(Q33840124)

29 July 2017

title

Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry (English)

1 reference

multicenter clinical trial

29 July 2017

main subject

0 references

author name string

Thomas Scheffold

1

1 reference

29 July 2017

Silke Kullmann

2

1 reference

29 July 2017

Andreas Huge

3

1 reference

29 July 2017

Priska Binner

4

1 reference

29 July 2017

Hermann R Ochs

5

1 reference

29 July 2017

Wolfgang Schöls

6

1 reference

29 July 2017

Joachim Thale

7

1 reference

29 July 2017

Wolfgang Motz

8

1 reference

29 July 2017

Franz Josef Hegge

9

1 reference

29 July 2017

Christoph Stellbrink

10

1 reference

29 July 2017

Thomas Dorsel

11

1 reference

29 July 2017

Hartmut Gülker

12

1 reference

29 July 2017

Hubertus Heuer

13

1 reference

29 July 2017

Wilfried Dinh

14

1 reference

29 July 2017

Monika Stoll

15

1 reference

29 July 2017

Georg Haltern

16

1 reference

29 July 2017

Forschungsverbund Herz-Kreislauf in NRW (Research Consortium Heart and Circulation in North Rhine-Westphalia)

17

1 reference

29 July 2017

publication date

7 March 2011

1 reference

BMC Cardiovascular Disorders

29 July 2017

published in

1 reference

29 July 2017

volume

11

1 reference

29 July 2017

page(s)

9

1 reference

Creative Commons Attribution 2.0 Generic

29 July 2017

copyright license

start time

7 March 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

exact match

https://scigraph.springernature.com/pub.10.1186/1471-2261-11-9

0 references

cites work

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Identifying the susceptibility genes for coronary artery disease: from hyperbole through doubt to cautious optimism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Whole genome analyses suggest ischemic stroke and heart disease share an association with polymorphisms on chromosome 9p21.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Risk factors for myocardial infarction in women and men: insights from the INTERHEART study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Chromosome 9p21.3 coronary heart disease locus genotype and prospective risk of CHD in healthy middle-aged men.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Genomewide association analysis of coronary artery disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

A common allele on chromosome 9 associated with coronary heart disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Genome-wide association studies for common diseases and complex traits

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Effect of potentially modifiable risk factors associated with myocardial infarction in 52 countries (the INTERHEART study): case-control study

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

Prediction of Coronary Heart Disease Using Risk Factor Categories

5 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

5 July 2018

https://api.crossref.org/works/10.1186%2F1471-2261-11-9

Menopause and risk of cardiovascular disease: the Framingham study.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3061953

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

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2261-11-9

Gene dosage of the common variant 9p21 predicts severity of coronary artery disease.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2261-11-9

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F1471-2261-11-9

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21385355

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Diabetes mellitus and hypertension in the elderly: concomitant hyperlipidemia and coronary heart disease risk

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21385355

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21385355

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2261-11-9

1 reference

Dimensions Publication ID

29 July 2017

0 references

1 reference

29 July 2017

1 reference