(Q35009487)

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Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment Study

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scholarly article

1 reference

Europe PubMed Central

5 August 2017

Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment Study (English)

1 reference

Europe PubMed Central

5 August 2017

Margaret A. Pericak-Vance

10

object named as

Margaret A Pericak-Vance

0 references

1

object named as

Dana C Crawford

1 reference

Europe PubMed Central

5 August 2017

Jonathan L Haines

16

object named as

Jonathan L Haines

1 reference

Europe PubMed Central

5 August 2017

Kristin Brown-Gentry

4

object named as

Kristin Brown-Gentry

1 reference

Europe PubMed Central

5 August 2017

author name string

Logan Dumitrescu

2

1 reference

Europe PubMed Central

5 August 2017

Robert Goodloe

3

1 reference

Europe PubMed Central

5 August 2017

Jonathan Boston

5

1 reference

Europe PubMed Central

5 August 2017

Bob McClellan

6

1 reference

Europe PubMed Central

5 August 2017

Cara Sutcliffe

7

1 reference

Europe PubMed Central

5 August 2017

Rachel Wiseman

8

1 reference

Europe PubMed Central

5 August 2017

Paxton Baker

9

1 reference

Europe PubMed Central

5 August 2017

William K Scott

11

1 reference

Europe PubMed Central

5 August 2017

Melissa Allen

12

1 reference

Europe PubMed Central

5 August 2017

Ping Mayo

13

1 reference

Europe PubMed Central

5 August 2017

Nathalie Schnetz-Boutaud

14

1 reference

Europe PubMed Central

5 August 2017

Holli H Dilks

15

1 reference

Europe PubMed Central

5 August 2017

Toni I Pollin

17

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Europe PubMed Central

5 August 2017

publication date

1 November 2014

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Europe PubMed Central

5 August 2017

Circulation: Cardiovascular Genetics

1 reference

Europe PubMed Central

5 August 2017

7

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Europe PubMed Central

5 August 2017

6

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Europe PubMed Central

5 August 2017

848-853

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Europe PubMed Central

5 August 2017

Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

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Implementing a successful data-management framework: the UK10K managed access model

1 reference

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Discovery and refinement of loci associated with lipid levels

1 reference

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Antisense oligonucleotide inhibition of apolipoprotein C-III reduces plasma triglycerides in rodents, nonhuman primates, and humans

1 reference

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8 July 2018

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

1 reference

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

1 reference

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8 July 2018

The Next PAGE in understanding complex traits: design for the analysis of Population Architecture Using Genetics and Epidemiology (PAGE) Study

1 reference

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8 July 2018

Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study

1 reference

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8 July 2018

Successful aging shows linkage to chromosomes 6, 7, and 14 in the Amish

1 reference

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8 July 2018

Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

Identification by whole-genome resequencing of gene defect responsible for severe hypercholesterolemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

Biological, clinical and population relevance of 95 loci for blood lipids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

METAL: fast and efficient meta-analysis of genomewide association scans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

Association of blood lipids with common DNA sequence variants at 19 genetic loci in the multiethnic United States National Health and Nutrition Examination Survey III.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

Plasma lipoproteins: genetic influences and clinical implications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

A spectrum of PCSK9 alleles contributes to plasma levels of low-density lipoprotein cholesterol.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

The effects of scale: variation in the APOA1/C3/A4/A5 gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

High-throughput genotyping with single nucleotide polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

8 July 2018

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

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8 July 2018

Maternal lineages and Alzheimer disease risk in the Old Order Amish.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4305446

26 October 2018

Identifiers

10.1161/CIRCGENETICS.113.000369

1 reference

Europe PubMed Central

5 August 2017

1 reference

Europe PubMed Central

5 August 2017

1 reference

Europe PubMed Central

5 August 2017

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