-
1
-
-
7144262383
-
Further support for an association between polymorphic CAG repeat in the hKCa3 gene and schizophrenia
-
1 Bowen T, Guy CA, Craddock N, Cardno AG, Williams NM, Spurlock G et al. Further support for an association between polymorphic CAG repeat in the hKCa3 gene and schizophrenia. Mol Psychiatry 1998; 3: 266-269.
-
(1998)
Mol Psychiatry
, vol.3
, pp. 266-269
-
-
Bowen, T.1
Guy, C.A.2
Craddock, N.3
Cardno, A.G.4
Williams, N.M.5
Spurlock, G.6
-
3
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosome
-
3 The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosome. Cell 1993; 72: 971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
4
-
-
0025800526
-
Androgen receptor gene mutation in X-linked spinal and bulbar muscular atrophy
-
4 La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH. Androgen receptor gene mutation in X-linked spinal and bulbar muscular atrophy. Nature 1991; 325: 77-79.
-
(1991)
Nature
, vol.325
, pp. 77-79
-
-
La Spada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
5
-
-
0027164698
-
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia typo 1
-
5 Orr HT, Chung MY, Banfi S, Kwiatkowski Jr J, Servadio A, Beudet AL et al. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia typo 1. Nat Genet 1933; 4: 221-226.
-
(1933)
Nat Genet
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.Y.2
Banfi, S.3
Kwiatkowski J., Jr.4
Servadio, A.5
Beudet, A.L.6
-
6
-
-
17344371397
-
Short GCC expansion in the PABP2 gene causes oculopharyngeal muscular dystrophy
-
6 Brais B, Bouchard JP, Xie YG, Rochefort DL, Chretien N, Tome FMS et al. Short GCC expansion in the PABP2 gene causes oculopharyngeal muscular dystrophy. Nat Genet 1998; 18: 164-166.
-
(1998)
Nat Genet
, vol.18
, pp. 164-166
-
-
Brais, B.1
Bouchard, J.P.2
Xie, Y.G.3
Rochefort, D.L.4
Chretien, N.5
Tome, F.M.S.6
-
7
-
-
0027256423
-
Direct detection of novel expanded trinucleotide repeats in the human genome
-
7 Schalling M, Hudson TJ, Buetow KH, Housman DE. Direct detection of novel expanded trinucleotide repeats in the human genome. Nat Genet 1993; 4: 135-139.
-
(1993)
Nat Genet
, vol.4
, pp. 135-139
-
-
Schalling, M.1
Hudson, T.J.2
Buetow, K.H.3
Housman, D.E.4
-
8
-
-
0028784037
-
CAG repeat expansion and schizophrenia: Association with the disease in females and with early age of onset
-
8 Morris AG, Gaitonde E, McKenna PJ, Mollon JD, Hunt D. CAG repeat expansion and schizophrenia: association with the disease in females and with early age of onset. Hum Mol Genet 1995; 4: 1957-1961.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1957-1961
-
-
Morris, A.G.1
Gaitonde, E.2
McKenna, P.J.3
Mollon, J.D.4
Hunt, D.5
-
9
-
-
10544244172
-
Confirmation of association between expanded CAG/CTG repeats both in schizophrenia and bipolar disorder
-
9 O'Donovan MC, Guy C, Craddock N, Bowen T, McKeon P, Macedo A et al. Confirmation of association between expanded CAG/CTG repeats both in schizophrenia and bipolar disorder. Psych Med 1996; 26: 1145-1153.
-
(1996)
Psych Med
, vol.26
, pp. 1145-1153
-
-
O'Donovan, M.C.1
Guy, C.2
Craddock, N.3
Bowen, T.4
McKeon, P.5
Macedo, A.6
-
10
-
-
0029240699
-
Detection of expanded CAG repeat in bipolar affective disorder using the repeat expansion detection (RED) method
-
10 Lindblad K, Nylander PO, Debruyn A, Sourey D, Zander C, Engstrom C et al. Detection of expanded CAG repeat in bipolar affective disorder using the repeat expansion detection (RED) method. Neurobiol Dis 1995; 2: 55-62.
