-
1
-
-
26844498125
-
Sequence variants in SLITRK1 are associated with Tourette's syndrome
-
Abelson J.F., Kwan K.Y., O'Roak B.J., et al. Sequence variants in SLITRK1 are associated with Tourette's syndrome. Science 310 (2005) 317-320
-
(2005)
Science
, vol.310
, pp. 317-320
-
-
Abelson, J.F.1
Kwan, K.Y.2
O'Roak, B.J.3
-
2
-
-
46149103853
-
Heterogeneous dysregulation of microRNAs across the autism spectrum
-
Abu-Elneel K., Liu T., Gazzaniga F.S., et al. Heterogeneous dysregulation of microRNAs across the autism spectrum. Neurogenetics 9 (2008) 153-161
-
(2008)
Neurogenetics
, vol.9
, pp. 153-161
-
-
Abu-Elneel, K.1
Liu, T.2
Gazzaniga, F.S.3
-
3
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir R.E., Van den Veyver I.B., Wan M., et al. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat. Genet. 23 (1999) 185-188
-
(1999)
Nat. Genet.
, vol.23
, pp. 185-188
-
-
Amir, R.E.1
Van den Veyver, I.B.2
Wan, M.3
-
4
-
-
0025736146
-
Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations
-
Archidiacono N., Lerone M., Rocchi M., et al. Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations. Hum. Genet. 86 (1991) 604-606
-
(1991)
Hum. Genet.
, vol.86
, pp. 604-606
-
-
Archidiacono, N.1
Lerone, M.2
Rocchi, M.3
-
6
-
-
0028906338
-
Autism as a strongly genetic disorder: evidence from a British twin study
-
Bailey A., Le Couteur A., Gottesman I., et al. Autism as a strongly genetic disorder: evidence from a British twin study. Psychol. Med. 25 (1995) 63-77
-
(1995)
Psychol. Med.
, vol.25
, pp. 63-77
-
-
Bailey, A.1
Le Couteur, A.2
Gottesman, I.3
-
7
-
-
0034873653
-
The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory
-
Bearden C.E., Woodin M.F., Wang P.P., et al. The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory. J. Clin. Exp. Neuropsychol. 23 (2001) 447-464
-
(2001)
J. Clin. Exp. Neuropsychol.
, vol.23
, pp. 447-464
-
-
Bearden, C.E.1
Woodin, M.F.2
Wang, P.P.3
-
8
-
-
78650238139
-
Schizophrenia is associated with an increase in cortical microRNA biogenesis
-
Advance online publication 1 September 2009. doi:10.1038/mp.2009.84
-
Beveridge N.J., Gardiner E., Carroll A.P., et al. Schizophrenia is associated with an increase in cortical microRNA biogenesis. Mol. Psychiatry (2009). http://doi:10.1038/mp.2009.84 Advance online publication 1 September 2009. doi:10.1038/mp.2009.84
-
(2009)
Mol. Psychiatry
-
-
Beveridge, N.J.1
Gardiner, E.2
Carroll, A.P.3
-
9
-
-
41849133938
-
Dysregulation of miRNA 181b in the temporal cortex in schizophrenia
-
Beveridge N.J., Tooney P.A., Carroll A.P., et al. Dysregulation of miRNA 181b in the temporal cortex in schizophrenia. Hum. Mol. Genet. 17 (2008) 1156-1168
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 1156-1168
-
-
Beveridge, N.J.1
Tooney, P.A.2
Carroll, A.P.3
-
10
-
-
52949109182
-
Excess protein synthesis in Drosophila fragile X mutants impairs long-term memory
-
Bolduc F.V., Bell K., Cox H., et al. Excess protein synthesis in Drosophila fragile X mutants impairs long-term memory. Nat. Neurosci. 11 (2008) 1143-1145
-
(2008)
Nat. Neurosci.
, vol.11
, pp. 1143-1145
-
-
Bolduc, F.V.1
Bell, K.2
Cox, H.3
-
11
-
-
41749090491
-
Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia
-
Brunet A., Armengol L., Pelaez T., et al. Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia. Behav. Brain Funct. 4 (2008) 10
-
(2008)
Behav. Brain Funct.
, vol.4
, pp. 10
-
-
Brunet, A.1
Armengol, L.2
Pelaez, T.3
-
12
-
-
67651233780
-
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes
-
Bucan M., Abrahams B.S., Wang K., et al. Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genet. 5 (2009) e1000536
-
(2009)
PLoS Genet.
, vol.5
-
-
Bucan, M.1
Abrahams, B.S.2
Wang, K.3
-
13
-
-
33745602880
-
Noncoding RNAs in the mammalian central nervous system
-
Cao X., Yeo G., Muotri A.R., et al. Noncoding RNAs in the mammalian central nervous system. Annu. Rev. Neurosci. 29 (2006) 77-103
-
(2006)
Annu. Rev. Neurosci.
, vol.29
, pp. 77-103
-
-
Cao, X.1
Yeo, G.2
Muotri, A.R.3
-
14
-
-
0032954610
-
International variation in reported livebirth prevalence rates of Down syndrome, adjusted for maternal age
-
Carothers A.D., Hecht C.A., and Hook E.B. International variation in reported livebirth prevalence rates of Down syndrome, adjusted for maternal age. J. Med. Genet. 36 (1999) 386-393
-
(1999)
J. Med. Genet.
, vol.36
, pp. 386-393
-
-
Carothers, A.D.1
Hecht, C.A.2
Hook, E.B.3
-
15
-
-
0036792769
-
Fragile X-related protein and VIG associate with the RNA interference machinery
-
Caudy A.A., Myers M., Hannon G.J., et al. Fragile X-related protein and VIG associate with the RNA interference machinery. Genes Dev. 16 (2002) 2491-2496
-
(2002)
Genes Dev.
