-
1
-
-
84860712363
-
Patterns and rates of exonic de novo mutations in autism spectrum disorders
-
1:CAS:528:DC%2BC38XmtVerurs%3D 22495311 3613847
-
Neale BM, Kou Y, Liu L, Ma'ayan A, Samocha KE, Sabo A, Lin CF, Stevens C, Wang LS, Makarov V, Polak P, Yoon S, Maguire J, Crawford EL, Campbell NG, Geller ET, Valladares O, Schafer C, Liu H, Zhao T, Cai G, Lihm J, Dannenfelser R, Jabado O, Peralta Z, Nagaswamy U, Muzny D, Reid JG, Newsham I, Wu Y, Lewis L, Han Y, Voight BF, Lim E, Rossin E, Kirby A, Flannick J, Fromer M, Shakir K, Fennell T, Garimella K, Banks E, Poplin R, Gabriel S, DePristo M, Wimbish JR, Boone BE, Levy SE, Betancur C, Sunyaev S, Boerwinkle E, Buxbaum JD, Cook Jr EH, Devlin B, Gibbs RA, Roeder K, Schellenberg GD, Sutcliffe JS, Daly MJ. Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature. 2012;485(7397):242-5.
-
(2012)
Nature
, vol.485
, Issue.7397
, pp. 242-245
-
-
Neale, B.M.1
Kou, Y.2
Liu, L.3
Ma'ayan, A.4
Samocha, K.E.5
Sabo, A.6
Lin, C.F.7
Stevens, C.8
Wang, L.S.9
Makarov, V.10
Polak, P.11
Yoon, S.12
Maguire, J.13
Crawford, E.L.14
Campbell, N.G.15
Geller, E.T.16
Valladares, O.17
Schafer, C.18
Liu, H.19
Zhao, T.20
Cai, G.21
Lihm, J.22
Dannenfelser, R.23
Jabado, O.24
Peralta, Z.25
Nagaswamy, U.26
Muzny, D.27
Reid, J.G.28
Newsham, I.29
Wu, Y.30
Lewis, L.31
Han, Y.32
Voight, B.F.33
Lim, E.34
Rossin, E.35
Kirby, A.36
Flannick, J.37
Fromer, M.38
Shakir, K.39
Fennell, T.40
Garimella, K.41
Banks, E.42
Poplin, R.43
Gabriel, S.44
DePristo, M.45
Wimbish, J.R.46
Boone, B.E.47
Levy, S.E.48
Betancur, C.49
Sunyaev, S.50
Boerwinkle, E.51
Buxbaum, J.D.52
Cook, E.H.53
Devlin, B.54
Gibbs, R.A.55
Roeder, K.56
Schellenberg, G.D.57
Sutcliffe, J.S.58
Daly, M.J.59
more..
-
2
-
-
84860741138
-
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
-
22495309 3350576 1:CAS:528:DC%2BC38XmtVeqsbc%3D
-
O'Roak BJ, Vives L, Girirajan S, Karakoc E, Krumm N, Coe BP, Levy R, Ko A, Lee C, Smith JD, Turner EH, Stanaway IB, Vernot B, Malig M, Baker C, Reilly B, Akey JM, Borenstein E, Rieder MJ, Nickerson DA, Bernier R, Shendure J, Eichler EE. Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations. Nature. 2012;485(7397):246-50.
-
(2012)
Nature
, vol.485
, Issue.7397
, pp. 246-250
-
-
O'Roak, B.J.1
Vives, L.2
Girirajan, S.3
Karakoc, E.4
Krumm, N.5
Coe, B.P.6
Levy, R.7
Ko, A.8
Lee, C.9
Smith, J.D.10
Turner, E.H.11
Stanaway, I.B.12
Vernot, B.13
Malig, M.14
Baker, C.15
Reilly, B.16
Akey, J.M.17
Borenstein, E.18
Rieder, M.J.19
Nickerson, D.A.20
Bernier, R.21
Shendure, J.22
Eichler, E.E.23
more..
-
3
-
-
84904635209
-
Disruptive CHD8 mutations define a subtype of autism early in development
-
1:CAS:528:DC%2BC2cXhtFWgtbbM 24998929 4136921
-
Bernier R, Golzio C, Xiong B, Stessman HA, Coe BP, Penn O, Witherspoon K, Gerdts J, Baker C, Vulto-van Silfhout AT, Schuurs-Hoeijmakers JH, Fichera M, Bosco P, Buono S, Alberti A, Failla P, Peeters H, Steyaert J, Vissers LE, Francescatto L, Mefford HC, Rosenfeld JA, Bakken T, O'Roak BJ, Pawlus M, Moon R, Shendure J, Amaral DG, Lein E, Rankin J, Romano C, de Vries BB, Katsanis N, Eichler EE. Disruptive CHD8 mutations define a subtype of autism early in development. Cell. 2014;158(2):263-76.
-
(2014)
Cell
, vol.158
, Issue.2
, pp. 263-276
-
-
Bernier, R.1
Golzio, C.2
Xiong, B.3
Stessman, H.A.4
Coe, B.P.5
Penn, O.6
Witherspoon, K.7
Gerdts, J.8
Baker, C.9
Vulto-Van Silfhout, A.T.10
Schuurs-Hoeijmakers, J.H.11
Fichera, M.12
Bosco, P.13
Buono, S.14
Alberti, A.15
Failla, P.16
Peeters, H.17
Steyaert, J.18
Vissers, L.E.19
Francescatto, L.20
Mefford, H.C.21
Rosenfeld, J.A.22
Bakken, T.23
O'Roak, B.J.24
Pawlus, M.25
Moon, R.26
Shendure, J.27
Amaral, D.G.28
Lein, E.29
Rankin, J.30
Romano, C.31
De Vries, B.B.32
Katsanis, N.33
Eichler, E.E.34
more..
-
4
-
-
84893708713
-
A de novo convergence of autism genetics and molecular neuroscience
-
1:CAS:528:DC%2BC2cXisVCruw%3D%3D 24387789
-
Krumm N, O'Roak BJ, Shendure J, Eichler EE. A de novo convergence of autism genetics and molecular neuroscience. Trends Neurosci. 2014;37(2):95-105.
-
(2014)
Trends Neurosci
, vol.37
, Issue.2
, pp. 95-105
-
-
Krumm, N.1
O'Roak, B.J.2
Shendure, J.3
Eichler, E.E.4
-
5
-
-
84901246368
-
De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability
-
1:CAS:528:DC%2BC2cXntlejtr0%3D 24776741 4031262
-
McCarthy SE, Gillis J, Kramer M, Lihm J, Yoon S, Berstein Y, Mistry M, Pavlidis P, Solomon R, Ghiban E, Antoniou E, Kelleher E, O'Brien C, Donohoe G, Gill M, Morris DW, McCombie WR, Corvin A. De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability. Mol Psychiatry. 2014;19(6):652-8.
-
(2014)
Mol Psychiatry
, vol.19
, Issue.6
, pp. 652-658
-
-
McCarthy, S.E.1
Gillis, J.2
Kramer, M.3
Lihm, J.4
Yoon, S.5
Berstein, Y.6
Mistry, M.7
Pavlidis, P.8
Solomon, R.9
Ghiban, E.10
Antoniou, E.11
Kelleher, E.12
O'Brien, C.13
Donohoe, G.14
Gill, M.15
Morris, D.W.16
McCombie, W.R.17
Corvin, A.18
-
6
-
-
84860347597
-
Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries
-
1:CAS:528:DC%2BC38XlvFyju7c%3D 22521361 3340505
-
Talkowski ME, Rosenfeld JA, Blumenthal I, Pillalamarri V, Chiang C, Heilbut A, Ernst C, Hanscom C, Rossin E, Lindgren AM, Pereira S, Ruderfer D, Kirby A, Ripke S, Harris DJ, Lee JH, Ha K, Kim HG, Solomon BD, Gropman AL, Lucente D, Sims K, Ohsumi TK, Borowsky ML, Loranger S, Quade B, Lage K, Miles J, Wu BL, Shen Y, Neale B, Shaffer LG, Daly MJ, Morton CC, Gusella JF. Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell. 2012;149(3):525-37.
