(Q43548774)

English

Identification of a common variant in the lipoprotein lipase gene in a large Utah kindred ascertained for coronary heart disease: the -93G/D9N variant predisposes to low HDL-C/high triglycerides

scientific article published in February 2001

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scholarly article

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Europe PubMed Central

PubMed publication ID

24 November 2017

Identification of a common variant in the lipoprotein lipase gene in a large Utah kindred ascertained for coronary heart disease: the -93G/D9N variant predisposes to low HDL-C/high triglycerides (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

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coronary artery disease

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author name string

Samuels ME

1

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24 November 2017

Forbey KC

2

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24 November 2017

Reid JE

3

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24 November 2017

Abkevich V

4

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24 November 2017

Bulka K

5

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24 November 2017

Wardell BR

6

1 reference

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24 November 2017

Bowen BR

7

1 reference

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24 November 2017

Hopkins PN

8

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24 November 2017

Hunt SC

9

1 reference

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24 November 2017

Ballinger DG

10

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24 November 2017

Skolnick MH

11

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24 November 2017

Wagner S

12

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24 November 2017

language of work or name

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publication date

1 February 2001

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24 November 2017

Clinical Genetics

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24 November 2017

59

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24 November 2017

2

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24 November 2017

88-98

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24 November 2017

Familial lipoprotein disorders in patients with premature coronary artery disease

1 reference

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21 January 2018

Lipoprotein lipase variants D9N and N291S are associated with increased plasma triglyceride and lower high-density lipoprotein cholesterol concentrations: studies in the fasting and postprandial states: the European Atherosclerosis Research Studies.

1 reference

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21 January 2018

A common mutation in the lipoprotein lipase gene promoter, -93T/G, is associated with lower plasma triglyceride levels and increased promoter activity in vitro

1 reference

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21 January 2018

Lipoprotein lipase mutations, plasma lipids and lipoproteins, and risk of ischemic heart disease. A meta-analysis

1 reference

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21 January 2018

Genetic localization to chromosome 1p32 of the third locus for familial hypercholesterolemia in a Utah kindred

1 reference

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21 January 2018

Mutations in the lipoprotein lipase gene associated with ischemic heart disease in men. The Copenhagen city heart study

1 reference

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21 January 2018

Higher triglycerides, lower high-density lipoprotein cholesterol, and higher systolic blood pressure in lipoprotein lipase-deficient heterozygotes. A preliminary report

1 reference

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21 January 2018

A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.

1 reference

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7 January 2021

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Evidence for a gene influencing the TG/HDL-C ratio on chromosome 7q32.3-qter: a genome-wide scan in the Framingham Study

1 reference

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7 January 2021

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A major susceptibility locus influencing plasma triglyceride concentrations is located on chromosome 15q in Mexican Americans

1 reference

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7 January 2021

based on heuristic

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Evidence of linkage of familial hypoalphalipoproteinemia to a novel locus on chromosome 11q23.

1 reference

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7 January 2021

based on heuristic

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Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

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Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

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Human pedigree-based quantitative-trait-locus mapping: localization of two genes influencing HDL-cholesterol metabolism

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Common variation in the lipoprotein lipase gene: effects on plasma lipids and risk of atherosclerosis.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Lipoprotein lipase gene mutations D9N and N291S in four pedigrees with familial combined hyperlipidaemia.

1 reference

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7 January 2021

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A comparison of positive family history definitions for defining risk of future disease

1 reference

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7 January 2021

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PedCheck: a program for identification of genotype incompatibilities in linkage analysis

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Tetranucleotide repeat polymorphism in the LPL gene

1 reference

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7 January 2021

based on heuristic

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Modulation of non-templated nucleotide addition by Taq DNA polymerase: primer modifications that facilitate genotyping

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage analysis in the presence of errors I: complex-valued recombination fractions and complex phenotypes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

A mutation in the promoter of the lipoprotein lipase (LPL) gene in a patient with familial combined hyperlipidemia and low LPL activity

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

The Asn9 variant of lipoprotein lipase is associated with the -93G promoter mutation and an increased risk of coronary artery disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Gender-related association between the -93T-->G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Two common mutations (D9N, N291S) in lipoprotein lipase: a cumulative analysis of their influence on plasma lipids and lipoproteins in men and women.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic dissection of complex traits

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2001.590205.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1034/J.1399-0004.2001.590205.X

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 November 2017

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