1993
Genomic and Yeast Artificial Chromosome Long-Range Regular Article Linking Six Loci in 10q11.2 and Spanning the Multiple Endocrine Neoplasia Type 2A (MEN2A) Region
Brooks-Wilson A, Lichter J, Ward D, Kidd K, Goodfellow P. Genomic and Yeast Artificial Chromosome Long-Range Regular Article Linking Six Loci in 10q11.2 and Spanning the Multiple Endocrine Neoplasia Type 2A (MEN2A) Region. Genomics 1993, 17: 611-617. PMID: 7902324, DOI: 10.1006/geno.1993.1380.Peer-Reviewed Original ResearchConceptsRestriction mappingIdentification of genesLong-range restriction mappingContig assemblyPhysical mapTumor-specific alterationsGenomic DNAYAC contigPhysical linkageCandidate intervalDistal lociLociProto-oncogeneD10S102GenesCandidate regionsRET proto-oncogeneFamilial medullary thyroid carcinomaType 2ARETD10S94Multiple endocrine neoplasia type 2AContigsGenomicsHereditary cancerA new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus
Lichter J, Wu J, Brooks-Wilson A, Difillipantonio M, Brewster S, Ward D, Goodfellow P, Kidd K. A new polymorphic marker (D10S97) tightly linked to the multiple endocrine neoplasia type 2A (MEN2A) locus. Human Genetics 1993, 90: 516-520. PMID: 8094065, DOI: 10.1007/bf00217451.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsBase SequenceChromosome MappingChromosomes, FungalChromosomes, Human, Pair 10Cloning, MolecularCricetinaeDeoxyribonuclease EcoRIDNADNA ProbesFemaleGene FrequencyGene LibraryGenetic LinkageGenetic MarkersGenome, HumanHumansHybrid CellsIn Situ Hybridization, FluorescenceLod ScoreMaleMolecular Sequence DataMultiple Endocrine NeoplasiaPedigreePolymorphism, GeneticPolymorphism, Restriction Fragment LengthSequence Analysis, DNA
1992
A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10
Lichter J, Wu J, Miller D, Goodfellow P, Kidd K. A high-resolution meiotic mapping panel for the pericentromeric region of chromosome 10. Genomics 1992, 13: 607-612. PMID: 1353475, DOI: 10.1016/0888-7543(92)90131-b.Peer-Reviewed Original ResearchMeSH KeywordsCentromereChromosome MappingChromosomes, Human, Pair 10Crossing Over, GeneticFemaleGenetic LinkageGenetic MarkersHumansMaleMeiosisMultiple Endocrine NeoplasiaPedigreeIsolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10
Miller D, Dill F, Lichter J, Kidd K, Goodfellow P. Isolation and high-resolution mapping of new DNA markers from the pericentromeric region of chromosome 10. Genomics 1992, 13: 601-606. PMID: 1353474, DOI: 10.1016/0888-7543(92)90130-k.Peer-Reviewed Original ResearchCentromereChromosome MappingChromosomes, Human, Pair 10DNADNA ProbesGenetic MarkersHumansHybrid CellsMultiple Endocrine NeoplasiaPresymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A
Lichter J, Wu J, Genel M, Flynn S, Pakstis A, Kidd J, Kidd K. Presymptomatic testing using DNA markers for individuals at risk for familial multiple endocrine neoplasia 2A. The Journal Of Clinical Endocrinology & Metabolism 1992, 74: 368-373. PMID: 1346145, DOI: 10.1210/jcem.74.2.1346145.Peer-Reviewed Original ResearchLocalization of the gene for MEN 2A.
Lichter J, Difilippantonio M, Wu J, Miller D, Ward D, Goodfellow P, Kidd K. Localization of the gene for MEN 2A. Henry Ford Hospital Medical Journal 1992, 40: 199-204. PMID: 1362405.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingChromosomes, Human, Pair 10Cloning, MolecularGenetic LinkageHumansIn Situ HybridizationMultiple Endocrine NeoplasiaPolymerase Chain ReactionPolymorphism, GeneticConceptsGene mapping techniquesYeast artificial chromosomesMapping panelPericentromeric regionArtificial chromosomesGenetic linkage studiesChromosome 10GenesSitu hybridizationLinkage studiesChromosomesMBMultiple endocrine neoplasia type 2A syndromeDNAHybridizationRegionConsistent orderSmall regionLocalizationFluorescenceMarkers
1990
The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10.
