Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree
Kennedy J, Giuffra L, Moises H, Cavalli-Sforza L, Pakstis A, Kidd J, Castiglione C, Sjogren B, Wetterberg L, Kidd K. Evidence against linkage of schizophrenia to markers on chromosome 5 in a northern Swedish pedigree. Nature 1988, 336: 167-170. PMID: 2903450, DOI: 10.1038/336167a0.Peer-Reviewed Original ResearchConceptsImportant pathogenic roleGenetic factorsSevere mental illnessAetiologic factorsChronic coursePathogenic roleProximal long armGlucocorticoid receptorMental illnessSchizophreniaSchizophrenia casesLinkage of schizophreniaGenetic linkage studiesFamily studiesLong armDistal long armMarkersChromosome 5Linkage studiesSwedish pedigreeArmLinkage ProjectIllnessStrong evidenceFactorsA linkage group of five DNA markers on human chromosome 10
Farrer L, Castiglione C, Kidd J, Myers S, Carson N, Simpson N, Kidd K. A linkage group of five DNA markers on human chromosome 10. Genomics 1988, 3: 72-77. PMID: 2906045, DOI: 10.1016/0888-7543(88)90162-0.Peer-Reviewed Original ResearchConceptsLinkage groupsDNA markersChromosome 10Recombination frequencySex-specific recombination frequenciesAccurate genetic mapHuman chromosome 10Three-locus analysisLong armChromosome 10 markersGenetic mapLinkage mapPericentric regionsMarker lociMap intervalPrevious localizationLinkage analysisProximal regionLociLarge pedigreeType 2APedigreeMultiple endocrine neoplasia type 2AD10S5MarkersD10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4
Miki T, Nishisho I, Tateishi H, Chen Y, Kidd J, Wu J, Pravtcheva D, Pakstis A, Takai S, Ruddle F, Kidd K. D10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4. Genomics 1988, 3: 78-81. PMID: 2906046, DOI: 10.1016/0888-7543(88)90163-2.Peer-Reviewed Original ResearchConceptsSomatic cell hybrid DNAsCell hybrid DNAsComparative mapping studiesTaqI RFLPMouse genomic DNASouthern blot analysisCM distalHybrid DNAChromosome 10Genomic DNARsaI RFLPGenetic linkageStrong linkage disequilibriumHuman cloneLinkage disequilibriumLong armBlot analysisRFLPMapping studiesLociDNAClonesBanIIDisequilibriumProbePredicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease
Farrer L, Bonne-Tamir B, Frydman M, Magazanik A, Kidd K, Bowcock A, Cavalli-Sforza L. Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease. Human Genetics 1988, 79: 109-117. PMID: 3164701, DOI: 10.1007/bf00280547.Peer-Reviewed Original ResearchConceptsWilson disease locusDisease locusUnaffected individualsChromosome 13 markersWND locusMultipoint linkage analysisDisease familiesWilson disease familiesGenetic markersLinkage analysisChromosome 13Long armLociSources of variationAutosomal recessive disorderMore variationGenotypesCopper concentrationRecessive disorderNormal homozygotesWilson's diseaseFamilial componentMarkersCopper levelsSubsequent analysis