(Q33620811)

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Underestimation of heritability using a mixed model with a polygenic covariance structure in a genome-wide association study for complex traits

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scholarly article

1 reference

Europe PubMed Central

28 July 2017

Underestimation of heritability using a mixed model with a polygenic covariance structure in a genome-wide association study for complex traits (English)

1 reference

Europe PubMed Central

28 July 2017

genome-wide association study

0 references

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24149545%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

author name string

Hyunju Ryoo

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24149545%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

language of work or name

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based on heuristic

inferred from title

publication date

23 October 2013

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Europe PubMed Central

28 July 2017

European Journal of Human Genetics

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24149545%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

22

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24149545%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24149545%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

851-854

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24149545%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

describes a project that uses

genome-wide association study

1 reference

based on heuristic

inferred from title

https://scigraph.springernature.com/pub.10.1038/ejhg.2013.236

0 references

The benefits of selecting phenotype-specific variants for applications of mixed models in genomics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

The genomic signature of trait-associated variants.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Heritability in the genome-wide association era

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Rare and common variants: twenty arguments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Five years of GWAS discovery

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

The mystery of missing heritability: Genetic interactions create phantom heritability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Genome partitioning of genetic variation for complex traits using common SNPs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Estimating missing heritability for disease from genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

GCTA: a tool for genome-wide complex trait analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Missing heritability and strategies for finding the underlying causes of complex disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Mixed linear model approach adapted for genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Variance component model to account for sample structure in genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Finding the missing heritability of complex diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Control of confounding of genetic associations in stratified populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

Genomic control for association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4023211

21 June 2018

A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.236

21 January 2018

Human copy number variation and complex genetic disease.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.236

21 January 2018

Computational neuroanatomy of speech production.

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2013.236

21 January 2018

Identifiers

10.1038/EJHG.2013.236

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24149545%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24149545%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24149545%20AND%20SRC:MED&resulttype=core&format=json

2 June 2020

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