Evaluating and improving power in whole-genome association studies using fixed marker sets. (Q53255191)

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scientific article published on 21 May 2006

Language	Label	Description	Also known as
English	Evaluating and improving power in whole-genome association studies using fixed marker sets.	scientific article published on 21 May 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

Evaluating and improving power in whole-genome association studies using fixed marker sets. (English)

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Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

whole genome sequencing

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based on heuristic

inferred from title

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Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

David Altshuler

5

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Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

Mark Joseph Daly

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object named as

Mark J Daly

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Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

Paul I W de Bakker

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object named as

Paul I W de Bakker

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

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object named as

Roman Yelensky

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Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

author name string

Itsik Pe'er

1

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

language of work or name

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publication date

21 May 2006

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Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

Nature Genetics

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PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

38

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Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

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Europe PubMed Central

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12 May 2018

http://europepmc.org/abstract/MED/16715096

663-667

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Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

A comparison of linkage disequilibrium measures for fine-scale mapping

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

The future of genetic studies of complex human diseases

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

A DNA Polymorphism Discovery Resource for Research on Human Genetic Variation: Table 1

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Database resources of the National Center for Biotechnology Information

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

A genome-wide scalable SNP genotyping assay using microarray technology

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Genome-wide association studies for common diseases and complex traits

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

A haplotype map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Power tools for human genetics

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Biases and reconciliation in estimates of linkage disequilibrium in the human genome

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Linkage disequilibrium in humans: models and data

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Efficiency and power in genetic association studies

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Ascertainment bias in studies of human genome-wide polymorphism.

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

The allelic architecture of human disease genes: common disease-common variant... or not?

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

1 reference

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21 January 2018

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Choosing haplotype-tagging SNPS based on unphased genotype data using a preliminary sample of unrelated subjects with an example from the Multiethnic Cohort Study

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Using linkage genome scans to improve power of association in genome scans

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

21 January 2018

Variation is the spice of life

1 reference

https://api.crossref.org/works/10.1038%2FNG1816

7 January 2021

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Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

12 May 2018

http://europepmc.org/abstract/MED/16715096

ResearchGate publication ID

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