Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease (Q38924697)

8 January 2018

title

Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease (English)

1 reference

8 January 2018

author

Rosanna Asselta

12

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8 January 2018

Stefano Duga

13

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Pradeep Natarajan

Pradeep Natarajan

7

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Hong-Hee Won

Hong-Hee Won

2

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Roberto Elosua

Roberto Elosua

31

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Jaume Marrugat

30

Jaume Marrugat

1 reference

8 January 2018

28

Nilesh J Samani

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42

Danish Saleheen

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44

Sekar Kathiresan

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29

Heribert Schunkert

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11

Ingrid B Borecki

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Adolfo Correa

15

Adolfo Correa

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James G. Wilson

17

James G Wilson

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John Danesh

37

John Danesh

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Diego Ardissino

38

Diego Ardissino

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author name string

Amit V Khera

1

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Gina M Peloso

3

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Colm O'Dushlaine

4

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Dajiang Liu

5

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Nathan O Stitziel

6

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Akihiro Nomura

8

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Connor A Emdin

9

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Namrata Gupta

10

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Piera Angelica Merlini

14

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Thorsten Kessler

16

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Matthew J Bown

18

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Peter S Braund

20

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David J Carey

21

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Michael F Murray

22

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H Lester Kirchner

23

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Joseph B Leader

24

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Daniel R Lavage

25

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J Neil Manus

26

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Dustin N Hartzel

27

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Ruth McPherson

32

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Martin Farrall

33

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Hugh Watkins

34

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Daniel J Rader

36

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Cristen Willer

40

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Gonçalo R Abecasis

41

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Frederick E Dewey

43

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8 January 2018

Myocardial Infarction Genetics Consortium, DiscovEHR Study Group, CARDIoGRAM Exome Consortium, and Global Lipids Genetics Consortium

45

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8 January 2018

language of work or name

English

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publication date

1 March 2017

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8 January 2018

The Journal of the American Medical Association

published in

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8 January 2018

volume

317

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8 January 2018

issue

9

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8 January 2018

page(s)

937-946

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8 January 2018

Analysis of protein-coding genetic variation in 60,706 humans

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Variant ASGR1 Associated with a Reduced Risk of Coronary Artery Disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Triglyceride-Rich Lipoproteins and Atherosclerotic Cardiovascular Disease: New Insights From Epidemiology, Genetics, and Biology

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

dbNSFP v3.0: A One-Stop Database of Functional Predictions and Annotations for Human Nonsynonymous and Splice-Site SNVs

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Inactivating mutations in NPC1L1 and protection from coronary heart disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Loss-of-function mutations in APOC3 and risk of ischemic vascular disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Loss-of-function mutations in APOC3, triglycerides, and coronary disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

A polygenic burden of rare disruptive mutations in schizophrenia

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Searching for missing heritability: designing rare variant association studies

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Meta-analysis of gene-level tests for rare variant association

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

ClinVar: public archive of relationships among sequence variation and human phenotype

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Mendelian randomization analysis with multiple genetic variants using summarized data

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Genetically elevated non-fasting triglycerides and calculated remnant cholesterol as causal risk factors for myocardial infarction

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

The Pakistan Risk of Myocardial Infarction Study: a resource for the study of genetic, lifestyle and other determinants of myocardial infarction in South Asia

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

S447X variant of the lipoprotein lipase gene, lipids, and risk of coronary heart disease in 3 prospective cohort studies

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Genomewide association analysis of coronary artery disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

A common allele on chromosome 9 associated with coronary heart disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Principal components analysis corrects for stratification in genome-wide association studies

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Lipoprotein lipase. A multifunctional enzyme relevant to common metabolic diseases

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Genetic variants associated with Lp(a) lipoprotein level and coronary disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Heterozygous lipoprotein lipase deficiency: frequency in the general population, effect on plasma lipid levels, and risk of ischemic heart disease

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Selective retention of VLDL, IDL, and LDL in the arterial intima of genetically hyperlipidemic rabbits in vivo. Molecular size as a determinant of fractional loss from the intima-inner media

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217

22 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5664181

Low nonfasting triglycerides and reduced all-cause mortality: a mendelian randomization study

2 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28267856

12 December 2020

inferred from PubMed ID database lookup

Reduced atherogenesis in cholesterol-fed diabetic rabbits. Giant lipoproteins do not enter the arterial wall

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28267856

12 December 2020

inferred from PubMed ID database lookup

Toward resolution of cardiovascular health disparities in African Americans: design and methods of the Jackson Heart Study

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/28267856

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1001/JAMA.2017.0972

1 reference

8 January 2018

release_ezqnmapzmjeh3dboqp7xl3nxmu

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ezqnmapzmjeh3dboqp7xl3nxmu

24 November 2022

mapped directly with Wikidata item

PMC publication ID

5664181

1 reference

8 January 2018

PubMed publication ID

28267856

1 reference

8 January 2018