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Volumn 63, Issue 3, 1998, Pages 839-846

Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population

Author keywords

[No Author keywords available]

Indexed keywords

AFRICA; ARTICLE; CHROMOSOME 11Q; CHROMOSOME 14Q; CHROMOSOME 2; CHROMOSOME 20Q; CHROMOSOME 21Q; CHROMOSOME 6P; CHROMOSOME 8Q; CONTROLLED STUDY; DNA POLYMORPHISM; GENE LOCUS; GENE MAPPING; GENETIC MARKER; GILLES DE LA TOURETTE SYNDROME; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

EID: 0032231676     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302002     Document Type: Article
Times cited : (75)

References (47)
  • 2
    • 0030008257 scopus 로고    scopus 로고
    • Integration of the cytogenetic, genetic, and physical maps of the human genome by FISH mapping of CEPH YAC clones
    • Bray-Ward P, Menninger J, Lieman J, Desai T, Mokady N, Banks A, Ward DC (1996) Integration of the cytogenetic, genetic, and physical maps of the human genome by FISH mapping of CEPH YAC clones. Genomics 32:1-14
    • (1996) Genomics , vol.32 , pp. 1-14
    • Bray-Ward, P.1    Menninger, J.2    Lieman, J.3    Desai, T.4    Mokady, N.5    Banks, A.6    Ward, D.C.7
  • 4
    • 0028673755 scopus 로고
    • Tourette syndrome: A hereditary neuropsychiatric spectrum disorder
    • Comings DE (1994) Tourette syndrome: a hereditary neuropsychiatric spectrum disorder. Ann Clin Psychiatry 6: 235-247
    • (1994) Ann Clin Psychiatry , vol.6 , pp. 235-247
    • Comings, D.E.1
  • 5
    • 0345030604 scopus 로고
    • A controlled study of Tourette syndrome - Revisited: A reply to the letter of Pauls et al
    • Comings DE, Comings BG (1988) A controlled study of Tourette syndrome - revisited: a reply to the letter of Pauls et al. Am J Hum Genet 43:209-217
    • (1988) Am J Hum Genet , vol.43 , pp. 209-217
    • Comings, D.E.1    Comings, B.G.2
  • 7
    • 0027468019 scopus 로고
    • Association between Tourette's syndrome and homozygosity at the dopamine D3 receptor gene
    • Comings DE, Muhleman D, Dietz G, Dino M, LeGro R, Gade R (1993) Association between Tourette's syndrome and homozygosity at the dopamine D3 receptor gene. Lancet 341: 906
    • (1993) Lancet , vol.341 , pp. 906
    • Comings, D.E.1    Muhleman, D.2    Dietz, G.3    Dino, M.4    LeGro, R.5    Gade, R.6
  • 8
    • 85031583400 scopus 로고    scopus 로고
    • Multiple childhood behavioral disorders (Tourette syndrome, multiple tics, ADHD, and OCD) presenting in a family with a balanced chromosome translocation (t1,8)(q21.1;q22.1)
    • in press
    • Devor EJ, Magee HJ. Multiple childhood behavioral disorders (Tourette syndrome, multiple tics, ADHD, and OCD) presenting in a family with a balanced chromosome translocation (t1,8)(q21.1;q22.1). Psychiatric Genet (in press)
    • Psychiatric Genet
    • Devor, E.J.1    Magee, H.J.2
  • 10
    • 0027318629 scopus 로고
    • Evidence for autosomal dominant transmission in Tourette's syndrome. United Kingdom Cohort Study
    • Eapen V, Pauls DL, Robertson MM (1993) Evidence for autosomal dominant transmission in Tourette's syndrome. United Kingdom Cohort Study. Br J Psychiatry 162:593-596
    • (1993) Br J Psychiatry , vol.162 , pp. 593-596
    • Eapen, V.1    Pauls, D.L.2    Robertson, M.M.3
  • 12
    • 0030935176 scopus 로고    scopus 로고
    • Genetic mapping using fluorescent quantification of allele frequencies in pooled DNA loaded by solid support
