-
1
-
-
0027161966
-
A pilot Swedish twin study of affective illness, including hospital- and population-ascertained subsamples
-
Kendler KS, Pedersen N, Johnson L, Neale MC, Mathe AA. A pilot Swedish twin study of affective illness, including hospital- and population-ascertained subsamples. Arch Gen Psychiatry 1993; 50: 699-700.
-
(1993)
Arch Gen Psychiatry
, vol.50
, pp. 699-700
-
-
Kendler, K.S.1
Pedersen, N.2
Johnson, L.3
Neale, M.C.4
Mathe, A.A.5
-
2
-
-
0344305525
-
Schizophrenia as a complex trait: Evidence from a meta-analysis of twin studies
-
Sullivan PF, Kendler KS, Neale MC. Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. Arch Gen Psychiatry 2003; 60: 1187-1192.
-
(2003)
Arch Gen Psychiatry
, vol.60
, pp. 1187-1192
-
-
Sullivan, P.F.1
Kendler, K.S.2
Neale, M.C.3
-
3
-
-
0025277392
-
Association within a family of a balanced autosomal translocation with major mental illness
-
St Clair D, Blackwood D, Muir W, Carothers A, Walker M, Spowart G et al. Association within a family of a balanced autosomal translocation with major mental illness. Lancet 1990; 336: 13-16.
-
(1990)
Lancet
, vol.336
, pp. 13-16
-
-
St. Clair, D.1
Blackwood, D.2
Muir, W.3
Carothers, A.4
Walker, M.5
Spowart, G.6
-
4
-
-
0034702026
-
Disruption of two novel genes by a translocation co-segregating with schizophrenia
-
Millar JK, Wilson-Annan JC, Anderson S, Christie S, Taylor MS, Semple CA et al. Disruption of two novel genes by a translocation co-segregating with schizophrenia. Hum Mol Genet 2000; 9: 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
-
5
-
-
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 DH, Fordyce A, Walker MT, St Clair DM, Porteous DJ, Muir WJ. 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 2001; 69: 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
-
6
-
-
3242806757
-
Clinical phenotypes associated with DISC1, a candidate gene for schizophrenia
-
Blackwood DH, Muir WJ. Clinical phenotypes associated with DISC1, a candidate gene for schizophrenia. Neurotox Res 2004; 6: 35-41.
-
(2004)
Neurotox Res
, vol.6
, pp. 35-41
-
-
Blackwood, D.H.1
Muir, W.J.2
-
7
-
-
0034235003
-
Chromosomal location and genomic structure of the human translin-associated factor X gene (TRAX; TSNAX) revealed by intergenic splicing to DISC1, a gene disrupted by a translocation segregating with schizophrenia
-
Millar JK, Christie S, Semple CA, Porteous DJ. Chromosomal location and genomic structure of the human translin-associated factor X gene (TRAX; TSNAX) revealed by intergenic splicing to DISC1, a gene disrupted by a translocation segregating with schizophrenia. Genomics 2000; 67: 69-77.
