-
1
-
-
0027272195
-
The Roscommon family study. I. Methods, diagnosis of probands, and risk of schizophrenia in relatives
-
Kendler K.S., McGuire M., Gruenberg A.M., O'Hare A., Spellman M., and Walsh D. The Roscommon family study. I. Methods, diagnosis of probands, and risk of schizophrenia in relatives. Arch Gen Psychiatry 50 (1993) 527-540
-
(1993)
Arch Gen Psychiatry
, vol.50
, pp. 527-540
-
-
Kendler, K.S.1
McGuire, M.2
Gruenberg, A.M.3
O'Hare, A.4
Spellman, M.5
Walsh, D.6
-
2
-
-
0031939076
-
The genetic epidemiology of schizophrenia in a Finnish twin cohort
-
Cannon T.D., Kaprio J., Lönnqvist J., Huttunen M., and Koskenvuo M. The genetic epidemiology of schizophrenia in a Finnish twin cohort. Arch Gen Psychiatry 55 (1998) 67-74
-
(1998)
Arch Gen Psychiatry
, vol.55
, pp. 67-74
-
-
Cannon, T.D.1
Kaprio, J.2
Lönnqvist, J.3
Huttunen, M.4
Koskenvuo, M.5
-
3
-
-
0028288450
-
The Finnish adoptive family study of schizophrenia. Implications for family research
-
Tienari P., Wynne L.C., Moring J., Lahti I., Naarala M., Sorri A., et al. The Finnish adoptive family study of schizophrenia. Implications for family research. Br J Psychiatry Suppl 23 (1994) 20-26
-
(1994)
Br J Psychiatry Suppl
, vol.23
, pp. 20-26
-
-
Tienari, P.1
Wynne, L.C.2
Moring, J.3
Lahti, I.4
Naarala, M.5
Sorri, A.6
-
4
-
-
0028964788
-
Evaluating the spectrum concept of schizophrenia in the Roscommon Family Study
-
Kendler K.S., Neale M.C., and Walsh D. Evaluating the spectrum concept of schizophrenia in the Roscommon Family Study. Am J Psychiatry 152 (1995) 749-754
-
(1995)
Am J Psychiatry
, vol.152
, pp. 749-754
-
-
Kendler, K.S.1
Neale, M.C.2
Walsh, D.3
-
5
-
-
0033916024
-
Toward reformulating the diagnosis of schizophrenia
-
Tsuang M.T., Stone W.S., and Faraone S.V. Toward reformulating the diagnosis of schizophrenia. Am J Psychiatry 157 (2000) 1041-1050
-
(2000)
Am J Psychiatry
, vol.157
, pp. 1041-1050
-
-
Tsuang, M.T.1
Stone, W.S.2
Faraone, S.V.3
-
6
-
-
0038823525
-
The endophenotype concept in psychiatry: Etymology and strategic intentions
-
Gottesman I.I., and Gould T.D. The endophenotype concept in psychiatry: Etymology and strategic intentions. Am J Psychiatry 160 (2003) 636-645
-
(2003)
Am J Psychiatry
, vol.160
, pp. 636-645
-
-
Gottesman, I.I.1
Gould, T.D.2
-
7
-
-
30344447674
-
Genes for schizophrenia and bipolar disorder?. Implications for psychiatric nosology
-
Craddock N., O'Donovan M.C., and Owen M.J. Genes for schizophrenia and bipolar disorder?. Implications for psychiatric nosology. Schizophr Bull 32 (2006) 9-16
-
(2006)
Schizophr Bull
, vol.32
, pp. 9-16
-
-
Craddock, N.1
O'Donovan, M.C.2
Owen, M.J.3
-
8
-
-
23944474042
-
Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit
-
Hallmeyer J.F., Kalaydjieva L., Badcock J., Dragovic M., Howell S., Michie P.T., et al. Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit. Am J Hum Genet 77 (2005) 468-476
-
(2005)
Am J Hum Genet
, vol.77
, pp. 468-476
-
-
Hallmeyer, J.F.1
Kalaydjieva, L.2
Badcock, J.3
Dragovic, M.4
Howell, S.5
Michie, P.T.6
-
9
-
-
4444332521
-
Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q
-
Paunio T., Tuulio-Henriksson A., Hiekkalinna T., Perola M., Varilo T., Partonen T., et al. Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q. Hum Mol Genet 13 (2004) 1693-1702
-
(2004)
Hum Mol Genet
