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Volumn 126 B, Issue 1, 2004, Pages 58-65

Modifier Effects in Autism at the MAO-A and DBH Loci

Author keywords

Autism; Catecholamires; DBH; Genetics; MAO A

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME A; CATECHOLAMINE DERIVATIVE; DOPAMINE BETA MONOOXYGENASE;

EID: 1842591872     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.20172     Document Type: Article
Times cited : (35)

References (55)
  • 4
    • 0023081468 scopus 로고
    • Monoamines in autism: An update of neurochemical research on a pervasive developmental disorder
    • Anderson GM. 1987. Monoamines in autism: An update of neurochemical research on a pervasive developmental disorder. Med Biol 65:67-74.
    • (1987) Med Biol , vol.65 , pp. 67-74
    • Anderson, G.M.1
  • 7
    • 0025115605 scopus 로고
    • Autism: Review of neurochemical investigation
    • Cook EH. 1990. Autism: Review of neurochemical investigation. Synapse 6:292-308.
    • (1990) Synapse , vol.6 , pp. 292-308
    • Cook, E.H.1
  • 11
    • 0032718084 scopus 로고    scopus 로고
    • Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene
    • Dean JC, Moore SJ, Osborne A, Howe J, Turnpenny PD. 1999. Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene. Clin Genet 56(3):216-220.
    • (1999) Clin Genet , vol.56 , Issue.3 , pp. 216-220
    • Dean, J.C.1    Moore, S.J.2    Osborne, A.3    Howe, J.4    Turnpenny, P.D.5
  • 13
    • 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(12):943-955.
    • (2001) Nat Rev Genet , vol.2 , Issue.12 , pp. 943-955
    • Folstein, S.E.1    Rosen-Sheidley, B.2
  • 15
    • 0034881171 scopus 로고    scopus 로고
    • Full-genome scans with autistic disorder: A review
    • Gutknecht L. 2001. Full-genome scans with autistic disorder: A review. Behav Genet 31(1):113-123.
    • (2001) Behav Genet , vol.31 , Issue.1 , pp. 113-123
    • Gutknecht, L.1
  • 16
    • 0017687903 scopus 로고
    • Hyperserotonemia and amine metabolites in autistic and retarded children
    • Hanley HG, Stahl SM, Freedman DX. 1977. Hyperserotonemia and amine metabolites in autistic and retarded children. Arch Gen Psychiatry 34:521-531.
    • (1977) Arch Gen Psychiatry , vol.34 , pp. 521-531
    • Hanley, H.G.1    Stahl, S.M.2    Freedman, D.X.3
  • 18
    • 0034309859 scopus 로고    scopus 로고
    • Genotype to phenotype: Challenges and opportunities
    • Holschneider DP, Shih JC. 2000. Genotype to phenotype: Challenges and opportunities. Int J Dev Neurosci 18(6):615-618.
    • (2000) Int J Dev Neurosci , vol.18 , Issue.6 , pp. 615-618
    • Holschneider, D.P.1    Shih, J.C.2
  • 19
    • 0031889466 scopus 로고    scopus 로고
    • Modifer genes in humans: Strategies for identification
    • Houlston RS, Tomlinson IP. 1998. Modifer genes in humans: Strategies for identification. Eur J Hum Genet 6(1):80-88.
    • (1998) Eur J Hum Genet , vol.6 , Issue.1 , pp. 80-88
    • Houlston, R.S.1    Tomlinson, I.P.2
  • 20
    • 0025727617 scopus 로고
    • Expression of two forms of human dopamine β-hydroxylase in COS cells
    • Ishii A, Kobayashi K, Kiuchi K, Nagatsu T. 1991. Expression of two forms of human dopamine β-hydroxylase in COS cells. Neurosci Lett 125:25-28.
    • (1991) Neurosci Lett , vol.125 , pp. 25-28
    • Ishii, A.1    Kobayashi, K.2    Kiuchi, K.3    Nagatsu, T.4
  • 22
    • 0021921891 scopus 로고
    • Serotonin relationships of autistic probands and their first-degree relatives
    • Kuperman S, Beeghly JH, Burns TL, Tsai LY. 1985. Serotonin relationships of autistic probands and their first-degree relatives. J Am Acad Child Psychiatry 24(2):186-190.
    • (1985) J Am Acad Child Psychiatry , vol.24 , Issue.2 , pp. 186-190
    • Kuperman, S.1    Beeghly, J.H.2    Burns, T.L.3    Tsai, L.Y.4
  • 23
    • 0023127061 scopus 로고
    • Association of serotonin concentration to behavior and IQ in autistic children
