(Q31115587)

3 October 2017

A powerful and efficient set test for genetic markers that handles confounders (English)

1 reference

3 October 2017

2

Christoph Lippert

1 reference

3 October 2017

Jennifer Listgarten

1

1 reference

3 October 2017

Eun Yong Kang

3

1 reference

3 October 2017

Jing Xiang

4

1 reference

3 October 2017

Carl M Kadie

5

1 reference

3 October 2017

David Heckerman

6

1 reference

3 October 2017

language of work or name

English

0 references

publication date

18 April 2013

1 reference

3 October 2017

1 reference

3 October 2017

29

1 reference

3 October 2017

12

1 reference

3 October 2017

1526-1533

1 reference

Creative Commons Attribution 3.0 Unported

3 October 2017

start time

2 October 2016

1 reference

April 2023 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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An exhaustive epistatic SNP association analysis on expanded Wellcome Trust data

21 June 2018

1 reference

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Patterns of methylation heritability in a genome-wide analysis of four brain regions.

21 June 2018

1 reference

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Optimal unified approach for rare-variant association testing with application to small-sample case-control whole-exome sequencing studies

21 June 2018

1 reference

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An efficient multi-locus mixed-model approach for genome-wide association studies in structured populations.

21 June 2018

1 reference

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Optimal tests for rare variant effects in sequencing association studies

21 June 2018

1 reference

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Improved linear mixed models for genome-wide association studies

21 June 2018

1 reference

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The UCSC Genome Browser database: extensions and updates 2011.

21 June 2018

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A general framework for detecting disease associations with rare variants in sequencing studies

21 June 2018

1 reference

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

21 June 2018

1 reference

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Pathways of distinction analysis: a new technique for multi-SNP analysis of GWAS 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=3673214

Genomic inflation factors under polygenic inheritance

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci

21 June 2018

1 reference

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The major genetic determinants of HIV-1 control affect HLA class I peptide presentation

21 June 2018

1 reference

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Statistical analysis strategies for association studies involving rare variants

21 June 2018

1 reference

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Correction for hidden confounders in the genetic analysis of gene expression

21 June 2018

1 reference

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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

Testing SNPs and sets of SNPs for importance in 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=3673214

Powerful SNP-set analysis for case-control genome-wide 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=3673214

New approaches to population stratification in genome-wide 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=3673214

Genome-wide association study of 107 phenotypes in Arabidopsis thaliana inbred lines.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

Variance component model to account for sample structure in genome-wide 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=3673214

GSEA-SNP: applying gene set enrichment analysis to SNP data from genome-wide 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=3673214

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=3673214

Accommodating linkage disequilibrium in genetic-association analyses via ridge regression

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

A tutorial on statistical methods for population 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=3673214

Principal components analysis corrects for stratification in genome-wide 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=3673214

Description of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

A unified mixed-model method for association mapping that accounts for multiple levels of relatedness

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

The human genome browser at UCSC

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

Genomic control for 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=3673214

GeneCards: integrating information about genes, proteins and diseases.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

FaST linear mixed models for genome-wide 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=3673214

Increased accuracy of artificial selection by using the realized relationship matrix.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

Likelihood ratio tests in behavioral genetics: problems and solutions.

25 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3673214

FaST-LMM-Select for addressing confounding from spatial structure and rare variants

25 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23599503

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/BIOINFORMATICS/BTT177

1 reference

journals/bioinformatics/ListgartenLKXKH13

3 October 2017

1 reference

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

3 October 2017

PubMed publication ID

23599503

1 reference