-
2
-
-
0029825936
-
Expansion of 50 CAG/CTG repeats excluded in schizophrenia by application of a highly efficient approach using repeat expansion detection and a PCR screening set
-
Bowen T, Guy C, Speight G, Jones L, Cardno A, Murphy K, McGuffin P, Owen MJ, O'Donovan MC. 1996. Expansion of 50 CAG/CTG repeats excluded in schizophrenia by application of a highly efficient approach using repeat expansion detection and a PCR screening set. Am J Hum Genet 59:912-917.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 912-917
-
-
Bowen, T.1
Guy, C.2
Speight, G.3
Jones, L.4
Cardno, A.5
Murphy, K.6
McGuffin, P.7
Owen, M.J.8
O'Donovan, M.C.9
-
3
-
-
0034082294
-
Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia
-
Bowen T, Guy CA, Cardno AG, Vincent JB, Kennedy JL, Jones LA, Gray M, Sanders RD, McCarthy G, Murphy KC, Owen MJ, O'Donovan MC. 2000. Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia. Psychiatr Genet 10:33-37.
-
(2000)
Psychiatr Genet
, vol.10
, pp. 33-37
-
-
Bowen, T.1
Guy, C.A.2
Cardno, A.G.3
Vincent, J.B.4
Kennedy, J.L.5
Jones, L.A.6
Gray, M.7
Sanders, R.D.8
McCarthy, G.9
Murphy, K.C.10
Owen, M.J.11
O'Donovan, M.C.12
-
4
-
-
0000818854
-
A novel, heritable, expanding CTG repeat in an intron of SEF2-1 localizes to human chromosome 18q21.1
-
Breschel T, McInnis MG, Margolis RL, Sirugo G, Corneliuseen B, Simpson SG, McMahon FJ, MacKinnon DF, Xu JF, Pleasant N, Huo Y, Ashworth RG, Grundstrom C, Grundstrom T, Kidd KK, DePaulo JR, Ross CA. 1997. A novel, heritable, expanding CTG repeat in an intron of SEF2-1 localizes to human chromosome 18q21.1. Hum Mol Genet 6:1855-1864.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1855-1864
-
-
Breschel, T.1
McInnis, M.G.2
Margolis, R.L.3
Sirugo, G.4
Corneliuseen, B.5
Simpson, S.G.6
McMahon, F.J.7
MacKinnon, D.F.8
Xu, J.F.9
Pleasant, N.10
Huo, Y.11
Ashworth, R.G.12
Grundstrom, C.13
Grundstrom, T.14
Kidd, K.K.15
DePaulo, J.R.16
Ross, C.A.17
-
5
-
-
0029737834
-
Autosomal dominant spastic paraplegia with anticipation maps to a 4-cm interval on chromosome 2p21-p24 in a large German family
-
Bürger J, Metzke H, Paternotte C, Schilling F, Hazan J, Reis A. 1996. Autosomal dominant spastic paraplegia with anticipation maps to a 4-cm interval on chromosome 2p21-p24 in a large German family. Hum Genet 98:371-375.
-
(1996)
Hum Genet
, vol.98
, pp. 371-375
-
-
Bürger, J.1
Metzke, H.2
Paternotte, C.3
Schilling, F.4
Hazan, J.5
Reis, A.6
-
6
-
-
6544269945
-
Isolation of a novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: A candidate for schizophrenia and bipolar disorder?
-
Chandy KG, Fantino E, Wittekindt O, Kalman K, Tong LL, Ho TH, Gutman GA, Crocq MA, Ganguli R, Nimgaonkar V, Morris-Rosendahl DJ, Gargus JJ. 1998. Isolation of a novel potassium channel gene hSKCa3 containing a polymorphic CAG repeat: A candidate for schizophrenia and bipolar disorder? Mol Psychiat 3:32-37.
