Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia (Q28943439)

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Robert A. Hegele

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Robert A. Hegele

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Sekar Kathiresan

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Sekar Kathiresan

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14 March 2017

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Salim Yusuf

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Benjamin F. Voight

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Adam D. McIntyre

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14 March 2017

Christopher J O'Donnell

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Christopher J. O'Donnell

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Christopher T. Johansen

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Jian Wang

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Matthew B. Lanktree

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Henian Cao

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Matthew R. Ban

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Rebecca A. Martins

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Brooke A. Kennedy

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Reina G. Hassell

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Maartje E. Visser

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Stephen M. Schwartz

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Geesje M. Dallinga-Thie

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Sonia S. Anand

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Murray W. Huff

describes a project that uses

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language of work or name

English

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publication date

1 August 2010

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14 March 2017

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684–687

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genome-wide association study

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Finding the missing heritability of complex diseases

inferred from title

cites work

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Chylomicronemia with a mutant GPIHBP1 (Q115P) that cannot bind lipoprotein lipase

16 March 2017

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Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

16 March 2017

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

16 March 2017

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Genome-wide association analysis of metabolic traits in a birth cohort from a founder population

16 March 2017

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Common variants at 30 loci contribute to polygenic dyslipidemia

16 March 2017

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Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

16 March 2017

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Newly identified loci that influence lipid concentrations and risk of coronary artery disease

16 March 2017

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Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia

16 March 2017

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PLINK: a tool set for whole-genome association and population-based linkage analyses

16 March 2017

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Hypertriglyceridemia: its etiology, effects and treatment

16 March 2017

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Population structure and eigenanalysis

16 March 2017

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

16 March 2017

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

16 March 2017

1 reference

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Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

16 March 2017

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Common disorders are quantitative traits

7 April 2017

1 reference

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A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia

3 June 2018

1 reference

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Plasma lipoproteins: genetic influences and clinical implications

3 June 2018

1 reference

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Polygenic determinants of severe hypertriglyceridemia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

3 June 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemia

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Common disorders are quantitative traits

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3017369

Resequencing genomic DNA of patients with severe hypertriglyceridemia (MIM 144650)

26 November 2018

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12 December 2020

Computing measures of explained variation for logistic regression models

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12 December 2020

APOA5 genetic variants are markers for classic hyperlipoproteinemia phenotypes and hypertriglyceridemia

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12 December 2020

Differences in risk factors, atherosclerosis, and cardiovascular disease between ethnic groups in Canada: the Study of Health Assessment and Risk in Ethnic groups (SHARE)

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12 December 2020

Identifiers

DOI

10.1038/NG.628

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299778

299778

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