    • Graff C, Persson A, Ulfendahl PJ, Wahlberg J, Wadelius C (1997) Genetic mapping using fluorescent quantification of allele frequencies in pooled DNA loaded by solid support. Clin Genet 51:145-152
    • (1997) Clin Genet , vol.51 , pp. 145-152
    • Graff, C.1    Persson, A.2    Ulfendahl, P.J.3    Wahlberg, J.4    Wadelius, C.5
  • 13
    • 19244363371 scopus 로고    scopus 로고
    • Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test
    • Grice DE, Leckman JF, Pauls DL, Kidd KK, Pakstis AJ, Chang FM, Buxbaum JD, et al (1996) Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test. Am J Hum Genet 59:644-652
    • (1996) Am J Hum Genet , vol.59 , pp. 644-652
    • Grice, D.E.1    Leckman, J.F.2    Pauls, D.L.3    Kidd, K.K.4    Pakstis, A.J.5    Chang, F.M.6    Buxbaum, J.D.7
  • 14
    • 0031971162 scopus 로고    scopus 로고
    • Linkage disequilibrium analysis in a recently founded population: Evaluation of the variegate porphyria founder in South African Afrikaners
    • Groenewald JZ, Liebenberg J, Groenewald IM, Warnich L (1998) Linkage disequilibrium analysis in a recently founded population: evaluation of the variegate porphyria founder in South African Afrikaners. Am J Hum Genet 62: 1254-1258
    • (1998) Am J Hum Genet , vol.62 , pp. 1254-1258
    • Groenewald, J.Z.1    Liebenberg, J.2    Groenewald, I.M.3    Warnich, L.4
  • 16
  • 19
    • 0026655039 scopus 로고
    • Relationship of birth weight to the phenotypic expression of Gilles de la Tourette's syndrome in monozygotic twins
    • Hyde TM, Aaronson BA, Randolph C, Rickler KC, Weinberger DR (1992) Relationship of birth weight to the phenotypic expression of Gilles de la Tourette's syndrome in monozygotic twins. Neurology 42:652-658
    • (1992) Neurology , vol.42 , pp. 652-658
    • Hyde, T.M.1    Aaronson, B.A.2    Randolph, C.3    Rickler, K.C.4    Weinberger, D.R.5
  • 20
    • 0025223040 scopus 로고
    • Medical genetics in South Africa
    • Jenkins T (1990) Medical genetics in South Africa. J Med Genet 27:760-779
    • (1990) J Med Genet , vol.27 , pp. 760-779
    • Jenkins, T.1
  • 21
    • 0029983636 scopus 로고    scopus 로고
    • The South African malady
    • Jenkins T (1996) The South African malady. Nat Genet 13: 7-9
    • (1996) Nat Genet , vol.13 , pp. 7-9
    • Jenkins, T.1
  • 22
    • 0030869377 scopus 로고    scopus 로고
    • What is significant in whole-genome linkage disequilibrium studies?
    • Krugylak L (1997) What is significant in whole-genome linkage disequilibrium studies? Am J Hum Genet 61:810-812
    • (1997) Am J Hum Genet , vol.61 , pp. 810-812
    • Krugylak, L.1
  • 23
    • 0022455402 scopus 로고
    • Familial Tourette's syndrome: Report of a large pedigree and potential for linkage analysis
    • Kurlan R, Behr J, Medved L, Shoulson I, Pauls D, Kidd JR, Kidd KK (1986) Familial Tourette's syndrome: report of a large pedigree and potential for linkage analysis. Neurology 36:772-776
    • (1986) Neurology , vol.36 , pp. 772-776
    • Kurlan, R.1    Behr, J.2    Medved, L.3    Shoulson, I.4    Pauls, D.5    Kidd, J.R.6    Kidd, K.K.7
  • 24
    • 0000803318 scopus 로고
    • Construction of multilocus genetic linkage maps in humans
    • Lander ES, Green P (1987) Construction of multilocus genetic linkage maps in humans. Proc Natl Acad Sci USA 84: 2363-2367
    • (1987) Proc Natl Acad Sci USA , vol.84 , pp. 2363-2367
