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Volumn 8, Issue 7, 2007, Pages 429-444

Genetic and environmental factors in complex neurodevelopmental disorders

Author keywords

Association studies; Environmental factors; Gene environment interactions; Linkage analysis; Neurodevelopmental disorders; Susceptibility genes

Indexed keywords

MESSENGER RNA;

EID: 41749125456     PISSN: 13892029     EISSN: None     Source Type: Journal    
DOI: 10.2174/138920207783591717     Document Type: Review
Times cited : (99)

References (216)
  • 1
    • 0029741063 scopus 로고    scopus 로고
    • The future of genetic studies of complex human diseases
    • Risch, N., Merikangas, K. The future of genetic studies of complex human diseases. Science 1996, 273: 1516-7.
    • (1996) Science , vol.273 , pp. 1516-1517
    • Risch, N.1    Merikangas, K.2
  • 2
    • 0029736803 scopus 로고    scopus 로고
    • Modern molecular genetic approaches to psychiatric disease
    • Craddock, N., Owen, M.J. Modern molecular genetic approaches to psychiatric disease. Br. Med. Bull. 1996, 52: 434-52.
    • (1996) Br. Med. Bull , vol.52 , pp. 434-452
    • Craddock, N.1    Owen, M.J.2
  • 3
    • 0030090443 scopus 로고    scopus 로고
    • Modern molecular genetic approaches to complex traits: Implications for psychiatric disorders
    • Owen, M.J., Craddock, N. Modern molecular genetic approaches to complex traits: implications for psychiatric disorders. Mol. Psychiatry 1996, 1: 21-6.
    • (1996) Mol. Psychiatry , vol.1 , pp. 21-26
    • Owen, M.J.1    Craddock, N.2
  • 4
    • 0034660559 scopus 로고    scopus 로고
    • Searching for genetic determinants in the new millennium
    • Risch, N.J. Searching for genetic determinants in the new millennium. Nature 2000, 405: 847-56.
    • (2000) Nature , vol.405 , pp. 847-856
    • Risch, N.J.1
  • 5
    • 33749043929 scopus 로고    scopus 로고
    • Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders
    • Lee, J.A., Lupski, J.R. Genomic rearrangements and gene copy-number alterations as a cause of nervous system disorders. Neuron 2006, 52: 103-21.
    • (2006) Neuron , vol.52 , pp. 103-121
    • Lee, J.A.1    Lupski, J.R.2
  • 6
    • 33751329250 scopus 로고    scopus 로고
    • Redon, R., Ishikawa, S., Fitch, K.R., Feuk, L., Perry, G.H., Andrews, T.D., Fiegler, H., Shapero, M.H., Carson, A.R., Chen, W., Cho, E.K., Dallaire, S., Freeman, J.L., Gonzalez, J.R., Gratacos, M., Huang, J., Kalaitzopoulos, D., Komura, D., MacDonald, J.R., Marshall, C.R., Mei, R., Montgomery, L., Nishimura, K., Okamura, K., Shen, F., Somerville, M.J., Tchinda, J., Valsesia, A., Woodwark, C., Yang, F., Zhang, J., Zerjal, T., Zhang, J., Armengol, L., Conrad, D.F., Estivill, X., Tyler-Smith, C., Carter, N.P., Aburatani, H., Lee, C., Jones, K.W., Scherer, S.W., Hurles, M.E. Global variation in copy number in the human genome. Nature 2006, 444: 444-54.
    • Redon, R., Ishikawa, S., Fitch, K.R., Feuk, L., Perry, G.H., Andrews, T.D., Fiegler, H., Shapero, M.H., Carson, A.R., Chen, W., Cho, E.K., Dallaire, S., Freeman, J.L., Gonzalez, J.R., Gratacos, M., Huang, J., Kalaitzopoulos, D., Komura, D., MacDonald, J.R., Marshall, C.R., Mei, R., Montgomery, L., Nishimura, K., Okamura, K., Shen, F., Somerville, M.J., Tchinda, J., Valsesia, A., Woodwark, C., Yang, F., Zhang, J., Zerjal, T., Zhang, J., Armengol, L., Conrad, D.F., Estivill, X., Tyler-Smith, C., Carter, N.P., Aburatani, H., Lee, C., Jones, K.W., Scherer, S.W., Hurles, M.E. Global variation in copy number in the human genome. Nature 2006, 444: 444-54.
  • 8
    • 33750079265 scopus 로고    scopus 로고
    • Characteristics of school-age children with autism
    • Montes, G., Halterman, J.S. Characteristics of school-age children with autism. J. Dev. Behav. Pediatr. 2006, 27: 379-85.
    • (2006) J. Dev. Behav. Pediatr , vol.27 , pp. 379-385
    • Montes, G.1    Halterman, J.S.2
  • 9
    • 33845797961 scopus 로고    scopus 로고
    • The genetics of autistic disorders and its clinical relevance: A review of the literature
    • Freitag, C.M. The genetics of autistic disorders and its clinical relevance: a review of the literature. Mol. Psychiatry 2007, 12: 2-22.
    • (2007) Mol. Psychiatry , vol.12 , pp. 2-22
    • Freitag, C.M.1
  • 10
    • 33847219669 scopus 로고    scopus 로고
    • A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence
    • Yang, M.S., Gill, M. A review of gene linkage, association and expression studies in autism and an assessment of convergent evidence. Int. J. Dev. Neurosci. 2007, 25: 69-85.
    • (2007) Int. J. Dev. Neurosci , vol.25 , pp. 69-85
    • Yang, M.S.1    Gill, M.2
  • 11
    • 32844454862 scopus 로고    scopus 로고
    • A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands
    • Lauritsen, M.B., Als, T.D., Dahl, H.A., Flint, T.J., Wang, A.G., Vang, M., Kruse, T.A., Ewald, H., Mors, O. A genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe Islands. Mol. Psychiatry 2006, 11: 37-46.
    • (2006) Mol. Psychiatry , vol.11 , pp. 37-46
    • Lauritsen, M.B.1    Als, T.D.2    Dahl, H.A.3    Flint, T.J.4    Wang, A.G.5    Vang, M.6    Kruse, T.A.7    Ewald, H.8    Mors, O.9
  • 12
    • 33847327313 scopus 로고    scopus 로고
    • Szatmari, P, Paterson, A.D, Zwaigenbaum, L, Roberts, W, Brian, J, Liu, X.Q, Vincent, J.B, Skaug, J.L, Thompson, A.P, Senman, L, Feuk, L, Qian, C, Bryson, S.E, Jones, M.B, Marshall, C.R, Scherer, S.W, Vieland, V.J, Bartlett, C, Mangin, L.V, Goedken, R, Segre, A, Pericak-Vance, M.A, Cuccaro, M.L, Gilbert, J.R, Wright, H.H, Abramson, R.K, Betancur, C, Bourgeron, T, Gillberg, C, Leboyer, M, Buxbaum, J.D, Davis, K.L, Hollander, E, Silverman, J.M, Hallmayer, J, Lotspeich, L, Sutcliffe, J.S, Haines, J.L, Folstein, S.E, Piven, J, Wassink, T.H, Sheffield, V, Geschwind, D.H, Bucan, M, Brown, W.T, Cantor, R.M, Constantino, J.N, Gilliam, T.C, Herbert, M, Lajonchere, C, Ledbetter, D.H, Lese-Martin, C, Miller, J, Nelson, S, Samango-Sprouse, C.A, Spence, S, State, M, Tanzi, R.E, Coon, H, Dawson, G, Devlin, B, Estes, A, Flodman, P, Klei, L, McMahon, W.M, Minshew, N, Munson, J, Korvatska, E, Rodier, P.M, Schellenberg, G.D, Smith, M
    • Szatmari, P., Paterson, A.D., Zwaigenbaum, L., Roberts, W., Brian, J., Liu, X.Q., Vincent, J.B., Skaug, J.L., Thompson, A.P., Senman, L., Feuk, L., Qian, C., Bryson, S.E., Jones, M.B., Marshall, C.R., Scherer, S.W., Vieland, V.J., Bartlett, C., Mangin, L.V., Goedken, R., Segre, A., Pericak-Vance, M.A., Cuccaro, M.L., Gilbert, J.R., Wright, H.H., Abramson, R.K., Betancur, C., Bourgeron, T., Gillberg, C., Leboyer, M., Buxbaum, J.D., Davis, K.L., Hollander, E., Silverman, J.M., Hallmayer, J., Lotspeich, L., Sutcliffe, J.S., Haines, J.L., Folstein, S.E., Piven, J., Wassink, T.H., Sheffield, V., Geschwind, D.H., Bucan, M., Brown, W.T., Cantor, R.M., Constantino, J.N., Gilliam, T.C., Herbert, M., Lajonchere, C., Ledbetter, D.H., Lese-Martin, C., Miller, J., Nelson, S., Samango-Sprouse, C.A., Spence, S., State, M., Tanzi, R.E., Coon, H., Dawson, G., Devlin, B., Estes, A., Flodman, P., Klei, L., McMahon, W.M., Minshew, N., Munson, J., Korvatska, E., Rodier, P.M., Schellenberg, G.D., Smith, M., Spence, M.A., Stodgell, C., Tepper, P.G., Wijsman, E.M., Yu, C.E., Roge, B., Mantoulan, C., Wittemeyer, K., Poustka, A., Felder, B., Klauck, S.M., Schuster, C., Poustka, F., Bolte, S., Feineis-Matthews, S., Herbrecht, E., Schmotzer, G., Tsiantis, J., Papanikolaou, K., Maestrini, E., Bacchelli, E., Blasi, F., Carone, S., Toma, C., Van Engeland, H., de Jonge, M., Kemner, et al., Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat. Genet. 2007, 39: 319-28.
