2012
Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs
Pakstis AJ, Fang R, Furtado MR, Kidd JR, Kidd KK. Mini-haplotypes as lineage informative SNPs and ancestry inference SNPs. European Journal Of Human Genetics 2012, 20: 1148-1154. PMID: 22535184, PMCID: PMC3476707, DOI: 10.1038/ejhg.2012.69.Peer-Reviewed Original Research
2004
The Genetic Architecture of Selection at the Human Dopamine Receptor D4 (DRD4) Gene Locus
Wang E, Ding Y, Flodman P, Kidd J, Kidd K, Grady D, Ryder O, Spence M, Swanson J, Moyzis R. The Genetic Architecture of Selection at the Human Dopamine Receptor D4 (DRD4) Gene Locus. American Journal Of Human Genetics 2004, 74: 931-944. PMID: 15077199, PMCID: PMC1181986, DOI: 10.1086/420854.Peer-Reviewed Original ResearchConceptsLittle linkage disequilibriumHuman dopamine receptor D4 genePolymorphic sitesDNA sequence organizationMost polymorphic sitesPatterns of recombinationObserved LD patternRare mutational eventsDRD4 locusGenetic architectureHaplotype diversityPositive selectionMore polymorphismsSequence organizationGene locusTandem repeatsMutational eventsLD patternsLinkage disequilibriumDopamine receptor D4 geneLociPhysiological differencesSame alleleReceptor variantsAlleles
2001
Insertional polymorphisms of full-length endogenous retroviruses in humans
Turner G, Barbulescu M, Su M, Jensen-Seaman M, Kidd K, Lenz J. Insertional polymorphisms of full-length endogenous retroviruses in humans. Current Biology 2001, 11: 1531-1535. PMID: 11591322, DOI: 10.1016/s0960-9822(01)00455-9.Peer-Reviewed Original Research
1997
Concerted evolution of the tandemly repeated genes encoding human U2 snRNA (the RNU2 locus) involves rapid intrachromosomal homogenization and rare interchromosomal gene conversion
Liao D, Pavelitz T, Kidd J, Kidd K, Weiner A. Concerted evolution of the tandemly repeated genes encoding human U2 snRNA (the RNU2 locus) involves rapid intrachromosomal homogenization and rare interchromosomal gene conversion. The EMBO Journal 1997, 16: 588-598. PMID: 9034341, PMCID: PMC1169662, DOI: 10.1093/emboj/16.3.588.Peer-Reviewed Original ResearchMeSH KeywordsAnimalsBase SequenceChromosomesCloning, MolecularDNA, SatelliteElectrophoresis, Agar GelEvolution, MolecularGenetic MarkersHaplotypesHumansLinkage DisequilibriumMolecular Sequence DataPedigreePolymorphism, GeneticPolymorphism, Restriction Fragment LengthPrimatesRecombination, GeneticRepetitive Sequences, Nucleic AcidRNA, Small NuclearSequence AnalysisConceptsU2 tandem arrayTandem arraysConcerted evolutionIntrachromosomal homogenizationU2 snRNAInterchromosomal gene conversionHuman U2 snRNARepeat unitsGenetic exchangeU2 genesGene conversionChromosome lineagesIndependent assortmentFlanking markersDiverse panelGenesMicrosatellite polymorphismSnRNACT alleleSacISacI polymorphismPolymorphismAllelesChromatid exchangesPrimary driving force
1996
Dynamics of the haplotype frequencies in populations: study using the Monte Carlo method.
