-
1
-
-
51349141278
-
A genome screen for quantitative trait loci influencing schizophrenia and neurocognitive phenotypes
-
Almasy L., Gur R.C., Haack K., Cole S.A., Calkins M.E., Peralta J.M., Hare E., Prasad K., Pogue-Geile M.F., Nimgaonkar V., et al. A genome screen for quantitative trait loci influencing schizophrenia and neurocognitive phenotypes. Am. J. Psychiatry 165 9 (2008) 1185-1192
-
(2008)
Am. J. Psychiatry
, vol.165
, Issue.9
, pp. 1185-1192
-
-
Almasy, L.1
Gur, R.C.2
Haack, K.3
Cole, S.A.4
Calkins, M.E.5
Peralta, J.M.6
Hare, E.7
Prasad, K.8
Pogue-Geile, M.F.9
Nimgaonkar, V.10
-
3
-
-
13444269543
-
Haploview: analysis and visualization of LD and haplotype maps
-
Barrett J.C., Fry B., Maller J., and Daly M.J. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21 2 (2005) 263-265
-
(2005)
Bioinformatics
, vol.21
, Issue.2
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
4
-
-
0041836207
-
Delusions and hallucinations in Alzheimer's disease: review of the brain decade
-
Bassiony M.M., and Lyketsos C.G. Delusions and hallucinations in Alzheimer's disease: review of the brain decade. Psychosomatics 44 5 (2003) 388-401
-
(2003)
Psychosomatics
, vol.44
, Issue.5
, pp. 388-401
-
-
Bassiony, M.M.1
Lyketsos, C.G.2
-
5
-
-
33750128290
-
Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome
-
Bittel D.C., Kibiryeva N., and Butler M.G. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome. Pediatrics 118 4 (2006) e1276-e1283
-
(2006)
Pediatrics
, vol.118
, Issue.4
-
-
Bittel, D.C.1
Kibiryeva, N.2
Butler, M.G.3
-
6
-
-
25144520082
-
Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression
-
Bray N.J., Preece A., Williams N.M., Moskvina V., Buckland P.R., Owen M.J., and O'Donovan M.C. Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression. Hum. Mol. Genet. 14 14 (2005) 1947-1954
-
(2005)
Hum. Mol. Genet.
, vol.14
, Issue.14
, pp. 1947-1954
-
-
Bray, N.J.1
Preece, A.2
Williams, N.M.3
Moskvina, V.4
Buckland, P.R.5
Owen, M.J.6
O'Donovan, M.C.7
-
7
-
-
0025099787
-
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
-
Call K.M., Glaser T., Ito C.Y., Buckler A.J., Pelletier J., Haber D.A., Rose E.A., Kral A., Yeger H., Lewis W.H., et al. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell 60 3 (1990) 509-520
-
(1990)
Cell
, vol.60
, Issue.3
, pp. 509-520
-
-
Call, K.M.1
Glaser, T.2
Ito, C.Y.3
Buckler, A.J.4
Pelletier, J.5
Haber, D.A.6
Rose, E.A.7
Kral, A.8
Yeger, H.9
Lewis, W.H.10
-
8
-
-
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., Verchinski B.A., Meyer-Lindenberg A., Balkissoon R., Kolachana B., et al. Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia. Proc. Natl. Acad. Sci. U. S. A. 102 24 (2005) 8627-8632
-
(2005)
Proc. Natl. Acad. Sci. U. S. A.