-
(1998)
Mol Psychiat
, 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
Gutman, G.A.7
Crocq, M.A.8
Ganguli, R.9
Nimgaonkar, V.10
Morris-Rosendahl, D.J.11
Gargus, J.J.12
-
7
-
-
85047698264
-
European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder
-
Del Favero J, Gestel SV, Borglum AD, Muir W, Ewald H, Mors O, Ivezic S, Oruc L, Adolfsson R, Blackwood D, Kruse T, Mendlewicz J, Schalling M, Van Broeckhoven C. 2002. European combined analysis of the CTG18.1 and the ERDA1 CAG/CTG repeats in bipolar disorder. Eur J Hum Genet 10:276-280.
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 276-280
-
-
Del Favero, J.1
Gestel, S.V.2
Borglum, A.D.3
Muir, W.4
Ewald, H.5
Mors, O.6
Ivezic, S.7
Oruc, L.8
Adolfsson, R.9
Blackwood, D.10
Kruse, T.11
Mendlewicz, J.12
Schalling, M.13
Van Broeckhoven, C.14
-
8
-
-
0036239387
-
A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder
-
DeLisi LE, Shaw SH, Crow TJ, Shields G, Smith AB, Larach VW, Wellman N, Loftus J, Nanthakumar B, Razi K, Stewart J, Comazzi M, Vita A, Heffner T, Sherrington R. 2002. A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder. Am J Psychiatry 159:803-812.
-
(2002)
Am J Psychiatry
, vol.159
, pp. 803-812
-
-
DeLisi, L.E.1
Shaw, S.H.2
Crow, T.J.3
Shields, G.4
Smith, A.B.5
Larach, V.W.6
Wellman, N.7
Loftus, J.8
Nanthakumar, B.9
Razi, K.10
Stewart, J.11
Comazzi, M.12
Vita, A.13
Heffner, T.14
Sherrington, R.15
-
9
-
-
0036699080
-
Hereditary spastic paraplegia
-
Fink JK. 2002. Hereditary spastic paraplegia. Neurol Clin 20:711-726.
-
(2002)
Neurol Clin
, vol.20
, pp. 711-726
-
-
Fink, J.K.1
-
10
-
-
0026345716
-
Variation of the CGG repeat at the Fragile X site results in genetic instability: Resolution of the Sherman paradox
-
Fu Y-H, Kuhl DPA, Pizzuti A, Pieretti M, Sutcliffe JS, Richards S, Verkerk AJMH, Holden JJA, Fenmwick RG, Warren ST, Nelson DL, Caskey CT. 1991. Variation of the CGG repeat at the Fragile X site results in genetic instability: Resolution of the Sherman paradox. Cell 67:1047-1058.
-
(1991)
Cell
, vol.67
, pp. 1047-1058
-
-
Fu, Y.-H.1
Kuhl, D.P.A.2
Pizzuti, A.3
Pieretti, M.4
Sutcliffe, J.S.5
Richards, S.6
Verkerk, A.J.M.H.7
Holden, J.J.A.8
Fenmwick, R.G.9
Warren, S.T.10
Nelson, D.L.11
Caskey, C.T.12
-
11
-
-
0035504265
-
Trinucleotide repeat expansions: Do they contribute to bipolar disorder?
-
Goossens D, Del Favero J, Van Broeckhoven C. 2001. Trinucleotide repeat expansions: Do they contribute to bipolar disorder? Brain Res Bull 56:243-257.
-
(2001)
Brain Res Bull
, vol.56
, pp. 243-257
-
-
Goossens, D.1
Del Favero, J.2
Van Broeckhoven, C.3
-
12
-
-
0032887046
-
CTG18.1 and ERDA-1 CAG/CTG repeat size in bipolar disorder
-
Guy CA, Bowen T, Jones I, McCandless F, Owen MJ, Craddock N, O'Donovan MC. 1999. CTG18.1 and ERDA-1 CAG/CTG repeat size in bipolar disorder. Neurobiol Dis 6:302-307.
