(Q28943353)

2

1 reference

14 March 2017

Ken Yamamoto

3

1 reference

14 March 2017

Eitaro Nakashima

4

1 reference

14 March 2017

Tomohiro Katsuya

5

1 reference

14 March 2017

Hiroyuki Asano

6

1 reference

14 March 2017

Masato Isono

7

1 reference

14 March 2017

Toru Nabika

8

1 reference

14 March 2017

Takao Sugiyama

9

1 reference

14 March 2017

Akihiro Fujioka

10

1 reference

14 March 2017

Nobuhisa Awata

11

1 reference

14 March 2017

Keizo Ohnaka

12

1 reference

14 March 2017

Masahiro Nakatochi

13

1 reference

14 March 2017

Hidetoshi Kitajima

14

1 reference

14 March 2017

Jiro Nakamura

16

1 reference

14 March 2017

Takayoshi Ohkubo

17

1 reference

14 March 2017

Yutaka Imai

18

1 reference

14 March 2017

Kazuaki Shimamoto

19

1 reference

14 March 2017

Shuhei Yamaguchi

21

1 reference

14 March 2017

Shotai Kobayashi

22

1 reference

14 March 2017

Ryoichi Takayanagi

23

1 reference

14 March 2017

Toshio Ogihara

24

1 reference

14 March 2017

Norihiro Kato

European Journal of Human Genetics

25

1 reference

14 March 2017

1 March 2012

1 reference

14 March 2017

1 reference

14 March 2017

20

1 reference

14 March 2017

3

1 reference

14 March 2017

333–340

1 reference

14 March 2017

describes a project that uses

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

Signals of recent positive selection in a worldwide sample of human populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Activation of aldehyde dehydrogenase-2 reduces ischemic damage to the heart

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

PLINK: a tool set for whole-genome association and population-based linkage analyses

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Subtle differences in HLA DQ haplotype-associated presentation of AChR alpha-chain peptides may suffice to mediate myasthenia gravis

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Genomic control for association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Dyslipidemia and cardiovascular disease: a series of epidemiologic studies in Japanese populations

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Genetics of myocardial infarction: a progress report

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Variance component model to account for sample structure in genome-wide association studies

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Magnitude of stratification in human populations and impacts on genome wide association studies

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

New susceptibility locus for coronary artery disease on chromosome 3q22.3.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Overcoming the winner's curse: estimating penetrance parameters from case-control data

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

DNA repair capacity measured by high throughput alkaline comet assays in EBV-transformed cell lines and peripheral blood cells from cancer patients and healthy volunteers

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283177

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

3 June 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2011.184

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/10.1038%2FEJHG.2011.184

SNPs in BRAP associated with risk of myocardial infarction in Asian populations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2011.184

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2011.184

Aldehyde dehydrogenase 2 gene is a risk factor for myocardial infarction in Japanese men.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2011.184

Lack of association between lymphotoxin-alpha, galectin-2 polymorphisms and coronary artery disease: a meta-analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2011.184

A Low Prevalence of Coronary Heart Disease among Subjects with Increased High-Density Lipoprotein Cholesterol Levels, Including Those with Plasma Cholesteryl Ester Transfer Protein Deficiency

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21971053

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Weak associations between human leucocyte antigen genotype and acute myocardial infarction

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21971053

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2011.184

1 reference

Dimensions Publication ID

1109666

1030923334

0 references

1109666

1 reference

1 reference

1 reference