Optimal tests for rare variant effects in sequencing association studies (Q31065241)

12 August 2017

Optimal tests for rare variant effects in sequencing association studies (English)

1 reference

12 August 2017

3

Xihong Lin

1 reference

12 August 2017

Seunggeun Lee

1

1 reference

PMCID

3440237

12 August 2017

Michael C Wu

series ordinal

2

1 reference

12 August 2017

14 June 2012

1 reference

12 August 2017

1 reference

12 August 2017

13

1 reference

12 August 2017

4

1 reference

12 August 2017

762-775

1 reference

Comparison of statistical tests for disease association with rare variants

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

Testing for an unusual distribution of rare variants

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

Pooled association tests for rare variants in exon-resequencing studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

An evaluation of statistical approaches to rare variant analysis in genetic association studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

A groupwise association test for rare mutations using a weighted sum statistic

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed models

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

Semiparametric regression of multidimensional genetic pathway data: least-squares kernel machines and linear mixed models

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

Haplotype-based association analysis via variance-components score test.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

Calibrating a coalescent simulation of human genome sequence variation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3440237

Algorithm AS 155: The Distribution of a Linear Combination of χ 2 Random Variables

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOSTATISTICS%2FKXS014

The Dallas Heart Study: a population-based probability sample for the multidisciplinary study of ethnic differences in cardiovascular health.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOSTATISTICS%2FKXS014

Hypothesis testing in semiparametric additive mixed models

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FBIOSTATISTICS%2FKXS014

Comparison of maximum statistics for hypothesis testing when a nuisance parameter is present only under the alternative

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22699862

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BIOSTATISTICS/KXS014

1 reference

12 August 2017

1 reference

12 August 2017

1 reference

PMCID

3440237