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Volumn 12, Issue 2, 1999, Pages 55-63

The Role of Genetics in Autism

Author keywords

Autism; Genetic studies; Genome screen; Multiplex families

Indexed keywords


EID: 0008406807     PISSN: 08963746     EISSN: None     Source Type: Journal    
DOI: 10.1097/00001163-199910000-00007     Document Type: Article
Times cited : (5)

References (35)
  • 1
    • 0000984981 scopus 로고
    • Autistic disturbances of affective contact
    • Kanner L. Autistic disturbances of affective contact. Nervous Child. 1943;2:217-250.
    • (1943) Nervous Child , vol.2 , pp. 217-250
    • Kanner, L.1
  • 2
    • 0031563047 scopus 로고    scopus 로고
    • Autism
    • Rapin I. Autism. NEJM. 1997;337:97-103.
    • (1997) NEJM , vol.337 , pp. 97-103
    • Rapin, I.1
  • 3
    • 0027101924 scopus 로고
    • The validity of autistic spectrum disorders: A literature review
    • Szatmari P. The validity of autistic spectrum disorders: A literature review. J Aut Dev Disord. 1992;22:583-600.
    • (1992) J Aut Dev Disord. , vol.22 , pp. 583-600
    • Szatmari, P.1
  • 6
    • 0032454027 scopus 로고    scopus 로고
    • Chromosomal disorders and autism
    • Gillberg C. Chromosomal disorders and autism. J Aut Dev Disord. 1998;28:415-425.
    • (1998) J Aut Dev Disord. , vol.28 , pp. 415-425
    • Gillberg, C.1
  • 7
    • 0032461803 scopus 로고    scopus 로고
    • Autism: The point of view from autism studies
    • Feinstein C, Reiss A. Autism: The point of view from autism studies. J Aut Dev Disord. 1998;28:393-405.
    • (1998) J Aut Dev Disord. , vol.28 , pp. 393-405
    • Feinstein, C.1    Reiss, A.2
  • 8
    • 0032453497 scopus 로고    scopus 로고
    • Autism and tuberous sclerosis
    • Smalley S.Autism and tuberous sclerosis. J Aut DevDisord. 1998;28:407-414.
    • (1998) J Aut DevDisord. , vol.28 , pp. 407-414
    • Smalley, S.1
  • 14
    • 0025008677 scopus 로고
    • Linkage studies for genetically complex traits. II. The power of affected sib pairs
    • Risch N. Linkage studies for genetically complex traits. II. The power of affected sib pairs. Am J Human Genet. 1990;46:229-241.
    • (1990) Am J Human Genet. , vol.46 , pp. 229-241
    • Risch, N.1
  • 15
    • 0025355888 scopus 로고
    • Genetic linkage and complex diseases, with special reference to psychiatric disorders
    • Risch N. Genetic linkage and complex diseases, with special reference to psychiatric disorders. Genet Epidemiol. 1990;7:1-16.
    • (1990) Genet Epidemiol. , vol.7 , pp. 1-16
    • Risch, N.1
  • 16
    • 0032461804 scopus 로고    scopus 로고
    • Finding specific genes that cause autism: A combination of approaches will be needed to maximize power
    • Folstein SE, Bisson E, Santangelo SL, Piven J. Finding specific genes that cause autism: A combination of approaches will be needed to maximize power. J Aut Dev Disord. 1998;28:439-445.
    • (1998) J Aut Dev Disord. , vol.28 , pp. 439-445
    • Folstein, S.E.1    Bisson, E.2    Santangelo, S.L.3    Piven, J.4
  • 17
    • 0030773652 scopus 로고    scopus 로고
    • Diagnosing autism: Analyses of data from the Autism Diagnostic Interview
    • Lord C, Pickles A, McLennan J, et al. Diagnosing autism: Analyses of data from the Autism Diagnostic Interview. J Aut Dev Disord. 1997;27:501-517.
    • (1997) J Aut Dev Disord. , vol.27 , pp. 501-517
    • Lord, C.1    Pickles, A.2    McLennan, J.3
  • 18
    • 0027997172 scopus 로고
    • Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
    • Lord C, Rutter M, LeCouteur A. Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Aut Dev Disord. 1994;24:659-685
    • (1994) J Aut Dev Disord. , vol.24 , pp. 659-685
    • Lord, C.1    Rutter, M.2    LeCouteur, A.3
  • 19
    • 0028012565 scopus 로고
    • Genetics of autism: Characteristics of affected and unaffected children from 37 multiplex families
    • Spiker D, Lotspeich L, Kraemer HC, et al. Genetics of autism: Characteristics of affected and unaffected children from 37 multiplex families. Am J Med Genet: Neuropsychia Genet. 1994;54:27-35.
    • (1994) Am J Med Genet: Neuropsychia Genet. , vol.54 , pp. 27-35
    • Spiker, D.1    Lotspeich, L.2    Kraemer, H.C.3
  • 20
    • 0028171490 scopus 로고
    • Molecular analysis and test for linkage between the FMR-1 gene and infantile autism in multiplex families
    • Hallmayer J, Pintado E, Lin A, et al. Molecular analysis and test for linkage between the FMR-1 gene and infantile autism in multiplex families. American Journal of Human Genet. 1994;55:951-959.
