메뉴 건너뛰기




Volumn 27, Issue 4, 1997, Pages 262-267

Candidate genes and psychiatric genetics: Tomorrow never knows

Author keywords

[No Author keywords available]

Indexed keywords


EID: 6244247470     PISSN: 00485713     EISSN: None     Source Type: Journal    
DOI: 10.3928/0048-5713-19970401-08     Document Type: Article
Times cited : (6)

References (36)
  • 1
    • 6244245468 scopus 로고    scopus 로고
    • Psychiatric epidemiology and information technology
    • Tien AY. Psychiatric epidemiology and information technology. Psychiatric Annals. 1997; 27:268-272.
    • (1997) Psychiatric Annals , vol.27 , pp. 268-272
    • Tien, A.Y.1
  • 2
    • 0031516496 scopus 로고    scopus 로고
    • An introductory overview of mutational analysis in psychiatric genetics
    • Cubells JF. An introductory overview of mutational analysis in psychiatric genetics. Psychiatric Annals. 1997; 27:273-278.
    • (1997) Psychiatric Annals , vol.27 , pp. 273-278
    • Cubells, J.F.1
  • 3
    • 0031483144 scopus 로고    scopus 로고
    • Review of gene mapping and molecular genetic studies of schizophrenia
    • Rao PA. Review of gene mapping and molecular genetic studies of schizophrenia. Psychiatric Annals. 1997; 27:279-284.
    • (1997) Psychiatric Annals , vol.27 , pp. 279-284
    • Rao, P.A.1
  • 4
    • 6244252925 scopus 로고    scopus 로고
    • The genetics of bipolar disorder
    • Kelsoe JR. The genetics of bipolar disorder. Psychiatric Annals. 1997; 27:285-292.
    • (1997) Psychiatric Annals , vol.27 , pp. 285-292
    • Kelsoe, J.R.1
  • 5
    • 0031519603 scopus 로고    scopus 로고
    • What genes confer vulnerability to Gilles de la Tourette's syndrome?
    • Leckman JF. What genes confer vulnerability to Gilles de la Tourette's syndrome? Psychiatric Annals. 1997; 27:293-296.
    • (1997) Psychiatric Annals , vol.27 , pp. 293-296
    • Leckman, J.F.1
  • 6
    • 0027442475 scopus 로고
    • Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A
    • Brunner HG, Nelen M, Breakefield XO, Ropers HH, van Oost BA. Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A. Science. 1993; 262:578-580.
    • (1993) Science , vol.262 , pp. 578-580
    • Brunner, H.G.1    Nelen, M.2    Breakefield, X.O.3    Ropers, H.H.4    Van Oost, B.A.5
  • 7
    • 0027370904 scopus 로고
    • X-linked borderline mental retardation with prominent behavior: Phenotype, genetic localization, and evidence for disturbed monoamine metabolism
    • Brunner HG, Nelen M, van Zandvoort P, et al. X-linked borderline mental retardation with prominent behavior: phenotype, genetic localization, and evidence for disturbed monoamine metabolism. Am J Hum Genet. 1993; 52:1032-1039.
    • (1993) Am J Hum Genet , vol.52 , pp. 1032-1039
    • Brunner, H.G.1    Nelen, M.2    Van Zandvoort, P.3
  • 8
    • 0027339609 scopus 로고
    • The A1 allele at the D2 dopamine receptor gene and alcoholism: A reappraisal
    • Gelernter J, Goldman D, Risch N. The A1 allele at the D2 dopamine receptor gene and alcoholism: a reappraisal. JAMA. 1993; 269:1673-1677.
    • (1993) JAMA , vol.269 , pp. 1673-1677
    • Gelernter, J.1    Goldman, D.2    Risch, N.3
  • 9
    • 0027450927 scopus 로고
    • Substance abuse vulnerability and D2 receptor genes
    • Uhl G, Blum K, Noble E, Smith S. Substance abuse vulnerability and D2 receptor genes. Trends Neurosci. 1993; 16:83-88.
    • (1993) Trends Neurosci , vol.16 , pp. 83-88
    • Uhl, G.1    Blum, K.2    Noble, E.3    Smith, S.4
  • 10
    • 0029000346 scopus 로고
    • Genetics of bipolar disorder: Time for another reinvention?
    • Gelernter J. Genetics of bipolar disorder: time for another reinvention? Am J Hum Genet. 1995; 56:1262-1266.