, vol.13
, pp. 1693-1702
-
-
Paunio, T.1
Tuulio-Henriksson, A.2
Hiekkalinna, T.3
Perola, M.4
Varilo, T.5
Partonen, T.6
-
10
-
-
38349025518
-
A dysbindin risk haplotype with less severe manic-type symptoms in psychosis
-
Corvin A., Donohoe G., Nangle J.M., Schwaiger S., Morris D., and Gill M. A dysbindin risk haplotype with less severe manic-type symptoms in psychosis. Neurosci Lett 431 (2008) 146-149
-
(2008)
Neurosci Lett
, vol.431
, pp. 146-149
-
-
Corvin, A.1
Donohoe, G.2
Nangle, J.M.3
Schwaiger, S.4
Morris, D.5
Gill, M.6
-
11
-
-
0028269088
-
The subtyping of schizophrenia in men and women: A latent class analysis
-
Castle D.J., Sham P.C., Wessely S., and Murray R.M. The subtyping of schizophrenia in men and women: A latent class analysis. Psychol Med 24 (1994) 41-51
-
(1994)
Psychol Med
, vol.24
, pp. 41-51
-
-
Castle, D.J.1
Sham, P.C.2
Wessely, S.3
Murray, R.M.4
-
12
-
-
16344369361
-
Five latent factors underlying schizophrenia: Analysis and relationship to illnesses in relatives
-
McGrath J.A., Nestadt G., Liang K.-Y., Lasseter V.K., Wolyniec P.S., Fallin M.D., et al. Five latent factors underlying schizophrenia: Analysis and relationship to illnesses in relatives. Schizophr Bull 30 (2004) 855-873
-
(2004)
Schizophr Bull
, vol.30
, pp. 855-873
-
-
McGrath, J.A.1
Nestadt, G.2
Liang, K.-Y.3
Lasseter, V.K.4
Wolyniec, P.S.5
Fallin, M.D.6
-
13
-
-
17344366490
-
Dimensions and classes of psychosis in a population cohort: A four-class, four-dimension model of schizophrenia and affective psychoses
-
Murray V., McKee I., Miller P.M., Young D., Muir W.J., Pelosi A.J., and Blackwood D.H. Dimensions and classes of psychosis in a population cohort: A four-class, four-dimension model of schizophrenia and affective psychoses. Psychol Med 35 (2005) 499-510
-
(2005)
Psychol Med
, vol.35
, pp. 499-510
-
-
Murray, V.1
McKee, I.2
Miller, P.M.3
Young, D.4
Muir, W.J.5
Pelosi, A.J.6
Blackwood, D.H.7
-
14
-
-
33847267269
-
Resolving the latent structure of schizophrenia endophenotypes using expectation-maximization-based finite mixture modeling
-
Lenzenweger M.F., McLachlan G., and Rubin D.B. Resolving the latent structure of schizophrenia endophenotypes using expectation-maximization-based finite mixture modeling. J Abnorm Psychol 116 (2007) 16-29
-
(2007)
J Abnorm Psychol
, vol.116
, pp. 16-29
-
-
Lenzenweger, M.F.1
McLachlan, G.2
Rubin, D.B.3
-
15
-
-
0033869708
-
Linkage disequilibrium in isolated populations: Finland and a young subpopulation of Kuusamo
-
Varilo T., Laan M., Hovatta I., Wiebe V., Terwilliger J.D., and Peltonen L. Linkage disequilibrium in isolated populations: Finland and a young subpopulation of Kuusamo. Eur J Hum Genet 8 (2000) 604-612
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 604-612
-
-
Varilo, T.1
Laan, M.2
Hovatta, I.3
Wiebe, V.4
Terwilliger, J.D.5
Peltonen, L.6
-
16
-
-
0033364825
-
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci
-
Hovatta I., Varilo T., Suvisaari J., Terwilliger J.D., Ollikainen V., Arajärvi R., et al. A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci. Am J Hum Genet 65 (1999) 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
Arajärvi, R.6
-
17
-
-
0004085199
-
-
American Psychiatric Press, Washington, DC
-