-
(2012)
Cell
, vol.149
, Issue.3
, pp. 525-537
-
-
Talkowski, M.E.1
Rosenfeld, J.A.2
Blumenthal, I.3
Pillalamarri, V.4
Chiang, C.5
Heilbut, A.6
Ernst, C.7
Hanscom, C.8
Rossin, E.9
Lindgren, A.M.10
Pereira, S.11
Ruderfer, D.12
Kirby, A.13
Ripke, S.14
Harris, D.J.15
Lee, J.H.16
Ha, K.17
Kim, H.G.18
Solomon, B.D.19
Gropman, A.L.20
Lucente, D.21
Sims, K.22
Ohsumi, T.K.23
Borowsky, M.L.24
Loranger, S.25
Quade, B.26
Lage, K.27
Miles, J.28
Wu, B.L.29
Shen, Y.30
Neale, B.31
Shaffer, L.G.32
Daly, M.J.33
Morton, C.C.34
Gusella, J.F.35
more..
-
7
-
-
34147158728
-
The Chd family of chromatin remodelers
-
1:CAS:528:DC%2BD2sXksFahuro%3D 17350655 1899158
-
Marfella CG, Imbalzano AN. The Chd family of chromatin remodelers. Mutat Res. 2007;618(1-2):30-40.
-
(2007)
Mutat Res
, vol.618
, Issue.1-2
, pp. 30-40
-
-
Marfella, C.G.1
Imbalzano, A.N.2
-
8
-
-
84944382599
-
CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment
-
26491539 4612430 1:CAS:528:DC%2BC28Xos1KrsbY%3D 015-0048-, eCollection 2015
-
Wang P, Lin M, Pedrosa E, Hrabovsky A, Zhang Z, Guo W, Lachman HM, Zheng D. CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in neurodevelopment. Mol Autism. 2015;6:55. 015-0048-, eCollection 2015.
-
(2015)
Mol Autism
, vol.6
, pp. 55
-
-
Wang, P.1
Lin, M.2
Pedrosa, E.3
Hrabovsky, A.4
Zhang, Z.5
Guo, W.6
Lachman, H.M.7
Zheng, D.8
-
9
-
-
84957554030
-
Genome-wide nucleosome specificity and function of chromatin remodellers in ES cells
-
26814966 4871117 1:CAS:528:DC%2BC28XhsFyitLs%3D
-
de Dieuleveult M, Yen K, Hmitou I, Depaux A, Boussouar F, Bou Dargham D, Jounier S, Humbertclaude H, Ribierre F, Baulard C, Farrell NP, Park B, Keime C, Carriere L, Berlivet S, Gut M, Gut I, Werner M, Deleuze JF, Olaso R, Aude JC, Chantalat S, Pugh BF, Gerard M. Genome-wide nucleosome specificity and function of chromatin remodellers in ES cells. Nature. 2016;530(7588):113-6.
-
(2016)
Nature
, vol.530
, Issue.7588
, pp. 113-116
-
-
De Dieuleveult, M.1
Yen, K.2
Hmitou, I.3
Depaux, A.4
Boussouar, F.5
Bou Dargham, D.6
Jounier, S.7
Humbertclaude, H.8
Ribierre, F.9
Baulard, C.10
Farrell, N.P.11
Park, B.12
Keime, C.13
Carriere, L.14
Berlivet, S.15
Gut, M.16
Gut, I.17
Werner, M.18
Deleuze, J.F.19
Olaso, R.20
Aude, J.C.21
Chantalat, S.22
Pugh, B.F.23
Gerard, M.24
more..
-
10
-
-
84856803144
-
Histone H1 recruitment by CHD8 is essential for suppression of the Wnt-beta-catenin signaling pathway
-
1:CAS:528:DC%2BC38XnvFOlsw%3D%3D 22083958 3255766
-
Nishiyama M, Skoultchi AI, Nakayama KI. Histone H1 recruitment by CHD8 is essential for suppression of the Wnt-beta-catenin signaling pathway. Mol Cell Biol. 2012;32(2):501-12.
-
(2012)
Mol Cell Biol
, vol.32
, Issue.2
, pp. 501-512
-
-
Nishiyama, M.1
Skoultchi, A.I.2
Nakayama, K.I.3
-
11
-
-
44949144048
-
CHD8 is an ATP-dependent chromatin remodeling factor that regulates beta-catenin target genes
-
1:CAS:528:DC%2BD1cXntFanurw%3D 18378692 2423111
-
Thompson BA, Tremblay V, Lin G, Bochar DA. CHD8 is an ATP-dependent chromatin remodeling factor that regulates beta-catenin target genes. Mol Cell Biol. 2008;28(12):3894-904.
-
(2008)
Mol Cell Biol
, vol.28
, Issue.12
, pp. 3894-3904
-
-
Thompson, B.A.1
Tremblay, V.2
Lin, G.3
Bochar, D.A.4
-
12
-
-
79958199264
-
Synaptic Wnt signaling-a contributor to major psychiatric disorders?
-
21533542 3180925
-
Okerlund ND, Cheyette BN. Synaptic Wnt signaling-a contributor to major psychiatric disorders? J Neurodev Disord. 2011;3(2):162-74.
-
(2011)
J Neurodev Disord
, vol.3
, Issue.2
, pp. 162-174
-
-
Okerlund, N.D.1
Cheyette, B.N.2
-
13
-
-
84962195201
-
Expression and functional analysis of the Wnt/beta-catenin induced miR-135a-2 locus in embryonic forebrain development
-
27048518 4822265 016-0065-y
-
Caronia-Brown G, Anderegg A, Awatramani R. Expression and functional analysis of the Wnt/beta-catenin induced mir-135a-2 locus in embryonic forebrain development. Neural Dev. 2016;11(1):9. 016-0065-y.
-
(2016)
Neural Dev
, vol.11
, Issue.1
, pp. 9
-
-
Caronia-Brown, G.1
Anderegg, A.2
Awatramani, R.3
-
14
-
-
84874094990
-
Functional corneal endothelium derived from corneal stroma stem cells of neural crest origin by retinoic acid and Wnt/beta-catenin signaling
-
1:CAS:528:DC%2BC3sXivVGgt7w%3D 22974347
-
Hatou S, Yoshida S, Higa K, Miyashita H, Inagaki E, Okano H, Tsubota K, Shimmura S. Functional corneal endothelium derived from corneal stroma stem cells of neural crest origin by retinoic acid and Wnt/beta-catenin signaling. Stem Cells Dev. 2013;22(5):828-39.
-
(2013)
Stem Cells Dev
, vol.22
, Issue.5
, pp. 828-839
-
-
Hatou, S.1
Yoshida, S.2
Higa, K.3
Miyashita, H.4
Inagaki, E.5
Okano, H.6
Tsubota, K.7
Shimmura, S.8
-
15
-
-
79951826167
-
Distinct roles for Wnt-4 and Wnt-11 during retinoic acid-induced neuronal differentiation
-
1:CAS:528:DC%2BC3MXjvFSltLY%3D 21280163
-
Elizalde C, Campa VM, Caro M, Schlangen K, Aransay AM, Vivanco M, Kypta RM. Distinct roles for Wnt-4 and Wnt-11 during retinoic acid-induced neuronal differentiation. Stem Cells. 2011;29(1):141-53.
-
(2011)
Stem Cells
, vol.29
, Issue.1
, pp. 141-153
-
-
Elizalde, C.1
Campa, V.M.2
Caro, M.3
Schlangen, K.4
Aransay, A.M.5
Vivanco, M.6
Kypta, R.M.7
-
16
-
-
79955884485
-
Modelling schizophrenia using human induced pluripotent stem cells
-
Brennand KJ, Simone A, Jou J, Gelboin-Burkhart C, Tran N, Sangar S, Li Y, Mu Y, Chen G, Yu D, McCarthy S, Sebat J, Gage FH. Modelling schizophrenia using human induced pluripotent stem cells. Nature. 2011;473(7346):221-5.