    • (1995) Am J Hum Genet , vol.56 , pp. 1262-1266
    • Gelernter, J.1
  • 11
    • 0027489981 scopus 로고
    • Excluding linkage between panic disorder and the gamma-aminobutyric acid beta 1 receptor locus in five Icelandic pedigrees
    • Schmidt SM, Zoega T, Crowe RR. Excluding linkage between panic disorder and the gamma-aminobutyric acid beta 1 receptor locus in five Icelandic pedigrees. Acta Psychiatr Scand. 1993; 88:225-228.
    • (1993) Acta Psychiatr Scand , vol.88 , pp. 225-228
    • Schmidt, S.M.1    Zoega, T.2    Crowe, R.R.3
  • 12
    • 0025925207 scopus 로고
    • The dopamine D2 receptor locus as a modifying gene in neuropsychiatric disorders
    • Comings DE, Comings BG, Muhleman D, et al. The dopamine D2 receptor locus as a modifying gene in neuropsychiatric disorders. JAMA. 1991; 266:1793-1800.
    • (1991) JAMA , vol.266 , pp. 1793-1800
    • Comings, D.E.1    Comings, B.G.2    Muhleman, D.3
  • 13
    • 0026651968 scopus 로고
    • Multiple dopamine D4 receptor variants in the human population
    • Van Tol HHM, Caren MW, Guan H-C, et al. Multiple dopamine D4 receptor variants in the human population. Nature. 1992; 358:149-152.
    • (1992) Nature , vol.358 , pp. 149-152
    • Van Tol, H.H.M.1    Caren, M.W.2    Guan, H.-C.3
  • 14
    • 13344275183 scopus 로고    scopus 로고
    • Dopamine D4 (D4DR) exon III polymorphism associated with the human personality trait of novelty seeking
    • Ebstein RP, Novick O, Umansky R, et al. Dopamine D4 (D4DR) exon III polymorphism associated with the human personality trait of novelty seeking. Nat Genet. 1996; 12:78-80.
    • (1996) Nat Genet , vol.12 , pp. 78-80
    • Ebstein, R.P.1    Novick, O.2    Umansky, R.3
  • 15
    • 0030033685 scopus 로고    scopus 로고
    • Population and familial association between the D4 dopamine receptor gene and measures of novelty seeking
    • Benjamin J, Li L, Patterson C, Greenberg BD, Murphy DL, Hamer DH. Population and familial association between the D4 dopamine receptor gene and measures of novelty seeking. Nat Genet. 1996; 12:81-84.
    • (1996) Nat Genet , vol.12 , pp. 81-84
    • Benjamin, J.1    Li, L.2    Patterson, C.3    Greenberg, B.D.4    Murphy, D.L.5    Hamer, D.H.6
  • 16
    • 19244363371 scopus 로고    scopus 로고
    • Linkage disequilibrium between an allele at the dopamine D4 receptor locus with Tourette's syndrome, by the transmission-disequilibrium test
    • Grice DE, Leckman JF, Pauls DL, et al. Linkage disequilibrium between an allele at the dopamine D4 receptor locus with Tourette's syndrome, by the transmission-disequilibrium test. Am J Hum Genet. 1996; 59:644-652.
    • (1996) Am J Hum Genet , vol.59 , pp. 644-652
    • Grice, D.E.1    Leckman, J.F.2    Pauls, D.L.3
  • 17
    • 0027078061 scopus 로고
    • Human dopamine transporter gene maps to chromosome 5p15.3 and displays a VNTR
    • Vandenbergh DJ, Persico AM, Hawkins AL, et al. Human dopamine transporter gene maps to chromosome 5p15.3 and displays a VNTR. Genomics. 1992; 14:1104-1106.
    • (1992) Genomics , vol.14 , pp. 1104-1106
    • Vandenbergh, D.J.1    Persico, A.M.2    Hawkins, A.L.3
  • 18
    • 0029157488 scopus 로고
    • Minisatellites and human disease
    • Krontiris TG. Minisatellites and human disease. Science. 1995; 269:1682-1683.
    • (1995) Science , vol.269 , pp. 1682-1683
    • Krontiris, T.G.1
  • 19
    • 0028042409 scopus 로고
    • Genetic association between dopamine transporter protein alleles and cocaine-induced paranoia
    • Gelernter J, Kranzler HR, Satel SL, Rao PA. Genetic association between dopamine transporter protein alleles and cocaine-induced paranoia. Neuropsychopharmacology. 1994; 11:195-200.
