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Volumn 48, Issue 8, 2003, Pages 526-537

Genetic and Neurodevelopmental Influences in Autistic Disorder

Author keywords

Autism; Genetics; Magnetic resonance imaging; Neurodevelopment; Phenotype expression

Indexed keywords

AUTISM; BRAIN DEVELOPMENT; BRAIN SIZE; CHILD; CORPUS CALLOSUM; GENE LOCATION; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; HEREDITY; HUMAN; NEUROBIOLOGY; PHENOTYPE; REVIEW;

EID: 0142073440     PISSN: 07067437     EISSN: None     Source Type: Journal    
DOI: 10.1177/070674370304800804     Document Type: Review
Times cited : (52)

References (117)
  • 2
    • 0142073438 scopus 로고    scopus 로고
    • Diagnosis and epidemiology of autism spectrum disorders
    • Tidmarsh L, Volkmar FR. Diagnosis and epidemiology of autism spectrum disorders. Can J Psychiatry 2003;48(8):517-25.
    • (2003) Can J Psychiatry , vol.48 , Issue.8 , pp. 517-525
    • Tidmarsh, L.1    Volkmar, F.R.2
  • 3
    • 0142136822 scopus 로고    scopus 로고
    • Autism spectrum disorders: Early detection and intervention, education, and psychopharmacological management
    • Bryson SE, Rogers SJ, Fombonne E. Autism spectrum disorders: early detection and intervention, education, and psychopharmacological management. Can J Psychiatry 2003;48:506-16.
    • (2003) Can J Psychiatry , vol.48 , pp. 506-516
    • Bryson, S.E.1    Rogers, S.J.2    Fombonne, E.3
  • 5
    • 0017530988 scopus 로고
    • Infantile autism: A genetic study of 21 twin pairs
    • Folstein S, Rutter M. Infantile autism: a genetic study of 21 twin pairs. J Child Psychol Psychiatry 1977;18:297-321.
    • (1977) J Child Psychol Psychiatry , vol.18 , pp. 297-321
    • Folstein, S.1    Rutter, M.2
  • 9
    • 0035653670 scopus 로고    scopus 로고
    • Genetics of autism: Complex etiology for a heterogeneous disorder
    • Folstein SE, Rosen-Sheidley B. Genetics of autism: complex etiology for a heterogeneous disorder. Nat Rev Genet 2001;2:943-55.
    • (2001) Nat Rev Genet , vol.2 , pp. 943-955
    • Folstein, S.E.1    Rosen-Sheidley, B.2
  • 11
    • 0033926492 scopus 로고    scopus 로고
    • The environment as an etiologic factor in autism: A new direction for research
    • London EA. The environment as an etiologic factor in autism: a new direction for research. Environ Health Perspect 2000;108:401-4.
    • (2000) Environ Health Perspect , vol.108 , pp. 401-404
    • London, E.A.1
  • 12
    • 0036471969 scopus 로고    scopus 로고
    • Maternal infection: Window on neuroimmune interactions in fetal brain development and mental illness
    • Patterson PH. Maternal infection: window on neuroimmune interactions in fetal brain development and mental illness. Curr Opin Neurobiol 2002;12:115-8.
    • (2002) Curr Opin Neurobiol , vol.12 , pp. 115-118
    • Patterson, P.H.1
  • 13
    • 0029134874 scopus 로고
    • Latent-class analysis of recurrence risks for complex phenotypes with select measurement error: A twin and family history study of autism
    • Pickles A, Bolton P, Macdonald H, Sim L, Rutter MI. Latent-class analysis of recurrence risks for complex phenotypes with select measurement error: a twin and family history study of autism. Am J Hum Genet 1995;57:717-26.
    • (1995) Am J Hum Genet , vol.57 , pp. 717-726
    • Pickles, A.1    Bolton, P.2    Macdonald, H.3    Sim, L.4    Rutter, M.I.5
  • 16
    • 0033667613 scopus 로고    scopus 로고
    • Discovery of allelic variants of HOXA1 and HOXB1: Genetic susceptibility to autism spectrum disorders
    • Ingram JL, Stodgell CJ, Hyman SL, Figlewicz DA, Weitkamp LR. Discovery of allelic variants of HOXA1 and HOXB1: genetic susceptibility to autism spectrum disorders. Teratology 2000;62:393-405.