, vol.102
, Issue.24
, 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
Verchinski, B.A.7
Meyer-Lindenberg, A.8
Balkissoon, R.9
Kolachana, B.10
-
9
-
-
0031793104
-
Regional gray matter, white matter, and cerebrospinal fluid distributions in schizophrenic patients, their siblings, and controls
-
Cannon T.D., van Erp T.G., Huttunen M., Lonnqvist J., Salonen O., Valanne L., Poutanen V.P., Standertskjold-Nordenstam C.G., Gur R.E., and Yan M. Regional gray matter, white matter, and cerebrospinal fluid distributions in schizophrenic patients, their siblings, and controls. Arch. Gen. Psychiatry 55 12 (1998) 1084-1091
-
(1998)
Arch. Gen. Psychiatry
, vol.55
, Issue.12
, pp. 1084-1091
-
-
Cannon, T.D.1
van Erp, T.G.2
Huttunen, M.3
Lonnqvist, J.4
Salonen, O.5
Valanne, L.6
Poutanen, V.P.7
Standertskjold-Nordenstam, C.G.8
Gur, R.E.9
Yan, M.10
-
10
-
-
0034060459
-
Twin studies of schizophrenia: from bow-and-arrow concordances to star wars Mx and functional genomics
-
Cardno A.G., and Gottesman II. Twin studies of schizophrenia: from bow-and-arrow concordances to star wars Mx and functional genomics. Am. J. Med. Genet. 97 1 (2000) 12-17
-
(2000)
Am. J. Med. Genet.
, vol.97
, Issue.1
, pp. 12-17
-
-
Cardno, A.G.1
Gottesman II2
-
11
-
-
6044246071
-
Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families
-
Chen X., Wang X., O'Neill A.F., Walsh D., and Kendler K.S. Variants in the catechol-o-methyltransferase (COMT) gene are associated with schizophrenia in Irish high-density families. Mol. Psychiatry 9 10 (2004) 962-967
-
(2004)
Mol. Psychiatry
, vol.9
, Issue.10
, pp. 962-967
-
-
Chen, X.1
Wang, X.2
O'Neill, A.F.3
Walsh, D.4
Kendler, K.S.5
-
12
-
-
34247569983
-
Disrupted in schizophrenia 1 genotype and positive symptoms in schizophrenia
-
DeRosse P., Hodgkinson C.A., Lencz T., Burdick K.E., Kane J.M., Goldman D., and Malhotra A.K. Disrupted in schizophrenia 1 genotype and positive symptoms in schizophrenia. Biol. Psychiatry 61 10 (2007) 1208-1210
-
(2007)
Biol. Psychiatry
, vol.61
, Issue.10
, pp. 1208-1210
-
-
DeRosse, P.1
Hodgkinson, C.A.2
Lencz, T.3
Burdick, K.E.4
Kane, J.M.5
Goldman, D.6
Malhotra, A.K.7
-
13
-
-
41649094148
-
Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data
-
Dudbridge F. Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data. Hum. Hered. 66 2 (2008) 87-98
-
(2008)
Hum. Hered.
, vol.66
, Issue.2
, pp. 87-98
-
-
Dudbridge, F.1
-
14
-
-
0035878561
-
Chromosome 1 loci in Finnish schizophrenia families
-
Ekelund J., Hovatta I., Parker A., Paunio T., Varilo T., Martin R., Suhonen J., Ellonen P., Chan G., Sinsheimer J.S., et al. Chromosome 1 loci in Finnish schizophrenia families. Hum. Mol. Genet. 10 15 (2001) 1611-1617
-
(2001)
Hum. Mol. Genet.
, vol.10
, Issue.15
, pp. 1611-1617
-
-
Ekelund, J.1
Hovatta, I.2
Parker, A.3
Paunio, T.4
Varilo, T.5
Martin, R.6
Suhonen, J.7
Ellonen, P.8
Chan, G.9
Sinsheimer, J.S.10
-
15
-
-
8744231685
-
Replication of 1q42 linkage in Finnish schizophrenia pedigrees
-
Ekelund J., Hennah W., Hiekkalinna T., Parker A., Meyer J., Lonnqvist J., and Peltonen L. Replication of 1q42 linkage in Finnish schizophrenia pedigrees. Mol. Psychiatry 9 11 (2004) 1037-1041
-
(2004)
Mol. Psychiatry
, vol.9
, Issue.11
, pp. 1037-1041
-
-
Ekelund, J.1
Hennah, W.2
Hiekkalinna, T.3
Parker, A.4
Meyer, J.5
Lonnqvist, J.6
Peltonen, L.7
-
16
-
-
0142244688
-
Schizophrenia
-
Freedman R. Schizophrenia. N. Engl. J. Med. 349 18 (2003) 1738-1749
-
(2003)
