-
1
-
-
0032874085
-
22q11 deletion syndrome: A geneticsubtype of schizophrenia
-
Bassett AS, Chow EW. 22q11 deletion syndrome: a geneticsubtype of schizophrenia. Biol Psychiatry. 1999;46:882-891.
-
(1999)
Biol Psychiatry.
, vol.46
, pp. 882-891
-
-
Bassett, A.S.1
Chow, E.W.2
-
2
-
-
9744258806
-
The molecular genetics of the22q11-associated schizophrenia
-
Karayiorgou M, Gogos JA. The molecular genetics of the22q11-associated schizophrenia. Brain Res Mol Brain Res.2004;132:95-104.
-
(2004)
Brain Res Mol Brain Res.
, vol.132
, pp. 95-104
-
-
Karayiorgou, M.1
Gogos, J.A.2
-
3
-
-
0033361897
-
Der(22) syndromeand velo-cardio-facial syndrome/DiGeorge syndrome sharea 1.5-Mb region of overlap on chromosome 22q11
-
Funke B, Edelmann L, McCain N, et al. Der(22) syndromeand velo-cardio-facial syndrome/DiGeorge syndrome sharea 1.5-Mb region of overlap on chromosome 22q11. Am JHum Genet. 1999;64:747-758.
-
(1999)
Am JHum Genet.
, vol.64
, pp. 747-758
-
-
Funke, B.1
Edelmann, L.2
McCain, N.3
-
4
-
-
0034161932
-
Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome:genomic organization and deletion endpoint analysis
-
Shaikh TH, Kurahashi H, Saitta SC, et al. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome:genomic organization and deletion endpoint analysis. Hum Mol Genet. 2000;9:489-501.
-
(2000)
Hum Mol Genet.
, vol.9
, pp. 489-501
-
-
Shaikh, T.H.1
Kurahashi, H.2
Saitta, S.C.3
-
5
-
-
10744223651
-
Role of TBX1 in humandel22q11.2 syndrome
-
Yagi H, Furutani Y, Hamada H, et al. Role of TBX1 in humandel22q11.2 syndrome. Lancet. 2003;362:1366-1373.
-
(2003)
Lancet.
, vol.362
, pp. 1366-1373
-
-
Yagi, H.1
Furutani, Y.2
Hamada, H.3
-
6
-
-
17344369067
-
Identification of a novel nuclear localizationsignal in Tbx1 that is deleted in DiGeorge syndromepatients harboring the 1223delC mutation
-
Stoller JZ, Epstein JA. Identification of a novel nuclear localizationsignal in Tbx1 that is deleted in DiGeorge syndromepatients harboring the 1223delC mutation. Hum Mol Genet.2005;14:885-892.
-
(2005)
Hum Mol Genet.
, vol.14
, pp. 885-892
-
-
Stoller, J.Z.1
Epstein, J.A.2
-
7
-
-
17744395906
-
TBX1 is responsiblefor cardiovascular defects in velo-cardio-facial/ DiGeorge syndrome
-
Merscher S, Funke B, Epstein JA, et al. TBX1 is responsiblefor cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.Cell. 2001;104:619-629.
-
(2001)
Cell.
, vol.104
, pp. 619-629
-
-
Merscher, S.1
Funke, B.2
Epstein, J.A.3
-
8
-
-
0035263599
-
Tbx1 haploinsufficieny inthe DiGeorge syndrome region causes aortic arch defects inmice
-
Lindsay EA, Vitelli F, Su H, et al. Tbx1 haploinsufficieny inthe DiGeorge syndrome region causes aortic arch defects inmice. Nature. 2001;410:97-101.
-
(2001)
Nature.
, vol.410
, pp. 97-101
-
-
Lindsay, E.A.1
Vitelli, F.2
Su, H.3
-
9
-
-
33646733029
-
Tbx1 haploinsufficiency islinked to behavioral disorders in mice and humans: Implicationsfor 22q11 deletion syndrome
-
Paylor R, Glaser B, Mupo A, et al. Tbx1 haploinsufficiency islinked to behavioral disorders in mice and humans: implicationsfor 22q11 deletion syndrome. Proc Natl Acad Sci U SA. 2006;103:7729-7734.
-
(2006)
Proc Natl Acad Sci U SA.
, vol.103
, pp. 7729-7734
-
-
Paylor, R.1
Glaser, B.2
Mupo, A.3
-
10
-
-
0035575658
-
Association of ZNF74gene genotypes with age-at-onset of schizophrenia
-
Takase K, Ohtsuki T, Migita O, et al. Association of ZNF74gene genotypes with age-at-onset of schizophrenia. Schizophr Res. 2001;52:161-165.
