(Q35004530)

5 August 2017

title

Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans (English)

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5 August 2017

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5 August 2017

Guy A Rouleau

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Françoise Le Deist

object named as

Françoise Le Deist

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Alan Hodgkinson

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Elie Haddad

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Daniel Sinnett

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Jacques L Michaud

1 reference

5 August 2017

Julie Hussin

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5 August 2017

Philip Awadalla

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5 August 2017

Youssef Idaghdour

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5 August 2017

Vanessa Bruat

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5 August 2017

Thibault de Maillard

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5 August 2017

Jean-Christophe Grenier

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5 August 2017

Elias Gbeha

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5 August 2017

Fadi F Hamdan

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5 August 2017

Simon Girard

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5 August 2017

Jean-François Spinella

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5 August 2017

Mathieu Larivière

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5 August 2017

Virginie Saillour

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5 August 2017

Jasmine Healy

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5 August 2017

Isabel Fernández

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5 August 2017

publication date

26 September 2013

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5 August 2017

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5 August 2017

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5 August 2017

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5 August 2017

page(s)

e1003815

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Creative Commons Attribution 4.0 International

5 August 2017

start time

26 September 2013

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April 2022 Public Data File from Crossref

copyrighted

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cites work

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8 July 2018

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8 July 2018

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8 July 2018

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Estimating the rate of adaptive molecular evolution in the presence of slightly deleterious mutations and population size change

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Proportionally more deleterious genetic variation in European than in African populations.

8 July 2018

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

8 July 2018

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

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Allelic variation in gene expression is common in the human genome

8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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21 January 2018

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21 January 2018

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21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003815

Comment on "Widespread RNA and DNA sequence differences in the human transcriptome".

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3784517

Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

26 October 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003815

Deep Human Genealogies Reveal a Selective Advantage to Be on an Expanding Wave Front

21 January 2018

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https://api.crossref.org/works/10.1371%2FJOURNAL.PGEN.1003815

Prevalence and distribution of genetic diseases in Quebec: impact of the past on the present

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3784517

Increased exonic de novo mutation rate in individuals with schizophrenia

9 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24086152

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Distributions of exons and introns in the human genome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24086152

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Comment on "Widespread RNA and DNA sequence differences in the human transcriptome"

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24086152

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PGEN.1003815

1 reference

5 August 2017

1 reference

5 August 2017

1 reference