, vol.16
, pp. 2491-2496
-
-
Caudy, A.A.1
Myers, M.2
Hannon, G.J.3
-
17
-
-
63649138643
-
miR-124 regulates adult neurogenesis in the subventricular zone stem cell niche
-
Cheng L.C., Pastrana E., Tavazoie M., et al. miR-124 regulates adult neurogenesis in the subventricular zone stem cell niche. Nat. Neurosci. 12 (2009) 399-408
-
(2009)
Nat. Neurosci.
, vol.12
, pp. 399-408
-
-
Cheng, L.C.1
Pastrana, E.2
Tavazoie, M.3
-
18
-
-
68949177123
-
Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization
-
Cho S.C., Yim S.H., Yoo H.K., et al. Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization. Psychiatr. Genet. 19 (2009) 177-185
-
(2009)
Psychiatr. Genet.
, vol.19
, pp. 177-185
-
-
Cho, S.C.1
Yim, S.H.2
Yoo, H.K.3
-
19
-
-
36048929095
-
Association of the Slit and Trk-like 1 gene in Taiwanese patients with Tourette syndrome
-
Chou I.C., Wan L., Liu S.C., et al. Association of the Slit and Trk-like 1 gene in Taiwanese patients with Tourette syndrome. Pediatr. Neurol. 37 (2007) 404-406
-
(2007)
Pediatr. Neurol.
, vol.37
, pp. 404-406
-
-
Chou, I.C.1
Wan, L.2
Liu, S.C.3
-
20
-
-
44349186162
-
Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder
-
Christian S.L., Brune C.W., Sudi J., et al. Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder. Biol. Psychiatry 63 (2008) 1111-1117
-
(2008)
Biol. Psychiatry
, vol.63
, pp. 1111-1117
-
-
Christian, S.L.1
Brune, C.W.2
Sudi, J.3
-
21
-
-
33144481470
-
Reciprocal actions of REST and a microRNA promote neuronal identity
-
Conaco C., Otto S., Han J.J., et al. Reciprocal actions of REST and a microRNA promote neuronal identity. Proc. Natl. Acad. Sci. U. S. A. 103 (2006) 2422-2427
-
(2006)
Proc. Natl. Acad. Sci. U. S. A.
, vol.103
, pp. 2422-2427
-
-
Conaco, C.1
Otto, S.2
Han, J.J.3
-
22
-
-
0027480909
-
X chromosome linkage studies in familial Rett syndrome
-
Curtis A.R., Headland S., Lindsay S., et al. X chromosome linkage studies in familial Rett syndrome. Hum. Genet. 90 (1993) 551-555
-
(1993)
Hum. Genet.
, vol.90
, pp. 551-555
-
-
Curtis, A.R.1
Headland, S.2
Lindsay, S.3
-
23
-
-
43749120042
-
Conditional loss of Dicer disrupts cellular and tissue morphogenesis in the cortex and hippocampus
-
Davis T.H., Cuellar T.L., Koch S.M., et al. Conditional loss of Dicer disrupts cellular and tissue morphogenesis in the cortex and hippocampus. J. Neurosci. 28 (2008) 4322-4330
-
(2008)
J. Neurosci.
, vol.28
, pp. 4322-4330
-
-
Davis, T.H.1
Cuellar, T.L.2
Koch, S.M.3
-
24
-
-
0027874350
-
Molecular mapping of twenty-four features of Down syndrome on chromosome 21
-
Delabar J.M., Theophile D., Rahmani Z., et al. Molecular mapping of twenty-four features of Down syndrome on chromosome 21. Eur. J. Hum. Genet. 1 (1993) 114-124
-
(1993)
Eur. J. Hum. Genet.
, vol.1
, pp. 114-124
-
-
Delabar, J.M.1
Theophile, D.2
Rahmani, Z.3
-
25
-
-
33750606811
-
Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome
-
Deng H., Le W.D., Xie W.J., et al. Examination of the SLITRK1 gene in Caucasian patients with Tourette syndrome. Acta Neurol. Scand. 114 (2006) 400-402
-
(2006)
Acta Neurol. Scand.
, vol.114
, pp. 400-402
-
-
Deng, H.1
Le, W.D.2
Xie, W.J.3
-
26
-
-
33748310866
-
Detection of mammalian microRNA expression by in situ hybridization with RNA oligonucleotides
-
Deo M., Yu J.Y., Chung K.H., et al. Detection of mammalian microRNA expression by in situ hybridization with RNA oligonucleotides. Dev. Dyn. 235 (2006) 2538-2548
-
(2006)
Dev. Dyn.
, vol.235
, pp. 2538-2548
-
-
Deo, M.1
Yu, J.Y.2
Chung, K.H.3
-
27
-
-
0027176361
-
The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation
-
Devys D., Lutz Y., Rouyer N., et al. The FMR-1 protein is cytoplasmic, most abundant in neurons and appears normal in carriers of a fragile X premutation. Nat. Genet. 4 (1993) 335-340
-
(1993)
Nat. Genet.
, vol.4
, pp. 335-340
-
-
Devys, D.1
Lutz, Y.2
Rouyer, N.3
-
28
-
-
44449121279
-
A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome
-
Dictenberg J.B., Swanger S.A., Antar L.N., et al. A direct role for FMRP in activity-dependent dendritic mRNA transport links filopodial-spine morphogenesis to fragile X syndrome. Dev. Cell 14 (2008) 926-939
-
(2008)
Dev. Cell
, vol.14
, pp. 926-939
-
-
Dictenberg, J.B.1
Swanger, S.A.2
Antar, L.N.3
-
29
-
-
75949101467
-
Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132
-
Edbauer D., Neilson J.R., Foster K.A., et al. Regulation of synaptic structure and function by FMRP-associated microRNAs miR-125b and miR-132. Neuron 65 (2010) 373-384
-
(2010)
Neuron
, vol.65
, pp. 373-384
-
-
Edbauer, D.1
Neilson, J.R.2
Foster, K.A.3
-
30
-
-
0026567450
-
Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis
-
Ellison K.A., Fill C.P., Terwilliger J., et al. Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis. Am. J. Hum. Genet. 50 (1992) 278-287
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 278-287
-
-
Ellison, K.A.1
Fill, C.P.2
Terwilliger, J.3
-
31
-
-
70350772348
-
MicroRNAs potentiate neural development
-
Fineberg S.K., Kosik K.S., and Davidson B.L. MicroRNAs potentiate neural development. Neuron 64 (2009) 303-309
-
(2009)
Neuron
, vol.64
, pp. 303-309
-
-
Fineberg, S.K.1
Kosik, K.S.2
Davidson, B.L.3
-
32
-
-
62649086993
-
Mef2-mediated transcription of the miR379-410 cluster regulates activity-dependent dendritogenesis by fine-tuning Pumilio2 protein levels
-
Fiore R., Khudayberdiev S., Christensen M., et al. Mef2-mediated transcription of the miR379-410 cluster regulates activity-dependent dendritogenesis by fine-tuning Pumilio2 protein levels. EMBO J. 28 (2009) 697-710
-
(2009)
EMBO J.
