(Q35708043)

9 August 2017

title

Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study (English)

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9 August 2017

6

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9 August 2017

Peter Holmans

5

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Valentina Escott-Price

series ordinal

1

object named as

Valentina Moskvina

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9 August 2017

3

Shaun Purcell

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9 August 2017

2

Colm O'Dushlaine

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9 August 2017

4

Nick Craddock

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9 August 2017

publication date

17 October 2011

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9 August 2017

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9 August 2017

volume

35

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9 August 2017

issue

8

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9 August 2017

page(s)

861-866

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A versatile gene-based test for genome-wide association studies

9 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268180

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268180

Identification of loci associated with schizophrenia by genome-wide association and follow-up

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268180

PLINK: a tool set for whole-genome association and population-based linkage analyses

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268180

Genomic control for association studies

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268180

Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268180

Rare chromosomal deletions and duplications increase risk of schizophrenia

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268180

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

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268180

Truncated product method for combining P-values.

25 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3268180

Combining dependent P-values

25 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.20636

Analysis of single-locus tests to detect gene/disease associations

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.20636

400: A Method for Combining Non-Independent, One-Sided Tests of Significance

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.20636

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/GEPI.20636

1 reference

9 August 2017

1 reference

9 August 2017

1 reference