First M.B., Spitzer R.L., Gibbon M., and Williams J.B.W. Structured Clinical Interview for DSM-IV Axis I Disorders-Clinician Version (SCID-CV) (1997), American Psychiatric Press, Washington, DC
-
(1997)
Structured Clinical Interview for DSM-IV Axis I Disorders-Clinician Version (SCID-CV)
-
-
First, M.B.1
Spitzer, R.L.2
Gibbon, M.3
Williams, J.B.W.4
-
20
-
-
0026410654
-
A polydiagnostic application of operational criteria in studies of psychotic illness: Development and reliability of the OPCRIT system
-
McGuffin P., Farmer A.E., and Harvey I. A polydiagnostic application of operational criteria in studies of psychotic illness: Development and reliability of the OPCRIT system. Arch Gen Psychiatry 48 (1991) 764-770
-
(1991)
Arch Gen Psychiatry
, vol.48
, pp. 764-770
-
-
McGuffin, P.1
Farmer, A.E.2
Harvey, I.3
-
21
-
-
0038218463
-
-
The Psychological Corporation, Harcourt Brace Jovanovich Inc, San Antonio, TX
-
Wechsler D. Wechsler Memory Scale-Revised (WMS-R) Manual (1987), The Psychological Corporation, Harcourt Brace Jovanovich Inc, San Antonio, TX
-
(1987)
Wechsler Memory Scale-Revised (WMS-R) Manual
-
-
Wechsler, D.1
-
23
-
-
0003545345
-
-
Psychological Corporation, Harcourt Brace & Company, San Antonio, TX
-
Delis D., Kramer J., Kaplan E., and Ober B. California Verbal Learning Test. Manual. Research Edition (1987), Psychological Corporation, Harcourt Brace & Company, San Antonio, TX
-
(1987)
California Verbal Learning Test. Manual. Research Edition
-
-
Delis, D.1
Kramer, J.2
Kaplan, E.3
Ober, B.4
-
24
-
-
0034702026
-
Disruption of two novel genes by a translocation co-segregating with schizophrenia
-
Millar J.K., Wilson-Annan J.C., Anderson S., Christie S., Taylor M.S., Semple C.A., et al. Disruption of two novel genes by a translocation co-segregating with schizophrenia. Hum Mol Genet 9 (2000) 1415-1423
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1415-1423
-
-
Millar, J.K.1
Wilson-Annan, J.C.2
Anderson, S.3
Christie, S.4
Taylor, M.S.5
Semple, C.A.6
-
25
-
-
18444364206
-
Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia
-
Straub R.E., Jiang Y., MacLean C.J., Ma Y., Webb B.T., Myakishev M.V., et al. 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 (2002) 337-348
-
(2002)
Am J Hum Genet
, vol.71
, pp. 337-348
-
-
Straub, R.E.1
Jiang, Y.2
MacLean, C.J.3
Ma, Y.4
Webb, B.T.5
Myakishev, M.V.6
-
26
-
-
0013375948
-
Neuregulin 1 and susceptibility to schizophrenia
-
Stefansson H., Sigurdsson E., Steinthorsdottir V., Bjornsdottir S., Sigmundsson T., Ghosh S., et al. Neuregulin 1 and susceptibility to schizophrenia. Am J Hum Genet 71 (2002) 877-892
-
(2002)
Am J Hum Genet
, vol.71
, pp. 877-892
-
-
Stefansson, H.1
Sigurdsson, E.2
Steinthorsdottir, V.3
Bjornsdottir, S.4
Sigmundsson, T.5
Ghosh, S.6
-
27
-
-
0345530985
-
Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects
-
Hennah W., Varilo T., Kestila M., Paunio T., Arajarvi R., Haukka J., et al. Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects. Hum Mol Genet 12 (2003) 3151-3159
-
(2003)
Hum Mol Genet
, vol.12
, pp. 3151-3159
-
-
Hennah, W.1
Varilo, T.2
Kestila, M.3
Paunio, T.4
Arajarvi, R.5
Haukka, J.6
-
28
-
-
33847401520
-
The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland
-
Turunen J., Peltonen J., Pietiläinen O., Hennah W., Loukola A., Paunio Y., et al. The role of DTNBP1, NRG1, and AKT1 in the genetics of schizophrenia in Finland. Schizophr Res 91 (2007) 27-36