    • (1994) Neuropsychopharmacology , vol.11 , pp. 195-200
    • Gelernter, J.1    Kranzler, H.R.2    Satel, S.L.3    Rao, P.A.4
  • 20
    • 0028987091 scopus 로고
    • Association of attention-deficit disorder and the dopamine transporter gene
    • Cook EH Jr, Stein MS, Krasowski MD, et al. Association of attention-deficit disorder and the dopamine transporter gene. Am J Hum Genet. 1995; 56:993-996.
    • (1995) Am J Hum Genet , vol.56 , pp. 993-996
    • Cook Jr., E.H.1    Stein, M.S.2    Krasowski, M.D.3
  • 21
    • 0344857708 scopus 로고
    • Biochemical instability in schizophrenia, II: The serotonin and gamma-aminobutyric acid systems
    • Meltzer, et al, eds. New York, NY: Raven Press
    • Van Kammen DP, Gelernter J. Biochemical instability in schizophrenia, II: the serotonin and gamma-aminobutyric acid systems. In: Meltzer, et al, eds. Psychopharmacology, The Third Generation of Progress, New York, NY: Raven Press; 1987.
    • (1987) Psychopharmacology, the Third Generation of Progress
    • Van Kammen, D.P.1    Gelernter, J.2
  • 22
    • 0029873266 scopus 로고    scopus 로고
    • Association between schizophrenia and the T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene
    • Williams J, Spurlock G, McGuffin P, et al. Association between schizophrenia and the T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. Lancet. 1996; 347:1294-1296.
    • (1996) Lancet , vol.347 , pp. 1294-1296
    • Williams, J.1    Spurlock, G.2    McGuffin, P.3
  • 23
    • 0029988749 scopus 로고    scopus 로고
    • Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia
    • Inayama Y, Yoneda H, Sakai T, et al. Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia. Am J Med Genet. 1996; 67:103-105.
    • (1996) Am J Med Genet , vol.67 , pp. 103-105
    • Inayama, Y.1    Yoneda, H.2    Sakai, T.3
  • 24
    • 0029880896 scopus 로고    scopus 로고
    • Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia
    • Erdmann J, Shimron-Abarbanell D, Rietschel M. Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: identification of two naturally occurring receptor variants and association analysis in schizophrenia. Hum Genet. 1996; 97:614-619.
    • (1996) Hum Genet , vol.97 , pp. 614-619
    • Erdmann, J.1    Shimron-Abarbanell, D.2    Rietschel, M.3
  • 25
    • 0029939169 scopus 로고    scopus 로고
    • Polymorphism in serotonin transporter gene associated with susceptibility to major depression
    • Ogilvie AD, Battersby S, Bubb VJ, et al. Polymorphism in serotonin transporter gene associated with susceptibility to major depression. Lancet. 1996; 347:731-733.
    • (1996) Lancet , vol.347 , pp. 731-733
    • Ogilvie, A.D.1    Battersby, S.2    Bubb, V.J.3
  • 26
    • 0029895783 scopus 로고    scopus 로고
    • Allelic variation of human serotonin transporter gene expression
    • Heils A, Teufel A, Petri S, et al. Allelic variation of human serotonin transporter gene expression. J Neurochem. 1996; 66:2621-2624.
    • (1996) J Neurochem , vol.66 , pp. 2621-2624
    • Heils, A.1    Teufel, A.2    Petri, S.3
  • 27
    • 0028117344 scopus 로고
    • Suicidality and 5-hydroxyindolacetic acid concentration associated with a tryptophan hydroxylase polymorphism
    • Nielsen DA, Goldman D, Virkkunen M, Tokola R, Rawlings R, Linnoila M. Suicidality and 5-hydroxyindolacetic acid concentration associated with a tryptophan hydroxylase polymorphism. Arch Gen Psychiatry. 1994; 51:34-38.
    • (1994) Arch Gen Psychiatry , vol.51 , pp. 34-38
    • Nielsen, D.A.1    Goldman, D.2    Virkkunen, M.3    Tokola, R.4    Rawlings, R.5    Linnoila, M.6
  • 28
    • 0027194791 scopus 로고
