(Q51575431)

7 April 2018

title

Evaluation of coverage variation of SNP chips for genome-wide association studies. (English)

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7 April 2018

genome-wide association study

main subject

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author name string

Mingyao Li

series ordinal

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7 April 2018

Chun Li

series ordinal

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7 April 2018

Weihua Guan

series ordinal

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7 April 2018

publication date

6 February 2008

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7 April 2018

European Journal of Human Genetics

published in

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7 April 2018

volume

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7 April 2018

issue

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7 April 2018

page(s)

635-643

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7 April 2018

Genome-wide association studies for common diseases and complex traits

cites work

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Genome-wide association studies: theoretical and practical concerns

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Whole-genome patterns of common DNA variation in three human populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Complement factor H polymorphism in age-related macular degeneration

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

A common genetic variant is associated with adult and childhood obesity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

A genome-wide association study identifies IL23R as an inflammatory bowel disease gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

A genome-wide association study identifies novel risk loci for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Evaluating coverage of genome-wide association studies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Finishing the euchromatic sequence of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Ascertainment bias in studies of human genome-wide polymorphism.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

The DNA sequence and biology of human chromosome 19

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

APOE and TGF-beta1 genes are associated with obesity phenotypes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokine.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Long-term prevention of renal insufficiency, excess matrix gene expression, and glomerular mesangial matrix expansion by treatment with monoclonal antitransforming growth factor-beta antibody in db/db diabetic mice

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Intron-exon structure of the human transforming growth factor-beta precursor gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Deficient Smad7 expression: a putative molecular defect in scleroderma

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

TGF-beta is a critical mediator of acute lung injury

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Anti-apoptotic function of a microRNA encoded by the HSV-1 latency-associated transcript

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Structural variation in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Sequence features in regions of weak and strong linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202007

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5202007

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7 April 2018

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7 April 2018