting SNPs in genomic selection: application to early mortality in broilers

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Identifiers

10.1371/JOURNAL.PGEN.1001146

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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