(Q24651685)

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Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study

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scholarly article

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Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study (English)

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genome-wide association study

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atherosclerosis

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based on heuristic

inferred from title

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based on heuristic

inferred from title

Eric Boerwinkle

5

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Aaron R. Folsom

2

object named as

Aaron R Folsom

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4

object named as

Kelly A Volcik

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author name string

Jan Bressler

1

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David J Couper

3

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language of work or name

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publication date

1 January 2010

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American Journal of Epidemiology

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171

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1

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14-23

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describes a project that uses

genome-wide association study

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based on heuristic

inferred from title

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

1 reference

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Genomewide association analysis of coronary artery disease

1 reference

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Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

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GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers

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A common allele on chromosome 9 associated with coronary heart disease

1 reference

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A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

1 reference

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Projections of global mortality and burden of disease from 2002 to 2030

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1 reference

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1 reference

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Variation in FTO contributes to childhood obesity and severe adult obesity

1 reference

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Sortilin is the major 110-kDa protein in GLUT4 vesicles from adipocytes

1 reference

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Evaluation of methods for the measurement of low-density lipoprotein cholesterol.

1 reference

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Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits

1 reference

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Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes

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A Coefficient of Agreement for Nominal Scales

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Identifiers

10.1093/AJE/KWP377

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