메뉴 건너뛰기




Volumn 75, Issue 4, 2004, Pages 545-560

Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; BRAIN MATURATION; CHROMOSOME 17Q; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE ASSOCIATION; EUROPE; FEMALE; GENE EXPRESSION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GILLES DE LA TOURETTE SYNDROME; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PATHOGENESIS; PEDIGREE ANALYSIS; PRIORITY JOURNAL; PROMOTER REGION; SCORING SYSTEM; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE;

EID: 4544358749     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/424389     Document Type: Article
Times cited : (53)

References (80)
  • 1
    • 0033197996 scopus 로고    scopus 로고
    • The insulin receptor tyrosine kinase substrate p58/53 and the insulin receptor are components of CNS synapses
    • Abbott MA, Wells DG, Fallon JR (1999) The insulin receptor tyrosine kinase substrate p58/53 and the insulin receptor are components of CNS synapses. J Neurosci 19:7300-7308
    • (1999) J Neurosci , vol.19 , pp. 7300-7308
    • Abbott, M.A.1    Wells, D.G.2    Fallon, J.R.3
  • 4
    • 0032032104 scopus 로고    scopus 로고
    • Bipolar disorder in adult patients with Tourette's syndrome: A clinical study
    • Berthier ML, Kulisevsky J, Campos VM (1998) Bipolar disorder in adult patients with Tourette's syndrome: a clinical study. Biol Psychiatry 43:364-370
    • (1998) Biol Psychiatry , vol.43 , pp. 364-370
    • Berthier, M.L.1    Kulisevsky, J.2    Campos, V.M.3
  • 5
    • 0036846301 scopus 로고    scopus 로고
    • ProSAP/Shank postsynaptic density proteins interact with insulin receptor tyrosine kinase substrate IRSp53
    • Bockmann J, Kreutz MR, Gundelfinger ED, Bockers TM (2002) ProSAP/Shank postsynaptic density proteins interact with insulin receptor tyrosine kinase substrate IRSp53. J Neurochem 83:1013-1017
    • (2002) J Neurochem , vol.83 , pp. 1013-1017
    • Bockmann, J.1    Kreutz, M.R.2    Gundelfinger, E.D.3    Bockers, T.M.4
  • 6
    • 0037175395 scopus 로고    scopus 로고
    • Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease
    • Bommel H, Xie G, Rossoll W, Wiese S, Jablonka S, Boehm T, Sendtner M (2002) Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease. J Cell Biol 159:563-569
    • (2002) J Cell Biol , vol.159 , pp. 563-569
    • Bommel, H.1    Xie, G.2    Rossoll, W.3    Wiese, S.4    Jablonka, S.5    Boehm, T.6    Sendtner, M.7
  • 7
    • 0029806344 scopus 로고    scopus 로고
    • Linkage analysis and exclusion of regions of chromosomes 3 and 8 in Gilles de la Tourette syndrome following the identification of a balanced translocation 46,XY,t(3;8) (p21.3;q24.1) in a case of Tourette syndrome
    • Brett PM, Curtis D, Robertson MM, Dahlitz M, Curling HM (1996) Linkage analysis and exclusion of regions of chromosomes 3 and 8 in Gilles de la Tourette syndrome following the identification of a balanced translocation 46,XY,t(3;8) (p21.3;q24.1) in a case of Tourette syndrome. Psychiatr Genet 6:99-105
    • (1996) Psychiatr Genet , vol.6 , pp. 99-105
    • Brett, P.M.1    Curtis, D.2    Robertson, M.M.3    Dahlitz, M.4    Curling, H.M.5
  • 8
    • 0028986830 scopus 로고
    • Exclusion of the 5-HT1A serotonin neuroreceptor and tryptophan oxygenase genes in a large British kindred multiply affected with Tourette's syndrome, chronic motor tics, and obsessive-compulsive behavior
    • Brett PM, Curtis D, Robertson MM, Curling HM (1995) Exclusion of the 5-HT1A serotonin neuroreceptor and tryptophan oxygenase genes in a large British kindred multiply affected with Tourette's syndrome, chronic motor tics, and obsessive-compulsive behavior. Am J Psychiatry 152:437-440