    • (2000) Teratology , vol.62 , pp. 393-405
    • Ingram, J.L.1    Stodgell, C.J.2    Hyman, S.L.3    Figlewicz, D.A.4    Weitkamp, L.R.5
  • 22
    • 0034615152 scopus 로고    scopus 로고
    • Analysis of linkage disequilibrium in γ-aminobutyric acid receptor subunit genes in autistic disorder
    • Martin ER, Menold MM, Wolpert CM, Bass MP, Donnelly SL. Ravan SA, and others. Analysis of linkage disequilibrium in γ-aminobutyric acid receptor subunit genes in autistic disorder. Am J Med Genet 2000;96:43-8.
    • (2000) Am J Med Genet , vol.96 , pp. 43-48
    • Martin, E.R.1    Menold, M.M.2    Wolpert, C.M.3    Bass, M.P.4    Donnelly, S.L.5    Ravan, S.A.6
  • 23
    • 0035417396 scopus 로고    scopus 로고
    • Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families
    • Nurmi EL, Bradford Y, Chen Y, Hall J, Arnone B. Gardiner MB, and others. Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families. Genomics 2001;77:105-13.
    • (2001) Genomics , vol.77 , pp. 105-113
    • Nurmi, E.L.1    Bradford, Y.2    Chen, Y.3    Hall, J.4    Arnone, B.5    Gardiner, M.B.6
  • 24
    • 0023912150 scopus 로고
    • Stoppage rules and genetic studies of autism
    • Jones MB, Szatmari P. Stoppage rules and genetic studies of autism. J Autism Dev Disord 1988;18:31-40.
    • (1988) J Autism Dev Disord , vol.18 , pp. 31-40
    • Jones, M.B.1    Szatmari, P.2
  • 25
    • 6844251000 scopus 로고    scopus 로고
    • A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International molecular genetic study of autism consortium
    • International Molecular Genetic Study of Autism Consortium (IMGSAC). A full genome screen for autism with evidence for linkage to a region on chromosome 7q. International molecular genetic study of autism consortium. Hum Mol Genet 1998;7:571-8.
    • (1998) Hum Mol Genet , vol.7 , pp. 571-578
  • 27
  • 28
    • 0033917433 scopus 로고    scopus 로고
    • Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families
    • Auranen M, Nieminen, Majuri S, Vanhala R, Peltonen L, Jarvela I. Analysis of autism susceptibility gene loci on chromosomes 1p, 4p, 6q, 7q, 13q, 15q, 16p, 17q, 19q and 22q in Finnish multiplex families. Mol Psychiatry 2000;5:320-22.
    • (2000) Mol Psychiatry , vol.5 , pp. 320-322
    • Auranen, M.1    Nieminen2    Majuri, S.3    Vanhala, R.4    Peltonen, L.5    Jarvela, I.6
  • 30
    • 0034883367 scopus 로고    scopus 로고
    • A Genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
    • International Molecular Genetic Study of Autism Consortium (IMGSAC). A Genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am J Hum Genet 2001;69:570-81.
    • (2001) Am J Hum Genet , vol.69 , pp. 570-581
  • 32
    • 0036138102 scopus 로고    scopus 로고
    • Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
    • Alarcon M, Cantor RM, Liu J, Gilliam TC, Geschwind DH, Autism Genetic Researth Exchange Consortium. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. Am J Hum Genet 2002;70:60-71.
    • (2002) Am J Hum Genet , vol.70 , pp. 60-71
    • Alarcon, M.1    Cantor, R.M.2    Liu, J.3    Gilliam, T.C.4    Geschwind, D.H.5
  • 34
    • 0028877463 scopus 로고
    • Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
    • Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 1995;11:241-7.
    • (1995) Nat Genet , vol.11 , pp. 241-247
    • Lander, E.1    Kruglyak, L.2
  • 36
    • 18344374001 scopus 로고    scopus 로고
    • Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disordrer
    • Shao Y, Raiford KL, Wolpert CM, Cope HA, Ravan SA, Ashley-Koch AA, and others. Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disordrer. Am J Hum Genet 2002;70:1058-61.