-
(2001)
Schizophr Res.
, vol.52
, pp. 161-165
-
-
Takase, K.1
Ohtsuki, T.2
Migita, O.3
-
11
-
-
33746954641
-
A complete genetic associationscan of the 22q11 deletion region and functional evidencereveal an association between DGCR2 andschizophrenia
-
Shifman S, Levit A, Chen ML, et al. A complete genetic associationscan of the 22q11 deletion region and functional evidencereveal an association between DGCR2 andschizophrenia. Hum Genet. 2006;120:160-170.
-
(2006)
Hum Genet.
, vol.120
, pp. 160-170
-
-
Shifman, S.1
Levit, A.2
Chen, M.L.3
-
12
-
-
33748927320
-
Transmission disequilibriumtest provides evidence of association between promoter polymorphismsin 22q11 gene DGCR14 and schizophrenia
-
Wang H, Duan S, Du J, et al. Transmission disequilibriumtest provides evidence of association between promoter polymorphismsin 22q11 gene DGCR14 and schizophrenia.J Neural Transm. 2006;113:1551-1561.
-
(2006)
J Neural Transm.
, vol.113
, pp. 1551-1561
-
-
Wang, H.1
Duan, S.2
Du, J.3
-
13
-
-
18544366528
-
PRODH mutations andhyperprolinemia in a subset of schizophrenic patients
-
Jacquet H, Raux G, Thibaut F, et al. PRODH mutations andhyperprolinemia 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
-
14
-
-
3042804077
-
Evidence that the gene encodingZDHHC8 contributes to the risk of schizophrenia
-
Mukai J, Liu H, Burt RA, et al. Evidence that the gene encodingZDHHC8 contributes to the risk of schizophrenia. NatGenet. 2004;36:725-731.
-
(2004)
NatGenet.
, vol.36
, pp. 725-731
-
-
Mukai, J.1
Liu, H.2
Burt, R.A.3
-
15
-
-
0038389841
-
A haplotype implicatedin schizophrenia susceptibility is associated with reducedCOMT expression in human brain
-
Bray NJ, Buckland PR, Williams NM, et al. A haplotype implicatedin schizophrenia susceptibility is associated with reducedCOMT expression in human brain. Am J HumGenet. 2003;73:152-161.
-
(2003)
Am J HumGenet.
, vol.73
, pp. 152-161
-
-
Bray, N.J.1
Buckland, P.R.2
Williams, N.M.3
-
16
-
-
33646247628
-
The quantificationof COMT mRNA in post mortem cerebellum tissue: Diagnosis, genotype, methylation and expression
-
Dempster EL, Mill J, Craig IW, Collier DA. The quantificationof COMT mRNA in post mortem cerebellum tissue: diagnosis, genotype, methylation and expression. BMC MedGenet. 2006;7:10.
-
(2006)
BMC MedGenet.
, vol.7
, pp. 10
-
-
Dempster, E.L.1
Mill, J.2
Craig, I.W.3
Collier, D.A.4
-
17
-
-
33846363929
-
Evidencefor statistical epistasis between catechol-O- methyltransferase(COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: Influence on risk of schizophrenia
-
Nicodemus KK, Kolachana BS, Vakkalanka R, et al. Evidencefor statistical epistasis between catechol-O-methyltransferase(COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: influence on risk of schizophrenia. HumGenet. 2007;120:889-906.
-
(2007)
HumGenet.
, vol.120
, pp. 889-906
-
-
Nicodemus, K.K.1
Kolachana, B.S.2
Vakkalanka, R.3
-
19
-
-
4444230582
-
The CLDN5 locus may be involved in the vulnerability to schizophrenia
-
DOI 10.1016/j.eurpsy.2004.06.007, PII S0924933804001385
-
Sun ZY, Wei J, Xie L, et al. The CLDN5 locus may be involvedin the vulnerability to schizophrenia. Eur Psychiatry.2004;19:354-357. (Pubitemid 39207962)
-
(2004)
European Psychiatry
, vol.19
, Issue.6
, pp. 354-357
-
-
Sun, Z.-Y.1
Wei, J.2
Xie, L.3
Shen, Y.4
Liu, S.-Z.5
Ju, G.-Z.6
Shi, J.-P.7
Yu, Y.-Q.8
Zhang, X.9
Xu, Q.10
Hemmings, G.P.11
-
20
-
-
20144388174
-
Further study of a genetic associationbetween the CLDN5 locus and schizophrenia
-
Ye L, Sun Z, Xie L, et al. Further study of a genetic associationbetween the CLDN5 locus and schizophrenia. Schizophr Res. 2005;75:139-141.