    • (1995) Am J Psychiatry , vol.152 , pp. 437-440
    • Brett, P.M.1    Curtis, D.2    Robertson, M.M.3    Curling, H.M.4
  • 9
    • 0034096555 scopus 로고    scopus 로고
    • Social and emotional adjustment in children affected with Gilles de la Tourette's syndrome: Associations with ADHD and family functioning
    • Carter AS, O'Donnell DA, Schultz RT, Scahill L, Leckman JF Pauls DL (2000) Social and emotional adjustment in children affected with Gilles de la Tourette's syndrome: associations with ADHD and family functioning. J Child Psychol Psychiatry 41:215-223
    • (2000) J Child Psychol Psychiatry , vol.41 , pp. 215-223
    • Carter, A.S.1    O'Donnell, D.A.2    Schultz, R.T.3    Scahill, L.4    Leckman, J.F.5    Pauls, D.L.6
  • 10
    • 0033237335 scopus 로고    scopus 로고
    • A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission
    • Clayton D (1999) A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission. Am J Hum Genet 65:1170-1177
    • (1999) Am J Hum Genet , vol.65 , pp. 1170-1177
    • Clayton, D.1
  • 11
    • 0024363750 scopus 로고
    • Hypothesis: Homozygosity in Tourette syndrome
    • Comings DE, Comings BG, Knell E (1989) Hypothesis: homozygosity in Tourette syndrome. Am J Med Genet 34:413-421
    • (1989) Am J Med Genet , vol.34 , pp. 413-421
    • Comings, D.E.1    Comings, B.G.2    Knell, E.3
  • 13
    • 0037559358 scopus 로고    scopus 로고
    • Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder
    • Crawford FC, Ait-Ghezala G, Morris M, Sutcliffe MJ, Hauser RA, Silver AA, Mullan MJ (2003) Translocation breakpoint in two unrelated Tourette syndrome cases, within a region previously linked to the disorder. Hum Genet 113:154-161
    • (2003) Hum Genet , vol.113 , pp. 154-161
    • Crawford, F.C.1    Ait-Ghezala, G.2    Morris, M.3    Sutcliffe, M.J.4    Hauser, R.A.5    Silver, A.A.6    Mullan, M.J.7
  • 14
    • 0030811382 scopus 로고    scopus 로고
    • Increased prevalence of the seven-repeat variant of the dopamine D4 receptor gene in patients with obsessive-compulsive disorder with tics
    • Cruz C, Camarena B, King N, Paez F, Sidenberg D, de la Fuente JR, Nicolini H (1997) Increased prevalence of the seven-repeat variant of the dopamine D4 receptor gene in patients with obsessive-compulsive disorder with tics. Neurosci Lett 231:1-4
    • (1997) Neurosci Lett , vol.231 , pp. 1-4
    • Cruz, C.1    Camarena, B.2    King, N.3    Paez, F.4    Sidenberg, D.5    De La Fuente, J.R.6    Nicolini, H.7
  • 16
    • 0038389850 scopus 로고    scopus 로고
    • Genomewide linkage analyses of bipolar disorder: A new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative
    • erratum 73:979
    • Dick DM, Foroud T, Flury L, Bowman ES, Miller MJ, Rau NL, Moe PR, et al (2003) Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative. Am J Hum Genet 73:107-114 (erratum 73:979)
    • (2003) Am J Hum Genet , vol.73 , pp. 107-114
    • Dick, D.M.1    Foroud, T.2    Flury, L.3    Bowman, E.S.4    Miller, M.J.5    Rau, N.L.6    Moe, P.R.7
  • 17
    • 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
  • 19
    • 0033824364 scopus 로고    scopus 로고
    • Function of tubulin binding proteins in vivo
    • Fleming JA, Vega LR, Solomon F (2000) Function of tubulin binding proteins in vivo. Genetics 156:69-80
    • (2000) Genetics , vol.156 , pp. 69-80
    • Fleming, J.A.1    Vega, L.R.2    Solomon, F.3
  • 20
    • 0031963425 scopus 로고    scopus 로고
    • Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse
    • Gade R, Muhleman D, Blake H, MacMurray J, Johnson P, Verde R, Saucier G, Comings DE (1998) Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse. Mol Psychiatry 3:50-60
    • (1998) Mol Psychiatry , vol.3 , pp. 50-60
    • Gade, R.1    Muhleman, D.2    Blake, H.3    MacMurray, J.4    Johnson, P.5    Verde, R.6    Saucier, G.7    Comings, D.E.8
  • 24
    • 0029372419 scopus 로고
    • HAPLO: A program using the EM algorithm to estimate the frequencies of multi-site haplotypes
    • Hawley ME, Kidd KK (1995) HAPLO: a program using the EM algorithm to estimate the frequencies of multi-site haplotypes. J Hered 86:409-411
    • (1995) J Hered , vol.86 , pp. 409-411
    • Hawley, M.E.1    Kidd, K.K.2
  • 26
    • 0036843239 scopus 로고    scopus 로고
    • Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome
    • HRD/Autosomal Recessive Kenny-Caffey Syndrome Consortium (2002) Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome. Nat Genet 32:448-452
    • (2002) Nat Genet , vol.32 , pp. 448-452
  • 27
    • 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
  • 28
    • 0028819689 scopus 로고
    • Comorbid Tourette's disorder and bipolar disorder: An etiologic perspective
    • Kerbeshian JB, Burd L, Klug M (1995) Comorbid Tourette's disorder and bipolar disorder: an etiologic perspective. Am J Psychiatry 152:1646-1651
    • (1995) Am J Psychiatry , vol.152 , pp. 1646-1651
    • Kerbeshian, J.B.1    Burd, L.2    Klug, M.3
  • 34
    • 0029886532 scopus 로고    scopus 로고
    • Parametric and nonparametric linkage analysis: A unified multipoint approach
    • Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES (1996) Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 58:1347-1363
    • (1996) Am J Hum Genet , vol.58 , pp. 1347-1363
    • Kruglyak, L.1    Daly, M.J.2    Reeve-Daly, M.P.3    Lander, E.S.4
  • 36
    • 0024836166 scopus 로고
    • Tourette's syndrome: Current concepts
    • Kurlan R (1989) Tourette's syndrome: current concepts. Neurology 39:1625-1630
    • (1989) Neurology , vol.39 , pp. 1625-1630
    • Kurlan, R.1
  • 37
    • 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
  • 40
    • 0037121261 scopus 로고    scopus 로고
    • Tourette's syndrome
    • Leckman JF (2002) Tourette's syndrome. Lancet 360:1577-1586
    • (2002) Lancet , vol.360 , pp. 1577-1586
    • Leckman, J.F.1
  • 41
    • 0033638136 scopus 로고    scopus 로고
    • Tourette's syndrome: When habit-forming systems form habits of their own?
    • Leckman JF, Riddle MA (2000) Tourette's syndrome: when habit-forming systems form habits of their own? Neuron 28:349-354
    • (2000) Neuron , vol.28 , pp. 349-354
    • Leckman, J.F.1    Riddle, M.A.2
  • 45
    • 0033006003 scopus 로고    scopus 로고
    • Allelic discrimination using fluorogenic probes and the 5′ nuclease assay
    • Livak KJ (1999) Allelic discrimination using fluorogenic probes and the 5′ nuclease assay. Genet Anal 14:143-149
    • (1999) Genet Anal , vol.14 , pp. 143-149
    • Livak, K.J.1
  • 46
    • 0034678076 scopus 로고    scopus 로고
    • Tubulin folding cofactor D is a microtubule destabilizing protein
    • Martin L, Fanarraga ML, Aloria K, Zabala JC (2000) Tubulin folding cofactor D is a microtubule destabilizing protein. FEBS Lett 470:93-95
    • (2000) FEBS Lett , vol.470 , pp. 93-95
    • Martin, L.1    Fanarraga, M.L.2    Aloria, K.3    Zabala, J.C.4
  • 49
    • 0034811199 scopus 로고    scopus 로고
    • Basal ganglia dysfunction in Tourette's syndrome: A new hypothesis
    • Mink JW (2001) Basal ganglia dysfunction in Tourette's syndrome: a new hypothesis. Pediatr Neurol 25:190-198
    • (2001) Pediatr Neurol , vol.25 , pp. 190-198