N. Engl. J. Med.
, vol.349
, Issue.18
, pp. 1738-1749
-
-
Freedman, R.1
-
17
-
-
18444369013
-
The structure of haplotype blocks in the human genome
-
Gabriel S.B., Schaffner S.F., Nguyen H., Moore J.M., Roy J., Blumenstiel B., Higgins J., DeFelice M., Lochner A., Faggart M., et al. The structure of haplotype blocks in the human genome. Science 296 5576 (2002) 2225-2229
-
(2002)
Science
, vol.296
, Issue.5576
, pp. 2225-2229
-
-
Gabriel, S.B.1
Schaffner, S.F.2
Nguyen, H.3
Moore, J.M.4
Roy, J.5
Blumenstiel, B.6
Higgins, J.7
DeFelice, M.8
Lochner, A.9
Faggart, M.10
-
18
-
-
33645986682
-
Schizophrenia susceptibility genes: emergence of positional candidates and future directions
-
Gogos J.A., and Gerber D.J. Schizophrenia susceptibility genes: emergence of positional candidates and future directions. Trends Pharmacol. Sci. 27 4 (2006) 226-233
-
(2006)
Trends Pharmacol. Sci.
, vol.27
, Issue.4
, pp. 226-233
-
-
Gogos, J.A.1
Gerber, D.J.2
-
19
-
-
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., Parker A., Martin R., Levitzky S., Partonen T., et al. Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects. Hum. Mol. Genet. 12 23 (2003) 3151-3159
-
(2003)
Hum. Mol. Genet.
, vol.12
, Issue.23
, pp. 3151-3159
-
-
Hennah, W.1
Varilo, T.2
Kestila, M.3
Paunio, T.4
Arajarvi, R.5
Haukka, J.6
Parker, A.7
Martin, R.8
Levitzky, S.9
Partonen, T.10
-
20
-
-
6344255274
-
Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder
-
Hodgkinson C.A., Goldman D., Jaeger J., Persaud S., Kane J.M., Lipsky R.H., and Malhotra A.K. Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder. Am. J. Hum. Genet. 75 5 (2004) 862-872
-
(2004)
Am. J. Hum. Genet.
, vol.75
, Issue.5
, pp. 862-872
-
-
Hodgkinson, C.A.1
Goldman, D.2
Jaeger, J.3
Persaud, S.4
Kane, J.M.5
Lipsky, R.H.6
Malhotra, A.K.7
-
21
-
-
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., Arajarvi R., Juvonen H., Kokko-Sahin M.L., Vaisanen L., Mannila H., et al. A genomewide screen for schizophrenia genes in an isolated Finnish subpopulation, suggesting multiple susceptibility loci. Am. J. Hum. Genet. 65 4 (1999) 1114-1124
-
(1999)
Am. J. Hum. Genet.