-
(1999)
Neurobiol Dis
, vol.6
, pp. 302-307
-
-
Guy, C.A.1
Bowen, T.2
Jones, I.3
McCandless, F.4
Owen, M.J.5
Craddock, N.6
O'Donovan, M.C.7
-
13
-
-
0032727249
-
Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12
-
Holmes SE, O'Hearn EE, McInnis MG, Gorelick-Feldman DA, Kleiderlein JJ, Callahan C, Kwak NG, Ingersoll-Ashworth RG, Sherr M, Sumner AJ, Sharp AH, Ananth U, Seltzer WK, Boss MA, Vieria-Saecker AM, Epplen JT, Riess O, Ross CA, Margolis RL. 1999. Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12. Nat Genet 23:391-392.
-
(1999)
Nat Genet
, vol.23
, pp. 391-392
-
-
Holmes, S.E.1
O'Hearn, E.E.2
McInnis, M.G.3
Gorelick-Feldman, D.A.4
Kleiderlein, J.J.5
Callahan, C.6
Kwak, N.G.7
Ingersoll-Ashworth, R.G.8
Sherr, M.9
Sumner, A.J.10
Sharp, A.H.11
Ananth, U.12
Seltzer, W.K.13
Boss, M.A.14
Vieria-Saecker, A.M.15
Epplen, J.T.16
Riess, O.17
Ross, C.A.18
Margolis, R.L.19
-
14
-
-
18344379670
-
A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2
-
Holmes SE, O'Hearn E, Rosenblatt A, Callahan C, Hwang HS, Ingersoll-Ashworth RG, Fleisher A, Stevanin G, Brice A, Potter NT, Ross CA, Margolis RL. 2001. A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2. Nat Genet 29:377-378.
-
(2001)
Nat Genet
, vol.29
, pp. 377-378
-
-
Holmes, S.E.1
O'Hearn, E.2
Rosenblatt, A.3
Callahan, C.4
Hwang, H.S.5
Ingersoll-Ashworth, R.G.6
Fleisher, A.7
Stevanin, G.8
Brice, A.9
Potter, N.T.10
Ross, C.A.11
Margolis, R.L.12
-
15
-
-
17644447664
-
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17
-
Ikeuchi T, Sanpei K, Takano H, Sasaki H, Tashiro K, Cancel G, Brice A, Bird TD, Schellenberg GD, Pericak-Vance MA, Welsh-Bohmer KA, Clark LN, Wilhelmsen K, Tsuji S. 1998. A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17. Genomics 49:321-326.
-
(1998)
Genomics
, vol.49
, pp. 321-326
-
-
Ikeuchi, T.1
Sanpei, K.2
Takano, H.3
Sasaki, H.4
Tashiro, K.5
Cancel, G.6
Brice, A.7
Bird, T.D.8
Schellenberg, G.D.9
Pericak-Vance, M.A.10
Welsh-Bohmer, K.A.11
Clark, L.N.12
Wilhelmsen, K.13
Tsuji, S.14
-
16
-
-
0031415105
-
No evidence for expanded polyglutamine sequences in bipolar disorder and schizophrenia
-
Jones AL, Middle F, Guy C, Spurlock G, Cairns NJ, McGuffin P, Craddock N, Owen M, O'Donovan MC. 1997. No evidence for expanded polyglutamine sequences in bipolar disorder and schizophrenia. Mol Psychiatry 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
Craddock, N.7
Owen, M.8
O'Donovan, M.C.9
-
18
-
-
0031984597
-
Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA
-
Koob MD, Benzow KA, Bird TD, Day JW, Moseley ML, Ranum LP. 1998. Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA. Nat Genet 18:72-75.
