1997
Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease.
Iyengar S, Kalinsky H, Weiss S, Korostishevsky M, Sadeh M, Zhao Y, Kidd K, Bonne-Tamir B. Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle disease. Journal Of Medical Genetics 1997, 34: 391. PMID: 9152836, PMCID: PMC1050946, DOI: 10.1136/jmg.34.5.391.Peer-Reviewed Original Research
1996
DNA Workbench: A Database Package to Manage Regional Physical Mapping
Nadkarni P, Cheung K, Castiglione C, Miller P, Kidd K. DNA Workbench: A Database Package to Manage Regional Physical Mapping. Journal Of Computational Biology 1996, 3: 319-329. PMID: 8811490, DOI: 10.1089/cmb.1996.3.319.Peer-Reviewed Original Research
1995
The CEPH Consortium Linkage Map of Human Chromosome 11
Litt M, Kramer P, Kort E, Fain P, Cox S, Root D, White R, Weissenbach J, Donis-Keller H, Gatti R, Weber J, Nakamura Y, Julier C, Hayashi K, Spurr N, Dean M, Mandel J, Kidd K, Kruse T, Retief A, Bale A, Meo T, Vergnaud G, Warren S, Willard H. The CEPH Consortium Linkage Map of Human Chromosome 11. Genomics 1995, 27: 101-112. PMID: 7665156, DOI: 10.1006/geno.1995.1011.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 Research
1989
Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish
Kelsoe J, Ginns E, Egeland J, Gerhard D, Goldstein A, Bale S, Pauls D, Long R, Kidd K, Conte G, Housman D, Paul S. Re-evaluation of the linkage relationship between chromosome 11p loci and the gene for bipolar affective disorder in the Old Order Amish. Nature 1989, 342: 238-243. PMID: 2682265, DOI: 10.1038/342238a0.Peer-Reviewed Original ResearchBipolar DisorderChromosomes, Human, Pair 11EthnicityGenes, rasGenetic LinkageGenotypeHumansInsulinPedigreePennsylvania
1988
Tyrosine hydroxylase maps to the short arm of chromosome 11 proximal to the insulin and HRAS1 loci
Xue F, Kidd J, Pakstis A, Castiglione C, Mallet J, Kidd K. Tyrosine hydroxylase maps to the short arm of chromosome 11 proximal to the insulin and HRAS1 loci. Genomics 1988, 2: 288-293. PMID: 2906039, DOI: 10.1016/0888-7543(88)90016-x.Peer-Reviewed Original Research
1987
Bipolar affective disorders linked to DNA markers on chromosome 11
Egeland J, Gerhard D, Pauls D, Sussex J, Kidd K, Alien C, Hostetter A, Housman D. Bipolar affective disorders linked to DNA markers on chromosome 11. Nature 1987, 325: 783-787. PMID: 2881209, DOI: 10.1038/325783a0.Peer-Reviewed Original ResearchMeSH KeywordsAdolescentAdultBipolar DisorderChristianityChromosomes, Human, Pair 11DNAEthnicityGenetic MarkersHumansPedigreePennsylvaniaPolymorphism, Restriction Fragment LengthReligion and MedicineThe anonymous RFLP locus D11S16 is tightly linked to catalase on 11p
Kidd J, Castiglione C, Pakstis A, Kidd K. The anonymous RFLP locus D11S16 is tightly linked to catalase on 11p. Cytogenetic And Genome Research 1987, 45: 63-64. PMID: 2885154, DOI: 10.1159/000132428.Peer-Reviewed Original ResearchExclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi‐point linkage analysis
Kramer P, Ozelius L, Gusella J, Fahn S, Kidd K, Breakefield X, Boerecki I. Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi‐point linkage analysis. Genetic Epidemiology 1987, 4: 377-386. PMID: 3692135, DOI: 10.1002/gepi.1370040506.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
Development of a map of chromosome 11p
Kramer P, Farrer L, Pakstis A, Kidd K. Development of a map of chromosome 11p. Genetic Epidemiology. Supplement 1986, 3: 153-158. PMID: 3471659, DOI: 10.1002/gepi.1370030724.Peer-Reviewed Original Research