(Q90227989)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

title

SumHer better estimates the SNP heritability of complex traits from summary statistics (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

1 reference

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

David J. Balding

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

publication date

3 December 2018

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

volume

51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

page(s)

277-284

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

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

12 April 2020

cites work

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7 January 2021

LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis.

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7 January 2021

Reevaluation of SNP heritability in complex human traits

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7 January 2021

Improved heritability estimation from genome-wide SNPs

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7 January 2021

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

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7 January 2021

Genome partitioning of genetic variation for complex traits using common SNPs

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7 January 2021

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

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7 January 2021

GCTA: a tool for genome-wide complex trait analysis

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7 January 2021

Genomic control for association studies

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7 January 2021

A map of human genome variation from population-scale sequencing

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7 January 2021

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

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7 January 2021

The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future

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7 January 2021

Dissecting the genetics of complex traits using summary association statistics

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7 January 2021

Describing the genetic architecture of epilepsy through heritability analysis

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7 January 2021

The fine-scale genetic structure of the British population

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7 January 2021

Genomic inflation factors under polygenic inheritance

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7 January 2021

FaST linear mixed models for genome-wide association studies

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7 January 2021

Advantages and pitfalls in the application of mixed-model association methods

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7 January 2021

Efficient Bayesian mixed-model analysis increases association power in large cohorts.

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7 January 2021

A unified mixed-model method for association mapping that accounts for multiple levels of relatedness

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7 January 2021

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

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7 January 2021

Genetic studies of body mass index yield new insights for obesity biology

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7 January 2021

Discovery and refinement of loci associated with lipid levels

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7 January 2021

Integrating common and rare genetic variation in diverse human populations

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7 January 2021

Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection.

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7 January 2021

A high-resolution map of human evolutionary constraint using 29 mammals

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https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

Evidence of abundant purifying selection in humans for recently acquired regulatory functions

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https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

Integrative annotation of chromatin elements from ENCODE data

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https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

PRSice: Polygenic Risk Score software

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https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

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7 January 2021

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

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7 January 2021

Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

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7 January 2021

Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations

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https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

Genome-wide meta-analyses identify multiple loci associated with smoking behavior

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https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

Genetics of rheumatoid arthritis contributes to biology and drug discovery

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7 January 2021

Biological insights from 108 schizophrenia-associated genetic loci

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7 January 2021

An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans

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https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture

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https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses

1 reference

https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

1 reference

https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways

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https://api.crossref.org/works/10.1038%2FS41588-018-0279-5

7 January 2021

Defining the role of common variation in the genomic and biological architecture of adult human height

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7 January 2021

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

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7 January 2021

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

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7 January 2021

Genome-wide association study identifies 74 loci associated with educational attainment

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7 January 2021

Estimating missing heritability for disease from genome-wide association studies

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7 January 2021

Bayes factors for genome-wide association studies: comparison with P-values

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7 January 2021

Joint analysis of functional genomic data and genome-wide association studies of 18 human traits

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7 January 2021

Improved whole-chromosome phasing for disease and population genetic studies

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7 January 2021

Genotype imputation with thousands of genomes

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7 January 2021

Population Structure and Cryptic Relatedness in Genetic Association Studies

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7 January 2021

Heritability of Threshold Characters.

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12 December 2020

Imputation and quality control steps for combining multiple genome-wide datasets

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12 December 2020

New genetic loci link adipose and insulin biology to body fat distribution

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12 December 2020

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

1 reference

12 December 2020

10.1038/S41588-018-0279-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:30510236%20AND%20SRC:MED&resulttype=core&format=json

12 April 2020

1 reference