    • Lander, E.S.1    Green, P.2
  • 26
    • 0026619049 scopus 로고
    • Tourette symptoms in 161 related family members
    • Chase TN, Friedhoff AJ, Cohen DJ (eds) Raven Press, New York
    • McMahon WM, Leppert M, Filloux F, van de Wetering BJM, Hasstedt S (1992) Tourette symptoms in 161 related family members. In: Chase TN, Friedhoff AJ, Cohen DJ (eds) Advances in neurology, vol 58. Raven Press, New York, pp 159-165
    • (1992) Advances in Neurology , vol.58 , pp. 159-165
    • McMahon, W.M.1    Leppert, M.2    Filloux, F.3    Van De Wetering, B.J.M.4    Hasstedt, S.5
  • 27
    • 0030140415 scopus 로고    scopus 로고
    • A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyria
    • Meissner PN, Dailey TA, Hift RJ, Ziman M, Corrigall AV, Roberts AG, Meissner DM, et al (1996) A R59W mutation in human protoporphyrinogen oxidase results in decreased enzyme activity and is prevalent in South Africans with variegate porphyria. Nat Genet 13:95-97
    • (1996) Nat Genet , vol.13 , pp. 95-97
    • Meissner, P.N.1    Dailey, T.A.2    Hift, R.J.3    Ziman, M.4    Corrigall, A.V.5    Roberts, A.G.6    Meissner, D.M.7
  • 29
    • 0027485238 scopus 로고
    • Determination of allele frequencies at loci with length polymorphism by quantitative analysis of DNA amplified from pooled samples
    • Pacek P, Sajantila A, Syvänen AC (1993) Determination of allele frequencies at loci with length polymorphism by quantitative analysis of DNA amplified from pooled samples. PCR Methods Appl 2:313-317
    • (1993) PCR Methods Appl , vol.2 , pp. 313-317
    • Pacek, P.1    Sajantila, A.2    Syvänen, A.C.3
  • 31
    • 0029962729 scopus 로고    scopus 로고
    • Quest for the elusive genetic basis of Tourette syndrome
    • Patel PI (1996) Quest for the elusive genetic basis of Tourette syndrome. Am J Hum Genet 59:980-982
    • (1996) Am J Hum Genet , vol.59 , pp. 980-982
    • Patel, P.I.1
  • 33
    • 0024061559 scopus 로고
    • Tourette syndrome and neuropsychiatric disorders: Is there a genetic relationship?
    • Pauls DL, Cohen DJ, Kidd KK, Leckman JF (1988) Tourette syndrome and neuropsychiatric disorders: Is there a genetic relationship? Am J Hum Genet 43:206-209
    • (1988) Am J Hum Genet , vol.43 , pp. 206-209
    • Pauls, D.L.1    Cohen, D.J.2    Kidd, K.K.3    Leckman, J.F.4
  • 34
    • 0022515798 scopus 로고
    • The inheritance of Gilles de la Tourette's syndrome and associated behaviors
    • Pauls DL, Leckman JF (1986) The inheritance of Gilles de la Tourette's syndrome and associated behaviors. N Engl J Med 315:993-997
    • (1986) N Engl J Med , vol.315 , pp. 993-997
    • Pauls, D.L.1    Leckman, J.F.2
  • 36
    • 0030954650 scopus 로고    scopus 로고
    • Rare disease genes - Lessons and challenges
    • Peltonen L, Uusitalo A (1997) Rare disease genes - lessons and challenges. Genome Res 7:765-767
    • (1997) Genome Res , vol.7 , pp. 765-767
    • Peltonen, L.1    Uusitalo, A.2
  • 39
    • 0026031188 scopus 로고
    • Gilles de la Tourette syndrome in the Middle East: Report of a cohort and a multiply affected large pedigree
    • Robertson MM, Trimble MR (1991) Gilles de la Tourette syndrome in the Middle East: report of a cohort and a multiply affected large pedigree. Br J Psychiatry 158:416-419
    • (1991) Br J Psychiatry , vol.158 , pp. 416-419
    • Robertson, M.M.1    Trimble, M.R.2
  • 41
    • 0028000502 scopus 로고
    • Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping
    • Sheffield VC, Carmi R, Kwitek-Black A, Rokhlina T, Nishimura D, Duyk GM, Elbedour K, et al (1994) Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping. Hum Mol Genet 3:1331-1335
    • (1994) Hum Mol Genet , vol.3 , pp. 1331-1335
    • Sheffield, V.C.1    Carmi, R.2    Kwitek-Black, A.3    Rokhlina, T.4    Nishimura, D.5    Duyk, G.M.6    Elbedour, K.7
  • 42
    • 16944365535 scopus 로고    scopus 로고
    • Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers
    • Starfield M, Hennies HC, Jung M, Jenkins T, Wienker T, Hull P, Spurdle A, et al (1997) Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers. Am J Hum Genet 61:370-378
    • (1997) Am J Hum Genet , vol.61 , pp. 370-378
    • Starfield, M.1    Hennies, H.C.2    Jung, M.3    Jenkins, T.4    Wienker, T.5    Hull, P.6    Spurdle, A.7
  • 43
    • 0021223733 scopus 로고
    • Association between familial hypercholesterolaemia and church affiliation
    • Torrington M, Botha JL, Pilcher GJ, Baker SG (1984) Association between familial hypercholesterolaemia and church affiliation. S Afr Med J 65:762-767
    • (1984) S Afr Med J , vol.65 , pp. 762-767
    • Torrington, M.1    Botha, J.L.2    Pilcher, G.J.3    Baker, S.G.4
  • 44
    • 0027191075 scopus 로고
    • The genetics of the Gilles de la Tourette syndrome: A review
    • van de Wetering BJM, Heutink P (1993) The genetics of the Gilles de la Tourette syndrome: a review. J Lab Clin Med 121:638-645
    • (1993) J Lab Clin Med , vol.121 , pp. 638-645
    • Van De Wetering, B.J.M.1    Heutink, P.2
  • 45
    • 0029759164 scopus 로고    scopus 로고
    • Family study and segregation analysis of Tourette syndrome: Evidence for a mixed model of inheritance
    • Walkup JT, LaBuda MC, Singer HS, Brown J, Riddle MA, Hurko O (1996) Family study and segregation analysis of Tourette syndrome: evidence for a mixed model of inheritance. Am J Hum Genet 59:684-693
    • (1996) Am J Hum Genet , vol.59 , pp. 684-693
    • Walkup, J.T.1    LaBuda, M.C.2    Singer, H.S.3    Brown, J.4    Riddle, M.A.5    Hurko, O.6
  • 46
    • 0029940761 scopus 로고    scopus 로고
    • Mapping of variegate porphyria (VP) gene: Contradictory evidence for linkage between VP and microsatellite markers at chromosome 14q32
    • Warnich L, Meissner PN, Hift RJ, Louw JH, van Heerden CJ, Retief AE (1996) Mapping of variegate porphyria (VP) gene: contradictory evidence for linkage between VP and microsatellite markers at chromosome 14q32. Hum Genet 97: 690-692
    • (1996) Hum Genet , vol.97 , pp. 690-692
    • Warnich, L.1    Meissner, P.N.2    Hift, R.J.3    Louw, J.H.4    Van Heerden, C.J.5    Retief, A.E.6
  • 47
    • 0026746637 scopus 로고
    • Application of microsatellite DNA polymorphisms to linkage mapping of Tourette syndrome gene(s)
    • Chase TN, Friedhoff AJ, Cohen DJ (eds) Raven Press, New York
    • Wilkie PJ, Ahmann PA, Hardacre J, LaPlant RJ, Hiner BC, Weber JL (1992) Application of microsatellite DNA polymorphisms to linkage mapping of Tourette syndrome gene(s). In: Chase TN, Friedhoff AJ, Cohen DJ (eds) Advances in neurology, vol 58. Raven Press, New York, pp 173-180
    • (1992) Advances in Neurology , vol.58 , pp. 173-180
    • Wilkie, P.J.1    Ahmann, P.A.2    Hardacre, J.3    Laplant, R.J.4    Hiner, B.C.5    Weber, J.L.6


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