-
(1998)
Nat Genet
, vol.18
, pp. 72-75
-
-
Koob, M.D.1
Benzow, K.A.2
Bird, T.D.3
Day, J.W.4
Moseley, M.L.5
Ranum, L.P.6
-
19
-
-
0032900772
-
An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)
-
Koob MD, Moseley ML, Schut LJ, Benzow KA, Bird TD, Day JW, Ranum LPW. 1999. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8). Nat Genet 21:379-384.
-
(1999)
Nat Genet
, vol.21
, pp. 379-384
-
-
Koob, M.D.1
Moseley, M.L.2
Schut, L.J.3
Benzow, K.A.4
Bird, T.D.5
Day, J.W.6
Ranum, L.P.W.7
-
20
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH. 1991. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 352:77-79.
-
(1991)
Nature
, vol.352
, pp. 77-79
-
-
La Spada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
21
-
-
0031712686
-
Two commonly expanded CAG/CTG repeat loci: Involvement in affective disorders?
-
Lindblad K, Nylander PO, Zander C, Yuan QP, Stahle L, Engstrom C, Balciuniene J, Pettersson U, Breschel T, McInnis M, Ross CA, Adolfsson R, Schalling M. 1998. Two commonly expanded CAG/CTG repeat loci: Involvement in affective disorders? Mol Psychiatry 3:405-410.
-
(1998)
Mol Psychiatry
, vol.3
, pp. 405-410
-
-
Lindblad, K.1
Nylander, P.O.2
Zander, C.3
Yuan, Q.P.4
Stahle, L.5
Engstrom, C.6
Balciuniene, J.7
Pettersson, U.8
Breschel, T.9
McInnis, M.10
Ross, C.A.11
Adolfsson, R.12
Schalling, M.13
-
22
-
-
0035800434
-
Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9
-
Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LP. 2001. Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9. Science 293:864-867.
-
(2001)
Science
, vol.293
, pp. 864-867
-
-
Liquori, C.L.1
Ricker, K.2
Moseley, M.L.3
Jacobsen, J.F.4
Kress, W.5
Naylor, S.L.6
Day, J.W.7
Ranum, L.P.8
-
23
-
-
0026603841
-
Myotonic dystrophy mutation: An unstable CTG repeat in the 3′ untranslated region of the gene
-
Mahadevan M, Tsilfidis C, Sabourin L, Shutler G, Amemiya C, Jonsen G, Neville C, Narang M, Barcel J, O'Hoy K, Leblond S, Earle-MacDonald J, De Jong PJ, Wieringa B, Korneluk RG. 1992. Myotonic dystrophy mutation: An unstable CTG repeat in the 3′ untranslated region of the gene. Science 255:1253-1255.
-
(1992)
Science
, vol.255
, pp. 1253-1255
-
-
Mahadevan, M.1
Tsilfidis, C.2
Sabourin, L.3
Shutler, G.4
Amemiya, C.5
Jonsen, G.6
Neville, C.7
Narang, M.8
Barcel, J.9
O'Hoy, K.10
Leblond, S.11
Earle-MacDonald, J.12
De Jong, P.J.13
Wieringa, B.14
Korneluk, R.G.15
-
24
-
-
0012473701
-
Detection of unstable trinucleotide repeat loci: Genome and cDNA screening
-
Wells RD, Warren ST, editors. San Diego: Academic Press, Inc
-
Margolis RL, Ross CA. 1998. Detection of unstable trinucleotide repeat loci: Genome and cDNA screening. In: Wells RD, Warren ST, editors. Genetic instabilities and hereditary neurological diseases. San Diego: Academic Press, Inc.
