메뉴 건너뛰기




Volumn 117 B, Issue 1, 2003, Pages 90-96

Defining the autism minimum candidate gene region on chromosome 7

Author keywords

Association analysis; Haplotype sharing; Microsatellite markers; Recombination breakpoint mapping

Indexed keywords

ARTICLE; AUTISM; CHROMOSOME 7Q; GENE MAPPING; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC RECOMBINATION; GENETIC SUSCEPTIBILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MICROSATELLITE MARKER; PRIORITY JOURNAL;

EID: 0042823957     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.10033     Document Type: Article
Times cited : (30)

References (44)
  • 1
    • 0004235298 scopus 로고
    • DSM-IV. Washington, DC: American Psychiatric Press, Inc
    • American Psychiatric Association. 1994. Diagnostic and statistical manual of mental disorders. DSM-IV. Washington, DC: American Psychiatric Press, Inc.
    • (1994) Diagnostic and Statistical Manual of Mental Disorders
  • 4
    • 0025835296 scopus 로고
    • Fast and sensitive silver staining of DNA in polyacrylamide gels
    • Bassam BJ, Caetano-Anolles G, Gresshoff PM. 1991. Fast and sensitive silver staining of DNA in polyacrylamide gels. Ann Biochem 196:80-83.
    • (1991) Ann Biochem , vol.196 , pp. 80-83
    • Bassam, B.J.1    Caetano-Anolles, G.2    Gresshoff, P.M.3
  • 7
    • 0033573212 scopus 로고    scopus 로고
    • An autosomal genomic screen for autism. Collaborative linkage study of autism
    • Collaborative Linkage Study of Autism. 1999. An autosomal genomic screen for autism. Collaborative linkage study of autism. Am J Med Genet 88:609-615.
    • (1999) Am J Med Genet , vol.88 , pp. 609-615
  • 8
    • 0013654741 scopus 로고    scopus 로고
    • Oxford: Cherwell Scientific Publishing
    • Cyrillic version 2.1. 1997. Cyrillic version 2.1. Oxford: Cherwell Scientific Publishing.
    • (1997) Cyrillic Version 2.1
  • 9
    • 0035653670 scopus 로고    scopus 로고
    • Genetics of autism: Complex aetiology for a heterogeneous disorder
    • Folstein SE, Rosen-Sheidley B. 2001. Genetics of autism: Complex aetiology for a heterogeneous disorder. Nat Rev Genet 2:943-955.
    • (2001) Nat Rev Genet , vol.2 , pp. 943-955
    • Folstein, S.E.1    Rosen-Sheidley, B.2
  • 10
    • 0032804766 scopus 로고    scopus 로고
    • The epidemiology of autism: A review
    • Fombonne E. 1999. The epidemiology of autism: A review. Psychol Med 29:769-786.
    • (1999) Psychol Med , vol.29 , pp. 769-786
    • Fombonne, E.1
  • 11
    • 0032975478 scopus 로고    scopus 로고
    • Autism: Not an extremely rare disorder
    • Gillberg C, Wing L. 1999. Autism: Not an extremely rare disorder. Acta Psychiatr Scand 99:399-406.
    • (1999) Acta Psychiatr Scand , vol.99 , pp. 399-406
    • Gillberg, C.1    Wing, L.2
  • 12
    • 0035162422 scopus 로고    scopus 로고
    • The null distribution of the heterogeneity lod score does depend on the assumed genetic model for the trait
    • Huang J, Vieland VJ. 2001. The null distribution of the heterogeneity lod score does depend on the assumed genetic model for the trait. Hum Hered 52:217-222.
    • (2001) Hum Hered , vol.52 , pp. 217-222
    • Huang, J.1    Vieland, V.J.2
  • 14
    • 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. 1998. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum Mol Genet 7:571-578.
    • (1998) Hum Mol Genet , vol.7 , pp. 571-578
  • 16
    • 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. 2001. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413:519-523.
    • (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
  • 20
  • 21
    • 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. 1994. Autism diagnostic interview-revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord 24:659-685.
    • (1994) J Autism Dev Disord , vol.24 , pp. 659-685
    • Lord, C.1    Rutter, M.2    LeCouteur, A.3
  • 22
    • 0030772982 scopus 로고    scopus 로고
    • Tests for linkage and association in nuclear families
    • Martin ER, Kaplan NL, Weir BS. 1997. Tests for linkage and association in nuclear families. Am J Hum Genet 61:439-448.
    • (1997) Am J Hum Genet , vol.61 , pp. 439-448