    • (2002) Am J Hum Genet , vol.70 , pp. 1058-1061
    • Shao, Y.1    Raiford, K.L.2    Wolpert, C.M.3    Cope, H.A.4    Ravan, S.A.5    Ashley-Koch, A.A.6
  • 37
    • 0035807360 scopus 로고    scopus 로고
    • A forkhead-domain gene is mutated in a severe speech and language disorder
    • Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 2001;413:519-23.
    • (2001) Nature , vol.413 , pp. 519-523
    • Lai, C.S.1    Fisher, S.E.2    Hurst, J.A.3    Vargha-Khadem, F.4    Monaco, A.P.5
  • 38
    • 0035002844 scopus 로고    scopus 로고
    • An investigation of language impairment in autism: Implications for genetic subgroups
    • Kjelgaard MG, Tager-Flusberg H. An investigation of language impairment in autism: implications for genetic subgroups. Language and Cognitive Processes 2001;16:287-308.
    • (2001) Language and Cognitive Processes , vol.16 , pp. 287-308
    • Kjelgaard, M.G.1    Tager-Flusberg, H.2
  • 40
    • 0036150925 scopus 로고    scopus 로고
    • Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7
    • Badner JA, Gershon ES. Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7. Mol Psychiatry 2002;7(1):56-66.
    • (2002) Mol Psychiatry , vol.7 , Issue.1 , pp. 56-66
    • Badner, J.A.1    Gershon, E.S.2
  • 41
    • 18344368187 scopus 로고    scopus 로고
    • FOXP2 is not a major susceptibility gene for autism or specific language impairment
    • Newbury DF, Bonora E, Lmab JA, Fisher SE, Lai SL, Baird G, and others. FOXP2 is not a major susceptibility gene for autism or specific language impairment. Am J Hum Genet 2002;70:1315-27.
    • (2002) Am J Hum Genet , vol.70 , pp. 1315-1327
    • Newbury, D.F.1    Bonora, E.2    Lmab, J.A.3    Fisher, S.E.4    Lai, S.L.5    Baird, G.6
  • 42
    • 0034766845 scopus 로고    scopus 로고
    • Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31
    • Cheung J, Petek E, Nakabayashi K. Tsui L-C, Vincent JB and Scherer SW. Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31. Genomics 2001;78:7-11.
    • (2001) Genomics , vol.78 , pp. 7-11
    • Cheung, J.1    Petek, E.2    Nakabayashi, K.3    Tsui, L.-C.4    Vincent, J.B.5    Scherer, S.W.6
  • 43
    • 0036731660 scopus 로고    scopus 로고
    • The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system
    • Vincent JB, Petek E, Thevarkunnel S, Kolozsvari D, Cheung J, Patel M, and others. The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system. Genomics 2002;80:283-94.
    • (2002) Genomics , vol.80 , pp. 283-294
    • Vincent, J.B.1    Petek, E.2    Thevarkunnel, S.3    Kolozsvari, D.4    Cheung, J.5    Patel, M.6
  • 44
    • 0033912327 scopus 로고    scopus 로고
    • Effects of stratification in the analysis of affected sib-pair data: Benefits and costs
    • Leal SM, Ott J. Effects of stratification in the analysis of affected sib-pair data: benefits and costs. Am J Hum Genet 2000;66:567-75.
    • (2000) Am J Hum Genet , vol.66 , pp. 567-575
    • Leal, S.M.1    Ott, J.2
  • 45
    • 0037083113 scopus 로고    scopus 로고
    • Regression models for allele sharing: Analysis of accumulating data in affected sib pair studies
    • Bull SB, Greenwood CMT, Mirea L, Morgan K. Regression models for allele sharing: analysis of accumulating data in affected sib pair studies. Statis Med 2002;21:431-44.
    • (2002) Statis Med , vol.21 , pp. 431-444
    • Bull, S.B.1    Greenwood, C.M.T.2    Mirea, L.3    Morgan, K.4
  • 46
    • 0036076138 scopus 로고    scopus 로고
    • Regression-based quantitative-trait-locus mapping in the 21st century
    • Feingold E. Regression-based quantitative-trait-locus mapping in the 21st century. Am J Hum Genet 2002;71:217-22.