-
(2000)
Genomics
, vol.67
, pp. 69-77
-
-
Millar, J.K.1
Christie, S.2
Semple, C.A.3
Porteous, D.J.4
-
8
-
-
0035878561
-
Chromosome 1 loci in Finnish schizophrenia families
-
Ekelund J, Hovatta I, Parker A, Paunio T, Varilo T, Martin R et al. Chromosome 1 loci in Finnish schizophrenia families. Hum Mol Genet 2001; 10: 1611-1617.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1611-1617
-
-
Ekelund, J.1
Hovatta, I.2
Parker, A.3
Paunio, T.4
Varilo, T.5
Martin, R.6
-
9
-
-
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 2003; 12: 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
-
10
-
-
8744231685
-
Replication of 1q42 linkage in Finnish schizophrenia pedigrees
-
Ekelund J, Hennah W, Hiekkalinna T, Parker A, Meyer J, Lonnqvist J et al. Replication of 1q42 linkage in Finnish schizophrenia pedigrees. Mol Psychiatry 2004; 9: 1037-1041.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 1037-1041
-
-
Ekelund, J.1
Hennah, W.2
Hiekkalinna, T.3
Parker, A.4
Meyer, J.5
Lonnqvist, J.6
-
11
-
-
0037953124
-
Linkage of schizophrenia with chromosome 1q loci in Taiwanese families
-
Hwu HG, Liu CM, Fann CS, Ou-Yang WC, Lee SF. Linkage of schizophrenia with chromosome 1q loci in Taiwanese families. Mol Psychiatry 2003; 8: 445-452.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 445-452
-
-
Hwu, H.G.1
Liu, C.M.2
Fann, C.S.3
Ou-Yang, W.C.4
Lee, S.F.5
-
12
-
-
6344255274
-
Disrupted in Schizophrenia 1 (DISC1): Association with schizophrenia, schizoaffective disorder, and bipolar disorder
-
Hodgkinson CA, Goldman D, Jaeger J, Persaud S, Kane JM, Lipsky RH et al. Disrupted in Schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder. Am J Hum Genet 2004; 75: 862-872.
-
(2004)
Am J Hum Genet
, vol.75
, pp. 862-872
-
-
Hodgkinson, C.A.1
Goldman, D.2
Jaeger, J.3
Persaud, S.4
Kane, J.M.5
Lipsky, R.H.6
-
13
-
-
12344327212
-
Schizophrenia genes, gene expression, and neuropathology: On the matter of their convergence
-
Harrison PJ, Weinberger DR. Schizophrenia genes, gene expression, and neuropathology: on the matter of their convergence. Mol Psychiatry 2005; 10: 40-68.
-
(2005)
Mol Psychiatry
, vol.10
, pp. 40-68
-
-
Harrison, P.J.1
Weinberger, D.R.2
-
14
-
-
0027186031
-
Linkage analysis of fifty-seven microsatellite loci to bipolar disorder
-
Gejman PV, Martinez M, Cao Q, Friedman E, Berrettini WH, Goldin LR et al. Linkage analysis of fifty-seven microsatellite loci to bipolar disorder. Neuropsychopharmacology 1993; 9: 31-40.
-
(1993)
Neuropsychopharmacology
, vol.9
, pp. 31-40
-
-
Gejman, P.V.1
Martinez, M.2
Cao, Q.3
Friedman, E.4
Berrettini, W.H.5
Goldin, L.R.6
-
15
-
-
12444256025
-
Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q
-
Curtis D, Kalsi G, Brynjolfsson J, McInnis M, O'Neill J, Smyth C et al. Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q. Psychiatr Genet 2003; 13: 77-84.
-
(2003)
Psychiatr Genet
, vol.13
, pp. 77-84
-
-
Curtis, D.1
Kalsi, G.2
Brynjolfsson, J.3
McInnis, M.4
O'Neill, J.5
Smyth, C.6
-
16
-
-
11244302487
-
A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42
-
Macgregor S, Visscher PM, Knott SA, Thomson P, Porteous DJ, Millar JK et al. A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42. Mol Psychiatry 2004; 9: 1083-1090.
-
(2004)
Mol Psychiatry
, vol.9
, pp. 1083-1090
-
-
Macgregor, S.1
Visscher, P.M.2
Knott, S.A.3
Thomson, P.4
Porteous, D.J.5
Millar, J.K.6
-
17
-
-
0037560038
-
DISC1 (Disrupted in Schizophrenia-1) is expressed in limbic regions of the primate brain
-
Austin CP, Ma L, Ky B, Morris JA, Shughrue PJ. DISC1 (Disrupted in Schizophrenia-1) is expressed in limbic regions of the primate brain. Neuroreport 2003; 14: 951-954.