-
(1995)
Neurobiol Dis
, vol.2
, pp. 55-62
-
-
Lindblad, K.1
Nylander, P.O.2
Debruyn, A.3
Sourey, D.4
Zander, C.5
Engstrom, C.6
-
11
-
-
0031030296
-
CAG repeat expansion in bipolar and unipolar disorder
-
11 Oruc L, Lindblad K, Verheyen G, Ahlberg S, Jakovljevic M, Ivezic S et al. CAG repeat expansion in bipolar and unipolar disorder. Am J Hum Genet 1997; 60: 730-733.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 730-733
-
-
Oruc, L.1
Lindblad, K.2
Verheyen, G.3
Ahlberg, S.4
Jakovljevic, M.5
Ivezic, S.6
-
12
-
-
0030133848
-
Frequency analysis of large CAG/CTG trinucleotide repeat in schizophrenia and bipolar affective disorder
-
12 Vincent JB, Klempan T, Parikh SS, Sasaki T, Meltzer HE, Sirugo G et al. Frequency analysis of large CAG/CTG trinucleotide repeat in schizophrenia and bipolar affective disorder. Mol Psychiatry 1996; 1: 141-148.
-
(1996)
Mol Psychiatry
, vol.1
, pp. 141-148
-
-
Vincent, J.B.1
Klempan, T.2
Parikh, S.S.3
Sasaki, T.4
Meltzer, H.E.5
Sirugo, G.6
-
13
-
-
0030961916
-
Exclusion of CAG/CTG trinucleotide repeat loci which map to chromosome 4 in bipolar disorder and schizophrenia
-
13 Speight G, Guy C, Bowen T, Asherson P, McGuffin P, Craddock N et al. Exclusion of CAG/CTG trinucleotide repeat loci which map to chromosome 4 in bipolar disorder and schizophrenia. Am J Med Genet (Neuropsych Genet) 1997; 74: 204-206.
-
(1997)
Am J Med Genet (Neuropsych Genet)
, vol.74
, pp. 204-206
-
-
Speight, G.1
Guy, C.2
Bowen, T.3
Asherson, P.4
McGuffin, P.5
Craddock, N.6
-
14
-
-
0000268002
-
Screening candidate chromosomes for expanded CAG/CTG repeat in schizophrenia and bipolar disorder
-
14 Guy C, Bowen T, Speight G, McGuffin P, Craddock N, Owen MJ et al. Screening candidate chromosomes for expanded CAG/CTG repeat in schizophrenia and bipolar disorder. Am J Med Genet (Neuropsych Genet) 1997; 74: 609.
-
(1997)
Am J Med Genet (Neuropsych Genet)
, vol.74
, pp. 609
-
-
Guy, C.1
Bowen, T.2
Speight, G.3
McGuffin, P.4
Craddock, N.5
Owen, M.J.6
-
15
-
-
0031415105
-
No evidence for expanded polyglutamine sequence in bipolar disorder and schizophrenia
-
15 Jones AL, Middle F, Guy C, Spurlock G, Cairns NJ, McGuffin P et al. No evidence for expanded polyglutamine sequence in bipolar disorder and schizophrenia. Mol Psychiatry 1997; 2; 478-482.
-
(1997)
Mol Psychiatry
, vol.2
, pp. 478-482
-
-
Jones, A.L.1
Middle, F.2
Guy, C.3
Spurlock, G.4
Cairns, N.J.5
McGuffin, P.6
-
16
-
-
0000226226
-
Investigating genes containing expressed repeats in bipolar disorder
-
16 Tureck G, Alda M, Joober R, Lafreniere RG, Grof B, Ahrens M et al. Investigating genes containing expressed repeats in bipolar disorder. Am J Med Genet (Neuropsych Genet) 1997; 74: 611.
-
(1997)
Am J Med Genet (Neuropsych Genet)
, vol.74
, pp. 611
-
-
Tureck, G.1
Alda, M.2
Joober, R.3
Lafreniere, R.G.4
Grof, B.5
Ahrens, M.6
-
17
-
-
6544269945
-
Isolation of novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: A candidate for schizophrenia and bipolar disorder
-
17 Chandy KG, Fantino E, Wittekindt O, Kalman K, Tong L-L, Ho T-H et al. Isolation of novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: a candidate for schizophrenia and bipolar disorder. Mol Psychiatry 1998; 3: 32-37.
-
(1998)
Mol Psychiatry
, vol.3
, pp. 32-37
-
-
Chandy, K.G.1
Fantino, E.2
Wittekindt, O.3
Kalman, K.4
Tong, L.-L.5
Ho, T.-H.6
-
18
-
-
0032129454
-
The human small conductance-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows possible association with schizophrenia
-
18 Wittekindt O, Jauch A, Burgert E, Sharer L et al. The human small conductance-regulated potassium channel gene (hSKCa3) contains two CAG repeats in exon 1, is on chromosome 1q21.3, and shows possible association with schizophrenia. Neurogenetics 1998; 1: 259-265.