-
(2011)
Nature
, vol.473
, Issue.7346
, pp. 221-225
-
-
Brennand, K.J.1
Simone, A.2
Jou, J.3
Gelboin-Burkhart, C.4
Tran, N.5
Sangar, S.6
Li, Y.7
Mu, Y.8
Chen, G.9
Yu, D.10
McCarthy, S.11
Sebat, J.12
Gage, F.H.13
-
17
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Wellcome Trust Case Control Consortium 1:CAS:528:DC%2BD2sXmtFelsb0%3D
-
Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature. 2007;447(7145):661-78.
-
(2007)
Nature
, vol.447
, Issue.7145
, pp. 661-678
-
-
-
18
-
-
77954874401
-
GSK3 signalling in neural development
-
1:CAS:528:DC%2BC3cXptVGisro%3D 20648061 3533361
-
Hur EM, Zhou FQ. GSK3 signalling in neural development. Nat Rev Neurosci. 2010;11(8):539-51.
-
(2010)
Nat Rev Neurosci
, vol.11
, Issue.8
, pp. 539-551
-
-
Hur, E.M.1
Zhou, F.Q.2
-
19
-
-
62149083806
-
Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling
-
1:CAS:528:DC%2BD1MXltFSntrs%3D 19303846 2704382
-
Mao Y, Ge X, Frank CL, Madison JM, Koehler AN, Doud MK, Tassa C, Berry EM, Soda T, Singh KK, Biechele T, Petryshen TL, Moon RT, Haggarty SJ, Tsai LH. Disrupted in schizophrenia 1 regulates neuronal progenitor proliferation via modulation of GSK3beta/beta-catenin signaling. Cell. 2009;136(6):1017-31.
-
(2009)
Cell
, vol.136
, Issue.6
, pp. 1017-1031
-
-
Mao, Y.1
Ge, X.2
Frank, C.L.3
Madison, J.M.4
Koehler, A.N.5
Doud, M.K.6
Tassa, C.7
Berry, E.M.8
Soda, T.9
Singh, K.K.10
Biechele, T.11
Petryshen, T.L.12
Moon, R.T.13
Haggarty, S.J.14
Tsai, L.H.15
-
20
-
-
84880641966
-
CHD8 is an independent prognostic indicator that regulates Wnt/beta-catenin signaling and the cell cycle in gastric cancer
-
1:CAS:528:DC%2BC3sXhsVygurrP 23835524
-
Sawada G, Ueo H, Matsumura T, Uchi R, Ishibashi M, Mima K, Kurashige J, Takahashi Y, Akiyoshi S, Sudo T, Sugimachi K, Doki Y, Mori M, Mimori K. CHD8 is an independent prognostic indicator that regulates Wnt/beta-catenin signaling and the cell cycle in gastric cancer. Oncol Rep. 2013;30(3):1137-42.
-
(2013)
Oncol Rep
, vol.30
, Issue.3
, pp. 1137-1142
-
-
Sawada, G.1
Ueo, H.2
Matsumura, T.3
Uchi, R.4
Ishibashi, M.5
Mima, K.6
Kurashige, J.7
Takahashi, Y.8
Akiyoshi, S.9
Sudo, T.10
Sugimachi, K.11
Doki, Y.12
Mori, M.13
Mimori, K.14
-
21
-
-
79954613030
-
Genetic and expressional alterations of CHD genes in gastric and colorectal cancers
-
21447119
-
Kim MS, Chung NG, Kang MR, Yoo NJ, Lee SH. Genetic and expressional alterations of CHD genes in gastric and colorectal cancers. Histopathology. 2011;58(5):660-8.
-
(2011)
Histopathology
, vol.58
, Issue.5
, pp. 660-668
-
-
Kim, M.S.1
Chung, N.G.2
Kang, M.R.3
Yoo, N.J.4
Lee, S.H.5
-
22
-
-
84892735426
-
Colorectal carcinomas with CpG island methylator phenotype 1 frequently contain mutations in chromatin regulators
-
1:CAS:528:DC%2BC2cXhsVynsbs%3D 24211491
-
Tahara T, Yamamoto E, Madireddi P, Suzuki H, Maruyama R, Chung W, Garriga J, Jelinek J, Yamano HO, Sugai T, Kondo Y, Toyota M, Issa JP, Estecio MR. Colorectal carcinomas with CpG island methylator phenotype 1 frequently contain mutations in chromatin regulators. Gastroenterology. 2014;146(2):530-38.e5.
-
(2014)
Gastroenterology
, vol.146
, Issue.2
, pp. 530-538
-
-
Tahara, T.1
Yamamoto, E.2
Madireddi, P.3
Suzuki, H.4
Maruyama, R.5
Chung, W.6
Garriga, J.7
Jelinek, J.8
Yamano, H.O.9
Sugai, T.10
Kondo, Y.11
Toyota, M.12
Issa, J.P.13
Estecio, M.R.14
-
23
-
-
85003220372
-
Frequent disruption of chromodomain helicase DNA-binding protein 8 (CHD8) and functionally associated chromatin regulators in prostate cancer
-
1:CAS:528:DC%2BC2MXlvFCltr8%3D 25499215 4309256
-
Damaschke NA, Yang B, Blute Jr ML, Lin CP, Huang W, Jarrard DF. Frequent disruption of chromodomain helicase DNA-binding protein 8 (CHD8) and functionally associated chromatin regulators in prostate cancer. Neoplasia. 2014;16(12):1018-27.
-
(2014)
Neoplasia
, vol.16
, Issue.12
, pp. 1018-1027
-
-
Damaschke, N.A.1
Yang, B.2
Blute, M.L.3
Lin, C.P.4
Huang, W.5
Jarrard, D.F.6
-
24
-
-
59649116006
-
CHD8 suppresses p53-mediated apoptosis through histone H1 recruitment during early embryogenesis
-
1:CAS:528:DC%2BD1MXht1Oqtrk%3D 19151705 3132516
-
Nishiyama M, Oshikawa K, Tsukada Y, Nakagawa T, Iemura S, Natsume T, Fan Y, Kikuchi A, Skoultchi AI, Nakayama KI. CHD8 suppresses p53-mediated apoptosis through histone H1 recruitment during early embryogenesis. Nat Cell Biol. 2009;11(2):172-82.
-
(2009)
Nat Cell Biol
, vol.11
, Issue.2
, pp. 172-182
-
-
Nishiyama, M.1
Oshikawa, K.2
Tsukada, Y.3
Nakagawa, T.4
Iemura, S.5
Natsume, T.6
Fan, Y.7
Kikuchi, A.8
Skoultchi, A.I.9
Nakayama, K.I.10
-
25
-
-
84895779640
-
The chromatin remodeller CHD8 is required for E2F-dependent transcription activation of S-phase genes
-
1:CAS:528:DC%2BC2cXjtlOrtbk%3D 24265227
-
Subtil-Rodriguez A, Vazquez-Chavez E, Ceballos-Chavez M, Rodriguez-Paredes M, Martin-Subero JI, Esteller M, Reyes JC. The chromatin remodeller CHD8 is required for E2F-dependent transcription activation of S-phase genes. Nucleic Acids Res. 2014;42(4):2185-96.
-
(2014)
Nucleic Acids Res
, vol.42
, Issue.4
, pp. 2185-2196
-
-
Subtil-Rodriguez, A.1
Vazquez-Chavez, E.2
Ceballos-Chavez, M.3
Rodriguez-Paredes, M.4
Martin-Subero, J.I.5
Esteller, M.6
Reyes, J.C.7
-
26
-
-
33747885707
-
CTCF-dependent chromatin insulator is linked to epigenetic remodeling
-
1:CAS:528:DC%2BD28XhtVSkt7rL 16949368
-
Ishihara K, Oshimura M, Nakao M. CTCF-dependent chromatin insulator is linked to epigenetic remodeling. Mol Cell. 2006;23(5):733-42.
-
(2006)
Mol Cell
, vol.23
, Issue.5
, pp. 733-742
-
-
Ishihara, K.1
Oshimura, M.2
Nakao, M.3
-
27
-
-
84924567722
-
The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment
-
1:CAS:528:DC%2BC2MXosVCrsL4%3D 25752243 4355952
-
Cotney J, Muhle RA, Sanders SJ, Liu L, Willsey AJ, Niu W, Liu W, Klei L, Lei J, Yin J, Reilly SK, Tebbenkamp AT, Bichsel C, Pletikos M, Sestan N, Roeder K, State MW, Devlin B, Noonan JP. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment. Nat Commun. 2015;6:6404.