    • (2002) Am J Hum Genet , vol.71 , pp. 217-222
    • Feingold, E.1
  • 49
    • 0033693172 scopus 로고    scopus 로고
    • Macrocephaly in autism and other pervasive developmental disorders
    • Fidler DJ, Bailey JN, Smalley SL. Macrocephaly in autism and other pervasive developmental disorders. Dev Med Child Neurol 2000;42:737-40.
    • (2000) Dev Med Child Neurol , vol.42 , pp. 737-740
    • Fidler, D.J.1    Bailey, J.N.2    Smalley, S.L.3
  • 57
    • 0142086580 scopus 로고    scopus 로고
    • Sibling risk ratios and correlations of social and cognitive traits in autistic sib pairs
    • Paper presented at; San Diego (CA)
    • Cantor-Chiu RM, Alarcon M, Geschwind D, AGRE Consortium. Sibling risk ratios and correlations of social and cognitive traits in autistic sib pairs. Paper presented at the Annual Meeting of the American Society of Human Genetics; 2001; San Diego (CA).
    • (2001) Annual Meeting of the American Society of Human Genetics
    • Cantor-Chiu, R.M.1    Alarcon, M.2    Geschwind, D.3
  • 59
    • 0037040451 scopus 로고    scopus 로고
    • Behavioral phenotype variation in autism multiplex families: Evidence for a severity gradient
    • Spiker D, Lotspeich LJ, Dimiceli S, Meres RM, Riseh N. Behavioral phenotype variation in autism multiplex families: Evidence for a severity gradient. Am J Med Genet 2002;114:129-36.
    • (2002) Am J Med Genet , vol.114 , pp. 129-136
    • Spiker, D.1    Lotspeich, L.J.2    Dimiceli, S.3    Meres, R.M.4    Riseh, N.5
  • 60
    • 0033913088 scopus 로고    scopus 로고
    • The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: A family history study
    • Szatmari P, MacLean JE, Jones MB, Bryson SE, Zwaigenbaum L, Bartolucci G, and others. The familial aggregation of the lesser variant in biological and nonbiological relatives of PDD probands: a family history study. J Child Psychol Psychiatry 2000;41:79-86.
    • (2000) J Child Psychol Psychiatry , vol.41 , pp. 79-86
    • Szatmari, P.1    MacLean, J.E.2    Jones, M.B.3    Bryson, S.E.4    Zwaigenbaum, L.5    Bartolucci, G.6
  • 63
    • 0035430886 scopus 로고    scopus 로고
    • A review of subtyping in autism and proposed dimensional classification model
    • Beglinger LJ, Smith TH. A review of subtyping in autism and proposed dimensional classification model. J Autism Dev Disord 2001;31:411-22.
    • (2001) J Autism Dev Disord , vol.31 , pp. 411-422
    • Beglinger, L.J.1    Smith, T.H.2
  • 65
    • 0031459372 scopus 로고    scopus 로고
    • Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p
    • Brzustowicz LM, Honer WG, Chow EW, Hogan J, Hodgkinson K, Bassett AS. Use of a quantitative trait to map a locus associated with severity of positive symptoms in familial schizophrenia to chromosome 6p. Am J Hum Genet 1997;61:1388-96.
    • (1997) Am J Hum Genet , vol.61 , pp. 1388-1396
    • Brzustowicz, L.M.1    Honer, W.G.2    Chow, E.W.3    Hogan, J.4    Hodgkinson, K.5    Bassett, A.S.6
  • 66
    • 0033758721 scopus 로고    scopus 로고
    • The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci
    • Watanabe RM, Ghosh S, Langefeld CD, Valle TT, Hauser ER, Magnuson VL, and others. The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci. Am J Hum Genet 2000;67:1186-200.
    • (2000) Am J Hum Genet , vol.67 , pp. 1186-1200
    • Watanabe, R.M.1    Ghosh, S.2    Langefeld, C.D.3    Valle, T.T.4    Hauser, E.R.5    Magnuson, V.L.6
  • 67
  • 69
    • 18244408330 scopus 로고    scopus 로고
    • A genomewide scan identifies two novel loci involved in specific language impairment
    • The SLI Consortium. A genomewide scan identifies two novel loci involved in specific language impairment. Am J Hum Genet 2002;70:384-98.