    • Gene dose of apolipoprotein e type 4 allele and the risk of Alzheimer's disease in late onset families
    • Corder EH, Saunders AM, Strittmatter WJ, et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science. 1993; 261:921-923.
    • (1993) Science , vol.261 , pp. 921-923
    • Corder, E.H.1    Saunders, A.M.2    Strittmatter, W.J.3
  • 29
    • 0028305380 scopus 로고
    • Protective effect of apolipoprotein e type 2 allele for late onset Alzheimer's disease
    • Corder EH, Saunders AM, Risch NJ, et al. Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer's disease. Nat Genet. 1994; 7:180-184.
    • (1994) Nat Genet , vol.7 , pp. 180-184
    • Corder, E.H.1    Saunders, A.M.2    Risch, N.J.3
  • 30
    • 0026088977 scopus 로고
    • Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease
    • Goate A, Chartier-Harlin MC, Mullan M, et al. Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease. Nature. 1991; 349:704-706.
    • (1991) Nature , vol.349 , pp. 704-706
    • Goate, A.1    Chartier-Harlin, M.C.2    Mullan, M.3
  • 31
    • 0026879650 scopus 로고
    • Presenile dementia and cerebral hemorrhage linked to a mutation at codon 692 of the β-amyloid precursor protein gene
    • Hendriks L, van Duijn CM, Cras P, et al. Presenile dementia and cerebral hemorrhage linked to a mutation at codon 692 of the β-amyloid precursor protein gene. Nat Genet. 1992; 1:218-221.
    • (1992) Nat Genet , vol.1 , pp. 218-221
    • Hendriks, L.1    Van Duijn, C.M.2    Cras, P.3
  • 32
    • 0027076725 scopus 로고
    • Association between schizophrenia and homozygosity at the dopamine D3 receptor gene
    • Crocq M-A, Mant R, Asherson P, et al. Association between schizophrenia and homozygosity at the dopamine D3 receptor gene. J Med Genet. 1992; 29:858-860.
    • (1992) J Med Genet , vol.29 , pp. 858-860
    • Crocq, M.-A.1    Mant, R.2    Asherson, P.3
  • 33
    • 0025852722 scopus 로고
    • Alcohol and aldehyde dehydrogenase genotypes and alcoholism in Chinese men
    • Thomasson HR, Edenberg HJ, Crabb DW, et al. Alcohol and aldehyde dehydrogenase genotypes and alcoholism in Chinese men. Am J Hum Genet. 1991; 48:677-681.
    • (1991) Am J Hum Genet , vol.48 , pp. 677-681
    • Thomasson, H.R.1    Edenberg, H.J.2    Crabb, D.W.3
  • 34
    • 0030026455 scopus 로고    scopus 로고
    • Association between a null mutation in the human ciliary neurotrophio factor (CNTF) gene and increased incidence of psychiatric diseases?
    • Thome J, Kornhuber J, Baumer A, Rösler M, Beckmann H, Riederer P. Association between a null mutation in the human ciliary neurotrophio factor (CNTF) gene and increased incidence of psychiatric diseases? Neurosci Lett. 1996b; 203:109-110.
    • (1996) Neurosci Lett , vol.203 , pp. 109-110
    • Thome, J.1    Kornhuber, J.2    Baumer, A.3    Rösler, M.4    Beckmann, H.5    Riederer, P.6
  • 35
    • 0028286735 scopus 로고
    • Neurotrophin-3 gene polymorphism associated with schizophrenia
    • Nanko S, Hattori M, Kuwata S, et al. Neurotrophin-3 gene polymorphism associated with schizophrenia. Acta Psychiatr Scand. 1994; 89:390-392.
    • (1994) Acta Psychiatr Scand , vol.89 , pp. 390-392
    • Nanko, S.1    Hattori, M.2    Kuwata, S.3
  • 36
    • 0027327267 scopus 로고
    • Association of apolipoprotein e allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease
    • Saunders AM, Strittmatter WJ, Schmechel D, et al. Association of apolipoprotein E allele epsilon 4 with late-onset familial and sporadic Alzheimer's disease. Neurology. 1993; 43:1467-1472.
    • (1993) Neurology , vol.43 , pp. 1467-1472
    • Saunders, A.M.1    Strittmatter, W.J.2    Schmechel, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.