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Volumn 12, Issue 3, 2002, Pages 121-126

Implications of multifactorial inheritance for identification of genetic mechanisms in major psychiatric disorders

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; BEHAVIOR DISORDER; BIPOLAR DISORDER; CHROMOSOMAL LOCALIZATION; DISEASE COURSE; EDITORIAL; FAMILY STUDY; FRAGILE X SYNDROME; GENETIC LINKAGE; HUMAN; HUMAN GENOME; HUNTINGTON CHOREA; LESCH NYHAN SYNDROME; MENTAL DISEASE; NEUROLOGIC DISEASE; NONHUMAN; PATHOPHYSIOLOGY; PHENOTYPE; PRIORITY JOURNAL; SCHIZOPHRENIA;

EID: 0036756052     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/00041444-200209000-00001     Document Type: Editorial
Times cited : (10)

References (61)
  • 1
    • 0036258079 scopus 로고    scopus 로고
    • Meta-analysis of whole-genone linkage scans of bipolar disorder and schizophrenia
    • Badner JA, Gershon ES (2002). Meta-analysis of whole-genone linkage scans of bipolar disorder and schizophrenia. Mol Psychiatry 7:405-411.
    • (2002) Mol Psychiatry , vol.7 , pp. 405-411
    • Badner, J.A.1    Gershon, E.S.2
  • 2
    • 0028871202 scopus 로고
    • Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus
    • Bennett ST, Lucassen AM, Gough SC, Powell EE, Undlien DE, Pritchard LE, et al. (1995). Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus. Nat Genet 9:284-292.
    • (1995) Nat Genet , vol.9 , pp. 284-292
    • Bennett, S.T.1    Lucassen, A.M.2    Gough, S.C.3    Powell, E.E.4    Undlien, D.E.5    Pritchard, L.E.6
  • 3
    • 0034666043 scopus 로고    scopus 로고
    • Are schizophrenic and bipolar disorders related? A review of family and molecular studies
    • Berrettini WH (2000). Are schizophrenic and bipolar disorders related? A review of family and molecular studies. Biol Psychiatry 48:531-538.
    • (2000) Biol Psychiatry , vol.48 , pp. 531-538
    • Berrettini, W.H.1
  • 4
    • 0027989690 scopus 로고
    • Quantitative trait loci mapping of three loci controlling morphine preference using inbred mouse strains
    • Berrettini WH, Ferraro TN, Alexander RC, Buchberg AM, Vogel WH (1994). Quantitative trait loci mapping of three loci controlling morphine preference using inbred mouse strains. Nat Genet 7:54-58.
    • (1994) Nat Genet , vol.7 , pp. 54-58
    • Berrettini, W.H.1    Ferraro, T.N.2    Alexander, R.C.3    Buchberg, A.M.4    Vogel, W.H.5
  • 5
    • 0034724924 scopus 로고    scopus 로고
    • Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22
    • Brzustowicz LM, Hodgkinson KA, Chow EW, Honer WG, Bassett AS (2000). Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science 288:678-682.
    • (2000) Science , vol.288 , pp. 678-682
    • Brzustowicz, L.M.1    Hodgkinson, K.A.2    Chow, E.W.3    Honer, W.G.4    Bassett, A.S.5
  • 6
    • 0023257348 scopus 로고
    • Neurogenetic adaptive mechanisms in alcoholism
    • Cloninger CR (1987). Neurogenetic adaptive mechanisms in alcoholism. Science 236:410-416.
    • (1987) Science , vol.236 , pp. 410-416
    • Cloninger, C.R.1
  • 7
    • 17344372511 scopus 로고    scopus 로고
    • A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus
    • Concannon P, Gogolin-Ewens KJ, Hinds DA, Wapelhorst B, Morrison VA, Stirling B, et al. (1998). A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nat Genet 19:292-296.