, vol.65
, Issue.4
, pp. 1114-1124
-
-
Hovatta, I.1
Varilo, T.2
Suvisaari, J.3
Terwilliger, J.D.4
Ollikainen, V.5
Arajarvi, R.6
Juvonen, H.7
Kokko-Sahin, M.L.8
Vaisanen, L.9
Mannila, H.10
-
22
-
-
0037953124
-
Linkage of schizophrenia with chromosome 1q loci in Taiwanese families
-
Hwu H.G., Liu C.M., Fann C.S., Ou-Yang W.C., and Lee S.F. Linkage of schizophrenia with chromosome 1q loci in Taiwanese families. Mol. Psychiatry 8 4 (2003) 445-452
-
(2003)
Mol. Psychiatry
, vol.8
, Issue.4
, pp. 445-452
-
-
Hwu, H.G.1
Liu, C.M.2
Fann, C.S.3
Ou-Yang, W.C.4
Lee, S.F.5
-
23
-
-
4444352846
-
Genetic and expression analyses of FZD3 in schizophrenia
-
Ide M., Muratake T., Yamada K., Iwayama-Shigeno Y., Iwamoto K., Takao H., Toyota T., Kaneko N., Minabe Y., Nakamura K., et al. Genetic and expression analyses of FZD3 in schizophrenia. Biol. Psychiatry 56 6 (2004) 462-465
-
(2004)
Biol. Psychiatry
, vol.56
, Issue.6
, pp. 462-465
-
-
Ide, M.1
Muratake, T.2
Yamada, K.3
Iwayama-Shigeno, Y.4
Iwamoto, K.5
Takao, H.6
Toyota, T.7
Kaneko, N.8
Minabe, Y.9
Nakamura, K.10
-
24
-
-
0019504748
-
Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21
-
Jacobs P.A., Hunt P.A., Mayer M., and Bart R.D. Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21. Am. J. Hum. Genet. 33 4 (1981) 513-518
-
(1981)
Am. J. Hum. Genet.
, vol.33
, Issue.4
, pp. 513-518
-
-
Jacobs, P.A.1
Hunt, P.A.2
Mayer, M.3
Bart, R.D.4
-
25
-
-
0023858453
-
Reliability and validity of the positive and negative syndrome scale for schizophrenics
-
Kay S.R., Opler L.A., and Lindenmayer J.P. Reliability and validity of the positive and negative syndrome scale for schizophrenics. Psychiatry Res. 23 1 (1988) 99-110
-
(1988)
Psychiatry Res.
, vol.23
, Issue.1
, pp. 99-110
-
-
Kay, S.R.1
Opler, L.A.2
Lindenmayer, J.P.3
-
26
-
-
62949108820
-
-
Kirov, G., Zaharieva, I., Georgieva, L., Moskvina, V., Nikolov, I., Cichon, S., Hillmer, A., Toncheva, D., Owen, M.J., O'Donovan, M.C., in press. A genome-wide association study in 574 schizophrenia trios using DNA pooling. Mol. Psychiatry (Mar 11: 1-8 (Electronic Publication)).
-
Kirov, G., Zaharieva, I., Georgieva, L., Moskvina, V., Nikolov, I., Cichon, S., Hillmer, A., Toncheva, D., Owen, M.J., O'Donovan, M.C., in press. A genome-wide association study in 574 schizophrenia trios using DNA pooling. Mol. Psychiatry (Mar 11: 1-8 (Electronic Publication)).
-
-
-
-
27
-
-
33846589304
-
Disease-associated intronic variants in the ErbB4 gene are related to altered ErbB4 splice-variant expression in the brain in schizophrenia
-
Law A.J., Kleinman J.E., Weinberger D.R., and Weickert C.S. Disease-associated intronic variants in the ErbB4 gene are related to altered ErbB4 splice-variant expression in the brain in schizophrenia. Hum. Mol. Genet. 16 2 (2007) 129-141
-
(2007)
Hum. Mol. Genet.
, vol.16
, Issue.2
, pp. 129-141
-
-
Law, A.J.1
Kleinman, J.E.2
Weinberger, D.R.3
Weickert, C.S.4
-
28
-
-
0023106062
-
Human retinoblastoma susceptibility gene: cloning, identification, and sequence
-
Lee W.H., Bookstein R., Hong F., Young L.J., Shew J.Y., and Lee E.Y. Human retinoblastoma susceptibility gene: cloning, identification, and sequence. Science 235 4794 (1987) 1394-1399
-
(1987)
Science
, vol.235
, Issue.4794
, pp. 1394-1399
-
-
Lee, W.H.1
Bookstein, R.2
Hong, F.3
Young, L.J.4
Shew, J.Y.5
Lee, E.Y.6
-
29
-
-
0037155219
-
Presenilin-dependent gamma-secretase-like intramembrane cleavage of ErbB4
-
Lee H.J., Jung K.M., Huang Y.Z., Bennett L.B., Lee J.S., Mei L., and Kim T.W. Presenilin-dependent gamma-secretase-like intramembrane cleavage of ErbB4. J. Biol. Chem. 277 8 (2002) 6318-6323
-
(2002)
