1996
DRD2 Haplotypes Containing the TaqI A1 Allele: Implications for Alcoholism Research
Kidd K, Pakstis A, Castiglione C, Kidd J, Speed W, Goldman D, Knowler W, Lu R, Bonne‐Tamir B. DRD2 Haplotypes Containing the TaqI A1 Allele: Implications for Alcoholism Research. Alcohol Clinical And Experimental Research 1996, 20: 697-705. PMID: 8800387, DOI: 10.1111/j.1530-0277.1996.tb01674.x.Peer-Reviewed Original ResearchMeSH KeywordsAlcoholismAllelesAnimalsChromosome MappingDeoxyribonucleases, Type II Site-SpecificEthnicityGene FrequencyGenetics, PopulationHaplotypesHumansPolymerase Chain ReactionPolymorphism, GeneticPolymorphism, Restriction Fragment LengthReceptors, Dopamine D2Repetitive Sequences, Nucleic AcidResearchConceptsGenetic variationAssociation studiesUnrelated control samplesDopamine D2 receptor locusDiversity of haplotypesShort tandem repeat polymorphismsDRD2 locusEvolutionary historyRestriction fragment length polymorphismPopulation geneticsPhylogenetic originFragment length polymorphismAncestral originReceptor locusHomologous regionsIntron 2LociAllelic systemHigher primatesHaplotypesTandem repeat polymorphismAllelesConsiderable diversityDRD2 haplotypesPolymorphism
1993
Assignment of the norepinephrine transporter protein (NET1) locusto chromosome 16
Gelernter J, Kruger S, Pakstis A, Pacholczyk T, Sparkes R, Kidd K, Amara S. Assignment of the norepinephrine transporter protein (NET1) locusto chromosome 16. Genomics 1993, 18: 690-692. PMID: 7905857, DOI: 10.1016/s0888-7543(05)80375-1.Peer-Reviewed Original ResearchMeSH KeywordsCarrier ProteinsChromosome MappingChromosomes, Human, Pair 16Deoxyribonucleases, Type II Site-SpecificDNA, ComplementaryGenetic LinkageGenetic MarkersHumansNorepinephrineNorepinephrine Plasma Membrane Transport ProteinsPolymorphism, Restriction Fragment LengthRestriction MappingSymportersConceptsNorepinephrine transporter proteinSomatic cell hybrid panelCell hybrid panelHybrid panelHP locusCEPH familiesLarge multigenerational familyTransporter proteinsLinkage analysisChromosome 16Provisional assignmentLinkage dataLociMultigenerational familiesGenetic polymorphismsSite of actionPreliminary assignmentNet1FamilyProteinRFLPSitesPolymorphismPCRLocalization
1992
Two RFLPs near HOX2@INGFR at locus D17S444E
Kennedy J, Honer W, Kaufmann C, Martignetti J, Brosius J, Kidd K. Two RFLPs near HOX2@INGFR at locus D17S444E. Nucleic Acids Research 1992, 20: 1171-1171. PMID: 1372406, PMCID: PMC312148, DOI: 10.1093/nar/20.5.1171.Peer-Reviewed Original Research
1991
A Hindi RFLP In the human D4 dopamine receptor locus (DRD4)
Kennedy J, Sidenberg D, Van Tol H, Kidd K. A Hindi RFLP In the human D4 dopamine receptor locus (DRD4). Nucleic Acids Research 1991, 19: 5801-5801. PMID: 1682888, PMCID: PMC329013, DOI: 10.1093/nar/19.20.5801.Peer-Reviewed Original ResearchChromosomes, Human, Pair 11Deoxyribonucleases, Type II Site-SpecificGene FrequencyHumansPolymorphism, Restriction Fragment LengthReceptors, DopamineReceptors, Dopamine D2Receptors, Dopamine D4An Mspl polymorphism for the HOX2F gene
Ogura T, Castiglione C, Pakstis A, Kidd K. An Mspl polymorphism for the HOX2F gene. Nucleic Acids Research 1991, 19: 1716-1716. PMID: 1709280, PMCID: PMC333945, DOI: 10.1093/nar/19.7.1716.Peer-Reviewed Original ResearchAllelesChromosome MappingChromosomes, Human, Pair 17Deoxyribonuclease HpaIIDeoxyribonucleases, Type II Site-SpecificDNA ProbesGenes, HomeoboxHumansPolymorphism, Restriction Fragment Length
1990
A HaeIII polymorphism at the D10S101 locus
Wu J, Kidd K. A HaeIII polymorphism at the D10S101 locus. Nucleic Acids Research 1990, 18: 5577-5577. PMID: 1977118, PMCID: PMC332269, DOI: 10.1093/nar/18.18.5577-a.Peer-Reviewed Original ResearchChromosomes, Human, Pair 10Deoxyribonucleases, Type II Site-SpecificHumansPolymorphism, Restriction Fragment LengthHincll polymorphism at the D10S95 locus
Wu J, Kidd K. Hincll polymorphism at the D10S95 locus. Nucleic Acids Research 1990, 18: 4965-4965. PMID: 1975682, PMCID: PMC332037, DOI: 10.1093/nar/18.16.4965-a.Peer-Reviewed Original ResearchChromosome MappingChromosomes, Human, Pair 10Deoxyribonucleases, Type II Site-SpecificGenetic LinkageHumansPolymorphism, Restriction Fragment LengthHaplotype of multiple polymorphisms resolved by enzymatic amplification of single DNA molecules.
