1992
Exclusion of Linkage Between the Serotonin2 Receptor and Schizophrenia in a Large Swedish Kindred
Hallmayer J, Kennedy J, Wetterberg L, Sjögren B, Kidd K, Cavalli-Sforza L. Exclusion of Linkage Between the Serotonin2 Receptor and Schizophrenia in a Large Swedish Kindred. JAMA Psychiatry 1992, 49: 216-219. PMID: 1348924, DOI: 10.1001/archpsyc.1992.01820030048006.Peer-Reviewed Original ResearchMeSH KeywordsChromosomes, Human, Pair 13DNA ProbesFemaleGenetic LinkageHumansLod ScoreMaleMiddle AgedPolymorphism, Restriction Fragment LengthReceptors, SerotoninSchizophreniaSweden
1988
Predicting 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 ResearchMeSH KeywordsCeruloplasminChromosome MappingChromosomes, Human, Pair 13CopperFemaleGenes, RecessiveGenetic LinkageGenetic MarkersGenotypeHepatolenticular DegenerationHumansMalePedigreeProbabilityConceptsWilson 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
1987
Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.
Bowcock A, Farrer L, Cavalli-Sforza L, Hebert J, Kidd K, Frydman M, Bonne-Tamir B. Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13. American Journal Of Human Genetics 1987, 41: 27-35. PMID: 3474893, PMCID: PMC1684171.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingChromosomes, Human, Pair 13DNAFemaleGenetic LinkageGenetic MarkersHepatolenticular DegenerationHumansMalePedigreePolymorphism, GeneticConceptsOrder of markersChromosome 13 markersMultipoint linkage analysisDNA markersRecombination frequencyMaximum lod scoreLinkage analysisPolymorphic markersChromosome 13LOD scoreLociD13S10Esterase DAutosomal recessive disorderWNDCopper metabolismRecessive disorderWilson's diseaseCentimorgansMarkersMetabolismKindredsAn efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13.
Farrer L, Goodfellow P, Lamarche C, Franjkovic I, Myers S, White B, Holden J, Kidd J, Simpson N, Kidd K. An efficient strategy for gene mapping using multipoint linkage analysis: exclusion of the multiple endocrine neoplasia 2A (MEN2A) locus from chromosome 13. American Journal Of Human Genetics 1987, 40: 329-37. PMID: 2883889, PMCID: PMC1684085.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingChromosomes, Human, Pair 13FemaleGenetic LinkageGenetic MarkersHumansLod ScoreMultiple Endocrine NeoplasiaConceptsMarker lociGenetic mapChromosome 13Red cell enzyme markersMapping disease genesLarger genetic mapMultipoint analysisLinkage mapMultipoint linkage analysisGene mappingDNA markersDisease genesTwo-point analysisLinkage analysisLociMEN2A locusClose linkageEnzyme markersType 2AMultiple endocrine neoplasia type 2ACMorganGenesMarkersMultiple endocrine neoplasia 2AFamilyA new human RFLP identified by 7D2 places D13S10 proximal to esterase D
Bowcock A, Farrer L, Hebert J, Bonne-Tamir B, Frydman M, Kidd K, Cavalli-Sforza L. A new human RFLP identified by 7D2 places D13S10 proximal to esterase D. Cytogenetic And Genome Research 1987, 44: 236-237. PMID: 2884079, DOI: 10.1159/000132379.Peer-Reviewed Original ResearchExclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi‐point linkage analysis
Kramer P, Ozelius L, Gusella J, Fahn S, Kidd K, Breakefield X, Boerecki I. Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi‐point linkage analysis. Genetic Epidemiology 1987, 4: 377-386. PMID: 3692135, DOI: 10.1002/gepi.1370040506.Peer-Reviewed Original Research