J. Biol. Chem.
, vol.277
, Issue.8
, pp. 6318-6323
-
-
Lee, H.J.1
Jung, K.M.2
Huang, Y.Z.3
Bennett, L.B.4
Lee, J.S.5
Mei, L.6
Kim, T.W.7
-
30
-
-
34249332776
-
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia
-
Lencz T., Morgan T.V., Athanasiou M., Dain B., Reed C.R., Kane J.M., Kucherlapati R., and Malhotra A.K. Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia. Mol. Psychiatry 12 6 (2007) 572-580
-
(2007)
Mol. Psychiatry
, vol.12
, Issue.6
, pp. 572-580
-
-
Lencz, T.1
Morgan, T.V.2
Athanasiou, M.3
Dain, B.4
Reed, C.R.5
Kane, J.M.6
Kucherlapati, R.7
Malhotra, A.K.8
-
31
-
-
0029087026
-
Candidate gene for the chromosome 1 familial Alzheimer's disease locus
-
Levy-Lahad E., Wasco W., Poorkaj P., Romano D.M., Oshima J., Pettingell W.H., Yu C.E., Jondro P.D., Schmidt S.D., Wang K., et al. Candidate gene for the chromosome 1 familial Alzheimer's disease locus. Science 269 5226 (1995) 973-977
-
(1995)
Science
, vol.269
, Issue.5226
, pp. 973-977
-
-
Levy-Lahad, E.1
Wasco, W.2
Poorkaj, P.3
Romano, D.M.4
Oshima, J.5
Pettingell, W.H.6
Yu, C.E.7
Jondro, P.D.8
Schmidt, S.D.9
Wang, K.10
-
32
-
-
0037168523
-
Genetic variation in the 22q11 locus and susceptibility to schizophrenia
-
Liu H., Abecasis G.R., Heath S.C., Knowles A., Demars S., Chen Y.J., Roos J.L., Rapoport J.L., Gogos J.A., and Karayiorgou M. Genetic variation in the 22q11 locus and susceptibility to schizophrenia. Proc. Natl. Acad. Sci. U. S. A. 99 26 (2002) 16859-16864
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, Issue.26
, pp. 16859-16864
-
-
Liu, H.1
Abecasis, G.R.2
Heath, S.C.3
Knowles, A.4
Demars, S.5
Chen, Y.J.6
Roos, J.L.7
Rapoport, J.L.8
Gogos, J.A.9
Karayiorgou, M.10
-
33
-
-
0842326677
-
Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia
-
Liu H., Heath S.C., Sobin C., Roos J.L., Galke B.L., Blundell M.L., Lenane M., Robertson B., Wijsman E.M., Rapoport J.L., 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. 99 6 (2002) 3717-3722
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, Issue.6
, pp. 3717-3722
-
-
Liu, H.1
Heath, S.C.2
Sobin, C.3
Roos, J.L.4
Galke, B.L.5
Blundell, M.L.6
Lenane, M.7
Robertson, B.8
Wijsman, E.M.9
Rapoport, J.L.10
-
34
-
-
33646229252
-
Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia
-
Mah S., Nelson M.R., Delisi L.E., Reneland R.H., Markward N., James M.R., Nyholt D.R., Hayward N., Handoko H., Mowry B., et al. Identification of the semaphorin receptor PLXNA2 as a candidate for susceptibility to schizophrenia. Mol. Psychiatry 11 5 (2006) 471-478
-
(2006)
Mol. Psychiatry
, vol.11
, Issue.5
, pp. 471-478
-
-
Mah, S.1
Nelson, M.R.2
Delisi, L.E.3
Reneland, R.H.4
Markward, N.5
James, M.R.6
Nyholt, D.R.7
Hayward, N.8
Handoko, H.9
Mowry, B.10
-
35
-
-
54249110309
-
Insight into neurocognitive dysfunction in Schizophrenia
-
Medalia A., and Thysen J. Insight into neurocognitive dysfunction in Schizophrenia. Schizophr. Bull. 34 6 (2008) 1221-1230
-
(2008)
Schizophr. Bull.