-
(2007)
Schizophr Res
, vol.91
, pp. 27-36
-
-
Turunen, J.1
Peltonen, J.2
Pietiläinen, O.3
Hennah, W.4
Loukola, A.5
Paunio, Y.6
-
31
-
-
0000354976
-
A comparative study of ordinary cross-validation, v-fold cross-validation and the repeated learning-testing methods
-
Burman P. A comparative study of ordinary cross-validation, v-fold cross-validation and the repeated learning-testing methods. Biometrika 76 (1989) 503-514
-
(1989)
Biometrika
, vol.76
, pp. 503-514
-
-
Burman, P.1
-
33
-
-
2342600219
-
Powerful allele sharing statistics for nonparmetric linkage analysis
-
Lange E.M., and Lange K. Powerful allele sharing statistics for nonparmetric linkage analysis. Hum Hered 57 (2004) 49-58
-
(2004)
Hum Hered
, vol.57
, pp. 49-58
-
-
Lange, E.M.1
Lange, K.2
-
34
-
-
0035071957
-
A new statistical method for haplotype reconstruction from population data
-
Stephens M., Smith N., and Donnelly P. A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 68 (2001) 978-989
-
(2001)
Am J Hum Genet
, vol.68
, pp. 978-989
-
-
Stephens, M.1
Smith, N.2
Donnelly, P.3
-
35
-
-
13844270527
-
Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation
-
Stephens M., and Scheet P. Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. Am J Hum Genet 76 (2005) 449-462
-
(2005)
Am J Hum Genet
, vol.76
, pp. 449-462
-
-
Stephens, M.1
Scheet, P.2
-
36
-
-
23944474042
-
Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit
-
Hallmayer J.F., Kalaydjieva L., Badcock J., Dragovic M., Howell S., Michie P.T., et al. Genetic evidence for a distinct subtype of schizophrenia characterized by pervasive cognitive deficit. Am J Hum Genet 77 (2005) 468-476
-
(2005)
Am J Hum Genet
, vol.77
, pp. 468-476
-
-
Hallmayer, J.F.1
Kalaydjieva, L.2
Badcock, J.3
Dragovic, M.4
Howell, S.5
Michie, P.T.6
-
37
-
-
33748052338
-
Subtyping schizophrenia: Implications for genetic research
-
Jablensky A. Subtyping schizophrenia: Implications for genetic research. Mol Psychiatry 11 (2006) 815-836
-
(2006)
Mol Psychiatry
, vol.11
, pp. 815-836
-
-
Jablensky, A.1
-
38
-
-
33845870419
-
Deconstructing schizophrenia: An overview of the use of endophenotypes in order to understand a complex disorder
-
Braff D.L., Freedman R., Schork N.J., and Gottesman I.I. Deconstructing schizophrenia: An overview of the use of endophenotypes in order to understand a complex disorder. Schizophr Bull 33 (2007) 21-32
-
(2007)
Schizophr Bull
, vol.33
, pp. 21-32
-
-
Braff, D.L.1
Freedman, R.2
Schork, N.J.3
Gottesman, I.I.4
-
39
-
-
34047244699
-
Adjudicating neurocognitive endophenotypes for schizophrenia
-
Glahn D.C., Almasy L., Blangero J., Burk G.M., Estrada J., Peralta J.M., et al. Adjudicating neurocognitive endophenotypes for schizophrenia. Am J Med Genet B Neuropsychiatr Genet 144 (2007) 242-249
-
(2007)
Am J Med Genet B Neuropsychiatr Genet
, vol.144
, pp. 242-249
-
-
Glahn, D.C.1
Almasy, L.2
Blangero, J.3
Burk, G.M.4
Estrada, J.5
Peralta, J.M.6
-
40
-
-
49649097104
-
Genetics of clinical features and subtypes of schizophrenia: A review of the recent literature
-
Fanous A.H., and Kendler K.S. Genetics of clinical features and subtypes of schizophrenia: A review of the recent literature. Curr Psychiatry Rep 10 (2008) 164-170
-
(2008)
Curr Psychiatry Rep
, vol.10
, pp. 164-170
-
-
Fanous, A.H.1