  • 13
    • 34247481814 scopus 로고    scopus 로고
    • Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., Walsh, T., Yamrom, B., Yoon, S., Krasnitz, A., Kendall, J., Leotta, A., Pai, D., Zhang, R., Lee, Y.H., Hicks, J., Spence, S.J., Lee, A.T., Puura, K., Lehtimaki, T., Ledbetter, D., Gregersen, P.K., Bregman, J., Sutcliffe, J.S., Jobanputra, V., Chung, W., Warburton, D., King, M.C., Skuse, D., Geschwind, D.H., Gilliam, T.C., Ye, K., Wigler, M. Strong association of de novo copy number mutations with autism. Science 2007, 316: 445-9.
    • Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., Walsh, T., Yamrom, B., Yoon, S., Krasnitz, A., Kendall, J., Leotta, A., Pai, D., Zhang, R., Lee, Y.H., Hicks, J., Spence, S.J., Lee, A.T., Puura, K., Lehtimaki, T., Ledbetter, D., Gregersen, P.K., Bregman, J., Sutcliffe, J.S., Jobanputra, V., Chung, W., Warburton, D., King, M.C., Skuse, D., Geschwind, D.H., Gilliam, T.C., Ye, K., Wigler, M. Strong association of de novo copy number mutations with autism. Science 2007, 316: 445-9.
  • 15
    • 0023359750 scopus 로고
    • The positive-negative dimension in schizophrenia: Its validity and significance
    • Kay, S.R., Opler, L.A. The positive-negative dimension in schizophrenia: its validity and significance. Psychiatr. Dev. 1987, 5: 79-103.
    • (1987) Psychiatr. Dev , vol.5 , pp. 79-103
    • Kay, S.R.1    Opler, L.A.2
  • 21
    • 33846160926 scopus 로고    scopus 로고
    • Molecular genetics of bipolar disorder and depression
    • Kato, T. Molecular genetics of bipolar disorder and depression. Psychiatry Clin. Neurosci. 2007, 61: 3-19.
    • (2007) Psychiatry Clin. Neurosci , vol.61 , pp. 3-19
    • Kato, T.1
  • 23
    • 0242385651 scopus 로고    scopus 로고
    • Evidence for shared susceptibility in bipolar disorder and schizophrenia
    • Berrettini, W. Evidence for shared susceptibility in bipolar disorder and schizophrenia. Am. J. Med. Genet. C Semin. Med. Genet. 2003, 123: 59-64.
    • (2003) Am. J. Med. Genet. C Semin. Med. Genet , vol.123 , pp. 59-64
    • Berrettini, W.1
  • 25
    • 84969213492 scopus 로고    scopus 로고
    • 000 cases of seven common diseases and 3,000 shared controls
    • Genome-wide association study of 14
    • Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007, 447: 661-78.
    • (2007) Nature , vol.447 , pp. 661-678
  • 26
    • 0037831023 scopus 로고    scopus 로고
    • The epidemiology of major depressive disorder: Results from the National Comorbidity Survey Replication (NCS-R)
    • Kessler, R.C., Berglund, P., Demler, O., Jin, R., Koretz, D., Merikangas, K.R., Rush, A.J., Walters, E.E., Wang, P.S. The epidemiology of major depressive disorder: results from the National Comorbidity Survey Replication (NCS-R). JAMA 2003, 289: 3095-105.
    • (2003) JAMA , vol.289 , pp. 3095-3105
    • Kessler, R.C.1    Berglund, P.2    Demler, O.3    Jin, R.4    Koretz, D.5    Merikangas, K.R.6    Rush, A.J.7    Walters, E.E.8    Wang, P.S.9
  • 27
    • 0030997314 scopus 로고    scopus 로고
    • Stressful life events and genetic liability to major depression: Genetic control of exposure to the environment?
    • Kendler, K.S., Karkowski-Shuman, L. Stressful life events and genetic liability to major depression: genetic control of exposure to the environment? Psychol. Med. 1997, 27: 539-47.
    • (1997) Psychol. Med , vol.27 , pp. 539-547
    • Kendler, K.S.1    Karkowski-Shuman, L.2
  • 31
    • 33846634095 scopus 로고    scopus 로고
    • No association between the BDNF Val66Met polymorphism and mood status in a non-clinical community sample of 7389 older adults
    • Surtees, P.G., Wainwright, N.W., Willis-Owen, S.A., Sandhu, M.S., Luben, R., Day, N.E., Flint, J. No association between the BDNF Val66Met polymorphism and mood status in a non-clinical community sample of 7389 older adults. J. Psychiatr. Res. 2007, 41: 404-9.
    • (2007) J. Psychiatr. Res , vol.41 , pp. 404-409
    • Surtees, P.G.1    Wainwright, N.W.2    Willis-Owen, S.A.3    Sandhu, M.S.4    Luben, R.5    Day, N.E.6    Flint, J.7
  • 32
    • 13444280555 scopus 로고    scopus 로고
    • The relationship between stressful life events, the serotonin transporter (5-HTTLPR) genotype and major depression
    • Gillespie, N.A., Whitfield, J.B., Williams, B., Heath, A.C., Martin, N.G. The relationship between stressful life events, the serotonin transporter (5-HTTLPR) genotype and major depression. Psychol. Med. 2005, 35: 101-11.
    • (2005) Psychol. Med , vol.35 , pp. 101-111
    • Gillespie, N.A.1    Whitfield, J.B.2    Williams, B.3    Heath, A.C.4    Martin, N.G.5
  • 34
    • 0034952023 scopus 로고    scopus 로고
    • Clinical and molecular genetics of ADHD and Tourette syndrome. Two related polygenic disorders
    • Comings, D.E. Clinical and molecular genetics of ADHD and Tourette syndrome. Two related polygenic disorders. Ann. N. Y. Acad. Sci. 2001, 931: 50-83.
    • (2001) Ann. N. Y. Acad. Sci , vol.931 , pp. 50-83
    • Comings, D.E.1
  • 36
    • 33748668214 scopus 로고    scopus 로고
    • Candidate gene studies of attention-deficit/ hyperactivity disorder
    • Faraone, S.V., Khan, S.A. Candidate gene studies of attention-deficit/ hyperactivity disorder. J. Clin. Psychiatry 2006, 67 Suppl 8: 13-20.
    • (2006) J. Clin. Psychiatry , vol.67 , Issue.SUPPL. 8 , pp. 13-20
    • Faraone, S.V.1    Khan, S.A.2
  • 37
    • 33748646825 scopus 로고    scopus 로고
    • Brookes, K, Xu, X, Chen, W, Zhou, K, Neale, B, Lowe, N, Anney, R, Franke, B, Gill, M, Ebstein, R, Buitelaar, J, Sham, P, Campbell, D, Knight, J, Andreou, P, Altink, M, Arnold, R, Boer, F, Buschgens, C, Butler, L, Christiansen, H, Feldman, L, Fleischman, K, Fliers, E, Howe-Forbes, R, Goldfarb, A, Heise, A, Gabriels, I, Korn-Lubetzki, I, Johansson, L, Marco, R, Medad, S, Minderaa, R, Mulas, F, Muller, U, Mulligan, A, Rabin, K, Rommelse, N, Sethna, V, Sorohan, J, Uebel, H, Psychogiou, L, Weeks, A, Barrett, R, Craig, I, Banaschewski, T, Sonuga-Barke, E, Eisenberg, J, Kuntsi, J, Manor, L, McGuffin, P, Miranda, A, Oades, R.D, Plomin, R, Roeyers, H, Rothenberger, A, Sergeant, J, Sternhausen, H.C, Taylor, E, Thompson, M, Faraone, S.V, Asherson, P. The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Mol. Psychiatry 2006, 11
    • Brookes, K., Xu, X., Chen, W., Zhou, K., Neale, B., Lowe, N., Anney, R., Franke, B., Gill, M., Ebstein, R., Buitelaar, J., Sham, P., Campbell, D., Knight, J., Andreou, P., Altink, M., Arnold, R., Boer, F., Buschgens, C., Butler, L., Christiansen, H., Feldman, L., Fleischman, K., Fliers, E., Howe-Forbes, R., Goldfarb, A., Heise, A., Gabriels, I., Korn-Lubetzki, I., Johansson, L., Marco, R., Medad, S., Minderaa, R., Mulas, F., Muller, U., Mulligan, A., Rabin, K., Rommelse, N., Sethna, V., Sorohan, J., Uebel, H., Psychogiou, L., Weeks, A., Barrett, R., Craig, I., Banaschewski, T., Sonuga-Barke, E., Eisenberg, J., Kuntsi, J., Manor, L, McGuffin, P., Miranda, A., Oades, R.D., Plomin, R., Roeyers, H., Rothenberger, A., Sergeant, J., Sternhausen, H.C., Taylor, E., Thompson, M., Faraone, S.V., Asherson, P. The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes. Mol. Psychiatry 2006, 11: 934-53.
  • 38
    • 0042090496 scopus 로고    scopus 로고
    • Diagnosing Tourette syndrome: Is it a common disorder?
    • Robertson, M.M. Diagnosing Tourette syndrome: is it a common disorder? J. Psychosom. Res. 2003, 55: 3-6.