-
(2003)
Neuroreport
, vol.14
, pp. 951-954
-
-
Austin, C.P.1
Ma, L.2
Ky, B.3
Morris, J.A.4
Shughrue, P.J.5
-
18
-
-
0442292274
-
Expression of Disrupted-In-Schizophrenia-1, a schizophrenia-associated gene, is prominent in the mouse hippocampus throughout brain development
-
Austin CP, Ky B, Ma L, Morris JA, Shughrue PJ. Expression of Disrupted-In-Schizophrenia-1, a schizophrenia-associated gene, is prominent in the mouse hippocampus throughout brain development. Neuroscience 2004; 124: 3-10.
-
(2004)
Neuroscience
, vol.124
, pp. 3-10
-
-
Austin, C.P.1
Ky, B.2
Ma, L.3
Morris, J.A.4
Shughrue, P.J.5
-
19
-
-
0037422609
-
Disrupted-in-Schizophrenia-1 (DISC-1): Mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth
-
Ozeki Y, Tomoda T, Kleiderlein J, Kamiya A, Bord L, Fujii K et al. Disrupted-in-Schizophrenia-1 (DISC-1): mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth. Proc Natl Acad Sci USA 2003; 100: 289-294.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 289-294
-
-
Ozeki, Y.1
Tomoda, T.2
Kleiderlein, J.3
Kamiya, A.4
Bord, L.5
Fujii, K.6
-
20
-
-
0042622356
-
Disrupted-in-schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth
-
Miyoshi K, Honda A, Baba K, Taniguchi M, Oono K, Fujita T et al. Disrupted-in-schizophrenia 1, a candidate gene for schizophrenia, participates in neurite outgrowth. Mol Pyschiatry 2003; 8: 685-694.
-
(2003)
Mol Pyschiatry
, vol.8
, pp. 685-694
-
-
Miyoshi, K.1
Honda, A.2
Baba, K.3
Taniguchi, M.4
Oono, K.5
Fujita, T.6
-
21
-
-
2342539835
-
Disrupted in Schizophrenia 1 is a multi-compartmentalised protein that predominantly localises to mitochondria
-
James R, Adams RR, Christie S, Buchanan SR, Porteous DJ, Millar JK. Disrupted in Schizophrenia 1 is a multi-compartmentalised protein that predominantly localises to mitochondria. Mol Cell Neurosci 2004; 26: 112-122.
-
(2004)
Mol Cell Neurosci
, vol.26
, pp. 112-122
-
-
James, R.1
Adams, R.R.2
Christie, S.3
Buchanan, S.R.4
Porteous, D.J.5
Millar, J.K.6
-
22
-
-
1342264187
-
Expression of fasciculation and elongation protein zeta-1 (FEZ1) in the developing rat brain
-
Honda A, Miyoshi K, Baba K, Taniguchi M, Koyama Y, Kuroda S et al. Expression of fasciculation and elongation protein zeta-1 (FEZ1) in the developing rat brain. Brain Res Mol Brain Bes 2004; 122: 89-92.
-
(2004)
Brain Res Mol Brain Bes
, vol.122
, pp. 89-92
-
-
Honda, A.1
Miyoshi, K.2
Baba, K.3
Taniguchi, M.4
Koyama, Y.5
Kuroda, S.6
-
23
-
-
0037766786
-
DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: Regulation and loss of interaction with mutation
-
Morris JA, Kandpal G, Ma L, Austin CP. DISC1 (Disrupted-In-Schizophrenia 1) is a centrosome-associated protein that interacts with MAP1A, MIPT3, ATF4/5 and NUDEL: regulation and loss of interaction with mutation. Hum Mol Genet 2003; 12: 1591-1608.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1591-1608
-
-
Morris, J.A.1
Kandpal, G.2
Ma, L.3
Austin, C.P.4
-
24
-
-
0242437914
-
Yeast two-hybrid screens implicate DISC1 in brain development and function
-
Millar JK, Christie S, Porteous DJ. Yeast two-hybrid screens implicate DISC1 in brain development and function. Biochem Biophys Res Commun 2003; 311: 1019-1025.