-
(2015)
Nat Commun
, vol.6
, pp. 6404
-
-
Cotney, J.1
Muhle, R.A.2
Sanders, S.J.3
Liu, L.4
Willsey, A.J.5
Niu, W.6
Liu, W.7
Klei, L.8
Lei, J.9
Yin, J.10
Reilly, S.K.11
Tebbenkamp, A.T.12
Bichsel, C.13
Pletikos, M.14
Sestan, N.15
Roeder, K.16
State, M.W.17
Devlin, B.18
Noonan, J.P.19
-
28
-
-
84908065133
-
CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors
-
1:CAS:528:DC%2BC2cXhslSrt73P 25294932 4210312
-
Sugathan A, Biagioli M, Golzio C, Erdin S, Blumenthal I, Manavalan P, Ragavendran A, Brand H, Lucente D, Miles J, Sheridan SD, Stortchevoi A, Kellis M, Haggarty SJ, Katsanis N, Gusella JF, Talkowski ME. CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors. Proc Natl Acad Sci U S A. 2014;111(42):E4468-77.
-
(2014)
Proc Natl Acad Sci U S A
, vol.111
, Issue.42
, pp. E4468-E4477
-
-
Sugathan, A.1
Biagioli, M.2
Golzio, C.3
Erdin, S.4
Blumenthal, I.5
Manavalan, P.6
Ragavendran, A.7
Brand, H.8
Lucente, D.9
Miles, J.10
Sheridan, S.D.11
Stortchevoi, A.12
Kellis, M.13
Haggarty, S.J.14
Katsanis, N.15
Gusella, J.F.16
Talkowski, M.E.17
-
29
-
-
84990990192
-
The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes
-
1:CAS:528:DC%2BC2MXotVeqt7w%3D 25989142 4471293
-
Wilkinson B, Grepo N, Thompson BL, Kim J, Wang K, Evgrafov OV, Lu W, Knowles JA, Campbell DB. The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes. Transl Psychiatry. 2015;5:e568.
-
(2015)
Transl Psychiatry
, vol.5
, pp. e568
-
-
Wilkinson, B.1
Grepo, N.2
Thompson, B.L.3
Kim, J.4
Wang, K.5
Evgrafov, O.V.6
Lu, W.7
Knowles, J.A.8
Campbell, D.B.9
-
30
-
-
84963718872
-
Pathway network analyses for autism reveal multisystem involvement, major overlaps with other diseases and convergence upon MAPK and calcium signaling
-
27055244 4824422 1:CAS:528:DC%2BC28Xht1yksL3N
-
Wen Y, Alshikho MJ, Herbert MR. Pathway network analyses for autism reveal multisystem involvement, major overlaps with other diseases and convergence upon MAPK and calcium signaling. PLoS One. 2016;11(4):e0153329.
-
(2016)
PLoS One
, vol.11
, Issue.4
, pp. e0153329
-
-
Wen, Y.1
Alshikho, M.J.2
Herbert, M.R.3
-
31
-
-
84920646061
-
Genetic risk for schizophrenia: convergence on synaptic pathways involved in plasticity
-
1:CAS:528:DC%2BC2cXhsV2lt7zE 25152434
-
Hall J, Trent S, Thomas KL, O'Donovan MC, Owen MJ. Genetic risk for schizophrenia: convergence on synaptic pathways involved in plasticity. Biol Psychiatry. 2015;77(1):52-8.
-
(2015)
Biol Psychiatry
, vol.77
, Issue.1
, pp. 52-58
-
-
Hall, J.1
Trent, S.2
Thomas, K.L.3
O'Donovan, M.C.4
Owen, M.J.5
-
32
-
-
85027906994
-
O'Donovan MC, Owen M. Genetic risk for schizophrenia: convergence on synaptic pathways involved in plasticity
-
Hall J, Trent S, Thomas KL, O'Donovan MC, Owen M. Genetic risk for schizophrenia: convergence on synaptic pathways involved in plasticity. Biol Psychiatry. 2014.
-
(2014)
Biol Psychiatry
-
-
Hall, J.1
Trent, S.2
Thomas, K.L.3
-
33
-
-
84904804929
-
Biological insights from 108 schizophrenia-associated genetic loci
-
Schizophrenia Working Group of the Psychiatric Genomics Consortium 4112379 1:CAS:528:DC%2BC2cXht1WlurrN
-
Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic loci. Nature. 2014;511(7510):421-7.
-
(2014)
Nature
, vol.511
, Issue.7510
, pp. 421-427
-
-
-
34
-
-
84871270974
-
Validation of schizophrenia-associated genes CSMD1, C10orf26, CACNA1C and TCF4 as miR-137 targets
-
1:CAS:528:DC%2BC38XhvVymsb%2FO 22182936
-
Kwon E, Wang W, Tsai LH. Validation of schizophrenia-associated genes CSMD1, C10orf26, CACNA1C and TCF4 as miR-137 targets. Mol Psychiatry. 2013;18(1):11-2.
-
(2013)
Mol Psychiatry
, vol.18
, Issue.1
, pp. 11-12
-
-
Kwon, E.1
Wang, W.2
Tsai, L.H.3
-
35
-
-
84899918742
-
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
-
1:CAS:528:DC%2BC2cXntVCjsr0%3D 24768552 4067558
-
Pinto D, Delaby E, Merico D, Barbosa M, Merikangas A, Klei L, Thiruvahindrapuram B, Xu X, Ziman R, Wang Z, Vorstman JA, Thompson A, Regan R, Pilorge M, Pellecchia G, Pagnamenta AT, Oliveira B, Marshall CR, Magalhaes TR, Lowe JK, Howe JL, Griswold AJ, Gilbert J, Duketis E, Dombroski BA, De Jonge MV, Cuccaro M, Crawford EL, Correia CT, Conroy J, Conceicao IC, Chiocchetti AG, Casey JP, Cai G, Cabrol C, Bolshakova N, Bacchelli E, Anney R, Gallinger S, Cotterchio M, Casey G, Zwaigenbaum L, Wittemeyer K, Wing K, Wallace S, van Engeland H, Tryfon A, Thomson S, Soorya L, Roge B, Roberts W, Poustka F, Mouga S, Minshew N, McInnes LA, McGrew SG, Lord C, Leboyer M, Le Couteur AS, Kolevzon A, Jimenez Gonzalez P, Jacob S, Holt R, Guter S, Green J, Green A, Gillberg C, Fernandez BA, Duque F, Delorme R, Dawson G, Chaste P, Cafe C, Brennan S, Bourgeron T, Bolton PF, Bolte S, Bernier R, Baird G, Bailey AJ, Anagnostou E, Almeida J, Wijsman EM, Vieland VJ, Vicente AM, Schellenberg GD, Pericak-Vance M, Paterson AD, Parr JR, Oliveira G, Nurnberger JI, Monaco AP, Maestrini E, Klauck SM, Hakonarson H, Haines JL, Geschwind DH, Freitag CM, Folstein SE, Ennis S, Coon H, Battaglia A, Szatmari P, Sutcliffe JS, Hallmayer J, Gill M, Cook EH, Buxbaum JD, Devlin B, Gallagher L, Betancur C, Scherer SW. Convergence of genes and cellular pathways dysregulated in autism spectrum disorders. Am J Hum Genet. 2014;94(5):677-94.
