(Q35882781)

English

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers

scientific article published in June 1996

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8651307%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8651307%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

Werner syndrome

1 reference

based on heuristic

inferred from title

lessons learned

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

linkage disequilibrium

1 reference

based on heuristic

inferred from title

author name string

K A Goddard

1

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16 October 2019

C E Yu

2

1 reference

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16 October 2019

J Oshima

3

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16 October 2019

T Miki

4

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16 October 2019

J Nakura

5

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16 October 2019

C Piussan

6

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16 October 2019

G M Martin

7

1 reference

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16 October 2019

G D Schellenberg

8

1 reference

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16 October 2019

E M Wijsman

9

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16 October 2019

language of work or name

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publication date

1 June 1996

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16 October 2019

American Journal of Human Genetics

1 reference

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16 October 2019

58

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16 October 2019

6

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16 October 2019

1286-1302

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8651307%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

Testing Hypotheses about Linkage Disequilibrium with Multiple Alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Mutation of human short tandem repeats

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Maximum-likelihood estimation of gene location by linkage disequilibrium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Design and sample-size considerations in the detection of linkage disequilibrium with a disease locus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Linkage disequilibrium between the FES, D15S127, and BLM loci in Ashkenazi Jews with Bloom syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Limits of resolution of genetic linkage studies: implications for the positional cloning of human disease genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Integrated mapping analysis of the Werner syndrome region of chromosome 8.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Likelihood methods for locating disease genes in nonequilibrium populations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

A single ataxia telangiectasia gene with a product similar to PI-3 kinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Sublocalization of an ataxia-telangiectasia gene distal to D11S384 by ancestral haplotyping in Costa Rican families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

The Bloom's syndrome gene product is homologous to RecQ helicases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Genetic association between chromosome 8 microsatellite (MS8-134) and Werner syndrome (WRN): chromosome microdissection and homozygosity mapping

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Replicative life-span of cultivated human cells. Effects of donor's age, tissue, and genotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

The sampling distribution of linkage disequilibrium under an infinite allele model without selection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Gametic disequilibrium measures: proceed with caution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Slipped-strand mispairing: a major mechanism for DNA sequence evolution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

On measures of gametic disequilibrium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

A disequilibrium coefficient approach to Hardy-Weinberg testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Identification of the cystic fibrosis gene: genetic analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Genetic linkage of Werner's syndrome to five markers on chromosome 8

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Performing the exact test of Hardy-Weinberg proportion for multiple alleles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Human chromosome 8 linkage map based on short tandem repeat polymorphisms: effect of genotyping errors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Nonrandom association between Huntington disease and two loci separated by about 3 Mb on 4p16.3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

The effect of combining alleles into electrophoretic classes on detecting linkage disequilibrium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Inferences about Linkage Disequilibrium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Genetic syndromes in man with potential relevance to the pathobiology of aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

11 July 2018

Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in Finland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

27 July 2018

A genetic analysis of the Werner syndrome region on human chromosome 8p.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

24 September 2018

Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1915073

24 September 2018

Close linkage of the gene for Werner's syndrome to ANK1 and D8S87 on the short arm of chromosome 8

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE ESTIMATION OF GENE FREQUENCIES IN A RANDOM-MATING POPULATION

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Monte Carlo tests for associations between disease and alleles at highly polymorphic loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage disequilibrium analysis of Friedreich's ataxia in 140 Caucasian families: positioning of the disease locus and evaluation of allelic heterogeneity

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype relative risks: an easy reliable way to construct a proper control sample for risk calculations

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity mapping of the Werner syndrome locus (WRN)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A 37-marker PCR-based genetic linkage map of human chromosome 9: observations on mutations and positive interference

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity mapping and Werner's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The stabilization of repetitive tracts of DNA by variant repeats requires a functional DNA mismatch repair system

1 reference

https://pubmed.ncbi.nlm.nih.gov/8651307

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8651307%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8651307%20AND%20SRC:MED&resulttype=core&format=json

16 October 2019

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