-
(1998)
Genetic Instabilities and Hereditary Neurological Diseases
-
-
Margolis, R.L.1
Ross, C.A.2
-
25
-
-
0029878412
-
cDNA cloning of a human homologue of the C. elegans cell fate-determining gene mab-21: Expression, chromosomal localization, and analysis of a highly polymorphic (CAG)n trinucleotide repeat
-
Margolis RL, Stine OC, McInnis MG, Ranen NG, Rubinsztein DC, Leggo J, Jones Brando LV, Kidwai AS, Loev SJ, Breschel TS, Callahan C, Simpson SG, DePaulo JR, McMahon FJ, Jain S, Paykel ES, Walsh C, DeLisi LE, Crow TJ, Torrey EF, Ashworth RG, Macke JP, Nathans J, Ross CA. 1996. cDNA cloning of a human homologue of the C. elegans cell fate-determining gene mab-21: Expression, chromosomal localization, and analysis of a highly polymorphic (CAG)n trinucleotide repeat. Hum Mol Genet 5:607-616.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 607-616
-
-
Margolis, R.L.1
Stine, O.C.2
McInnis, M.G.3
Ranen, N.G.4
Rubinsztein, D.C.5
Leggo, J.6
Jones Brando, L.V.7
Kidwai, A.S.8
Loev, S.J.9
Breschel, T.S.10
Callahan, C.11
Simpson, S.G.12
DePaulo, J.R.13
McMahon, F.J.14
Jain, S.15
Paykel, E.S.16
Walsh, C.17
DeLisi, L.E.18
Crow, T.J.19
Torrey, E.F.20
Ashworth, R.G.21
Macke, J.P.22
Nathans, J.23
Ross, C.A.24
more..
-
26
-
-
0030840917
-
cDNAs with long CAG trinucleotide repeats from human brain
-
Margolis RL, Abraham MA, Gatchell SB, Li S-H, Kidwai AS, Breschel TS, Stine OC, Callahan C, McInnis MG, Ross CA. 1997. cDNAs with long CAG trinucleotide repeats from human brain. Hum Genet 100:114-122.
-
(1997)
Hum Genet
, vol.100
, pp. 114-122
-
-
Margolis, R.L.1
Abraham, M.A.2
Gatchell, S.B.3
Li, S.-H.4
Kidwai, A.S.5
Breschel, T.S.6
Stine, O.C.7
Callahan, C.8
McInnis, M.G.9
Ross, C.A.10
-
28
-
-
0033771685
-
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
-
Matsuura T, Yamagata T, Burgess DL, Rasmussen A, Grewal RP, Watase K, Khajavi M, McCall AE, Davis CF, Zu L, Achari M, Pulst SM, Alonso E, Noebels JL, Nelson DL, Zoghbi HY, Ashizawa T. 2000. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nat Genet 26:191-194.
-
(2000)
Nat Genet
, vol.26
, pp. 191-194
-
-
Matsuura, T.1
Yamagata, T.2
Burgess, D.L.3
Rasmussen, A.4
Grewal, R.P.5
Watase, K.6
Khajavi, M.7
McCall, A.E.8
Davis, C.F.9
Zu, L.10
Achari, M.11
Pulst, S.M.12
Alonso, E.13
Noebels, J.L.14
Nelson, D.L.15
Zoghbi, H.Y.16
Ashizawa, T.17
-
29
-
-
0032969384
-
Family-based association analysis of the hSKCa3 potassium channel gene in bipolar disorder
-
McInnis MG, Breschel TS, Margolis RL, Chellis J, MacKinnon DF, McMahon FJ, Simpson SG, Lan TH, Chen H, Ross CA, DePaulo JR. 1999. Family-based association analysis of the hSKCa3 potassium channel gene in bipolar disorder. Mol Psychiatry 4:217-219.
-
(1999)
Mol Psychiatry
, vol.4
, pp. 217-219
-
-
McInnis, M.G.1
Breschel, T.S.2
Margolis, R.L.3
Chellis, J.4
MacKinnon, D.F.5
McMahon, F.J.6
Simpson, S.G.7
Lan, T.H.8
Chen, H.9
Ross, C.A.10
DePaulo, J.R.11
-
30
-
-
0033949096
-
Allelic distribution of CTG18.1 in Caucasian populations: Association studies in bipolar disorder, schizophrenia, and ataxia
-
McInnis MG, Swift-Scanlanl T, Mahoney AT, Vincent J, Verheyen G, Lan TH, Oruc L, Riess O, Broeckhoven CV, Chen H, Kennedy JL, MacKinnon DF, Margolis RL, Simpson SG, McMahon FJ, Gershon E, Jr., Reich T, DePaulo JR, Ross CA. 2000. Allelic distribution of CTG18.1 in Caucasian populations: Association studies in bipolar disorder, schizophrenia, and ataxia. Mol Psychiatry 5:439-442.