-
(2003)
Biochem Biophys Res Commun
, vol.311
, pp. 1019-1025
-
-
Millar, J.K.1
Christie, S.2
Porteous, D.J.3
-
25
-
-
10744229990
-
Disrupted in Schizophrenia 1 and Nudel form a neurodevelopmentally regulated protein complex: Implications for schizophrenia and other major neurological disorders
-
Brandon NJ, Handford EJ, Schurov I, Rain JC, Pelling M, Duran-Jimeniz B et al. Disrupted in Schizophrenia 1 and Nudel form a neurodevelopmentally regulated protein complex: implications for schizophrenia and other major neurological disorders. Mol Cell Neurosci 2004; 25: 42-55.
-
(2004)
Mol Cell Neurosci
, vol.25
, pp. 42-55
-
-
Brandon, N.J.1
Handford, E.J.2
Schurov, I.3
Rain, J.C.4
Pelling, M.5
Duran-Jimeniz, B.6
-
26
-
-
4544339685
-
DISC1 and DISC2: Discovering and dissecting molecular mechanisms underlying psychiatric illness
-
Millar JK, James R, Brandon NJ, Thomson PA. DISC1 and DISC2: discovering and dissecting molecular mechanisms underlying psychiatric illness. Ann Med 2004; 36: 367-378.
-
(2004)
Ann Med
, vol.36
, pp. 367-378
-
-
Millar, J.K.1
James, R.2
Brandon, N.J.3
Thomson, P.A.4
-
27
-
-
0031023837
-
Isolation and characterisation of a cDNA encoding a translin-like protein, TRAX
-
Aoki K, Ishida R, Kasai M. Isolation and characterisation of a cDNA encoding a translin-like protein, TRAX. FEBS Lett 1997; 401: 109-112.
-
(1997)
FEBS Lett
, vol.401
, pp. 109-112
-
-
Aoki, K.1
Ishida, R.2
Kasai, M.3
-
28
-
-
0029166131
-
Testis-brain RNA-binding protein, a testicular translational regulatory RNA-binding protein, is present in the brain and binds to the 3′ untranslated regions of transported brain mRNAs
-
Han JR, Gu W, Hecht NB. Testis-brain RNA-binding protein, a testicular translational regulatory RNA-binding protein, is present in the brain and binds to the 3′ untranslated regions of transported brain mRNAs. Biol Reprod 1995; 53: 707-717.
-
(1995)
Biol Reprod
, vol.53
, pp. 707-717
-
-
Han, J.R.1
Gu, W.2
Hecht, N.B.3
-
29
-
-
0032545356
-
The dendritic translocation of translin protein in the form of BC1 RNA protein particles in developing rat hippocampal neurons in primary culture
-
Kobayashi S, Takashima A, Anzai K. The dendritic translocation of translin protein in the form of BC1 RNA protein particles in developing rat hippocampal neurons in primary culture. Biochem Biophys Res Commun 1998; 253: 448-453.
-
(1998)
Biochem Biophys Res Commun
, vol.253
, pp. 448-453
-
-
Kobayashi, S.1
Takashima, A.2
Anzai, K.3
-
30
-
-
1842477453
-
Translin-associated factor X is post-transcriptionally regulated by its partner protein TB-RBP, and both are essential for normal cell proliferation
-
Yang S, Cho YS, Chennathukuzhi VM, Underkoffler LA, Loonies K, Hecht NB. Translin-associated factor X is post-transcriptionally regulated by its partner protein TB-RBP, and both are essential for normal cell proliferation. J Biol Chem 2004; 279: 12605-12614.
-
(2004)
J Biol Chem
, vol.279
, pp. 12605-12614
-
-
Yang, S.1
Cho, Y.S.2
Chennathukuzhi, V.M.3
Underkoffler, L.A.4
Loonies, K.5
Hecht, N.B.6
-
31
-
-
0042190668
-
Mice deficient for testis-brain RNA-binding protein exhibit a coordinate loss of TRAX, reduced fertility, altered gene expression in the brain, and behavioral changes
-
Chennathukuzhi V, Stein JM, Abel T, Donlon S, Yang S, Miller JP et al. Mice deficient for testis-brain RNA-binding protein exhibit a coordinate loss of TRAX, reduced fertility, altered gene expression in the brain, and behavioral changes. Mol Cell Biol 2003; 23: 6419-6434.