    • (2003) J. Psychosom. Res , vol.55 , pp. 3-6
    • Robertson, M.M.1
  • 39
    • 0042090498 scopus 로고    scopus 로고
    • An update on the genetics of Gilles de la Tourette syndrome
    • Pauls, D.L. An update on the genetics of Gilles de la Tourette syndrome. J. Psychosom. Res. 2003, 55: 7-12.
    • (2003) J. Psychosom. Res , vol.55 , pp. 7-12
    • Pauls, D.L.1
  • 44
    • 0027468019 scopus 로고
    • Association between Tourette's syndrome and homozygosity at the dopamine D3 receptor gene
    • Comings, D.E., Muhleman, D., Dietz, G., Dino, M., LeGro, R., Gade, R. Association between Tourette's syndrome and homozygosity at the dopamine D3 receptor gene. Lancet 1993, 341: 906.
    • (1993) Lancet , vol.341 , pp. 906
    • Comings, D.E.1    Muhleman, D.2    Dietz, G.3    Dino, M.4    LeGro, R.5    Gade, R.6
  • 46
    • 0029947141 scopus 로고    scopus 로고
    • Polygenic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder: The additive and subtractive effect of the three dopaminergic genes - DRD2, D beta H, and DAT1
    • Comings, D.E., Wu, S., Chiu, C., Ring, R.H., Gade, R., Ahn, C., MacMurray, J.P., Dietz, G., Muhleman, D. Polygenic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder: the additive and subtractive effect of the three dopaminergic genes - DRD2, D beta H, and DAT1. Am. J. Med. Genet. 1996, 67: 264-88.
    • (1996) Am. J. Med. Genet , vol.67 , pp. 264-288
    • Comings, D.E.1    Wu, S.2    Chiu, C.3    Ring, R.H.4    Gade, R.5    Ahn, C.6    MacMurray, J.P.7    Dietz, G.8    Muhleman, D.9
  • 47
    • 0031963425 scopus 로고    scopus 로고
    • Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse
    • Gade, R., Muhleman, D., Blake, H., MacMurray, J., Johnson, P., Verde, R., Saucier, G., Comings, D.E. Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse. Mol. Psychiatry 1998, 3: 50-60.
    • (1998) Mol. Psychiatry , vol.3 , pp. 50-60
    • Gade, R.1    Muhleman, D.2    Blake, H.3    MacMurray, J.4    Johnson, P.5    Verde, R.6    Saucier, G.7    Comings, D.E.8
  • 50
    • 0029931471 scopus 로고    scopus 로고
    • No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families
    • Barr, C.L., Wigg, K.G., Zovko, E., Sandor, P., Tsui, L.C. No evidence for a major gene effect of the dopamine D4 receptor gene in the susceptibility to Gilles de la Tourette syndrome in five Canadian families. Am. J. Med. Genet. 1996, 67: 301-5.
    • (1996) Am. J. Med. Genet , vol.67 , pp. 301-305
    • Barr, C.L.1    Wigg, K.G.2    Zovko, E.3    Sandor, P.4    Tsui, L.C.5
  • 51
    • 0027316068 scopus 로고
    • Failure to find linkage and increased homozygosity for the dopamine D3 receptor gene in Tourette's syndrome
    • Brett, P., Robertson, M., Gurling, H., Curtis, D. Failure to find linkage and increased homozygosity for the dopamine D3 receptor gene in Tourette's syndrome. Lancet 1993, 341: 1225.
    • (1993) Lancet , vol.341 , pp. 1225
    • Brett, P.1    Robertson, M.2    Gurling, H.3    Curtis, D.4
  • 52
    • 0031014917 scopus 로고    scopus 로고
    • Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome
    • Barr, C.L., Wigg, K.G., Zovko, E., Sandor, P., Tsui, L.C. Linkage study of the dopamine D5 receptor gene and Gilles de la Tourette syndrome. Am. J. Med. Genet. 1997, 74: 58-61.
    • (1997) Am. J. Med. Genet , vol.74 , pp. 58-61
    • Barr, C.L.1    Wigg, K.G.2    Zovko, E.3    Sandor, P.4    Tsui, L.C.5
  • 53
    • 0028939968 scopus 로고
    • The genetic susceptibility to Gilles de la Tourette syndrome in a large multiple affected British kindred: Linkage analysis excludes a role for the genes coding for dopamine D1, D2, D3, D4, D5 receptors, dopamine beta hydroxylase, tyrosinase, and tyrosine hydroxylase
    • Brett, P.M., Curtis, D., Robertson, M.M., Gurling, H.M. The genetic susceptibility to Gilles de la Tourette syndrome in a large multiple affected British kindred: linkage analysis excludes a role for the genes coding for dopamine D1, D2, D3, D4, D5 receptors, dopamine beta hydroxylase, tyrosinase, and tyrosine hydroxylase. Biol. Psychiatry 1995, 37: 533-40.
    • (1995) Biol. Psychiatry , vol.37 , pp. 533-540
    • Brett, P.M.1    Curtis, D.2    Robertson, M.M.3    Gurling, H.M.4
  • 54
    • 26844498125 scopus 로고    scopus 로고
    • Abelson, J.F., Kwan, K.Y., O'Roak, B.J., Baek, D.Y., Stillman, A.A., Morgan, T.M., Mathews, C.A., Pauls, D.L., Rasin, M.R., Gunel, M., Davis, N.R., Ercan-Sencicek, A.G., Guez, D.H., Spertus, J.A., Leckman, J.F., Dure, L.S.t., Kurlan, R., Singer, H.S., Gilbert, D.L., Farhi, A., Louvi, A., Lifton, R.P., Sestan, N., State, M.W. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science 2005, 310: 317-20.
    • Abelson, J.F., Kwan, K.Y., O'Roak, B.J., Baek, D.Y., Stillman, A.A., Morgan, T.M., Mathews, C.A., Pauls, D.L., Rasin, M.R., Gunel, M., Davis, N.R., Ercan-Sencicek, A.G., Guez, D.H., Spertus, J.A., Leckman, J.F., Dure, L.S.t., Kurlan, R., Singer, H.S., Gilbert, D.L., Farhi, A., Louvi, A., Lifton, R.P., Sestan, N., State, M.W. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science 2005, 310: 317-20.
  • 55
    • 0025181072 scopus 로고
    • Prevalence of reading disability in boys and girls. Results of the Connecticut Longitudinal Study
    • Shaywitz, S.E., Shaywitz, B.A., Fletcher, J.M., Escobar, M.D. Prevalence of reading disability in boys and girls. Results of the Connecticut Longitudinal Study. Jama 1990, 264: 998-1002.
    • (1990) Jama , vol.264 , pp. 998-1002
    • Shaywitz, S.E.1    Shaywitz, B.A.2    Fletcher, J.M.3    Escobar, M.D.4
  • 56
    • 35148862570 scopus 로고    scopus 로고
    • A review of association and linkage studies for genetical analyses of learning disorders
    • Caylak, E. A review of association and linkage studies for genetical analyses of learning disorders. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2007, 144: 923-43.
    • (2007) Am. J. Med. Genet. B Neuropsychiatr. Genet , vol.144 , pp. 923-943
    • Caylak, E.1
  • 60
    • 0036752812 scopus 로고    scopus 로고
    • Genetic and environmental factors in febrile seizures: A Danish population-based twin study
    • Kjeldsen, M.J., Kyvik, K.O., Friis, M.L., Christensen, K. Genetic and environmental factors in febrile seizures: a Danish population-based twin study. Epilepsy Res. 2002, 51: 167-77.
    • (2002) Epilepsy Res , vol.51 , pp. 167-177
    • Kjeldsen, M.J.1    Kyvik, K.O.2    Friis, M.L.3    Christensen, K.4
  • 67
    • 0030749655 scopus 로고    scopus 로고
    • Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies
    • Steinlein, O., Sander, T., Stoodt, J., Kretz, R., Janz, D., Propping, P. Possible association of a silent polymorphism in the neuronal nicotinic acetylcholine receptor subunit alpha4 with common idiopathic generalized epilepsies. Am. J. Med. Genet. 1997, 74: 445-9.
    • (1997) Am. J. Med. Genet , vol.74 , pp. 445-449
    • Steinlein, O.1    Sander, T.2    Stoodt, J.3    Kretz, R.4    Janz, D.5    Propping, P.6
  • 68
    • 0033625146 scopus 로고    scopus 로고
    • Interleukin (IL)1beta, IL-1alpha, and IL-1 receptor antagonist gene polymorphisms in patients with temporal lobe epilepsy
    • Kanemoto, K., Kawasaki, J., Miyamoto, T., Obayashi, H., Nishimura, M. Interleukin (IL)1beta, IL-1alpha, and IL-1 receptor antagonist gene polymorphisms in patients with temporal lobe epilepsy. Ann. Neurol. 2000, 47: 571-4.
    • (2000) Ann. Neurol , vol.47 , pp. 571-574
    • Kanemoto, K.1    Kawasaki, J.2    Miyamoto, T.3    Obayashi, H.4    Nishimura, M.5
  • 69
    • 0036263088 scopus 로고    scopus 로고
    • Polymorphisms for interleukin 1 beta exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions
    • Tsai, F.J., Hsieh, Y.Y., Chang, C.C., Lin, C.C., Tsai, C.H. Polymorphisms for interleukin 1 beta exon 5 and interleukin 1 receptor antagonist in Taiwanese children with febrile convulsions. Arch. Pediatr. Adolesc. Med. 2002, 156: 545-8.
