(Q42948366)

11 November 2017

Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'. (English)

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11 November 2017

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11 November 2017

Carolina Medina-Gomez

6

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11 November 2017

12

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11 November 2017

16

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11 November 2017

13

Jessica van Setten

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11 November 2017

David van Enckevort

17

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Lennart C Karssen

Lennart C Karssen

9

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Cisca Wijmenga

Cisca Wijmenga

23

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Morris A Swertz

24

Morris A Swertz

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11 November 2017

Cornelia M. van Duijn

20

Cornelia M van Duijn

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11 November 2017

8

Jouke Jan Hottenga

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11 November 2017

11

Eskil Kreiner-Møller

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11 November 2017

7

Laurent C Francioli

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11 November 2017

22

Paul I W de Bakker

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11 November 2017

Javier Gutierrez-Achury

14

Javier Gutierrez-Achury

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11 November 2017

5

Freerk van Dijk

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11 November 2017

19

Heorhiy Byelas

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11 November 2017

18

Martijn Dijkstra

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11 November 2017

Alexandros Kanterakis

4

Alexandros Kanterakis

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11 November 2017

2

Androniki Menelaou

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11 November 2017

Elisabeth M van Leeuwen

3

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11 November 2017

Karol Estrada

10

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11 November 2017

Harm-Jan Westra

15

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11 November 2017

Genome of Netherlands Consortium

21

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11 November 2017

4 June 2014

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European Journal of Human Genetics

11 November 2017

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11 November 2017

22

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11 November 2017

11

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11 November 2017

1321-1326

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Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported

11 November 2017

start time

4 June 2014

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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exact match

https://scigraph.springernature.com/pub.10.1038/ejhg.2014.19

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cites work

The Genome of the Netherlands: design, and project goals

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Bayesian refinement of association signals for 14 loci in 3 common diseases

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Efficiency and power as a function of sequence coverage, SNP array density, and imputation

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Optimal tests for rare variant effects in sequencing association studies

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Genotype imputation with thousands of genomes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Performance of genotype imputation for rare variants identified in exons and flanking regions of genes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Promise and pitfalls of the Immunochip

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

A comparison of approaches to account for uncertainty in analysis of imputed genotypes

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Uncovering the roles of rare variants in common disease through whole-genome sequencing

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Concept, design and implementation of a cardiovascular gene-centric 50 k SNP array for large-scale genomic association studies

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

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

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Efficiency and power in genetic association studies

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4200431

16 August 2018

Identifiers

DOI

10.1038/EJHG.2014.19

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Dimensions Publication ID

11 November 2017

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11 November 2017

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