    • Mink, J.W.1
  • 50
    • 0032891376 scopus 로고    scopus 로고
    • Identification of BAIAP2 (BAI-associated protein 2), a novel human homologue of hamster IRSp53, whose SH3 domain interacts with the cytoplasmic domain of BAI1
    • Oda K, Shiratsuchi T, Nishimori H, Inazawa J, Yoshikawa H, Taketani Y, Nakamura Y, Tokino T (1999) Identification of BAIAP2 (BAI-associated protein 2), a novel human homologue of hamster IRSp53, whose SH3 domain interacts with the cytoplasmic domain of BAI1. Cytogenet Cell Genet 84:75-82
    • (1999) Cytogenet Cell Genet , vol.84 , pp. 75-82
    • Oda, K.1    Shiratsuchi, T.2    Nishimori, H.3    Inazawa, J.4    Yoshikawa, H.5    Taketani, Y.6    Nakamura, Y.7    Tokino, T.8
  • 51
    • 0033012401 scopus 로고    scopus 로고
    • Dentatorubral-pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate
    • Okamura-Oho Y, Miyashita T, Ohmi K, Yamada M (1999) Dentatorubral- pallidoluysian atrophy protein interacts through a proline-rich region near polyglutamine with the SH3 domain of an insulin receptor tyrosine kinase substrate. Hum Mol Genet 8:947-957
    • (1999) Hum Mol Genet , vol.8 , pp. 947-957
    • Okamura-Oho, Y.1    Miyashita, T.2    Ohmi, K.3    Yamada, M.4
  • 52
    • 0030587462 scopus 로고    scopus 로고
    • Mouse and human neuronal pentraxin 1 (NPTX1): Conservation, genomic structure, and chromosomal localization
    • Omeis IA, Hsu YC, Perin MS (1996) Mouse and human neuronal pentraxin 1 (NPTX1): conservation, genomic structure, and chromosomal localization. Genomics 36:543-545
    • (1996) Genomics , vol.36 , pp. 543-545
    • Omeis, I.A.1    Hsu, Y.C.2    Perin, M.S.3
  • 54
    • 0042090498 scopus 로고    scopus 로고
    • An update on the genetics of Gilles de la Tourette syndrome
    • Pauls DL (2003) An update on the genetics of Gilles de la Tourette syndrome. J Psychosom Res 55:7-12
    • (2003) J Psychosom Res , vol.55 , pp. 7-12
    • Pauls, D.L.1
  • 56
    • 0022515798 scopus 로고
    • The inheritance of Gilles de la Tourette's syndrome and associated behaviors: Evidence for autosomal dominant transmission
    • Pauls DL, Leckman JF (1986) The inheritance of Gilles de la Tourette's syndrome and associated behaviors: evidence for autosomal dominant transmission. 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
  • 60
    • 0035000925 scopus 로고    scopus 로고
    • Prospective, longitudinal study of tic, obsessive-compulsive, and attention-deficit/hyperactivity disorders in an epidemiological sample
    • Peterson BS, Pine DS, Cohen P, Brook JS (2001) Prospective, longitudinal study of tic, obsessive-compulsive, and attention-deficit/hyperactivity disorders in an epidemiological sample. J Am Acad Child Adolesc Psychiatry 40:685-695
    • (2001) J Am Acad Child Adolesc Psychiatry , vol.40 , pp. 685-695
    • Peterson, B.S.1    Pine, D.S.2    Cohen, P.3    Brook, J.S.4
  • 62
    • 0034977045 scopus 로고    scopus 로고
    • Linkage disequilibrium in humans: Models and data
    • Pritchard JK, Przeworski M (2001) Linkage disequilibrium in humans: models and data. Am J Hum Genet 69:1-14
    • (2001) Am J Hum Genet , vol.69 , pp. 1-14
    • Pritchard, J.K.1    Przeworski, M.2
  • 63
    • 0033983916 scopus 로고    scopus 로고
    • Tourette syndrome, associated conditions and the complexities of treatment
    • Robertson MM (2000) Tourette syndrome, associated conditions and the complexities of treatment. Brain 123:425-462
    • (2000) Brain , vol.123 , pp. 425-462
    • Robertson, M.M.1
  • 64
    • 0042090496 scopus 로고    scopus 로고
    • Diagnosing Tourette syndrome: Is it a common disorder?
