-
1
-
-
0034060459
-
Twin studies of schizophrenia: From bow-and-arrow concordances to Star Wars Mx and functional genomics
-
Cardno AG, Gottesman H: Twin studies of schizophrenia: from bow-and-arrow concordances to Star Wars Mx and functional genomics. Am J Med Genet 2000, 97:12-17.
-
(2000)
Am. J. Med. Genet.
, vol.97
, pp. 12-17
-
-
Cardno, A.G.1
Gottesman, I.I.2
-
2
-
-
0023255401
-
Twin concordance for DSM-III schizophrenia.: Scrutinizing the validity of the definition
-
Farmer AE, McGuffin P, Gottesman H: Twin concordance for DSM-III schizophrenia.: scrutinizing the validity of the definition. Arch Gen Psychiatry 1987, 44:634-641.
-
(1987)
Arch. Gen. Psychiatry
, vol.44
, pp. 634-641
-
-
Farmer, A.E.1
McGuffin, P.2
Gottesman, H.3
-
3
-
-
0022587915
-
Genetic markers in schizophrenia
-
McGuffin P, Sturt E: Genetic markers in schizophrenia. Hum Hered 1986, 36:65-88.
-
(1986)
Hum. Hered.
, vol.36
, pp. 65-88
-
-
McGuffin, P.1
Sturt, E.2
-
4
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
The International Human Genome Mapping Consortium
-
The International Human Genome Mapping Consortium: Initial sequencing and analysis of the human genome. Nature 2000, 409:860-921.
-
(2000)
Nature
, vol.409
, pp. 860-921
-
-
-
5
-
-
0842348300
-
Linkage and association
-
Edited by McGuffin P, Owen MJ, Gottesman H. Oxford: Oxford University Press
-
Sham P, McGuffin P: Linkage and association. In Psychiatric Genetics and Genomics. Edited by McGuffin P, Owen MJ, Gottesman H. Oxford: Oxford University Press; 2002:55-73.
-
(2002)
Psychiatric Genetics and Genomics
, pp. 55-73
-
-
Sham, P.1
McGuffin, P.2
-
6
-
-
0347970947
-
The dementias
-
Edited by McGuffin P, Owen MJ, Gottesman H. Oxford: Oxford University Press
-
Liddell MB, Williams J, Owen MJ: The dementias. In Psychiatric Genetics and Genomics. Edited by McGuffin P, Owen MJ, Gottesman H. Oxford: Oxford University Press; 2002:341-396.
-
(2002)
Psychiatric Genetics and Genomics
, pp. 341-396
-
-
Liddell, M.B.1
Williams, J.2
Owen, M.J.3
-
7
-
-
0035220164
-
Significance levels in genome scans
-
Thomson G: Significance levels in genome scans. Adv Genet 2001, 42:475-486.
-
(2001)
Adv. Genet.
, vol.42
, pp. 475-486
-
-
Thomson, G.1
-
8
-
-
0034018285
-
Linkage and associated studies of schizophrenia
-
Riley BP, McGuffin P: Linkage and associated studies of schizophrenia. Am J Med Genet 2000, 97:23-44.
-
(2000)
Am. J. Med. Genet.
, vol.97
, pp. 23-44
-
-
Riley, B.P.1
McGuffin, P.2
-
9
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L: Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet 1995, 11:241-247.
-
(1995)
Nat. Genet.
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
10
-
-
0034724924
-
Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22
-
Brzustowicz LM, Hodgkinson KA, Chow EW, et al.: Location of a major susceptibility locus for familial schizophrenia on chromosome 1q21-q22. Science 2000, 288:678-682.
-
(2000)
Science
, vol.288
, pp. 678-682
-
-
Brzustowicz, L.M.1
Hodgkinson, K.A.2
Chow, E.W.3
-
11
-
-
0035089756
-
Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23
-
Gurling HM, Kalsi G, Brynjolfson J, et al.: Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23. Am J Hum Genet 2001, 68:661-673.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 661-673
-
-
Gurling, H.M.1
Kalsi, G.2
Brynjolfson, J.3
-
12
-
-
18344389404
-
No major schizophrenia locus detected on chromosome 1q in a large multicenter sample
-
Levinson DF, Holmans PA, Laurent C, et al.: No major schizophrenia locus detected on chromosome 1q in a large multicenter sample. Science 2002, 296:739-741.
