(Q37167765)

18 August 2017

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title

Genetics of premature myocardial infarction (English)

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18 August 2017

main subject

myocardial infarction

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Robert Roberts

1

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18 August 2017

publication date

1 June 2008

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Current Atherosclerosis Reports

18 August 2017

published in

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18 August 2017

volume

10

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18 August 2017

issue

3

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18 August 2017

page(s)

186-193

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https://scigraph.springernature.com/pub.10.1007/s11883-008-0030-2

18 August 2017

exact match

0 references

cites work

Familial lipoprotein disorders in patients with premature coronary artery disease

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11883-008-0030-2

Lack of MEF2A mutations in coronary artery disease

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11883-008-0030-2

A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study

21 January 2018

1 reference

12 December 2020

Genome-wide association studies for common diseases and complex traits

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12 December 2020

Molecular cardiology and genetics in the 21st century--a primer

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12 December 2020

Genetics and prevention: a new look at high-density lipoprotein cholesterol

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12 December 2020

The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease

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12 December 2020

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

1 reference

12 December 2020

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.

1 reference

12 December 2020

The familial occurrence of hypertension and coronary artery disease, with observations concerning obesity and diabetes

1 reference

12 December 2020

Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol

1 reference

12 December 2020

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

1 reference

12 December 2020

Whole-genome patterns of common DNA variation in three human populations

1 reference

12 December 2020

Tangier disease as a test of the reverse cholesterol transport hypothesis

1 reference

12 December 2020

Measures of twin concordance

1 reference

12 December 2020

Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysis.

1 reference

12 December 2020

Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100

1 reference

12 December 2020

Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study

1 reference

12 December 2020

Personalized genomic medicine: a future prerequisite for the prevention of coronary artery disease.

1 reference

12 December 2020

Familial hypercholesterolemia and coronary heart disease: a HuGE association review

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12 December 2020

Association studies in an era of too much information: clinical analysis of new biomarker and genetic data

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12 December 2020

Genome-wide association studies: theoretical and practical concerns

1 reference

12 December 2020

A genomewide scan for early-onset coronary artery disease in 438 families: the GENECARD Study

1 reference

12 December 2020

Familial defective apolipoprotein B100: clinical characteristics of 54 cases

1 reference

12 December 2020

Family history assessment: strategies for prevention of cardiovascular disease

1 reference

12 December 2020

Incidence of coronary artery disease in siblings of patients with premature coronary artery disease: 10 years of follow-up.

1 reference

12 December 2020

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

1 reference

12 December 2020

Genes influencing HDL metabolism: new perspectives and implications for atherosclerosis prevention

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12 December 2020

A common allele on chromosome 9 associated with coronary heart disease

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12 December 2020

FAMILIAL PATTERNS IN ISCHAEMIC HEART DISEASE.

1 reference

12 December 2020

Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia

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12 December 2020

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

1 reference

12 December 2020

Genomewide association analysis of coronary artery disease

1 reference

12 December 2020

Peakwide mapping on chromosome 3q13 identifies the kalirin gene as a novel candidate gene for coronary artery disease

1 reference

12 December 2020

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

1 reference

12 December 2020

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.

1 reference

12 December 2020

Genomewide scans of complex human diseases: true linkage is hard to find

1 reference

12 December 2020

Myozenin 2 is a novel gene for human hypertrophic cardiomyopathy

1 reference

12 December 2020

A gene harvest revealing the archeology and complexity of human disease

1 reference

12 December 2020

Phenotypic variability in familial hypercholesterolaemia: an update

1 reference

12 December 2020

Inhibition of experimental intimal thickening in mice lacking a novel G-protein-coupled receptor

1 reference

12 December 2020

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

12 December 2020

Kalirin expression is regulated by multiple promoters

1 reference

12 December 2020

Genetics of familial combined hyperlipidemia and risk of coronary heart disease

1 reference

12 December 2020

10.1007/S11883-008-0030-2

Identifiers

DOI

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18 August 2017

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