The association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's Heart and Health cohort study and a meta-analysis (Q24801635)

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English	The association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's Heart and Health cohort study and a meta-analysis	scientific article

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scholarly article

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4 references

30 June 2019

14 September 2019

28 September 2019

19 November 2019

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based on heuristic

inferred from title

The association of the PON1 Q192R polymorphism with coronary heart disease: findings from the British Women's Heart and Health cohort study and a meta-analysis (English)

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17 June 2019

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aryldialkylphosphatases

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genetic polymorphism

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genetic variation

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14 September 2019

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28 September 2019

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19 November 2019

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based on heuristic

inferred from title

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based on heuristic

inferred from title

coronary artery disease

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based on heuristic

inferred from title

George Davey Smith

8

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Deborah A. Lawlor

1

object named as

Debbie A Lawlor

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object named as

Tom R Gaunt

3

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9

object named as

Shah Ebrahim

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4

object named as

Lesley J Hinks

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7

object named as

Nick Timpson

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author name string

Ian N M Day

2

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Patricia J Briggs

5

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Matthew Kiessling

6

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language of work or name

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publication date

23 June 2004

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14 March 2019

19 March 2019

22 March 2019

17 June 2019

19 June 2019

30 June 2019

14 September 2019

28 September 2019

19 November 2019

9 references

14 March 2019

19 March 2019

22 March 2019

17 June 2019

19 June 2019

30 June 2019

14 September 2019

28 September 2019

19 November 2019

5

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1

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17

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Association between the severity of angiographic coronary artery disease and paraoxonase gene polymorphisms in the National Heart, Lung, and Blood Institute-sponsored Women's Ischemia Syndrome Evaluation (WISE) study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

7 April 2017

DNA polymorphisms in two paraoxonase genes (PON1 and PON2) are associated with the risk of coronary heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

7 April 2017

Empirical evidence of bias. Dimensions of methodological quality associated with estimates of treatment effects in controlled trials

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

7 April 2017

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

7 April 2017

Geographical variation in cardiovascular disease, risk factors, and their control in older women: British Women's Heart and Health Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

7 April 2017

Socioeconomic position in childhood and adulthood and insulin resistance: cross sectional survey using data from British women's heart and health study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

7 April 2017

Genetic variations of the paraoxonase gene in patients with coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

7 April 2017

Mice lacking serum paraoxonase are susceptible to organophosphate toxicity and atherosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

7 April 2017

‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease?*

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

7 April 2017

Beyond cholesterol. Modifications of low-density lipoprotein that increase its atherogenicity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

7 April 2017

Mendelian randomization: prospects, potentials, and limitations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

Fibrinogen, C-reactive protein and coronary heart disease: does Mendelian randomization suggest the associations are non-causal?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

Problems of reporting genetic associations with complex outcomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

Paraoxonase and atherosclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

Paraoxonase1-192 polymorphism modulates the nonfatal myocardial infarction risk associated with decreased HDLs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

How high-density lipoprotein protects against the effects of lipid peroxidation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

Polymorphism in high density lipoprotein paraoxonase gene and risk of acute myocardial infarction in men: prospective nested case-control study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

Coronary heart disease. At the interface of molecular genetics and preventive medicine

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

Serum paraoxonase after myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

Effect of the molecular polymorphisms of human paraoxonase (PON1) on the rate of hydrolysis of paraoxon

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

Whole genome amplification using a degenerate oligonucleotide primer allows hundreds of genotypes to be performed on less than one nanogram of genomic DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

The Gln-Arg191 polymorphism of the human paraoxonase gene (HUMPONA) is not associated with the risk of coronary artery disease in Finns

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

A variant of human paraoxonase/arylesterase (HUMPONA) gene is a risk factor for coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

Molecular basis for the polymorphic forms of human serum paraoxonase/arylesterase: glutamine or arginine at position 191, for the respective A or B allozymes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 September 2017

The Gln-Arg 191 polymorphism of the human paraoxonase gene is not associated with the risk of coronary artery disease among Chinese in Taiwan.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