    • (2002) Arch. Pediatr. Adolesc. Med , vol.156 , pp. 545-548
    • Tsai, F.J.1    Hsieh, Y.Y.2    Chang, C.C.3    Lin, C.C.4    Tsai, C.H.5
  • 72
    • 0037032589 scopus 로고    scopus 로고
    • Association analysis between the human interleukin 1beta (-511) gene polymorphism and susceptibility to febrile convulsions
    • Tilgen, N., Pfeiffer, H., Cobilanschi, J., Rau, B., Horvath, S., Elger, C.E., Propping, P., Heils, A. Association analysis between the human interleukin 1beta (-511) gene polymorphism and susceptibility to febrile convulsions. Neurosci. Lett. 2002, 334: 68-70.
    • (2002) Neurosci. Lett , vol.334 , pp. 68-70
    • Tilgen, N.1    Pfeiffer, H.2    Cobilanschi, J.3    Rau, B.4    Horvath, S.5    Elger, C.E.6    Propping, P.7    Heils, A.8
  • 73
    • 2342644850 scopus 로고    scopus 로고
    • Febrile convulsions and genetic susceptibility: Role of the neuronal nicotinic acetylcholine receptor alpha 4 subunit
    • author reply 561-2
    • Mulley, J., Heron, S., Scheffer, I., Berkovic, S. Febrile convulsions and genetic susceptibility: role of the neuronal nicotinic acetylcholine receptor alpha 4 subunit. Epilepsia 2004, 45: 561; author reply 561-2.
    • (2004) Epilepsia , vol.45 , pp. 561
    • Mulley, J.1    Heron, S.2    Scheffer, I.3    Berkovic, S.4
  • 74
    • 24344435545 scopus 로고    scopus 로고
    • Interleukin-1alpha, interleukin-1beta, and interleukin-1Ra polymorphisms in febrile seizures
    • Haspolat, S., Baysal, Y., Duman, O., Coskun, M., Tosun, O., Yegin, O. Interleukin-1alpha, interleukin-1beta, and interleukin-1Ra polymorphisms in febrile seizures. J. Child Neurol. 2005, 20: 565-8.
    • (2005) J. Child Neurol , vol.20 , pp. 565-568
    • Haspolat, S.1    Baysal, Y.2    Duman, O.3    Coskun, M.4    Tosun, O.5    Yegin, O.6
  • 75
    • 33947099991 scopus 로고    scopus 로고
    • Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy
    • Hempelmann, A., Cobilanschi, J., Heils, A., Muhle, H., Stephani, U., Weber, Y., Lerche, H., Sander, T. Lack of evidence of an allelic association of a functional GABRB3 exon 1a promoter polymorphism with idiopathic generalized epilepsy. Epilepsy Res. 2007, 74: 28-32.
    • (2007) Epilepsy Res , vol.74 , pp. 28-32
    • Hempelmann, A.1    Cobilanschi, J.2    Heils, A.3    Muhle, H.4    Stephani, U.5    Weber, Y.6    Lerche, H.7    Sander, T.8
  • 76
    • 0035464960 scopus 로고    scopus 로고
    • Monogenic causes of X-linked mental retardation
    • Chelly, J., Mandel, J.L. Monogenic causes of X-linked mental retardation. Nat. Rev. Genet. 2001, 2: 669-80.
    • (2001) Nat. Rev. Genet , vol.2 , pp. 669-680
    • Chelly, J.1    Mandel, J.L.2
  • 78
    • 0021052051 scopus 로고
    • Epidemiology of mental retardation - a Swedish survey
    • Hagberg, B., Kyllerman, M. Epidemiology of mental retardation - a Swedish survey. Brain Dev. 1983, 5: 441-9.
    • (1983) Brain Dev , vol.5 , pp. 441-449
    • Hagberg, B.1    Kyllerman, M.2
  • 79
    • 0030137717 scopus 로고    scopus 로고
    • Identification of the gene FMR2, associated with FRAXE mental retardation
    • Gecz, J., Gedeon, A.K., Sutherland, G.R., Mulley, J.C. Identification of the gene FMR2, associated with FRAXE mental retardation. Nat. Genet. 1996, 13: 105-8.
    • (1996) Nat. Genet , vol.13 , pp. 105-108
    • Gecz, J.1    Gedeon, A.K.2    Sutherland, G.R.3    Mulley, J.C.4
  • 86
    • 0033968407 scopus 로고    scopus 로고
    • Zemni, R., Bienvenu, T., Vinet, M.C., Sefiani, A., Carrie, A., Billuart, P., McDonell, N., Couvert, P., Francis, F., Chafey, P., Fauchereau, F., Friocourt, G., des Portes, V., Cardona, A., Frints, S., Meindl, A., Brandau, O., Ronce, N., Moraine, C., van Bokhoven, H., Ropers, H.H., Sudbrak, R., Kahn, A., Fryns, J.P., Beldjord, C., Chelly, J. A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation. Nat. Genet. 2000, 24: 167-70.
    • Zemni, R., Bienvenu, T., Vinet, M.C., Sefiani, A., Carrie, A., Billuart, P., McDonell, N., Couvert, P., Francis, F., Chafey, P., Fauchereau, F., Friocourt, G., des Portes, V., Cardona, A., Frints, S., Meindl, A., Brandau, O., Ronce, N., Moraine, C., van Bokhoven, H., Ropers, H.H., Sudbrak, R., Kahn, A., Fryns, J.P., Beldjord, C., Chelly, J. A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation. Nat. Genet. 2000, 24: 167-70.
  • 90
    • 16844381297 scopus 로고    scopus 로고
    • Genetic susceptibility to substance dependence
    • Hiroi, N., Agatsuma, S. Genetic susceptibility to substance dependence. Mol. Psychiatry 2005, 10: 336-44.
    • (2005) Mol. Psychiatry , vol.10 , pp. 336-344
    • Hiroi, N.1    Agatsuma, S.2
  • 91
    • 0033301678 scopus 로고    scopus 로고
    • The genetic epidemiology of smoking
    • discussion S69-70
    • Sullivan, P.F., Kendler, K.S. The genetic epidemiology of smoking. Nicotine Tob. Res. 1999, 1 Suppl 2: S51-7; discussion S69-70.
    • (1999) Nicotine Tob. Res , vol.1 , Issue.SUPPL. 2
    • Sullivan, P.F.1    Kendler, K.S.2
  • 93
    • 0029021015 scopus 로고
    • Dopamine transporter gene polymorphism and alcoholism
    • Muramatsu, T., Higuchi, S. Dopamine transporter gene polymorphism and alcoholism. Biochem. Biophys. Res. Commun. 1995, 211: 28-32.
    • (1995) Biochem. Biophys. Res. Commun , vol.211 , pp. 28-32
    • Muramatsu, T.1    Higuchi, S.2
  • 94
    • 33645784017 scopus 로고    scopus 로고
    • An association between the DAT1 polymorphism and smoking behavior in young adults from the National Longitudinal Study of Adolescent Health
    • Timberlake, D.S., Haberstick, B.C., Lessem, J.M., Smolen, A., Ehringer, M., Hewitt, J.K., Hopfer, C. An association between the DAT1 polymorphism and smoking behavior in young adults from the National Longitudinal Study of Adolescent Health. Health Psychol. 2006, 25: 190-7.
    • (2006) Health Psychol , vol.25 , pp. 190-197
    • Timberlake, D.S.1    Haberstick, B.C.2    Lessem, J.M.3    Smolen, A.4    Ehringer, M.5    Hewitt, J.K.6    Hopfer, C.7
  • 101
    • 0034626405 scopus 로고    scopus 로고
    • Confirmation of an excess of the high enzyme activity COMT val allele in heroin addicts in a family-based haplotype relative risk study
    • Horowitz, R., Kotler, M., Shufman, E., Aharoni, S., Kremer, I., Cohen, H., Ebstein, R.P. Confirmation of an excess of the high enzyme activity COMT val allele in heroin addicts in a family-based haplotype relative risk study. Am. J. Med. Genet. 2000, 96: 599-603.
    • (2000) Am. J. Med. Genet , vol.96 , pp. 599-603
    • Horowitz, R.1    Kotler, M.2    Shufman, E.3    Aharoni, S.4    Kremer, I.5    Cohen, H.6    Ebstein, R.P.7
  • 102
    • 4544328497 scopus 로고    scopus 로고
    • The genetic basis for smoking behavior: A systematic review and meta-analysis
    • Munafo, M., Clark, T., Johnstone, E., Murphy, M., Walton, R. The genetic basis for smoking behavior: a systematic review and meta-analysis. Nicotine Tob. Res. 2004, 6: 583-97.
    • (2004) Nicotine Tob. Res , vol.6 , pp. 583-597
    • Munafo, M.1    Clark, T.2    Johnstone, E.3    Murphy, M.4    Walton, R.5
  • 103
    • 34247542196 scopus 로고    scopus 로고
    • Association of the DRD2 gene Taq1A polymorphism and alcoholism: A meta-analysis of case-control studies and evidence of publication bias
    • Munafo, M.R., Matheson, I.J., Flint, J. Association of the DRD2 gene Taq1A polymorphism and alcoholism: a meta-analysis of case-control studies and evidence of publication bias. Mol. Psychiatry 2007, 12: 454-61.
    • (2007) Mol. Psychiatry , vol.12 , pp. 454-461
    • Munafo, M.R.1    Matheson, I.J.2    Flint, J.3
  • 104
    • 34347269144 scopus 로고    scopus 로고
    • Alcohol dehydrogenase 1B genotype and fetal alcohol syndrome: A HuGE minireview
    • Green, R.F., Stoler, J.M. Alcohol dehydrogenase 1B genotype and fetal alcohol syndrome: a HuGE minireview. Am. J. Obstet. Gynecol. 2007, 197: 12-25.