-
(2014)
Am J Hum Genet
, vol.94
, Issue.5
, pp. 677-694
-
-
Pinto, D.1
Delaby, E.2
Merico, D.3
Barbosa, M.4
Merikangas, A.5
Klei, L.6
Thiruvahindrapuram, B.7
Xu, X.8
Ziman, R.9
Wang, Z.10
Vorstman, J.A.11
Thompson, A.12
Regan, R.13
Pilorge, M.14
Pellecchia, G.15
Pagnamenta, A.T.16
Oliveira, B.17
Marshall, C.R.18
Magalhaes, T.R.19
Lowe, J.K.20
Howe, J.L.21
Griswold, A.J.22
Gilbert, J.23
Duketis, E.24
Dombroski, B.A.25
De Jonge, M.V.26
Cuccaro, M.27
Crawford, E.L.28
Correia, C.T.29
Conroy, J.30
Conceicao, I.C.31
Chiocchetti, A.G.32
Casey, J.P.33
Cai, G.34
Cabrol, C.35
Bolshakova, N.36
Bacchelli, E.37
Anney, R.38
Gallinger, S.39
Cotterchio, M.40
Casey, G.41
Zwaigenbaum, L.42
Wittemeyer, K.43
Wing, K.44
Wallace, S.45
Van Engeland, H.46
Tryfon, A.47
Thomson, S.48
Soorya, L.49
Roge, B.50
Roberts, W.51
Poustka, F.52
Mouga, S.53
Minshew, N.54
McInnes, L.A.55
McGrew, S.G.56
Lord, C.57
Leboyer, M.58
Le Couteur, A.S.59
Kolevzon, A.60
Jimenez Gonzalez, P.61
Jacob, S.62
Holt, R.63
Guter, S.64
Green, J.65
Green, A.66
Gillberg, C.67
Fernandez, B.A.68
Duque, F.69
Delorme, R.70
Dawson, G.71
Chaste, P.72
Cafe, C.73
Brennan, S.74
Bourgeron, T.75
Bolton, P.F.76
Bolte, S.77
Bernier, R.78
Baird, G.79
Bailey, A.J.80
Anagnostou, E.81
Almeida, J.82
Wijsman, E.M.83
Vieland, V.J.84
Vicente, A.M.85
Schellenberg, G.D.86
Pericak-Vance, M.87
Paterson, A.D.88
Parr, J.R.89
Oliveira, G.90
Nurnberger, J.I.91
Monaco, A.P.92
Maestrini, E.93
Klauck, S.M.94
Hakonarson, H.95
Haines, J.L.96
Geschwind, D.H.97
Freitag, C.M.98
Folstein, S.E.99
Ennis, S.100
Coon, H.101
Battaglia, A.102
Szatmari, P.103
Sutcliffe, J.S.104
Hallmayer, J.105
Gill, M.106
Cook, E.H.107
Buxbaum, J.D.108
Devlin, B.109
Gallagher, L.110
Betancur, C.111
Scherer, S.W.112
more..
-
36
-
-
84922396236
-
Molecular convergence of neurodevelopmental disorders
-
1:CAS:528:DC%2BC2cXhslelsrbJ 25307298 4225591
-
Chen ES, Gigek CO, Rosenfeld JA, Diallo AB, Maussion G, Chen GG, Vaillancourt K, Lopez JP, Crapper L, Poujol R, Shaffer LG, Bourque G, Ernst C. Molecular convergence of neurodevelopmental disorders. Am J Hum Genet. 2014;95(5):490-508.
-
(2014)
Am J Hum Genet
, vol.95
, Issue.5
, pp. 490-508
-
-
Chen, E.S.1
Gigek, C.O.2
Rosenfeld, J.A.3
Diallo, A.B.4
Maussion, G.5
Chen, G.G.6
Vaillancourt, K.7
Lopez, J.P.8
Crapper, L.9
Poujol, R.10
Shaffer, L.G.11
Bourque, G.12
Ernst, C.13
-
37
-
-
84990937732
-
A molecular model for neurodevelopmental disorders
-
1:CAS:528:DC%2BC2MXotVeqt7s%3D 25966365 4471287
-
Gigek CO, Chen ES, Ota VK, Maussion G, Peng H, Vaillancourt K, Diallo AB, Lopez JP, Crapper L, Vasuta C, Chen GG, Ernst C. A molecular model for neurodevelopmental disorders. Transl Psychiatry. 2015;5:e565.
-
(2015)
Transl Psychiatry
, vol.5
, pp. e565
-
-
Gigek, C.O.1
Chen, E.S.2
Ota, V.K.3
Maussion, G.4
Peng, H.5
Vaillancourt, K.6
Diallo, A.B.7
Lopez, J.P.8
Crapper, L.9
Vasuta, C.10
Chen, G.G.11
Ernst, C.12
-
38
-
-
84882960508
-
Knockdown of human TCF4 affects multiple signaling pathways involved in cell survival, epithelial to mesenchymal transition and neuronal differentiation
-
1:CAS:528:DC%2BC3sXhtl2iu7bF 24058414 3751932
-
Forrest MP, Waite AJ, Martin-Rendon E, Blake DJ. Knockdown of human TCF4 affects multiple signaling pathways involved in cell survival, epithelial to mesenchymal transition and neuronal differentiation. PLoS One. 2013;8(8):e73169.
-
(2013)
PLoS One
, vol.8
, Issue.8
, pp. e73169
-
-
Forrest, M.P.1
Waite, A.J.2
Martin-Rendon, E.3
Blake, D.J.4
-
39
-
-
84899669003
-
Heat shock alters the expression of schizophrenia and autism candidate genes in an induced pluripotent stem cell model of the human telencephalon
-
24736721 3988108 1:CAS:528:DC%2BC2cXhsFemtL%2FK
-
Lin M, Zhao D, Hrabovsky A, Pedrosa E, Zheng D, Lachman HM. Heat shock alters the expression of schizophrenia and autism candidate genes in an induced pluripotent stem cell model of the human telencephalon. PLoS One. 2014;9(4):e94968.
-
(2014)
PLoS One
, vol.9
, Issue.4
, pp. e94968
-
-
Lin, M.1
Zhao, D.2
Hrabovsky, A.3
Pedrosa, E.4
Zheng, D.5
Lachman, H.M.6
-
40
-
-
84864506775
-
Modeling human cortical development in vitro using induced pluripotent stem cells
-
1:CAS:528:DC%2BC38XhtlelsbfE 22761314 3411972
-
Mariani J, Simonini MV, Palejev D, Tomasini L, Coppola G, Szekely AM, Horvath TL, Vaccarino FM. Modeling human cortical development in vitro using induced pluripotent stem cells. Proc Natl Acad Sci U S A. 2012;109(31):12770-5.
-
(2012)
Proc Natl Acad Sci U S A
, vol.109
, Issue.31
, pp. 12770-12775
-
-
Mariani, J.1
Simonini, M.V.2
Palejev, D.3
Tomasini, L.4
Coppola, G.5
Szekely, A.M.6
Horvath, T.L.7
Vaccarino, F.M.8
-
41
-
-
84884414984
-
Cerebral organoids model human brain development and microcephaly
-
1:CAS:528:DC%2BC3sXhtlCntb3F 23995685
-
Lancaster MA, Renner M, Martin CA, Wenzel D, Bicknell LS, Hurles ME, Homfray T, Penninger JM, Jackson AP, Knoblich JA. Cerebral organoids model human brain development and microcephaly. Nature. 2013;501(7467):373-9.
-
(2013)
Nature
, vol.501
, Issue.7467
, pp. 373-379
-
-
Lancaster, M.A.1
Renner, M.2
Martin, C.A.3
Wenzel, D.4
Bicknell, L.S.5
Hurles, M.E.6
Homfray, T.7
Penninger, J.M.8
Jackson, A.P.9
Knoblich, J.A.10
-
42
-
-
84937212591
-
FOXG1-dependent dysregulation of GABA/glutamate neuron differentiation in autism spectrum disorders
-
1:CAS:528:DC%2BC2MXht1KgtLrN 26186191 4519016
-
Mariani J, Coppola G, Zhang P, Abyzov A, Provini L, Tomasini L, Amenduni M, Szekely A, Palejev D, Wilson M, Gerstein M, Grigorenko EL, Chawarska K, Pelphrey KA, Howe JR, Vaccarino FM. FOXG1-dependent dysregulation of GABA/glutamate neuron differentiation in autism spectrum disorders. Cell. 2015;162(2):375-90.
-
(2015)
Cell
, vol.162
, Issue.2
, pp. 375-390
-
-
Mariani, J.1
Coppola, G.2
Zhang, P.3
Abyzov, A.4
Provini, L.5
Tomasini, L.6
Amenduni, M.7
Szekely, A.8
Palejev, D.9
Wilson, M.10
Gerstein, M.11
Grigorenko, E.L.12
Chawarska, K.13
Pelphrey, K.A.14
Howe, J.R.15
Vaccarino, F.M.16
-
43
-
-
84885579222
-
Evf2 (Dlx6as) lncRNA regulates ultraconserved enhancer methylation and the differential transcriptional control of adjacent genes
-
1:CAS:528:DC%2BC3sXhvV2itL3N 24089468 4007716
-
Berghoff EG, Clark MF, Chen S, Cajigas I, Leib DE, Kohtz JD. Evf2 (Dlx6as) lncRNA regulates ultraconserved enhancer methylation and the differential transcriptional control of adjacent genes. Development. 2013;140(21):4407-16.