, vol.34
, Issue.6
, pp. 1221-1230
-
-
Medalia, A.1
Thysen, J.2
-
36
-
-
2942648152
-
Schizophrenia
-
Mueser K.T., and McGurk S.R. Schizophrenia. Lancet 363 9426 (2004) 2063-2072
-
(2004)
Lancet
, vol.363
, Issue.9426
, pp. 2063-2072
-
-
Mueser, K.T.1
McGurk, S.R.2
-
37
-
-
3042804077
-
Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia
-
Mukai J., Liu H., Burt R.A., Swor D.E., Lai W.S., Karayiorgou M., and Gogos J.A. Evidence that the gene encoding ZDHHC8 contributes to the risk of schizophrenia. Nat. Genet. 36 7 (2004) 725-731
-
(2004)
Nat. Genet.
, vol.36
, Issue.7
, pp. 725-731
-
-
Mukai, J.1
Liu, H.2
Burt, R.A.3
Swor, D.E.4
Lai, W.S.5
Karayiorgou, M.6
Gogos, J.A.7
-
38
-
-
0842329756
-
The molecular genetics of schizophrenia: new findings promise new insights
-
Owen M.J., Williams N.M., O, and ' Donovan M.C. The molecular genetics of schizophrenia: new findings promise new insights. Mol. Psychiatry 9 1 (2004) 14-27
-
(2004)
Mol. Psychiatry
, vol.9
, Issue.1
, pp. 14-27
-
-
Owen, M.J.1
Williams, N.M.2
O3
' Donovan, M.C.4
-
39
-
-
62949145896
-
-
Potkin, S.G., Turner, J.A., Fallon, J.A., Lakatos, A., Keator, D.B., Guffanti, G., Macciardi, F., in press. Gene discovery through imaging genetics: identification of two novel genes associated with schizophrenia. Mol. Psychiatry. (Dec 9: 1-13 (Electronic Publication)).
-
Potkin, S.G., Turner, J.A., Fallon, J.A., Lakatos, A., Keator, D.B., Guffanti, G., Macciardi, F., in press. Gene discovery through imaging genetics: identification of two novel genes associated with schizophrenia. Mol. Psychiatry. (Dec 9: 1-13 (Electronic Publication)).
-
-
-
-
40
-
-
0029101491
-
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
-
Rogaev E.I., Sherrington R., Rogaeva E.A., Levesque G., Ikeda M., Liang Y., Chi H., Lin C., Holman K., Tsuda T., et al. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Nature 376 6543 (1995) 775-778
-
(1995)
Nature
, vol.376
, Issue.6543
, pp. 775-778
-
-
Rogaev, E.I.1
Sherrington, R.2
Rogaeva, E.A.3
Levesque, G.4
Ikeda, M.5
Liang, Y.6
Chi, H.7
Lin, C.8
Holman, K.9
Tsuda, T.10
-
41
-
-
0031593685
-
Inhibition of presenilin 1 expression is promoted by p53 and p21WAF-1 and results in apoptosis and tumor suppression
-
Roperch J.P., Alvaro V., Prieur S., Tuynder M., Nemani M., Lethrosne F., Piouffre L., Gendron M.C., Israeli D., Dausset J., et al. Inhibition of presenilin 1 expression is promoted by p53 and p21WAF-1 and results in apoptosis and tumor suppression. Nat. Med. 4 7 (1998) 835-838
-
(1998)
Nat. Med.