    • (2007) Am. J. Obstet. Gynecol , vol.197 , pp. 12-25
    • Green, R.F.1    Stoler, J.M.2
  • 105
    • 0031172819 scopus 로고    scopus 로고
    • Variation in induction of human placental CYP2E1: Possible role in susceptibility to fetal alcohol syndrome?
    • Rasheed, A., Hines, R.N., McCarver-May, D.G. Variation in induction of human placental CYP2E1: possible role in susceptibility to fetal alcohol syndrome? Toxicol. Appl. Pharmacol. 1997, 144: 396-400.
    • (1997) Toxicol. Appl. Pharmacol , vol.144 , pp. 396-400
    • Rasheed, A.1    Hines, R.N.2    McCarver-May, D.G.3
  • 106
    • 0031577540 scopus 로고    scopus 로고
    • Expression of CYP2E1 during embryogenesis and fetogenesis in human cephalic tissues: Implications for the fetal alcohol syndrome
    • Boutelet-Bochan, H., Huang, Y., Juchau, M.R. Expression of CYP2E1 during embryogenesis and fetogenesis in human cephalic tissues: implications for the fetal alcohol syndrome. Biochem. Biophys. Res. Commun. 1997, 238: 443-7.
    • (1997) Biochem. Biophys. Res. Commun , vol.238 , pp. 443-447
    • Boutelet-Bochan, H.1    Huang, Y.2    Juchau, M.R.3
  • 108
    • 0034810295 scopus 로고    scopus 로고
    • A review and meta-analysis of the genetic epidemiology of anxiety disorders
    • Hettema, J.M., Neale, M.C., Kendler, K.S. A review and meta-analysis of the genetic epidemiology of anxiety disorders. Am. J. Psychiatry 2001, 158: 1568-78.
    • (2001) Am. J. Psychiatry , vol.158 , pp. 1568-1578
    • Hettema, J.M.1    Neale, M.C.2    Kendler, K.S.3
  • 113
    • 34047157648 scopus 로고    scopus 로고
    • Samuels, J., Shugart, Y.Y., Grados, M.A., Willour, V.L., Bienvenu, O.J., Greenberg, B.D., Knowles, J.A., McCracken, J.T., Rauch, S.L., Murphy, D.L., Wang, Y., Pinto, A., Fyer, A.J., Piacentini, J., Pauls, D.L., Cullen, B., Rasmussen, S.A., Hoehn-Saric, R., Valle, D., Liang, K.Y., Riddle, M.A., Nestadt, G. Significant linkage to compulsive hoarding on chromosome 14 in families with obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study. Am. J. Psychiatry 2007, 164: 493-9.
    • Samuels, J., Shugart, Y.Y., Grados, M.A., Willour, V.L., Bienvenu, O.J., Greenberg, B.D., Knowles, J.A., McCracken, J.T., Rauch, S.L., Murphy, D.L., Wang, Y., Pinto, A., Fyer, A.J., Piacentini, J., Pauls, D.L., Cullen, B., Rasmussen, S.A., Hoehn-Saric, R., Valle, D., Liang, K.Y., Riddle, M.A., Nestadt, G. Significant linkage to compulsive hoarding on chromosome 14 in families with obsessive-compulsive disorder: results from the OCD Collaborative Genetics Study. Am. J. Psychiatry 2007, 164: 493-9.
  • 114
    • 33746545576 scopus 로고    scopus 로고
    • Shugart, Y.Y., Samuels, J., Willour, V.L., Grados, M.A., Greenberg, B.D., Knowles, J.A., McCracken, J.T., Rauch, S.L., Murphy, D.L., Wang, Y., Pinto, A., Fyer, A.J., Piacentini, J., Pauls, D.L., Cullen, B., Page, J., Rasmussen, S.A., Bienvenu, O.J., Hoehn-Saric, R., Valle, D., Liang, K.Y., Riddle, M.A., Nestadt, G. Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q. Mol. Psychiatry 2006, 11: 763-70.
    • Shugart, Y.Y., Samuels, J., Willour, V.L., Grados, M.A., Greenberg, B.D., Knowles, J.A., McCracken, J.T., Rauch, S.L., Murphy, D.L., Wang, Y., Pinto, A., Fyer, A.J., Piacentini, J., Pauls, D.L., Cullen, B., Page, J., Rasmussen, S.A., Bienvenu, O.J., Hoehn-Saric, R., Valle, D., Liang, K.Y., Riddle, M.A., Nestadt, G. Genomewide linkage scan for obsessive-compulsive disorder: evidence for susceptibility loci on chromosomes 3q, 7p, 1q, 15q, and 6q. Mol. Psychiatry 2006, 11: 763-70.
  • 116
    • 1442289923 scopus 로고    scopus 로고
    • Genome-wide linkage scan for loci predisposing to social phobia: Evidence for a chromosome 16 risk locus
    • Gelernter, J., Page, G.P., Stein, M.B., Woods, S.W. Genome-wide linkage scan for loci predisposing to social phobia: evidence for a chromosome 16 risk locus. Am. J. Psychiatry 2004, 161: 59-66.
    • (2004) Am. J. Psychiatry , vol.161 , pp. 59-66
    • Gelernter, J.1    Page, G.P.2    Stein, M.B.3    Woods, S.W.4
  • 120
    • 33645470916 scopus 로고    scopus 로고
    • Genome scan for loci predisposing to anxiety disorders using a novel multivariate approach: Strong evidence for a chromosome 4 risk locus
    • Kaabi, B., Gelernter, J., Woods, S.W., Goddard, A., Page, G.P., Elston, R.C. Genome scan for loci predisposing to anxiety disorders using a novel multivariate approach: strong evidence for a chromosome 4 risk locus. Am. J. Hum. Genet. 2006, 78: 543-53.
    • (2006) Am. J. Hum. Genet , vol.78 , pp. 543-553
    • Kaabi, B.1    Gelernter, J.2    Woods, S.W.3    Goddard, A.4    Page, G.P.5    Elston, R.C.6
  • 125
    • 0031984203 scopus 로고    scopus 로고
    • Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease
    • Deckert, J., Nothen, M.M., Franke, P., Delmo, C., Fritze, J., Knapp, M., Maier, W., Beckmann, H., Propping, P. Systematic mutation screening and association study of the A1 and A2a adenosine receptor genes in panic disorder suggest a contribution of the A2a gene to the development of disease. Mol. Psychiatry 1998, 3: 81-5.
    • (1998) Mol. Psychiatry , vol.3 , pp. 81-85
    • Deckert, J.1    Nothen, M.M.2    Franke, P.3    Delmo, C.4    Fritze, J.5    Knapp, M.6    Maier, W.7    Beckmann, H.8    Propping, P.9
  • 127
    • 0037904330 scopus 로고    scopus 로고
    • Domschke, K., Kuhlenbaumer, G., Schirmacher, A., Lorenzi, C., Armengol, L., DiBella, D., Gratacos, M., Garritsen, H.S., Nothen, M.M., Franke, P., Sand, P., Fritze, J., Perez, G., Maier, W., Sibrowski, W., Estivill, X., Bellodi, L., Ringelstein, E.B., Arolt, V., Martin-Santos, R., Catalano, M., Stogbauer, F., Deckert, J. Human nuclear transcription factor gene CREM: genomic organization, mutation screening, and association analysis in panic disorder. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2003, 117: 70-8.
    • Domschke, K., Kuhlenbaumer, G., Schirmacher, A., Lorenzi, C., Armengol, L., DiBella, D., Gratacos, M., Garritsen, H.S., Nothen, M.M., Franke, P., Sand, P., Fritze, J., Perez, G., Maier, W., Sibrowski, W., Estivill, X., Bellodi, L., Ringelstein, E.B., Arolt, V., Martin-Santos, R., Catalano, M., Stogbauer, F., Deckert, J. Human nuclear transcription factor gene CREM: genomic organization, mutation screening, and association analysis in panic disorder. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2003, 117: 70-8.
  • 129
    • 33746498349 scopus 로고    scopus 로고
    • Association between glutamic acid decarboxylase genes and anxiety disorders, major depression, and neuroticism
    • Hettema, J.M., An, S.S., Neale, M.C., Bukszar, J., van den Oord, E.J., Kendler, K.S., Chen, X. Association between glutamic acid decarboxylase genes and anxiety disorders, major depression, and neuroticism. Mol. Psychiatry 2006, 11: 752-62.
    • (2006) Mol. Psychiatry , vol.11 , pp. 752-762
    • Hettema, J.M.1    An, S.S.2    Neale, M.C.3    Bukszar, J.4    van den Oord, E.J.5    Kendler, K.S.6    Chen, X.7
  • 134
    • 1942475408 scopus 로고    scopus 로고
    • A family-based association study of the 5-HT-1Dbeta receptor gene in obsessive-compulsive disorder
    • Camarena, B., Aguilar, A., Loyzaga, C., Nicolini, H. A family-based association study of the 5-HT-1Dbeta receptor gene in obsessive-compulsive disorder. Int. J. Neuropsychopharmacol. 2004, 7: 49-53.