-
(2002)
Science
, vol.296
, pp. 739-741
-
-
Levinson, D.F.1
Holmans, P.A.2
Laurent, C.3
-
13
-
-
0034988163
-
Genetic studies of bipolar affective disorder in large families
-
Blackwood DH, Visscher PM, Muir WJ: Genetic studies of bipolar affective disorder in large families. Br J Psychiatry 2001, 41:134-136.
-
(2001)
Br. J. Psychiatry
, vol.41
, pp. 134-136
-
-
Blackwood, D.H.1
Visscher, P.M.2
Muir, W.J.3
-
14
-
-
0033364825
-
A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci
-
Hovatta I, Varilo T, Suvisaari J, et al.: A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci. Am J Hum Genet 1999, 65:1114-1124.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1114-1124
-
-
Hovatta, I.1
Varilo, T.2
Suvisaari, J.3
-
15
-
-
18144434579
-
Genome-wide scan for schizophrenia in the Finnish population: Evidence for a locus on chromosome 7q22
-
Ekelund J, Lichtermann D, Hovatta I, et al.: Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22. Hum Mol Genet 2000, 9:1049-1057.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1049-1057
-
-
Ekelund, J.1
Lichtermann, D.2
Hovatta, I.3
-
16
-
-
0012150654
-
Schizophrenia
-
Edited by McGuffin P, Owen MJ, Gottesman I.I. Oxford: Oxford University Press
-
Owen MJ, O'Donovan MC, Gottesman H: Schizophrenia. In Psychiatric Genetics and Genomics. Edited by McGuffin P, Owen MJ, Gottesman H. Oxford: Oxford University Press; 2002:247-266.
-
(2002)
Psychiatric Genetics and Genomics
, pp. 247-266
-
-
Owen, M.J.1
O'Donovan, M.C.2
Gottesman, I.I.3
-
17
-
-
0032882849
-
High rates of schizophrenia in adults with velo-cardio-facial syndrome
-
Murphy KC, Jones LA, Owen MJ: High rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch Gen Psychiatry 1999, 56:940-945.
-
(1999)
Arch. Gen. Psychiatry
, vol.56
, pp. 940-945
-
-
Murphy, K.C.1
Jones, L.A.2
Owen, M.J.3
-
18
-
-
0036258079
-
Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia
-
Badner JA, Gershon ES: Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia. Mol Psychiatry 2002, 7:405-411.
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 405-411
-
-
Badner, J.A.1
Gershon, E.S.2
-
19
-
-
0002710362
-
Problems of replivating linkage claims in psychiatry
-
Edited by Gershon ES, Cloninger CR. Washington DC; American Psychiatric Press
-
Suarez BK, Hamper CL, Van Eeerdewegh P: Problems of replivating linkage claims in psychiatry. In Genetic Approaches to Mental Disorders. Edited by Gershon ES, Cloninger CR. Washington DC; American Psychiatric Press: 1994.
-
(1994)
Genetic Approaches to Mental Disorders
-
-
Suarez, B.K.1
Hamper, C.L.2
Van Eeerdewegh, P.3
-
20
-
-
0035121790
-
Genetics of schizophrenia and the new millennium: Progress and pitfalls
-
Baron M: Genetics of schizophrenia and the new millennium: progress and pitfalls. Am J Hum Genet 2001, 68:299-312.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 299-312
-
-
Baron, M.1
-
21
-
-
0037086178
-
Differential expression of the "C" and "T" alleles of the 5-HT2A receptor gene in the temporal cortex of normal individuals and schizophrenics
-
Polesskaya OO, Sokolov BP: Differential expression of the "C" and "T" alleles of the 5-HT2A receptor gene in the temporal cortex of normal individuals and schizophrenics. J Neurosci Res 2002, 67:812-822.
