GEE-based SNP set association test for continuous and discrete traits in family-based association studies (Q33556485)

28 July 2017

GEE-based SNP set association test for continuous and discrete traits in family-based association studies (English)

1 reference

28 July 2017

1 reference

Xiaofeng Zhu

3

0 references

Susan Redline

series ordinal

4

object named as

Susan Redline

1 reference

28 July 2017

5

Xihong Lin

1 reference

28 July 2017

Xuefeng Wang

1

1 reference

PubMed ID

24166731

28 July 2017

Seunggeun Lee

series ordinal

2

1 reference

28 July 2017

25 October 2013

1 reference

28 July 2017

1 reference

28 July 2017

37

1 reference

28 July 2017

8

1 reference

28 July 2017

778-786

1 reference

Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

A variance component based multi-marker association test using family and unrelated data.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Family-based association tests for sequence data, and comparisons with population-based association tests

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Sequence kernel association test for quantitative traits in family samples

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

SNP set association analysis for familial data

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Optimal tests for rare variant effects in sequencing association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

A comparison of strategies for analyzing dichotomous outcomes in genome-wide association studies with general pedigrees

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Family-based designs for genome-wide association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Detecting rare and common variants for complex traits: sibpair and odds ratio weighted sum statistics (SPWSS, ORWSS).

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

A rapid generalized least squares model for a genome-wide quantitative trait association analysis in families

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Combined admixture mapping and association analysis identifies a novel blood pressure genetic locus on 5p13: contributions from the CARe consortium

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

GATES: a rapid and powerful gene-based association test using extended Simes procedure

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

On combining family-based and population-based case-control data in association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

ROADTRIPS: case-control association testing with partially or completely unknown population and pedigree structure

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

GWAF: an R package for genome-wide association analyses with family data

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Detecting rare variants for complex traits using family and unrelated data

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Avoiding the high Bonferroni penalty in genome-wide association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Pathway analysis by adaptive combination of P-values

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

A partial least-square approach for modeling gene-gene and gene-environment interactions when multiple markers are genotyped

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

A unified association analysis approach for family and unrelated samples correcting for stratification.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Generalized genomic distance-based regression methodology for multilocus association analysis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Family-based designs in the age of large-scale gene-association studies

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

A whole-genome scan for obstructive sleep apnea and obesity

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

Rank truncated product of P-values, with application to genomewide association scans.

14 July 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21763

Powerful multi-marker association tests: unifying genomic distance-based regression and logistic regression

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21763

Single marker family-based association analysis not conditional on parental information

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21763

On combining family and case-control studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21763

HAPGEN2: simulation of multiple disease SNPs

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21763

Truncated product method for combining P-values.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21763

Identification of association between disease and multiple markers via sparse partial least-squares regression

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

An approximate distribution of estimates of variance components.

31 October 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4007511

31 October 2018

https://api.crossref.org/works/10.1002%2FGEPI.21763

inferred from DOI database lookup

7 January 2021

based on heuristic

A principal components regression approach to multilocus genetic association studies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24166731

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/GEPI.21763

1 reference

28 July 2017

1 reference

28 July 2017

1 reference

PubMed ID

24166731