(Q39334653)

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A Fast Method that Uses Polygenic Scores to Estimate the Variance Explained by Genome-wide Marker Panels and the Proportion of Variants Affecting a Trait

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scholarly article

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Europe PubMed Central

PMC publication ID

11 September 2017

A Fast Method that Uses Polygenic Scores to Estimate the Variance Explained by Genome-wide Marker Panels and the Proportion of Variants Affecting a Trait (English)

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

author name string

Luigi Palla

1

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Europe PubMed Central

PMC publication ID

11 September 2017

Frank Dudbridge

2

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Europe PubMed Central

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11 September 2017

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publication date

16 July 2015

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Europe PubMed Central

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11 September 2017

American Journal of Human Genetics

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Europe PubMed Central

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11 September 2017

97

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Europe PubMed Central

PMC publication ID

11 September 2017

2

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Europe PubMed Central

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11 September 2017

250-259

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

An atlas of genetic correlations across human diseases and traits

1 reference

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11 September 2017

LD Score regression distinguishes confounding from polygenicity in genome-wide association studies

1 reference

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11 September 2017

Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder

1 reference

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11 September 2017

Measuring missing heritability: inferring the contribution of common variants

1 reference

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Structural architecture of SNP effects on complex traits

1 reference

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11 September 2017

Research review: Polygenic methods and their application to psychiatric traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573448

11 September 2017

Biological insights from 108 schizophrenia-associated genetic loci

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573448

11 September 2017

MultiBLUP: improved SNP-based prediction for complex traits

1 reference

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11 September 2017

Statistical power to detect genetic (co)variance of complex traits using SNP data in unrelated samples.

1 reference

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11 September 2017

Explaining additional genetic variation in complex traits

1 reference

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11 September 2017

Searching for missing heritability: designing rare variant association studies

1 reference

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11 September 2017

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

1 reference

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11 September 2017

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

1 reference

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11 September 2017

Power and predictive accuracy of polygenic risk scores.

1 reference

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11 September 2017

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

1 reference

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

1 reference

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11 September 2017

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

1 reference

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11 September 2017

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

1 reference

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11 September 2017

The mystery of missing heritability: Genetic interactions create phantom heritability

1 reference

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11 September 2017

Environment-sensitive epigenetics and the heritability of complex diseases

1 reference

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11 September 2017

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

1 reference

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11 September 2017

Adaptation - not by sweeps alone

1 reference

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11 September 2017

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

1 reference

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11 September 2017

The genetics of human adaptation: hard sweeps, soft sweeps, and polygenic adaptation

1 reference

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11 September 2017

Common polygenic variation contributes to risk of schizophrenia and bipolar disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573448

11 September 2017

Personal genomes: The case of the missing heritability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573448

11 September 2017

PLINK: a tool set for whole-genome association and population-based linkage analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4573448

11 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=4573448

11 September 2017

The genetic theory of adaptation: a brief history

1 reference

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11 September 2017

Genome-wide efficient mixed-model analysis for association studies

1 reference

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17 June 2018

Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis

1 reference

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21 August 2018

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

1 reference

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21 August 2018

Identifiers

10.1016/J.AJHG.2015.06.005

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 September 2017

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