(Q33879523)

29 July 2017

Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families (English)

1 reference

29 July 2017

6

Gail P Jarvik

0 references

Ellen M. Wijsman

object named as

Ellen M Wijsman

series ordinal

1

0 references

John D Brunzell

series ordinal

4

object named as

John D Brunzell

1 reference

29 July 2017

2

Joseph H Rothstein

1 reference

29 July 2017

Robert P Igo

3

1 reference

PubMed ID

20383777

29 July 2017

Arno G Motulsky

series ordinal

5

1 reference

29 July 2017

11 April 2010

1 reference

29 July 2017

1 reference

29 July 2017

127

1 reference

29 July 2017

6

1 reference

29 July 2017

705-719

1 reference

https://scigraph.springernature.com/pub.10.1007/s00439-010-0819-2

29 July 2017

0 references

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5 July 2018

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Common variants at 30 loci contribute to polygenic dyslipidemia

5 July 2018

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Carboxypeptidase E mediates palmitate-induced beta-cell ER stress and apoptosis

5 July 2018

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5 July 2018

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Identifying the susceptibility genes for coronary artery disease: from hyperbole through doubt to cautious optimism

5 July 2018

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

5 July 2018

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

5 July 2018

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A genome-wide association study of global gene expression

5 July 2018

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Association of neuropeptide Y receptor Y5 polymorphisms with dyslipidemia in Mexican Americans

5 July 2018

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Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees

5 July 2018

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Genetics of high-density lipoproteins

5 July 2018

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Segregation analysis of a complex quantitative trait: approaches for identifying influential data points

5 July 2018

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Genetics of apolipoprotein B and apolipoprotein AI and premature coronary artery disease

5 July 2018

1 reference

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Comparison of single-nucleotide polymorphisms and microsatellite markers for linkage analysis in the COGA and simulated data sets for Genetic Analysis Workshop 14: Presentation Groups 1, 2, and 3.

5 July 2018

1 reference

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Familial hypobetalipoproteinemia: genetics and metabolism

5 July 2018

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Genome-wide search for new genes controlling plasma lipid concentrations in mice and humans

5 July 2018

1 reference

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Joint oligogenic segregation and linkage analysis using bayesian Markov chain Monte Carlo methods

5 July 2018

1 reference

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Ignoring linkage disequilibrium among tightly linked markers induces false-positive evidence of linkage for affected sib pair analysis

5 July 2018

1 reference

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Compendium of genome-wide scans of lipid-related phenotypes: adding a new genome-wide search of apolipoprotein levels

5 July 2018

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Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

5 July 2018

1 reference

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Haploview: analysis and visualization of LD and haplotype maps

5 July 2018

1 reference

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Genetics of LDL particle heterogeneity: from genetic epidemiology to DNA-based variations

5 July 2018

1 reference

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Testing for serial correlation in least squares regression. I

5 July 2018

1 reference

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Genetics of familial combined hyperlipidemia and risk of coronary heart disease

5 July 2018

1 reference

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Sequential tests for the detection of linkage

5 July 2018

1 reference

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Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia

5 July 2018

1 reference

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Genetic dissection of familial combined hyperlipidemia

5 July 2018

1 reference

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Genetic linkage methods for quantitative traits

5 July 2018

1 reference

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Genetics of lipoprotein abnormalities associated with coronary artery disease susceptibility

5 July 2018

1 reference

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Linkage of a gene for familial hypobetalipoproteinemia to chromosome 3p21.1-22.

5 July 2018

1 reference

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Comprehensive human genetic maps: individual and sex-specific variation in recombination

5 July 2018

1 reference

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DNA sequence diversity in a 9.7-kb region of the human lipoprotein lipase gene.

5 July 2018

1 reference

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Genetic analysis of simulated oligogenic traits in nuclear and extended pedigrees: summary of GAW10 contributions

5 July 2018

1 reference

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Markov chain Monte Carlo segregation and linkage analysis for oligogenic models

5 July 2018

1 reference

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Testing association between candidate-gene markers and phenotype in related individuals, by use of estimating equations

5 July 2018

1 reference

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The central role of dietary fat, not carbohydrate, in the insulin resistance syndrome

5 July 2018

1 reference

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Inherited susceptibility determines the distribution of dense low-density lipoprotein subfraction profiles in familial combined hyperlipidemia

5 July 2018

1 reference

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Inheritance of plasma apolipoprotein B levels in families of patients undergoing coronary arteriography at an early age.

5 July 2018

1 reference

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Limits of resolution of genetic linkage studies: implications for the positional cloning of human disease genes

5 July 2018

1 reference

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Genetic predictors of FCHL in four large pedigrees. Influence of ApoB level major locus predicted genotype and LDL subclass phenotype.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Effects of misspecifying genetic parameters in lod score analysis.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Sources of interindividual variation in the quantitative levels of apolipoprotein B in pedigrees ascertained through a lipid clinic

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Inheritance of low density lipoprotein subclass patterns in familial combined hyperlipidemia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Estimating low-density lipoprotein cholesterol by the Friedewald equation is adequate for classifying patients on the basis of nationally recommended cutpoints.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Familial combined hyperlipidemia and abnormal lipoprotein lipase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Variability of human linkage data

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Ascertainment in the sequential sampling of pedigrees

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Genetic heterogeneity in familial hypercholesterolemia: evidence for two different mutations affecting functions of low-density lipoprotein receptor

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex.

