Haplotype fine mapping by evolutionary trees (Q34145172)

31 July 2017

Haplotype fine mapping by evolutionary trees (English)

1 reference

31 July 2017

K Roeder

2

0 references

author name string

J C Lam

series ordinal

1

1 reference

PubMed ID

10677324

31 July 2017

B Devlin

series ordinal

3

1 reference

PubMed ID

10677324

31 July 2017

language of work or name

English

0 references

publication date

1 February 2000

1 reference

American Journal of Human Genetics

31 July 2017

1 reference

31 July 2017

66

1 reference

31 July 2017

2

1 reference

31 July 2017

659-673

1 reference

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

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Linkage-disequilibrium mapping of disease genes by reconstruction of ancestral haplotypes in founder populations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Linkage disequilibrium mapping in isolated populations: the example of Finland revisited

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Likelihood analysis of disequilibrium mapping, and related problems

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Gene genealogies within mutant allelic classes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

A comparison of linkage disequilibrium measures for fine-scale mapping

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Mutation of human short tandem repeats

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Likelihood methods for locating disease genes in nonequilibrium populations.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Identification of the cystic fibrosis gene: genetic analysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Repositioning the hereditary paraganglioma critical region on chromosome band 11q23.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Linkage disequilibrium as a gene-mapping tool.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Highly polymorphic minisatellite sequences: allele frequencies and mutation rates for five locus-specific probes in a Caucasian population

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Disequilibrium Mapping: Composite Likelihood for Pairwise Disequilibrium

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1288117

Partition structures, Polya urns, the Ewens sampling formula, and the ages of alleles

28 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10677324

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2-cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10677324

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/10677324

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/302756

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

PubMed ID

10677324