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A powerful and adaptive association test for rare variants
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Europe PubMed Central
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4125385
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24831820%20AND%20SRC:MED&resulttype=core&format=json
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18 March 2020
title
A powerful and adaptive association test for rare variants
(English)
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PMC publication ID
4125385
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18 March 2020
author
Peng Wei
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5
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4125385
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18 March 2020
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Wei Pan
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1
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4125385
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24831820%20AND%20SRC:MED&resulttype=core&format=json
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18 March 2020
Junghi Kim
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2
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18 March 2020
Yiwei Zhang
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3
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18 March 2020
Xiaotong Shen
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4
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4125385
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24831820%20AND%20SRC:MED&resulttype=core&format=json
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18 March 2020
language of work or name
English
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publication date
15 May 2014
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4125385
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24831820%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
published in
Genetics
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4125385
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24831820%20AND%20SRC:MED&resulttype=core&format=json
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18 March 2020
volume
197
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18 March 2020
issue
4
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4125385
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18 March 2020
page(s)
1081-1095
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4125385
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18 March 2020
cites work
Functional linear models for association analysis of quantitative traits
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Sequence kernel association tests for the combined effect of rare and common variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
A unified mixed-effects model for rare-variant association in sequencing studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
An exponential combination procedure for set-based association tests in sequencing studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Adjustment for population stratification via principal components in association analysis of rare variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Incorporating predicted functions of nonsynonymous variants into gene-based analysis of exome sequencing data: a comparative study
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Genetic Analysis Workshop 17 mini-exome simulation
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Hierarchical generalized linear models for multiple groups of rare and common variants: jointly estimating group and individual-variant effects
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Adaptive tests for detecting gene-gene and gene-environment interactions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
A general framework for detecting disease associations with rare variants in sequencing studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
A data-driven method for identifying rare variants with heterogeneous trait effects
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Comparison of statistical tests for disease association with rare variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Rare-variant association testing for sequencing data with the sequence kernel association test
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Association studies for next-generation sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Assessment of rare BRCA1 and BRCA2 variants of unknown significance using hierarchical modeling
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Adaptive tests for association analysis of rare variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Testing for an unusual distribution of rare variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Relationship between genomic distance-based regression and kernel machine regression for multi-marker association testing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
A new testing strategy to identify rare variants with either risk or protective effect on disease
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Efficient utilization of rare variants for detection of disease-related genomic regions
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Analysing biological pathways in genome-wide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Comprehensive approach to analyzing rare genetic variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
To identify associations with rare variants, just WHaIT: Weighted haplotype and imputation-based tests
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
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
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Statistical analysis strategies for association studies involving rare variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Association screening of common and rare genetic variants by penalized regression
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Powerful SNP-set analysis for case-control genome-wide association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Pooled association tests for rare variants in exon-resequencing studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
A data-adaptive sum test for disease association with multiple common or rare variants
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Test selection with application to detecting disease association with multiple SNPs
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Detecting rare variants for complex traits using family and unrelated data
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
A groupwise association test for rare mutations using a weighted sum statistic
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Asymptotic tests of association with multiple SNPs in linkage disequilibrium
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed models
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
So many correlated tests, so little time! Rapid adjustment of P values for multiple correlated tests
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Improved power by use of a weighted score test for linkage disequilibrium mapping
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
An efficient resampling method for assessing genome-wide statistical significance in mapping quantitative trait Loci
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
Empirical threshold values for quantitative trait mapping
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
5 July 2018
A new expectation-maximization statistical test for case-control association studies considering rare variants obtained by high-throughput sequencing
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
29 October 2018
A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST).
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
29 October 2018
Rapid simulation of P values for product methods and multiple-testing adjustment in association studies
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4125385
retrieved
29 October 2018
Robust and powerful tests for rare variants using Fisher's method to combine evidence of association from two or more complementary tests
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24831820
retrieved
12 December 2020
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inferred from PubMed ID database lookup
Identifiers
DOI
10.1534/GENETICS.114.165035
1 reference
stated in
Europe PubMed Central
PMC publication ID
4125385
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24831820%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
PMC publication ID
4125385
1 reference
stated in
Europe PubMed Central
PMC publication ID
4125385
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24831820%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
PubMed publication ID
24831820
1 reference
stated in
Europe PubMed Central
PMC publication ID
4125385
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24831820%20AND%20SRC:MED&resulttype=core&format=json
retrieved
18 March 2020
ResearchGate publication ID
262382394
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