    • (1998) Nat Genet , vol.19 , pp. 292-296
    • Concannon, P.1    Gogolin-Ewens, K.J.2    Hinds, D.A.3    Wapelhorst, B.4    Morrison, V.A.5    Stirling, B.6
  • 8
    • 0032928542 scopus 로고    scopus 로고
    • Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans
    • Cox NJ, Frigge M, Nicolae DL, Concannon P, Hanis CL, Bell GI, Kong A (1999). Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans. Nat Genet 21:213-215.
    • (1999) Nat Genet , vol.21 , pp. 213-215
    • Cox, N.J.1    Frigge, M.2    Nicolae, D.L.3    Concannon, P.4    Hanis, C.L.5    Bell, G.I.6    Kong, A.7
  • 9
    • 0034640718 scopus 로고    scopus 로고
    • Update on chromosomal locations for psychiatric disorders: Report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics
    • Monterey, California, October: 14-18, 1999
    • DeLisi LE, Craddock NJ, Detera-Wadleigh S, Forund T, Gejman P, Kennedy JL, et al. (2000). Update on chromosomal locations for psychiatric disorders: Report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics, Monterey, California, October: 14-18, 1999. Am J Med Genet 96:434-449.
    • (2000) Am J Med Genet , vol.96 , pp. 434-449
    • DeLisi, L.E.1    Craddock, N.J.2    Detera-Wadleigh, S.3    Forund, T.4    Gejman, P.5    Kennedy, J.L.6
  • 10
    • 0030784524 scopus 로고    scopus 로고
    • Genetics and developmental psychopathology: 2. The main effects of genes and environment on behavioral problems in the Virginia Twin Study of Adolescent Behavioral Development
    • Eaves LJ, Silberg JL, Meyer JM, Maes HH, Simonoff E, Pickles A, et al. (1997). Genetics and developmental psychopathology: 2. The main effects of genes and environment on behavioral problems in the Virginia Twin Study of Adolescent Behavioral Development. J Child Psychol Psychiatry 38:965-980.
    • (1997) J Child Psychol Psychiatry , vol.38 , pp. 965-980
    • Eaves, L.J.1    Silberg, J.L.2    Meyer, J.M.3    Maes, H.H.4    Simonoff, E.5    Pickles, A.6
  • 11
    • 77955058518 scopus 로고
    • The inheritance of liability to certain diseases, estimated from the incidence among relatives
    • Falconer DS (1965). The inheritance of liability to certain diseases, estimated from the incidence among relatives. Ann Hum Genet 29:51-76.
    • (1965) Ann Hum Genet , vol.29 , pp. 51-76
    • Falconer, D.S.1
  • 12
    • 0033868423 scopus 로고    scopus 로고
    • Alcoholism susceptibility loci: Confirmation studies in a replicate sample and further mapping
    • Foroud T, Edenberg HJ, Goate A, Rice J, Flury L, Koller DL, et al. (2000). Alcoholism susceptibility loci: Confirmation studies in a replicate sample and further mapping. Alcohol Clin Exp Res 24:933-945.
    • (2000) Alcohol Clin Exp Res , vol.24 , pp. 933-945
    • Foroud, T.1    Edenberg, H.J.2    Goate, A.3    Rice, J.4    Flury, L.5    Koller, D.L.6
  • 14
    • 0019975573 scopus 로고
    • A family study of schizoaffective, bipolar I, bipolar II, unipolar, and normal control probands
    • Gershon ES, Hamovit J, Guroff JJ, Dibble E, Leckman JF, Sceery W, et al. (1982). A family study of schizoaffective, bipolar I, bipolar II, unipolar, and normal control probands. Arch Gen Psychiatry 39:1157-1167.
    • (1982) Arch Gen Psychiatry , vol.39 , pp. 1157-1167
    • Gershon, E.S.1    Hamovit, J.2    Guroff, J.J.3    Dibble, E.4    Leckman, J.F.5    Sceery, W.6
  • 16
    • 0343296426 scopus 로고    scopus 로고
    • Clinical and genetic findings in responders to long-term lithium treatment
    • Park City, Utah, February 2000
    • Grof P (2000). Clinical and genetic findings in responders to long-term lithium treatment. Presented at the Meeting of the Psychiatric Research Society, Park City, Utah, February 2000.
