(Q41957125)

14 October 2017

Correction for multiple testing in a gene region (English)

1 reference

14 October 2017

2

1 reference

14 October 2017

Audrey E Hendricks

1

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Kathryn L. Lunetta

object named as

Kathryn L Lunetta

series ordinal

5

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author name string

Mark W Logue

series ordinal

3

1 reference

PMCID

3925272

14 October 2017

Richard H Myers

series ordinal

4

1 reference

14 October 2017

10 July 2013

1 reference

European Journal of Human Genetics

14 October 2017

1 reference

14 October 2017

22

1 reference

14 October 2017

3

1 reference

14 October 2017

414-418

1 reference

https://scigraph.springernature.com/pub.10.1038/ejhg.2013.144

14 October 2017

0 references

cites work

Rare-variant association testing for sequencing data with the sequence kernel association test

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

Statistical analysis strategies for association studies involving rare variants

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

Pooled association tests for rare variants in exon-resequencing studies

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

Avoiding the high Bonferroni penalty in genome-wide association studies

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

A new measure of the effective number of tests, a practical tool for comparing families of non-independent significance tests

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

On multiple-testing correction in genome-wide association studies

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

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

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925272

Adjusting multiple testing in multilocus analyses using the eigenvalues of a correlation matrix

18 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FEJHG.2013.144

Evaluation of Nyholt's procedure for multiple testing correction

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23838599

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/EJHG.2013.144

1 reference

PMCID

3925272

Dimensions Publication ID

14 October 2017

0 references

1 reference

14 October 2017

1 reference

PMCID

3925272