Grigorenko E, Shikanian A, Kidd D, Dorig R, Kidd K. Dynamics of the haplotype frequencies in populations: study using the Monte Carlo method. Genetika 1996, 32: 1705-13. PMID: 9102365.Peer-Reviewed Original ResearchMeSH KeywordsAllelesChromosome MappingComputer SimulationGene FrequencyHaplotypesHumansModels, GeneticMonte Carlo MethodRecombination, GeneticSelection, GeneticSoftwareConceptsNatural selectionEffective population sizeRandom genetic driftMonte Carlo methodHaplotype frequenciesGenetic driftRandom matingEvolutionary dynamicsCarlo methodPopulation sizeRecurrent mutationsMutation processHarmonic meanFrequency dynamicsDifferent populationsSimulation resultsExperimental dataDynamicsMatingPopulationMutationsHaplotypesAllelesColonizationNew World colonization
1995
The CEPH consortium linkage map of human chromosome 16
Kozman H, Keith T, Donis-keller H, White R, Weissenbach J, Dean M, Vergnaud G, Kidd K, Gusella J, Royle N, Sutherland G, Mulley J. The CEPH consortium linkage map of human chromosome 16. Genomics 1995, 25: 44-58. PMID: 7774955, DOI: 10.1016/0888-7543(95)80108-x.Peer-Reviewed Original ResearchConceptsHuman chromosome 16Genetic mapLinkage mapMap lengthSomatic cell hybrid panelFemale map lengthsChromosome 16Male map lengthFramework genetic mapCell hybrid panelMean genetic distanceSex-averaged mapRestriction enzyme combinationsGenetic distanceAverage heterozygosityEntire chromosomesHybrid panelPhysical mapCEPH consortium linkage mapFamily DNACEPH family DNAsPrimer pairsMarker genotypesLociEnzyme combinations
1993
Physical and Genetic Maps for Chromosome 10
Lichter J, Difilippantonio M, Pakstis A, Goodfellow P, Ward D, Kidd K. Physical and Genetic Maps for Chromosome 10. Genomics 1993, 16: 320-324. PMID: 8314570, DOI: 10.1006/geno.1993.1192.Peer-Reviewed Original ResearchConceptsChromosome 10Physical mapOrder of lociGenetic mapLinkage mapGenetic distanceFemale mapGenetic linkage studiesMetaphase chromosomesPolymorphic lociNew lociQ armLociFractional lengthCentromeresLinkage studiesFishPhysical distanceRecombinationCentimorgansChromosomesDistance estimatesFemalesMalesFluorescence
1990
A 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 ResearchThe CEPH consortium primary linkage map of human chromosome 10
White R, Lalouel J, Nakamura Y, Donis-Keller H, Green P, Bowden D, Mathew C, Easton D, Robson E, Morton N, Gusella J, Haines J, Retief A, Kidd K, Murray J, Lathrop G, Cann H. The CEPH consortium primary linkage map of human chromosome 10. Genomics 1990, 6: 393-412. PMID: 1970325, DOI: 10.1016/0888-7543(90)90469-b.Peer-Reviewed Original Research
1989
Estimation of segregation and linkage parameters in simulated data. II. Simultaneous estimation with one linked marker.
Price R, Kramer P, Pauls D, Kidd K. Estimation of segregation and linkage parameters in simulated data. II. Simultaneous estimation with one linked marker. American Journal Of Human Genetics 1989, 45: 95-105. PMID: 2741954, PMCID: PMC1683382.Peer-Reviewed Original ResearchClosing 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 Research
1988
A polymorphic DNA marker on chromosome 10 linked to RBP3 on the MEN2A side
Wu J, Cavenee W, Miki T, Kidd K. A polymorphic DNA marker on chromosome 10 linked to RBP3 on the MEN2A side. Cytogenetic And Genome Research 1988, 48: 246-247. PMID: 2907872, DOI: 10.1159/000132639.Peer-Reviewed Original Research
1987
One 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
1984
Identification of a recent recombination event within the human beta-globin gene cluster.
Gerhard D, Kidd K, Kidd J, Egeland J, Housman D. Identification of a recent recombination event within the human beta-globin gene cluster. Proceedings Of The National Academy Of Sciences Of The United States Of America 1984, 81: 7875-7879. PMID: 6096866, PMCID: PMC392255, DOI: 10.1073/pnas.81.24.7875.Peer-Reviewed Original ResearchMeSH KeywordsAllelesBase SequenceDNA Restriction EnzymesFemaleGenesGenetic LinkageGenotypeGlobinsHumansMalePedigreePolymorphism, GeneticRecombination, GeneticConceptsBeta-globin gene clusterHuman beta-globin gene clusterGene clusterRecombination eventsChromosome 11DNA sequence polymorphismsRecent recombination eventsGenetic recombination eventsMeiotic crossingDNA regionsDNA markersC-Ha-rasSequence polymorphismsReference pedigreesCrossover eventsOncogene c-Ha-rasPreproparathyroid hormoneSegment 12PedigreeD11S12HaplotypesInheritanceClustersRegionHot spotsEstimating the Recombination Frequency for the MN and the Ss Loci
Spence A, Field L, Marazita M, Joseph J, Sparkes M, Crist M, Crandall B, Anderson C, Bateman J, Rotter J, Kidd K, Hodge S, Sparkes R. Estimating the Recombination Frequency for the MN and the Ss Loci. Human Heredity 1984, 34: 343-347. PMID: 6510930, DOI: 10.1159/000153494.Peer-Reviewed Original ResearchMeSH KeywordsFemaleGene FrequencyGenetic LinkageHumansLod ScoreMaleMNSs Blood-Group SystemRecombination, Genetic
1979
Genetic Linkage and Hemochromatosis
Kidd K. Genetic Linkage and Hemochromatosis. New England Journal Of Medicine 1979, 301: 209-210. PMID: 449978, DOI: 10.1056/nejm197907263010409.Peer-Reviewed Original Research