-
(2013)
Development
, vol.140
, Issue.21
, pp. 4407-4416
-
-
Berghoff, E.G.1
Clark, M.F.2
Chen, S.3
Cajigas, I.4
Leib, D.E.5
Kohtz, J.D.6
-
44
-
-
84940780822
-
MicroRNA profiling of neurons generated using induced pluripotent stem cells derived from patients with schizophrenia and schizoaffective disorder, and 22q11.2 Del
-
26173148 4501820 1:CAS:528:DC%2BC2MXhsVemu7fI
-
Zhao D, Lin M, Chen J, Pedrosa E, Hrabovsky A, Fourcade HM, Zheng D, Lachman HM. MicroRNA profiling of neurons generated using induced pluripotent stem cells derived from patients with schizophrenia and schizoaffective disorder, and 22q11.2 Del. PLoS One. 2015;10(7):e0132387.
-
(2015)
PLoS One
, vol.10
, Issue.7
, pp. e0132387
-
-
Zhao, D.1
Lin, M.2
Chen, J.3
Pedrosa, E.4
Hrabovsky, A.5
Fourcade, H.M.6
Zheng, D.7
Lachman, H.M.8
-
45
-
-
84952674076
-
Human cerebral organoids recapitulate gene expression programs of fetal neocortex development
-
1:CAS:528:DC%2BC2MXhvFKqsLfO 26644564 4697386
-
Camp JG, Badsha F, Florio M, Kanton S, Gerber T, Wilsch-Brauninger M, Lewitus E, Sykes A, Hevers W, Lancaster M, Knoblich JA, Lachmann R, Paabo S, Huttner WB, Treutlein B. Human cerebral organoids recapitulate gene expression programs of fetal neocortex development. Proc Natl Acad Sci U S A. 2015;112(51):15672-7.
-
(2015)
Proc Natl Acad Sci U S A
, vol.112
, Issue.51
, pp. 15672-15677
-
-
Camp, J.G.1
Badsha, F.2
Florio, M.3
Kanton, S.4
Gerber, T.5
Wilsch-Brauninger, M.6
Lewitus, E.7
Sykes, A.8
Hevers, W.9
Lancaster, M.10
Knoblich, J.A.11
Lachmann, R.12
Paabo, S.13
Huttner, W.B.14
Treutlein, B.15
-
46
-
-
84966283954
-
Near-optimal probabilistic RNA-seq quantification
-
1:CAS:528:DC%2BC28XlsVansL8%3D 27043002
-
Bray NL, Pimentel H, Melsted P, Pachter L. Near-optimal probabilistic RNA-seq quantification. Nat Biotechnol. 2016;34(5):525-7.
-
(2016)
Nat Biotechnol
, vol.34
, Issue.5
, pp. 525-527
-
-
Bray, N.L.1
Pimentel, H.2
Melsted, P.3
Pachter, L.4
-
47
-
-
84865760395
-
GENCODE: the reference human genome annotation for The ENCODE Project
-
1:CAS:528:DC%2BC38XhtlentLvN 22955987 3431492
-
Harrow J, Frankish A, Gonzalez JM, Tapanari E, Diekhans M, Kokocinski F, Aken BL, Barrell D, Zadissa A, Searle S, Barnes I, Bignell A, Boychenko V, Hunt T, Kay M, Mukherjee G, Rajan J, Despacio-Reyes G, Saunders G, Steward C, Harte R, Lin M, Howald C, Tanzer A, Derrien T, Chrast J, Walters N, Balasubramanian S, Pei B, Tress M, Rodriguez JM, Ezkurdia I, van Baren J, Brent M, Haussler D, Kellis M, Valencia A, Reymond A, Gerstein M, Guigo R, Hubbard TJ. GENCODE: the reference human genome annotation for The ENCODE Project. Genome Res. 2012;22(9):1760.
-
(2012)
Genome Res
, vol.22
, Issue.9
, pp. 1760
-
-
Harrow, J.1
Frankish, A.2
Gonzalez, J.M.3
Tapanari, E.4
Diekhans, M.5
Kokocinski, F.6
Aken, B.L.7
Barrell, D.8
Zadissa, A.9
Searle, S.10
Barnes, I.11
Bignell, A.12
Boychenko, V.13
Hunt, T.14
Kay, M.15
Mukherjee, G.16
Rajan, J.17
Despacio-Reyes, G.18
Saunders, G.19
Steward, C.20
Harte, R.21
Lin, M.22
Howald, C.23
Tanzer, A.24
Derrien, T.25
Chrast, J.26
Walters, N.27
Balasubramanian, S.28
Pei, B.29
Tress, M.30
Rodriguez, J.M.31
Ezkurdia, I.32
Van Baren, J.33
Brent, M.34
Haussler, D.35
Kellis, M.36
Valencia, A.37
Reymond, A.38
Gerstein, M.39
Guigo, R.40
Hubbard, T.J.41
more..
-
48
-
-
84924629414
-
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
-
25516281 4302049 1:CAS:528:DC%2BC2MXjtVCrsL8%3D
-
Love MI, Huber W, Anders S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014;15(12):550.
-
(2014)
Genome Biol
, vol.15
, Issue.12
, pp. 550
-
-
Love, M.I.1
Huber, W.2
Anders, S.3
-
49
-
-
61449172037
-
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
-
1:CAS:528:DC%2BD1cXhsFCkurnI
-
da Huang W, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc. 2009;4(1):44-57.
-
(2009)
Nat Protoc
, vol.4
, Issue.1
, pp. 44-57
-
-
Da Huang, W.1
Sherman, B.T.2
Lempicki, R.A.3
-
50
-
-
58549112996
-
Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists
-
1:CAS:528:DC%2BD1MXktlenuw%3D%3D
-
da Huang W, Sherman BT, Lempicki RA. Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists. Nucleic Acids Res. 2009;37(1):1-13.
-
(2009)
Nucleic Acids Res
, vol.37
, Issue.1
, pp. 1-13
-
-
Da Huang, W.1
Sherman, B.T.2
Lempicki, R.A.3
-
51
-
-
84928398433
-
ZNF804A transcriptional networks in differentiating neurons derived from induced pluripotent stem cells of human origin
-
25905630 4408091 1:CAS:528:DC%2BC28Xot1WltL8%3D
-
Chen J, Lin M, Hrabovsky A, Pedrosa E, Dean J, Jain S, Zheng D, Lachman HM. ZNF804A transcriptional networks in differentiating neurons derived from induced pluripotent stem cells of human origin. PLoS One. 2015;10(4):e0124597.
-
(2015)
PLoS One
, vol.10
, Issue.4
, pp. e0124597
-
-
Chen, J.1
Lin, M.2
Hrabovsky, A.3
Pedrosa, E.4
Dean, J.5
Jain, S.6
Zheng, D.7
Lachman, H.M.8
-
52
-
-
84884826708
-
Transcriptome comparison of human neurons generated using induced pluripotent stem cells derived from dental pulp and skin fibroblasts
-
1:CAS:528:DC%2BC3sXhsF2ku7zJ 24098394 3789755
-
Chen J, Lin M, Foxe JJ, Pedrosa E, Hrabovsky A, Carroll R, Zheng D, Lachman HM. Transcriptome comparison of human neurons generated using induced pluripotent stem cells derived from dental pulp and skin fibroblasts. PLoS One. 2013;8(10):e75682.
-
(2013)
PLoS One
, vol.8
, Issue.10
, pp. e75682
-
-
Chen, J.1
Lin, M.2
Foxe, J.J.3
Pedrosa, E.4
Hrabovsky, A.5
Carroll, R.6
Zheng, D.7
Lachman, H.M.8
-
53
-
-
84862224852
-
AutismKB: an evidence-based knowledgebase of autism genetics
-
1:CAS:528:DC%2BC3MXhs12htbnM 22139918
-
Xu LM, Li JR, Huang Y, Zhao M, Tang X, Wei L. AutismKB: an evidence-based knowledgebase of autism genetics. Nucleic Acids Res. 2012;40(Database issue):D1016-22.