, vol.4
, Issue.7
, pp. 835-838
-
-
Roperch, J.P.1
Alvaro, V.2
Prieur, S.3
Tuynder, M.4
Nemani, M.5
Lethrosne, F.6
Piouffre, L.7
Gendron, M.C.8
Israeli, D.9
Dausset, J.10
-
42
-
-
33749072714
-
Presenilin-dependent ErbB4 nuclear signaling regulates the timing of astrogenesis in the developing brain
-
Sardi S.P., Murtie J., Koirala S., Patten B.A., and Corfas G. Presenilin-dependent ErbB4 nuclear signaling regulates the timing of astrogenesis in the developing brain. Cell 127 1 (2006) 185-197
-
(2006)
Cell
, vol.127
, Issue.1
, pp. 185-197
-
-
Sardi, S.P.1
Murtie, J.2
Koirala, S.3
Patten, B.A.4
Corfas, G.5
-
43
-
-
40149105889
-
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women
-
Shifman S., Johanneson, nnesson M., Bronstein M., Chen S.X., Collier D.A., Craddock N.J., Kendler K.S., Li T., O'Donovan M., O'Neill F.A., et al. Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. PLoS Genet. 4 2 (2008) e28
-
(2008)
PLoS Genet.
, vol.4
, Issue.2
-
-
Shifman, S.1
Johanneson2
nnesson, M.3
Bronstein, M.4
Chen, S.X.5
Collier, D.A.6
Craddock, N.J.7
Kendler, K.S.8
Li, T.9
O'Donovan, M.10
O'Neill, F.A.11
-
44
-
-
0035911156
-
Presenilin 1 negatively regulates beta-catenin/T cell factor/lymphoid enhancer factor-1 signaling independently of beta-amyloid precursor protein and notch processing
-
Soriano S., Kang D.E., Fu M., Pestell R., Chevallier N., Zheng H., and Koo E.H. Presenilin 1 negatively regulates beta-catenin/T cell factor/lymphoid enhancer factor-1 signaling independently of beta-amyloid precursor protein and notch processing. J. Cell Biol. 152 4 (2001) 785-794
-
(2001)
J. Cell Biol.
, vol.152
, Issue.4
, pp. 785-794
-
-
Soriano, S.1
Kang, D.E.2
Fu, M.3
Pestell, R.4
Chevallier, N.5
Zheng, H.6
Koo, E.H.7
-
45
-
-
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., Gosden C., and Evans H.J. Association within a family of a balanced autosomal translocation with major mental illness. Lancet 336 8706 (1990) 13-16
-
(1990)
Lancet
, vol.336
, Issue.8706
, pp. 13-16
-
-
St Clair, D.1
Blackwood, D.2
Muir, W.3
Carothers, A.4
Walker, M.5
Spowart, G.6
Gosden, C.7
Evans, H.J.8
-
46
-
-
43949122950
-
Genomewide association for schizophrenia in the CATIE study: results of stage 1
-
Sullivan P.F., Lin D., Tzeng J.Y., van den Oord E., Perkins D., Stroup T.S., Wagner M., Lee S., Wright F.A., Zou F., et al. Genomewide association for schizophrenia in the CATIE study: results of stage 1. Mol. Psychiatry 13 6 (2008) 570-584
-
(2008)
Mol. Psychiatry
, vol.13
, Issue.6
, pp. 570-584
-
-
Sullivan, P.F.1
Lin, D.2
Tzeng, J.Y.3
van den Oord, E.4
Perkins, D.5
Stroup, T.S.6
Wagner, M.7
Lee, S.8
Wright, F.A.9
Zou, F.10
-
47
-
-
13144265717
-
Presenilin 1 associates with glycogen synthase kinase-3beta and its substrate tau
-
Takashima A., Murayama M., Murayama O., Kohno T., Honda T., Yasutake K., Nihonmatsu N., Mercken M., Yamaguchi H., Sugihara S., et al. Presenilin 1 associates with glycogen synthase kinase-3beta and its substrate tau. Proc. Natl. Acad. Sci. U. S. A. 95 16 (1998) 9637-9641
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, Issue.16
, pp. 9637-9641
-
-
Takashima, A.1
Murayama, M.2
Murayama, O.3
Kohno, T.4
Honda, T.5
Yasutake, K.6
Nihonmatsu, N.7
Mercken, M.8
Yamaguchi, H.9
Sugihara, S.10
-
48
-
-
4043052896
-
Identification of the role of presenilins beyond Alzheimer's disease.