    • Kuperman S, Beeghly JH, Burns TL, Tsai L. 1987. Association of serotonin concentration to behavior and IQ in autistic children. J Autism Dev Disord 17:133-140.
    • (1987) J Autism Dev Disord , vol.17 , pp. 133-140
    • Kuperman, S.1    Beeghly, J.H.2    Burns, T.L.3    Tsai, L.4
  • 26
    • 0021040495 scopus 로고
    • Effects of untreated maternal phenylketonuria and hyperphenylalaninenemia on the fetus
    • Levy HL, Waisbren SE. 1983. Effects of untreated maternal phenylketonuria and hyperphenylalaninenemia on the fetus. N Engl J Med 309:1269-1274.
    • (1983) N Engl J Med , vol.309 , pp. 1269-1274
    • Levy, H.L.1    Waisbren, S.E.2
  • 28
    • 0024369122 scopus 로고
    • Autism diagnostic observation schedule: A standardized observation of communicative and social behavior
    • Lord C, Rutter M, Goode S, Heemsbergen J, Jordan H, Mawhood L, Scholper E. 1989. Autism diagnostic observation schedule: A standardized observation of communicative and social behavior. J Autism Dev Disord 19(2):185-212.
    • (1989) J Autism Dev Disord , vol.19 , Issue.2 , pp. 185-212
    • Lord, C.1    Rutter, M.2    Goode, S.3    Heemsbergen, J.4    Jordan, H.5    Mawhood, L.6    Scholper, E.7
  • 29
    • 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, Le Couteur A. 1994. Autism Diagnostic Interview-Revised: A revised version of a diagnostic interview for caregivers of individuals with possible Pervasive Developmental Disorders. J Aut Dev Disord 24:659-685.
    • (1994) J Aut Dev Disord , vol.24 , pp. 659-685
    • Lord, C.1    Rutter, M.2    Le Couteur, A.3
  • 30
    • 0033802632 scopus 로고    scopus 로고
    • The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism
    • Lord C, Risi S, Lambrecht L, Cook EH Jr, Leventhal BL, DiLavore P, Pickles A, Rutter M. 2000. The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disord 30(3):205-223.
    • (2000) J Autism Dev Disord , vol.30 , Issue.3 , pp. 205-223
    • Lord, C.1    Risi, S.2    Lambrecht, L.3    Cook Jr., E.H.4    Leventhal, B.L.5    DiLavore, P.6    Pickles, A.7    Rutter, M.8
  • 33
    • 0027397393 scopus 로고
    • Phenylketonuria due to phenylalanine hydroxylase deficiency: An unfolding story. Education and debate
    • Medical Research Council Working Party on Phenylketonuria. 1993. Phenylketonuria due to phenylalanine hydroxylase deficiency: An unfolding story. Education and debate. BMJ 306:115-119.
    • (1993) BMJ , vol.306 , pp. 115-119
  • 34
    • 0031051256 scopus 로고    scopus 로고
    • Did Asperger's cases have Asperger disorder? A research note
    • Miller JN, Ozonoff S. 1997. Did Asperger's cases have Asperger disorder? A research note. J Child Psychol Psychiatry 38(2):247-251.
    • (1997) J Child Psychol Psychiatry , vol.38 , Issue.2 , pp. 247-251
    • Miller, J.N.1    Ozonoff, S.2
  • 35
    • 0030938599 scopus 로고    scopus 로고
    • Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium
    • Mitchell LE. 1997. Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium. Am J Hum Genet 60(4):1006-1007.
    • (1997) Am J Hum Genet , vol.60 , Issue.4 , pp. 1006-1007
    • Mitchell, L.E.1
  • 36
    • 0035287508 scopus 로고    scopus 로고
    • Modifer genes in mice and humans
    • Nadeau JH. 2001. Modifer genes in mice and humans. Nat Rev Genet 2(3):165-174.
    • (2001) Nat Rev Genet , vol.2 , Issue.3 , pp. 165-174
    • Nadeau, J.H.1
  • 37
    • 0042318559 scopus 로고    scopus 로고
    • Genetics: Modifying the message
    • Nadeau JH. 2003. Genetics: Modifying the message. Science 301(5635):927-928.
    • (2003) Science , vol.301 , Issue.5635 , pp. 927-928
    • Nadeau, J.H.1
  • 39
    • 0035825185 scopus 로고    scopus 로고
    • The broad autism phenotype: A complementary strategy for molecular genetic studies of autism
    • Piven J. 2001. The broad autism phenotype: A complementary strategy for molecular genetic studies of autism. Am J Med Genet 105(1):34-35.