, vol.28
, pp. 697-710
-
-
Fiore, R.1
Khudayberdiev, S.2
Christensen, M.3
-
33
-
-
0017530988
-
Infantile autism: a genetic study of 21 twin pairs
-
Folstein S., and Rutter M. Infantile autism: a genetic study of 21 twin pairs. J. Child Psychol. Psychiatry 18 (1977) 297-321
-
(1977)
J. Child Psychol. Psychiatry
, vol.18
, pp. 297-321
-
-
Folstein, S.1
Rutter, M.2
-
34
-
-
18244385475
-
MicroRNAs regulate brain morphogenesis in zebrafish
-
Giraldez A.J., Cinalli R.M., Glasner M.E., et al. MicroRNAs regulate brain morphogenesis in zebrafish. Science 308 (2005) 833-838
-
(2005)
Science
, vol.308
, pp. 833-838
-
-
Giraldez, A.J.1
Cinalli, R.M.2
Glasner, M.E.3
-
35
-
-
67349182343
-
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
-
Glessner J.T., Wang K., Cai G., et al. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature 459 (2009) 569-573
-
(2009)
Nature
, vol.459
, pp. 569-573
-
-
Glessner, J.T.1
Wang, K.2
Cai, G.3
-
36
-
-
0034753368
-
Excess of twins among affected sibling pairs with autism: implications for the etiology of autism
-
Greenberg D.A., Hodge S.E., Sowinski J., et al. Excess of twins among affected sibling pairs with autism: implications for the etiology of autism. Am. J. Hum. Genet. 69 (2001) 1062-1067
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 1062-1067
-
-
Greenberg, D.A.1
Hodge, S.E.2
Sowinski, J.3
-
37
-
-
0021782655
-
Rett syndrome: Swedish approach to analysis of prevalence and cause
-
Hagberg B. Rett syndrome: Swedish approach to analysis of prevalence and cause. Brain Dev. 7 (1985) 276-280
-
(1985)
Brain Dev.
, vol.7
, pp. 276-280
-
-
Hagberg, B.1
-
38
-
-
0020507697
-
A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases
-
Hagberg B., Aicardi J., Dias K., et al. A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases. Ann. Neurol. 14 (1983) 471-479
-
(1983)
Ann. Neurol.
, vol.14
, pp. 471-479
-
-
Hagberg, B.1
Aicardi, J.2
Dias, K.3
-
39
-
-
58149097010
-
Posttranscriptional crossregulation between Drosha and DGCR8
-
Han J., Pedersen J.S., Kwon S.C., et al. Posttranscriptional crossregulation between Drosha and DGCR8. Cell 136 (2009) 75-84
-
(2009)
Cell
, vol.136
, pp. 75-84
-
-
Han, J.1
Pedersen, J.S.2
Kwon, S.C.3
-
40
-
-
40449084022
-
Brain expressed microRNAs implicated in schizophrenia etiology
-
Hansen T., Olsen L., Lindow M., et al. Brain expressed microRNAs implicated in schizophrenia etiology. PLoS ONE 2 (2007) e873
-
(2007)
PLoS ONE
, vol.2
-
-
Hansen, T.1
Olsen, L.2
Lindow, M.3
-
41
-
-
41349096445
-
Gene regulation by transcription factors and microRNAs
-
Hobert O. Gene regulation by transcription factors and microRNAs. Science 319 (2008) 1785-1786
-
(2008)
Science
, vol.319
, pp. 1785-1786
-
-
Hobert, O.1
-
42
-
-
0037188502
-
Altered synaptic plasticity in a mouse model of fragile X mental retardation
-
Huber K.M., Gallagher S.M., Warren S.T., et al. Altered synaptic plasticity in a mouse model of fragile X mental retardation. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 7746-7750
-
(2002)
Proc. Natl. Acad. Sci. U. S. A.
, vol.99
, pp. 7746-7750
-
-
Huber, K.M.1
Gallagher, S.M.2
Warren, S.T.3
-
43
-
-
0035800521
-
A cellular function for the RNA-interference enzyme Dicer in the maturation of the let-7 small temporal RNA
-
Hutvagner G., McLachlan J., Pasquinelli A.E., et al. A cellular function for the RNA-interference enzyme Dicer in the maturation of the let-7 small temporal RNA. Science 293 (2001) 834-838
-
(2001)
Science
, vol.293
, pp. 834-838
-
-
Hutvagner, G.1
McLachlan, J.2
Pasquinelli, A.E.3
-
44
-
-
78650514762
-
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
-
Ingason A., Rujescu D., Cichon S., et al. Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Mol. Psychiatry (2009)
-
(2009)
Mol. Psychiatry
-
-
Ingason, A.1
Rujescu, D.2
Cichon, S.3
-
45
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
ISC. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455 (2008) 237-241
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
ISC1
-
46
-
-
0036791671
-
A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins
-
Ishizuka A., Siomi M.C., and Siomi H. A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins. Genes Dev. 16 (2002) 2497-2508
-
(2002)
Genes Dev.