    • (2004) Int. J. Neuropsychopharmacol , vol.7 , pp. 49-53
    • Camarena, B.1    Aguilar, A.2    Loyzaga, C.3    Nicolini, H.4
  • 136
    • 1642503730 scopus 로고    scopus 로고
    • Association analysis of the catechol-o-methyltransferase (COMT), serotonin transporter (5-HTT) and serotonin 2A receptor (5HT2A) gene polymorphisms with obsessive-compulsive disorder
    • Meira-Lima, I., Shavitt, R.G., Miguita, K., Ikenaga, E., Miguel, E.C., Vallada, H. Association analysis of the catechol-o-methyltransferase (COMT), serotonin transporter (5-HTT) and serotonin 2A receptor (5HT2A) gene polymorphisms with obsessive-compulsive disorder. Genes Brain Behav. 2004, 3: 75-9.
    • (2004) Genes Brain Behav , vol.3 , pp. 75-79
    • Meira-Lima, I.1    Shavitt, R.G.2    Miguita, K.3    Ikenaga, E.4    Miguel, E.C.5    Vallada, H.6
  • 138
    • 1542314848 scopus 로고    scopus 로고
    • A meta-analysis of the association between the serotonin transporter gene polymorphism (5-HTTLPR) and trait anxiety
    • Schinka, J.A., Busch, R.M., Robichaux-Keene, N. A meta-analysis of the association between the serotonin transporter gene polymorphism (5-HTTLPR) and trait anxiety. Mol. Psychiatry 2004, 9: 197-202.
    • (2004) Mol. Psychiatry , vol.9 , pp. 197-202
    • Schinka, J.A.1    Busch, R.M.2    Robichaux-Keene, N.3
  • 139
    • 2142817209 scopus 로고    scopus 로고
    • Meta-analysis of the association between a serotonin transporter promoter polymorphism (5-HTTLPR) and anxiety-related personality traits
    • Sen, S., Burmeister, M., Ghosh, D. Meta-analysis of the association between a serotonin transporter promoter polymorphism (5-HTTLPR) and anxiety-related personality traits. Am. J. Med. Genet. B Neuropsychiatr. Genet. 2004, 127: 85-9.
    • (2004) Am. J. Med. Genet. B Neuropsychiatr. Genet , vol.127 , pp. 85-89
    • Sen, S.1    Burmeister, M.2    Ghosh, D.3
  • 143
    • 36248971736 scopus 로고    scopus 로고
    • Interaction between BDNF Val66Met and dopamine transporter gene variation influences anxiety-related traits
    • Hunnerkopf R., Strobel, A., Gutknecht, L., Brocke, B., Lesch, K.P. Interaction between BDNF Val66Met and dopamine transporter gene variation influences anxiety-related traits. Neuropsychopharmacology 2007, 32: 2552-60.
    • (2007) Neuropsychopharmacology , vol.32 , pp. 2552-2560
    • Hunnerkopf, R.1    Strobel, A.2    Gutknecht, L.3    Brocke, B.4    Lesch, K.P.5
  • 148
    • 0027410515 scopus 로고
    • A twin study of genetic and environmental contributions to liability for posttraumatic stress symptoms
    • True, W.R., Rice, J., Eisen, S.A., Heath, A.C., Goldberg, J., Lyons, M.J., Nowak, J. A twin study of genetic and environmental contributions to liability for posttraumatic stress symptoms. Arch. Gen. Psychiatry 1993, 50: 257-64.
    • (1993) Arch. Gen. Psychiatry , vol.50 , pp. 257-264
    • True, W.R.1    Rice, J.2    Eisen, S.A.3    Heath, A.C.4    Goldberg, J.5    Lyons, M.J.6    Nowak, J.7
  • 153
    • 0030222484 scopus 로고    scopus 로고
    • Dopamine D2 receptor (DRD2) gene and susceptibility to posttraumatic stress disorder: A study and replication
    • Comings, D.E., Muhleman, D., Gysin, R. Dopamine D2 receptor (DRD2) gene and susceptibility to posttraumatic stress disorder: a study and replication. Biol. Psychiatry 1996, 40: 368-72.
    • (1996) Biol. Psychiatry , vol.40 , pp. 368-372
    • Comings, D.E.1    Muhleman, D.2    Gysin, R.3
  • 154
    • 0032535420 scopus 로고    scopus 로고
    • Heritability of binge-eating and broadly defined bulimia nervosa
    • Bulik, C.M., Sullivan, P.F., Kendler, K.S. Heritability of binge-eating and broadly defined bulimia nervosa. Biol. Psychiatry 1998, 44: 1210-8.
    • (1998) Biol. Psychiatry , vol.44 , pp. 1210-1218
    • Bulik, C.M.1    Sullivan, P.F.2    Kendler, K.S.3
  • 155
    • 0035002124 scopus 로고    scopus 로고
    • Genetic and environmental influences on anorexia nervosa syndromes in a population-based twin sample
    • Klump, K.L., Miller, K.B., Keel, P.K., McGue, M., Iacono, W.G. Genetic and environmental influences on anorexia nervosa syndromes in a population-based twin sample. Psychol. Med. 2001, 31: 737-40.
    • (2001) Psychol. Med , vol.31 , pp. 737-740
    • Klump, K.L.1    Miller, K.B.2    Keel, P.K.3    McGue, M.4    Iacono, W.G.5
  • 158
    • 0031561157 scopus 로고    scopus 로고
    • Association between 5-HT2A gene promoter polymorphism and anorexia nervosa
    • Collier, D.A., Arranz, M.J., Li, T., Mupita, D., Brown, N., Treasure, J. Association between 5-HT2A gene promoter polymorphism and anorexia nervosa. Lancet 1997, 350: 412.
    • (1997) Lancet , vol.350 , pp. 412
    • Collier, D.A.1    Arranz, M.J.2    Li, T.3    Mupita, D.4    Brown, N.5    Treasure, J.6
  • 160
    • 0033937156 scopus 로고    scopus 로고
    • Serotonin transporter linked polymorphic region in anorexia nervosa and bulimia nervosa
    • Di Bella, D.D., Catalano, M., Cavallini, M.C., Riboldi, C., Bellodi, L. Serotonin transporter linked polymorphic region in anorexia nervosa and bulimia nervosa. Mol. Psychiatry 2000, 5: 233-4.
    • (2000) Mol. Psychiatry , vol.5 , pp. 233-234
    • Di Bella, D.D.1    Catalano, M.2    Cavallini, M.C.3    Riboldi, C.4    Bellodi, L.5
  • 161
    • 0032515550 scopus 로고    scopus 로고
    • Lack of association between 5-HT2A gene promoter polymorphism and susceptibility to anorexia nervosa
    • Campbell, D.A., Sundaramurthy, D., Markham, A.F., Pieri, L.F. Lack of association between 5-HT2A gene promoter polymorphism and susceptibility to anorexia nervosa. Lancet 1998, 351: 499.
    • (1998) Lancet , vol.351 , pp. 499
    • Campbell, D.A.1    Sundaramurthy, D.2    Markham, A.F.3    Pieri, L.F.4
  • 162
    • 0032725028 scopus 로고    scopus 로고
    • Allelic variation of the 5-HT2C receptor (HTR2C) in bulimia nervosa and binge eating disorder
    • Burnet, P.W., Smith, K.A., Cowen, P.J., Fairburn, C.G., Harrison, P.J. Allelic variation of the 5-HT2C receptor (HTR2C) in bulimia nervosa and binge eating disorder. Psychiatr. Genet. 1999, 9: 101-4.
    • (1999) Psychiatr. Genet , vol.9 , pp. 101-104
    • Burnet, P.W.1    Smith, K.A.2    Cowen, P.J.3    Fairburn, C.G.4    Harrison, P.J.5
  • 164
    • 3042736862 scopus 로고    scopus 로고
    • Ribases, M., Gratacos, M., Fernandez-Aranda, F., Bellodi, L., Boni, C., Anderluh, M., Cavallini, M.C., Cellini, E., Di Bella, D., Erzegovesi, S., Foulon, C., Gabrovsek, M., Gorwood, P., Hebebrand, J., Hinney, A., Holliday, J., Hu, X., Karwautz, A., Kipman, A., Komel, R., Nacmias, B., Remschmidt, H., Ricca, V., Sorbi, S., Wagner, G., Treasure, J., Collier, D.A., Estivill, X. Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations. Hum. Mol. Genet. 2004, 13: 1205-12.
    • Ribases, M., Gratacos, M., Fernandez-Aranda, F., Bellodi, L., Boni, C., Anderluh, M., Cavallini, M.C., Cellini, E., Di Bella, D., Erzegovesi, S., Foulon, C., Gabrovsek, M., Gorwood, P., Hebebrand, J., Hinney, A., Holliday, J., Hu, X., Karwautz, A., Kipman, A., Komel, R., Nacmias, B., Remschmidt, H., Ricca, V., Sorbi, S., Wagner, G., Treasure, J., Collier, D.A., Estivill, X. Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations. Hum. Mol. Genet. 2004, 13: 1205-12.
  • 166
    • 33748751178 scopus 로고    scopus 로고
    • Association of catecholamine-O-methyltransferase and 5-HTTLPR genotype with eating disorder-related behavior and attitudes in females with eating disorders
    • Frieling, H., Romer, K.D., Wilhelm, J., Hillemacher, T., Kornhuber, J., de Zwaan, M., Jacoby, G.E., Bleich, S. Association of catecholamine-O-methyltransferase and 5-HTTLPR genotype with eating disorder-related behavior and attitudes in females with eating disorders. Psychiatr. Genet. 2006, 16: 205-8.
