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  • Abecasis, G.R., Burt, R.A., Hall, D., Bochum, S., Doheny, K.F., Lundy, S.L., Torrington, M., Roos, J.L., Gogos, J.A. & Karayiorgou, M. (2004) Genome-wide scan in schizophrenia families from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1. Am J Hum Genet 74, 403417.
  • Altshuler, D., Hirschhorn, J.N., Klannemark, M., Lindgren, C.M., Vohl, M.C., Nemesh, J., Lane, C.R., Schaffner, S.F., Bolk, S., Brewer, C., Tuomi, T., Gaudet, D., Hudson, T.J., Daly, M., Groop, L. & Lander, E.S. (2000) The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat Genet 26, 7680.
  • American Psychiatric Association (1994) Diagnostic and Statistical Manual, 4th edn. American Psychiatric Association, Washington, DC.
  • Badner, J.A. & Gershon, E.S. (2002) Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia. Mol Psychiatry 7, 405411.
  • Benson, M.A., Newey, S.E., Martin-Rendon, E., Hawkes, R. & Blake, D.J. (2001) Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain. J Biol Chem 276, 2423224241.
  • Blouin, J.L., Dombroski, B.A., Nath, S.K., Lasseter, V.K., Wolyniec, P.S., Nestadt, G., Thornquist, M., Ullrich, G., McGrath, J., Kasch, L., Lamacz, M., Thomas, M.G., Gehrig, C., Radhakrishna, U., Snyder, S.E., Balk, K.G., Neufeld, K., Swartz, K.L., DeMarchi, N., Papadimitriou, G.N., Dikeos, D.G., Stefanis, C.N., Chakravarti, A., Childs, B., Housman, D.E., Kazazian, H.H., Antonarakis, S.E. & Pulver, A.E. (1998) Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nat Genet 20, 7073.
  • Brownstein, M.J., Carpten, J.D. & Smith, J.R. (1996) Modulation of non-templated nucleotide addition by Taq DNA polymerase: primer modifications that facilitate genotyping. Biotechniques 20, 10081010.
  • Brzustowicz, L.M., Honer, W.G., Chow, E.W., Little, D., Hogan, J., Hodgkinson, K. & Bassett, A.S. (1999) Linkage of familial schizophrenia to chromosome 13q32. Am J Hum Genet 65, 10961103.
  • Chen, X., Levine, L. & Kwok, P.Y. (1999) Fluorescence polarization in homogeneous nucleic acid analysis. Genome Res 9, 492498.
  • Chumakov, I., Blumenfeld, M., Guerassimenko, O., Cavarec, L., Palicio, M., Abderrahim, H., Bougueleret, L., Barry, C., Tanaka, H., La Rosa, P., Puech, A., Tahri, N., Cohen-Akenine, A., Delabrosse, S., Lissarrague, S., Picard, F.P., Maurice, K., Essioux, L., Millasseau, P., Grel, P., Debailleul, V., Simon, A.M., Caterina, D., Dufaure, I., Malekzadeh, K., Belova, M., Luan. J.J., Bouillot, M., Sambucy, J.L., Primas, G., Saumier, M., Boubkiri, N., Martin- Saumier, S., Nasroune, M., Peixoto, H., Delaye, A., Pinchot, V., Bastucci, M., Guillou, S., Chevillon, M., Sainz-Fuertes, R., Meguenni, S., Aurich-Costa, J., Cherif, D., Gimalac, A., Van Duijn, C., Gauvreau, D., Ouellette, G., Fortier, I., Raelson, J., Sherbatich, T., Riazanskaia, N., Rogaev, E., Raeymaekers, P., Aerssens, J., Konings, F., Luyten, W., Macciardi, F., Sham, P.C., Straub, R.E., Weinberger, D.R., Cohen, N., Cohen, D., Ouelette, G. & Realson, J. (2002) Genetic and physiological data implicating the new human gene G72 and the gene for d-amino acid oxidase in schizophrenia. Proc Natl Acad Sci USA 99, 1367513680. Erratum in Proc Natl Acad Sci USA 2002 99, 17221.
