(Q46724519)

24 December 2017

title

Uncovering the total heritability explained by all true susceptibility variants in a genome-wide association study (English)

1 reference

24 December 2017

genome-wide association study

main subject

0 references

1 reference

Hon-Cheong So

1

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author name string

Miaoxin Li

series ordinal

2

1 reference

24 December 2017

Pak C Sham

series ordinal

3

1 reference

24 December 2017

language of work or name

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26 May 2011

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24 December 2017

published in

Genetic Epidemiology

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24 December 2017

volume

35

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24 December 2017

issue

6

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24 December 2017

page(s)

447-456

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24 December 2017

describes a project that uses

genome-wide association study

1 reference

based on heuristic

inferred from title

cites work

Broad and narrow heritabilities of quantitative traits in a founder population

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Bootstrap Methods: Another Look at the Jackknife

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Large-Scale Simultaneous Hypothesis Testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Empirical Bayes Estimates for Large-Scale Prediction Problems

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Common variants at 30 loci contribute to polygenic dyslipidemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Update on the incidence and prevalence of Crohn's disease and ulcerative colitis in Olmsted County, Minnesota, 1940-2000.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

A HapMap harvest of insights into the genetics of common disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Crohn's disease: the genetic contribution

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Sizing up human height variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Empirical Bayes Analysis of a Microarray Experiment

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

Admissible Estimators, Recurrent Diffusions, and Insoluble Boundary Value Problems

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

inferred from DOI database lookup

7 January 2021

based on heuristic

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.20593

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/GEPI.20593

1 reference

24 December 2017

1 reference

24 December 2017