    • (1994) American Journal of Human Genet. , vol.55 , pp. 951-959
    • Hallmayer, J.1    Pintado, E.2    Lin, A.3
  • 22
    • 0041122971 scopus 로고
    • Autism and pervasive developmental disorders
    • Bloom FE, Kupfer DJ, eds. New York: Raven Press
    • Lotspeich LJ. Autism and pervasive developmental disorders. In: Bloom FE, Kupfer DJ, eds. Psychopharmacology: The Fourth Generation of Progress. New York: Raven Press; 1995: 1653-1663.
    • (1995) Psychopharmacology: The Fourth Generation of Progress , pp. 1653-1663
    • Lotspeich, L.J.1
  • 23
    • 8244234472 scopus 로고    scopus 로고
    • Evidence of linkage between the serotonin transporter and autistic disorder
    • Cook Jr EH, Courchesne RY, Lord C, et. Evidence of linkage between the serotonin transporter and autistic disorder. Mole Psychia. 1997;2:247-250.
    • (1997) Mole Psychia. , vol.2 , pp. 247-250
    • Cook Jr., E.H.1    Courchesne, R.Y.2    Lord, C.3
  • 25
    • 16944364326 scopus 로고    scopus 로고
    • Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
    • Cook Jr H, Lindgren V, Leventhal BL, et al. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Human Genet. 1997;60:928-934.
    • (1997) Am J Human Genet. , vol.60 , pp. 928-934
    • Cook Jr., H.1    Lindgren, V.2    Leventhal, B.L.3
  • 26
    • 17344364660 scopus 로고    scopus 로고
    • Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers
    • Cook Jr EH, Courchesne RY, Cox NJ, et al. Linkage-disequilibrium mapping of autistic disorder, with 15q11-13 markers. Am J Human Genet. 1998;62:1077-1083.
    • (1998) Am J Human Genet. , vol.62 , pp. 1077-1083
    • Cook Jr., E.H.1    Courchesne, R.Y.2    Cox, N.J.3
  • 27
    • 0001777849 scopus 로고    scopus 로고
    • Linkage evidence supports the involvement of chromosome 15 in autistic disorder (AUT)
    • Pericak-Vance MA, Wolpert CM, Menold MM, et al. Linkage evidence supports the involvement of chromosome 15 in autistic disorder (AUT). Am J Human Genet. Suppl. 1997;A40:208.
    • (1997) Am J Human Genet. , vol.A40 , Issue.SUPPL. , pp. 208
    • Pericak-Vance, M.A.1    Wolpert, C.M.2    Menold, M.M.3
  • 28
    • 85034562292 scopus 로고    scopus 로고
    • Absence of linkage to chromosome 15q11-q13 markers in ninety multiplex families with autism
    • In press
    • Salmon B, Hallmayer J, Rogers T, et al. Absence of linkage to chromosome 15q11-q13 markers in ninety multiplex families with autism. Neuropsychia Genet. In press.
    • Neuropsychia Genet.
    • Salmon, B.1    Hallmayer, J.2    Rogers, T.3
  • 29
    • 0030200135 scopus 로고    scopus 로고
    • Strong association of the third hypervariable region of HLA-DRB1 with autism
    • Warren RP, Odell JD, Warren L, et al. Strong association of the third hypervariable region of HLA-DRB1 with autism. J Neuroimmun. 1996;67:97-102.
    • (1996) J Neuroimmun. , vol.67 , pp. 97-102
    • Warren, R.P.1    Odell, J.D.2    Warren, L.3
  • 31
    • 0029120604 scopus 로고
    • Increased frequency of the extended or ancestral Haplotype B44-SC30-DR4 in autism
    • Daniels WW, Warren RP, Odell J.D, et al. Increased frequency of the extended or ancestral Haplotype B44-SC30-DR4 in autism. Neuropsychobio. 1995;32:120-123.
    • (1995) Neuropsychobio , vol.32 , pp. 120-123
    • Daniels, W.W.1    Warren, R.P.2    Odell, J.D.3
  • 32
    • 85031582946 scopus 로고    scopus 로고
    • Exclusion of linkage to the HLA region in ninety multiplex sibships with autism
    • In press
    • Rogers T, Kalaydjieva L, Hallmayer J, et al. Exclusion of linkage to the HLA region in ninety multiplex sibships with autism. J Aut Dev Disord. In press.
    • J Aut Dev Disord.
    • Rogers, T.1    Kalaydjieva, L.2    Hallmayer, J.3
  • 34
    • 6844251000 scopus 로고    scopus 로고
    • A full genome screen for autism with evidence of linkage to a region of chromosome 7p
    • International Molecular Genetic Study of Autism Consortium. A full genome screen for autism with evidence of linkage to a region of chromosome 7p. Human Mole Gene. 1998;7:571-578.
    • (1998) Human Mole Gene , vol.7 , pp. 571-578
  • 35
    • 0033362024 scopus 로고    scopus 로고
    • A genomic screen of autism: Evidence for polygenic inheritance
    • Risch R, Spiker D, Lotspeich L, et al. A genomic screen of autism: Evidence for polygenic inheritance. Am J Human Genet. 1999;65:493-507.
    • (1999) Am J Human Genet. , vol.65 , pp. 493-507
    • Risch, R.1    Spiker, D.2    Lotspeich, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.