Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression (Q30428383)

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English	Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression	scientific article

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scholarly article

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Europe PubMed Central

PMC publication ID

8 November 2017

Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression (English)

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

quantitative trait

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based on heuristic

inferred from title

Jung-Ying Tzeng

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Jung-Ying Tzeng

1

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Mark I McCarthy

5

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Chris Tyler-Smith

4

object named as

Chris Smith

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Europe PubMed Central

PMC publication ID

8 November 2017

Patrick F. Sullivan

10

object named as

Patrick F Sullivan

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Europe PubMed Central

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8 November 2017

author name string

Daowen Zhang

2

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Europe PubMed Central

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8 November 2017

Monnat Pongpanich

3

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Europe PubMed Central

PMC publication ID

8 November 2017

Michèle M Sale

6

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Europe PubMed Central

PMC publication ID

8 November 2017

Bradford B Worrall

7

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Europe PubMed Central

PMC publication ID

8 November 2017

Fang-Chi Hsu

8

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8 November 2017

Duncan C Thomas

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8 November 2017

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publication date

1 August 2011

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8 November 2017

American Journal of Human Genetics

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8 November 2017

89

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Europe PubMed Central

PMC publication ID

8 November 2017

2

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

277-288

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Europe PubMed Central

PMC publication ID

8 November 2017

Transcobalamin 2 variant associated with poststroke homocysteine modifies recurrent stroke risk

1 reference

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Testing for an unusual distribution of rare variants

1 reference

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20 June 2018

Self-Contained Gene-Set Analysis of Expression Data: An Evaluation of Existing and Novel Methods

1 reference

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20 June 2018

Genomic similarity and kernel methods I: advancements by building on mathematical and statistical foundations

1 reference

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20 June 2018

Genomic similarity and kernel methods II: methods for genomic information

1 reference

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Powerful SNP-set analysis for case-control genome-wide association studies

1 reference

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20 June 2018

Pooled association tests for rare variants in exon-resequencing studies

1 reference

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20 June 2018

Gene--environment-wide association studies: emerging approaches

1 reference

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Methods for investigating gene-environment interactions in candidate pathway and genome-wide association studies

1 reference

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Gene, region and pathway level analyses in whole-genome studies

1 reference

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Comparisons of multi-marker association methods to detect association between a candidate region and disease

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20 June 2018

Association tests using kernel-based measures of multi-locus genotype similarity between individuals

1 reference

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The impact of gene-environment dependence and misclassification in genetic association studies incorporating gene-environment interactions

1 reference

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

1 reference

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20 June 2018

Gene-trait similarity regression for multimarker-based association analysis.

1 reference

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ATOM: a powerful gene-based association test by combining optimally weighted markers

1 reference

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

1 reference

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20 June 2018

U-statistics-based tests for multiple genes in genetic association studies

1 reference

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20 June 2018

Gene-environment interactions for complex traits: definitions, methodological requirements and challenges

1 reference

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Comparison of the power of haplotype-based versus single- and multilocus association methods for gene x environment (gene x sex) interactions and application to gene x smoking and gene x sex interactions in rheumatoid arthritis

1 reference

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20 June 2018

Analysis of multiple SNPs in a candidate gene or region

1 reference

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A powerful and flexible multilocus association test for quantitative traits

1 reference

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

1 reference

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Group additive regression models for genomic data analysis

1 reference

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20 June 2018

Improved power by use of a weighted score test for linkage disequilibrium mapping

1 reference

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20 June 2018

Powerful multilocus tests of genetic association in the presence of gene-gene and gene-environment interactions

1 reference

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20 June 2018

Generalized genomic distance-based regression methodology for multilocus association analysis

1 reference

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20 June 2018

An entropy-based statistic for genomewide association studies

1 reference

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Nonparametric tests of association of multiple genes with human disease

1 reference

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Genome-wide association studies for common diseases and complex traits

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On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit.

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Epistasis: what it means, what it doesn't mean, and statistical methods to detect it in humans

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Genome scan of complex traits by haplotype sharing correlation.

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20 June 2018

Score tests for association between traits and haplotypes when linkage phase is ambiguous

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On multiple-testing correction in genome-wide association studies

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26 November 2018

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A 31 bp VNTR in the cystathionine beta-synthase (CBS) gene is associated with reduced CBS activity and elevated post-load homocysteine levels

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Haplotype sharing analysis using mantel statistics

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12 December 2020

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Exploiting gene-environment interaction to detect genetic associations

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12 December 2020

based on heuristic

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A principal components regression approach to multilocus genetic association studies

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https://pubmed.ncbi.nlm.nih.gov/21835306

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.AJHG.2011.07.007

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

8 November 2017

ResearchGate publication ID

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