A genome-wide association study primer for clinicians (Q37539400)

20 August 2017

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title

A genome-wide association study primer for clinicians (English)

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genome-wide association study

20 August 2017

main subject

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author name string

Tzu-Hao Wang

series ordinal

1

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20 August 2017

Hsin-Shih Wang

series ordinal

2

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20 August 2017

publication date

1 June 2009

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Taiwanese Journal of Obstetrics & Gynecology

20 August 2017

published in

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20 August 2017

volume

48

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20 August 2017

issue

2

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20 August 2017

page(s)

89-95

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describes a project that uses

20 August 2017

genome-wide association study

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How to interpret a genome-wide association study

inferred from title

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New links to the pathogenesis of Crohn disease provided by genome-wide association scans

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The structure of haplotype blocks in the human genome

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A haplotype map of the human genome

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Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

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Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

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Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer

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Genome-wide association study identifies novel breast cancer susceptibility loci

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Genome-wide association study of prostate cancer identifies a second risk locus at 8q24

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Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

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Multiple regions within 8q24 independently affect risk for prostate cancer

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A common variant on chromosome 9p21 affects the risk of myocardial infarction

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Variants conferring risk of atrial fibrillation on chromosome 4q25.

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Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

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Genomewide association analysis of coronary artery disease

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Whole-genome analysis of sporadic amyotrophic lateral sclerosis

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Risk alleles for multiple sclerosis identified by a genomewide study

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STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosus

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Genome-wide association studies provide new insights into type 2 diabetes aetiology

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Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes

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Selection of controls in case-control studies. I. Principles

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7 January 2021

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Identifiers

DOI

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20 August 2017

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