(Q56903797)

4

object named as

David A Hafler

David A. Hafler

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John D. Rioux

object named as

John D. Rioux

John D Rioux

5

0 references

author name string

Sheila Guschwan-McMahon

2

0 references

Emily C. Walsh

Genetic analysis of multiple sclerosis

1

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language of work or name

English

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publication date

September 2003

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published in

Journal of Autoimmunity

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volume

21

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issue

2

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page(s)

111-6

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111-116

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cites work

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

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

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A full genome search in multiple sclerosis

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A genome screen for multiple sclerosis in Sardinian multiplex families

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A genome screen for multiple sclerosis in Italian families.

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

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Genomewide scan of multiple sclerosis in Finnish multiplex families

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A genome screen for linkage in Australian sibling-pairs with multiple sclerosis

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Meta-analysis of genome searches

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The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen

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Genetic basis for clinical expression in multiple sclerosis

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APOE epsilon2-4 and -491 polymorphisms are not associated with MS

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Transverse myelopathy, a rare complication of mixed connective tissue disease: comparison with SLE related transverse myelopathy

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CTLA4 exon 1 dimorphism is associated with primary progressive multiple sclerosis

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CTLA-4 gene polymorphism may modulate disease in Japanese multiple sclerosis patients.

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Genetic variation at position -1082 of the interleukin 10 (IL10) promotor and the outcome of multiple sclerosis

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Combined effect of HLA-DRB1*1501 and interleukin-1 receptor antagonist gene allele 2 in susceptibility to relapsing/remitting multiple sclerosis

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Analysis of an IFN- gamma gene (IFNG) Polymorphism in Multiple Sclerosis in Europe: Effect of Population Structure on Association with Disease

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Lack of association between IL-1A and IL-1B promoter polymorphisms and multiple sclerosis

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Association of two variants in IL-1beta and IL-1 receptor antagonist genes with multiple sclerosis

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

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Genetic polymorphisms of IL-1beta and IL-1 receptor antagonist in association with multiple sclerosis in Japanese patients

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Association of interleukin-1beta and interleukin-1 receptor antagonist genes with disease severity in MS

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CTLA4 mediates antigen-specific apoptosis of human T cells

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No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study

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Chromosome 19q13 and multiple sclerosis susceptibility in Finland: a linkage and two-stage association study

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Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12.

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Calculating confidence intervals for relative risks (odds ratios) and standardised ratios and rates

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