(Q33689020)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

title

The rs1333049 polymorphism on locus 9p21.3 and extreme longevity in Spanish and Japanese cohorts (English)

1 reference

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28 February 2020

19

1 reference

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28 February 2020

Noriyuki Fuku

2

1 reference

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28 February 2020

Yolanda Cámara

3

1 reference

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28 February 2020

Nuria Garatachea

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Alejandro Santos-Lozano

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Haruka Murakami

12

1 reference

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28 February 2020

Motohiko Miyachi

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

author name string

Tomàs Pinós

1

1 reference

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28 February 2020

Yasumichi Arai

4

1 reference

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28 February 2020

Yukiko Abe

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Gabriel Rodríguez-Romo

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Elisabet Miro-Casas

9

1 reference

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28 February 2020

Marisol Ruiz-Meana

10

1 reference

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28 February 2020

Imanol Otaegui

11

1 reference

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28 February 2020

David Garcia-Dorado

14

1 reference

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28 February 2020

Kunihiko Hinohara

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Antoni L Andreu

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Akinori Kimura

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Nobuyoshi Hirose

18

1 reference

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28 February 2020

publication date

28 October 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

volume

36

1 reference

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28 February 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

page(s)

933-943

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

Genetic signatures of exceptional longevity in humans

28 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

Genome-wide association study for coronary artery calcification with follow-up in 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=4039251

Are centenarians genetically predisposed to lower disease risk?

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

The coronary artery disease-associated 9p21 variant and later life 20-year survival to cohort extinction

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

Chromosome 9p21.3 polymorphism in a Chinese Han population is associated with angiographic coronary plaque progression in non-diabetic but not in type 2 diabetic patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

Association of an allele on chromosome 9 and abdominal aortic aneurysm

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

Association of the 9p21.3 locus with risk of first-ever myocardial infarction in Pakistanis: case-control study in South Asia and updated meta-analysis of Europeans

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

A variant at chromosome 9p21 is associated with recurrent myocardial infarction and cardiac death after acute coronary syndrome: the GRACE Genetics 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=4039251

Association between 9p21 genomic markers and heart disease: a meta-analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

The 9p21 myocardial infarction risk allele increases risk of peripheral artery disease in older people

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities 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=4039251

Chromosome 9p21.3 genotype is associated with vascular dementia and Alzheimer's 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=4039251

Lack of association of chromosome 9p21.3 genotype with cardiovascular structure and function in persons with stable coronary artery disease: The Heart and Soul 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=4039251

Large scale association analysis of novel genetic loci for 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=4039251

The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

Exceptional longevity does not result in excessive levels of disability

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

Association of genetic variation on chromosome 9p21 with susceptibility and progression of atherosclerosis: a population-based, prospective 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=4039251

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=4039251

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=4039251

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=4039251

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=4039251

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=4039251

Polymorphisms of the genes encoding CD40 and growth differentiation factor 15 and in the 9p21.3 region in patients with rheumatoid arthritis and cardiovascular disease

21 June 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

A common variant at chromosome 9P21.3 is associated with age of onset of coronary disease but not subsequent mortality

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

Preliminary evidence of a genetic association between chromosome 9p21.3 and human longevity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

Functional status of centenarians in Tokyo, Japan: developing better phenotypes of exceptional longevity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

Validation of the association of genetic variants on chromosome 9p21 and 1q41 with myocardial infarction in a Japanese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

Chromosome 9p21 and coronary artery disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

Effect of the functional toll-like receptor 4 Asp299Gly polymorphism on susceptibility to late-onset Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

Evaluation of the association of genetic variants on the chromosomal loci 9p21.3, 6q25.1, and 2q36.3 with angiographically characterized coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

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/10.1007%2FS11357-013-9593-0

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

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/10.1007%2FS11357-013-9593-0

Independent association of the variant rs1333049 at the 9p21 locus and coronary heart disease.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

Single nucleotide polymorphism rs1333049 on chromosome 9p21.3 is associated with Alzheimer's disease in Han Chinese.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4039251

Single polymorphism nucleotide rs1333049 on chromosome 9p21 is associated with carotid plaques but not with common carotid intima-media thickness in older adults. A combined analysis of the Three-City and the EVA studies

30 October 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11357-013-9593-0

A common variant in chromosome 9p21 associated with coronary artery disease in Asian Indians

21 January 2018

1 reference

12 December 2020

Chromosome 9p21 polymorphism is associated with myocardial infarction but not with clinical outcome in Han Chinese

1 reference

12 December 2020

The chromosome 9p21 region and myocardial infarction in a European population

1 reference

12 December 2020

Association between the coronary artery disease risk locus on chromosome 9p21.3 and abdominal aortic aneurysm

1 reference

12 December 2020

Common genetic variants on chromosome 9p21 confers risk of ischemic stroke: a large-scale genetic association study

1 reference

12 December 2020

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

1 reference

12 December 2020

Morbidity of Tokyo-area centenarians and its relationship to functional status

1 reference

12 December 2020

10.1007/S11357-013-9593-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

PubMed publication ID

24163049

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24163049%20AND%20SRC:MED&resulttype=core&format=json