-
(2012)
Nucleic Acids Res
, vol.40
, Issue.Database issue
, pp. D1016-D1022
-
-
Xu, L.M.1
Li, J.R.2
Huang, Y.3
Zhao, M.4
Tang, X.5
Wei, L.6
-
54
-
-
84889583293
-
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism
-
1:CAS:528:DC%2BC3sXhvFWis7zP 24267886 3995413
-
Willsey AJ, Sanders SJ, Li M, Dong S, Tebbenkamp AT, Muhle RA, Reilly SK, Lin L, Fertuzinhos S, Miller JA, Murtha MT, Bichsel C, Niu W, Cotney J, Ercan-Sencicek AG, Gockley J, Gupta AR, Han W, He X, Hoffman EJ, Klei L, Lei J, Liu W, Liu L, Lu C, Xu X, Zhu Y, Mane SM, Lein ES, Wei L, Noonan JP, Roeder K, Devlin B, Sestan N, State MW. Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell. 2013;155(5):997-1007.
-
(2013)
Cell
, vol.155
, Issue.5
, pp. 997-1007
-
-
Willsey, A.J.1
Sanders, S.J.2
Li, M.3
Dong, S.4
Tebbenkamp, A.T.5
Muhle, R.A.6
Reilly, S.K.7
Lin, L.8
Fertuzinhos, S.9
Miller, J.A.10
Murtha, M.T.11
Bichsel, C.12
Niu, W.13
Cotney, J.14
Ercan-Sencicek, A.G.15
Gockley, J.16
Gupta, A.R.17
Han, W.18
He, X.19
Hoffman, E.J.20
Klei, L.21
Lei, J.22
Liu, W.23
Liu, L.24
Lu, C.25
Xu, X.26
Zhu, Y.27
Mane, S.M.28
Lein, E.S.29
Wei, L.30
Noonan, J.P.31
Roeder, K.32
Devlin, B.33
Sestan, N.34
State, M.W.35
more..
-
55
-
-
84899472749
-
DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics
-
24602502 4016412 1:CAS:528:DC%2BC2MXivVWltLY%3D-2392-5-22
-
Liu L, Lei J, Sanders SJ, Willsey AJ, Kou Y, Cicek AE, Klei L, Lu C, He X, Li M, Muhle RA, Ma'ayan A, Noonan JP, Sestan N, McFadden KA, State MW, Buxbaum JD, Devlin B, Roeder K. DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics. Mol Autism. 2014;5(1):22. -2392-5-22.
-
(2014)
Mol Autism
, vol.5
, Issue.1
, pp. 22
-
-
Liu, L.1
Lei, J.2
Sanders, S.J.3
Willsey, A.J.4
Kou, Y.5
Cicek, A.E.6
Klei, L.7
Lu, C.8
He, X.9
Li, M.10
Muhle, R.A.11
Ma'ayan, A.12
Noonan, J.P.13
Sestan, N.14
McFadden, K.A.15
State, M.W.16
Buxbaum, J.D.17
Devlin, B.18
Roeder, K.19
-
56
-
-
84912101541
-
The contribution of de novo coding mutations to autism spectrum disorder
-
1:CAS:528:DC%2BC2cXhvVemtrnN 25363768 4313871
-
Iossifov I, O'Roak BJ, Sanders SJ, Ronemus M, Krumm N, Levy D, Stessman HA, Witherspoon KT, Vives L, Patterson KE, Smith JD, Paeper B, Nickerson DA, Dea J, Dong S, Gonzalez LE, Mandell JD, Mane SM, Murtha MT, Sullivan CA, Walker MF, Waqar Z, Wei L, Willsey AJ, Yamrom B, Lee YH, Grabowska E, Dalkic E, Wang Z, Marks S, Andrews P, Leotta A, Kendall J, Hakker I, Rosenbaum J, Ma B, Rodgers L, Troge J, Narzisi G, Yoon S, Schatz MC, Ye K, McCombie WR, Shendure J, Eichler EE, State MW, Wigler M. The contribution of de novo coding mutations to autism spectrum disorder. Nature. 2014;515(7526):216-21.
-
(2014)
Nature
, vol.515
, Issue.7526
, pp. 216-221
-
-
Iossifov, I.1
O'Roak, B.J.2
Sanders, S.J.3
Ronemus, M.4
Krumm, N.5
Levy, D.6
Stessman, H.A.7
Witherspoon, K.T.8
Vives, L.9
Patterson, K.E.10
Smith, J.D.11
Paeper, B.12
Nickerson, D.A.13
Dea, J.14
Dong, S.15
Gonzalez, L.E.16
Mandell, J.D.17
Mane, S.M.18
Murtha, M.T.19
Sullivan, C.A.20
Walker, M.F.21
Waqar, Z.22
Wei, L.23
Willsey, A.J.24
Yamrom, B.25
Lee, Y.H.26
Grabowska, E.27
Dalkic, E.28
Wang, Z.29
Marks, S.30
Andrews, P.31
Leotta, A.32
Kendall, J.33
Hakker, I.34
Rosenbaum, J.35
Ma, B.36
Rodgers, L.37
Troge, J.38
Narzisi, G.39
Yoon, S.40
Schatz, M.C.41
Ye, K.42
McCombie, W.R.43
Shendure, J.44
Eichler, E.E.45
State, M.W.46
Wigler, M.47
more..
-
57
-
-
84912144889
-
Synaptic, transcriptional and chromatin genes disrupted in autism
-
DDD Study Homozygosity Mapping Collaborative for Autism UK10K Consortium 25363760 4402723 1:CAS:528:DC%2BC2cXhvVemtrnJ
-
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, Biscaldi M, Bolton PF, Brownfeld JM, Cai J, Campbell NG, Carracedo A, Chahrour MH, Chiocchetti AG, Coon H, Crawford EL, Curran SR, Dawson G, Duketis E, Fernandez BA, Gallagher L, Geller E, Guter SJ, Hill RS, Ionita-Laza J, Jimenz Gonzalez P, Kilpinen H, Klauck SM, Kolevzon A, Lee I, Lei I, Lei J, Lehtimaki T, Lin CF, Ma'ayan A, Marshall CR, McInnes AL, Neale B, Owen MJ, Ozaki N, Parellada M, Parr JR, Purcell S, Puura K, Rajagopalan D, Rehnstrom K, Reichenberg A, Sabo A, Sachse M, Sanders SJ, Schafer C, Schulte-Ruther M, Skuse D, Stevens C, Szatmari P, Tammimies K, Valladares O, Voran A, Li-San W, Weiss LA, Willsey AJ, Yu TW, Yuen RK, DDD Study, Homozygosity Mapping Collaborative for Autism, UK10K Consortium, Cook EH, Freitag CM, Gill M, Hultman CM, Lehner T, Palotie A, Schellenberg GD, Sklar P, State MW, Sutcliffe JS, Walsh CA, Scherer SW, Zwick ME, Barett JC, Cutler DJ, Roeder K, Devlin B, Daly MJ, Buxbaum JD. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 2014;515(7526):209-15.
