(Q42698511)

5 November 2017

Progress and challenges in genome-wide association studies in humans (English)

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genome-wide association study

5 November 2017

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author name string

Peter Donnelly

series ordinal

1

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PubMed ID

19079049

5 November 2017

language of work or name

English

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publication date

1 December 2008

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5 November 2017

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5 November 2017

456

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5 November 2017

728-731

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5 November 2017

7223

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https://scigraph.springernature.com/pub.10.1038/nature07631

5 November 2017

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cites work

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Genome-wide association analysis identifies 20 loci that influence adult height

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Identification of ten loci associated with height highlights new biological pathways in human growth

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

A HapMap harvest of insights into the genetics of common disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Newly identified genetic risk variants for celiac disease related to the immune response

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Personal genomes: The case of the missing heritability

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Genetic predisposition to breast cancer: past, present, and future

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Beta-cell dysfunction, rather than insulin insensitivity, is the primary defect in familial type 2 diabetes.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Newly identified loci highlight beta cell dysfunction as a key cause of type 2 diabetes: where are the insulin resistance genes?

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

The emerging landscape of breast cancer susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

A common allele on chromosome 9 associated with coronary heart disease

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Multiple loci identified in a genome-wide association study of prostate cancer

1 reference

https://api.crossref.org/works/10.1038%2FNATURE07631

7 January 2021

Identifiers

DOI

10.1038/NATURE07631

1 reference

PubMed ID

19079049

Dimensions Publication ID

5 November 2017

0 references

1 reference

PubMed ID

19079049