, vol.16
, pp. 2497-2508
-
-
Ishizuka, A.1
Siomi, M.C.2
Siomi, H.3
-
47
-
-
1642540373
-
Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway
-
Jin P., Zarnescu D.C., Ceman S., et al. Biochemical and genetic interaction between the fragile X mental retardation protein and the microRNA pathway. Nat. Neurosci. 7 (2004) 113-117
-
(2004)
Nat. Neurosci.
, vol.7
, pp. 113-117
-
-
Jin, P.1
Zarnescu, D.C.2
Ceman, S.3
-
48
-
-
62549120015
-
Genome-wide identification of targets of the drosha-pasha/DGCR8 complex
-
Kadener S., Rodriguez J., Abruzzi K.C., et al. Genome-wide identification of targets of the drosha-pasha/DGCR8 complex. Rna 15 (2009) 537-545
-
(2009)
Rna
, vol.15
, pp. 537-545
-
-
Kadener, S.1
Rodriguez, J.2
Abruzzi, K.C.3
-
49
-
-
0029102665
-
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
-
Karayiorgou M., Morris M.A., Morrow B., et al. Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc. Natl. Acad. Sci. U. S. A. 92 (1995) 7612-7616
-
(1995)
Proc. Natl. Acad. Sci. U. S. A.
, vol.92
, pp. 7612-7616
-
-
Karayiorgou, M.1
Morris, M.A.2
Morrow, B.3
-
50
-
-
0035043250
-
Developmental roles and molecular characterization of a Drosophila homologue of Arabidopsis Argonaute1, the founder of a novel gene superfamily
-
Kataoka Y., Takeichi M., and Uemura T. Developmental roles and molecular characterization of a Drosophila homologue of Arabidopsis Argonaute1, the founder of a novel gene superfamily. Genes Cells 6 (2001) 313-325
-
(2001)
Genes Cells
, vol.6
, pp. 313-325
-
-
Kataoka, Y.1
Takeichi, M.2
Uemura, T.3
-
51
-
-
34547428532
-
The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome)
-
Kates W.R., Krauss B.R., AbdulSabur N., et al. The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome). Neuropsychologia 45 (2007) 2863-2873
-
(2007)
Neuropsychologia
, vol.45
, pp. 2863-2873
-
-
Kates, W.R.1
Krauss, B.R.2
AbdulSabur, N.3
-
52
-
-
33750444633
-
Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses
-
Keen-Kim D., Mathews C.A., Reus V.I., et al. Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses. Hum. Mol. Genet. 15 (2006) 3324-3328
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 3324-3328
-
-
Keen-Kim, D.1
Mathews, C.A.2
Reus, V.I.3
-
53
-
-
70449363623
-
Tourette syndrome and comorbid early-onset schizophrenia
-
Kerbeshian J., Peng C.Z., and Burd L. Tourette syndrome and comorbid early-onset schizophrenia. J. Psychosom. Res. 67 (2009) 515-523
-
(2009)
J. Psychosom. Res.
, vol.67
, pp. 515-523
-
-
Kerbeshian, J.1
Peng, C.Z.2
Burd, L.3
-
54
-
-
34548537573
-
A MicroRNA feedback circuit in midbrain dopamine neurons
-
Kim J., Inoue K., Ishii J., et al. A MicroRNA feedback circuit in midbrain dopamine neurons. Science 317 (2007) 1220-1224
-
(2007)
Science
, vol.317
, pp. 1220-1224
-
-
Kim, J.1
Inoue, K.2
Ishii, J.3
-
55
-
-
18344369543
-
MicroRNA biogenesis: coordinated cropping and dicing
-
Kim V.N. MicroRNA biogenesis: coordinated cropping and dicing. Nat. Rev. Mol. Cell Biol. 6 (2005) 376-385
-
(2005)
Nat. Rev. Mol. Cell Biol.
, vol.6
, pp. 376-385
-
-
Kim, V.N.1
-
56
-
-
38349106160
-
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
-
Kirov G., Gumus D., Chen W., et al. Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Hum. Mol. Genet. 17 (2008) 458-465
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 458-465
-
-
Kirov, G.1
Gumus, D.2
Chen, W.3
-
57
-
-
64549147485
-
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
-
Kirov G., Grozeva D., Norton N., et al. Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. Hum Mol Genet. 18 (2009) 1497-1503
-
(2009)
Hum Mol Genet.
, vol.18
, pp. 1497-1503
-
-
Kirov, G.1
Grozeva, D.2
Norton, N.3
-
58
-
-
36448969801
-
Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA
-
Klein M.E., Lioy D.T., Ma L., et al. Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA. Nat. Neurosci. 10 (2007) 1513-1514
-
(2007)
Nat. Neurosci.
, vol.10
, pp. 1513-1514
-
-
Klein, M.E.1
Lioy, D.T.2
Ma, L.3
-
60
-
-
42749095242
-
Human chromosome 21-derived miRNAs are overexpressed in down syndrome brains and hearts
-
Kuhn D.E., Nuovo G.J., Martin M.M., et al. Human chromosome 21-derived miRNAs are overexpressed in down syndrome brains and hearts. Biochem. Biophys. Res. Commun. 370 (2008) 473-477
-
(2008)
Biochem. Biophys. Res. Commun.
, vol.370
, pp. 473-477
-
-
Kuhn, D.E.1
Nuovo, G.J.2
Martin, M.M.3
-
61
-
-
74049098309
-
Chromosome 21-derived microRNAs provide an etiological basis for aberrant protein expression in human Down syndrome brains
-
Kuhn D.E., Nuovo G.J., Terry Jr. A.V., et al. Chromosome 21-derived microRNAs provide an etiological basis for aberrant protein expression in human Down syndrome brains. J. Biol. Chem. 285 (2009) 1529-1543
-
(2009)
J. Biol. Chem.
, vol.285
, pp. 1529-1543
-
-
Kuhn, D.E.1
Nuovo, G.J.2
Terry Jr., A.V.3
-
63
-
-
0037197803
-
Identification of tissue-specific microRNAs from mouse
-
Lagos-Quintana M., Rauhut R., Yalcin A., et al. Identification of tissue-specific microRNAs from mouse. Curr. Biol. 12 (2002) 735-739
-
(2002)
Curr. Biol.
