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Volumn 72, Issue , 2006, Pages 165-178

Shared Susceptibility Region On Chromosome 15 Between Autism And Catatonia

Author keywords

[No Author keywords available]

Indexed keywords

AUTISM; CATATONIC SCHIZOPHRENIA; CHROMOSOME 15; COMPARATIVE STUDY; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENETICS; HUMAN; REVIEW; SCHIZOPHRENIA;

EID: 33646269516     PISSN: 00747742     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0074-7742(05)72010-9     Document Type: Review
Times cited : (29)

References (72)
  • 1
    • 0017187975 scopus 로고
    • Catatonia. A prospective clinical study
    • Abrams R., and Taylor M.A. Catatonia. A prospective clinical study. Arch. Gen. Psychiat. 33 (1976) 579-581
    • (1976) Arch. Gen. Psychiat. , vol.33 , pp. 579-581
    • Abrams, R.1    Taylor, M.A.2
  • 2
    • 0036138102 scopus 로고    scopus 로고
    • Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families
    • Alarcon M., Cantor R.M., Liu J., Gilliam T.C., and Geschwind D.H. Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families. Am. J. Hum. Genet. 70 (2002) 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
  • 8
    • 0032231877 scopus 로고    scopus 로고
    • Comprehensive human genetic maps: Individual and sex-specific variation in recombination
    • Broman K.W., Murray J.C., Sheffield V.C., White R.L., and Weber J.L. Comprehensive human genetic maps: Individual and sex-specific variation in recombination. Am. J. Hum. Genet. 63 (1998) 861-869
    • (1998) Am. J. Hum. Genet. , vol.63 , pp. 861-869
    • Broman, K.W.1    Murray, J.C.2    Sheffield, V.C.3    White, R.L.4    Weber, J.L.5
  • 12
    • 6044246071 scopus 로고    scopus 로고
    • Variants in the catechol-O-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families
    • Chen X., Wang X., O'Neill A.F., Walsh D., and Kendler K.S. Variants in the catechol-O-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families. Mol. Psychiatr. 9 (2004) 962-967
    • (2004) Mol. Psychiatr. , vol.9 , pp. 962-967
    • Chen, X.1    Wang, X.2    O'Neill, A.F.3    Walsh, D.4    Kendler, K.S.5
  • 16
    • 0031852985 scopus 로고    scopus 로고
    • Brief report: Catatonia in autistic disorders
    • Dhossche D. Brief report: Catatonia in autistic disorders. J. Autism Dev. Disord. 28 (1998) 329-331
    • (1998) J. Autism Dev. Disord. , vol.28 , pp. 329-331
    • Dhossche, D.1
  • 18
    • 0037335094 scopus 로고    scopus 로고
    • Genetic origins of anxiety in women: A role for a functional catechol-O-methyltransferase polymorphism
    • Enoch M.A., Xu K., Ferro E., Harris C.R., and Goldman D. Genetic origins of anxiety in women: A role for a functional catechol-O-methyltransferase polymorphism. Psychiatr. Genet. 13 (2003) 33-41
    • (2003) Psychiatr. Genet. , vol.13 , pp. 33-41
    • Enoch, M.A.1    Xu, K.2    Ferro, E.3    Harris, C.R.4    Goldman, D.5
  • 23
    • 0037365978 scopus 로고    scopus 로고
    • Association between a functional catechol-O-methyltransferase gene polymorphism and schizophrenia: Meta-analysis of case-control and family-based studies
    • Glatt S.J., Faraone S.V., and Tsuang M.T. Association between a functional catechol-O-methyltransferase gene polymorphism and schizophrenia: Meta-analysis of case-control and family-based studies. Am. J. Psychiatry 160 (2003) 469-476
    • (2003) Am. J. Psychiatry , vol.160 , pp. 469-476
    • Glatt, S.J.1    Faraone, S.V.2    Tsuang, M.T.3
  • 24
    • 0041819686 scopus 로고    scopus 로고
    • CAG-repeat length in exon 1 of KCNN3 does not influence risk for schizophrenia or bipolar disorder: A meta-analysis of association studies
    • Glatt S.J., Faraone S.V., and Tsuang M.T. CAG-repeat length in exon 1 of KCNN3 does not influence risk for schizophrenia or bipolar disorder: A meta-analysis of association studies. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 121 (2003) 14-20
    • (2003) Am. J. Med. Genet. B. Neuropsychiatr. Genet. , vol.121 , pp. 14-20
    • Glatt, S.J.1    Faraone, S.V.2    Tsuang, M.T.3
  • 25
    • 6844251000 scopus 로고    scopus 로고
    • A full genome screen for autism with evidence for linkage to a region on chromosome 7q
    • IMGSAC
    • IMGSAC. A full genome screen for autism with evidence for linkage to a region on chromosome 7q. Hum. Mol. Genet. 7 (1998) 571-578
