(Q34269759)

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Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients

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scholarly article

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Europe PubMed Central

1 August 2017

Evidence for substantial effect modification by gender in a large-scale genetic association study of the metabolic syndrome among coronary heart disease patients (English)

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Europe PubMed Central

1 August 2017

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metabolic syndrome

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inferred from title

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coronary artery disease

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6

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1 August 2017

David J Moliterno

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object named as

David J Moliterno

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Europe PubMed Central

1 August 2017

L Kristin Newby

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object named as

L Kristin Newby

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Europe PubMed Central

1 August 2017

author name string

Jeanette J McCarthy

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Europe PubMed Central

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Joanne Meyer

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Europe PubMed Central

1 August 2017

William J Rogers

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Europe PubMed Central

1 August 2017

GenQuest multicenter study

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1 August 2017

publication date

14 October 2003

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Europe PubMed Central

1 August 2017

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Europe PubMed Central

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114

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1

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87-98

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1 August 2017

https://scigraph.springernature.com/pub.10.1007/s00439-003-1026-1

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A genome-wide scan for coronary heart disease suggests in Indo-Mauritians a susceptibility locus on chromosome 16p13 and replicates linkage with the metabolic syndrome on 3q27.

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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Cardiovascular morbidity and mortality associated with the metabolic syndrome

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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Quantitative trait loci on chromosomes 3 and 17 influence phenotypes of the metabolic syndrome.

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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Prospective analysis of the insulin-resistance syndrome (syndrome X).

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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Genetic versus environmental aetiology of the metabolic syndrome among male and female twins

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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SBE-TAGS: an array-based method for efficient single-nucleotide polymorphism genotyping

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https://pubmed.ncbi.nlm.nih.gov/14557872

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SNP genotyping by the 5'-nuclease reaction

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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Prevalence of the metabolic syndrome among US adults: findings from the third National Health and Nutrition Examination Survey

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

based on heuristic

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Sex-specific and sex-independent quantitative trait loci for facets of the metabolic syndrome in WOKW rats

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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The metabolic syndrome: prevalence and associated risk factor findings in the US population from the Third National Health and Nutrition Examination Survey, 1988-1994.

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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The Interaction of Selection and Linkage. I. General Considerations; Heterotic Models

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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Genome scan for blood pressure in Dutch dyslipidemic families reveals linkage to a locus on chromosome 4p.

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

based on heuristic

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Variation in the lipoprotein receptor-related protein, alpha2-macroglobulin and lipoprotein receptor-associated protein genes in relation to plasma lipid levels and risk of early myocardial infarction

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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LRP: a multifunctional scavenger and signaling receptor

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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Executive Summary of The Third Report of The National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, And Treatment of High Blood Cholesterol In Adults (Adult Treatment Panel III)

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

based on heuristic

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Functional expression of low density lipoprotein receptor-related protein is controlled by receptor-associated protein in vivo

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

based on heuristic

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Genetics of the metabolic syndrome

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

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https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

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Variation in the LRP-associated protein gene (LRPAP1) is associated with late-onset Alzheimer disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

based on heuristic

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Association of genetic variants in the HDL receptor, SR-B1, with abnormal lipids in women with coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

based on heuristic

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Update on managing hypercholesterolemia. The new NCEP guidelines

1 reference

https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

based on heuristic

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Characterization of single-nucleotide polymorphisms in coding regions of human genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

based on heuristic

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Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction

1 reference

https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

based on heuristic

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A comprehensive linkage analysis for myocardial infarction and its related risk factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/14557872

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-003-1026-1

1 reference

Europe PubMed Central

1 August 2017

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0 references

1 reference

Europe PubMed Central

1 August 2017

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