2008
The expanding genetic overlap between multiple sclerosis and type I diabetes
Booth D, Heard R, Stewart G, Goris A, Dobosi R, Dubois B, Lorentzen Å, Celius E, Harbo H, Spurkland A, Olsson T, Kockum I, Link J, Hillert J, Ban M, Baker A, Sawcer S, Compston A, Mihalova T, Strange R, Hawkins C, Ingram G, Robertson N, De Jager P, Hafler D, Barcellos L, Ivinson A, Pericak-Vance M, Oksenberg J, Hauser S, McCauley J, Sexton D, Haines J. The expanding genetic overlap between multiple sclerosis and type I diabetes. Genes & Immunity 2008, 10: 11-14. PMID: 18987646, PMCID: PMC2718424, DOI: 10.1038/gene.2008.83.Peer-Reviewed Original ResearchMeSH KeywordsAdaptor Proteins, Signal TransducingAdultAllelesAmino Acid SubstitutionAntigens, Differentiation, T-LymphocyteAustraliaBelgiumCase-Control StudiesConfidence IntervalsDiabetes Mellitus, Type 1FamilyGenetic Predisposition to DiseaseHumansLectins, C-TypeLinkage DisequilibriumMiddle AgedMonosaccharide Transport ProteinsMultiple SclerosisNorwayOdds RatioPolymorphism, Single NucleotideProbabilitySwedenTryptophanUnited KingdomUnited StatesConceptsSingle nucleotide polymorphismsSusceptibility genesAutoimmune susceptibility genesMultiple sclerosis susceptibility genesClustering of autoimmune diseasesAssociated with type I diabetesTrio familiesCD226 geneEvidence of associationNucleotide polymorphismsCLEC16A geneGenetic overlapGenesMultiple sclerosis dataType I diabetesMultiple sclerosisAutoimmune diseasesFamilial clusteringRs12708716CLEC16ARs763361
2005
Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis
De Jager PL, Sawcer S, Waliszewska A, Farwell L, Wild G, Cohen A, Langelier D, Bitton A, Compston A, Hafler DA, Rioux JD. Evaluating the role of the 620W allele of protein tyrosine phosphatase PTPN22 in Crohn's disease and multiple sclerosis. European Journal Of Human Genetics 2005, 14: 317-321. PMID: 16391555, DOI: 10.1038/sj.ejhg.5201548.Peer-Reviewed Original ResearchMeSH KeywordsAllelesCanadaCase-Control StudiesCrohn DiseaseGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansInflammationModels, StatisticalMultiple SclerosisOdds RatioPolymorphism, GeneticProtein Tyrosine Phosphatase, Non-Receptor Type 1Protein Tyrosine Phosphatase, Non-Receptor Type 22Protein Tyrosine PhosphatasesRiskUnited KingdomConceptsSystemic lupus erythematosusCases of CDCrohn's diseaseMultiple sclerosisPTPN22 620W alleleAutoimmune thyroiditisRheumatoid arthritisInflammatory diseasesEvidence of associationCases of MSProtein tyrosine phosphatase PTPN22Chronic inflammatory diseaseType 1 diabetesTyrosine phosphatase PTPN22PTPN22 alleleLupus erythematosusPooled analysisControl subjectsModest odds ratiosOdds ratioDiseaseRisk allelesPhosphatase PTPN22SclerosisPossible role
2004
Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping
Sawcer SJ, Maranian M, Singlehurst S, Yeo T, Compston A, Daly MJ, De Jager PL, Gabriel S, Hafler DA, Ivinson AJ, Lander ES, Rioux JD, Walsh E, Gregory SG, Schmidt S, Pericak-Vance MA, Barcellos L, Hauser SL, Oksenberg JR, Kenealy SJ, Haines JL. Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping. Human Molecular Genetics 2004, 13: 1943-1949. PMID: 15238506, DOI: 10.1093/hmg/ddh202.Peer-Reviewed Original Research