, vol.12
, pp. 735-739
-
-
Lagos-Quintana, M.1
Rauhut, R.2
Yalcin, A.3
-
64
-
-
0027751663
-
The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14
-
Lee R.C., Feinbaum R.L., and Ambros V. The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14. Cell 75 (1993) 843-854
-
(1993)
Cell
, vol.75
, pp. 843-854
-
-
Lee, R.C.1
Feinbaum, R.L.2
Ambros, V.3
-
65
-
-
0031937997
-
Is the girl with Rett syndrome normal at birth?
-
Leonard H., and Bower C. Is the girl with Rett syndrome normal at birth?. Dev. Med. Child Neurol. 40 (1998) 115-121
-
(1998)
Dev. Med. Child Neurol.
, vol.40
, pp. 115-121
-
-
Leonard, H.1
Bower, C.2
-
66
-
-
33846340841
-
Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome
-
Lewandowski K.E., Shashi V., Berry P.M., et al. Schizophrenic-like neurocognitive deficits in children and adolescents with 22q11 deletion syndrome. Am. J. Med. Genet. B Neuropsychiatr. Genet. 144 (2007) 27-36
-
(2007)
Am. J. Med. Genet. B Neuropsychiatr. Genet.
, vol.144
, pp. 27-36
-
-
Lewandowski, K.E.1
Shashi, V.2
Berry, P.M.3
-
67
-
-
13944282215
-
Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs
-
Lim L.P., Lau N.C., Garrett-Engele P., et al. Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs. Nature 433 (2005) 769-773
-
(2005)
Nature
, vol.433
, pp. 769-773
-
-
Lim, L.P.1
Lau, N.C.2
Garrett-Engele, P.3
-
68
-
-
4444368187
-
Argonaute2 is the catalytic engine of mammalian RNAi
-
Liu J., Carmell M.A., Rivas F.V., et al. Argonaute2 is the catalytic engine of mammalian RNAi. Science 305 (2004) 1437-1441
-
(2004)
Science
, vol.305
, pp. 1437-1441
-
-
Liu, J.1
Carmell, M.A.2
Rivas, F.V.3
-
69
-
-
51649130773
-
Expression of microRNAs and their precursors in synaptic fractions of adult mouse forebrain
-
Lugli G., Torvik V.I., Larson J., et al. Expression of microRNAs and their precursors in synaptic fractions of adult mouse forebrain. J. Neurochem. 106 (2008) 650-661
-
(2008)
J. Neurochem.
, vol.106
, pp. 650-661
-
-
Lugli, G.1
Torvik, V.I.2
Larson, J.3
-
70
-
-
34547212309
-
The MicroRNA miR-124 promotes neuronal differentiation by triggering brain-specific alternative pre-mRNA splicing
-
Makeyev E.V., Zhang J., Carrasco M.A., et al. The MicroRNA miR-124 promotes neuronal differentiation by triggering brain-specific alternative pre-mRNA splicing. Mol. Cell. 27 (2007) 435-448
-
(2007)
Mol. Cell.
, vol.27
, pp. 435-448
-
-
Makeyev, E.V.1
Zhang, J.2
Carrasco, M.A.3
-
71
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall C.R., Noor A., Vincent J.B., et al. Structural variation of chromosomes in autism spectrum disorder. Am. J. Hum. Genet. 82 (2008) 477-488
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
Noor, A.2
Vincent, J.B.3
-
72
-
-
67349117808
-
Molecular determinants of dysregulated GABAergic gene expression in the prefrontal cortex of subjects with schizophrenia
-
Mellios N., Huang H.S., Baker S.P., et al. Molecular determinants of dysregulated GABAergic gene expression in the prefrontal cortex of subjects with schizophrenia. Biol. Psychiatry 65 (2009) 1006-1014
-
(2009)
Biol. Psychiatry
, vol.65
, pp. 1006-1014
-
-
Mellios, N.1
Huang, H.S.2
Baker, S.P.3
-
73
-
-
0029895568
-
Molecular-clinical correlations in males with an expanded FMR1 mutation
-
Merenstein S.A., Sobesky W.E., Taylor A.K., et al. Molecular-clinical correlations in males with an expanded FMR1 mutation. Am. J. Med. Genet. 64 (1996) 388-394
-
(1996)
Am. J. Med. Genet.
, vol.64
, pp. 388-394
-
-
Merenstein, S.A.1
Sobesky, W.E.2
Taylor, A.K.3
-
74
-
-
65949085347
-
Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders
-
Miller D.T., Shen Y., Weiss L.A., et al. Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders. J. Med. Genet. 46 (2009) 242-248
-
(2009)
J. Med. Genet.
, vol.46
, pp. 242-248
-
-
Miller, D.T.1
Shen, Y.2
Weiss, L.A.3
-
78
-
-
0032882849
-
High rates of schizophrenia in adults with velo-cardio-facial syndrome
-
Murphy K.C., Jones L.A., and Owen M.J. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch. Gen. Psychiatry 56 (1999) 940-945
-
(1999)
Arch. Gen. Psychiatry
, vol.56
, pp. 940-945
-
-
Murphy, K.C.1
Jones, L.A.2
Owen, M.J.3
-
79
-
-
51549108502
-
The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP
-
Napoli I., Mercaldo V., Boyl P.P., et al. The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP. Cell 134 (2008) 1042-1054
-
(2008)
Cell
, vol.134
, pp. 1042-1054
-
-
Napoli, I.1
Mercaldo, V.2
Boyl, P.P.3
-
80
-
-
41849119117
-
MeCP2-dependent repression of an imprinted miR-184 released by depolarization
-
Nomura T., Kimura M., Horii T., et al. MeCP2-dependent repression of an imprinted miR-184 released by depolarization. Hum. Mol. Genet. 17 (2008) 1192-1199
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 1192-1199
-
-
Nomura, T.1
Kimura, M.2
Horii, T.3
-
81
-
-
70449361669
-
The genetics of Tourette syndrome: a review
-
O'Rourke J.A., Scharf J.M., Yu D., et al. The genetics of Tourette syndrome: a review. J. Psychosom. Res. 67 (2009) 533-545
-
(2009)