-
Thinakaran G., and Parent A.T. Identification of the role of presenilins beyond Alzheimer's disease. Pharmacol. Res. 50 4 (2004) 411-418
-
(2004)
Pharmacol. Res.
, vol.50
, Issue.4
, pp. 411-418
-
-
Thinakaran, G.1
Parent, A.T.2
-
49
-
-
0025297599
-
Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients
-
Wallace M.R., Marchuk D.A., Andersen L.B., Letcher R., Odeh H.M., Saulino A.M., Fountain J.W., Brereton A., Nicholson J., Mitchell A.L., et al. Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients. Science 249 4965 (1990) 181-186
-
(1990)
Science
, vol.249
, Issue.4965
, pp. 181-186
-
-
Wallace, M.R.1
Marchuk, D.A.2
Andersen, L.B.3
Letcher, R.4
Odeh, H.M.5
Saulino, A.M.6
Fountain, J.W.7
Brereton, A.8
Nicholson, J.9
Mitchell, A.L.10
-
50
-
-
42349088634
-
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
-
Walsh T., McClellan J.M., McCarthy S.E., Addington A.M., Pierce S.B., Cooper G.M., Nord A.S., Kusenda M., Malhotra D., Bhandari A., et al. Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 320 5875 (2008) 539-543
-
(2008)
Science
, vol.320
, Issue.5875
, pp. 539-543
-
-
Walsh, T.1
McClellan, J.M.2
McCarthy, S.E.3
Addington, A.M.4
Pierce, S.B.5
Cooper, G.M.6
Nord, A.S.7
Kusenda, M.8
Malhotra, D.9
Bhandari, A.10
-
51
-
-
67149146923
-
Evidence of epistasis between the catechol-O-methyltransferase and aldehyde dehydrogenase 3B1 genes in paranoid schizophrenia
-
in press
-
Wang, Y., Hu, Y., Yue, F., Zhnag, K.R., Yang, H., Ma, J.T., Xu, Q., Shen, Y., in press. Evidence of epistasis between the catechol-O-methyltransferase and aldehyde dehydrogenase 3B1 genes in paranoid schizophrenia. Biol. Psychiatry.
-
Biol. Psychiatry
-
-
Wang, Y.1
Hu, Y.2
Yue, F.3
Zhnag, K.R.4
Yang, H.5
Ma, J.T.6
Xu, Q.7
Shen, Y.8
-
52
-
-
0034426026
-
The NOTCH4 locus is associated with susceptibility to schizophrenia
-
Wei J., and Hemmings G.P. The NOTCH4 locus is associated with susceptibility to schizophrenia. Nat. Genet. 25 4 (2000) 376-377
-
(2000)
Nat. Genet.
, vol.25
, Issue.4
, pp. 376-377
-
-
Wei, J.1
Hemmings, G.P.2
-
53
-
-
55349093318
-
A family- and population-based study of the UFD1L gene for schizophrenia
-
Xie L., Ye L., Ju G.Z., Xu Q., Zhang X., Liu Z.L., Shi J.P., Yu Y.Q., Wang Z.Q., Shen Y., et al. A family- and population-based study of the UFD1L gene for schizophrenia. Am. J. Med. Genet. 147B 7 (2008) 1076-1079
-
(2008)
Am. J. Med. Genet.
, vol.147 B
, Issue.7
, pp. 1076-1079
-
-
Xie, L.1
Ye, L.2
Ju, G.Z.3
Xu, Q.4
Zhang, X.5
Liu, Z.L.6
Shi, J.P.7
Yu, Y.Q.8
Wang, Z.Q.9
Shen, Y.10
|