    • (2002) Am J Hum Genet , vol.70 , pp. 384-398
  • 70
    • 0036201494 scopus 로고    scopus 로고
    • Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourettc Syndrome
    • Zhang H, Leckman JF, Pauls DL, Tsai CP, Kidd KK, Campos MR, Tourette Syndrome Association International Consortium for Genetics. Genomewide scan of hoarding in sib pairs in which both sibs have Gilles de la Tourettc Syndrome. Am J Hum Genet 2002;70:896-905.
    • (2002) Am J Hum Genet , vol.70 , pp. 896-905
    • Zhang, H.1    Leckman, J.F.2    Pauls, D.L.3    Tsai, C.P.4    Kidd, K.K.5    Campos, M.R.6
  • 71
    • 0029046177 scopus 로고    scopus 로고
    • Complete multipoint sib-pair analysis of qualitative and quantitative traits
    • Kruglyak L, Lander ES. Complete multipoint sib-pair analysis of qualitative and quantitative traits. Am J Hum Genet 1997;57:439-54.
    • (1997) Am J Hum Genet , vol.57 , pp. 439-454
    • Kruglyak, L.1    Lander, E.S.2
  • 74
    • 0024336203 scopus 로고
    • The UCLA-University of Utah epidemiologic survey of autism: Recurrence risk estimates and genetic counseling
    • Ritvo ER, Jorde LB, Mason-Brothers A, Freeman BJ, Pingree C, Jones MB, and others. The UCLA-University of Utah epidemiologic survey of autism: recurrence risk estimates and genetic counseling Am J Psychiatry 1989;146:1032-6.
    • (1989) Am J Psychiatry , vol.146 , pp. 1032-1036
    • Ritvo, E.R.1    Jorde, L.B.2    Mason-Brothers, A.3    Freeman, B.J.4    Pingree, C.5    Jones, M.B.6
  • 75
    • 0029872978 scopus 로고    scopus 로고
    • Autism: Towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives
    • Bailey A, Phillips W, Rutter M. Autism: towards an integration of clinical, genetic, neuropsychological, and neurobiological perspectives. J Child Psychol Psychiatry 1996;37:89-126.
    • (1996) J Child Psychol Psychiatry , vol.37 , pp. 89-126
    • Bailey, A.1    Phillips, W.2    Rutter, M.3
  • 76
    • 0035986909 scopus 로고    scopus 로고
    • Structural and functional magnetic resonance imaging of autism
    • Cody H, Pelphrey K, Piven J. Structural and functional magnetic resonance imaging of autism. Int J Dev Neurosci 2002;20:421-38.
    • (2002) Int J Dev Neurosci , vol.20 , pp. 421-438
    • Cody, H.1    Pelphrey, K.2    Piven, J.3
  • 77
    • 0000984981 scopus 로고
    • Autistic disturbances of affective contact
    • Kanner L. Autistic disturbances of affective contact. Nervous Child 1943;2:217-50.
    • (1943) Nervous Child , vol.2 , pp. 217-250
    • Kanner, L.1
  • 81
    • 0026531964 scopus 로고
    • Magnetic resonance imaging in autism: Measurement of the cerebellum, pons, and fourth ventricle
    • Piven J, Nehme E, Simon J, Barta P, Pearlson G, Folstein S. Magnetic resonance imaging in autism: measurement of the cerebellum, pons, and fourth ventricle. Biol Psychiatry 1992;31:491-504.
    • (1992) Biol Psychiatry , vol.31 , pp. 491-504
    • Piven, J.1    Nehme, E.2    Simon, J.3    Barta, P.4    Pearlson, G.5    Folstein, S.6
  • 85
    • 0035943033 scopus 로고    scopus 로고
    • Unusual brain growth patterns in early life in patients with autistic disorder: An MRI study
    • Courchesne E, Karns C, Davis H, Ziccardi R, Carper R, Tigue Z, and others. Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study. Neurology 2001;57:245-54.