    • (2000) Meeting of the Psychiatric Research Society
    • Grof, P.1
  • 17
    • 0035089756 scopus 로고    scopus 로고
    • Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23
    • Gurling H, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo B, et al. (2001). Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23. Am J Hum Genet 68:661-673.
    • (2001) Am J Hum Genet , vol.68 , pp. 661-673
    • Gurling, H.1    Kalsi, G.2    Brynjolfson, J.3    Sigmundsson, T.4    Sherrington, R.5    Mankoo, B.6
  • 20
    • 0033772073 scopus 로고    scopus 로고
    • Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
    • Horikawa Y, Oda N, Cox NJ, Li X, Orho-Melander M, Hara M, et al. (2000). Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus. Nat Genet 26:163-175.
    • (2000) Nat Genet , vol.26 , pp. 163-175
    • Horikawa, Y.1    Oda, N.2    Cox, N.J.3    Li, X.4    Orho-Melander, M.5    Hara, M.6
  • 21
    • 0033364825 scopus 로고    scopus 로고
    • A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci
    • Hovatta I, Varilo T, Suvisaari J, Terwilliger JD, Ollikainen V, Arajarvi R, et al. (1999). A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci. Am J Hum Genet 65:1114-1124.
    • (1999) Am J Hum Genet , vol.65 , pp. 1114-1124
    • Hovatta, I.1    Varilo, T.2    Suvisaari, J.3    Terwilliger, J.D.4    Ollikainen, V.5    Arajarvi, R.6
  • 22
    • 0035978651 scopus 로고    scopus 로고
    • Association of NOD2 leucinerich repeat variants with susceptibility to Crohn's disease
    • Hugot JP, Chamaillard M, Zouali H, Lesage S, Cezard JP, Belaiche J, et al. (2001). Association of NOD2 leucinerich repeat variants with susceptibility to Crohn's disease. Nature 411:599-603.
    • (2001) Nature , vol.411 , pp. 599-603
    • Hugot, J.P.1    Chamaillard, M.2    Zouali, H.3    Lesage, S.4    Cezard, J.P.5    Belaiche, J.6
  • 23
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
    • Huntington's Disease Collaborative Research Group (1993). A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72:971-983.
    • (1993) Cell , vol.72 , pp. 971-983
  • 24
    • 2042437650 scopus 로고    scopus 로고
    • Initial sequencing and analysis of the human genome
    • International Human Genome Sequencing Consortium (2001). Initial sequencing and analysis of the human genome. Nature 409:860-921.
    • (2001) Nature , vol.409 , pp. 860-921
  • 26
    • 0031745437 scopus 로고    scopus 로고
    • Twin studies of adult psychiatric and substance dependence disorders: Are they biased by differences in the environmental experiences of monozygotic and dizygotic twins in childhood and adolescence?
    • Kendler KS, Gardner CO (1998). Twin studies of adult psychiatric and substance dependence disorders: Are they biased by differences in the environmental experiences of monozygotic and dizygotic twins in childhood and adolescence? Psychol Med 28:625-633.
    • (1998) Psychol Med , vol.28 , pp. 625-633
    • Kendler, K.S.1    Gardner, C.O.2
  • 27
    • 0032954516 scopus 로고    scopus 로고
    • A population-based twin study of lifetime major depression in men and women
    • Kendler KS, Prescott CA (1999). A population-based twin study of lifetime major depression in men and women. Arch Gen Psychiatry 56:39-44.
    • (1999) Arch Gen Psychiatry , vol.56 , pp. 39-44
    • Kendler, K.S.1    Prescott, C.A.2
  • 28
    • 0034077236 scopus 로고    scopus 로고
    • A multi-dimensional twin study of mental health in women
    • Kendler KS, Myers JM, Neale MC (2000). A multi-dimensional twin study of mental health in women. Am J Psychiatry 157:506-513.
