(Q30393812)

15 September 2017

Rare coding variation in paraoxonase-1 is associated with ischemic stroke in the NHLBI Exome Sequencing Project (English)

1 reference

15 September 2017

17

Gail P Jarvik

0 references

Daniel Seung Kim

1

object named as

Daniel Seung Kim

1 reference

15 September 2017

12

Rebecca F Gottesman

1 reference

15 September 2017

14

Ulrike Peters

1 reference

15 September 2017

16

Deborah A Nickerson

1 reference

15 September 2017

8

James F Meschia

1 reference

15 September 2017

William T. Longstreth

11

object named as

W T Longstreth

1 reference

15 September 2017

David R Crosslin

2

1 reference

15 September 2017

Paul L Auer

3

1 reference

15 September 2017

Stephanie M Suzuki

4

1 reference

15 September 2017

Judit Marsillach

5

1 reference

15 September 2017

Amber A Burt

6

1 reference

15 September 2017

Adam S Gordon

7

1 reference

15 September 2017

Mike A Nalls

9

1 reference

15 September 2017

Bradford B Worrall

10

1 reference

15 September 2017

Clement E Furlong

13

1 reference

15 September 2017

Stephen S Rich

15

1 reference

15 September 2017

NHLBI Exome Sequencing Project

18

1 reference

15 September 2017

7 April 2014

1 reference

Journal of Lipid Research

15 September 2017

1 reference

15 September 2017

55

1 reference

15 September 2017

6

1 reference

15 September 2017

1173-1178

1 reference

Heart disease and stroke statistics--2014 update: a report from the American Heart Association

15 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Novel gene-by-environment interactions: APOB and NPC1L1 variants affect the relationship between dietary and total plasma cholesterol

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

A high-performance computing toolset for relatedness and principal component analysis of SNP data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Dietary cholesterol increases paraoxonase 1 enzyme activity

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Additional Common Polymorphisms in the PON Gene Cluster Predict PON1 Activity but Not Vascular Disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Evolution and functional impact of rare coding variation from deep sequencing of human exomes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

The mystery of missing heritability: Genetic interactions create phantom heritability

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Niacin in patients with low HDL cholesterol levels receiving intensive statin therapy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Rare-variant association testing for sequencing data with the sequence kernel association test

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Missing heritability and strategies for finding the underlying causes of complex disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Distribution and intensity of constraint in mammalian genomic sequence

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Effects of 5' regulatory-region polymorphisms on paraoxonase-gene (PON1) expression

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4031948

Paraoxonase (PON1) phenotype is a better predictor of vascular disease than is PON1(192) or PON1(55) genotype.

20 June 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P049247

Novel paraoxonase (PON1) nonsense and missense mutations predicted by functional genomic assay of PON1 status

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P049247

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P049247

Four genetic polymorphisms of paraoxonase gene and risk of coronary heart disease: a meta-analysis based on 88 case-control studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P049247

Race/ethnicity, quality of care, and outcomes in ischemic stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1194%2FJLR.P049247

Paraoxonase activity, but not haplotype utilizing the linkage disequilibrium structure, predicts vascular disease

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24711634

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1194/JLR.P049247

1 reference

15 September 2017

1 reference

15 September 2017

PubMed publication ID

24711634

1 reference