(Q38005008)

26 August 2017

title

The complex genetic basis of plasma triglycerides (English)

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26 August 2017

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2

Robert A Hegele

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author name string

Christopher T Johansen

series ordinal

1

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26 August 2017

publication date

1 June 2012

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Current Atherosclerosis Reports

26 August 2017

published in

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26 August 2017

volume

14

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26 August 2017

issue

3

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26 August 2017

page(s)

227-234

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Fasting compared with nonfasting triglycerides and risk of cardiovascular events in women

26 August 2017

cites work

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https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Triglycerides and heart disease: still a hypothesis?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

The role of triglycerides in atherosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Triglyceride-mediated pathways and coronary disease: collaborative analysis of 101 studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Genetic determinants of LDL, lipoprotein(a), triglyceride-rich lipoproteins and HDL: concordance and discordance with cardiovascular disease risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Hypertriglyceridemia: its etiology, effects and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

A specific apoprotein activator for lipoprotein lipase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Inherited apolipoprotein A-V deficiency in severe hypertriglyceridemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Hypertriglyceridaemia and low plasma HDL in a patient with apolipoprotein A-V deficiency due to a novel mutation in the APOA5 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Novel LMF1 nonsense mutation in a patient with severe hypertriglyceridemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Chylomicronemia with low postheparin lipoprotein lipase levels in the setting of GPIHBP1 defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Mutation of conserved cysteines in the Ly6 domain of GPIHBP1 in familial chylomicronemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Homozygous missense mutation (G56R) in glycosylphosphatidylinositol-anchored high-density lipoprotein-binding protein 1 (GPI-HBP1) in two siblings with fasting chylomicronemia (MIM 144650).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Genetic determinants of plasma triglycerides

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

An increased burden of common and rare lipid-associated risk alleles contributes to the phenotypic spectrum of hypertriglyceridemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Genetic bases of hypertriglyceridemic phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Regulation of hepatic gluconeogenesis by an ER-bound transcription factor, CREBH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

The transcription factor cyclic AMP-responsive element-binding protein H regulates triglyceride metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Quantitative trait locus mapping and identification of Zhx2 as a novel regulator of plasma lipid metabolism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Exome sequencing, ANGPTL3 mutations, and familial combined hypolipidemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11883-012-0243-2

Genetic and developmental regulation of the lipoprotein lipase gene: loci both distal and proximal to the lipoprotein lipase structural gene control enzyme expression

21 January 2018

1 reference

12 December 2020

Apolipoprotein A5 and hypertriglyceridemia

1 reference

12 December 2020

Rare loss-of-function mutations in ANGPTL family members contribute to plasma triglyceride levels in humans.

1 reference

12 December 2020

Common and rare gene variants affecting plasma LDL cholesterol

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12 December 2020

New wrinkles in lipoprotein lipase biology.

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12 December 2020

Excess of rare variants in non-genome-wide association study candidate genes in patients with hypertriglyceridemia

1 reference

12 December 2020

Nonfasting Triglycerides and Risk of Myocardial Infarction, Ischemic Heart Disease, and Death in Men and Women

1 reference

12 December 2020

Characterization of three kindreds with familial combined hypolipidemia caused by loss-of-function mutations of ANGPTL3.

1 reference

12 December 2020

Childhood-onset chylomicronaemia with reduced plasma lipoprotein lipase activity and mass: identification of a novel GPIHBP1 mutation

1 reference

12 December 2020

10.1007/S11883-012-0243-2

Identifiers

DOI

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Dimensions Publication ID

26 August 2017

1008492484

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