(Q33553419)

28 July 2017

A reference panel of 64,976 haplotypes for genotype imputation (English)

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Cornelia M. van Duijn

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Cornelia M van Duijn

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David Schlessinger

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David Schlessinger

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Samuli Ripatti

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Samuli Ripatti

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Alexander Teumer

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Alexander Teumer

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Nicole Soranzo

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Nicole Soranzo

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Jaakko Tuomilehto

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Stacey Gabriel

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Francis S Collins

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Cisca Wijmenga

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Cisca Wijmenga

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Eleftheria Zeggini

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Eleftheria Zeggini

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Kristian Hveem

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Charles Kooperberg

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Andrew Hattersley

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Laura J. Corbin

Laura J Corbin

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Arthur Gilly

Arthur Gilly

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Yang Luo

Yang Luo

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Shane McCarthy

Shane McCarthy

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Ilaria Gandin

Ilaria Gandin

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Lukas Forer

Lukas Forer

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Massimiliano Cocca

Massimiliano Cocca

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Matthew G Sampson

Matthew G Sampson

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Tabitha A Harrison

Tabitha Harrison

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Anubha Mahajan

Anubha Mahajan

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Chad M Brummett

Chad M Brummett

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Kerrin S. Small

Kerrin Small

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Shawn Levy

Shawn Levy

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Gerome Breen

Gerome Breen

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George Davey Smith

George Davey Smith

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He Zhang

He Zhang

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Andrea Angius

Andrea Angius

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Karen L Mohlke

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Karen L Mohlke

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Francesco Cucca

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Veikko Salomaa

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Veikko Salomaa

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Morris A Swertz

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Mark I McCarthy

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Carl A Anderson

Carl A Anderson

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Michael Boehnke

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Michael Boehnke

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Aarno Palotie

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Dwight Stambolian

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Luigi Ferrucci

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Leif Groop

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Christian Fuchsberger

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Christian Fuchsberger

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David Altshuler

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Jan Veldink

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Kari Branham

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Haplotype Reference Consortium

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Haplotype Reference Consortium

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Emily Chew

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Seppo Koskinen

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Timothy Frayling

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Steven McCarroll

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Matthias Kretzler

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Petr Danecek

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P Eline Slagboom

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James F Wilson

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Ulrike Peters

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Timothy Spector

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Deborah Nickerson

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Matt McGue

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William Iacono

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Michele Pato

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James C Lee

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Andrew R Wood

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Ross M Fraser

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Cristen Willer

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Scott Vrieze

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Hyun Min Kang

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Sayantan Das

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Carlo Sidore

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Laura J Scott

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Fabio Busonero

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Matthias Nauck

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Andrew Chan

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George Dedoussis

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Oddgeir L Holmen

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John B Vincent

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Richard M Myers

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Cinzia Sala

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Daniela Toniolo

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David Melzer

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Klaudia Walter

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Josine L Min

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Harry Campbell

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Aliki-Eleni Farmaki

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Jeffrey C Barrett

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Paul I W de Bakker

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Warren Kretzschmar

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Olivier Delaneau

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Kevin Sharp

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Alan Kwong

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Carlos Pato

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Christopher E Gillies

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Massimo Mezzavilla

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Michela Traglia

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Dorrett Boomsma

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Sai Chen

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Marcus Dorr

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Nicola Pirastu

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Melvin McInnis

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Marcus Tuke

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Leonard H Van den Berg

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Wouter Van Rheenen

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Paolo Gasparini

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language of work or name

English

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publication date

22 August 2016

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10

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1279-1283

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https://scigraph.springernature.com/pub.10.1038/ng.3643

28 July 2017

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cites work

Phasing for medical sequencing using rare variants and large haplotype reference panels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

A global reference for human genetic variation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

Sparse whole-genome sequencing identifies two loci for major depressive disorder

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

A genome-wide association study identifies protein quantitative trait loci (pQTLs)

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

A new multipoint method for genome-wide association studies by imputation of genotypes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

Genetic structure of human populations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

Subsystems contributing to the decline in ability to walk: bridging the gap between epidemiology and geriatric practice in the InCHIANTI study.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

A second generation human haplotype map of over 3.1 million SNPs

28 July 2018

1 reference

Improved whole-chromosome phasing for disease and population genetic studies

21 January 2018

1 reference

minimac2: faster genotype imputation

21 January 2018

1 reference

Haplotype estimation for biobank-scale data sets

21 January 2018

1 reference

The African Genome Variation Project shapes medical genetics in Africa

21 January 2018

1 reference

Cohort Profile: The Study of Health in Pomerania

21 January 2018

1 reference

Genotype imputation for genome-wide association studies

21 January 2018

1 reference

Serum levels and genotype distribution of α1-antitrypsin in the general population

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5388176

Structural and functional characterization of the abnormal Z alpha 1-antitrypsin isolated from human liver

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27548312

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG.3643

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Dimensions Publication ID

28 July 2017

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28 July 2017

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