(Q42614413)

English

Genome-wide TDT analysis in a localized population with a high prevalence of multiple sclerosis indicates the importance of a region on chromosome 14q.

scientific article published on December 2003

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scholarly article

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Europe PubMed Central

PubMed publication ID

3 November 2017

Genome-wide TDT analysis in a localized population with a high prevalence of multiple sclerosis indicates the importance of a region on chromosome 14q. (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Kári Stefánsson

6

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Stefansson K

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Europe PubMed Central

PubMed publication ID

3 November 2017

author name string

Giedraitis V

1

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Modin H

2

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Callander M

3

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Landtblom AM

4

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

Fossdal R

5

1 reference

Europe PubMed Central

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3 November 2017

Hillert J

7

1 reference

Europe PubMed Central

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3 November 2017

Gulcher J

8

1 reference

Europe PubMed Central

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3 November 2017

publication date

1 December 2003

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Europe PubMed Central

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3 November 2017

Genes and Immunity

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Europe PubMed Central

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3 November 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

8

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Europe PubMed Central

PubMed publication ID

3 November 2017

559-563

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

A polymorphic DNA marker genetically linked to Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

Identification of the cystic fibrosis gene: chromosome walking and jumping

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

A population-based study of multiple sclerosis in twins: update

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

Human leukocyte antigen studies in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

HLA class II-associated genetic susceptibility in multiple sclerosis: a critical evaluation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

Gene finding in genetically isolated populations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

Use of population isolates for mapping complex traits

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

Sharing of a conserved haplotype suggests a susceptibility gene for multiple sclerosis at chromosome 17p11.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

Genomewide Scan of Multiple Sclerosis in Finnish Multiplex Families

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

The CTLA-4 gene is associated with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

21 January 2018

A population-based study of multiple sclerosis in twins

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

7 January 2021

based on heuristic

inferred from DOI database lookup

Distribution of multiple sclerosis in Sweden based on mortality and disability compensation statistics

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

7 January 2021

based on heuristic

inferred from DOI database lookup

A meta-analysis of genomic screens in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

7 January 2021

based on heuristic

inferred from DOI database lookup

Fine mapping of a multiple sclerosis locus to 2.5 Mb on chromosome 17q22-q24

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

7 January 2021

based on heuristic

inferred from DOI database lookup

CTLA4 is associated with susceptibility to multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

7 January 2021

based on heuristic

inferred from DOI database lookup

CTLA4 exon 1 dimorphism is associated with primary progressive multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

7 January 2021

based on heuristic

inferred from DOI database lookup

A high-resolution recombination map of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.GENE.6364024

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.GENE.6364024

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 November 2017

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