    • (1998) Hum. Mol. Genet. , vol.7 , pp. 571-578
  • 26
    • 0034883367 scopus 로고    scopus 로고
    • A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p
    • IMGSAC
    • IMGSAC. A genomewide screen for autism: Strong evidence for linkage to chromosomes 2q, 7q, and 16p. Am. J. Hum. Genet. 69 (2001) 570-581
    • (2001) Am. J. Hum. Genet. , vol.69 , pp. 570-581
  • 27
    • 0035830310 scopus 로고    scopus 로고
    • An autosomal genomic screen for autism
    • IMGSAC
    • IMGSAC. An autosomal genomic screen for autism. Am. J. Med. Genet. 105 (2001) 609-615
    • (2001) Am. J. Med. Genet. , vol.105 , pp. 609-615
  • 28
    • 3042722158 scopus 로고    scopus 로고
    • Linkage disequilibrium in the DTNBP1 (dysbindin) gene region and on chromosome 1p36 among psychotic patients from a genetic isolate in Israel: Findings from identity by descent haplotype sharing analysis
    • Kohn Y., Danilovich E., Filon D., Oppenheim A., Karni O., Kanyas K., Turetsky N., Korner M., and Lerer B. Linkage disequilibrium in the DTNBP1 (dysbindin) gene region and on chromosome 1p36 among psychotic patients from a genetic isolate in Israel: Findings from identity by descent haplotype sharing analysis. Am. J. Med. Genet. B. Neuropsychiatr. Genet. 128 (2004) 65-70
    • (2004) Am. J. Med. Genet. B. Neuropsychiatr. Genet. , vol.128 , pp. 65-70
    • Kohn, Y.1    Danilovich, E.2    Filon, D.3    Oppenheim, A.4    Karni, O.5    Kanyas, K.6    Turetsky, N.7    Korner, M.8    Lerer, B.9
  • 29
    • 0344196966 scopus 로고    scopus 로고
    • Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15
    • Kury S., Rubie C., Moisan J.P., and Stober G. Mutation analysis of the zinc transporter gene SLC30A4 reveals no association with periodic catatonia on chromosome 15q15. J. Neural. Transm. 110 (2003) 1329-1332
    • (2003) J. Neural. Transm. , vol.110 , pp. 1329-1332
    • Kury, S.1    Rubie, C.2    Moisan, J.P.3    Stober, G.4
  • 32
    • 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 IMGSAC families. The International Molecular Genetic Study of Autism Consortium
    • Maestrini E., Lai C., Marlow A., Matthews N., Wallace S., Bailey A., Cook E.H., Weeks D.E., and Monaco A.P. Serotonin transporter (5-HTT) and gamma-aminobutyric acid receptor subunit beta3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSAC families. The International Molecular Genetic Study of Autism Consortium. Am. J. Med. Genet. 88 (1999) 492-496
    • (1999) Am. J. Med. Genet. , vol.88 , pp. 492-496
    • Maestrini, E.1    Lai, C.2    Marlow, A.3    Matthews, N.4    Wallace, S.5    Bailey, A.6    Cook, E.H.7    Weeks, D.E.8    Monaco, A.P.9
  • 38
    • 85047697752 scopus 로고    scopus 로고
    • Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus
    • Meyer J., Ortega G., Schraut K., Nurnberg G., Ruschendorf F., Saar K., Mossner R., Wienker T.F., Reis A., Stober G., and Lesch K.P. Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus. Mol. Psychiatr. 7 (2002) 220-223
    • (2002) Mol. Psychiatr. , vol.7 , pp. 220-223
    • Meyer, J.1    Ortega, G.2    Schraut, K.3    Nurnberg, G.4    Ruschendorf, F.5    Saar, K.6    Mossner, R.7    Wienker, T.F.8    Reis, A.9    Stober, G.10    Lesch, K.P.11
  • 39
    • 0033637841 scopus 로고    scopus 로고
    • Molecular characterization of schizophrenia viewed by microarray analysis of gene expression in prefrontal cortex
    • Mirnics K., Middleton F.A., Marquez A., Lewis D.A., and Levitt P. Molecular characterization of schizophrenia viewed by microarray analysis of gene expression in prefrontal cortex. Neuron 28 (2000) 53-67
    • (2000) Neuron , vol.28 , pp. 53-67
    • Mirnics, K.1    Middleton, F.A.2    Marquez, A.3    Lewis, D.A.4    Levitt, P.5
  • 40
    • 0042611650 scopus 로고    scopus 로고
    • Genomic organization and single-nucleotide polymorphism map of desmuslin, a novel intermediate filament protein on chromosome 15q26.3
    • Mizuno Y., Puca A.A., O'Brien K.F., Beggs A.H., and Kunkel L.M. Genomic organization and single-nucleotide polymorphism map of desmuslin, a novel intermediate filament protein on chromosome 15q26.3. BMC Genet. 2 (2001) 8
    • (2001) BMC Genet. , vol.2 , pp. 8
    • Mizuno, Y.1    Puca, A.A.2    O'Brien, K.F.3    Beggs, A.H.4    Kunkel, L.M.5
  • 47
    • 0035826542 scopus 로고    scopus 로고
    • GABA-A receptor beta3 and alpha5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: A genetic association study
