(Q33377253)

English

Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study

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scholarly article

1 reference

Europe PubMed Central

26 July 2017

Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study (English)

1 reference

Europe PubMed Central

26 July 2017

coronary artery disease

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

26 July 2017

3

1 reference

Europe PubMed Central

26 July 2017

Cornelia M. van Duijn

6

object named as

Cornelia M van Duijn

0 references

5

object named as

Albert Hofman

1 reference

Europe PubMed Central

26 July 2017

Jacqueline C M Witteman

7

object named as

Jacqueline C M Witteman

1 reference

Europe PubMed Central

26 July 2017

4

object named as

Ben A Oostra

1 reference

Europe PubMed Central

26 July 2017

author name string

Mandy van Hoek

2

1 reference

Europe PubMed Central

26 July 2017

language of work or name

0 references

publication date

16 October 2008

1 reference

Europe PubMed Central

26 July 2017

1 reference

Europe PubMed Central

26 July 2017

6

1 reference

Europe PubMed Central

26 July 2017

30

1 reference

Europe PubMed Central

26 July 2017

https://scigraph.springernature.com/pub.10.1186/1741-7015-6-30

0 references

Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2579294

21 June 2018

Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 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=2579294

21 June 2018

The Rotterdam Study: objectives and design update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2579294

21 June 2018

Genomewide association analysis 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=2579294

21 June 2018

A common allele on chromosome 9 associated with coronary heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2579294

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2579294

21 June 2018

The increased risk of death from ischaemic heart disease in first degree relatives of 121 men and 96 women with ischaemic heart disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2579294

21 June 2018

Prevalence, determinants, and misclassification of myocardial infarction in the elderly

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2579294

21 June 2018

Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-6-30

21 January 2018

Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-6-30

21 January 2018

Predictive value of noninvasive measures of atherosclerosis for incident myocardial infarction: the Rotterdam Study.

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-6-30

21 January 2018

Sample size requirements for matched case-control studies of gene-environment interaction

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-6-30

21 January 2018

Role of the CDKN1A/p21, CDKN1C/p57, and CDKN2A/p16 genes in the risk of atherosclerosis and myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925945

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A common variant on chromosome 9p21 affects the risk of early-onset coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925945

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1741-7015-6-30

1 reference

Europe PubMed Central

26 July 2017

1 reference

Europe PubMed Central

26 July 2017

1 reference

Europe PubMed Central

26 July 2017

ResearchGate publication ID

0 references

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