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Volumn 39, Issue 8, 2000, Pages 946-962

The genetics of childhood psychiatric disorders: A decade of progress

Author keywords

Attention deficit hyperactivity disorder; Autism; Childhood psychiatric disorders; Dyslexia; Genetics; Tourette's disorder

Indexed keywords

ATTENTION DEFICIT DISORDER; AUTISM; CHILDHOOD DISEASE; DYSLEXIA; GENE FREQUENCY; GENE MAPPING; GENETIC LINKAGE; GENETICS; GENOME IMPRINTING; GILLES DE LA TOURETTE SYNDROME; HUMAN; MENTAL DISEASE; PRIORITY JOURNAL; QUANTITATIVE TRAIT; REVIEW;

EID: 0033888971     PISSN: 08908567     EISSN: None     Source Type: Journal    
DOI: 10.1097/00004583-200008000-00006     Document Type: Article
Times cited : (25)

References (128)
  • 2
    • 0029867499 scopus 로고    scopus 로고
    • Diagnostic testing for Prader-Willi and Angelman syndromes: Report of the ASHG/ACMG Test and Technology Transfer Committee
    • (1996) Am J Hum Genet , vol.58 , pp. 1085-1088
  • 18
  • 19
    • 0002046974 scopus 로고
    • Evidence that Tourette syndrome gene is at 18 22.1
    • Human Genetics: Proceedings of the 7th International Congress of Human Genetics Abstract Part II, Vogel F, Sperling K, eds. Berlin: Springer
    • (1986) , pp. 620
    • Comings, D.E.1    Comings, B.G.2    Dietz, G.3
  • 26
    • 0023094073 scopus 로고
    • Gene location in Tourette syndrome
    • (1987) Lancet , vol.14 , pp. 627
    • Donnai1
  • 29
  • 35
    • 0026345716 scopus 로고
    • Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
    • (1991) Cell , vol.67 , pp. 1047-1058
    • Fu, Y.H.1    Kuhl, D.P.2    Pizzuti, A.3
  • 49
    • 6844251000 scopus 로고    scopus 로고
    • A full genome screen for autism with evidence for linkage to a region on chromosome 7q
    • (1998) Hum Mol Genet , vol.7 , pp. 571-578
  • 59
    • 0028877463 scopus 로고
    • Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
    • (1995) Nat Genet , vol.11 , pp. 241-247
    • Lander, E.1    Kruglyak, L.2
  • 61
    • 0032859009 scopus 로고    scopus 로고
    • Incremental progress in developmental psychopathology: Simply complex
    • (1999) Am J Psychiatry , vol.156 , pp. 1495-1498
    • Leckman, J.1
  • 63
    • 0032403843 scopus 로고    scopus 로고
    • Analysis of CAG/CTG repeat size in Chinese subjects with schizophrenia and bipolar affective disorder using the repeat expansion detection method
    • (1998) Biol Psychiatry , vol.44 , pp. 1160-1165
    • Li, T.1    Vallada, H.P.2    Liu, X.3
  • 65
    • 0030068024 scopus 로고    scopus 로고
    • Molecular genetics of human blood pressure variation
    • (1996) Science , vol.272 , pp. 676-680
    • Lifton, R.P.1
  • 69
    • 0033569931 scopus 로고    scopus 로고
    • Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families: The International Molecular Genetic Study of Autism Consortium
    • (1999) Am J Med Genet , vol.88 , pp. 492-496
    • Maestrini, E.1    Lai, C.2    Marlow, A.3
  • 76
    • 0032807087 scopus 로고    scopus 로고
    • Quantitative trait loci analysis for the differences in susceptibility to atherosclerosis and diabetes between inbred mouse strains C57BL/6J and C57BLKS/J
    • (1999) J Lipid Res , vol.40 , pp. 1328-1335
    • Mu, J.L.1    Naggert, J.K.2    Svenson, K.L.3
  • 77
    • 0027474137 scopus 로고
    • Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: A review
    • (1993) Am J Med Genet , vol.46 , pp. 16-25
    • Nicholls, R.D.1
  • 81
    • 85031606605 scopus 로고
    • Analysis of Human Genetic Linkage. Baltimore: Johns Hopkins University Press
    • (1991)
    • Ott, J.1
  • 85
    • 0022515798 scopus 로고
    • The inheritance of Gilles de la Tourette's syndrome and associated behaviors: Evidence for autosomal dominant transmission
    • (1986) N Engl J Med , vol.315 , pp. 993-997
    • Pauls, D.L.1    Leckman, J.F.2
  • 87
    • 0031409125 scopus 로고    scopus 로고
    • Molecular background of the Finnish disease heritage
    • (1997) Ann Med , vol.29 , pp. 553-556
    • Peltonen, L.1
  • 88
    • 0000877874 scopus 로고
    • The detection of autosomal linkage data which consists of pairs of brothers and sisters of unspecified parentage
    • (1935) Ann Eugen , vol.6 , pp. 133-138
    • Penrose, L.S.1
  • 91
    • 0025019555 scopus 로고
    • Linkage strategies for genetically complex traits, I: Multilocus models
    • (1990) Am J Hum Genet , vol.46 , pp. 222-228
    • Risch, N.1
  • 92
    • 0025008677 scopus 로고
    • Linkage strategies for genetically complex traits, II: The power of affected relative pairs
    • (1990) Am J Hum Genet , vol.46 , pp. 229-241
    • Risch, N.1
  • 93
    • 0025020461 scopus 로고
    • Linkage strategies for genetically complex traits, III: The effect of marker polymorphism on analysis of affected relative pairs
    • (1990) Am J Hum Genet , vol.46 , pp. 242-253
    • Risch, N.1
  • 96
    • 0029001682 scopus 로고
    • Extreme discordant sib pairs for mapping quantitative trait loci in humans
    • (1995) Science , vol.268 , pp. 1584-1589
    • Risch, N.1    Zhang, H.2
  • 118
    • 85031609703 scopus 로고    scopus 로고
    • Cloning of a candidate gene (ARG1) from the breakpoint of t(7;20) in an autistic twin pair
    • Abstracts of the Annual Meeting of the American Society for Human Genetics, program no. 230
    • (1999)
    • Sultana, R.1    Yu, J.2    Raskind, W.3    Disteche, C.4
  • 120
    • 0033365190 scopus 로고    scopus 로고
    • A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome
    • (1999) Am J Hum Genet , vol.65 , pp. 1428-1436
  • 122
    • 0025905795 scopus 로고
    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, A.J.1    Pieretti, M.2    Sutcliffe, J.S.3
  • 124
    • 0031440856 scopus 로고    scopus 로고
    • Linkage disequilibrium between the dopamine transporter gene (DAT1) and bipolar disorder: Extending the transmission disequilibrium test (TDT) to examine genetic heterogeneity
    • (1997) Genet Epidemiol , vol.14 , pp. 699-704
    • Waldman, I.D.1    Robinson, B.F.2    Feigon, S.A.3
  • 125
    • 0032217057 scopus 로고    scopus 로고
    • Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: Heterogeneity owing to diagnostic subtype and severity
    • (1998) Am J Hum Genet , vol.63 , pp. 1767-1776
    • Waldman, I.D.1    Rowe, D.C.2    Abramowitz, A.3
  • 127
    • 85031609995 scopus 로고
    • Nongenetic factors associated with the expression of Tourette's syndrome
    • Proceedings of the 34th Annual Meeting of the American Academy of Child and Adolescent Psychiatry
    • (1987)
    • Walkup, J.T.1    Leckman, J.F.2    Price, R.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.