    • (2006) Psychiatr. Genet , vol.16 , pp. 205-208
    • Frieling, H.1    Romer, K.D.2    Wilhelm, J.3    Hillemacher, T.4    Kornhuber, J.5    de Zwaan, M.6    Jacoby, G.E.7    Bleich, S.8
  • 167
    • 33750729945 scopus 로고    scopus 로고
    • Association of eating disorders with catechol-o-methyltransferase gene functional polymorphism
    • Mikolajczyk, E., Smiarowska, M., Grzywacz, A., Samochowiec, J. Association of eating disorders with catechol-o-methyltransferase gene functional polymorphism. Neuropsychobiology 2006, 54: 82-6.
    • (2006) Neuropsychobiology , vol.54 , pp. 82-86
    • Mikolajczyk, E.1    Smiarowska, M.2    Grzywacz, A.3    Samochowiec, J.4
  • 168
    • 0037974499 scopus 로고    scopus 로고
    • Epidemiology of neural tube defects
    • Frey, L., Hauser, W.A. Epidemiology of neural tube defects. Epilepsia 2003, 44 Suppl 3: 4-13.
    • (2003) Epilepsia , vol.44 , Issue.SUPPL. 3 , pp. 4-13
    • Frey, L.1    Hauser, W.A.2
  • 169
    • 33646749888 scopus 로고    scopus 로고
    • Etiology, pathogenesis and prevention of neural tube defects
    • Padmanabhan, R. Etiology, pathogenesis and prevention of neural tube defects. Congenit. Anom. (Kyoto) 2006, 46: 55-67.
    • (2006) Congenit. Anom. (Kyoto) , vol.46 , pp. 55-67
    • Padmanabhan, R.1
  • 174
    • 29344447985 scopus 로고    scopus 로고
    • A known functional polymorphism (Ile 120Val) of the human PCMT1 gene and risk of spina bifida
    • Zhu, H., Yang, W., Lu, W., Zhang, J., Shaw, G.M., Lammer, E.J., Finnell, R.H. A known functional polymorphism (Ile 120Val) of the human PCMT1 gene and risk of spina bifida. Mol. Genet. Metab. 2006, 87: 66-70.
    • (2006) Mol. Genet. Metab , vol.87 , pp. 66-70
    • Zhu, H.1    Yang, W.2    Lu, W.3    Zhang, J.4    Shaw, G.M.5    Lammer, E.J.6    Finnell, R.H.7
  • 175
    • 33947682250 scopus 로고    scopus 로고
    • Association between CFL1 gene polymorphisms and spina bifida risk in a California population
    • Zhu, H., Enaw, J.O., Ma, C., Shaw, G.M., Lammer, E.J., Finnell, R.H. Association between CFL1 gene polymorphisms and spina bifida risk in a California population. BMC Med. Genet. 2007, 8: 12.
    • (2007) BMC Med. Genet , vol.8 , pp. 12
    • Zhu, H.1    Enaw, J.O.2    Ma, C.3    Shaw, G.M.4    Lammer, E.J.5    Finnell, R.H.6
  • 176
    • 0023038860 scopus 로고
    • Epidemiology of infantile hydrocephalus in Sweden. I. Birth prevalence and general data
    • Fernell, E., Hagberg, B., Hagberg, G., von Wendt, L. Epidemiology of infantile hydrocephalus in Sweden. I. Birth prevalence and general data. Acta Paediatr. Scand. 1986, 75: 975-81.
    • (1986) Acta Paediatr. Scand , vol.75 , pp. 975-981
    • Fernell, E.1    Hagberg, B.2    Hagberg, G.3    von Wendt, L.4
  • 177
    • 0022571148 scopus 로고
    • X linked hydrocephalus: A survey of a 20 year period in Victoria, Australia
    • Halliday, J., Chow, CW., Wallace, D., Danks, D.M. X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia. J. Med. Genet. 1986, 23: 23-31.
    • (1986) J. Med. Genet , vol.23 , pp. 23-31
    • Halliday, J.1    Chow, C.W.2    Wallace, D.3    Danks, D.M.4
  • 178
    • 0024103321 scopus 로고
    • Heterogeneity in familial hydrocephalus
    • Willems, P.J. Heterogeneity in familial hydrocephalus. Am. J. Med. Genet. 1988, 31: 471-3.
    • (1988) Am. J. Med. Genet , vol.31 , pp. 471-473
    • Willems, P.J.1
  • 179
    • 0027080958 scopus 로고
    • An epidemiologic study of environmental and genetic factors in congenital hydrocephalus
    • Stoll, C., Alembik, Y., Dott, B., Roth, M.P. An epidemiologic study of environmental and genetic factors in congenital hydrocephalus. Eur. J. Epidemiol. 1992, 8: 797-803.
    • (1992) Eur. J. Epidemiol , vol.8 , pp. 797-803
    • Stoll, C.1    Alembik, Y.2    Dott, B.3    Roth, M.P.4
  • 180
    • 0033047253 scopus 로고    scopus 로고
    • Congenital hydrocephalus internus and aqueduct stenosis: Aetiology and implications for genetic counselling
    • Haverkamp, F., Wolfle, J., Aretz, M., Kramer, A., Hohmann, B., Fahnenstich, H., Zerres, K. Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counselling. Eur. J. Pediatr. 1999, 158: 474-8.
    • (1999) Eur. J. Pediatr , vol.158 , pp. 474-478
    • Haverkamp, F.1    Wolfle, J.2    Aretz, M.3    Kramer, A.4    Hohmann, B.5    Fahnenstich, H.6    Zerres, K.7
  • 181
    • 33750633677 scopus 로고    scopus 로고
    • Genetics of human hydrocephalus
    • Zhang, J., Williams, M.A., Rigamonti, D. Genetics of human hydrocephalus. J. Neurol. 2006, 253: 1255-66.
    • (2006) J. Neurol , vol.253 , pp. 1255-1266
    • Zhang, J.1    Williams, M.A.2    Rigamonti, D.3
  • 182
    • 0033910448 scopus 로고    scopus 로고
    • Mental retardation and developmental disabilities influenced by environmental neurotoxic insults
    • Schroeder, S.R. Mental retardation and developmental disabilities influenced by environmental neurotoxic insults. Environ. Health Perspect. 2000, 108 Suppl 3: 395-9.
    • (2000) Environ. Health Perspect , vol.108 , Issue.SUPPL. 3 , pp. 395-399
    • Schroeder, S.R.1
  • 183
    • 0036015019 scopus 로고    scopus 로고
    • Prenatal viral infection leads to pyramidal cell atrophy and macrocephaly in adulthood: Implications for genesis of autism and schizophrenia
    • Fatemi, S.H., Earle, J., Kanodia, R., Kist, D., Emamian, E.S., Patterson, P.H., Shi, L., Sidwell, R. Prenatal viral infection leads to pyramidal cell atrophy and macrocephaly in adulthood: implications for genesis of autism and schizophrenia. Cell. Mol. Neurobiol. 2002, 22: 25-33.
    • (2002) Cell. Mol. Neurobiol , vol.22 , pp. 25-33
    • Fatemi, S.H.1    Earle, J.2    Kanodia, R.3    Kist, D.4    Emamian, E.S.5    Patterson, P.H.6    Shi, L.7    Sidwell, R.8
  • 184
    • 2442505571 scopus 로고    scopus 로고
    • Obstetrical complications and subsequent schizophrenia in adolescent and young adult offsprings: Is there a relationship?
    • Boog, G. Obstetrical complications and subsequent schizophrenia in adolescent and young adult offsprings: is there a relationship? Eur. J. Obstet. Gynecol. Reprod. Biol. 2004, 114: 130-6.
    • (2004) Eur. J. Obstet. Gynecol. Reprod. Biol , vol.114 , pp. 130-136
    • Boog, G.1
  • 185
    • 0029150724 scopus 로고
    • Risk factors for the co-occurrence of partial epilepsy, cerebral palsy and mental retardation
    • Curatolo, P., Arpino, C., Stazi, M.A., Medda, E. Risk factors for the co-occurrence of partial epilepsy, cerebral palsy and mental retardation. Dev. Med. Child Neurol. 1995, 37: 776-82.
    • (1995) Dev. Med. Child Neurol , vol.37 , pp. 776-782
    • Curatolo, P.1    Arpino, C.2    Stazi, M.A.3    Medda, E.4
  • 186
    • 0030592318 scopus 로고    scopus 로고
    • Birth seasonality in bipolar disorder, schizophrenia, schizoaffective disorder and stillbirths
    • Torrey, E.F., Rawlings, R.R., Ennis, J.M., Merrill, D.D., Flores, D.S. Birth seasonality in bipolar disorder, schizophrenia, schizoaffective disorder and stillbirths. Schizophr. Res. 1996, 21: 141-9.
    • (1996) Schizophr. Res , vol.21 , pp. 141-149
    • Torrey, E.F.1    Rawlings, R.R.2    Ennis, J.M.3    Merrill, D.D.4    Flores, D.S.5
  • 187
    • 0031558802 scopus 로고    scopus 로고
    • Seasonality of births in schizophrenia and bipolar disorder: A review of the literature
    • Torrey, E.F., Miller, J., Rawlings, R., Yolken, R.H. Seasonality of births in schizophrenia and bipolar disorder: a review of the literature. Schizophr. Res. 1997, 28: 1-38.
    • (1997) Schizophr. Res , vol.28 , pp. 1-38
    • Torrey, E.F.1    Miller, J.2    Rawlings, R.3    Yolken, R.H.4
  • 189
    • 34249850973 scopus 로고    scopus 로고
    • Immigrant youth at risk for disorders of mood: Recognizing complex dynamics
    • Yearwood, E.L., Crawford, S., Kelly, M., Moreno, N. Immigrant youth at risk for disorders of mood: recognizing complex dynamics. Arch. Psychiatr. Nurs. 2007, 21: 162-71.
