(Q34024421)

30 July 2017

title

A genetic risk variant for myocardial infarction on chromosome 6p24 is associated with impaired central hemodynamic indexes (English)

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30 July 2017

main subject

myocardial infarction

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1 reference

10

Viola Vaccarino

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30 July 2017

13

Arshed A Quyyumi

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30 July 2017

1

Riyaz S Patel

1 reference

30 July 2017

Alanna A Morris

2

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30 July 2017

Yusuf Ahmed

3

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30 July 2017

Nino Kavtaradze

4

1 reference

30 July 2017

Salman Sher

5

1 reference

30 July 2017

Shaoyong Su

6

1 reference

30 July 2017

A Maziar Zafari

7

1 reference

30 July 2017

Rebecca Din-Dzietham

8

1 reference

30 July 2017

Salina P Waddy

9

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30 July 2017

R Wayne Alexander

11

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30 July 2017

Gary Gibbons

12

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30 July 2017

publication date

19 April 2012

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Journal of Clinical Hypertension

30 July 2017

published in

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30 July 2017

volume

25

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30 July 2017

issue

7

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30 July 2017

page(s)

797-803

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Association between depression and inflammation--differences by race and sex: the META-Health study

30 July 2017

cites work

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5 July 2018

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

5 July 2018

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5 July 2018

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5 July 2018

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COL4A1 is associated with arterial stiffness by genome-wide association scan

5 July 2018

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

5 July 2018

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Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction

5 July 2018

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

5 July 2018

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

5 July 2018

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Genetics and pathophysiology of arterial stiffness

5 July 2018

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Common variants at 30 loci contribute to polygenic dyslipidemia

5 July 2018

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Future use of genomics in coronary artery disease

5 July 2018

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5 July 2018

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Genomewide association analysis of 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=4127881

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

5 July 2018

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A common allele on chromosome 9 associated with coronary heart 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=4127881

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127881

A novel endonuclease IV post-PCR genotyping system

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4127881

Arterial stiffness and stroke in hypertension: therapeutic implications for stroke prevention

5 July 2018

1 reference

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Phactrs 1-4: A family of protein phosphatase 1 and actin regulatory proteins

5 July 2018

1 reference

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The novel genetic variant predisposing to coronary artery disease in the region of the PSRC1 and CELSR2 genes on chromosome 1 associates with serum cholesterol

5 July 2018

1 reference

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Relation of pulse pressure and arterial stiffness to concentric left ventricular hypertrophy in young men (from the Bogalusa Heart Study).

21 January 2018

1 reference

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Heritability of central systolic pressure augmentation: a twin study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJH.2012.41

Increased wave reflection rather than central arterial stiffness is the main determinant of raised pulse pressure in women and relates to mismatch in arterial dimensions: a twin study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FAJH.2012.41

SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery

21 January 2018

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12 December 2020

Chronically decreased aortic distensibility causes deterioration of coronary perfusion during increased left ventricular contraction

1 reference

12 December 2020

Variation in the human matrix metalloproteinase-9 gene is associated with arterial stiffness in healthy individuals

1 reference

12 December 2020

The influence of heart rate on augmentation index and central arterial pressure in humans

1 reference

12 December 2020

Identifiers

DOI

10.1038/AJH.2012.41

1 reference

30 July 2017

1 reference

30 July 2017

1 reference