-
(2005)
Schizophr Res.
, vol.75
, pp. 139-141
-
-
Ye, L.1
Sun, Z.2
Xie, L.3
-
21
-
-
27744572389
-
ZDHHC8 as a candidategene for schizophrenia: Analysis of a putative functionalintronic marker in case-control and family-based associationstudies
-
Faul T, Gawlik M, Bauer M, et al. ZDHHC8 as a candidategene for schizophrenia: analysis of a putative functionalintronic marker in case-control and family-based associationstudies. BMC Psychiatry. 2005;5:35.
-
(2005)
BMC Psychiatry.
, vol.5
, pp. 35
-
-
Faul, T.1
Gawlik, M.2
Bauer, M.3
-
22
-
-
33749185252
-
Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individualor interactive effects on schizophrenia susceptibility
-
Glaser B, Moskvina V, Kirov G, et al. Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individualor interactive effects on schizophrenia susceptibility.Schizophr Res. 2006;87:21-27.
-
(2006)
Schizophr Res.
, vol.87
, pp. 21-27
-
-
Glaser, B.1
Moskvina, V.2
Kirov, G.3
-
23
-
-
33749052718
-
Association study of the G-protein signaling 4(RGS4) and proline dehydrogenase (PRODH) genes withschizophrenia: A meta-analysis
-
Li D, He L. Association study of the G-protein signaling 4(RGS4) and proline dehydrogenase (PRODH) genes withschizophrenia: a meta-analysis. Eur J Hum Genet. 2006;14:1130-1135.
-
(2006)
Eur J Hum Genet.
, vol.14
, pp. 1130-1135
-
-
Li, D.1
He, L.2
-
24
-
-
23744517092
-
Lack of associationof the COMT (Val158/108 Met) gene and schizophrenia:A meta-analysis of case-control studies
-
Munafo MR, Bowes L, Clark TG, Flint J. Lack of associationof the COMT (Val158/108 Met) gene and schizophrenia:a meta-analysis of case-control studies. Mol Psychiatry. 2005;10:765-770.
-
(2005)
Mol Psychiatry.
, vol.10
, pp. 765-770
-
-
Munafo, M.R.1
Bowes, L.2
Clark, T.G.3
Flint, J.4
-
25
-
-
30044449524
-
A 200-kb region of humanchromosome 22q11.2 confers antipsychotic- responsive behavioralabnormalities in mice
-
Hiroi N, Zhu H, Lee M, et al. A 200-kb region of humanchromosome 22q11.2 confers antipsychotic-responsive behavioralabnormalities in mice. Proc Natl Acad Sci U S A. 2005;102:19132-19137.
-
(2005)
Proc Natl Acad Sci U S A.
, vol.102
, pp. 19132-19137
-
-
Hiroi, N.1
Zhu, H.2
Lee, M.3
-
26
-
-
38849191674
-
Strong evidencethat GNB1L is associated with schizophrenia
-
Williams NM, Glaser B, Norton N, et al. Strong evidencethat GNB1L is associated with schizophrenia. Hum Mol Genet. 2008;17:555-566.
-
(2008)
Hum Mol Genet.
, vol.17
, pp. 555-566
-
-
Williams, N.M.1
Glaser, B.2
Norton, N.3
-
27
-
-
4644333848
-
Chronic haloperidolpromotes corticostriatal long-term potentiation by targetingdopamine D2L receptors
-
Centonze D, Usiello A, Costa C, et al. Chronic haloperidolpromotes corticostriatal long-term potentiation by targetingdopamine D2L receptors. J Neurosci. 2004;24:8214-8222.
-
(2004)
J Neurosci.
, vol.24
, pp. 8214-8222
-
-
Centonze, D.1
Usiello, A.2
Costa, C.3
-
28
-
-
37349036431
-
Aripiprazole, an atypicalantipsychotic, prevents the motor hyperactivity inducedby psychotomimetics and psychostimulants in mice
-
Leite JV, Guimaraes FS, Moreira FA. Aripiprazole, an atypicalantipsychotic, prevents the motor hyperactivity inducedby psychotomimetics and psychostimulants in mice. Eur JPharmacol. 2008;578:222-227.
-
(2008)
Eur JPharmacol.
