(Q48538210)

12 February 2018

title

Does haplotype diversity predict power for association mapping of disease susceptibility? (English)

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12 February 2018

author

Andrew Collins

series ordinal

2

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12 February 2018

Newton Ennis Morton

series ordinal

3

object named as

Newton E Morton

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12 February 2018

Weihua Zhang

1

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12 February 2018

publication date

4 June 2004

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12 February 2018

published in

Human Genetics

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12 February 2018

volume

115

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12 February 2018

page(s)

157-164

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12 February 2018

issue

2

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12 February 2018

https://scigraph.springernature.com/pub.10.1007/s00439-004-1122-x

exact match

0 references

cites work

The usefulness of different density SNP maps for disease association studies of common variants

1 reference

12 December 2020

The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis

1 reference

12 December 2020

Positional cloning by linkage disequilibrium

1 reference

12 December 2020

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

1 reference

12 December 2020

A dynamic programming algorithm for haplotype block partitioning

1 reference

12 December 2020

Linkage disequilibrium and the mapping of complex human traits.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Haplotypic analysis of the TNF locus by association efficiency and entropy

1 reference

12 December 2020

Using haplotype blocks to map human complex trait loci

1 reference

12 December 2020

Sequential tests for the detection of linkage

1 reference

12 December 2020

Disequilibrium Mapping: Composite Likelihood for Pairwise Disequilibrium

1 reference

12 December 2020

Are rare variants responsible for susceptibility to complex diseases?

1 reference

12 December 2020

Statistical significance for genomewide studies

1 reference

12 December 2020

Haplotype block structure and its applications to association studies: power and study designs

1 reference

12 December 2020

Minimal haplotype tagging

1 reference

12 December 2020

A likelihood-based extended admixture model of oligogenic inheritance in 'model-based' and 'model-free' analysis.

1 reference

12 December 2020

Genomics. New mapping project splits the community.

1 reference

12 December 2020

Variation is the spice of life

1 reference

12 December 2020

Linkage disequilibrium in human populations

1 reference

12 December 2020

The future of genetic studies of complex human diseases

1 reference

12 December 2020

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

12 December 2020

Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals.

1 reference

12 December 2020

Finding genes underlying risk of complex disease by linkage disequilibrium mapping

1 reference

12 December 2020

The impact of SNP density on fine-scale patterns of linkage disequilibrium

1 reference

12 December 2020

Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

1 reference

12 December 2020

Properties of linkage disequilibrium (LD) maps

1 reference

12 December 2020

Nucleotide and haplotypic diversity of the NOS2A promoter region and its relationship to cerebral malaria.

1 reference

12 December 2020

Selection of genetic markers for association analyses, using linkage disequilibrium and haplotypes.

1 reference

12 December 2020

The optimal measure of allelic association

1 reference

12 December 2020

High-resolution haplotype structure in the human genome

1 reference

12 December 2020

Fine-scale mapping of disease loci via shattered coalescent modeling of genealogies.

1 reference

12 December 2020

Mapping a disease locus by allelic association

1 reference

12 December 2020

On the allelic spectrum of human disease

1 reference

12 December 2020

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

1 reference

12 December 2020

Haplotype tagging for the identification of common disease genes

1 reference

12 December 2020

10.1007/S00439-004-1122-X

Identifiers

DOI

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12 February 2018

PubMed ID

15221450

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12 February 2018