J. Psychosom. Res.
, vol.67
, pp. 533-545
-
-
O'Rourke, J.A.1
Scharf, J.M.2
Yu, D.3
-
82
-
-
33745623128
-
Post-transcriptional regulation of microRNA expression
-
Obernosterer G., Leuschner P.J., Alenius M., et al. Post-transcriptional regulation of microRNA expression. RNA 12 (2006) 1161-1167
-
(2006)
RNA
, vol.12
, pp. 1161-1167
-
-
Obernosterer, G.1
Leuschner, P.J.2
Alenius, M.3
-
84
-
-
34249736846
-
microRNA expression in the prefrontal cortex of individuals with schizophrenia and schizoaffective disorder
-
Perkins D.O., Jeffries C.D., Jarskog L.F., et al. microRNA expression in the prefrontal cortex of individuals with schizophrenia and schizoaffective disorder. Genome Biol. 8 (2007) R27
-
(2007)
Genome Biol.
, vol.8
-
-
Perkins, D.O.1
Jeffries, C.D.2
Jarskog, L.F.3
-
85
-
-
33947537457
-
Fragile X mental retardation protein induces synapse loss through acute postsynaptic translational regulation
-
Pfeiffer B.E., and Huber K.M. Fragile X mental retardation protein induces synapse loss through acute postsynaptic translational regulation. J. Neurosci. 27 (2007) 3120-3130
-
(2007)
J. Neurosci.
, vol.27
, pp. 3120-3130
-
-
Pfeiffer, B.E.1
Huber, K.M.2
-
86
-
-
4644310115
-
Tethering of human Ago proteins to mRNA mimics the miRNA-mediated repression of protein synthesis
-
Pillai R.S., Artus C.G., and Filipowicz W. Tethering of human Ago proteins to mRNA mimics the miRNA-mediated repression of protein synthesis. Rna 10 (2004) 1518-1525
-
(2004)
Rna
, vol.10
, pp. 1518-1525
-
-
Pillai, R.S.1
Artus, C.G.2
Filipowicz, W.3
-
87
-
-
60349108540
-
Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of Fmr1 knockout mice
-
Pilpel Y., Kolleker A., Berberich S., et al. Synaptic ionotropic glutamate receptors and plasticity are developmentally altered in the CA1 field of Fmr1 knockout mice. J. Physiol. 587 (2009) 787-804
-
(2009)
J. Physiol.
, vol.587
, pp. 787-804
-
-
Pilpel, Y.1
Kolleker, A.2
Berberich, S.3
-
88
-
-
0028082293
-
Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1
-
Pulver A.E., Karayiorgou M., Wolyniec P.S., et al. Sequential strategy to identify a susceptibility gene for schizophrenia: report of potential linkage on chromosome 22q12-q13.1: Part 1. Am. J. Med. Genet. 54 (1994) 36-43
-
(1994)
Am. J. Med. Genet.
, vol.54
, pp. 36-43
-
-
Pulver, A.E.1
Karayiorgou, M.2
Wolyniec, P.S.3
-
89
-
-
70349117273
-
Characterization of small RNAs in aplysia reveals a role for miR-124 in constraining synaptic plasticity through CREB
-
Rajasethupathy P., Fiumara F., Sheridan R., et al. Characterization of small RNAs in aplysia reveals a role for miR-124 in constraining synaptic plasticity through CREB. Neuron 63 (2009) 803-817
-
(2009)
Neuron
, vol.63
, pp. 803-817
-
-
Rajasethupathy, P.1
Fiumara, F.2
Sheridan, R.3
-
90
-
-
51749093103
-
Degradation of microRNAs by a family of exoribonucleases in Arabidopsis
-
Ramachandran V., and Chen X. Degradation of microRNAs by a family of exoribonucleases in Arabidopsis. Science 321 (2008) 1490-1492
-
(2008)
Science
, vol.321
, pp. 1490-1492
-
-
Ramachandran, V.1
Chen, X.2
-
91
-
-
0042090496
-
Diagnosing Tourette syndrome: is it a common disorder?
-
Robertson M.M. Diagnosing Tourette syndrome: is it a common disorder?. J. Psychosom. Res. 55 (2003) 3-6
-
(2003)
J. Psychosom. Res.
, vol.55
, pp. 3-6
-
-
Robertson, M.M.1
-
92
-
-
34447261382
-
Cerebellar neurodegeneration in the absence of microRNAs
-
Schaefer A., O'Carroll D., Tan C.L., et al. Cerebellar neurodegeneration in the absence of microRNAs. J. Exp. Med. 204 (2007) 1553-1558
-
(2007)
J. Exp. Med.
, vol.204
, pp. 1553-1558
-
-
Schaefer, A.1
O'Carroll, D.2
Tan, C.L.3
-
93
-
-
42049101407
-
Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample
-
Scharf J.M., Moorjani P., Fagerness J., et al. Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample. Neurology 70 (2008) 1495-1496
-
(2008)
Neurology
, vol.70
, pp. 1495-1496
-
-
Scharf, J.M.1
Moorjani, P.2
Fagerness, J.3
-
94
-
-
70450248489
-
microRNAs at the synapse
-
Schratt G. microRNAs at the synapse. Nat. Rev. Neurosci. 10 (2009) 842-849
-
(2009)
Nat. Rev. Neurosci.