    • (2000) Am J Psychiatry , vol.157 , pp. 506-513
    • Kendler, K.S.1    Myers, J.M.2    Neale, M.C.3
  • 29
    • 0029745410 scopus 로고    scopus 로고
    • Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome
    • Lachman HM, Morrow B, Shprintzen R, Veit S, Parsia SS, Faedda G, et al. (1996). Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome. Am J Med Genet 67:468-472.
    • (1996) Am J Med Genet , vol.67 , pp. 468-472
    • Lachman, H.M.1    Morrow, B.2    Shprintzen, R.3    Veit, S.4    Parsia, S.S.5    Faedda, G.6
  • 31
    • 0036357391 scopus 로고    scopus 로고
    • Comorbid bipolar disorder and panic disorder in families with a high prevalence of bipolar disorder
    • MacKinnon DF, Zandi PP, Cooper J, Potash JB, Simpson SG, Gershon E, et al. (2002). Comorbid bipolar disorder and panic disorder in families with a high prevalence of bipolar disorder. Am J Psychiat 159:30-35.
    • (2002) Am J Psychiat , vol.159 , pp. 30-35
    • MacKinnon, D.F.1    Zandi, P.P.2    Cooper, J.3    Potash, J.B.4    Simpson, S.G.5    Gershon, E.6
  • 35
  • 37
    • 0035018761 scopus 로고    scopus 로고
    • Evidence for locus on chromosome 1 that influences vulnerability to alcoholism and affective disorder
    • Nurnberger JI, Foroud T, Flury L, Su J, Meyer ET, Hu KL, et al. (2001). Evidence for locus on chromosome 1 that influences vulnerability to alcoholism and affective disorder. Am J Psychiatry 158:718-724.
    • (2001) Am J Psychiatry , vol.158 , pp. 718-724
    • Nurnberger, J.I.1    Foroud, T.2    Flury, L.3    Su, J.4    Meyer, E.T.5    Hu, K.L.6
  • 38
    • 0031849496 scopus 로고    scopus 로고
    • Ultra-ultra rapid cycling bipolar disorder is associated with the low activity catecholamine-O-methyltransferase allele
    • Papolos DF, Veit S, Faedda GL, Saito T, Lachman HM (1998). Ultra-ultra rapid cycling bipolar disorder is associated with the low activity catecholamine-O-methyltransferase allele. Mol Psychiatry 3:346-349.
    • (1998) Mol Psychiatry , vol.3 , pp. 346-349
    • Papolos, D.F.1    Veit, S.2    Faedda, G.L.3    Saito, T.4    Lachman, H.M.5
  • 40
  • 42
    • 0029826621 scopus 로고    scopus 로고
    • A genomic survey of alcohol dependence and related phenotypes: Results from the Collaborative Study on the Genetics of Alcoholism (COGA)
    • Reich T (1996). A genomic survey of alcohol dependence and related phenotypes: Results from the Collaborative Study on the Genetics of Alcoholism (COGA). Alcohol Clin Exp Res 20(8 Suppl):133A-137A.
    • (1996) Alcohol Clin Exp Res , vol.20 , Issue.8 SUPPL.
    • Reich, T.1
  • 43
    • 0015422250 scopus 로고
    • The use of multiple thresholds in determining the mode of transmission of semi-continuous traits
    • Reich T, James JW, Morris CA (1972). The use of multiple thresholds in determining the mode of transmission of semi-continuous traits. Ann Hum Genet 36:163-184.
    • (1972) Ann Hum Genet , vol.36 , pp. 163-184
    • Reich, T.1    James, J.W.2    Morris, C.A.3
  • 44
    • 0016530209 scopus 로고
    • The multifactorial model of disease transmission: I. Description of the model and its use in psychiatry
    • Reich R, Cloninger CR, Guze SB (1975). The multifactorial model of disease transmission: I. Description of the model and its use in psychiatry. Br J Psychiatry 127:1-10.