-
(1998)
Neurogenetics
, vol.1
, pp. 259-265
-
-
Wittekindt, O.1
Jauch, A.2
Burgert, E.3
Sharer, L.4
-
19
-
-
0032552863
-
Transmission disequilibrium analysis of a triplet repeat within the hSKCa3 gene using family trios with schizophrenia
-
19 Li T, Hu X, Chandy KG, Fantino E et al. Transmission disequilibrium analysis of a triplet repeat within the hSKCa3 gene using family trios with schizophrenia. Biochem Biophys Res Com 1998; 251: 662-665.
-
(1998)
Biochem Biophys Res Com
, vol.251
, pp. 662-665
-
-
Li, T.1
Hu, X.2
Chandy, K.G.3
Fantino, E.4
-
20
-
-
0030965076
-
Analysis of the CAG repeats in the SCA1 and B37 gene in schizophrenia and bipolar I disorder patients - Tentative association between B37 and schizophrenia
-
20 Morris-Rosendahl D, Burgert E, Uyanik G, Mayerova A, Duval F, Macher JP et al. Analysis of the CAG repeats in the SCA1 and B37 gene in schizophrenia and bipolar I disorder patients - tentative association between B37 and schizophrenia. Am J Med Genet (Neuropsych Genet) 1997; 74: 324-330.
-
(1997)
Am J Med Genet (Neuropsych Genet)
, vol.74
, pp. 324-330
-
-
Morris-Rosendahl, D.1
Burgert, E.2
Uyanik, G.3
Mayerova, A.4
Duval, F.5
Macher, J.P.6
-
21
-
-
0027142626
-
Association study of schizophrenia with dopamine D3 receptor gene polymorphism: Probable effect of family history of schizophrenia
-
21 Nimgaonkar VL, Zhang XR, Caldwell JG, Ganguli R, Chakravarti A. Association study of schizophrenia with dopamine D3 receptor gene polymorphism: probable effect of family history of schizophrenia. Am J Med Genet (Neuropsych Genet) 1993; 48: 214-217.
-
(1993)
Am J Med Genet (Neuropsych Genet)
, vol.48
, pp. 214-217
-
-
Nimgaonkar, V.L.1
Zhang, X.R.2
Caldwell, J.G.3
Ganguli, R.4
Chakravarti, A.5
-
22
-
-
0031750241
-
A triple repeat on 17q account from most expansion detected by the repeat expansion detection technique
-
22 Sidransky E, Burgess C, Ikeuchi T, Linblad K et al. A triple repeat on 17q account from most expansion detected by the repeat expansion detection technique. Am J Hum Genet 1998; 62: 1548-1551.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1548-1551
-
-
Sidransky, E.1
Burgess, C.2
Ikeuchi, T.3
Linblad, K.4
-
23
-
-
0029983060
-
The Irish study of high density schizophrenia families: Field methods and power to detect linkage
-
23 Kendler KS, O'Neil FA, Murphy B, Duke F, Straub RE, Shinkwin R et al. The Irish study of high density schizophrenia families: field methods and power to detect linkage. Am J Med Genet (Neuropsych Genet) 1996; 57: 179-190.
-
(1996)
Am J Med Genet (Neuropsych Genet)
, vol.57
, pp. 179-190
-
-
Kendler, K.S.1
O'Neil, F.A.2
Murphy, B.3
Duke, F.4
Straub, R.E.5
Shinkwin, R.6
-
24
-
-
0028820161
-
A potential vulnerability locus for schizophrenia on chromosome 6p24-22: Evidence for genetic heterogeneity
-
24 Straub RE, MacLean CJ, O'Neill AF, Burke J, Murphy B, Duke F et al. A potential vulnerability locus for schizophrenia on chromosome 6p24-22: evidence for genetic heterogeneity. Nat Genet 1995; 11: 287-292.
-
(1995)
Nat Genet
, vol.11
, pp. 287-292
-
-
Straub, R.E.1
MacLean, C.J.2
O'Neill, A.F.3
Burke, J.4
Murphy, B.5
Duke, F.6
-
26
-
-
0028981182
-
An extended transmission/disequilibrium test (TDT) for multi-allele marker loci
-
26 Sham PC, Curtis D. An extended transmission/disequilibrium test (TDT) for multi-allele marker loci. Ann Hum Genet 1995; 59: 323-336.
-
(1995)
Ann Hum Genet
, vol.59
, pp. 323-336
-
-
Sham, P.C.1
Curtis, D.2
|