Kendler, K.S.2
-
41
-
-
26444474920
-
Relationship between a high-risk haplotype in the DTNBP1 (dysbindin) gene and clinical features of schizophrenia
-
Fanous A.H., van den Oord E.J., Riley B.P., Aggen S.H., Neale M.C., O'Neill F.A., et al. Relationship between a high-risk haplotype in the DTNBP1 (dysbindin) gene and clinical features of schizophrenia. Am J Psychiatry 162 (2005) 1824-1832
-
(2005)
Am J Psychiatry
, vol.162
, pp. 1824-1832
-
-
Fanous, A.H.1
van den Oord, E.J.2
Riley, B.P.3
Aggen, S.H.4
Neale, M.C.5
O'Neill, F.A.6
-
42
-
-
33645927927
-
Dysbindin genotype and negative symptoms in schizophrenia
-
DeRosse P., Funke B., Burdick K.E., Lencz T., Ekholm J., Kane J.M., et al. Dysbindin genotype and negative symptoms in schizophrenia. Am J Psychiatry 163 (2006) 532-534
-
(2006)
Am J Psychiatry
, vol.163
, pp. 532-534
-
-
DeRosse, P.1
Funke, B.2
Burdick, K.E.3
Lencz, T.4
Ekholm, J.5
Kane, J.M.6
-
43
-
-
33645905721
-
Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS)
-
Gornick M.C., Addington A.M., Sporn A., Gogtay N., Greenstein D., Lenane M., et al. Dysbindin (DTNBP1, 6p22.3) is associated with childhood-onset psychosis and endophenotypes measured by the Premorbid Adjustment Scale (PAS). J Autism Dev Disord 35 (2005) 831-838
-
(2005)
J Autism Dev Disord
, vol.35
, pp. 831-838
-
-
Gornick, M.C.1
Addington, A.M.2
Sporn, A.3
Gogtay, N.4
Greenstein, D.5
Lenane, M.6
-
44
-
-
20144387173
-
Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1)
-
Raybould R., Green E.K., MacGregor S., Gordon-Smith K., Heron J., Hyde S., et al. Bipolar disorder and polymorphisms in the dysbindin gene (DTNBP1). Biol Psychiatry 57 (2005) 696-701
-
(2005)
Biol Psychiatry
, vol.57
, pp. 696-701
-
-
Raybould, R.1
Green, E.K.2
MacGregor, S.3
Gordon-Smith, K.4
Heron, J.5
Hyde, S.6
-
45
-
-
33745192557
-
Genetic variation in DTNBP1 influences general cognitive ability
-
Burdick K.E., Lencz T., Funke B., Finn C.T., Szeszko P.R., Kane J.M., et al. Genetic variation in DTNBP1 influences general cognitive ability. Hum Mol Genet 15 (2006) 1563-1568
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1563-1568
-
-
Burdick, K.E.1
Lencz, T.2
Funke, B.3
Finn, C.T.4
Szeszko, P.R.5
Kane, J.M.6
-
46
-
-
38949126972
-
Early visual processing deficits in dysbindin associated schizophrenia
-
Donohoe G., Morris D.W., De Sanctis P., Magno E., Montesi J.L., Garavan H.P., et al. Early visual processing deficits in dysbindin associated schizophrenia. Biol Psychiatry 63 (2008) 484-489
-
(2008)
Biol Psychiatry
, vol.63
, pp. 484-489
-
-
Donohoe, G.1
Morris, D.W.2
De Sanctis, P.3
Magno, E.4
Montesi, J.L.5
Garavan, H.P.6
-
47
-
-
34247170190
-
Variance in neurocognitive performance is associated with dysbindin-1 in schizophrenia: A preliminary study
-
Donohoe G., Morris D.W., Clarke S., McGhee K.A., Schwaiger S., Nangle J.M., et al. Variance in neurocognitive performance is associated with dysbindin-1 in schizophrenia: A preliminary study. Neuropsychologia 45 (2007) 454-458
-
(2007)
Neuropsychologia
, vol.45
, pp. 454-458
-
-
Donohoe, G.1
Morris, D.W.2
Clarke, S.3
McGhee, K.A.4
Schwaiger, S.5
Nangle, J.M.6
-
48
-
-
38949126972
-
Early visual processing deficits in dysbindin-associated schizophrenia
-