30 May 2018

Paraoxonase Polymorphism (Gln192-Arg) Is Associated with Coronary Heart Disease in Japanese Noninsulin-Dependent Diabetes Mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

30 May 2018

Genetic polymorphism of paraoxonase and the risk of coronary heart disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

30 May 2018

The role of high-density lipoprotein and lipid-soluble antioxidant vitamins in inhibiting low-density lipoprotein oxidation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

30 May 2018

High-density lipoprotein inhibits the oxidative modification of low-density lipoprotein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

30 May 2018

Four paraoxonase gene polymorphisms in 11212 cases of coronary heart disease and 12786 controls: meta-analysis of 43 studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

Human paraoxonase gene cluster polymorphisms as predictors of coronary heart disease risk in the prospective Northwick Park Heart Study II.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

Low paraoxonase activity predicts coronary events in the Caerphilly Prospective Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

[The paraoxonase Gln-Arg192 polymorphism in patients with coronary heart disease in Chinese population].

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

Prediction of the risk of myocardial infarction from polymorphisms in candidate genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

Human paraoxonase 1 gene polymorphisms and the risk of coronary heart disease: a community-based study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

Paraoxonase Gln-Arg(192) and Leu-Met(55) gene polymorphisms and enzyme activity in a population with a low rate of coronary heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

Paraoxonase status in coronary heart disease: are activity and concentration more important than genotype?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

PON2 gene variants are associated with clinical manifestations of cardiovascular disease in familial hypercholesterolemia patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

A prospective study of paraoxonase gene Q/R192 polymorphism and severity, progression and regression of coronary atherosclerosis, plasma lipid levels, clinical events and response to fluvastatin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

Risk of myocardial infarction associated with Gln/Arg 192 polymorphism in the human paraoxonase gene and diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

Paraoxonase gene polymorphism and coronary artery disease in Indian subjects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

Lack of protection against oxidative modification of LDL by avian HDL.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

The paraoxonase Gln-Arg 192 polymorphism in subjects with ischaemic heart disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

The molecular basis of the human serum paraoxonase activity polymorphism.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=449704

28 November 2018

Common paraoxonase gene variants, mortality risk and fatal cardiovascular events in elderly subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for association between paraoxonase gene polymorphisms and atherosclerotic diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential effects of smoking on myocardial infarction risk according to the Gln/Arg 192 variants of the human paraoxonase gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human paraoxonase Gln-Argl92 (Q/R) polymorphism in turkish patients with coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tobacco smoking modifies association between Gln-Arg192 polymorphism of human paraoxonase gene and risk of myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The paraoxonase Leu-Met54 and Gln-Arg191 gene polymorphisms are not associated with the risk of coronary heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gln-Arg192 polymorphism of paraoxonase and coronary heart disease in type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Gln/Arg polymorphism of human paraoxonase (PON 192) is not related to myocardial infarction in the ECTIM Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraoxonase gene polymorphism in Japanese subjects with coronary heart disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alloenzymes of paraoxonase and effectiveness of high-density lipoproteins in protecting low-density lipoprotein against lipid peroxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 192Arg variant of the human paraoxonase (HUMPONA) gene polymorphism is associated with an increased risk for coronary artery disease in the Japanese

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gln-Arg192 polymorphism of human paraoxonase gene is not associated with coronary artery disease in italian patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraoxonase active site required for protection against LDL oxidation involves its free sulfhydryl group and is different from that required for its arylesterase/paraoxonase activities: selective action of human paraoxonase allozymes Q and R

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraoxonase 192 Gln/Arg gene polymorphism, coronary artery disease, and myocardial infarction in type 2 diabetes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paraoxonase polymorphisms are not associated with cardiovascular risk in renal transplant recipients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Coronary artery disease risk in Chinese type 2 diabetics: is there a role for paraxonase 1 gene (Q192R) polymorphism?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum paraoxonase activity and paraoxonase gene polymorphism in type 2 diabetic patients with or without vascular complications

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extensive association analysis between polymorphisms of PON gene cluster with coronary heart disease in Chinese Han population

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the human paraoxonase 1 gene: frequencies, allelic linkages, and association with coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/15214960

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1186/1471-2156-5-17

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