-
(2002)
J. Neurosci. Res.
, vol.67
, pp. 812-822
-
-
Polesskaya, O.O.1
Sokolov, B.P.2
-
22
-
-
1542336569
-
Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia
-
EMASS Collaborative Group. European Multicentre Association Study of Schizophrenia
-
Williams J, McGuffin P, Nothen M, Owen MJ: Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia. EMASS Collaborative Group. European Multicentre Association Study of Schizophrenia. Lancet 1997, 349:1221.
-
(1997)
Lancet
, vol.349
, pp. 1221
-
-
Williams, J.1
McGuffin, P.2
Nothen, M.3
Owen, M.J.4
-
23
-
-
0035981177
-
No association between T102C polymorphism of serotonin-2A receptor gene and clinical phenotypes of Chinese schizophrenic patients
-
Chen RY, Sham P, Chen EY, et al.: No association between T102C polymorphism of serotonin-2A receptor gene and clinical phenotypes of Chinese schizophrenic patients. Psychiatry Res 2001, 105:175-185.
-
(2001)
Psychiatry Res.
, vol.105
, pp. 175-185
-
-
Chen, R.Y.1
Sham, P.2
Chen, E.Y.3
-
24
-
-
0036345529
-
No evidence for an association between the 5-hydroxytryptamine 5-HT2a receptor gene and schizophrenia in Kuwaiti Arabs
-
Haider MZ, Zahid MA: No evidence for an association between the 5-hydroxytryptamine 5-HT2a receptor gene and schizophrenia in Kuwaiti Arabs. Psychiatry Clin Neurosci 2002, 56:465-467.
-
(2002)
Psychiatry Clin. Neurosci.
, vol.56
, pp. 465-467
-
-
Haider, M.Z.1
Zahid, M.A.2
-
25
-
-
6844222858
-
A meta-analysis and transmission dysequilibrium study of association between the dopamine D3 receptor gene and schizophrenia
-
Williams J, Spurlock G, Holmans P, et al.: A meta-analysis and transmission dysequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Mol Psychiatry 1998, 3:141-149.
-
(1998)
Mol. Psychiatry
, vol.3
, pp. 141-149
-
-
Williams, J.1
Spurlock, G.2
Holmans, P.3
-
26
-
-
0035985480
-
Characterization, mutation detection, and association analysis of alternative promoters and 5′ UTRs of the human dopamine D3 receptor gene in schizophrenia
-
Anney RJ, Rees MI, Bryan E, et al.: Characterization, mutation detection, and association analysis of alternative promoters and 5′ UTRs of the human dopamine D3 receptor gene in schizophrenia. Mol Psychiatry 2002, 7:493-502.
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 493-502
-
-
Anney, R.J.1
Rees, M.I.2
Bryan, E.3
-
27
-
-
0035985470
-
Determination of the genomic structure and mutation screening in schizophrenic individuals for five subunits of the N-methyl-D-aspartate glutamate receptor
-
Williams NM, Bowen T, Spurlock G, et al.: Determination of the genomic structure and mutation screening in schizophrenic individuals for five subunits of the N-methyl-D-aspartate glutamate receptor. Mol Psychiatry 2002, 7:508-514.
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 508-514
-
-
Williams, N.M.1
Bowen, T.2
Spurlock, G.3
-
28
-
-
0036261211
-
Association between the ionotropic glutamate receptor kainate 3 (GRIK3) ser310ala polymorphism and schizophrenia
-
Begni S, Popoli M, Moraschi S, et al.: Association between the ionotropic glutamate receptor kainate 3 (GRIK3) ser310ala polymorphism and schizophrenia. Mol Psychiatry 2002, 7:416-418.
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 416-418
-
-
Begni, S.1
Popoli, M.2
Moraschi, S.3
-
29
-
-
0035056929
-
The genomic organization of the metabotropic glutamate receptor subtype 5 gene, and its association with schizophrenia
-
Devon RS, Anderson S, Teague PW, et al.: The genomic organization of the metabotropic glutamate receptor subtype 5 gene, and its association with schizophrenia. Mol Psychiatry 2001, 6:311-314.
