(Q37074287)

18 August 2017

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title

Progress in unraveling the genetics of coronary artery disease and myocardial infarction (English)

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18 August 2017

main subject

myocardial infarction

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4

Paul N Hopkins

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18 August 2017

Jeffrey L Anderson

1

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18 August 2017

John F Carlquist

series ordinal

2

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18 August 2017

Benjamin D Horne

series ordinal

3

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18 August 2017

language of work or name

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1 September 2007

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Current Atherosclerosis Reports

18 August 2017

published in

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18 August 2017

volume

9

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18 August 2017

issue

3

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18 August 2017

page(s)

179-186

1 reference

https://scigraph.springernature.com/pub.10.1007/s11883-007-0017-4

18 August 2017

exact match

0 references

cites work

Preventing myocardial infarction in the young adult in the first place: how do the national cholesterol education panel iii guidelines perform?

1 reference

12 December 2020

Plasma triglycerides and type III hyperlipidemia are independently associated with premature familial coronary artery disease

1 reference

12 December 2020

Lack of MEF2A mutations in coronary artery disease

1 reference

12 December 2020

Genotypes of the cytochrome p450 isoform, CYP2C9, and the vitamin K epoxide reductase complex subunit 1 conjointly determine stable warfarin dose: a prospective study.

1 reference

12 December 2020

Genomic medicine--a primer

1 reference

12 December 2020

MTHFR 677C-->T polymorphism and risk of coronary heart disease: a meta-analysis.

1 reference

12 December 2020

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

1 reference

12 December 2020

Prevalence of conventional risk factors in patients with coronary heart disease

1 reference

12 December 2020

A haplotype map of the human genome

1 reference

12 December 2020

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

12 December 2020

A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol.

1 reference

12 December 2020

A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration

1 reference

12 December 2020

Heterozygous familial hypercholesterolemia: Failure of normal allele to compensate for mutant allele at a regulated genetic locus

1 reference

12 December 2020

Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution

1 reference

12 December 2020

Major apolipoprotein B-100 mutations in lipoprotein metabolism and atherosclerosis

1 reference

12 December 2020

Heart disease and stroke statistics--2006 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

1 reference

12 December 2020

The structure of haplotype blocks in the human genome

1 reference

12 December 2020

The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction

1 reference

12 December 2020

A variant of the gene encoding leukotriene A4 hydrolase confers ethnicity-specific risk of myocardial infarction

1 reference

12 December 2020

Genetic susceptibility to myocardial infarction and coronary artery disease

1 reference

12 December 2020

Generating genetic risk scores from intermediate phenotypes for use in association studies of clinically significant endpoints

1 reference

12 December 2020

Positive association of the beta fibrinogen H1/H2 gene variation to basal fibrinogen levels and to the increase in fibrinogen concentration during acute phase reaction but not to coronary artery disease and myocardial infarction

1 reference

12 December 2020

Heritability of death from coronary heart disease: a 36-year follow-up of 20 966 Swedish twins

1 reference

12 December 2020

Update on low density lipoprotein receptor mutations

1 reference

12 December 2020

The heritability of mortality due to heart diseases: a correlated frailty model applied to Danish twins

1 reference

12 December 2020

Familial defective apolipoprotein B100: clinical characteristics of 54 cases

1 reference

12 December 2020

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

1 reference

12 December 2020

Cardiovascular pharmacogenomics: current status, future prospects

1 reference

12 December 2020

A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study

1 reference

12 December 2020

An utter refutation of the "fundamental theorem of the HapMap".

1 reference

12 December 2020

Gene variants of VAMP8 and HNRPUL1 are associated with early-onset myocardial infarction

1 reference

12 December 2020

The gene encoding 5-lipoxygenase activating protein confers risk of myocardial infarction and stroke

1 reference

12 December 2020

Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro

1 reference

12 December 2020

SNP judgments and freedom of association

1 reference

12 December 2020

Major risk factors as antecedents of fatal and nonfatal coronary heart disease events

1 reference

12 December 2020

Mutation of MEF2A in an inherited disorder with features of coronary artery disease

1 reference

12 December 2020

Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

1 reference

12 December 2020

Replication validity of genetic association studies

1 reference

12 December 2020

Usefulness of cardiovascular family history data for population-based preventive medicine and medical research (the Health Family Tree Study and the NHLBI Family Heart Study).

1 reference

12 December 2020

The Sequence of the Human Genome

1 reference

12 December 2020

Phenotypic variability in familial hypercholesterolaemia: an update

1 reference

12 December 2020

Candidate gene susceptibility variants predict intermediate end points but not angiographic coronary artery disease

1 reference

12 December 2020

Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration

1 reference

12 December 2020

Identification of four gene variants associated with myocardial infarction

1 reference

12 December 2020

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

12 December 2020

Large-scale test of hypothesised associations between the angiotensin-converting-enzyme insertion/deletion polymorphism and myocardial infarction in about 5000 cases and 6000 controls. International Studies of Infarct Survival (ISIS) Collaborators

1 reference

12 December 2020

Initial sequencing and analysis of the human genome

1 reference

12 December 2020

High-Resolution Characterization of Linkage Disequilibrium Structure and Selection of Tagging Single Nucleotide Polymorphisms: Application to the Cholesteryl Ester Transfer Protein Gene

1 reference

12 December 2020

10.1007/S11883-007-0017-4

Identifiers

DOI

1 reference

18 August 2017

1 reference