  • Clayton, D. (1999) A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission. Am J Hum Genet 65, 11701177.
  • Cloninger, C.R. (1989) Schizophrenia: genetic etiological factors. In Kaplan, H.I. & Saddock, B.J. (eds), Comprehensive Textbook of Psychiatry, 5th edn. William & Wilkins, Baltimore, pp. 732744.
  • Collier, D.A. & Sham, P.C. (1997) Catch me if you can: are catechol- and indoleamine genes pleiotropic QTLs for common mental disorders? Mol Psychiatry 2, 181183.
  • Detera-Wadleigh, S.D., Badner, J.A., Berrettini, W.H., Yoshikawa, T., Goldin, L.R., Turner, G., Rollins, D.Y., Moses, T., Sanders, A.R., Karkera, J.D., Esterling, L.E., Zeng, J., Ferraro, T.N., Guroff, J.J., Kazuba, D., Maxwell, M.E., Nurnberger, J.I. Jr & Gershon, E.S. (1999) A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2. Proc Natl Acad Sci USA 96, 56045609.
  • Dudbridge, F. (2002) Methods and software for association tests of uncertain haplotypes in case-parent trios. Am J Hum Genet 71, A2338.
  • Dudbridge, F. (2003) Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 25, 115121.
  • Gogos, J.A., Santha, M., Takacs, Z., Beck, K.D., Luine, V., Lucas, L.R., Nadler, J.V. & Karayiorgou, M. (1999) The gene encoding proline dehydrogenase modulates sensorimotor gating in mice. Nat Genet 21, 434439.
  • Hall, D., Wijsman, E.M., Roos, J.L., Gogos, J.A. & Karayiorgou, M. (2002) Extended intermarker linkage disequilibrium in the Afrikaners. Genome Res 12, 956961.
  • Hattori, E., Liu, C., Badner, J.A., Bonner, T.I., Christian, S.L., Maheshwari, M., Detera-Wadleigh, S.D., Gibbs, R.A. & Gershon, E.S. (2003) Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series. Am J Hum Genet 72, 11311140.
  • Jacquet, H., Raux, G., Thibaut, F., Hecketsweiler, B., Houy, E., Demilly, C., Haouzir, S., Allio, G., Fouldrin, G., Drouin, V., Bou, J., Petit, M., Campion, D. & Frebourg, T. (2002) PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. Hum Mol Genet 11, 22432249.
  • Karayiorgou, M., Torrington, M., Abecasis, G.R., Pretorius, H., Robertson, B., Kaliski, S., Lay, S., Sobin, C., Möller, N., Lundy, S.L., Blundell, M.L., Gogos, J.A. & Roos, J.L. (2004) Phenotypic characterization and genealogical tracing in an Afrikaner schizophrenia database. Am J Med Genet 124B, 2028.
  • Liu, H., Abecasis, G.R., Heath, S.C., Knowles, A., Demars, S., Chen, Y.J., Roos, J.L., Rapoport, J.L., Gogos, J.A. & Karayiorgou, M. (2002b) Genetic variation in the 22q11 locus and susceptibility to schizophrenia. Proc Natl Acad Sci USA 99, 1685916864.
  • Liu, C., Badner, J.A., Christian, S.L., Guroff, J.J., Detera-Wadleigh, S.D. & Gershon, E.S. (2001) Fine mapping supports previous linkage evidence for a bipolar disorder susceptibility locus on 13q32. Am J Med Genet 105, 375380.
  • Liu, H., Heath, S.C., Sobin, C., Roos, J.L., Galke, B.L., Blundell, M.L., Lenane, M., Robertson, B., Wijsman, E.M., Rapoport, J.L., Gogos, J.A. & Karayiorgou, M. (2002a) Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia. Proc Natl Acad Sci USA 99, 37173722.
  • Martin, E.R., Monks, S.A., Warren, L.L. & Kaplan, N.L. (2000) A test for linkage and association in general pedigrees: the pedigree disequilibrium test. Am J Hum Genet 67, 146154.
