2016
Proposed nomenclature for microhaplotypes
Kidd KK. Proposed nomenclature for microhaplotypes. Human Genomics 2016, 10: 16. PMID: 27316555, PMCID: PMC4912715, DOI: 10.1186/s40246-016-0078-y.Peer-Reviewed Original ResearchConceptsSingle nucleotide polymorphismsHUGO Gene Nomenclature CommitteeGene Nomenclature CommitteeGroup of genesGene familyPopulation geneticsChromosome numberChromosome 1Related genesGenetic markersNucleotide polymorphismsNomenclature CommitteeGenesMicrohaplotypesRootsChromosomesFamilyLociUnique characterStandardized nomenclatureGeneticsNomenclatureSequencePolymorphism
2005
Normal DNA sequence variations in humans
Kidd K. Normal DNA sequence variations in humans. 2005 DOI: 10.1002/047001153x.g206101.Peer-Reviewed Original Research
2001
Race, Genes and Human Origins: How Genetically Diverse Are We?
Kidd K. Race, Genes and Human Origins: How Genetically Diverse Are We? 2001, 11-24. DOI: 10.1007/978-1-4615-1591-3_2.Peer-Reviewed Original Research
1993
A hypervariable segment in the human dopamine receptor D4 (DRD4) gene
Lichter J, Barr C, Kennedy J, Van Tol H, Kidd K, Livak K. A hypervariable segment in the human dopamine receptor D4 (DRD4) gene. Human Molecular Genetics 1993, 2: 767-773. PMID: 8353495, DOI: 10.1093/hmg/2.6.767.Peer-Reviewed Original ResearchConceptsHuman dopamine receptor D4 geneAmino acid sequenceThird cytoplasmic loopNumber of repeatsPutative third cytoplasmic loopFunctional proteinsCytoplasmic loopAcid sequenceRepeat regionDifferent repeatsHypervariable segmentDifferent haplotypesRepeatsDopamine receptor D4 geneUnrelated chromosomesNovel polymorphismsD4 geneGenesProteinHuman dopamine D4 receptorPolymorphic variantsSequencePolymorphismChromosomesReceptors
1992
DNA sequence polymorphism within hominoid species exceeds the number of phylogenetically informative characters for a HOX2 locus.
Ruano G, Rogers J, Ferguson-Smith A, Kidd K. DNA sequence polymorphism within hominoid species exceeds the number of phylogenetically informative characters for a HOX2 locus. Molecular Biology And Evolution 1992, 9: 575-586. PMID: 1352841, DOI: 10.1093/oxfordjournals.molbev.a040743.Peer-Reviewed Original ResearchConceptsSeparate speciation eventsDNA sequence polymorphismsMaximum parsimony methodsBase pair differencesDenaturing gradient gelGene treesSpeciation eventsSpecies clustersBase pair substitutionsPhylogenetic treeInformative charactersComplete sequenceSequence polymorphismsHominoid speciesSpecies variabilityDifferent allelesG. gorillaSpeciesP. troglodytesAllelesGradient gelsGorillasSequenceTreesGenus
1986
Linkage Analysis in a Family with Dominantly Inherited Torsion Dystonia: Exclusion of the Pro-Opiomelanocortin and Glutamic Acid Decarboxylase Genes and Other Chromosomal Regions Using DNA Polymorphisms
Breakefield X, Bressman S, Kramer P, Ozelius L, Moskowitz C, Tanzi R, Brin M, Hobbs W, Kaufman D, Tobin A, Kidd K, Fahn S, Gusella J. Linkage Analysis in a Family with Dominantly Inherited Torsion Dystonia: Exclusion of the Pro-Opiomelanocortin and Glutamic Acid Decarboxylase Genes and Other Chromosomal Regions Using DNA Polymorphisms. Journal Of Neurogenetics 1986, 3: 159-175. PMID: 3016220, DOI: 10.3109/01677068609106846.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentAdultAgedChildChild, PreschoolChromosome DeletionChromosome MappingCloning, MolecularDNADNA Restriction EnzymesDystonia Musculorum DeformansFemaleGenesGenes, DominantGenetic LinkageGlutamate DecarboxylaseHumansLymphocytesMaleMiddle AgedPedigreePolymorphism, GeneticPro-OpiomelanocortinConceptsLinkage analysisGlutamic acid decarboxylase geneRestriction fragment length polymorphismDecarboxylase geneDNA sequencesMode of inheritanceChromosomal regionsDNA polymorphismsFragment length polymorphismDefective geneLod score methodGenesDNA probesLength polymorphismLymphoblast linesInheritanceDisease statesAutosomal dominant modeGene penetranceSequenceFamilyPolymorphismGenomeAcid decarboxylaseRequisite assumptions
1982
Recombinant DNA approach to neurogenetic disorders
Housman D, Kidd K, Gusella J. Recombinant DNA approach to neurogenetic disorders. Trends In Neurosciences 1982, 5: 320-323. DOI: 10.1016/0166-2236(82)90192-8.Peer-Reviewed Original ResearchHuman neurogenetic disordersRecombinant DNA techniquesDNA techniquesGenetic linkage methodsRecombinant DNA approachesCharacterization of sequencesNeurogenetic disordersSingle locusDNA sequencesDNA approachAbnormal phenotypeDNA copiesNeurological phenotypeOrganismsPolypeptidePhenotypeHuntington's diseaseSequenceGENETIC LINKAGE MARKERS IN THE STUDY OF PSYCHIATRIC DISORDERS
Kidd K. GENETIC LINKAGE MARKERS IN THE STUDY OF PSYCHIATRIC DISORDERS. 1982, 459-466. DOI: 10.1016/b978-0-08-027987-9.50049-4.Peer-Reviewed Original Research