(Q34787709)

4 August 2017

1 reference

title

Genetic cardiovascular risk prediction: will we get there? (English)

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4 August 2017

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Ramachandran S. Vasan

object named as

Ramachandran S Vasan

series ordinal

2

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author name string

George Thanassoulis

series ordinal

1

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4 August 2017

language of work or name

English

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publication date

1 November 2010

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4 August 2017

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4 August 2017

volume

122

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4 August 2017

issue

22

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4 August 2017

page(s)

2323-2334

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The genetic interpretation of area under the ROC curve in genomic profiling

4 August 2017

cites work

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8 July 2018

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General Cardiovascular Risk Profile identifies advanced coronary artery calcium and is improved by family history: the multiethnic study of atherosclerosis

8 July 2018

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

8 July 2018

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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

8 July 2018

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Prediction of cardiovascular disease outcomes and established cardiovascular risk factors by genome-wide association markers

8 July 2018

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Sequencing technologies - the next generation

8 July 2018

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Large, rare chromosomal deletions associated with severe early-onset obesity

8 July 2018

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Assessment of claims of improved prediction beyond the Framingham risk score

8 July 2018

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Sporadic cases are the norm for complex disease

8 July 2018

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Finding the missing heritability of complex diseases

8 July 2018

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Genetic scoring analysis: a way forward in genome wide association studies?

8 July 2018

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A genome-wide association study of hypertension and blood pressure in African Americans

8 July 2018

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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

8 July 2018

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

8 July 2018

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Challenges of translating genetic tests into clinical and public health practice

8 July 2018

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Predicting the 30-year risk of cardiovascular disease: the framingham heart study

8 July 2018

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A composite scoring of genotypes discriminates coronary heart disease risk beyond conventional risk factors in the Boston Puerto Rican Health Study

8 July 2018

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Advances in measuring the effect of individual predictors of cardiovascular risk: the role of reclassification measures

8 July 2018

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Detecting gene-gene interactions that underlie human diseases

8 July 2018

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

8 July 2018

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Genome-wide association study of blood pressure and hypertension

8 July 2018

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Common genetic variation and human traits

8 July 2018

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

8 July 2018

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Genome-based prediction of common diseases: methodological considerations for future research

8 July 2018

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Lowering mortality in ST-elevation myocardial infarction and non-ST-elevation myocardial infarction: key prehospital and emergency room treatment strategies

8 July 2018

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

8 July 2018

1 reference

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Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

8 July 2018

1 reference

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

8 July 2018

1 reference

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Adverse consequences of the 50% misconception

8 July 2018

1 reference

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

8 July 2018

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Heart disease and stroke statistics--2009 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

8 July 2018

1 reference

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

8 July 2018

1 reference

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Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

8 July 2018

1 reference

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Common variants at 30 loci contribute to polygenic dyslipidemia

8 July 2018

1 reference

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Invited commentary: from genome-wide association studies to gene-environment-wide interaction studies--challenges and opportunities

8 July 2018

1 reference

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C-reactive protein and parental history improve global cardiovascular risk prediction: the Reynolds Risk Score for men.

8 July 2018

1 reference

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Genome-based prediction of common diseases: advances and prospects

8 July 2018

1 reference

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Integrated detection and population-genetic analysis of SNPs and copy number variation

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Prediction of individual genetic risk of complex disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Size matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Why Most Discovered True Associations Are Inflated

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Genetic predisposition, nongenetic risk factors, and coronary infarct

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Why study gene-environment interactions?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

'Deep phenotyping': characterizing populations in the era of genomics and systems biology

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Heritability in the genomics era — concepts and misconceptions

8 July 2018

1 reference

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Heterogeneity in meta-analyses of genome-wide association investigations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Prediction of individual genetic risk to disease from genome-wide association studies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Genomewide association analysis of coronary artery disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Derivation and validation of QRISK, a new cardiovascular disease risk score for the United Kingdom: prospective open cohort study.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Evaluating the added predictive ability of a new marker: from area under the ROC curve to reclassification and beyond

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

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

8 July 2018

1 reference

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A common allele on chromosome 9 associated with coronary heart disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

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

8 July 2018

1 reference

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

8 July 2018

1 reference

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Overcoming the winner's curse: estimating penetrance parameters from case-control data

8 July 2018

1 reference

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Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

8 July 2018

1 reference

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Use and misuse of the receiver operating characteristic curve in risk prediction

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Predictive testing for complex diseases using multiple genes: fact or fiction?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Commentary: grading the credibility of molecular evidence for complex diseases

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Sibling cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

A haplotype map of the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Clinical trial designs for predictive marker validation in cancer treatment trials

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Parental cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults: a prospective study of parents and offspring

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Factors of risk in the development of coronary heart disease--six year follow-up experience. The Framingham Study

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Initial sequencing and analysis of the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

The Sequence of the Human Genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Prediction of Coronary Heart Disease Using Risk Factor Categories

8 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

8 July 2018

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Fatality outside hospital from acute coronary events in three British health districts, 1994-5. United Kingdom Heart Attack Study Collaborative Group

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Biased Selection of Controls for Case-Control Analyses of Cohort Studies

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Population-wide generalizability of genome-wide discovered associations

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Value of genetic profiling for the prediction of coronary heart disease

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

A simulation study of control sampling methods for nested case-control studies of genetic and molecular biomarkers and prostate cancer progression

26 October 2018

1 reference

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Polymorphisms associated with cholesterol and risk of cardiovascular events

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Mapping the cancer genome. Pinpointing the genes involved in cancer will help chart a new course across the complex landscape of human malignancies.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Development and validation of improved algorithms for the assessment of global cardiovascular risk in women: the Reynolds Risk Score.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Candidate gene genotypes, along with conventional risk factor assessment, improve estimation of coronary heart disease risk in healthy UK men.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Prevalence of conventional risk factors in patients with coronary heart disease

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Prediction of the risk of myocardial infarction from polymorphisms in candidate genes

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

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

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Distinct Heritable Patterns of Angiographic Coronary Artery Disease in Families With Myocardial Infarction

9 December 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3075800

Health care provider and consumer awareness, perceptions, and use of direct-to-consumer personal genomic tests, United States, 2008

9 December 2018

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12 December 2020

Pharmacogenetics in cardiovascular antithrombotic therapy

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12 December 2020

Cohort studies and the genetics of complex disease

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12 December 2020

Genetic--epidemiologic study of early-onset ischemic heart disease

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12 December 2020

Genetic effects versus bias for candidate polymorphisms in myocardial infarction: case study and overview of large-scale evidence

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12 December 2020

Genetic risk prediction--are we there yet?

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12 December 2020

Population genetics--making sense out of sequence

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12 December 2020

Polygenic susceptibility to breast cancer and implications for prevention

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12 December 2020

10.1161/CIRCULATIONAHA.109.909309

Identifiers

DOI

1 reference

release_ij7ppenfenhr5d33bxxkk4uq6i

4 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ij7ppenfenhr5d33bxxkk4uq6i

24 November 2022

mapped directly with Wikidata item

PMC publication ID

3075800

1 reference

4 August 2017

1 reference