    • Martin, E.R.1    Kaplan, N.L.2    Weir, B.S.3
  • 23
    • 0033910787 scopus 로고    scopus 로고
    • A test for linkage and association in general pedigrees: The pedigree disequilibrium test
    • Martin ER, Monks SA, Warren LL, Kaplan NL. 2000. A test for linkage and association in general pedigrees: The pedigree disequilibrium test. Am J Hum Genet 67(1):146-154.
    • (2000) Am J Hum Genet , vol.67 , Issue.1 , pp. 146-154
    • Martin, E.R.1    Monks, S.A.2    Warren, L.L.3    Kaplan, N.L.4
  • 28
    • 0029134874 scopus 로고
    • Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: A twin and family history study of autism
    • Pickles A, Bolton P, Macdonald H, Bailey A, Le Couteur A, Sim CH, Rutter M. 1995. Latent-class analysis of recurrence risks for complex phenotypes with selection and measurement error: A twin and family history study of autism. Am J Hum Genet 57:717-726.
    • (1995) Am J Hum Genet , vol.57 , pp. 717-726
    • Pickles, A.1    Bolton, P.2    Macdonald, H.3    Bailey, A.4    Le Couteur, A.5    Sim, C.H.6    Rutter, M.7
  • 32
    • 0029935399 scopus 로고    scopus 로고
    • Estimating linkage heterogeneity
    • Smith CA, Stephens DA. 1996. Estimating linkage heterogeneity. Ann Hum Genet 60(Pt 2):161-169.
    • (1996) Ann Hum Genet , vol.60 , Issue.PART 2 , pp. 161-169
    • Smith, C.A.1    Stephens, D.A.2
  • 33
    • 0029945706 scopus 로고    scopus 로고
    • Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics
    • Sobel E, Lange K. 1996. Descent graphs in pedigree analysis: Applications to haplotyping, location scores, and marker-sharing statistics. Am J Hum Genet 58:1323-1337.
    • (1996) Am J Hum Genet , vol.58 , pp. 1323-1337
    • Sobel, E.1    Lange, K.2
  • 36
    • 0035829982 scopus 로고    scopus 로고
    • A balanced reciprocal translocation t(5; 7)(q14;q32) associated with autistic disorder: Molecular analysis of the chromosome 7 breakpoint
    • Tentler D, Brandberg G, Betancur C, Gillberg C, Anneren G, Orsmark C, Green ED, Carlsson B, Dahl N. 2001. A balanced reciprocal translocation t(5; 7)(q14;q32) associated with autistic disorder: Molecular analysis of the chromosome 7 breakpoint. Am J Med Genet 105:729-736.
    • (2001) Am J Med Genet , vol.105 , pp. 729-736
    • Tentler, D.1    Brandberg, G.2    Betancur, C.3    Gillberg, C.4    Anneren, G.5    Orsmark, C.6    Green, E.D.7    Carlsson, B.8    Dahl, N.9
  • 37
    • 18244408330 scopus 로고    scopus 로고
    • A genomewide scan identifies two novel loci involved in specific language impairment
    • The SLI Consortium. 2002. A genomewide scan identifies two novel loci involved in specific language impairment. Am J Hum Genet 70:384-398.
    • (2002) Am J Hum Genet , vol.70 , pp. 384-398
  • 39
    • 4243283491 scopus 로고    scopus 로고
    • Identification of genes at translocation breakpoints on chromosome 7q31 in autistic individuals
    • Vincent JB, Herbrick JA, Gurling HMD, Scherer SW. 1999. Identification of genes at translocation breakpoints on chromosome 7q31 in autistic individuals. Am J Hum Genet (Suppl)64:A471.
    • (1999) Am J Hum Genet (Suppl) , vol.64
    • Vincent, J.B.1    Herbrick, J.A.2    Gurling, H.M.D.3    Scherer, S.W.4
  • 40
    • 0033859129 scopus 로고    scopus 로고
    • Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual
    • Vincent JB, Herbrick JA, Gurling HM, Bolton PF, Roberts W, Scherer SW. 2000. Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual. Am J Hum Genet 67:510-514.
    • (2000) Am J Hum Genet , vol.67 , pp. 510-514
    • Vincent, J.B.1    Herbrick, J.A.2    Gurling, H.M.3    Bolton, P.F.4    Roberts, W.5    Scherer, S.W.6
  • 41
    • 0034599736 scopus 로고    scopus 로고
    • Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31
    • Warburton P, Baird G, Chen W, Morris K, Jacobs BW, Hodgson S, Docherty Z. 2000. Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31. Am J Med Genet 96:228-234.
    • (2000) Am J Med Genet , vol.96 , pp. 228-234
    • Warburton, P.1    Baird, G.2    Chen, W.3    Morris, K.4    Jacobs, B.W.5    Hodgson, S.6    Docherty, Z.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.