    • - (2003) Diagnosing Tourette syndrome: is it a common disorder? J Psychosom Res 55:3-6
    • (2003) J Psychosom Res , vol.55 , pp. 3-6
  • 65
    • 0030741184 scopus 로고    scopus 로고
    • Huntington's disease and dentatorubralpallidoluysian atrophy: Proteins, pathogenesis and pathology
    • Ross CA, Becher MW, Colomer V, Engelender S, Wood JD, Sharp AH (1997) Huntington's disease and dentatorubralpallidoluysian atrophy: proteins, pathogenesis and pathology. Brain Pathol 7:1003-1016
    • (1997) Brain Pathol , vol.7 , pp. 1003-1016
    • Ross, C.A.1    Becher, M.W.2    Colomer, V.3    Engelender, S.4    Wood, J.D.5    Sharp, A.H.6
  • 67
    • 0032231676 scopus 로고    scopus 로고
    • Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population
    • Simonic I, Gericke GS, Ott J, Weber JL (1998) Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population. Am J Hum Genet 63:839-846
    • (1998) Am J Hum Genet , vol.63 , pp. 839-846
    • Simonic, I.1    Gericke, G.S.2    Ott, J.3    Weber, J.L.4
  • 68
    • 0035825981 scopus 로고    scopus 로고
    • Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners
    • Simonic I, Nyholt DR, Gericke GS, Gordon D, Matsumoto N, Ledbetter DH, Ott J, Weber JL (2001) Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners. Am J Med Genet 105:163-167
    • (2001) Am J Med Genet , vol.105 , pp. 163-167
    • Simonic, I.1    Nyholt, D.R.2    Gericke, G.S.3    Gordon, D.4    Matsumoto, N.5    Ledbetter, D.H.6    Ott, J.7    Weber, J.L.8
  • 69
    • 0033677539 scopus 로고    scopus 로고
    • Current issues in Tourette syndrome
    • Singer HS (2000) Current issues in Tourette syndrome. Mov Disord 15:1051-1063
    • (2000) Mov Disord , vol.15 , pp. 1051-1063
    • Singer, H.S.1
  • 70
    • 4544229530 scopus 로고    scopus 로고
    • Neurobiology of Tourette's syndrome: Concepts of neuroanatomic localization and neurochemical abnormalities
    • Singer HS, Minzer K (2003) Neurobiology of Tourette's syndrome: concepts of neuroanatomic localization and neurochemical abnormalities. Brain Dev Suppl 25:S70-S84
    • (2003) Brain Dev Suppl , vol.25
    • Singer, H.S.1    Minzer, K.2
  • 72
    • 0027377799 scopus 로고
    • Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
    • Spielman RS, McGinnis RE, Ewens WJ (1993) Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 52:506-516
    • (1993) Am J Hum Genet , vol.52 , pp. 506-516
    • Spielman, R.S.1    McGinnis, R.E.2    Ewens, W.J.3
  • 75
    • 0033365190 scopus 로고    scopus 로고
    • A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome
    • Tourette Syndrome Association International Consortium for Genetics (TSAICG) (1999) A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome. Am J Hum Genet 65:1428-1436
    • (1999) Am J Hum Genet , vol.65 , pp. 1428-1436
  • 76
    • 0038278610 scopus 로고    scopus 로고
    • CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder
    • Verkerk AJ, Mathews CA, Joosse M, Bussen BH, Heutink P, Oostra BA, Tourette Syndrome Association International Consortium for Genetics (2003) CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. Genomics 82:1-9
    • (2003) Genomics , vol.82 , pp. 1-9
    • Verkerk, A.J.1    Mathews, C.A.2    Joosse, M.3    Bussen, B.H.4    Heutink, P.5    Oostra, B.A.6
  • 77
    • 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
  • 79
    • 0036201494 scopus 로고    scopus 로고
    • Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourette syndrome
    • Zhang H, Leckman JF, Pauls DL, Tsai C-P, Kidd KK, Campos MR, Tourette Syndrome Association International Consortium for Genetics (2002) Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourette syndrome. Am J Hum Genet 70:896-904
    • (2002) Am J Hum Genet , vol.70 , pp. 896-904
    • Zhang, H.1    Leckman, J.F.2    Pauls, D.L.3    Tsai, C.-P.4    Kidd, K.K.5    Campos, M.R.6
  • 80
    • 0032779692 scopus 로고    scopus 로고
    • Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random association
    • Zhao H, Pakstis AJ, Kidd JR, Kidd KK (1999) Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random association. Ann Hum Genet 63:167-179
    • (1999) Ann Hum Genet , vol.63 , pp. 167-179
    • Zhao, H.1    Pakstis, A.J.2    Kidd, J.R.3    Kidd, K.K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.