(Q41890222)

13 October 2017

Disease model distortion in association studies (English)

1 reference

13 October 2017

4

Peter Donnelly

1 reference

13 October 2017

Damjan Vukcevic

1

1 reference

PMCID

3110308

13 October 2017

Eliana Hechter

series ordinal

2

1 reference

PMCID

3110308

13 October 2017

Chris Spencer

series ordinal

3

1 reference

13 October 2017

17 March 2011

1 reference

13 October 2017

1 reference

13 October 2017

35

1 reference

13 October 2017

4

1 reference

13 October 2017

278-290

1 reference

Prioritizing GWAS results: A review of statistical methods and recommendations for their application

13 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

Bayesian statistical methods for genetic association studies

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

Estimating coverage and power for genetic association studies using near-complete variation data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

What can genome-wide association studies tell us about the genetics of common disease?

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

Data and theory point to mainly additive genetic variance for complex traits

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

A second generation human haplotype map of over 3.1 million SNPs

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

A tutorial on statistical methods for population association studies

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

A haplotype map of the human genome

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

The ENCODE (ENCyclopedia Of DNA Elements) Project

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

The complex interplay among factors that influence allelic association.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

Linkage disequilibrium in humans: models and data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

From genotypes to genes: doubling the sample size

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

The effects of SNP genotyping errors on the power of the Cochran-Armitage linear trend test for case/control association studies.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

Genome-wide strategies for detecting multiple loci that influence complex diseases.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3110308

Risk ratio and rate ratio estimation in case-cohort designs: Hypertension and cardiovascular mortality

18 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.20576

Tests for Linear Trends in Proportions and Frequencies

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FGEPI.20576

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/GEPI.20576

1 reference

13 October 2017

0 references

1 reference

13 October 2017

1 reference

PMCID

3110308