Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population (Q35046461)

6 August 2017

title

Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population (English)

1 reference

6 August 2017

Annabel Z Wang

1

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6 August 2017

Lin Li

2

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6 August 2017

Bin Zhang

3

1 reference

6 August 2017

Gong-Qing Shen

4

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6 August 2017

Qing Kenneth Wang

5

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6 August 2017

language of work or name

English

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publication date

4 April 2011

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6 August 2017

published in

Annals of Human Genetics

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6 August 2017

volume

75

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6 August 2017

issue

4

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6 August 2017

page(s)

475-482

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From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locus

6 August 2017

cites work

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8 July 2018

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TANGO1 facilitates cargo loading at endoplasmic reticulum exit sites

8 July 2018

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

8 July 2018

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8 July 2018

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8 July 2018

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Large scale association analysis of novel genetic loci for coronary artery disease

8 July 2018

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Identification of association of common AGGF1 variants with susceptibility for Klippel-Trenaunay syndrome using the structure association program

8 July 2018

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

8 July 2018

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8 July 2018

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8 July 2018

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An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction

8 July 2018

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Reduced expression of TANGO in colon and hepatocellular carcinomas.

8 July 2018

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Interactions of TANGO and leukocyte integrin CD11c/CD18 regulate the migration of human monocytes

8 July 2018

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8 July 2018

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A common allele on chromosome 9 associated with coronary heart disease

8 July 2018

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

8 July 2018

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8 July 2018

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Molecular genetics of coronary artery disease

8 July 2018

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Advances in the genetic basis of coronary artery disease

8 July 2018

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Premature myocardial infarction novel susceptibility locus on chromosome 1P34-36 identified by genomewide linkage analysis

8 July 2018

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Association of the single nucleotide polymorphism rs599839 in the vicinity of the sortilin 1 gene with LDL and triglyceride metabolism, coronary heart disease and myocardial infarction. The Ludwigshafen Risk and Cardiovascular Health Study

8 July 2018

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Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease

21 January 2018

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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

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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

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

21 January 2018

1 reference

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Minor allele C of chromosome 1p32 single nucleotide polymorphism rs11206510 confers risk of ischemic stroke in the Chinese Han population.

21 January 2018

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Genetic--epidemiologic study of early-onset ischemic heart disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21463265

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1111/J.1469-1809.2011.00646.X

1 reference

6 August 2017

1 reference

6 August 2017

1 reference