(Q34170897)

31 July 2017

1 reference

23 July 2020

1 reference

systematic review

1 reference

title

Variants in exon 11 of MEF2A gene and coronary artery disease: evidence from a case-control study, systematic review, and meta-analysis (English)

1 reference

myogenic regulatory factors

31 July 2017

main subject

coronary artery disease

1 reference

23 July 2020

1 reference

14 September 2019

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11 December 2019

1 reference

22 December 2019

genetic predisposition to disease

1 reference

10 September 2020

1 reference

1 reference

1 reference

Yan Liu

1

1 reference

31 July 2017

Wenquan Niu

2

1 reference

31 July 2017

Zhijun Wu

3

1 reference

31 July 2017

Xiuxiu Su

4

1 reference

31 July 2017

Qiujin Chen

5

1 reference

31 July 2017

Lin Lu

6

1 reference

31 July 2017

Wei Jin

7

1 reference

31 July 2017

language of work or name

English

0 references

publication date

21 February 2012

11 references

31 July 2017

14 March 2019

19 March 2019

22 March 2019

17 June 2019

30 June 2019

14 September 2019

11 December 2019

22 December 2019

23 July 2020

10 September 2020

10 references

31 July 2017

14 March 2019

19 March 2019

22 March 2019

17 June 2019

30 June 2019

14 September 2019

11 December 2019

22 December 2019

23 July 2020

7

1 reference

31 July 2017

issue

2

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31 July 2017

page(s)

e31406

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Creative Commons Attribution 4.0 International

31 July 2017

copyright license

9 references

14 March 2019

19 March 2019

22 March 2019

17 June 2019

30 June 2019

14 September 2019

11 December 2019

22 December 2019

on focus list of Wikimedia project

23 July 2020

copyright status

copyrighted

0 references

ScienceSource

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cites work

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The relative importance of common and rare genetic variants in the development of hypertriglyceridemia

5 July 2018

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Emerging genomic applications in coronary artery disease

5 July 2018

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

5 July 2018

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Genetic contribution of the leukotriene pathway to coronary artery disease

5 July 2018

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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

5 July 2018

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GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE - Session Introduction

5 July 2018

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Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review

5 July 2018

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Structural changes in exon 11 of MEF2A are not related to sporadic coronary artery disease in Han Chinese population

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3283621

Association and functional analyses of MEF2A as a susceptibility gene for premature myocardial infarction and coronary artery disease

5 July 2018

1 reference

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Common vs. rare allele hypotheses for complex diseases

5 July 2018

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Functional SNPs in HSPA1A gene predict risk of coronary heart disease

5 July 2018

1 reference

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Molecular genetics of myocardial infarction

5 July 2018

1 reference

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Common and rare alleles as causes of complex phenotypes

5 July 2018

1 reference

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The genetic basis of complex traits: rare variants or "common gene, common disease"?

5 July 2018

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Lack of association between the platelet glycoprotein Ia C807T gene polymorphism and coronary artery disease: a meta-analysis

5 July 2018

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Genetic susceptibility to myocardial infarction and coronary artery disease

5 July 2018

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Lack of MEF2A Delta7aa mutation in Irish families with early onset ischaemic heart disease, a family based study

5 July 2018

1 reference

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Genome-wide association study to identify SNPs conferring risk of myocardial infarction and their functional analyses.

5 July 2018

1 reference

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Miscues on the "lack of MEF2A mutations" in coronary artery disease

5 July 2018

1 reference

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Lack of MEF2A mutations in 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=3283621

MEF2A sequence variants and coronary artery disease: a change of heart?

5 July 2018

1 reference

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Genome-wide association studies for common diseases and complex traits

5 July 2018

1 reference

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Transcription factor MEF2A mutations in patients with 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=3283621

Mutation of MEF2A in an inherited disorder with features of coronary artery disease

5 July 2018

1 reference

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Genetic factors in cardiovascular disease. 10 questions

5 July 2018

1 reference

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5 July 2018

1 reference

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Genetic evaluation for coronary artery disease

5 July 2018

1 reference

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5 July 2018

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5 July 2018

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5 July 2018

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5 July 2018

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Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21.

5 July 2018

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The Pro279Leu variant in the transcription factor MEF2A is associated with myocardial infarction

21 January 2018

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CAG repeat polymorphism of the MEF2A gene is not associated with the risk of coronary artery disease among Taiwanese.

21 January 2018

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Lack of Association Between the MEF2A Gene and Myocardial Infarction

21 January 2018

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21 January 2018

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How meta-analysis increases statistical power

21 January 2018

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12 December 2020

[Study on novel mutations of MEF2A gene in Chinese patients with coronary artery disease]

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12 December 2020

MEF2A gene and susceptibility to coronary artery disease in the Chinese people

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12 December 2020

Assessment of MEF2A mutations in myocardial infarction in Japanese patients

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12 December 2020

A study of the role of the Myocyte-specific Enhancer Factor-2A gene in coronary artery disease

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12 December 2020

Relationship of the CAG repeat polymorphism of the MEF2A gene and coronary artery disease in a Chinese population

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12 December 2020

MEF2A sequence variants in Turkish population

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12 December 2020

Exon 11 deletion in the myocyte enhancer factor (MEF)2A and early onset coronary artery disease gene in a Sicilian family

1 reference

12 December 2020

10.1371/JOURNAL.PONE.0031406

Identifiers

DOI

1 reference

release_jgttuemga5ft7caqdsmj2j5rvm

31 July 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jgttuemga5ft7caqdsmj2j5rvm

24 November 2022

mapped directly with Wikidata item

PMC publication ID

3283621

1 reference

31 July 2017

1 reference