Donohoe G., Morris D.W., De Sanctis P., Magno E., Montesi J.L., Garavan H.P., et al. Early visual processing deficits in dysbindin-associated schizophrenia. Biol Psychiatry 63 (2007) 484-489
-
(2007)
Biol Psychiatry
, vol.63
, pp. 484-489
-
-
Donohoe, G.1
Morris, D.W.2
De Sanctis, P.3
Magno, E.4
Montesi, J.L.5
Garavan, H.P.6
-
49
-
-
34447535547
-
Association study of dysbindin gene with clinical and outcome measures in a representative cohort of Italian schizophrenic patients
-
Tosato S., Ruggeri M., Bonetto C., Bertani M., Marrella G., Lasalvia A., et al. Association study of dysbindin gene with clinical and outcome measures in a representative cohort of Italian schizophrenic patients. Am J Med Genet B Neuropsychiatr Genet 144B (2007) 647-659
-
(2007)
Am J Med Genet B Neuropsychiatr Genet
, vol.144 B
, pp. 647-659
-
-
Tosato, S.1
Ruggeri, M.2
Bonetto, C.3
Bertani, M.4
Marrella, G.5
Lasalvia, A.6
-
50
-
-
33747350777
-
DTNBP1 (dysbindin) gene variants modulate prefrontal brain function in healthy individuals
-
Fallgatter A.J., Herrmann M.J., Hohoff C., Ehlis A.C., Jarczok T.A., Freitag C.M., and Deckert J. DTNBP1 (dysbindin) gene variants modulate prefrontal brain function in healthy individuals. Neuropsychopharmacology 31 (2006) 2002-2010
-
(2006)
Neuropsychopharmacology
, vol.31
, pp. 2002-2010
-
-
Fallgatter, A.J.1
Herrmann, M.J.2
Hohoff, C.3
Ehlis, A.C.4
Jarczok, T.A.5
Freitag, C.M.6
Deckert, J.7
-
51
-
-
6344237686
-
Association of the DTNBP1 locus with schizophrenia in a U.S. population
-
Funke B., Finn C.T., Plocik A.M., Lake S., DeRosse P., Kane J.M., et al. Association of the DTNBP1 locus with schizophrenia in a U.S. population. Am J Hum Genet 75 (2004) 891-899
-
(2004)
Am J Hum Genet
, vol.75
, pp. 891-899
-
-
Funke, B.1
Finn, C.T.2
Plocik, A.M.3
Lake, S.4
DeRosse, P.5
Kane, J.M.6
-
52
-
-
38949090696
-
Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction
-
Vilella E., Costas J., Sanjuan J., Guitart M., De Diego Y., and Carracedo A. Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction. J Psychiatr Res 42 (2008) 278-288
-
(2008)
J Psychiatr Res
, vol.42
, pp. 278-288
-
-
Vilella, E.1
Costas, J.2
Sanjuan, J.3
Guitart, M.4
De Diego, Y.5
Carracedo, A.6
-
53
-
-
43349097737
-
No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: Implications for psychiatric genetics
-
Sanders A.R., Duan J., Levinson D., Shi J., He D., and Hou C. No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: Implications for psychiatric genetics. Am J Psychiatry 165 (2008) 497-506
-
(2008)
Am J Psychiatry
, vol.165
, pp. 497-506
-
-
Sanders, A.R.1
Duan, J.2
Levinson, D.3
Shi, J.4
He, D.5
Hou, C.6
-
54
-
-
37449007716
-
The DISC locus in psychiatric illness
-
Chubb J.E., Bradshaw N.J., Soares D.C., Porteous D.J., and Millar J.K. The DISC locus in psychiatric illness. Mol Psychiatry 13 (2008) 36-64
-
(2008)
Mol Psychiatry
, vol.13
, pp. 36-64
-
-
Chubb, J.E.1
Bradshaw, N.J.2
Soares, D.C.3
Porteous, D.J.4
Millar, J.K.5
-
55
-
-
0034927864
-
Schizophrenia and affective disorders-cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: Clinical and P300 findings in a family
-
Blackwood D.H., Fordyce A., Walker M.T., St Clair D.M., Porteous D.J., and Muir W.J. Schizophrenia and affective disorders-cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: Clinical and P300 findings in a family. Am J Hum Genet 69 (2001) 428-433
-
(2001)
Am J Hum Genet