-
(2000)
Mol Psychiatry
, vol.5
, pp. 439-442
-
-
McInnis, M.G.1
Swift-Scanlanl, T.2
Mahoney, A.T.3
Vincent, J.4
Verheyen, G.5
Lan, T.H.6
Oruc, L.7
Riess, O.8
Broeckhoven, C.V.9
Chen, H.10
Kennedy, J.L.11
MacKinnon, D.F.12
Margolis, R.L.13
Simpson, S.G.14
McMahon, F.J.15
Gershon Jr., E.16
Reich, T.17
DePaulo, J.R.18
Ross, C.A.19
-
31
-
-
0034880799
-
Association and linkage studies between bipolar affective disorder and the polymorphic CAG/CTG repeat loci ERDA1, SEF2-1B, MAB21L and KCNN3
-
Meira-Lima IV, Zhao J, Sham P, Pereira AC, Krieger JE, Vallada H. 2001. Association and linkage studies between bipolar affective disorder and the polymorphic CAG/CTG repeat loci ERDA1, SEF2-1B, MAB21L and KCNN3. Mol Psychiatry 6:565-569.
-
(2001)
Mol Psychiatry
, vol.6
, pp. 565-569
-
-
Meira-Lima, I.V.1
Zhao, J.2
Sham, P.3
Pereira, A.C.4
Krieger, J.E.5
Vallada, H.6
-
32
-
-
0031439034
-
A CAG/CTG expansion in the normal population
-
Nakamoto M, Takebayashi H, Kawaguchi Y, Narumiya S, Taniwaki M, Nakamura Y, Ishikawa Y, Akiguchi I, Kimura J, Kakizuka A. 1997. A CAG/CTG expansion in the normal population. Nat Genet 17:385-386.
-
(1997)
Nat Genet
, vol.17
, pp. 385-386
-
-
Nakamoto, M.1
Takebayashi, H.2
Kawaguchi, Y.3
Narumiya, S.4
Taniwaki, M.5
Nakamura, Y.6
Ishikawa, Y.7
Akiguchi, I.8
Kimura, J.9
Kakizuka, A.10
-
33
-
-
0027164698
-
Expansion of a trinucleotide CAG repeat in spinocerebellar ataxia type 1
-
Orr HT, Chung MY, Banfi S, Kwiatkowski TJ, Jr., Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LP, Zoghbi HY. 1993. Expansion of a trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet 4:221-226.
-
(1993)
Nat Genet
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.Y.2
Banfi, S.3
Kwiatkowski Jr., T.J.4
Servadio, A.5
Beaudet, A.L.6
McCall, A.E.7
Duvick, L.A.8
Ranum, L.P.9
Zoghbi, H.Y.10
-
34
-
-
0027300219
-
Genes with triplet repeats: Candidate mediators of neuropsychiatric disorders
-
Ross CA, McInnis MG, Margolis RL, Li S-H. 1993. Genes with triplet repeats: Candidate mediators of neuropsychiatric disorders. Trend Neurosci 16:254-260.
-
(1993)
Trend Neurosci
, vol.16
, pp. 254-260
-
-
Ross, C.A.1
McInnis, M.G.2
Margolis, R.L.3
Li, S.-H.4
-
35
-
-
0027256423
-
Direct detection of novel expanded trinucleotide repeats in the human genome
-
Schalling M, Hudson TJ, Buetow KW, Housman DE. 1993. Direct detection of novel expanded trinucleotide repeats in the human genome. Nat Genet 4:135-139.