Carson N, Wu J, Jackson C, Kidd K, Simpson N. The mutation for medullary thyroid carcinoma with parathyroid tumors (MTC with PTs) is closely linked to the centromeric region of chromosome 10. American Journal Of Human Genetics 1990, 47: 946-51. PMID: 1978560, PMCID: PMC1683917.Peer-Reviewed Original ResearchA refined linkage map for DNA markers around the pericentromeric region of chromosome 10
Wu J, Myers S, Carson N, Kidd J, Anderson L, Castiglione C, Hoyle L, Lichter J, Sukhatme V, Simpson N, Kidd K. A refined linkage map for DNA markers around the pericentromeric region of chromosome 10. Genomics 1990, 8: 461-468. PMID: 1981049, DOI: 10.1016/0888-7543(90)90032-p.Peer-Reviewed Original Research
1989
The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies
Wu J, Giuffra L, Goodfellow P, Myers S, Carson N, Anderson L, Hoyle L, Simpson N, Kidd K. The β subunit locus of the human fibronectin receptor: DNA restriction fragment length polymorphism and linkage mapping studies. Human Genetics 1989, 83: 383-390. PMID: 2572537, DOI: 10.1007/bf00291386.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingChromosomes, Human, Pair 1Chromosomes, Human, Pair 10Chromosomes, Human, Pair 17Chromosomes, Human, Pair 21DNADNA ProbesDNA, NeoplasmFemaleGenetic LinkageGenetic MarkersHaplotypesHumansMaleMultiple Endocrine NeoplasiaPolymorphism, Restriction Fragment LengthReceptors, FibronectinReceptors, ImmunologicConceptsRestriction fragment length polymorphismHuman fibronectin receptorCDNA clonesFragment length polymorphismLinkage analysisDNA restriction fragment length polymorphismsMultiple restriction fragment length polymorphismsPolymorphism information content (PIC) valuesFibronectin receptorHighest polymorphism information content valuePartial cDNA cloneInformation content valuesLength polymorphismLinkage studiesPairwise linkage analysisSouthern blot analysisTypes of polymorphismsChromosome 10 markersGenomic clonesPericentromeric regionTransmembrane proteinDNA markersGenetic linkage studiesDNA sequencesSingle locusClosing in on the MEN2A locus.
Simpson N, Kidd K. Closing in on the MEN2A locus. Henry Ford Hospital Medical Journal 1989, 37: 100-5. PMID: 2576936.Peer-Reviewed Original ResearchThe mapping of the locus for multiple endocrine neoplasia type 2A by linkage with chromosome 10 markers.
Simpson N, Kidd K. The mapping of the locus for multiple endocrine neoplasia type 2A by linkage with chromosome 10 markers. Hormone And Metabolic Research. Supplement Series 1989, 21: 5-9. PMID: 2572529.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingChromosomes, Human, Pair 10Genetic LinkageGenetic MarkersHumansMultiple Endocrine NeoplasiaConceptsDisease locusInterstitial retinol-binding proteinChromosome 10 markersTest of linkageChromosome 10Disease genesDeletion siteChromosome 20Additional family dataBinding proteinLociGenesExclusion of linkageSitu hybridizationD10S5Ultimate identificationRetinol-binding proteinType 2AMultiple endocrine neoplasia type 2AGenomeMarkersFamily dataLinkageProteinHybridization
1988
A 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 2AD10S5Markers
1987
Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: Evidence against synteny
Farrer L, Goodfellow P, White B, Holden J, Kidd J, Simpson N, Kidd K. Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: Evidence against synteny. Cancer Genetics 1987, 27: 327-334. PMID: 2885081, DOI: 10.1016/0165-4608(87)90015-x.Peer-Reviewed Original ResearchAn 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 2AFamilyWhere is the locus for multiple endocrine neoplasia type 2A?
Simpson N, Kidd K. Where is the locus for multiple endocrine neoplasia type 2A? Henry Ford Hospital Medical Journal 1987, 35: 168-71. PMID: 2891652.Peer-Reviewed Original ResearchOne large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map.
Pakstis A, Kidd J, Castiglione C, Pletcher B, Murphy P, Farrer L, Genel M, Kidd K. One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map. Henry Ford Hospital Medical Journal 1987, 35: 164-7. PMID: 2891651.Peer-Reviewed Original Research
1986
Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group‐specific loci: Use of restriction fragment length polymorphisms extends exclusion region
Kidd K, Kidd J, Castiglione C, Pakstis A, Sparkes R, Rao D. Progress toward resolving the possible linkage of multiple endocrine neoplasia type 2A to haptoglobin and group‐specific loci: Use of restriction fragment length polymorphisms extends exclusion region. Genetic Epidemiology 1986, 3: 195-200. PMID: 2873080, DOI: 10.1002/gepi.1370030306.Peer-Reviewed Original ResearchLinkage Analyses of Multiple Endocrine Neoplasia, Type 2 (MEN-2) with 23 Classical Genetic Polymorphisms
Kruger S, Gertner J, Sparkes R, Haedt L, Crist M, Sparkes M, Genel M, Kidd K. Linkage Analyses of Multiple Endocrine Neoplasia, Type 2 (MEN-2) with 23 Classical Genetic Polymorphisms. Human Heredity 1986, 36: 6-11. PMID: 2868987, DOI: 10.1159/000153592.Peer-Reviewed Original ResearchAllelesFemaleGene FrequencyGenes, DominantGenetic LinkageHumansMaleMultiple Endocrine NeoplasiaPedigreePhenotypePolymorphism, GeneticLinkage Analyses of Multiple Endocrine Neoplasia, Type 2A (MEN-2A) with 20 DNA Polymorphisms: 5% of the Genome Excluded
Kidd K, Kidd J, Castiglione C, Genel M, Darby J, Cavalli-Sforza L, Gusella J. Linkage Analyses of Multiple Endocrine Neoplasia, Type 2A (MEN-2A) with 20 DNA Polymorphisms: 5% of the Genome Excluded. Human Heredity 1986, 36: 243-249. PMID: 2875939, DOI: 10.1159/000153634.Peer-Reviewed Original ResearchMeSH KeywordsChromosome MappingGenetic LinkageGenetic MarkersHumansMultiple Endocrine NeoplasiaPolymorphism, GeneticPolymorphism, Restriction Fragment Length
1985
Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.
Goodfellow P, White B, Holden J, Duncan A, Sears E, Wang H, Berlin L, Kidd K, Simpson N. Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A. American Journal Of Human Genetics 1985, 37: 890-7. PMID: 2864854, PMCID: PMC1684696.Peer-Reviewed Original Research