(Q57259513)

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To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?

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title

To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies? (English)

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main subject

genome-wide association study

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Jeffrey C Barrett

2

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David M. Evans

object named as

David M Evans

series ordinal

1

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author name string

Lon R Cardon

series ordinal

3

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publication date

16 January 2008

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published in

European Journal of Human Genetics

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volume

16

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page(s)

718-723

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issue

6

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exact match

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5202011

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cites work

A haplotype map of the human genome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

Genome-wide association study identifies novel breast cancer susceptibility loci

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

Genomewide association analysis of coronary artery disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

Mutation in blood coagulation factor V associated with resistance to activated protein C.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

A common coding variant in CASP8 is associated with breast cancer risk

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

Evaluating coverage of genome-wide association studies

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

Genetic Power Calculator: design of linkage and association genetic mapping studies of complex traits

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5202011

retrieved

7 January 2021

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Identifiers

DOI

10.1038/SJ.EJHG.5202011

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PubMed ID

18197186

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(Q57259513)

To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?

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