-
(2003)
Mol Cell Biol
, vol.23
, pp. 6419-6434
-
-
Chennathukuzhi, V.1
Stein, J.M.2
Abel, T.3
Donlon, S.4
Yang, S.5
Miller, J.P.6
-
32
-
-
0031460857
-
An allelic association study of two polymorphic markers in close proximity to a balanced translocation t(1:11) that co-segregates with mental illness
-
Wilson-Annan JC, Blackwood DH, Muir W, Millar JK, Porteous DJ. An allelic association study of two polymorphic markers in close proximity to a balanced translocation t(1:11) that co-segregates with mental illness. Psychiatr Genet 1997; 7: 171-174.
-
(1997)
Psychiatr Genet
, vol.7
, pp. 171-174
-
-
Wilson-Annan, J.C.1
Blackwood, D.H.2
Muir, W.3
Millar, J.K.4
Porteous, D.J.5
-
33
-
-
0034941967
-
Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar affective disorder
-
Devon RS, Anderson S, Teague PW, Burgess P, Kipari TM, Semple CA et al. Identification of polymorphisms within Disrupted in Schizophrenia 1 and Disrupted in Schizophrenia 2, and an investigation of their association with schizophrenia and bipolar affective disorder. Psychiatr Genet 2001; 11: 71-78.
-
(2001)
Psychiatr Genet
, vol.11
, pp. 71-78
-
-
Devon, R.S.1
Anderson, S.2
Teague, P.W.3
Burgess, P.4
Kipari, T.M.5
Semple, C.A.6
-
35
-
-
0018119373
-
A diagnostic interview: The schedule for affective disorders and schizophrenia
-
Endicott J, Spitzer RL. A diagnostic interview: the schedule for affective disorders and schizophrenia. Arch Gen Psychiatry 1978; 35: 837-862.
-
(1978)
Arch Gen Psychiatry
, vol.35
, pp. 837-862
-
-
Endicott, J.1
Spitzer, R.L.2
-
37
-
-
85062143268
-
-
NCBI Entrz SNP, http://www.ncbi.nlm.nih.gov/entrez.
-
-
-
-
40
-
-
0034789532
-
Haplotype tagging for the identification of common disease genes
-
Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G et al. Haplotype tagging for the identification of common disease genes. Nat Genet 2001; 29: 233-237.
-
(2001)
Nat Genet
, vol.29
, pp. 233-237
-
-
Johnson, G.C.1
Esposito, L.2
Barratt, B.J.3
Smith, A.N.4
Heward, J.5
Di Genova, G.6
-
41
-
-
85062141941
-
-
http://www.hapmap.org/thehapmap.html.en.
-
-
-
-
42
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005; 21: 263-265.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
43
-
-
0041857847
-
Pedigree disequilibrium tests for multilocus haplotypes
-
Dudbridge F. Pedigree disequilibrium tests for multilocus haplotypes. Genet Epidemiol 2003; 25: 115-221. http://www.hgmp.mrc.ac.uk/~fdudbrid/software/ unphased/.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 115-221
-
-
Dudbridge, F.1
-
44
-
-
1942504197
-
DISC1 localizes to the centrosome by binding to kendrin
-
Miyoshi K, Asanuma M, Miyazaki I, Diaz-Corrales FJ, Katayama T, Tohyama M et al. DISC1 localizes to the centrosome by binding to kendrin. Biochem Biophys Res Commun 2004; 317: 1195-1199.
-
(2004)
Biochem Biophys Res Commun
, vol.317
, pp. 1195-1199
-
-
Miyoshi, K.1
Asanuma, M.2
Miyazaki, I.3
Diaz-Corrales, F.J.4
Katayama, T.5
Tohyama, M.6
-
45
-
-
1242314858
-
Neuregulin 1 and schizophrenia
-
Stefansson H, Steinthorsdottir V, Thorgeirsson TE, Gulcher JR, Stefansson K. Neuregulin 1 and schizophrenia. Ann Med 2004; 36: 62-71.
