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Rare-variant association analysis: study designs and statistical tests
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title
Rare-variant association analysis: study designs and statistical tests
(English)
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PubMed
main subject
statistics
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author
Michael Boehnke
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3
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Xihong Lin
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4
object named as
Xihong Lin
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Crossref
author name string
Seunggeung Lee
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1
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Gonçalo R. Abecasis
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2
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language of work or name
English
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PubMed
publication date
3 July 2014
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published in
American Journal of Human Genetics
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PubMed
volume
95
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PubMed
issue
1
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PubMed
page(s)
5-23
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4085641
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28 September 2017
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits
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28 September 2017
Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies
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28 September 2017
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28 September 2017
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis
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28 September 2017
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28 September 2017
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28 September 2017
ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
SNP detection and genotyping from low-coverage sequencing data on multiple diploid samples
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4085641
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28 September 2017
A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions
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28 September 2017
Powerful SNP-set analysis for case-control genome-wide association studies
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28 September 2017
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28 September 2017
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28 September 2017
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4085641
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28 September 2017
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4085641
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28 September 2017
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4085641
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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28 September 2017
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31 May 2018
Detecting rare variant effects using extreme phenotype sampling in sequencing association studies
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31 May 2018
An exponential combination procedure for set-based association tests in sequencing studies
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31 May 2018
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4085641
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31 May 2018
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4085641
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31 May 2018
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31 May 2018
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31 May 2018
Asymptotic tests of association with multiple SNPs in linkage disequilibrium
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4085641
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31 May 2018
Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4085641
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28 November 2018
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28 November 2018
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28 November 2018
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28 November 2018
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28 November 2018
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28 November 2018
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28 November 2018
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28 November 2018
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28 November 2018
Extreme Selection Strategies in Gene Mapping Studies of Oligogenic Quantitative Traits Do Not Always Increase Power
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28 November 2018
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based on heuristic
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Identifiers
DOI
10.1016/J.AJHG.2014.06.009
1 reference
stated in
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OpenCitations bibliographic resource ID
984670
OpenCitations bibliographic resource ID
984670
1 reference
stated in
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OpenCitations bibliographic resource ID
984670
PMCID
4085641
1 reference
stated in
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OpenCitations bibliographic resource ID
984670
PubMed ID
24995866
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
984670
ResearchGate publication ID
263712346
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