, vol.578
, pp. 222-227
-
-
Leite, J.V.1
Guimaraes, F.S.2
Moreira, F.A.3
-
29
-
-
30544437565
-
Effects of haloperidol, clozapine, and quetiapine on sensorimotor gatingin a genetic model of reduced NMDA receptor function
-
Duncan GE, Moy SS, Lieberman JA, Koller BH. Effects of haloperidol, clozapine, and quetiapine on sensorimotor gatingin a genetic model of reduced NMDA receptor function.Psychopharmacology (Berl). 2006;184:190-200.
-
(2006)
Psychopharmacology (Berl).
, vol.184
, pp. 190-200
-
-
Duncan, G.E.1
Moy, S.S.2
Lieberman, J.A.3
Koller, B.H.4
-
30
-
-
33947217962
-
Chronichaloperidol treatmentresults in a decrease in the expression of myelin/oligodendrocyterelatedgenes in themouse brain
-
Narayan S, Kass KE, Thomas EA.Chronichaloperidol treatmentresults in a decrease in the expression of myelin/oligodendrocyterelatedgenes in themouse brain. J Neurosci Res. 2007;85:757-765.
-
(2007)
J Neurosci Res.
, vol.85
, pp. 757-765
-
-
Narayan, S.1
Kass, K.E.2
Thomas, E.A.3
-
31
-
-
59449096993
-
Aripiprazole amelioratesphencyclidine-induced impairment of recognition memorythrough dopamine D(1) and serotonin 5-HT (1A) receptors
-
First published ib August6, 2008, DOI:10.1007/s00213-008-1240-6
-
Nagai T, Murai R, Matsui K, et al. Aripiprazole amelioratesphencyclidine- induced impairment of recognition memorythrough dopamine D(1) and serotonin 5-HT (1A) receptors.Psychopharmacology (Berl). 2008 First published ib August6, 2008, DOI:10.1007/s00213-008-1240-6.
-
(2008)
Psychopharmacology (Berl).
-
-
Nagai, T.1
Murai, R.2
Matsui, K.3
-
32
-
-
0035888654
-
Mice overexpressinggenes from the 22q11 region deleted in velo-cardio-facialsyndrome/DiGeorge syndrome have middle and inner eardefects
-
Funke B, Epstein JA, Kochilas LK, et al. Mice overexpressinggenes from the 22q11 region deleted in velo-cardio-facialsyndrome/DiGeorge syndrome have middle and inner eardefects. Hum Mol Genet. 2001;10:2549-2556.
-
(2001)
Hum Mol Genet.
, vol.10
, pp. 2549-2556
-
-
Funke, B.1
Epstein, J.A.2
Kochilas, L.K.3
-
33
-
-
8844244726
-
Genetic inheritanceof gene expression in human cell lines
-
Monks SA, Leonardson A, Zhu H, et al. Genetic inheritanceof gene expression in human cell lines. Am J Hum Genet.2004;75:1094-1105.
-
(2004)
Am J Hum Genet.
, vol.75
, pp. 1094-1105
-
-
Monks, S.A.1
Leonardson, A.2
Zhu, H.3
-
34
-
-
4043128071
-
Genetic analysis of genome-wide variation in human gene expression
-
Morley M, Molony CM, Weber TM, et al. Genetic analysis of genome-wide variation in human gene expression. Nature.2004;430:743-747.
-
(2004)
Nature.
, vol.430
, pp. 743-747
-
-
Morley, M.1
Molony, C.M.2
Weber, T.M.3
-
35
-
-
49749117889
-
Micro-RNA(interference) networks are embedded in the gene regulatorynetworks
-
Pitto L, Ripoli A, Cremisi F, Simili M, Rainaldi G. Micro- RNA(interference) networks are embedded in the gene regulatorynetworks. Cell Cycle. 2008;7(16):2458-2461.
-
(2008)
Cell Cycle.
, vol.7
, Issue.16
, pp. 2458-2461
-
-
Pitto, L.1
Ripoli, A.2
Cremisi, F.3
Simili, M.4
Rainaldi, G.5
-
36
-
-
41849115577
-
Cis- andtrans-loci influence expression of the schizophrenia susceptibilitygene DTNBP1
-
Bray NJ, Holmans PA, van den Bree MB, et al. Cis- andtrans-loci influence expression of the schizophrenia susceptibilitygene DTNBP1. Hum Mol Genet. 2008;17:1169-11
-
(2008)
Hum Mol Genet.
, vol.17
, pp. 1169-11
-
-
Bray, N.J.1
Holmans, P.A.2
Van Den Bree, M.B.3
|