(Q31108294)

20 August 2017

Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set (English)

1 reference

20 August 2017

Masahiro Kanai

1

0 references

Toshihiro Tanaka

object named as

Toshihiro Tanaka

series ordinal

2

0 references

author name string

Yukinori Okada

series ordinal

3

1 reference

20 August 2017

16 June 2016

1 reference

Journal of Human Genetics

20 August 2017

1 reference

20 August 2017

61

1 reference

20 August 2017

10

1 reference

20 August 2017

861-866

1 reference

Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International

20 August 2017

start time

16 June 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Genomic Insights into the Ancestry and Demographic History of South America

1 reference

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An integrated map of structural variation in 2,504 human genomes

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

A global reference for human genetic variation

14 July 2018

1 reference

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Sparse whole-genome sequencing identifies two loci for major depressive disorder

14 July 2018

1 reference

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Large-scale whole-genome sequencing of the Icelandic population

14 July 2018

1 reference

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Second-generation PLINK: rising to the challenge of larger and richer datasets

14 July 2018

1 reference

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Addressing population-specific multiple testing burdens in genetic 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=5090169

Genetics of rheumatoid arthritis contributes to biology and drug discovery

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

A comprehensive SNP and indel imputability database

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

Correcting away the hidden heritability

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

Genotype imputation 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=5090169

Uncovering the roles of rare variants in common disease through whole-genome sequencing

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

Practical aspects of imputation-driven meta-analysis of 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=5090169

Multiple testing in the genomics era: findings from Genetic Analysis Workshop 15, Group 15.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

A second generation human haplotype map of over 3.1 million SNPs

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

PLINK: a tool set for whole-genome association and population-based linkage analyses

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

Non-replication and inconsistency in the genome-wide association setting

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

Principal components analysis corrects for stratification 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=5090169

Statistical significance for genomewide 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=5090169

Genomic control for 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=5090169

Multiple significance tests: the Bonferroni method

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5090169

A multiple testing correction method for genetic association studies using correlated single nucleotide polymorphisms

14 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2016.72

What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2016.72

SmileFinder: a resampling-based approach to evaluate signatures of selection from genome-wide sets of matching allele frequency data in two or more diploid populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2016.72

Long-range LD can confound genome scans in admixed populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2016.72

21 January 2018

Identifiers

DOI

10.1038/JHG.2016.72

1 reference

PMC publication ID

5090169

Dimensions Publication ID

20 August 2017

0 references

1 reference

PMC publication ID

5090169

20 August 2017

PubMed publication ID

27305981

1 reference

PMC publication ID

5090169