(Q33403360)

26 July 2017

The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosis (English)

1 reference

26 July 2017

1 reference

1 reference

coronary artery disease

1 reference

inferred from title

author

Christie M. Ballantyne

series ordinal

2

object named as

Christie M Ballantyne

1 reference

26 July 2017

Suet Nee Chen

1

1 reference

26 July 2017

Antonio M Gotto

series ordinal

3

1 reference

26 July 2017

Ali J Marian

series ordinal

4

1 reference

26 July 2017

language of work or name

1 reference

27 January 2009

1 reference

BMC Cardiovascular Disorders

26 July 2017

1 reference

26 July 2017

9

1 reference

26 July 2017

3

1 reference

Creative Commons Attribution 2.0 Generic

26 July 2017

start time

27 January 2009

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.10.1186/1471-2261-9-3

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

Inactivation of the p19(ARF) tumor suppressor affects intestinal epithelial cell proliferation and integrity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

p15Ink4b is a critical tumour suppressor in the absence of p16Ink4a

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

Genomewide association analysis of coronary artery disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

A common allele on chromosome 9 associated with coronary heart disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

Tracking atherosclerosis regression: a clinical tool in preventive cardiology

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

Role of the p16 tumor suppressor gene in cancer

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

Prevalence of germ-line mutations in p16, p19ARF, and CDK4 in familial melanoma: analysis of a clinic-based population

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

Testing for linkage disequilibrium in genotypic data using the Expectation-Maximization algorithm

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2637231

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

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-9-3

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-9-3

Role of the INK4a locus in tumor suppression and cell mortality.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-9-3

Specific haplotypes of the P-selectin gene are associated with myocardial infarction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-9-3

A new algorithm for haplotype-based association analysis: the Stochastic-EM algorithm.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-9-3

Coronary Artery Disease-Associated Locus on Chromosome 9p21 and Early Markers of Atherosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-9-3

Genetic determination of osteoporosis: lessons learned from a large genome-wide linkage study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-9-3

A first-generation linkage disequilibrium map of human chromosome 22

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-9-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-9-3

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/19173706

12 December 2020

inferred from PubMed ID database lookup

Effects of fluvastatin on coronary atherosclerosis in patients with mild to moderate cholesterol elevations (Lipoprotein and Coronary Atherosclerosis Study [LCAS])

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19173706

12 December 2020

inferred from PubMed ID database lookup

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/19173706

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1186/1471-2261-9-3

1 reference

Dimensions Publication ID

26 July 2017

0 references

1 reference

26 July 2017

1 reference