-
(1993)
Nat Genet
, vol.4
, pp. 135-139
-
-
Schalling, M.1
Hudson, T.J.2
Buetow, K.W.3
Housman, D.E.4
-
37
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's Disease chromosomes
-
The Huntington's Disease Collaborative Research group. 1993. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's Disease chromosomes. Cell 72:971-983.
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
38
-
-
0033046558
-
Analysis of genome-wide CAG/CTG repeats, and at SEF2-1B and ERDA1 in schizophrenia and bipolar affective disorder
-
Vincent JB, Petronis A, Strong E, Parikh SV, Meltzer HY, Lieberman J, Kennedy JL. 1999. Analysis of genome-wide CAG/CTG repeats, and at SEF2-1B and ERDA1 in schizophrenia and bipolar affective disorder. Mol Psychiatry 4:229-234.
-
(1999)
Mol Psychiatry
, vol.4
, pp. 229-234
-
-
Vincent, J.B.1
Petronis, A.2
Strong, E.3
Parikh, S.V.4
Meltzer, H.Y.5
Lieberman, J.6
Kennedy, J.L.7
-
39
-
-
0033939994
-
An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: A common expansion locus
-
Vincent JB, Neves-Pereira ML, Paterson AD, Yamamoto E, Parikh SV, Macciardi F, Gurling HM, Potkin SG, Pato CN, Macedo A, Kovacs M, Davies M, Lieberman JA, Meltzer HY, Petronis A, Kennedy JL. 2000a. An unstable trinucleotide-repeat region on chromosome 13 implicated in spinocerebellar ataxia: A common expansion locus. Am J Hum Genet 66:819-829.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 819-829
-
-
Vincent, J.B.1
Neves-Pereira, M.L.2
Paterson, A.D.3
Yamamoto, E.4
Parikh, S.V.5
Macciardi, F.6
Gurling, H.M.7
Potkin, S.G.8
Pato, C.N.9
Macedo, A.10
Kovacs, M.11
Davies, M.12
Lieberman, J.A.13
Meltzer, H.Y.14
Petronis, A.15
Kennedy, J.L.16
-
40
-
-
0034606271
-
Long repeat tracts at SCA8 in major psychosis
-
Vincent JB, Yuan QP, Schalling M, Adolfsson R, Azevedo MH, Macedo A, Bauer A, DallaTorre C, Medeiros HM, Pato MT, Pato CN, Bowen T, Guy CA, Owen MJ, O'Donovan MC, Paterson AD, Petronis A, Kennedy JL. 2000b. Long repeat tracts at SCA8 in major psychosis. Am J Med Genet 96:873-876.
-
(2000)
Am J Med Genet
, vol.96
, pp. 873-876
-
-
Vincent, J.B.1
Yuan, Q.P.2
Schalling, M.3
Adolfsson, R.4
Azevedo, M.H.5
Macedo, A.6
Bauer, A.7
DallaTorre, C.8
Medeiros, H.M.9
Pato, M.T.10
Pato, C.N.11
Bowen, T.12
Guy, C.A.13
Owen, M.J.14
O'Donovan, M.C.15
Paterson, A.D.16
Petronis, A.17
Kennedy, J.L.18
-
41
-
-
0031012399
-
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
-
Zhuchenko O, Bailey J, Bonnen P, Ashizawa T, Stockton DW, Amos C, Dobyns WB, Subramony SH, Zoghbi HY, Lee CC. 1997. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. Nat Genet 15:62-69.
-
(1997)
Nat Genet
, vol.15
, pp. 62-69
-
-
Zhuchenko, O.1
Bailey, J.2
Bonnen, P.3
Ashizawa, T.4
Stockton, D.W.5
Amos, C.6
Dobyns, W.B.7
Subramony, S.H.8
Zoghbi, H.Y.9
Lee, C.C.10
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