(Q38401224)

English

A flexible Bayesian framework for modeling haplotype association with disease, allowing for dominance effects of the underlying causative variants

scientific article published on 31 August 2006

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scholarly article

1 reference

Europe PubMed Central

2 September 2017

A flexible Bayesian framework for modeling haplotype association with disease, allowing for dominance effects of the underlying causative variants (English)

1 reference

Europe PubMed Central

2 September 2017

author name string

Andrew P Morris

1

1 reference

Europe PubMed Central

2 September 2017

language of work or name

0 references

publication date

31 August 2006

1 reference

Europe PubMed Central

2 September 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

2 September 2017

79

1 reference

Europe PubMed Central

2 September 2017

679-694

1 reference

Europe PubMed Central

2 September 2017

4

1 reference

Europe PubMed Central

2 September 2017

A haplotype map of the human genome

1 reference

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1 reference

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1 reference

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Recent developments in genomewide association scans: a workshop summary and review

1 reference

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1 reference

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Use of unphased multilocus genotype data in indirect association studies

1 reference

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The role of haplotypes in candidate gene studies

1 reference

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The complex interplay among factors that influence allelic association.

1 reference

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The International HapMap Project

1 reference

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1 reference

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1 reference

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A comparison of bayesian methods for haplotype reconstruction from population genotype data

1 reference

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Modeling and E-M estimation of haplotype-specific relative risks from genotype data for a case-control study of unrelated individuals

1 reference

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1 reference

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1 reference

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Score tests for association between traits and haplotypes when linkage phase is ambiguous

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592560

6 September 2017

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592560

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A candidate prostate cancer susceptibility gene at chromosome 17p

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592560

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Pharmacogenomics: translating functional genomics into rational therapeutics

1 reference

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Cytochrome P450 2D6 variants in a Caucasian population: allele frequencies and phenotypic consequences

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The future of genetic studies of complex human diseases

1 reference

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6 September 2017

A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. IV. Nested analyses with cladogram uncertainty and recombination.

1 reference

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6 September 2017

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

1 reference

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6 September 2017

A cladistic analysis of phenotype associations with haplotypes inferred from restriction endonuclease mapping. II. The analysis of natural populations

1 reference

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A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping. I. Basic theory and an analysis of alcohol dehydrogenase activity in Drosophila

1 reference

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A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping and DNA sequence data. III. Cladogram estimation

1 reference

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Linkage disequilibrium mapping via cladistic analysis of single-nucleotide polymorphism haplotypes

1 reference

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Fine mapping of disease genes via haplotype clustering.

1 reference

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Maximum likelihood estimation of haplotype effects and haplotype-environment interactions in association studies.

1 reference

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1 reference

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31 August 2018

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

1 reference

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31 August 2018

Bayesian partitioning for estimating disease risk.

1 reference

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31 August 2018

Linkage disequilibrium mapping identifies a 390 kb region associated with CYP2D6 poor drug metabolising activity

1 reference

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12 December 2020

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Europe PubMed Central

2 September 2017

1 reference

Europe PubMed Central

2 September 2017

1 reference

Europe PubMed Central

2 September 2017

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