(Q39763886)

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Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability

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scholarly article

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Europe PubMed Central

14 September 2017

Novel method to estimate the phenotypic variation explained by genome-wide association studies reveals large fraction of the missing heritability (English)

1 reference

Europe PubMed Central

14 September 2017

genome-wide association study

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2

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Zoltán Kutalik

1

object named as

Zoltán Kutalik

1 reference

Europe PubMed Central

14 September 2017

Jacques S Beckmann

object named as

Jacques S Beckmann

5

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6

object named as

Sven Bergmann

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Europe PubMed Central

14 September 2017

Dawn Waterworth

3

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Dawn Waterworth

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Europe PubMed Central

14 September 2017

author name string

GIANT consortium

4

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Europe PubMed Central

14 September 2017

publication date

4 April 2011

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Europe PubMed Central

14 September 2017

Genetic Epidemiology

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Europe PubMed Central

14 September 2017

35

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Europe PubMed Central

14 September 2017

341-349

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Europe PubMed Central

14 September 2017

5

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Europe PubMed Central

14 September 2017

Rare genetic variants and the risk of cancer

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

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The Convergence of a Class of Double-rank Minimization Algorithms 1. General Considerations

1 reference

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

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

21 January 2018

The CoLaus study: a population-based study to investigate the epidemiology and genetic determinants of cardiovascular risk factors and metabolic syndrome

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

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Common genetic variation and human traits

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

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Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

21 January 2018

Hundreds of variants clustered in genomic loci and biological pathways affect human height

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

21 January 2018

Personal genomes: The case of the missing heritability

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

21 January 2018

Finding the missing heritability of complex diseases

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

21 January 2018

A new multipoint method for genome-wide association studies by imputation of genotypes

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

21 January 2018

Estimation of effect size distribution from genome-wide association studies and implications for future discoveries

1 reference

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21 January 2018

How many genetic variants remain to be discovered?

1 reference

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21 January 2018

Pooled association tests for rare variants in exon-resequencing studies

1 reference

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21 January 2018

The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

21 January 2018

Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

21 January 2018

Mapping allele-specific DNA methylation: a new tool for maximizing information from GWAS.

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

21 January 2018

Common SNPs explain a large proportion of the heritability for human height

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

21 January 2018

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

1000 Genomes project

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20582

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/GEPI.20582

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

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