(Q77892102)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914228%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

review article

1 reference

title

Inheritance of susceptibility to multiple sclerosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914228%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

author name string

S Sawcer

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914228%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

P N Goodfellow

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914228%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

publication date

1 December 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914228%20AND%20SRC:MED&resulttype=core&format=json

Current Opinion in Immunology

9 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914228%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914228%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914228%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

page(s)

697-703

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914228%20AND%20SRC:MED&resulttype=core&format=json

The epidemiology of multiple sclerosis

9 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The British Isles survey of multiple sclerosis in twins

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Evidence for genetic basis of multiple sclerosis. The Canadian Collaborative Study Group.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Offspring recurrence rates and clinical characteristics of conjugal multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Multiple sclerosis among immigrants in Greater London

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Multiple sclerosis in Iceland: 1. Evidence of a postwar epidemic.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

HL-A antigens and multiple sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

B-cell alloantigen Ag 7a in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

B-lymphocyte alloantigens associated with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Extended major histocompatibility complex haplotypes in patients with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

HLA-DQ polymorphisms do not explain HLA class II associations with multiple sclerosis in two Canadian patient groups

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Association of susceptibility to multiple sclerosis in Sweden with HLA class II DRB1 and DQB1 alleles

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

An evaluation of tumor necrosis factor microsatellite alleles in genetic susceptibility to multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Tumour necrosis factor microsatellites show association with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Genetic predisposition to multiple sclerosis as revealed by immunoprinting

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

DRB1-DQA1-DQB1 loci and multiple sclerosis predisposition in the Sardinian population

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

HLA typing in the United Kingdom multiple sclerosis genome screen

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The familial nature of multiple sclerosis: Age-corrected empiric recurrence risks for children and siblings of patients

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Age-adjusted recurrence risks for relatives of patients with multiple sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Risks of multiple sclerosis in relatives of patients in Flanders, Belgium

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Multiple sclerosis: updated risks for relatives

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Application of automated DNA sizing technology for genotyping microsatellite loci

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

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/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

A full genome search in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Genomewide scan of multiple sclerosis in Finnish multiplex families

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Empirical genomewide significance levels established by whole genome simulations.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The future of genetic studies of complex human diseases

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The genetic analysis of multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Genetics of multiple sclerosis [published erratum appears in Hum Mol Genet 1997 Nov;6(12):2189]

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The Huntington's disease candidate region exhibits many different haplotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The origin of the major cystic fibrosis mutation (delta F508) in European populations.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patients

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

What is significant in whole-genome linkage disequilibrium studies?

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Association mapping of disease loci, by use of a pooled DNA genomic screen

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

A cerebellar ataxia locus identified by DNA pooling to search for linkage disequilibrium in an isolated population from the Cayman Islands

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Detection of obesity QTLs on mouse chromosomes 1 and 7 by selective DNA pooling.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

DNA variation and the future of human genetics

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The use of a genetic map of biallelic markers in linkage studies

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Identification of murine loci associated with susceptibility to chronic experimental autoimmune encephalomyelitis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Genetic analysis of inflammation, cytokine mRNA expression and disease course of relapsing experimental autoimmune encephalomyelitis in DA rats

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Polygenic control of experimental allergic encephalomyelitis in Biozzi ABH and BALB/c mice

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Mapping loci influencing the persistence of Theiler's virus in the murine central nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Association between susceptibility to Theiler's virus-induced demyelination and T-cell receptor Jbeta1-Cbeta1 polymorphism rather than Vbeta deletion.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

TNF is a potent anti-inflammatory cytokine in autoimmune-mediated demyelination.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

HLA-DR and -DQ associations with multiple sclerosis in Turkey

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The HLA-DQ(alpha 1*0102, beta 1*0602) heterodimer may confer susceptibility to multiple sclerosis in the absence of the HLA-DR(alpha 1*01, beta 1*1501) heterodimer

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

HLA-DR, -DQA1 and -DQB1 associations in Australian multiple sclerosis patients

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

HLA associations with multiple sclerosis in the Canary Islands.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Tumor necrosis factor (TNF) microsatellite haplotypes in relation to extended haplotypes, susceptibility to diseases associated with the major histocompatibility complex and TNF secretion

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

TNF-alpha promoter polymorphisms, production and susceptibility to multiple sclerosis in different groups of patients

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

HLA-DM polymorphisms do not associate with multiple sclerosis: an association study with analysis of myelin basic protein T cell specificity

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Susceptibility to relapsing-progressive multiple sclerosis is associated with inheritance of genes linked to the variable region of the TcR beta locus: use of affected family-based controls

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The germline repertoire of T cell receptor beta-chain genes in patients with chronic progressive multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

A susceptibility locus for multiple sclerosis is linked to the T cell receptor beta chain complex

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Further localization of a multiple sclerosis susceptibility gene on chromosome 7q using a new T cell receptor beta-chain DNA polymorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Susceptibility for multiple sclerosis is determined, in part, by inheritance of a 175-kb region of the TcR V beta chain locus and HLA class II genes

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The germline repertoire of T-cell receptor beta chain genes in patients with relapsing/remitting multiple sclerosis or optic neuritis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

No association with germline T cell receptor beta-chain gene alleles or haplotypes in Swedish patients with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Discordance of T-cell receptor ?-chain genes in familial multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

HLA and T-cell receptor polymorphisms in Belgian multiple sclerosis patients: no evidence for disease association with the T-cell receptor

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

T-cell receptor alpha, beta, gamma, and delta chain gene microsatellites show no association with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

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/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Susceptibility to multiple sclerosis and the immunoglobulin heavy chain gene cluster

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

No linkage or association of a VNTR marker in the junction region of the immunoglobulin heavy chain genes in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Multiple sclerosis: the increased frequency of the ICAM-1 exon 6 gene point mutation genetic type K469.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Occurrence and clinical relevance of an interleukin-4 gene polymorphism in patients with multiple sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Immunohistochemical and genetic evidence of myeloperoxidase involvement in multiple sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The CCR5 deletion mutation fails to protect against multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Golli-MBP gene in multiple sclerosis susceptibility

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

PCR typing of two short tandem repeat (STR) structures upstreams of the human myelin basic protein (MBP) gene; the genetic susceptibility in multiple sclerosis and monosymptomatic idiopathic optic neuritis in Danes

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Role of myelin basic protein and proteolipid protein genes in multiple sclerosis: single strand conformation polymorphism analysis of the human sequences

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The myelin basic protein gene in multiple sclerosis: identification of discrete alleles of a 1.3 kb tetranucleotide repeat sequence

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Identification of a Val I 45 IIe substitution in the human myelin oligodendrocyte glycoprotein: lack of association with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Analysis of polymorphisms of the 2',3'-cyclic nucleotide-3'-phosphodiesterase gene in patients with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Genetic susceptibility to the development of autoimmune disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Leber's hereditary optic neuropathy mitochondrial DNA mutations in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Mitochondrial DNA mutations in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

No association of the 11778 mitochondrial DNA mutation and multiple sclerosis in Japan

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Screening for Leber's hereditary optic neuropathy associated mitochondrial DNA mutations in patients with prominent optic neuritis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

Neuromyelitis optica (Devic's syndrome): no association with the primary mitochondrial DNA mutations found in Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

LHON mutations in Italian patients affected by multiple sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0952-7915%2898%2980091-5

7 January 2021

10.1016/S0952-7915(98)80091-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9914228%20AND%20SRC:MED&resulttype=core&format=json

9 December 2019

1 reference