(Q40015281)

16 September 2017

title

Weighting sequence variants based on their annotation increases power of whole-genome association studies (English)

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16 September 2017

main subject

whole genome sequencing

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2

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16 September 2017

Daníel F. Guðbjartsson

11

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16 September 2017

Unnur Þorsteinsdóttir

9

object named as

Unnur Thorsteinsdottir

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16 September 2017

Gísli Másson

6

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Augustine Kong

object named as

Augustine Kong

8

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Patrick Sulem

10

object named as

Patrick Sulem

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16 September 2017

12

Kari Stefansson

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16 September 2017

author name string

Gardar Sveinbjornsson

1

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16 September 2017

Florian Zink

3

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16 September 2017

Sigurjón A Gudjonsson

4

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16 September 2017

Asmundur Oddson

5

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16 September 2017

Hilma Holm

7

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16 September 2017

language of work or name

English

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publication date

8 February 2016

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16 September 2017

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16 September 2017

volume

48

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16 September 2017

issue

3

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16 September 2017

page(s)

314-317

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Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

16 September 2017

cites work

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The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

21 January 2018

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Large-scale whole-genome sequencing of the Icelandic population

21 January 2018

1 reference

An integrated map of genetic variation from 1,092 human genomes

21 January 2018

1 reference

Estimation of the multiple testing burden for genomewide association studies of nearly all common variants

21 January 2018

1 reference

The International HapMap Project

21 January 2018

1 reference

Whole-genome sequence variation, population structure and demographic history of the Dutch population

21 January 2018

1 reference

A global reference for human genetic variation

21 January 2018

1 reference

Statistical power and significance testing in large-scale genetic studies

21 January 2018

1 reference

Coding single-nucleotide polymorphisms associated with complex vs. Mendelian disease: evolutionary evidence for differences in molecular effects.

21 January 2018

1 reference

All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs

21 January 2018

1 reference

Genome partitioning of genetic variation for complex traits using common SNPs

21 January 2018

1 reference

Importance of different types of prior knowledge in selecting genome-wide findings for follow-up

21 January 2018

1 reference

Rare mutations associating with serum creatinine and chronic kidney disease

21 January 2018

1 reference

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

21 January 2018

1 reference

The Sequence Ontology: a tool for the unification of genome annotations

21 January 2018

1 reference

An integrated encyclopedia of DNA elements in the human genome

21 January 2018

1 reference

Systematic localization of common disease-associated variation in regulatory DNA

21 January 2018

1 reference

Integrative analysis of 111 reference human epigenomes

21 January 2018

1 reference

Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases

21 January 2018

1 reference

ChromHMM: automating chromatin-state discovery and characterization

21 January 2018

1 reference

Distribution and intensity of constraint in mammalian genomic sequence

21 January 2018

1 reference

Evolutionary constraint facilitates interpretation of genetic variation in resequenced human genomes

21 January 2018

1 reference

A general framework for estimating the relative pathogenicity of human genetic variants

21 January 2018

1 reference

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

21 January 2018

1 reference

Functional annotation signatures of disease susceptibility loci improve SNP association analysis

21 January 2018

1 reference

Integrating functional data to prioritize causal variants in statistical fine-mapping studies

21 January 2018

1 reference

Genome-Wide Significance Levels and Weighted Hypothesis Testing

21 January 2018

1 reference

Using linkage genome scans to improve power of association in genome scans

21 January 2018

1 reference

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

21 January 2018

1 reference

Partitioning heritability by functional annotation using genome-wide association summary statistics

21 January 2018

1 reference

Common variants of FUT2 are associated with plasma vitamin B12 levels

21 January 2018

1 reference

A Simplex Method for Function Minimization

21 January 2018

1 reference

False discovery control with p-value weighting

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1038/NG.3507

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Dimensions Publication ID

16 September 2017

1043168111

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