    • (2001) Neurology , vol.57 , pp. 245-254
    • Courchesne, E.1    Karns, C.2    Davis, H.3    Ziccardi, R.4    Carper, R.5    Tigue, Z.6
  • 89
    • 0033973481 scopus 로고    scopus 로고
    • How can we learn about developmental processes from cross-sectional studies, or can we?
    • Kraemer HC, Yesavage JA, Taylor JL, Kupfer D. How can we learn about developmental processes from cross-sectional studies, or can we? Am J Psychiatry 2000;157:163-71.
    • (2000) Am J Psychiatry , vol.157 , pp. 163-171
    • Kraemer, H.C.1    Yesavage, J.A.2    Taylor, J.L.3    Kupfer, D.4
  • 91
    • 0035021249 scopus 로고    scopus 로고
    • Neuropeptides and neurotrophins in neonatal blood of children with autism or mental retardation
    • Nelson KB, Grether JK, Croen LA, Dambrosia JM, Dickens BF, Jellife LL, and others. Neuropeptides and neurotrophins in neonatal blood of children with autism or mental retardation. Ann Neurol 2001;49:597-606.
    • (2001) Ann Neurol , vol.49 , pp. 597-606
    • Nelson, K.B.1    Grether, J.K.2    Croen, L.A.3    Dambrosia, J.M.4    Dickens, B.F.5    Jellife, L.L.6
  • 93
    • 0029135317 scopus 로고
    • Reduced size of corpus callosum in autism
    • Egaas B, Courchesne E, Saitoh O. Reduced size of corpus callosum in autism. Arch Neurol 1995;52:794-801.
    • (1995) Arch Neurol , vol.52 , pp. 794-801
    • Egaas, B.1    Courchesne, E.2    Saitoh, O.3
  • 94
  • 97
    • 0033919413 scopus 로고    scopus 로고
    • Cerebral specialization and intrahemispheric communication: Does the corpus callosum enable the human condition?
    • Gazzinaga M. Cerebral specialization and intrahemispheric communication: does the corpus callosum enable the human condition? Brain 2000;123:1293-326.
    • (2000) Brain , vol.123 , pp. 1293-1326
    • Gazzinaga, M.1
  • 98
    • 0142022807 scopus 로고
    • Cerebral lateralization in autism: Clues to its role in language and affective development
    • Molfese DL, Segalowitz SJ, editors. New York: Guilford Press
    • Dawson G. Cerebral lateralization in autism: clues to its role in language and affective development. In: Molfese DL, Segalowitz SJ, editors. Brain lateralization in children: developmental implications. New York: Guilford Press, 1988. p 437-61.
    • (1988) Brain Lateralization in Children: Developmental Implications , pp. 437-461
    • Dawson, G.1
  • 100
  • 101
    • 0028884697 scopus 로고
    • SPECT study of the brain in childhood autism: Evidence for a lack of normal hemispheric asymmetry
    • Chiron C, Leboyer M, Leon F, Jambaque I, Nuttin C, Syrota A. SPECT study of the brain in childhood autism: evidence for a lack of normal hemispheric asymmetry. Dev Med Child Neurol 1995;37:849-60.
    • (1995) Dev Med Child Neurol , vol.37 , pp. 849-860
    • Chiron, C.1    Leboyer, M.2    Leon, F.3    Jambaque, I.4    Nuttin, C.5    Syrota, A.6
  • 103
    • 0031976207 scopus 로고    scopus 로고
    • The cerebellar cognitive affective syndrome
    • Schmahmann JD, Sherman JC. The cerebellar cognitive affective syndrome. Brain 1998;121:561-79.
    • (1998) Brain , vol.121 , pp. 561-579
    • Schmahmann, J.D.1    Sherman, J.C.2
  • 105
    • 0034122498 scopus 로고    scopus 로고
    • Inverse correlation between frontal lobe and cerebellum sizes in children with autism
    • Carper RA, Courchesne E. Inverse correlation between frontal lobe and cerebellum sizes in children with autism. Brain 2000;123:836-44.