5 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00439-010-0819-2

Familial-combined hyperlipidaemia in very young myocardial infarction survivors (< or =40 years of age).

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Small dense low-density lipoprotein in familial combined hyperlipidemia: Independent of metabolic syndrome and related to history of cardiovascular events.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Molecular scanning of the human carboxypeptidase E gene for mutations in Chinese subjects with coronary atherosclerosis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Evidence for a quantitative trait locus affecting low levels of apolipoprotein B and low density lipoprotein on chromosome 10 in Caucasian families.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Empirical significance values for linkage analysis: trait simulation using posterior model distributions from MCMC oligogenic segregation analysis.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Ascertainment correction for Markov chain Monte Carlo segregation and linkage analysis of a quantitative trait.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Genome scan for quantitative trait loci influencing HDL levels: evidence for multilocus inheritance in familial combined hyperlipidemia

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Evidence of QTLs on chromosomes 1q42 and 8q24 for LDL-cholesterol and apoB levels in the HERITAGE family study

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Low-density lipoprotein particle size loci in familial combined hyperlipidemia: evidence for multiple loci from a genome scan

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Quantitative trait loci for apolipoprotein B, cholesterol, and triglycerides in familial combined hyperlipidemia pedigrees

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Exploring positional candidate genes: linkage conditional on measured genotype

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Evidence of linkage of HDL level variation to APOC3 in two samples with different ascertainment

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Small, Dense LDL and Elevated Apolipoprotein B Are the Common Characteristics for the Three Major Lipid Phenotypes of Familial Combined Hyperlipidemia

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Novel neuropeptide Y1 and Y5 receptor gene variants: associations with serum triglyceride and high-density lipoprotein cholesterol levels

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Genetic influences contributing to LDL particle size in familial combined hyperlipidaemia

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

The power to detect linkage in complex disease by means of simple LOD-score analyses

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Spectrum of LDL receptor gene mutations in heterozygous familial hypercholesterolemia.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

The use of measured genotype information in the analysis of quantitative phenotypes in man. I. Models and analytical methods.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

A survey of genetic human cortical gene expression

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Accounting for Linkage Disequilibrium among Markers in Linkage Analysis: Impact of Haplotype Frequency Estimation and Molecular Haplotypes for a Gene in a Candidate Region for Alzheimer’s Disease

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2877194

Replication of linkage of familial hypobetalipoproteinemia to chromosome 3p in six kindreds

29 October 2018

1 reference

12 December 2020

Very low density lipoprotein overproduction in genetic forms of hypertriglyceridaemia

1 reference

12 December 2020

Identification of multiple subclasses of plasma low density lipoproteins in normal humans

1 reference

12 December 2020

Plasma lipoproteins in familial combined hyperlipidemia and monogenic familial hypertriglyceridemia

1 reference

12 December 2020

Enzymatic methods for quantification of lipoprotein lipids

1 reference

12 December 2020

Major locus inheritance of apolipoprotein B in Utah pedigrees

1 reference

12 December 2020

Evidence for a new pathophysiological mechanism for coronary artery disease regression: hepatic lipase-mediated changes in LDL density

1 reference

12 December 2020

Familial combined hyperlipidaemia: under - defined and under - diagnosed?

1 reference

12 December 2020

Association of the mutation for the human carboxypeptidase E gene exon 4 with the severity of coronary artery atherosclerosis

1 reference

12 December 2020

The molecular basis of familial hypercholesterolemia in The Netherlands

1 reference

12 December 2020

Detection and characterization of the heterozygote state for lipoprotein lipase deficiency

1 reference

12 December 2020

Regression of coronary artery disease as a result of intensive lipid-lowering therapy in men with high levels of apolipoprotein B

1 reference

12 December 2020

Familial combined hyperlipidaemia linked to the apolipoprotein AI–CIII–AIV gene cluster on chromosome 11q23q–q24

1 reference

12 December 2020

Plasma triglyceride and LDL heterogeneity in familial combined hyperlipidemia

1 reference

12 December 2020

Stable isotopes show a direct relation between VLDL apoB overproduction and serum triglyceride levels and indicate a metabolically and biochemically coherent basis for familial combined hyperlipidemia

1 reference

12 December 2020

Genotype at a major locus with large effects on apolipoprotein B levels predicts familial combined hyperlipidemia

1 reference

12 December 2020

No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families

1 reference

12 December 2020

10.1007/S00439-010-0819-2

Identifiers

DOI

1 reference

PubMed ID

20383777

Dimensions Publication ID

29 July 2017

0 references

1 reference

29 July 2017

1 reference

PubMed ID

20383777