  • Morris, D.W., McGhee, K.A., Schwaiger, S., Scully, P., Quinn, J., Meagher, D., Waddington, J.L., Gill, M. & Corvin, A.P. (2003) No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study. Schizophr Res 60, 167172.
  • Nurnberger, J.I., Blehar, M.C., Kaufmann, C.A., York-Cooler, C., Simpson, S.G., Harkavy-Friedman, J., Severe, J.B., Malaspina, D. & Reich, T. & Collaborators from the NIMH Genetics Initiative (1994) Diagnostic interview for genetic studies, rationale, unique features, and training. Arch General Psychiatry 51, 949.
  • Schwab, S.G., Knapp, M., Mondabon, S., Hallmayer, J., Borrmann-Hassenbach, M., Albus, M., Lerer, B., Rietschel, M., Trixler, M., Maier, W. & Wildenauer, D.B. (2003) Support for association of schizophrenia with genetic variation in the 6p22.3 gene, dysbindin, in sib-pair families with linkage and in an additional sample of triad families. Am J Hum Genet 72, 185190.
  • Stefansson, H., Sarginson, J., Kong, A., Yates, P., Steinthorsdottir, V., Gudfinnsson, E.K., Gunnarsdottir, S., Walker, N., Petursson, H., Crombie, C., Ingason, A., Gulcher, J.R., Stefansson, K. & St Clair, D. (2002b) Association of neuregulin 1 with schizophrenia confirmed in a Scottish population. Am J Hum Genet 72, 8387.
  • Stefansson, H., Sigurdsson, E., Steinthorsdottir, V., Bjornsdottir, S., Sigmundsson, T., Ghosh, S., Brynjolfsson, J., Gunnarsdottir, S., Ivarsson, O., Chou, T.T., Hjaltason, O., Birgisdottir, B., Jonsson, H., Gudnadottir, V.G., Gudmundsdottir, E., Bjornsson, A., Ingvarsson, B., Ingason, A., Sigfusson, S., Hardardottir, H., Harvey, R.P., Lai, D., Zhou, M., Brunner, D., Mutel, V., Gonzalo, A., Lemke, G., Sainz, J., Johannesson, G., Andresson, T., Gudbjartsson, D., Manolescu, A., Frigge, M.L., Gurney, M.E., Kong, A., Gulcher, J.R., Petursson, H. & Stefansson, K. (2002a) Neuregulin 1 and susceptibility to schizophrenia. Am J Hum Genet 71, 877892.
  • Straub, R.E., Jiang, Y., MacLean, C.J., Ma, Y., Webb, B.T., Myakishev, M.V., Harris-Kerr, C., Wormley, B., Sadek, H., Kadambi, B., Cesare, A.J., Gibberman, A., Wang, X., O'Neill, F.A., Walsh, D. & Kendler, K.S. (2002) Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia. Am J Hum Genet 71, 337348. Erratum in Am J Hum Genet 2002 72, 1007.
  • Straub, R.E., MacLean, C.J., O'Neill, F.A., Burke, J., Murphy, B., Duke, F., Shinkwin, R., Webb, B.T., Zhang, J., Walsh, D et al. (1995) A potential vulnerability locus for schizophrenia on chromosome 6p24–22: evidence for genetic heterogeneity. Nat Genet 11, 287293.
  • Tsai, G., Yang, P., Chung, L.C., Lange, N. & Coyle, J.T. (1998) d-serine added to antipsychotics for the treatment of schizophrenia. Biol Psychiatry 44, 10811089.
  • Van Den Bogaert, A., Schumacher, J., Schulze, T.G., Otte, A.C., Ohlraun, S., Kovalenko, S., Becker, T., Freudenberg, J., Jonsson, E.G., Mattila-Evenden, M., Sedvall, G.C., Czerski, P.M., Kapelski, P., Hauser, J., Maier, W., Rietschel, M., Propping, P., Nothen, M.M. & Cichon, S. (2003) The DTNBP1 (Dysbindin) gene contributes to schizophrenia, depending on family history of the disease. Am J Hum Genet 73, 14381443.