(Q37636303)

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The deleterious mutation load is insensitive to recent population history.

scientific article published on 09 February 2014

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Europe PubMed Central

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21 August 2017

The deleterious mutation load is insensitive to recent population history. (English)

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Michael C Turchin

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509481%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

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Yuval B Simons

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509481%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Jonathan K Pritchard

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509481%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

Guy Sella

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509481%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

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publication date

9 February 2014

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Europe PubMed Central

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21 August 2017

Nature Genetics

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509481%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

46

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Europe PubMed Central

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4 June 2020

3

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Europe PubMed Central

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4 June 2020

220-224

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509481%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

https://scigraph.springernature.com/pub.10.1038/ng.2896

0 references

Properties and modeling of GWAS when complex disease risk is due to non-complementing, deleterious mutations in genes of large effect.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Evolution and functional impact of rare coding variation from deep sequencing of human exomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Rare and common variants: twenty arguments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

The functional spectrum of low-frequency coding variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

A map of human genome variation from population-scale sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

MutationTaster evaluates disease-causing potential of sequence alterations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

A method and server for predicting damaging missense mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Evolution in health and medicine Sackler colloquium: Genetic architecture of a complex trait and its implications for fitness and genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Inferring the joint demographic history of multiple populations from multidimensional SNP frequency data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Finding the missing heritability of complex diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Identification of deleterious mutations within three human genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Widespread genomic signatures of natural selection in hominid evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Interrogating multiple aspects of variation in a full resequencing data set to infer human population size changes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Theoretical models of selection and mutation on quantitative traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Are rare variants responsible for susceptibility to complex diseases?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

When did the human population size start increasing?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

23 August 2017

Calibrating a coalescent simulation of human genome sequence variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

14 September 2017

Recent explosive human population growth has resulted in an excess of rare genetic variants

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

25 June 2018

Deep resequencing reveals excess rare recent variants consistent with explosive population growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

25 June 2018

Genetics. Human genetic variation, shared and private

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

1 September 2018

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3953611

1 September 2018

Computational neuroanatomy of speech production.

1 reference

https://api.crossref.org/works/10.1038%2FNG.2896

21 January 2018

Deleterious mutations can surf to high densities on the wave front of an expanding population

1 reference

https://pubmed.ncbi.nlm.nih.gov/24509481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational Meltdowns in Sexual Populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/24509481

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/NG.2896

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509481%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

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PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509481%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24509481%20AND%20SRC:MED&resulttype=core&format=json

4 June 2020

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