(Q35053963)

English

Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes

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scholarly article

1 reference

Europe PubMed Central

6 August 2017

Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes (English)

1 reference

Europe PubMed Central

6 August 2017

1 reference

based on heuristic

inferred from title

coronary artery disease

1 reference

based on heuristic

inferred from title

13

object named as

E J Topol

1 reference

Europe PubMed Central

6 August 2017

L Kristin Newby

10

object named as

L K Newby

1 reference

Europe PubMed Central

6 August 2017

author name string

J J McCarthy

1

1 reference

Europe PubMed Central

6 August 2017

A Parker

2

1 reference

Europe PubMed Central

6 August 2017

R Salem

3

1 reference

Europe PubMed Central

6 August 2017

D J Moliterno

4

1 reference

Europe PubMed Central

6 August 2017

Q Wang

5

1 reference

Europe PubMed Central

6 August 2017

E F Plow

6

1 reference

Europe PubMed Central

6 August 2017

S Rao

7

1 reference

Europe PubMed Central

6 August 2017

G Shen

8

1 reference

Europe PubMed Central

6 August 2017

W J Rogers

9

1 reference

Europe PubMed Central

6 August 2017

R Cannata

11

1 reference

Europe PubMed Central

6 August 2017

K Glatt

12

1 reference

Europe PubMed Central

6 August 2017

GeneQuest Investigators

14

1 reference

Europe PubMed Central

6 August 2017

language of work or name

0 references

publication date

1 May 2004

1 reference

Europe PubMed Central

6 August 2017

Journal of Medical Genetics

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Europe PubMed Central

6 August 2017

41

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Europe PubMed Central

6 August 2017

334-341

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Europe PubMed Central

6 August 2017

5

1 reference

Europe PubMed Central

6 August 2017

The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Thrombospondin-4 and its variants: expression and differential effects on endothelial cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Problems of reporting genetic associations with complex outcomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Genetic associations in large versus small studies: an empirical assessment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Prevalence of coronary heart disease associated with HFE mutations in adults attending a health appraisal center

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

A comprehensive review of genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Genetic risk factors of venous thrombosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Detecting association in a case-control study while correcting for population stratification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Characterization of single-nucleotide polymorphisms in coding regions of human genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

The P-selectin gene is highly polymorphic: reduced frequency of the Pro715 allele carriers in patients with myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Family history as a risk factor of coronary heart disease in patients under 60 years of age.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Polymorphism of the NADH/NADPH oxidase p22 phox gene in patients with coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

DNA polymorphisms in the apolipoprotein C-III and insulin genes and atherosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

Coronary artery disease and its risk factors in families of young men with angina pectoris and in controls

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

8 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

A comprehensive linkage analysis for myocardial infarction and its related risk factors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

The interleukin-6 -174 G/C promoter polymorphism is associated with risk of coronary heart disease and systolic blood pressure in healthy men.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

A new promoter polymorphism in the gene of lipopolysaccharide receptor CD14 is associated with expired myocardial infarction in patients with low atherosclerotic risk profile

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

Polymorphisms of platelet membrane glycoprotein Ib associated with arterial thrombotic disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

Association of the platelet Pl(A) polymorphism of glycoprotein IIb/IIIa and the fibrinogen Bbeta 448 polymorphism with myocardial infarction and extent of coronary artery disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

Relationship of polymorphisms in the renin-angiotensin system and in E-selectin of patients with early severe coronary heart disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

Impact of apolipoprotein E polymorphism on lipoproteins and risk of myocardial infarction. The ECTIM Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1579684

25 October 2018

Tobacco smoking modifies association between Gln-Arg192 polymorphism of human paraoxonase gene and risk of myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Associations between lipoprotein lipase gene polymorphisms and plasma correlations of lipids, lipoproteins and lipase activities in young myocardial infarction survivors and age-matched healthy individuals from Sweden

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Beta fibrinogen gene polymorphisms are associated with plasma fibrinogen and coronary artery disease in patients with myocardial infarction. The ECTIM Study. Etude Cas-Temoins sur l'Infarctus du Myocarde

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisome proliferator-activated receptor gamma C161-->T polymorphism and coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The relationship between angiotensin II type 1 receptor gene and coronary heart disease, hypertension and diabetes mellitus in Chinese]

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

E-selectin polymorphism and atherosclerosis: an association study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between HaeIII polymorphism of scavenger receptor class B type I gene and plasma HDL-cholesterol concentration

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An insertion/deletion polymorphism in the α2b-adrenergic receptor gene is a novel genetic risk factor for acute coronary events

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Allelic discrimination using fluorogenic probes and the 5' nuclease assay

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common variant of the endothelial nitric oxide synthase (Glu298-->Asp) is a major risk factor for coronary artery disease in the UK

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in the Coagulation Factor VII Gene and the Risk of Myocardial Infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein A1 gene polymorphisms and risk of early coronary disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The LDL receptor-related protein (LRP1/A2MR) and coronary atherosclerosis--novel genomic variants and functional consequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interleukin-1 receptor antagonist gene polymorphism and coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of cholesteryl ester transfer protein-TaqIB polymorphism with variations in lipoprotein subclasses and coronary heart disease risk: the Framingham study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15121769

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.2003.016584

1 reference

Europe PubMed Central

6 August 2017

1 reference

Europe PubMed Central

6 August 2017

1 reference

Europe PubMed Central

6 August 2017

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