Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies (Q30946038)

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English	Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies	scientific article

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Efficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies (English)

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

author name string

Frank Dudbridge

1

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Bobby P C Koeleman

2

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

language of work or name

0 references

publication date

19 July 2004

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

75

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

3

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

424-435

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182021

14 July 2018

The International HapMap Project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182021

14 July 2018

Mathematical multi-locus approaches to localizing complex human trait genes

1 reference

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

1 reference

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14 July 2018

Statistical significance for genomewide studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182021

14 July 2018

Estimating the occurrence of false positives and false negatives in microarray studies by approximating and partitioning the empirical distribution of p-values

1 reference

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14 July 2018

False discovery rate in linkage and association genome screens for complex disorders.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182021

14 July 2018

Genebanks: A Comparison of Eight Proposed International Genetic Databases

1 reference

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14 July 2018

Cost-effective designs for linkage disequilibrium mapping of complex traits

1 reference

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Multiplex relative risk and estimation of the number of loci underlying an inherited disease

1 reference

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14 July 2018

DNA Pooling: a tool for large-scale association studies

1 reference

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14 July 2018

Limitations of stratifying sib-pair data in common disease linkage studies: an example using chromosome 10p14-10q11 in type 1 diabetes

1 reference

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14 July 2018

Genomewide linkage disequilibrium mapping of severe bipolar disorder in a population isolate

1 reference

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14 July 2018

Trimming, weighting, and grouping SNPs in human case-control association studies

1 reference

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14 July 2018

A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetes

1 reference

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14 July 2018

Navigating gene expression using microarrays--a technology review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182021

14 July 2018

Are rare variants responsible for susceptibility to complex diseases?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182021

14 July 2018

Linkage disequilibrium in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182021

14 July 2018

Searching for genetic determinants in the new millennium

1 reference

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14 July 2018

Methods of correcting for multiple testing: operating characteristics

1 reference

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14 July 2018

The future of genetic studies of complex human diseases

1 reference

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14 July 2018

Empirical threshold values for quantitative trait mapping

1 reference

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Methods for assessing the statistical significance of molecular sequence features by using general scoring schemes

1 reference

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14 July 2018

Power estimation of multiple SNP association test of case-control study and application

1 reference

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25 November 2018

Rank truncated product of P-values, with application to genomewide association scans.

1 reference

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25 November 2018

Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1182021

25 November 2018

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

1 reference

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Pedigree disequilibrium tests for multilocus haplotypes.

1 reference

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Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

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A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility

1 reference

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25 November 2018

Truncated product method for combining P-values.

1 reference

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A simple correction for multiple comparisons in interval mapping genome scans.

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Two-Stage Designs for Gene-Disease Association Studies

1 reference

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12 December 2020

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1 reference

19 June 2022

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1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

ResearchGate publication ID

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