(Q43764697)

26 November 2017

title

Association of polymorphisms in 9p21 region with CAD in North Indian population: replication of SNPs identified through GWAS. (English)

1 reference

genome-wide association study

26 November 2017

0 references

1 reference

5

1 reference

26 November 2017

J Kumar

1

1 reference

26 November 2017

S Yumnam

2

1 reference

26 November 2017

T Basu

3

1 reference

26 November 2017

A Ghosh

4

1 reference

26 November 2017

G Karthikeyan

6

1 reference

26 November 2017

S Sengupta

7

1 reference

26 November 2017

publication date

1 June 2011

1 reference

26 November 2017

1 reference

26 November 2017

volume

79

1 reference

26 November 2017

issue

6

1 reference

26 November 2017

page(s)

588-593

1 reference

describes a project that uses

26 November 2017

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

Predictors of change in plasma total cysteine: longitudinal findings from the Hordaland homocysteine study

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

Plasma total cysteine as a risk factor for vascular disease: The European Concerted Action Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

Vitamin B12 deficiency is associated with coronary artery disease in an Indian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

Molecular genetics of coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

Human Genome Variation 2006: emerging views on structural variation and large-scale SNP analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

A common allele on chromosome 9 associated with coronary heart disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

Genomewide association analysis of coronary artery disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

Homocysteine levels are associated with MTHFR A1298C polymorphism in Indian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

Functional analysis of the chromosome 9p21.3 coronary artery disease risk locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

The common genetic variant upstream of INSIG2 gene is not associated with obesity in Indian population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

Single nucleotide polymorphisms in homocysteine metabolism pathway genes: association of CHDH A119C and MTHFR C677T with hyperhomocysteinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2010.01509.X

10.1111/J.1399-0004.2010.01509.X

21 January 2018

Identifiers

DOI

1 reference

26 November 2017

1 reference