, vol.69
, pp. 428-433
-
-
Blackwood, D.H.1
Fordyce, A.2
Walker, M.T.3
St Clair, D.M.4
Porteous, D.J.5
Muir, W.J.6
-
56
-
-
20844463251
-
Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia
-
Callicott J.H., Straub R.E., Pezawas L., Egan M.F., Mattay V.S., Hariri A.R., et al. Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia. Proc Natl Acad Sci U S A 102 (2005) 8627-8632
-
(2005)
Proc Natl Acad Sci U S A
, vol.102
, pp. 8627-8632
-
-
Callicott, J.H.1
Straub, R.E.2
Pezawas, L.3
Egan, M.F.4
Mattay, V.S.5
Hariri, A.R.6
-
57
-
-
33750058844
-
Differential expression of disrupted-in-schizophrenia (DISC1) in bipolar disorder
-
Maeda K., Nwulia E., Chang J., Balkissoon R., Ishizuka K., Chen H., et al. Differential expression of disrupted-in-schizophrenia (DISC1) in bipolar disorder. Biol Psychiatry 60 (2006) 929-935
-
(2006)
Biol Psychiatry
, vol.60
, pp. 929-935
-
-
Maeda, K.1
Nwulia, E.2
Chang, J.3
Balkissoon, R.4
Ishizuka, K.5
Chen, H.6
-
58
-
-
34848875136
-
Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments
-
Palo O.M., Antila M., Silander K., Hennah W., Kilpinen H., Soronen P., et al. Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments. Hum Mol Genet 16 (2007) 2517-2528
-
(2007)
Hum Mol Genet
, vol.16
, pp. 2517-2528
-
-
Palo, O.M.1
Antila, M.2
Silander, K.3
Hennah, W.4
Kilpinen, H.5
Soronen, P.6
-
59
-
-
33749576292
-
Impact of the DISC1 Ser704Cys polymorphism on risk for major depression, brain morphology and ERK signaling
-
Hashimoto R., Numakawa T., Ohnishi T., Kumamaru E., Yagasaki Y., Ishimoto T., et al. Impact of the DISC1 Ser704Cys polymorphism on risk for major depression, brain morphology and ERK signaling. Hum Mol Genet 15 (2006) 3024-3033
-
(2006)
Hum Mol Genet
, vol.15
, pp. 3024-3033
-
-
Hashimoto, R.1
Numakawa, T.2
Ohnishi, T.3
Kumamaru, E.4
Yagasaki, Y.5
Ishimoto, T.6
-
60
-
-
32844455739
-
A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia
-
Hennah W., Tuulio-Henriksson A., Paunio T., Ekelund J., Varilo T., Partonen T., et al. A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia. Mol Psychiatry 10 (2005) 1097-1103
-
(2005)
Mol Psychiatry
, vol.10
, pp. 1097-1103
-
-
Hennah, W.1
Tuulio-Henriksson, A.2
Paunio, T.3
Ekelund, J.4
Varilo, T.5
Partonen, T.6
-
61
-
-
33748741474
-
A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention
-
Liu Y.L., Fann C.S., Liu C.M., Chen W.J., Wu J.Y., Hung S.I., et al. A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention. Biol Psychiatry 60 (2006) 554-562
-
(2006)
Biol Psychiatry
, vol.60
, pp. 554-562
-
-
Liu, Y.L.1
Fann, C.S.2
Liu, C.M.3
Chen, W.J.4
Wu, J.Y.5
Hung, S.I.6
-
62
-
-
27744554247
-
Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory
-
Cannon T.D., Hennah W., van Erp T.G., Thompson P.M., Lonnqvist J., Huttunen M., et al. Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory. Arch Gen Psychiatry 62 (2005) 1205-1213
-
(2005)
Arch Gen Psychiatry
, vol.62
, pp. 1205-1213
-
-
Cannon, T.D.1
Hennah, W.2
van Erp, T.G.3
Thompson, P.M.4
Lonnqvist, J.5
Huttunen, M.6
-
63
-
-
43349108259
-
Schizophrenia candidate genes: Are we really coming up blank?
-
[Editorial]
-
Hamilton S.P. Schizophrenia candidate genes: Are we really coming up blank?. [Editorial]. Am J Psychiatry 165 (2008) 420-423
-
(2008)
Am J Psychiatry
, vol.165
, pp. 420-423
-
-
Hamilton, S.P.1
|