(Q33299387)

English

Genetic variants of complement factor H gene are not associated with premature coronary heart disease: a family-based study in the Irish population

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Genetic variants of complement factor H gene are not associated with premature coronary heart disease: a family-based study in the Irish population (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

population genetics

0 references

1 reference

based on heuristic

inferred from title

coronary artery disease

1 reference

based on heuristic

inferred from title

author name string

Weihua Meng

1

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Anne Hughes

2

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Chris C Patterson

3

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Christine Belton

4

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Muhammad S Kamaruddin

5

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Paul G Horan

6

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Frank Kee

7

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Pascal P McKeown

8

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

publication date

18 September 2007

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

BMC Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

8

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

62

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

A common CFH haplotype, with deletion of CFHR1 and CFHR3, is associated with lower risk of age-related macular degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

Genetic susceptibility to myocardial infarction and coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

Complement factor H Y402H gene polymorphism, C-reactive protein, and risk of incident myocardial infarction, ischaemic stroke, and venous thromboembolism: a nested case-control study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

Bruch's membrane and the vascular intima: is there a common basis for age-related changes and disease?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

Complement factor H polymorphism in age-related macular degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

Complement factor H polymorphism and age-related macular degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

Complement factor H variant increases the risk of age-related macular degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

The human complement factor H: functional roles, genetic variations and disease associations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

Role of complement activation in atherosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2048938

21 June 2018

A common site within factor H SCR 7 responsible for binding heparin, C-reactive protein and streptococcal M protein.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-62

21 January 2018

Family-based investigation of the C677T polymorphism of the methylenetetrahydrofolate reductase gene in ischaemic heart disease.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-62

21 January 2018

Intracranial arteries of human fetuses are more resistant to hypercholesterolemia-induced fatty streak formation than extracranial arteries.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-62

21 January 2018

C-reactive protein is a marker for a complex culprit lesion anatomy in unstable angina

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-62

21 January 2018

The role of the atherosclerotic process in the pathogenesis of age-related macular degeneration

1 reference

https://pubmed.ncbi.nlm.nih.gov/17877809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of association between complement factor H polymorphisms and coronary artery disease or myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/17877809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between complement factor H and proteoglycans in early human coronary atherosclerotic lesions: implications for local regulation of complement activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/17877809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The electrocardiogram in population studies. A classification system

1 reference

https://pubmed.ncbi.nlm.nih.gov/17877809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement factor H Y402H gene polymorphism in coronary artery disease and atherosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17877809

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2350-8-62

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 July 2017

ResearchGate publication ID

0 references

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