(Q36294045)

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Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood

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scholarly article

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Europe PubMed Central

PMC publication ID

13 August 2017

Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (English)

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Peter M. Visscher

4

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

object named as

J Yang

2

0 references

5

object named as

N R Wray

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

author name string

S H Lee

1

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

M E Goddard

3

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

language of work or name

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publication date

26 July 2012

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Europe PubMed Central

PMC publication ID

13 August 2017

number of pages

3

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based on heuristic

inferred from page(s)

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Europe PubMed Central

PMC publication ID

13 August 2017

28

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Europe PubMed Central

PMC publication ID

13 August 2017

19

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Europe PubMed Central

PMC publication ID

13 August 2017

2540-2542

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

Estimating the proportion of variation in susceptibility to schizophrenia captured by common SNPs.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463125

30 September 2017

Impact of diagnostic misclassification on estimation of genetic correlations using genome-wide genotypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463125

30 September 2017

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=3463125

30 September 2017

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=3463125

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463125

30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463125

30 September 2017

Heritability of Threshold Characters.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463125

30 September 2017

An efficient variance component approach implementing an average information REML suitable for combined LD and linkage mapping with a general complex pedigree

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3463125

30 September 2017

Identifiers

10.1093/BIOINFORMATICS/BTS474

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

DBLP publication ID

journals/bioinformatics/LeeYGVW12

1 reference

DBLP Dataset 2021-01-02

28 January 2021

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

13 August 2017

ResearchGate publication ID

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