(Q40143010)

17 September 2017

The (in)famous GWAS P-value threshold revisited and updated for low-frequency variants (English)

1 reference

genome-wide association study

17 September 2017

0 references

1 reference

4

Leif Groop

1 reference

17 September 2017

2

Alisa K Manning

1 reference

17 September 2017

João Fadista

1

1 reference

17 September 2017

Jose C Florez

series ordinal

3

1 reference

17 September 2017

6 January 2016

1 reference

European Journal of Human Genetics

17 September 2017

1 reference

17 September 2017

24

1 reference

17 September 2017

8

1 reference

17 September 2017

1202-1205

1 reference

Statistical power and significance testing in large-scale genetic studies

17 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

An integrated map of genetic variation from 1,092 human genomes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

A high-performance computing toolset for relatedness and principal component analysis of SNP data

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

The variant call format and VCFtools

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

Bayesian statistical methods for genetic association studies

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

A second generation human haplotype map of over 3.1 million SNPs

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

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

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

A haplotype map of the human genome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

Assessing the probability that a positive report is false: an approach for molecular epidemiology studies

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

Statistical significance for genomewide studies

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

Molecular genetics of the Finnish disease heritage.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4970684

20 August 2018

Identifiers

DOI

10.1038/EJHG.2015.269

1 reference

Dimensions Publication ID

17 September 2017

0 references

1 reference

17 September 2017

PubMed publication ID

26733288

1 reference