Estimating missing heritability for disease from genome-wide association studies (Q34687621)

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English	Estimating missing heritability for disease from genome-wide association studies	scientific article

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scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

title

Estimating missing heritability for disease from genome-wide association studies (English)

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stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

main subject

genome-wide association study

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heritability

1 reference

based on heuristic

inferred from title

author

Peter M. Visscher

series ordinal

4

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stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

Sang Hong Lee

object named as

Sang Hong Lee

series ordinal

1

0 references

Michael Goddard

object named as

Michael E Goddard

series ordinal

3

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Naomi R. Wray

object named as

Naomi R Wray

series ordinal

2

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language of work or name

English

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publication date

3 March 2011

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

published in

American Journal of Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

volume

88

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stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

issue

3

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stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

page(s)

294-305

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stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

cites work

GCTA: a tool for genome-wide complex trait analysis

1 reference

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PubMed Central

reference URL

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7 July 2018

A Commentary on ‘Common SNPs Explain a Large Proportion of the Heritability for Human Height’ by Yang et al. (2010)

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PubMed Central

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7 July 2018

A simple and fast two-locus quality control test to detect false positives due to batch effects in genome-wide association studies

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PubMed Central

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7 July 2018

Reconciling the analysis of IBD and IBS in complex trait studies

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PubMed Central

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7 July 2018

Genomewide association studies and assessment of the risk of disease

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3059431

retrieved

7 July 2018

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

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PubMed Central

reference URL

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7 July 2018

The genetic interpretation of area under the ROC curve in genomic profiling

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7 July 2018

Finding the missing heritability of complex diseases

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PubMed Central

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7 July 2018

Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

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7 July 2018

Personal genomes: The case of the missing heritability

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PubMed Central

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7 July 2018

Accuracy of predicting the genetic risk of disease using a genome-wide approach

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PubMed Central

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7 July 2018

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

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7 July 2018

Heritability in the genomics era — concepts and misconceptions

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7 July 2018

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

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7 July 2018

Heritability of Threshold Characters.

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7 July 2018

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

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7 July 2018

Genetic liability of type 1 diabetes and the onset age among 22,650 young Finnish twin pairs: a nationwide follow-up study

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7 July 2018

Severe mental disorders in offspring with 2 psychiatrically ill parents.

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retrieved

26 October 2018

Identifiers

DOI

10.1016/J.AJHG.2011.02.002

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

PMC publication ID

3059431

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

PubMed publication ID

21376301

1 reference

stated in

Europe PubMed Central

PubMed publication ID

21376301

retrieved

3 August 2017

ResearchGate publication ID

50287498

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