    • (2000) Brain , vol.123 , pp. 836-844
    • Carper, R.A.1    Courchesne, E.2
  • 106
    • 0037317443 scopus 로고    scopus 로고
    • Differential effects of developmental cerebellar abnormality on cognitive and motor functions in the cerebellum: An fMRI study of autism
    • Allen G, Courchesne E. Differential effects of developmental cerebellar abnormality on cognitive and motor functions in the cerebellum: an fMRI study of autism. Am J Psychiatry 2003;160:262-73.
    • (2003) Am J Psychiatry , vol.160 , pp. 262-273
    • Allen, G.1    Courchesne, E.2
  • 109
    • 0028342512 scopus 로고
    • Medial temporal lobe structures and autism: A review of clinical and experimental findings
    • Bachevelier J. Medial temporal lobe structures and autism: a review of clinical and experimental findings. Neuropsychologia 1994;32:627-48.
    • (1994) Neuropsychologia , vol.32 , pp. 627-648
    • Bachevelier, J.1
  • 110
    • 0034950953 scopus 로고    scopus 로고
    • Development of the hippocampal formation from 2 to 42 years: MRI evidence of smaller area
    • Saitoh O, Karns C, Courchesne E. Development of the hippocampal formation from 2 to 42 years: MRI evidence of smaller area. Brain 2001;124:1317-24.
    • (2001) Brain , vol.124 , pp. 1317-1324
    • Saitoh, O.1    Karns, C.2    Courchesne, E.3
  • 112
    • 0034119076 scopus 로고    scopus 로고
    • Abnormal ventral temporal cortical activity during face discrimination among individuals with autism and Asperger syndrome
    • Schultz RT, Gauthier I, Klin A, Fulbright RK, Anderson AW, Volkmar F, and others. Abnormal ventral temporal cortical activity during face discrimination among individuals with autism and Asperger syndrome. Arch Gen Psychiatry 2000;57:331-40.
    • (2000) Arch Gen Psychiatry , vol.57 , pp. 331-340
    • Schultz, R.T.1    Gauthier, I.2    Klin, A.3    Fulbright, R.K.4    Anderson, A.W.5    Volkmar, F.6
  • 113
    • 0033763695 scopus 로고    scopus 로고
    • The functional neuroanatomy of social behaviour: Changes in cerebral blood flow when people with autistic disorder process facial expressions
    • Critchley HD, Daly EM, Bullmore ET, Williams SC, Van Amelsvoort T, Robertson DM, and others. The functional neuroanatomy of social behaviour: changes in cerebral blood flow when people with autistic disorder process facial expressions. Brain 2000;123:2203-12.
    • (2000) Brain , vol.123 , pp. 2203-2212
    • Critchley, H.D.1    Daly, E.M.2    Bullmore, E.T.3    Williams, S.C.4    Van Amelsvoort, T.5    Robertson, D.M.6
  • 114
    • 0034783917 scopus 로고    scopus 로고
    • Face processing occurs outside the fusiform 'face area' in autism: Evidence from functional MRI
    • Pierce K, Muller RA, Ambrose J, Allen G, Courchesne E. Face processing occurs outside the fusiform 'face area' in autism: evidence from functional MRI. Brain 2001;124:2059-73.
    • (2001) Brain , vol.124 , pp. 2059-2073
    • Pierce, K.1    Muller, R.A.2    Ambrose, J.3    Allen, G.4    Courchesne, E.5
  • 116
    • 0025908096 scopus 로고
    • The genetics of schizophrenia is the genetics of neurodevelopment
    • Jones P, Murray RM. The genetics of schizophrenia is the genetics of neurodevelopment. Br J Psychiatry 1991;158:615-23.
    • (1991) Br J Psychiatry , vol.158 , pp. 615-623
    • Jones, P.1    Murray, R.M.2
  • 117
    • 0037135137 scopus 로고    scopus 로고
    • Serotonin transporter genetic variation and the response of the human amygdala
    • Hariri AR, Mattay VS, Tessitore A, Kolachana B, Fera F, Goldman D, and others. Serotonin transporter genetic variation and the response of the human amygdala. Science 2002;97:400-2.
    • (2002) Science , vol.97 , pp. 400-402
    • Hariri, A.R.1    Mattay, V.S.2    Tessitore, A.3    Kolachana, B.4    Fera, F.5    Goldman, D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.