A method for detecting recent selection in the human genome from allele age estimates (Q34264356)

1 August 2017

title

A method for detecting recent selection in the human genome from allele age estimates (English)

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1 August 2017

3

Lynn B Jorde

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1 August 2017

Christopher Toomajian

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author name string

Christopher Toomajian

1

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1 August 2017

Richard S Ajioka

2

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1 August 2017

James P Kushner

4

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1 August 2017

Martin Kreitman

5

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1 August 2017

language of work or name

English

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publication date

1 September 2003

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1 August 2017

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1 August 2017

volume

165

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1 August 2017

issue

1

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1 August 2017

page(s)

287-297

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Detecting recent positive selection in the human genome from haplotype structure

1 August 2017

cites work

1 reference

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Sequence variation and haplotype structure at the human HFE locus

6 July 2018

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Patterns of linkage disequilibrium in the human genome

6 July 2018

1 reference

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Linkage disequilibrium: what history has to tell us.

6 July 2018

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Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.

6 July 2018

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6 July 2018

Estimating allele age.

1 reference

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Bayesian analysis of haplotypes for linkage disequilibrium mapping

6 July 2018

1 reference

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Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

6 July 2018

1 reference

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High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequence

6 July 2018

1 reference

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Linkage disequilibrium in humans: models and data

6 July 2018

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The use of intraallelic variability for testing neutrality and estimating population growth rate

6 July 2018

1 reference

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Linkage disequilibrium in the human genome

6 July 2018

1 reference

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High-resolution HLA class I typing in the CEPH families: analysis of linkage disequilibrium among HLA loci

6 July 2018

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Unusual haplotype structure at the proximal breakpoint of In(2L)t in a natural population of Drosophila melanogaster

6 July 2018

1 reference

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Assessment of linkage disequilibrium by the decay of haplotype sharing, with application to fine-scale genetic mapping

6 July 2018

1 reference

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The genetic basis for the association of the 8.1 ancestral haplotype (A1, B8, DR3) with multiple immunopathological diseases

6 July 2018

1 reference

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Recombination within the human MHC.

6 July 2018

1 reference

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Transferrin receptor is negatively modulated by the hemochromatosis protein HFE: implications for cellular iron homeostasis

6 July 2018

1 reference

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The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

6 July 2018

1 reference

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Estimating the age of mutant disease alleles based on linkage disequilibrium

6 July 2018

1 reference

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Heterogeneity in rates of recombination in the 6-Mb region telomeric to the human major histocompatibility complex

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

Global prevalence of putative haemochromatosis mutations

6 July 2018

1 reference

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Clinical and biochemical abnormalities in people heterozygous for hemochromatosis

6 July 2018

1 reference

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Structural analysis of the HLA-A/HLA-F subregion: precise localization of two new multigene families closely associated with the HLA class I sequences

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

6 July 2018

1 reference

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Mitochondrial portraits of human populations using median networks

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

Allele frequencies at microsatellite loci: the stepwise mutation model revisited

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

Evidence for positive selection in the superoxide dismutase (Sod) region of Drosophila melanogaster

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

A powerful likelihood method for the analysis of linkage disequilibrium between trait loci and one or more polymorphic marker loci

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population

6 July 2018

1 reference

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The hitch-hiking effect of a favourable gene

6 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

6 July 2018

12 December 2020

What maintains the frequencies of human genetic diseases?

1 reference

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Phenylketonuria. Population genetics of a disease

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

Studies of RFLP closely linked to the cystic fibrosis locus throughout Europe lead to new considerations in populations genetics

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

Frequency analysis and allele map in favor of the celtic origin of the C282Y mutation of hemochromatosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

Linkage disequilibrium in HLA cannot be explained by selective recombination.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1462736

A model of mutation appropriate to estimate the number of electrophoretically detectable alleles in a finite population

28 October 2018

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12 December 2020

The age of an allele in a finite population

1 reference

12 December 2020

Prevalence of Hemochromatosis among 11,065 Presumably Healthy Blood Donors

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12 December 2020

The HLA A1-B8 haplotype extends 6 Mb beyond HLA-A: associations between HLA-A, B, F and 15 microsatellite markers

1 reference

12 December 2020

A haplotype and linkage disequilibrium analysis of the hereditary hemochromatosis gene region

1 reference

12 December 2020

Identifiers

PMC publication ID

1462736

1 reference

1 August 2017

1 reference