, vol.10
, pp. 842-849
-
-
Schratt, G.1
-
95
-
-
31144479591
-
A brain-specific microRNA regulates dendritic spine development
-
Schratt G.M., Tuebing F., Nigh E.A., et al. A brain-specific microRNA regulates dendritic spine development. Nature 439 (2006) 283-289
-
(2006)
Nature
, vol.439
, pp. 283-289
-
-
Schratt, G.M.1
Tuebing, F.2
Nigh, E.A.3
-
96
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
Sebat J., Lakshmi B., Malhotra D., et al. Strong association of de novo copy number mutations with autism. Science 316 (2007) 445-449
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
-
97
-
-
0032231652
-
Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28
-
Sirianni N., Naidu S., Pereira J., et al. Rett syndrome: confirmation of X-linked dominant inheritance, and localization of the gene to Xq28. Am. J. Hum. Genet. 63 (1998) 1552-1558
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1552-1558
-
-
Sirianni, N.1
Naidu, S.2
Pereira, J.3
-
98
-
-
17144423635
-
Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis
-
Sobin C., Kiley-Brabeck K., Daniels S., et al. Neuropsychological characteristics of children with the 22q11 Deletion Syndrome: a descriptive analysis. Child Neuropsychol. 11 (2005) 39-53
-
(2005)
Child Neuropsychol.
, vol.11
, pp. 39-53
-
-
Sobin, C.1
Kiley-Brabeck, K.2
Daniels, S.3
-
99
-
-
0031020846
-
Tourette disorder: a cross-cultural review
-
Staley D., Wand R., and Shady G. Tourette disorder: a cross-cultural review. Compr. Psychiatry 38 (1997) 6-16
-
(1997)
Compr. Psychiatry
, vol.38
, pp. 6-16
-
-
Staley, D.1
Wand, R.2
Shady, G.3
-
100
-
-
43949124669
-
Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model
-
Stark K.L., Xu B., Bagchi A., et al. Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model. Nat. Genet. 40 (2008) 751-760
-
(2008)
Nat. Genet.
, vol.40
, pp. 751-760
-
-
Stark, K.L.1
Xu, B.2
Bagchi, A.3
-
101
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson H., Rujescu D., Cichon S., et al. Large recurrent microdeletions associated with schizophrenia. Nature 455 (2008) 232-236
-
(2008)
Nature
, vol.455
, pp. 232-236
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
-
102
-
-
0024523493
-
A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden
-
Steffenburg S., Gillberg C., Hellgren L., et al. A twin study of autism in Denmark, Finland, Iceland, Norway and Sweden. J. Child Psychol. Psychiatry 30 (1989) 405-416
-
(1989)
J. Child Psychol. Psychiatry
, vol.30
, pp. 405-416
-
-
Steffenburg, S.1
Gillberg, C.2
Hellgren, L.3
-
103
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
Szatmari P., Paterson A.D., Zwaigenbaum L., et al. Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nat. Genet. 39 (2007) 319-328
-
(2007)
Nat. Genet.
, vol.39
, pp. 319-328
-
-
Szatmari, P.1
Paterson, A.D.2
Zwaigenbaum, L.3
-
104
-
-
66349107637
-
Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism
-
Talebizadeh Z., Butler M.G., and Theodoro M.F. Feasibility and relevance of examining lymphoblastoid cell lines to study role of microRNAs in autism. Autism Res. 1 (2008) 307
-
(2008)
Autism Res.
, vol.1
, pp. 307
-
-
Talebizadeh, Z.1
Butler, M.G.2
Theodoro, M.F.3
-
105
-
-
33747334621
-
Extensive post-transcriptional regulation of microRNAs and its implications for cancer
-
Thomson J.M., Newman M., Parker J.S., et al. Extensive post-transcriptional regulation of microRNAs and its implications for cancer. Genes Dev. 20 (2006) 2202-2207
-
(2006)
Genes Dev.
, vol.20
, pp. 2202-2207
-
-
Thomson, J.M.1
Newman, M.2
Parker, J.S.3
-
106
-
-
66449118741
-
Post-transcriptional control of DGCR8 expression by the Microprocessor
-
Triboulet R., Chang H.M., Lapierre R.J., et al. Post-transcriptional control of DGCR8 expression by the Microprocessor. Rna 15 (2009) 1005-1011
-
(2009)
Rna
, vol.15
, pp. 1005-1011
-
-
Triboulet, R.1
Chang, H.M.2
Lapierre, R.J.3
-
107
-
-
4544306641
-
Neuropsychiatric symptoms of fragile X syndrome: pathophysiology and pharmacotherapy
-
Tsiouris J.A., and Brown W.T. Neuropsychiatric symptoms of fragile X syndrome: pathophysiology and pharmacotherapy. CNS Drugs. 18 (2004) 687-703
-
(2004)
CNS Drugs.
, vol.18
, pp. 687-703
-
-
Tsiouris, J.A.1
Brown, W.T.2
-
109
-
-
33749143420
-
Genetic and clinical analysis of a large Dutch Gilles de la Tourette family
-
Verkerk A.J., Cath D.C., van der Linde H.C., et al. Genetic and clinical analysis of a large Dutch Gilles de la Tourette family. Mol. Psychiatry 11 (2006) 954-964
-
(2006)
Mol. Psychiatry
, vol.11
, pp. 954-964
-
-
Verkerk, A.J.1
Cath, D.C.2
van der Linde, H.C.3
-
110
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk A.J., Pieretti M., Sutcliffe J.S., et al. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65 (1991) 905-914
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.1
Pieretti, M.2
Sutcliffe, J.S.3
-
111
-
-
28044439909
-
A cAMP-response element binding protein-induced microRNA regulates neuronal morphogenesis
-
Vo N., Klein M.E., Varlamova O., et al. A cAMP-response element binding protein-induced microRNA regulates neuronal morphogenesis. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 16426-16431
-
(2005)
Proc. Natl. Acad. Sci. U. S. A.
