Integrating common and rare genetic variation in diverse human populations (Q29547220)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20811451%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

title

Integrating common and rare genetic variation in diverse human populations (English)

2 references

PubMed

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20811451

23 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20811451%20AND%20SRC:MED&resulttype=core&format=json

human population genetics

13 February 2020

main subject

1 reference

1 reference

1 reference

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13 February 2020

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13 February 2020

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13 February 2020

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13 February 2020

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13 February 2020

1 reference

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13 February 2020

Claudia Gonzaga-Jauregui

1 reference

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13 February 2020

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13 February 2020

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13 February 2020

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13 February 2020

1 reference

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13 February 2020

Pardis C Sabeti

1 reference

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13 February 2020

Stephen F Schaffner

1 reference

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13 February 2020

Stephen F Schaffner

1 reference

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13 February 2020

Stephen F Schaffner

1 reference

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13 February 2020

Michael Inouye

1 reference

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13 February 2020

Leena Peltonen-Palotie

object named as

Leena Peltonen

1 reference

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13 February 2020

Leena Peltonen-Palotie

object named as

Leena Peltonen

1 reference

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13 February 2020

Leena Peltonen-Palotie

object named as

Leena Peltonen

1 reference

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13 February 2020

Mark J Daly

1 reference

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13 February 2020

Matthew Hurles

1 reference

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13 February 2020

Vivian Ota Wang

1 reference

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13 February 2020

Lora R Lewis

1 reference

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13 February 2020

Alicia Hawes

1 reference

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13 February 2020

David Wheeler

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13 February 2020

Stephen Leslie

1 reference

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13 February 2020

Richard A Gibbs

1 reference

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13 February 2020

Richard A Gibbs

1 reference

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13 February 2020

Richard A Gibbs

1 reference

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13 February 2020

Richard A Gibbs

1 reference

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13 February 2020

Richard A Gibbs

1 reference

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13 February 2020

author name string

International HapMap 3 Consortium

1 reference

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13 February 2020

David M Altshuler

1 reference

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13 February 2020

David M Altshuler

1 reference

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13 February 2020

Emmanouil Dermitzakis

1 reference

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13 February 2020

Fuli Yu

1 reference

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13 February 2020

Emmanouil Dermitzakis

1 reference

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13 February 2020

Penelope E Bonnen

1 reference

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13 February 2020

David M Altshuler

1 reference

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13 February 2020

Paul I W de Bakker

1 reference

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13 February 2020

Stacey B Gabriel

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13 February 2020

Rhian Gwilliam

1 reference

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13 February 2020

Xiaoming Jia

1 reference

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13 February 2020

Aarno Palotie

1 reference

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13 February 2020

Melissa Parkin

1 reference

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13 February 2020

Pamela Whittaker

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13 February 2020

Fuli Yu

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13 February 2020

Yanru Ren

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13 February 2020

Donna Marie Muzny

1 reference

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13 February 2020

Katayoon Darvishi

1 reference

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13 February 2020

Joshua M Korn

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13 February 2020

Charles Lee

1 reference

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13 February 2020

Steven A McCarrol

1 reference

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13 February 2020

James Nemesh

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13 February 2020

Emmanouil Dermitzakis

1 reference

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13 February 2020

Alon Keinan

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Stephen B Montgomery

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Samuela Pollack

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13 February 2020

Alkes L Price

1 reference

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13 February 2020

Penelope E Bonnen

1 reference

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13 February 2020

Alon Keinan

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13 February 2020

Alkes L Price

1 reference

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Fuli Yu

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13 February 2020

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Morris W Foster

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13 February 2020

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13 February 2020

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13 February 2020

Charmaine D Royal

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13 February 2020

Richard R Sharp

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13 February 2020

Changqing Zeng

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Lisa D Brooks

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Jean E McEwen

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13 February 2020

language of work or name

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23 April 2017

publication date

1 September 2010

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13 February 2020

0 references

2 references

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23 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20811451%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

volume

467

2 references

PubMed

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23 April 2017

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13 February 2020

issue

7311

2 references

PubMed

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23 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20811451%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

page(s)

52-58

1 reference

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Finding the missing heritability of complex diseases

13 February 2020

cites work

1 reference

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Origins and functional impact of copy number variation in the human genome

23 April 2017

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Signals of recent positive selection in a worldwide sample of human populations

23 April 2017

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African genetic diversity: implications for human demographic history, modern human origins, and complex disease mapping

23 April 2017

1 reference

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A second generation human haplotype map of over 3.1 million SNPs

23 April 2017

1 reference

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Measurement of the human allele frequency spectrum demonstrates greater genetic drift in East Asians than in Europeans

23 April 2017

1 reference

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A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

23 April 2017

1 reference

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

23 April 2017

1 reference

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Global variation in copy number in the human genome

23 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

SLC24A5, a putative cation exchanger, affects pigmentation in zebrafish and humans

23 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

SNPdetector: a software tool for sensitive and accurate SNP detection

23 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

A haplotype map of the human genome

23 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

23 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

Initial sequencing and analysis of the human genome

23 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

Integrated detection and population-genetic analysis of SNPs and copy number variation

23 April 2017

1 reference

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Positive natural selection in the human lineage

23 April 2017

1 reference

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A composite of multiple signals distinguishes causal variants in regions of positive selection

23 April 2017

1 reference

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A genome scan for positive selection in thoroughbred horses

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

Constructing genomic maps of positive selection in humans: where do we go from here?

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

Progress and challenges in genome-wide association studies in humans

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

A robust statistical method for case-control association testing with copy number variation

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

A genotype calling algorithm for the Illumina BeadArray platform

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

Biases and reconciliation in estimates of linkage disequilibrium in the human genome

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

Genomic regions exhibiting positive selection identified from dense genotype data

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173859

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20811451

3 June 2018

Identifiers

3 references

23 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20811451%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

13 February 2020

1052674054

0 references

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20811451

3 references

23 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20811451%20AND%20SRC:MED&resulttype=core&format=json

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20811451

13 February 2020

PubMed publication ID

3 references

23 April 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20811451%20AND%20SRC:MED&resulttype=core&format=json