    • (1975) Br J Psychiatry , vol.127 , pp. 1-10
    • Reich, R.1    Cloninger, C.R.2    Guze, S.B.3
  • 47
    • 0034785352 scopus 로고    scopus 로고
    • Genetic variation in the 5q31 cytokine gene cluster confers susceptibility in Crohn's Disease
    • Rioux JD, Daly MJ, Silverberg MS, Lindblad K, Steinhart H, Cohen Z, et al. (2001). Genetic variation in the 5q31 cytokine gene cluster confers susceptibility in Crohn's Disease. Nat Genet 29:223-228.
    • (2001) Nat Genet , vol.29 , pp. 223-228
    • Rioux, J.D.1    Daly, M.J.2    Silverberg, M.S.3    Lindblad, K.4    Steinhart, H.5    Cohen, Z.6
  • 48
    • 0029741063 scopus 로고    scopus 로고
    • The future of genetic studies of complex human diseases
    • Risch N, Merikangas K (1996). The future of genetic studies of complex human diseases. Science 273:1516-1517.
    • (1996) Science , vol.273 , pp. 1516-1517
    • Risch, N.1    Merikangas, K.2
  • 49
    • 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 52:506-516.
    • (1993) Am J Hum Genet , vol.52 , pp. 506-516
    • Spielman, R.S.1    McGinnis, R.E.2    Ewens, W.J.3
  • 51
    • 0028875316 scopus 로고
    • Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect
    • Stine OC, Xu J, Koskela R, McMahon FJ, Gschwend M, Friddle C, et al. (1995). Evidence for linkage of bipolar disorder to chromosome 18 with a parent-of-origin effect. Am J Hum Genet 57:1384-1394.
    • (1995) Am J Hum Genet , vol.57 , pp. 1384-1394
    • Stine, O.C.1    Xu, J.2    Koskela, R.3    McMahon, F.J.4    Gschwend, M.5    Friddle, C.6
  • 53
    • 0002710362 scopus 로고
    • Problems replicating linkage claims in psychiatry
    • Gershon ES, Cloninger CR, editors. Washington, DC: American Psychiatric Press
    • Suarez B, Harpe CL, Van Eerdewegh P (1994). Problems replicating linkage claims in psychiatry. In: Gershon ES, Cloninger CR, editors. Genetic Approaches to Mental Disorder. Washington, DC: American Psychiatric Press. pp. 23-46.
    • (1994) Genetic Approaches to Mental Disorder , pp. 23-46
    • Suarez, B.1    Harpe, C.L.2    Van Eerdewegh, P.3
  • 54
    • 0033365190 scopus 로고    scopus 로고
    • A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome
    • Tourette Syndrome Association International Consortium for Genetics (1999). A complete genome screen in sib pairs affected by Gilles de la Tourette syndrome. Am J Hum Genet 65:1428-1436.
    • (1999) Am J Hum Genet , vol.65 , pp. 1428-1436
  • 55
    • 17944371887 scopus 로고    scopus 로고
    • Mapping susceptibility genes for bipolar disorder: A pharmacogenetic approach based on excellent response to lithium
    • Turecki G, Grof P, Grof E, D'Souza V, Lebuis S, Marineau C (2001). Mapping susceptibility genes for bipolar disorder: A pharmacogenetic approach based on excellent response to lithium. Mol Psychiat 6:570-578.
    • (2001) Mol Psychiat , vol.6 , pp. 570-578
    • Turecki, G.1    Grof, P.2    Grof, E.3    D'Souza, V.4    Lebuis, S.5    Marineau, C.6
  • 61
    • 0027461605 scopus 로고
    • Production of a model for Lesch-Nyhan syndrome in hypoxanthine phosphoribosyltransferase-deficient mice
    • Wu CL, Melton DW (1993). Production of a model for Lesch-Nyhan syndrome in hypoxanthine phosphoribosyltransferase-deficient mice. Nat Genet 3:235-240.
    • (1993) Nat Genet , vol.3 , pp. 235-240
    • Wu, C.L.1    Melton, D.W.2


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