(Q37880143)

24 August 2017

1 reference

title

The relative importance of common and rare genetic variants in the development of hypertriglyceridemia (English)

1 reference

24 August 2017

1 reference

David Evans

1

1 reference

24 August 2017

Jens Aberle

series ordinal

2

1 reference

24 August 2017

Frank-Ulrich Beil

series ordinal

3

1 reference

24 August 2017

publication date

1 May 2011

1 reference

Expert Review of Cardiovascular Therapy

24 August 2017

published in

1 reference

24 August 2017

volume

9

1 reference

24 August 2017

issue

5

1 reference

24 August 2017

page(s)

637-644

1 reference

Relation of coronary heart disease incidence and total mortality to plasma cholesterol reduction in randomised trials: use of meta-analysis

24 August 2017

cites work

1 reference

The Collaborative Lipid Research Clinics Family Study: biological and cultural determinants of familial resemblance for plasma lipids and lipoproteins.

21 January 2018

1 reference

Genetic and environmental influences on serum lipid levels in twins.

21 January 2018

1 reference

Monogenic dyslipidemias: window on determinants of plasma lipoprotein metabolism

21 January 2018

1 reference

Plasma lipoproteins: genetic influences and clinical implications

21 January 2018

1 reference

Common and rare variants in multifactorial susceptibility to common diseases

21 January 2018

1 reference

Common vs. rare allele hypotheses for complex diseases

21 January 2018

1 reference

Common genetic variation and human traits

21 January 2018

1 reference

Finding the missing heritability of complex diseases

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides

21 January 2018

1 reference

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

21 January 2018

1 reference

Common variants at 30 loci contribute to polygenic dyslipidemia

21 January 2018

1 reference

Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication

21 January 2018

1 reference

Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis

21 January 2018

1 reference

Genetic variants influencing circulating lipid levels and risk of coronary artery disease

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Uncovering the roles of rare variants in common disease through whole-genome sequencing

21 January 2018

1 reference

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

21 January 2018

1 reference

Lipoprotein lipase: from gene to obesity

21 January 2018

1 reference

APOA5 and triglyceride metabolism, lesson from human APOA5 deficiency

21 January 2018

1 reference

Seven lipoprotein lipase gene polymorphisms, lipid fractions, and coronary disease: a HuGE association review and meta-analysis

21 January 2018

1 reference

Apolipoprotein A5 and triglyceridemia. Focus on the effects of the common variants

21 January 2018

1 reference

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

21 January 2018

1 reference

Large scale replication analysis of loci associated with lipid concentrations in a Japanese population

21 January 2018

1 reference

Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples

21 January 2018

1 reference

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.

21 January 2018

1 reference

Polymorphisms associated with cholesterol and risk of cardiovascular events

21 January 2018

1 reference

Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample

21 January 2018

1 reference

Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip

21 January 2018

1 reference

Rare APOA5 mutations--clinical consequences, metabolic and functional effects: an ENID review

21 January 2018

1 reference

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

21 January 2018

1 reference

Lipoprotein lipase: genetics, lipid uptake, and regulation.

21 January 2018

1 reference

Prediction of deleterious human alleles

21 January 2018

1 reference

Accurate prediction of the functional significance of single nucleotide polymorphisms and mutations in the ABCA1 gene

21 January 2018

1 reference

The single nucleotide polymorphism -1131T>C in the apolipoprotein A5 (APOA5) gene is associated with elevated triglycerides in patients with hyperlipidemia

21 January 2018

1 reference

Sequencing technologies - the next generation

21 January 2018

1 reference

Resequencing of pooled DNA for detecting disease associations with rare variants

21 January 2018

1 reference

Statistical analysis strategies for association studies involving rare variants

21 January 2018

1 reference

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

21 January 2018

1 reference

Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein

21 January 2018

1 reference

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

21 January 2018

1 reference

Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia

21 January 2018

1 reference

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

21 January 2018

1 reference

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1586/ERC.11.53

1 reference

24 August 2017

1 reference