2015
Genetic markers for massively parallel sequencing in forensics
Kidd K, Speed W, Wootton S, Lagace R, Langit R, Haigh E, Chang J, Pakstis A. Genetic markers for massively parallel sequencing in forensics. Forensic Science International Genetics Supplement Series 2015, 5: e677-e679. DOI: 10.1016/j.fsigss.2015.12.004.Peer-Reviewed Original ResearchShort tandem repeat polymorphismsSingle nucleotide polymorphismsParallel sequencingSingle single-nucleotide polymorphismSequence readsMore haplotypesSNP panelGenetic markersMultiple allelesAncestry inferenceNucleotide polymorphismsCodominant systemsTandem repeat polymorphismMicrohaplotypesLociSequencingIndividual identificationRepeat polymorphismPolymorphismField of forensicsDNAHaplotypesReadsPhenotypeAlleles
2010
Vegetable Intake in College-Aged Adults Is Explained by Oral Sensory Phenotypes and TAS2R38 Genotype
Duffy VB, Hayes JE, Davidson AC, Kidd JR, Kidd KK, Bartoshuk LM. Vegetable Intake in College-Aged Adults Is Explained by Oral Sensory Phenotypes and TAS2R38 Genotype. Chemosensory Perception 2010, 3: 137-148. PMID: 21157576, PMCID: PMC3000691, DOI: 10.1007/s12078-010-9079-8.Peer-Reviewed Original ResearchVegetable intakeTAS2R38 genotypeFood frequency questionnaireFungiform papillaeGreater vegetable consumptionAVI/AVIFrequency questionnaireFood recordsCollege-Aged AdultsAnterior tongueVegetable consumptionSensory phenotypesHealthy adultsPropylthiouracilVegetable likingOral sensationIntakeMore papillaeReceptor geneLaboratory-based studiesPapillaeGreater consumptionPhenotypeAdultsNontasters
1995
Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population
Baldwin C, Weiss S, Farrer L, De Stefano A, Adair R, Franklyn B, Kidd K, Korostishevsky M, Bonné-Tamir B. Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population. Human Molecular Genetics 1995, 4: 1637-1642. PMID: 8541853, DOI: 10.1093/hmg/4.9.1637.Peer-Reviewed Original ResearchConceptsHuman chromosome 7q31Genetic linkage analysisNon-syndromic deafnessChromosomal locationGene locationNon-syndromic formsRecessive non-syndromic deafnessLinkage analysisChromosome 7q31Nonallelic mutationsGenetic isolateLarge familyLOD scoreGenetic heterogeneityGenetic causeRecessive deafnessGenesRecognizable phenotypeFirst evidenceDruze familyFamilyAffected individualsSpecific patternsMutationsPhenotype
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 diseaseSequence
1978
Research Designs for the Study of Gene-Environment Interactions in Psychiatric Disorders: Report of a Foundations Fund for Research in Psychiatry Panel
Kidd K, Matthysee S. Research Designs for the Study of Gene-Environment Interactions in Psychiatric Disorders: Report of a Foundations Fund for Research in Psychiatry Panel. JAMA Psychiatry 1978, 35: 925-932. PMID: 678045, DOI: 10.1001/archpsyc.1978.01770320019001.Peer-Reviewed Original ResearchConceptsGenetic variantsUnrelated individualsIndividual genetic variantsGenetic variationDifferent genetic variantsExtended pedigreesGenetic heterogeneityGene-environment interactionsGenetic hypothesisPhenotypeDiagnostic phenotypesFamilyGeneticsVariantsTraitsIndividual susceptibilitySpecific hypothesesSuch studiesHypothesisEnvironmental contributionsPedigreeGenotypesSusceptibility