(Q36980303)

17 August 2017

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title

Genetic determinants of plasma lipoproteins (English)

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17 August 2017

2

Robert A Hegele

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Rebecca L Pollex

series ordinal

1

object named as

Rebecca L Pollex

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17 August 2017

publication date

1 November 2007

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Nature Clinical Practice Cardiovascular Medicine

17 August 2017

published in

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17 August 2017

volume

4

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17 August 2017

issue

11

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17 August 2017

page(s)

600-609

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Apolipoprotein E in hyperlipidemia

17 August 2017

cites work

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Heterozygous familial hypercholesterolemia: an underrecognized cause of early cardiovascular disease

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Apolipoprotein E gene polymorphism effects triglycerides but not CAD risk in Caucasian women younger than 65 years

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Genetics of atherosclerosis

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Genetic basis of lipoprotein disorders

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7 January 2021

Genetic polymorphisms, lipoproteins and coronary artery disease risk

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7 January 2021

Apolipoprotein E polymorphisms predict low density lipoprotein cholesterol levels and carotid artery wall thickness but not incident coronary heart disease in 12,491 ARIC study participants

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7 January 2021

Cholesteryl ester transfer protein TaqIB variant, high-density lipoprotein cholesterol levels, cardiovascular risk, and efficacy of pravastatin treatment: individual patient meta-analysis of 13,677 subjects.

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7 January 2021

Effects of an inhibitor of cholesteryl ester transfer protein on HDL cholesterol

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7 January 2021

Effect of torcetrapib on the progression of coronary atherosclerosis

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7 January 2021

Variation at the hepatic lipase and apolipoprotein AI/CIII/AIV loci is a major cause of genetically determined variation in plasma HDL cholesterol levels

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7 January 2021

Linkage between cholesterol 7alpha-hydroxylase and high plasma low-density lipoprotein cholesterol concentrations

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7 January 2021

A hepatic lipase (LIPC) allele associated with high plasma concentrations of high density lipoprotein cholesterol

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7 January 2021

Absence of association between genetic variation in the LIPC gene promoter and plasma lipoproteins in three Canadian populations

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7 January 2021

Variable association between genetic variation in the CYP7 gene promoter and plasma lipoproteins in three Canadian populations

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7 January 2021

Small genetic effects in complex diseases: a review of regulatory sequence variants in dyslipoproteinemia and atherosclerosis

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7 January 2021

Common genetic variation in the promoter of the human apo CIII gene abolishes regulation by insulin and may contribute to hypertriglyceridemia

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7 January 2021

Metabolic syndrome in aboriginal Canadians: prevalence and genetic associations

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7 January 2021

Maturity-onset diabetes of the young (MODY) mutation in type 2 diabetes and latent autoimmune diabetes of the adult

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7 January 2021

Genetic determinants of high density lipoprotein levels.

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7 January 2021

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

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7 January 2021

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

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7 January 2021

Mutations in PCSK9 cause autosomal dominant hypercholesterolemia

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7 January 2021

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

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7 January 2021

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

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7 January 2021

Protease variants, LDL, and coronary heart disease

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7 January 2021

LRP6 mutation in a family with early coronary disease and metabolic risk factors

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7 January 2021

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

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7 January 2021

NPC1L1: evolution from pharmacological target to physiological sterol transporter

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7 January 2021

Compound heterozygosity for two non-synonymous polymorphisms in NPC1L1 in a non-responder to ezetimibe

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https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

NPC1L1 haplotype is associated with inter-individual variation in plasma low-density lipoprotein response to ezetimibe

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Sequence variation in NPC1L1 and association with improved LDL-cholesterol lowering in response to ezetimibe treatment

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7 January 2021

Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

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7 January 2021

GENE SEQUENCING: The Race for the $1000 Genome

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7 January 2021

Global variation in copy number in the human genome

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7 January 2021

‘Mendelian randomization’: can genetic epidemiology contribute to understanding environmental determinants of disease?*

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7 January 2021

Biomedicine. Lowering LDL--not only how low, but how long?