-
(2001)
Mol. Psychiatry
, vol.6
, pp. 311-314
-
-
Devon, R.S.1
Anderson, S.2
Teague, P.W.3
-
30
-
-
0034426026
-
The NOTCH4 focus is associated with susceptibility to schizophrenia
-
Wei J, Hemmings GP: The NOTCH4 focus is associated with susceptibility to schizophrenia. Nat Genet 2000, 25:376-377.
-
(2000)
Nat. Genet.
, vol.25
, pp. 376-377
-
-
Wei, J.1
Hemmings, G.P.2
-
31
-
-
0035871539
-
Association study of CAG repeats in the KCNN3 gene in Japanese patients with schizophrenia, schizoaffective disorder and bipolar disorder
-
Ujike H, Yamamoto A, Tanaka Y, et al.: Association study of CAG repeats in the KCNN3 gene in Japanese patients with schizophrenia, schizoaffective disorder and bipolar disorder. Psychiatry Res 2001, 101:203-207.
-
(2001)
Psychiatry Res.
, vol.101
, pp. 203-207
-
-
Ujike, H.1
Yamamoto, A.2
Tanaka, Y.3
-
32
-
-
0034975491
-
Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls
-
Sklar P, Schwab SG, Williams NM, et al.: Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls. Nat Genet 2001, 28:126-128.
-
(2001)
Nat. Genet.
, vol.28
, pp. 126-128
-
-
Sklar, P.1
Schwab, S.G.2
Williams, N.M.3
-
33
-
-
85047697720
-
A family-based and case-control association study of the NOTCH4 gene and schizophrenia
-
Fan JB, Tang JX, Gu NF, et al.: A family-based and case-control association study of the NOTCH4 gene and schizophrenia. Mol Psychiatry 2002, 7:100-103.
-
(2002)
Mol. Psychiatry
, vol.7
, pp. 100-103
-
-
Fan, J.B.1
Tang, J.X.2
Gu, N.F.3
-
35
-
-
0037221589
-
Association of neuregulin-1 with schizophrenia confirmed in a Scottish population
-
Stefansson H, Sarginson J, Kong A, et al.: Association of neuregulin-1 with schizophrenia confirmed in a Scottish population. Am J Hum Genet 2003, 72:83-87.
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 83-87
-
-
Stefansson, H.1
Sarginson, J.2
Kong, A.3
-
36
-
-
0037108758
-
Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia
-
Chumakov I, Blumenfeld M, Guerassimenko O, et al.: Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. Proc Natl Acad Sci U S A 2002, 99:13675-13680.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 13675-13680
-
-
Chumakov, I.1
Blumenfeld, M.2
Guerassimenko, O.3
-
37
-
-
18444364206
-
Genetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophrenia
-
Straub RE, Jiang Y, MacLean CJ, 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 2002, 71:337-348.
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 337-348
-
-
Straub, R.E.1
Jiang, Y.2
MacLean, C.J.3
-
38
-
-
0842326677
-
Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia
-
Liu H, Heath SC, Sobin C, et al.: Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia. Proc Natl Acad Sci U S A 2002, 99:3717-3722.
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 3717-3722
-
-
Liu, H.1
Heath, S.C.2
Sobin, C.3
-
39
-
-
18544366528
-
PRODH mutations and hyperprolinemia in a subset of schizophrenic patients
-
Jacquet H, Raux G, Thibaut F, et al.: PRODH mutations and hyperprolinemia in a subset of schizophrenic patients. Hum Mol Genet 2002, 11:2243-2249.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 2243-2249
-
-
Jacquet, H.1
Raux, G.2
Thibaut, F.3
-
40
-
-
0030004521
-
Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders
-
Lachman HM, Papolos DF, Saito T, et al.: Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders. Pharmacogenetics 1996, 6:243-250.
-
(1996)
Pharmacogenetics
, vol.6
, pp. 243-250
-
-
Lachman, H.M.1
Papolos, D.F.2
Saito, T.3
-
41
-
-
0029851636
-
Preferential transmission of the high activity allele of COMT in schizophrenia
-
Li T, Sham PC, Vallada H, Xie T: Preferential transmission of the high activity allele of COMT in schizophrenia. Psychiatr Genet 1996, 6:131-133.