Ruano G, Kidd K, Stephens J. Haplotype of multiple polymorphisms resolved by enzymatic amplification of single DNA molecules. Proceedings Of The National Academy Of Sciences Of The United States Of America 1990, 87: 6296-6300. PMID: 1974719, PMCID: PMC54520, DOI: 10.1073/pnas.87.16.6296.Peer-Reviewed Original ResearchBase SequenceDeoxyribonucleases, Type II Site-SpecificDNAGenetic Carrier ScreeningGenetic LinkageHaplotypesHumansMolecular Sequence DataNucleic Acid Amplification TechniquesOligonucleotide ProbesPolymerase Chain ReactionPolymorphism, GeneticPolymorphism, Restriction Fragment LengthTourette SyndromeWhite PeopleHigh frequency Pvull and Pstl polymorphisms identified by KW31 (D10S96) on chromosome 10
Wu J, Kidd K. High frequency Pvull and Pstl polymorphisms identified by KW31 (D10S96) on chromosome 10. Nucleic Acids Research 1990, 18: 1316-1316. PMID: 1969625, PMCID: PMC330480, DOI: 10.1093/nar/18.5.1316-a.Peer-Reviewed Original ResearchBacteriophage lambdaChromosomes, Human, Pair 10Deoxyribonucleases, Type II Site-SpecificHumansPolymorphism, Restriction Fragment Length
1988
An MPO cDNA clone identifies an RFLP with PstI
Miki T, Weil S, Rosner G, Reid M, Kidd K. An MPO cDNA clone identifies an RFLP with PstI. Nucleic Acids Research 1988, 16: 1649-1649. PMID: 2894639, PMCID: PMC336369, DOI: 10.1093/nar/16.4.1649.Peer-Reviewed Original ResearchCell LineChromosomes, Human, Pair 17Deoxyribonucleases, Type II Site-SpecificDNADNA Restriction EnzymesGenesHumansPeroxidasePolymorphism, GeneticPolymorphism, Restriction Fragment Length
1987
A second useful polymorphism for the cytosolic thymidine kinase gene (TK1) with the enzyme BstEII which will allow haplotying at this locus on chromosome 17 (q21-q22)
Murphy P, Lin P, Ruddle F, Kidd K. A second useful polymorphism for the cytosolic thymidine kinase gene (TK1) with the enzyme BstEII which will allow haplotying at this locus on chromosome 17 (q21-q22). Nucleic Acids Research 1987, 15: 7212-7212. PMID: 2889186, PMCID: PMC306236, DOI: 10.1093/nar/15.17.7212.Peer-Reviewed Original ResearchMeSH KeywordsChromosomes, Human, Pair 17CytosolDeoxyribonucleases, Type II Site-SpecificDNA Restriction EnzymesHumansPolymorphism, GeneticPolymorphism, Restriction Fragment LengthThymidine KinaseA moderately frequent RFLP identified by both SacI and BanII with a probe from the HOX2 locus in man (17q11–17q22)
Murphy P, Ferguson-Smith A, Miki T, Feinberg A, Ruddle F, Kidd K. A moderately frequent RFLP identified by both SacI and BanII with a probe from the HOX2 locus in man (17q11–17q22). Nucleic Acids Research 1987, 15: 6311-6311. PMID: 2888083, PMCID: PMC306101, DOI: 10.1093/nar/15.15.6311.Peer-Reviewed Original ResearchChromosomes, Human, Pair 17Deoxyribonucleases, Type II Site-SpecificDNA Restriction EnzymesHumansPolymorphism, GeneticPolymorphism, Restriction Fragment LengthA 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 Research
1986
A frequent polymorphism for the cytosolic thymidine kinase gene, TK1, (17q21-q22) detected by the enzyme Taql
Murphy P, Kidd J, Castiglione C, Lin P, Ruddle F, Kidd K. A frequent polymorphism for the cytosolic thymidine kinase gene, TK1, (17q21-q22) detected by the enzyme Taql. Nucleic Acids Research 1986, 14: 4381-4381. PMID: 3012471, PMCID: PMC339879, DOI: 10.1093/nar/14.10.4381.Peer-Reviewed Original ResearchMeSH KeywordsChromosomes, Human, 16-18Deoxyribonucleases, Type II Site-SpecificDNA Restriction EnzymesHumansPolymorphism, GeneticThymidine Kinase