(Q34988777)

5 August 2017

Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk (English)

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genome-wide association study

5 August 2017

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author

David M. Evans

series ordinal

1

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5 August 2017

2

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5 August 2017

Naomi R Wray

3

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publication date

24 June 2009

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5 August 2017

Human Molecular Genetics

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5 August 2017

18

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5 August 2017

3525-3531

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18

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Genetic testing in clinical practice

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Implications of the Human Genome Project for medical science.

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Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration

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Personal genomes: The case of the missing heritability

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1 reference

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The impact of genotype frequencies on the clinical validity of genomic profiling for predicting common chronic diseases

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1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP295

Prediction of individual genetic risk to disease from genome-wide association studies

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1 reference

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Schizophrenia genetics: the search for a hard lead

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Prediction of individual genetic risk of complex disease

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1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP295

PLINK: a tool set for whole-genome association and population-based linkage analyses

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1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP295

The meaning and use of the area under a receiver operating characteristic (ROC) curve

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1 reference

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Will Genetics Revolutionize Medicine?

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Identifiers

DOI

10.1093/HMG/DDP295

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5 August 2017

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PubMed ID

19553258