-
(1996)
Psychiatr. Genet.
, vol.6
, pp. 131-133
-
-
Li, T.1
Sham, P.C.2
Vallada, H.3
Xie, T.4
-
42
-
-
9844257590
-
Catechol-O-methyltransferase polymorphisms and schizophrenia: A transmission disequilibrium study in multiply affected families
-
Kunugi H, Vallada HP, Sham PC, et al.: Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families. Psychiatr Genet 1997, 7:97-101.
-
(1997)
Psychiatr. Genet.
, vol.7
, pp. 97-101
-
-
Kunugi, H.1
Vallada, H.P.2
Sham, P.C.3
-
43
-
-
0035810850
-
Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia
-
Egan MF, Goldberg TE, Kolachana BS, et al.: Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia. Proc Natl Acad Sci U S A 2001, 98:6917-6922.
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 6917-6922
-
-
Egan, M.F.1
Goldberg, T.E.2
Kolachana, B.S.3
-
44
-
-
13344284664
-
No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol-O-methyltransferase activity
-
Daniels JK, Williams NM, Williams J, et al.: No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol-O-methyltransferase activity. Am J Psychiatry 1996, 153:268-270.
-
(1996)
Am. J. Psychiatry
, vol.153
, pp. 268-270
-
-
Daniels, J.K.1
Williams, N.M.2
Williams, J.3
-
45
-
-
0030978628
-
Neuropsychological correlates of sustained attention in schizophrenia
-
Chen EY, Lam LC, Chen RY, et al.: Neuropsychological correlates of sustained attention in schizophrenia. Schizophr Res 1997, 24:299-310.
-
(1997)
Schizophr. Res.
, vol.24
, pp. 299-310
-
-
Chen, E.Y.1
Lam, L.C.2
Chen, R.Y.3
-
46
-
-
0031568907
-
Lack of association of a functional catechol-O-methyltransferase gene polymorphism in schizophrenia
-
Strous RD, Bark N, Woerner M, Lachman HM: Lack of association of a functional catechol-O-methyltransferase gene polymorphism in schizophrenia. Biol Psychiatry 1997, 41:493-495.
-
(1997)
Biol. Psychiatry
, vol.41
, pp. 493-495
-
-
Strous, R.D.1
Bark, N.2
Woerner, M.3
Lachman, H.M.4
-
47
-
-
0037043064
-
Schizophrenia and functional polymorphisms in the MAOA and COMT genes: No evidence for association or epistasis
-
Norton N, Kirov G, Zammit S, et al.: Schizophrenia and functional polymorphisms in the MAOA and COMT genes: no evidence for association or epistasis. Am J Med Genet 2002, 114:491-496.
-
(2002)
Am. J. Med. Genet.
, vol.114
, pp. 491-496
-
-
Norton, N.1
Kirov, G.2
Zammit, S.3
-
48
-
-
0031910582
-
Association study of a functional catechol-O-methyltransferase gene polymorphism in Japanese schizophrenics
-
Ohmori O, Shinkai T, Kojima H, et al.: Association study of a functional catechol-O-methyltransferase gene polymorphism in Japanese schizophrenics. Neurosci Lett 1998, 243:109-112.
-
(1998)
Neurosci. Lett.
, vol.243
, pp. 109-112
-
-
Ohmori, O.1
Shinkai, T.2
Kojima, H.3
-
49
-
-
0036913209
-
A highly significant association between a COMT haplotype and schizophrenia
-
Shifman S, Bronstein M, Sternfeld M, et al.: A highly significant association between a COMT haplotype and schizophrenia. Am J Hum Genet 2002, 71:1296-1302.
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 1296-1302
-
-
Shifman, S.1
Bronstein, M.2
Sternfeld, M.3
-
50
-
-
0002820468
-
The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia
-
Moises HW, Zoega T, Gottesman H: The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia. BMC Psychiatry 2002, 2:8.
-
(2002)
BMC Psychiatry
, vol.2
, pp. 8
-
-
Moises, H.W.1
Zoega, T.2
Gottesman, I.I.3
|