, vol.102
, pp. 16426-16431
-
-
Vo, N.1
Klein, M.E.2
Varlamova, O.3
-
112
-
-
33847323881
-
DGCR8 is essential for microRNA biogenesis and silencing of embryonic stem cell self-renewal
-
Wang Y., Medvid R., Melton C., et al. DGCR8 is essential for microRNA biogenesis and silencing of embryonic stem cell self-renewal. Nat. Genet. 39 (2007) 380-385
-
(2007)
Nat. Genet.
, vol.39
, pp. 380-385
-
-
Wang, Y.1
Medvid, R.2
Melton, C.3
-
113
-
-
48249095979
-
An activity-regulated microRNA controls dendritic plasticity by down-regulating p250GAP
-
Wayman G.A., Davare M., Ando H., et al. An activity-regulated microRNA controls dendritic plasticity by down-regulating p250GAP. Proc. Natl. Acad. Sci. U. S. A. 105 (2008) 9093-9098
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 9093-9098
-
-
Wayman, G.A.1
Davare, M.2
Ando, H.3
-
114
-
-
39049163023
-
Association between microdeletion and microduplication at 16p11.2 and autism
-
Weiss L.A., Shen Y., Korn J.M., et al. Association between microdeletion and microduplication at 16p11.2 and autism. N. Engl. J. Med. 358 (2008) 667-675
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 667-675
-
-
Weiss, L.A.1
Shen, Y.2
Korn, J.M.3
-
115
-
-
33748092355
-
Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder
-
Wendland J.R., Kruse M.R., and Murphy D.L. Functional SLITRK1 var321, varCDfs and SLC6A4 G56A variants and susceptibility to obsessive-compulsive disorder. Mol. Psychiatry 11 (2006) 802-804
-
(2006)
Mol. Psychiatry
, vol.11
, pp. 802-804
-
-
Wendland, J.R.1
Kruse, M.R.2
Murphy, D.L.3
-
116
-
-
0021956826
-
Occurrence of neuropathological changes and dementia of Alzheimer's disease in Down's syndrome
-
Wisniewski K.E., Wisniewski H.M., and Wen G.Y. Occurrence of neuropathological changes and dementia of Alzheimer's disease in Down's syndrome. Ann. Neurol. 17 (1985) 278-282
-
(1985)
Ann. Neurol.
, vol.17
, pp. 278-282
-
-
Wisniewski, K.E.1
Wisniewski, H.M.2
Wen, G.Y.3
-
117
-
-
0026765446
-
Age-related occurrence of signs and symptoms in the Rett syndrome
-
Witt Engerstrom I. Age-related occurrence of signs and symptoms in the Rett syndrome. Brain Dev. 14 Suppl (1992) S11-S20
-
(1992)
Brain Dev.
, vol.14 SUPPL
-
-
Witt Engerstrom, I.1
-
118
-
-
33750432857
-
Comparative sequence analysis reveals an intricate network among REST, CREB and miRNA in mediating neuronal gene expression
-
Wu J., and Xie X. Comparative sequence analysis reveals an intricate network among REST, CREB and miRNA in mediating neuronal gene expression. Genome Biol. 7 (2006) R85
-
(2006)
Genome Biol.
, vol.7
-
-
Wu, J.1
Xie, X.2
-
119
-
-
46249093584
-
Strong association of de novo copy number mutations with sporadic schizophrenia
-
Xu B., Roos J.L., Levy S., et al. Strong association of de novo copy number mutations with sporadic schizophrenia. Nat. Genet. 40 (2008) 880-885
-
(2008)
Nat. Genet.
, vol.40
, pp. 880-885
-
-
Xu, B.1
Roos, J.L.2
Levy, S.3
-
120
-
-
58149357047
-
The steady-state level of the nervous-system-specific microRNA-124a is regulated by dFMR1 in Drosophila
-
Xu X.L., Li Y., Wang F., et al. The steady-state level of the nervous-system-specific microRNA-124a is regulated by dFMR1 in Drosophila. J. Neurosci. 28 (2008) 11883-11889
-
(2008)
J. Neurosci.
, vol.28
, pp. 11883-11889
-
-
Xu, X.L.1
Li, Y.2
Wang, F.3
-
121
-
-
48849103603
-
MicroRNA miR-124 regulates neurite outgrowth during neuronal differentiation
-
Yu J.Y., Chung K.H., Deo M., et al. MicroRNA miR-124 regulates neurite outgrowth during neuronal differentiation. Exp. Cell Res. 314 (2008) 2618-2633
-
(2008)
Exp. Cell Res.
, vol.314
, pp. 2618-2633
-
-
Yu, J.Y.1
Chung, K.H.2
Deo, M.3
-
122
-
-
0035977134
-
Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function
-
Zhang Y.Q., Bailey A.M., Matthies H.J., et al. Drosophila fragile X-related gene regulates the MAP1B homolog Futsch to control synaptic structure and function. Cell 107 (2001) 591-603
-
(2001)
Cell
, vol.107
, pp. 591-603
-
-
Zhang, Y.Q.1
Bailey, A.M.2
Matthies, H.J.3
-
123
-
-
64949159019
-
Evidence for selective microRNAs and their effectors as common long-term targets for the actions of mood stabilizers
-
Zhou R., Yuan P., Wang Y., et al. Evidence for selective microRNAs and their effectors as common long-term targets for the actions of mood stabilizers. Neuropsychopharmacology 34 (2009) 1395-1405
-
(2009)
Neuropsychopharmacology
, vol.34
, pp. 1395-1405
-
-
Zhou, R.1
Yuan, P.2
Wang, Y.3
-
124
-
-
57149124492
-
Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder
-
Zimprich A., Hatala K., Riederer F., et al. Sequence analysis of the complete SLITRK1 gene in Austrian patients with Tourette's disorder. Psychiatr. Genet. 18 (2008) 308-309
-
(2008)
Psychiatr. Genet.
, vol.18
, pp. 308-309
-
-
Zimprich, A.1
Hatala, K.2
Riederer, F.3
|