-
(2004)
Ann Med
, vol.36
, pp. 62-71
-
-
Stefansson, H.1
Steinthorsdottir, V.2
Thorgeirsson, T.E.3
Gulcher, J.R.4
Stefansson, K.5
-
46
-
-
2342477899
-
Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria
-
Kirov G, Ivanov D, Williams NM, Preece A, Nikolov I, Milev R et al. Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria. Biol Psychiatry 2004; 55: 971-975.
-
(2004)
Biol Psychiatry
, vol.55
, pp. 971-975
-
-
Kirov, G.1
Ivanov, D.2
Williams, N.M.3
Preece, A.4
Nikolov, I.5
Milev, R.6
-
47
-
-
12144286724
-
Is NOTCH4 associated with schizophrenia?
-
Zhang X, Wei J, Yu YQ, Liu SZ, Shi JP, Liu LL et al. Is NOTCH4 associated with schizophrenia? Psychiatr Genet 2004; 14: 43-46.
-
(2004)
Psychiatr Genet
, vol.14
, pp. 43-46
-
-
Zhang, X.1
Wei, J.2
Yu, Y.Q.3
Liu, S.Z.4
Shi, J.P.5
Liu, L.L.6
-
48
-
-
0742288585
-
The complex interplay among factors that influence allelic association
-
Zondervan KT, Cardon LR. The complex interplay among factors that influence allelic association. Nat Rev Genet 2004; 5: 89-100.
-
(2004)
Nat Rev Genet
, vol.5
, pp. 89-100
-
-
Zondervan, K.T.1
Cardon, L.R.2
-
49
-
-
18344389404
-
No major schizophrenia locus detected on chromosome 1q in a large multicenter sample
-
Levinson DF, Holmans PA, Laurent C, Riley B, Pulver AE, Gejman PV 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
Riley, B.4
Pulver, A.E.5
Gejman, P.V.6
-
50
-
-
18744424564
-
Is schizophrenia linked to chromosome 1q?
-
author reply 2277
-
Macgregor S, Visscher PM, Knott S, Porteous D, Muir W, Millar K et al. Is schizophrenia linked to chromosome 1q? Science 2002; 298: 2277, author reply 2277.
-
(2002)
Science
, vol.298
, pp. 2277
-
-
Macgregor, S.1
Visscher, P.M.2
Knott, S.3
Porteous, D.4
Muir, W.5
Millar, K.6
-
51
-
-
0037320652
-
Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor
-
Duan J, Wainwright MS, Comeron JM, Saitou N, Sanders AR, Gelernter J et al. Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor. Hum Mol Genet 2003; 12: 205-216.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 205-216
-
-
Duan, J.1
Wainwright, M.S.2
Comeron, J.M.3
Saitou, N.4
Sanders, A.R.5
Gelernter, J.6
-
52
-
-
3042804077
-
Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia
-
Mukai J, Liu H, Burt RA, Swor DE, Lai WS, Karayiorgou M et al. Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia. Nat Genet 2004; 36: 725-731.
-
(2004)
Nat Genet
, vol.36
, pp. 725-731
-
-
Mukai, J.1
Liu, H.2
Burt, R.A.3
Swor, D.E.4
Lai, W.S.5
Karayiorgou, M.6
-
53
-
-
85047693249
-
Dysbindin-1 and schizophrenia: From genetics to neuropathology
-
Owen MJ, Williams NM, O'Donovan MC. Dysbindin-1 and schizophrenia: from genetics to neuropathology. J Clin Invest 2004; 113: 1255-1257.
-
(2004)
J Clin Invest
, vol.113
, pp. 1255-1257
-
-
Owen, M.J.1
Williams, N.M.2
O'Donovan, M.C.3
|