(Q42676998)

4 November 2017

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

1 reference

4 November 2017

5

Peter M Andersen

1 reference

4 November 2017

2

Vilmantas Giedraitis

1 reference

4 November 2017

Bing He

1

1 reference

4 November 2017

Arturs Ligers

3

1 reference

4 November 2017

Michael Binzer

4

1 reference

4 November 2017

Lars Forsgren

6

1 reference

4 November 2017

Lodewijk A Sandkuijl

7

1 reference

4 November 2017

Jan Hillert

8

1 reference

4 November 2017

1 April 2002

1 reference

European Journal of Human Genetics

4 November 2017

1 reference

4 November 2017

10

1 reference

4 November 2017

4

1 reference

4 November 2017

271-275

1 reference

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5200802

4 November 2017

0 references

cites work

The role of genetic factors in multiple sclerosis susceptibility.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Evidence of linkage with HLA-DR in DRB1*15-negative families with multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Linkage and association analysis of genes encoding cytokines and myelin proteins in multiple sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Genomewide scan of multiple sclerosis in Finnish multiplex families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Genome screening by searching for shared segments: mapping a gene for benign recurrent intrahepatic cholestasis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Genetic mapping using haplotype, association and linkage methods suggests a locus for severe bipolar disorder (BPI) at 18q22-q23.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Familial clustering of multiple sclerosis in a northern Swedish rural district.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

A comprehensive genetic map of the human genome based on 5,264 microsatellites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Localization of the EPM1 gene for progressive myoclonus epilepsy on chromosome 21: linkage disequilibrium allows high resolution mapping

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Linkage disequilibrium mapping of a type 1 diabetes susceptibility gene (IDDM7) to chromosome 2q31-q33.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Genome scanning for segments shared identical by descent among distant relatives in isolated populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Human leukocyte antigen studies in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

A full genome search in multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

Inheritance of susceptibility to multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

7 January 2021

A study of interleukin-1 cluster genes in susceptibility to and severity of multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

7 January 2021

Immune system genes in multiple sclerosis: genetic association and linkage analyses on TCR beta, IGH, IFN-gamma and IL-1ra/IL-1 beta loci

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

7 January 2021

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

7 January 2021

A meta-analysis of genomic screens in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

7 January 2021

Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

7 January 2021

HLA-DR-DQ haplotypes defined by restriction fragment analysis. Correlation to serology

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

7 January 2021

Linkage analysis of HLA class II genes in Swedish multiplex families with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

7 January 2021

Linkage disequilibrium mapping of complex disease: fantasy or reality?

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5200802

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5200802

1 reference

Dimensions Publication ID

4 November 2017

0 references

1 reference