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7 January 2021

Candidate genes, small effects, and the prediction of atherosclerosis

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7 January 2021

Simon Dack Lecture. The genomic basis of myocardial infarction

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7 January 2021

Candidate gene genotypes, along with conventional risk factor assessment, improve estimation of coronary heart disease risk in healthy UK men.

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7 January 2021

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

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7 January 2021

Associations between two common polymorphisms in the ABCA1 gene and subclinical atherosclerosis: Multi-Ethnic Study of Atherosclerosis (MESA)

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7 January 2021

Consistent effects of genes involved in reverse cholesterol transport on plasma lipid and apolipoprotein levels in CARDIA participants

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https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Candidate gene susceptibility variants predict intermediate end points but not angiographic coronary artery disease

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https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Common polymorphisms of ATP binding cassette transporter A1, including a functional promoter polymorphism, associated with plasma high density lipoprotein cholesterol levels in Turks

1 reference

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7 January 2021

Associations of the apolipoprotein A1/C3/A4/A5 gene cluster with triglyceride and HDL cholesterol levels in women with type 2 diabetes

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https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Sex-specific effect of APOAV variant (Val153>Met) on plasma levels of high-density lipoprotein cholesterol

1 reference

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7 January 2021

Genetic variations of apolipoprotein A5 gene is associated with the risk of coronary artery disease among Chinese in Taiwan

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Apolipoprotein E polymorphism and changes in serum lipids during a family-based counselling intervention

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

The effect of the APOE polymorphism on HDL-C concentrations depends on the cholesterol ester transfer protein gene variation in a Southern European population.

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Association of apolipoprotein E genotype with early onset of coronary heart disease in Greek men.

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Common variants of Cholesteryl ester transfer protein gene and their association with lipid parameters in healthy volunteers of Tamilian population

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

An increased coronary risk is paradoxically associated with common cholesteryl ester transfer protein gene variations that relate to higher high-density lipoprotein cholesterol: a population-based study

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

The association between high-density lipoprotein cholesterol level and cholesteryl ester transfer protein TaqIB gene polymorphism is influenced by alcohol drinking in a population-based sample.

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Functional interaction between -629C/A, -971G/A and -1337C/T polymorphisms in the CETP gene is a major determinant of promoter activity and plasma CETP concentration in the REGRESS Study.

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

An interaction between the TaqIB polymorphism of cholesterol ester transfer protein and smoking is associated with changes in plasma high-density lipoprotein cholesterol levels in Turks

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

The effect of cholesteryl ester transfer protein -629C->A promoter polymorphism on high-density lipoprotein cholesterol is dependent on serum triglycerides.

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Cholesteryl ester transfer protein variants have differential stability but uniform inhibition by torcetrapib.

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Effects of cholesterol ester transfer protein Taq1B gene polymorphism on serum lipoprotein levels in Turkish coronary artery disease patients

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

The C-480T hepatic lipase polymorphism is associated with HDL-C but not with risk of coronary heart disease

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Lipoprotein subclass and particle size differences in Afro-Caribbeans, African Americans, and white Americans: associations with hepatic lipase gene variation

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Association of APOA5 c.553G>T polymorphism with type 2 diabetes mellitus in a Chinese population

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Genetic variations of the apolipoprotein B gene in Turkish patients with coronary artery disease

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Relations of APOE promoter polymorphisms to LDL cholesterol and markers of subclinical atherosclerosis in young adults

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

The effect of apolipoprotein E polymorphism on lipid levels in Korean adults

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Apolipoprotein E polymorphism in Vietnamese children and its relationship to plasma lipid and lipoprotein levels

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Effects of cholesteryl ester transfer protein TAQ1B polymorphism in renal transplant patients

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

A common PCSK9 haplotype, encompassing the E670G coding single nucleotide polymorphism, is a novel genetic marker for plasma low-density lipoprotein cholesterol levels and severity of coronary atherosclerosis

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Evidence for consistent intragenic and intergenic interactions between SNP effects in the APOA1/C3/A4/A5 gene cluster

1 reference

https://api.crossref.org/works/10.1038%2FNCPCARDIO1005

7 January 2021

Identifiers

DOI

10.1038/NCPCARDIO1005

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17 August 2017

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