    • (2001) Am J Med Genet , vol.105 , Issue.1 , pp. 34-35
    • Piven, J.1
  • 40
    • 0031711343 scopus 로고    scopus 로고
    • A functional polymorphism in the monoamine oxidase A gene promoter
    • Sabol SZ, Hu S, Hamer D. 1998. A functional polymorphism in the monoamine oxidase A gene promoter. Hum Genet 103:273-279.
    • (1998) Hum Genet , vol.103 , pp. 273-279
    • Sabol, S.Z.1    Hu, S.2    Hamer, D.3
  • 41
    • 0027367005 scopus 로고
    • Genotype relative risks: Methods for design and analysis of candidate-gene association studies
    • Schaid DJ, Sommer SS. 1993. Genotype relative risks: Methods for design and analysis of candidate-gene association studies. Am J Hum Genet 53:1114-1126.
    • (1993) Am J Hum Genet , vol.53 , pp. 1114-1126
    • Schaid, D.J.1    Sommer, S.S.2
  • 43
    • 0027377799 scopus 로고
    • Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
    • Spielman RS, McGinnis RE, Ewens WJ. 1993. Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 52(3):506-516.
    • (1993) Am J Hum Genet , vol.52 , Issue.3 , pp. 506-516
    • Spielman, R.S.1    McGinnis, R.E.2    Ewens, W.J.3
  • 44
    • 0037297040 scopus 로고    scopus 로고
    • Stability and change among high functioning children with pervasive developmental disorders: A two-year outcome study
    • Starr E, Szatmari P, Bryson SE, Zwaigenbaum L. 2003. Stability and change among high functioning children with pervasive developmental disorders: A two-year outcome study. J Aut Develop Disord 33(1):15-22.
    • (2003) J Aut Develop Disord , vol.33 , Issue.1 , pp. 15-22
    • Starr, E.1    Szatmari, P.2    Bryson, S.E.3    Zwaigenbaum, L.4
  • 45
    • 0014106330 scopus 로고
    • Congenital malformations in offspring of phenylketonuric mothers
    • Stevenson RE, Huntley CC. 1967. Congenital malformations in offspring of phenylketonuric mothers. Pediatrics 40(1):33-45.
    • (1967) Pediatrics , vol.40 , Issue.1 , pp. 33-45
    • Stevenson, R.E.1    Huntley, C.C.2
  • 49
    • 0033848821 scopus 로고    scopus 로고
    • Pervasive developmental disorders: A 10 year review
    • Tanguay PE. 2000. Pervasive developmental disorders: A 10 year review. J Am Acad Child Adolesc Psychiatry 39(9):1079-1095.
    • (2000) J Am Acad Child Adolesc Psychiatry , vol.39 , Issue.9 , pp. 1079-1095
    • Tanguay, P.E.1
  • 50
    • 0028935117 scopus 로고
    • Noradrenaline is essential for mouse fetal development
    • Thomas SA, Matsumoto AM, Palmiter RD. 1995. Noradrenaline is essential for mouse fetal development. Nature 374(6523):643-646.
    • (1995) Nature , vol.374 , Issue.6523 , pp. 643-646
    • Thomas, S.A.1    Matsumoto, A.M.2    Palmiter, R.D.3
  • 52
    • 0031949066 scopus 로고    scopus 로고
    • A log-linear approach to case-parent-triad data: Assessing effective disease genes that act either directly or through maternal effect and that may be subject to parental imprinting
    • Weinberg CR, Wilcox AJ, Lie RT. 1998. A log-linear approach to case-parent-triad data: Assessing effective disease genes that act either directly or through maternal effect and that may be subject to parental imprinting. Am J Hum Genet 62(4):969-978.
    • (1998) Am J Hum Genet , vol.62 , Issue.4 , pp. 969-978
    • Weinberg, C.R.1    Wilcox, A.J.2    Lie, R.T.3
  • 54
    • 0037041302 scopus 로고    scopus 로고
    • Family-based and population study of a functional promotor-region monoamine oxidase A polymorphism in autism: Possible association with IQ
    • Yirmiya N, Pilowsky T, Tidhar S, Nemanov L, Altmark L, Ebstein RP. 2002. Family-based and population study of a functional promotor-region monoamine oxidase A polymorphism in autism: Possible association with IQ. Am J Med Genet 114(3):284-287.
    • (2002) Am J Med Genet , vol.114 , Issue.3 , pp. 284-287
    • Yirmiya, N.1    Pilowsky, T.2    Tidhar, S.3    Nemanov, L.4    Altmark, L.5    Ebstein, R.P.6


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