    • (2007) Arch. Psychiatr. Nurs , vol.21 , pp. 162-171
    • Yearwood, E.L.1    Crawford, S.2    Kelly, M.3    Moreno, N.4
  • 190
    • 36049039253 scopus 로고    scopus 로고
    • Risk for schizophrenia in intercountry adoptees: A Danish population-based cohort study
    • Cantor-Graae, E., Pedersen, C.B. Risk for schizophrenia in intercountry adoptees: a Danish population-based cohort study. J. Child Psychol. Psychiatry 2007, 48: 1053-60.
    • (2007) J. Child Psychol. Psychiatry , vol.48 , pp. 1053-1060
    • Cantor-Graae, E.1    Pedersen, C.B.2
  • 191
    • 20944446077 scopus 로고    scopus 로고
    • Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: Longitudinal evidence of a gene X environment interaction
    • Caspi, A., Moffitt, T.E., Cannon, M., McClay, J., Murray, R., Harrington, H., Taylor, A., Arseneault, L., Williams, B., Braithwaite, A., Poulton, R., Craig, I.W. Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: longitudinal evidence of a gene X environment interaction. Biol. Psychiatry 2005, 57: 1117-27.
    • (2005) Biol. Psychiatry , vol.57 , pp. 1117-1127
    • Caspi, A.1    Moffitt, T.E.2    Cannon, M.3    McClay, J.4    Murray, R.5    Harrington, H.6    Taylor, A.7    Arseneault, L.8    Williams, B.9    Braithwaite, A.10    Poulton, R.11    Craig, I.W.12
  • 192
    • 0033569641 scopus 로고    scopus 로고
    • Epigenetics: Regulation through repression
    • Wolffe, A.P., Matzke, M.A. Epigenetics: regulation through repression. Science 1999, 286: 481-6.
    • (1999) Science , vol.286 , pp. 481-486
    • Wolffe, A.P.1    Matzke, M.A.2
  • 193
    • 0027374296 scopus 로고
    • Adult phenotype in the mouse can be affected by epigenetic events in the early embryo
    • Reik, W., Romer, L, Barton, S.C., Surani, M.A., Howlett, S.K., Klose, J. Adult phenotype in the mouse can be affected by epigenetic events in the early embryo. Development 1993, 119: 933-42.
    • (1993) Development , vol.119 , pp. 933-942
    • Reik, W.1    Romer, L.2    Barton, S.C.3    Surani, M.A.4    Howlett, S.K.5    Klose, J.6
  • 194
    • 0035839106 scopus 로고    scopus 로고
    • Nuclear cloning and epigenetic reprogramming of the genome
    • Rideout, W.M., 3rd, Eggan, K., Jaenisch, R. Nuclear cloning and epigenetic reprogramming of the genome. Science 2001, 293: 1093-8.
    • (2001) Science , vol.293 , pp. 1093-1098
    • Rideout 3rd, W.M.1    Eggan, K.2    Jaenisch, R.3
  • 195
    • 0032830639 scopus 로고    scopus 로고
    • Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
    • Amir, R.E., Van den Veyver, I.B., Wan, M., Tran, C.Q., Francke, U., Zoghbi, H.Y. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat. Genet. 1999, 23: 185-8.
    • (1999) Nat. Genet , vol.23 , pp. 185-188
    • Amir, R.E.1    Van den Veyver, I.B.2    Wan, M.3    Tran, C.Q.4    Francke, U.5    Zoghbi, H.Y.6
  • 197
    • 0034069652 scopus 로고    scopus 로고
    • Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation
    • Gibbons, R.J., McDowell, T.L., Raman, S., O'Rourke, D.M., Garrick, D., Ayyub, H., Higgs, D.R. Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation. Nat. Genet. 2000, 24: 368-71.
    • (2000) Nat. Genet , vol.24 , pp. 368-371
    • Gibbons, R.J.1    McDowell, T.L.2    Raman, S.3    O'Rourke, D.M.4    Garrick, D.5    Ayyub, H.6    Higgs, D.R.7
  • 198
    • 0034639857 scopus 로고    scopus 로고
    • Understanding the molecular basis of fragile X syndrome
    • Jin, P., Warren, S.T. Understanding the molecular basis of fragile X syndrome. Hum. Mol. Genet. 2000, 9: 901-8.
    • (2000) Hum. Mol. Genet , vol.9 , pp. 901-908
    • Jin, P.1    Warren, S.T.2
  • 199
    • 33846056133 scopus 로고    scopus 로고
    • Folate and neural tube defects
    • Pitkin, R.M. Folate and neural tube defects. Am. J. Clin. Nutr. 2007, 85: 285S-288S.
    • (2007) Am. J. Clin. Nutr , vol.85
    • Pitkin, R.M.1
  • 203
    • 0038823525 scopus 로고    scopus 로고
    • The endophenotype concept in psychiatry: Etymology and strategic intentions
    • Gottesman, II, Gould, T.D. The endophenotype concept in psychiatry: etymology and strategic intentions. Am. J. Psychiatry 2003, 160: 636-45.
    • (2003) Am. J. Psychiatry , vol.160 , pp. 636-645
    • Gottesman, I.1    Gould, T.D.2
  • 204
    • 33846525474 scopus 로고    scopus 로고
    • The endophenotype concept in psychiatric genetics
    • Flint, J., Munafo, M.R. The endophenotype concept in psychiatric genetics. Psychol. Med. 2007, 37: 163-80.
    • (2007) Psychol. Med , vol.37 , pp. 163-180
    • Flint, J.1    Munafo, M.R.2
  • 205
    • 0025019555 scopus 로고
    • Linkage strategies for genetically complex traits. I. Multilocus models
    • Risch, N. Linkage strategies for genetically complex traits. I. Multilocus models. Am. J. Hum. Genet. 1990, 46: 222-8.
    • (1990) Am. J. Hum. Genet , vol.46 , pp. 222-228
    • Risch, N.1
  • 206
    • 34047236641 scopus 로고    scopus 로고
    • Simulations provide support for the common disease-common variant hypothesis
    • Peng, B., Kimmel, M. Simulations provide support for the common disease-common variant hypothesis. Genetics 2007, 175: 763-76.
    • (2007) Genetics , vol.175 , pp. 763-776
    • Peng, B.1    Kimmel, M.2
  • 207
    • 0035451780 scopus 로고    scopus 로고
    • On the allelic spectrum of human disease
    • Reich, D.E., Lander, E.S. On the allelic spectrum of human disease. Trends Genet. 2001, 17: 502-10.
    • (2001) Trends Genet , vol.17 , pp. 502-510
    • Reich, D.E.1    Lander, E.S.2
  • 208
    • 0034969437 scopus 로고    scopus 로고
    • Are rare variants responsible for susceptibility to complex diseases?
    • Pritchard, J.K. Are rare variants responsible for susceptibility to complex diseases? Am. J. Hum. Genet. 2001, 69: 124-37.
    • (2001) Am. J. Hum. Genet , vol.69 , pp. 124-137
    • Pritchard, J.K.1
  • 209
    • 0033969453 scopus 로고    scopus 로고
    • Effect of allelic heterogeneity on the power of the transmission disequilibrium test
    • Slager, S.L., Huang, J., Vieland, V.J. Effect of allelic heterogeneity on the power of the transmission disequilibrium test. Genet. Epidemiol. 2000, 18: 143-56.
    • (2000) Genet. Epidemiol , vol.18 , pp. 143-156
    • Slager, S.L.1    Huang, J.2    Vieland, V.J.3
  • 212
    • 0020822755 scopus 로고
    • Epidemiology and genetics of neural tube defects: An application of the Utah Genealogical Data Base
    • Jorde, L.B., Fineman, R.M., Martin, R.A. Epidemiology and genetics of neural tube defects: an application of the Utah Genealogical Data Base. Am. J. Phys. Anthropol. 1983, 62: 23-31.
    • (1983) Am. J. Phys. Anthropol , vol.62 , pp. 23-31
    • Jorde, L.B.1    Fineman, R.M.2    Martin, R.A.3
  • 213
    • 33344462433 scopus 로고    scopus 로고
    • Genetic influences on reading difficulties in boys and girls: The Colorado twin study
    • Hawke, J.L., Wadsworth, S.J., DeFries, J.C. Genetic influences on reading difficulties in boys and girls: the Colorado twin study. Dyslexia 2006, 12: 21-9.
    • (2006) Dyslexia , vol.12 , pp. 21-29
    • Hawke, J.L.1    Wadsworth, S.J.2    DeFries, J.C.3
  • 215
    • 0021739656 scopus 로고
    • Genetic and environmental influences on obsessional traits and symptoms
    • Clifford, C.A., Murray, R.M., Fulker, D.W. Genetic and environmental influences on obsessional traits and symptoms. Psychol. Med. 1984, 14: 791-800.
    • (1984) Psychol. Med , vol.14 , pp. 791-800
    • Clifford, C.A.1    Murray, R.M.2    Fulker, D.W.3
  • 216
    • 0034605991 scopus 로고    scopus 로고
    • Obsessive and compulsive symptoms in a general population sample of female twins
    • Jonnal, A.H., Gardner, C.O., Prescott, C.A., Kendler, K.S. Obsessive and compulsive symptoms in a general population sample of female twins. Am. J. Med. Genet. 2000, 96: 791-6.
    • (2000) Am. J. Med. Genet , vol.96 , pp. 791-796
    • Jonnal, A.H.1    Gardner, C.O.2    Prescott, C.A.3    Kendler, K.S.4


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