    • Papadimitriou G.N., Dikeos D.G., Karadima G., Avramopoulos D., Daskalopoulou E.G., and Stefanis C.N. GABA-A receptor beta3 and alpha5 subunit gene cluster on chromosome 15q11-q13 and bipolar disorder: A genetic association study. Am. J. Med. Genet. 105 (2001) 317-320
    • (2001) Am. J. Med. Genet. , vol.105 , pp. 317-320
    • Papadimitriou, G.N.1    Dikeos, D.G.2    Karadima, G.3    Avramopoulos, D.4    Daskalopoulou, E.G.5    Stefanis, C.N.6
  • 49
    • 0035856428 scopus 로고    scopus 로고
    • Postmortem brain abnormalities of the glutamate neurotransmitter system in autism
    • Purcell A.E., Jeon O.H., Zimmerman A.W., Blue M.E., and Pevsner J. Postmortem brain abnormalities of the glutamate neurotransmitter system in autism. Neurology 57 (2001) 1618-1628
    • (2001) Neurology , vol.57 , pp. 1618-1628
    • Purcell, A.E.1    Jeon, O.H.2    Zimmerman, A.W.3    Blue, M.E.4    Pevsner, J.5
  • 51
    • 0026348447 scopus 로고
    • Catatonia in autistic disorder: A sign of comorbidity or variable expression?
    • Realmuto G.M., and August G.J. Catatonia in autistic disorder: A sign of comorbidity or variable expression?. J. Autism Dev. Disord. 21 (1991) 517-528
    • (1991) J. Autism Dev. Disord. , vol.21 , pp. 517-528
    • Realmuto, G.M.1    August, G.J.2
  • 53
    • 8844248677 scopus 로고    scopus 로고
    • Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: Association is more significant in women
    • Sazci A., Ergul E., Kucukali I., Kilic G., Kaya G., and Kara I. Catechol-O-methyltransferase gene Val108/158Met polymorphism, and susceptibility to schizophrenia: Association is more significant in women. Brain. Res. Mol. Brain. Res. 132 (2004) 51-56
    • (2004) Brain. Res. Mol. Brain. Res. , vol.132 , pp. 51-56
    • Sazci, A.1    Ergul, E.2    Kucukali, I.3    Kilic, G.4    Kaya, G.5    Kara, I.6
  • 57
    • 0034606205 scopus 로고    scopus 로고
    • Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: Identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13
    • Smith M., Filipek P.A., Wu C., Bocian M., Hakim S., Modahl C., and Spence M.A. Analysis of a 1-megabase deletion in 15q22-q23 in an autistic patient: Identification of candidate genes for autism and of homologous DNA segments in 15q22-q23 and 15q11-q13. Am. J. Med. Genet. 96 (2000) 765-770
    • (2000) Am. J. Med. Genet. , vol.96 , pp. 765-770
    • Smith, M.1    Filipek, P.A.2    Wu, C.3    Bocian, M.4    Hakim, S.5    Modahl, C.6    Spence, M.A.7
  • 58
  • 62
    • 0036780845 scopus 로고    scopus 로고
    • Periodic catatonia: Confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity
    • Stöber G., Seelow D., Ruschendorf F., Ekici A., Beckmann H., and Reis A. Periodic catatonia: Confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity. Hum. Genet. 111 (2002) 323-330
    • (2002) Hum. Genet. , vol.111 , pp. 323-330
    • Stöber, G.1    Seelow, D.2    Ruschendorf, F.3    Ekici, A.4    Beckmann, H.5    Reis, A.6
  • 65
    • 0035957960 scopus 로고    scopus 로고
    • N-methyl-D-aspartate receptors regulate a group of transiently expressed genes in the developing brain
    • Sugiura N., Patel R.G., and Corriveau R.A. N-methyl-D-aspartate receptors regulate a group of transiently expressed genes in the developing brain. J. Biol. Chem. 276 (2001) 14,257-14,263
    • (2001) J. Biol. Chem. , vol.276
    • Sugiura, N.1    Patel, R.G.2    Corriveau, R.A.3
  • 67
    • 0038235907 scopus 로고    scopus 로고
    • Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families
    • van den Oord E.J., Sullivan P.F., Jiang Y., Walsh D., O'Neill F.A., Kendler K.S., and Riley B.P. Identification of a high-risk haplotype for the dystrobrevin binding protein 1 (DTNBP1) gene in the Irish study of high-density schizophrenia families. Mol. Psychiatr. 8 (2003) 499-510
    • (2003) Mol. Psychiatr. , vol.8 , pp. 499-510
    • van den Oord, E.J.1    Sullivan, P.F.2    Jiang, Y.3    Walsh, D.4    O'Neill, F.A.5    Kendler, K.S.6    Riley, B.P.7
  • 69
    • 0033625728 scopus 로고    scopus 로고
    • Catatonia in autistic spectrum disorders
    • Wing L., and Shah A. Catatonia in autistic spectrum disorders. Br. J. Psychiatry 176 (2000) 357-362
    • (2000) Br. J. Psychiatry , vol.176 , pp. 357-362
    • Wing, L.1    Shah, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.