-
(2014)
Nature
, vol.515
, Issue.7526
, pp. 209-215
-
-
De Rubeis, S.1
He, X.2
Goldberg, A.P.3
Poultney, C.S.4
Samocha, K.5
Cicek, A.E.6
Kou, Y.7
Liu, L.8
Fromer, M.9
Walker, S.10
Singh, T.11
Klei, L.12
Kosmicki, J.13
Shih-Chen, F.14
Aleksic, B.15
Biscaldi, M.16
Bolton, P.F.17
Brownfeld, J.M.18
Cai, J.19
Campbell, N.G.20
Carracedo, A.21
Chahrour, M.H.22
Chiocchetti, A.G.23
Coon, H.24
Crawford, E.L.25
Curran, S.R.26
Dawson, G.27
Duketis, E.28
Fernandez, B.A.29
Gallagher, L.30
Geller, E.31
Guter, S.J.32
Hill, R.S.33
Ionita-Laza, J.34
Jimenz Gonzalez, P.35
Kilpinen, H.36
Klauck, S.M.37
Kolevzon, A.38
Lee, I.39
Lei, I.40
Lei, J.41
Lehtimaki, T.42
Lin, C.F.43
Ma'ayan, A.44
Marshall, C.R.45
McInnes, A.L.46
Neale, B.47
Owen, M.J.48
Ozaki, N.49
Parellada, M.50
Parr, J.R.51
Purcell, S.52
Puura, K.53
Rajagopalan, D.54
Rehnstrom, K.55
Reichenberg, A.56
Sabo, A.57
Sachse, M.58
Sanders, S.J.59
Schafer, C.60
Schulte-Ruther, M.61
Skuse, D.62
Stevens, C.63
Szatmari, P.64
Tammimies, K.65
Valladares, O.66
Voran, A.67
Li-San, W.68
Weiss, L.A.69
Willsey, A.J.70
Yu, T.W.71
Yuen, R.K.72
Cook, E.H.73
Freitag, C.M.74
Gill, M.75
Hultman, C.M.76
Lehner, T.77
Palotie, A.78
Schellenberg, G.D.79
Sklar, P.80
State, M.W.81
Sutcliffe, J.S.82
Walsh, C.A.83
Scherer, S.W.84
Zwick, M.E.85
Barett, J.C.86
Cutler, D.J.87
Roeder, K.88
Devlin, B.89
Daly, M.J.90
Buxbaum, J.D.91
more..
-
58
-
-
46249104490
-
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database
-
1:CAS:528:DC%2BD1cXnslKku7w%3D 18583979
-
Allen NC, Bagade S, McQueen MB, Ioannidis JP, Kavvoura FK, Khoury MJ, Tanzi RE, Bertram L. Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database. Nat Genet. 2008;40(7):827-34.
-
(2008)
Nat Genet
, vol.40
, Issue.7
, pp. 827-834
-
-
Allen, N.C.1
Bagade, S.2
McQueen, M.B.3
Ioannidis, J.P.4
Kavvoura, F.K.5
Khoury, M.J.6
Tanzi, R.E.7
Bertram, L.8
-
59
-
-
84946239187
-
Differential responses to lithium in hyperexcitable neurons from patients with bipolar disorder
-
Pharmacogenomics of Bipolar Disorder Study 1:CAS:528:DC%2BC2MXhslynurrL 26524527 4742055
-
Mertens J, Wang QW, Kim Y, Yu DX, Pham S, Yang B, Zheng Y, Diffenderfer KE, Zhang J, Soltani S, Eames T, Schafer ST, Boyer L, Marchetto MC, Nurnberger JI, Calabrese JR, Odegaard KJ, McCarthy MJ, Zandi PP, Alba M, Nievergelt CM, Pharmacogenomics of Bipolar Disorder Study, Mi S, Brennand KJ, Kelsoe JR, Gage FH, Yao J. Differential responses to lithium in hyperexcitable neurons from patients with bipolar disorder. Nature. 2015;527(7576):95-9.
-
(2015)
Nature
, vol.527
, Issue.7576
, pp. 95-99
-
-
Mertens, J.1
Wang, Q.W.2
Kim, Y.3
Yu, D.X.4
Pham, S.5
Yang, B.6
Zheng, Y.7
Diffenderfer, K.E.8
Zhang, J.9
Soltani, S.10
Eames, T.11
Schafer, S.T.12
Boyer, L.13
Marchetto, M.C.14
Nurnberger, J.I.15
Calabrese, J.R.16
Odegaard, K.J.17
McCarthy, M.J.18
Zandi, P.P.19
Alba, M.20
Nievergelt, C.M.21
Mi, S.22
Brennand, K.J.23
Kelsoe, J.R.24
Gage, F.H.25
Yao, J.26
more..
-
60
-
-
71149108056
-
Correlation of mRNA and protein in complex biological samples
-
1:CAS:528:DC%2BD1MXhsFams7bJ 19850042
-
Maier T, Guell M, Serrano L. Correlation of mRNA and protein in complex biological samples. FEBS Lett. 2009;583(24):3966-73.
-
(2009)
FEBS Lett
, vol.583
, Issue.24
, pp. 3966-3973
-
-
Maier, T.1
Guell, M.2
Serrano, L.3
-
61
-
-
53949085577
-
Progressive loss of PAX6, TBR2, NEUROD and TBR1 mRNA gradients correlates with translocation of EMX2 to the cortical plate during human cortical development
-
18973570 2675014
-
Bayatti N, Sarma S, Shaw C, Eyre JA, Vouyiouklis DA, Lindsay S, Clowry GJ. Progressive loss of PAX6, TBR2, NEUROD and TBR1 mRNA gradients correlates with translocation of EMX2 to the cortical plate during human cortical development. Eur J Neurosci. 2008;28(8):1449-56.
-
(2008)
Eur J Neurosci
, vol.28
, Issue.8
, pp. 1449-1456
-
-
Bayatti, N.1
Sarma, S.2
Shaw, C.3
Eyre, J.A.4
Vouyiouklis, D.A.5
Lindsay, S.6
Clowry, G.J.7
-
62
-
-
68449090594
-
Common variants conferring risk of schizophrenia
-
Stefansson H, Ophoff RA, Steinberg S, Andreassen OA, Cichon S, Rujescu D, Werge T, Pietilainen OP, Mors O, Mortensen PB, Sigurdsson E, Gustafsson O, Nyegaard M, Tuulio-Henriksson A, Ingason A, Hansen T, Suvisaari J, Lonnqvist J, Paunio T, Borglum AD, Hartmann A, Fink-Jensen A, Nordentoft M, Hougaard D, Norgaard-Pedersen B, Bottcher Y, Olesen J, Breuer R, Moller HJ, Giegling I, Rasmussen HB, Timm S, Mattheisen M, Bitter I, Rethelyi JM, Magnusdottir BB, Sigmundsson T, Olason P, Masson G, Gulcher JR, Haraldsson M, Fossdal R, Thorgeirsson TE, Thorsteinsdottir U, Ruggeri M, Tosato S, Franke B, Strengman E, Kiemeney LA, Group, Melle I, Djurovic S, Abramova L, Kaleda V, Sanjuan J, de Frutos R, Bramon E, Vassos E, Fraser G, Ettinger U, Picchioni M, Walker N, Toulopoulou T, Need AC, Ge D, Lim Yoon J, Shianna KV, Freimer NB, Cantor RM, Murray R, Kong A, Golimbet V, Carracedo A, Arango C, Costas J, Jonsson EG, Terenius L, Agartz I, Petursson H, Nothen MM, Rietschel M, Matthews PM, Muglia P, Peltonen L, St Clair D, Goldstein DB, Stefansson K, Collier DA, Genetic Risk and Outcome in Psychosis (GROUP), Kahn RS, Linszen DH, van Os J, Wiersma D, Bruggeman R, Cahn W, de Haan L, Krabbendam L, Myin-Germeys I. Common variants conferring risk of schizophrenia. Nature. 2009;460(7256):744-7.
-
(2009)
Nature
, vol.460
, Issue.7256
, pp. 744-747
-
-
Stefansson, H.1
Ophoff, R.A.2
Steinberg, S.3
Andreassen, O.A.4
Cichon, S.5
Rujescu, D.6
Werge, T.7
Pietilainen, O.P.8
Mors, O.9
Mortensen, P.B.10
Sigurdsson, E.11
Gustafsson, O.12
Nyegaard, M.13
Tuulio-Henriksson, A.14
Ingason, A.15
Hansen, T.16
Suvisaari, J.17
Lonnqvist, J.18
Paunio, T.19
Borglum, A.D.20
Hartmann, A.21
Fink-Jensen, A.22
Nordentoft, M.23
Hougaard, D.24
Norgaard-Pedersen, B.25
Bottcher, Y.26
Olesen, J.27
Breuer, R.28
Moller, H.J.29
Giegling, I.30
Rasmussen, H.B.31
Timm, S.32
Mattheisen, M.33
Bitter, I.34
Rethelyi, J.M.35
Magnusdottir, B.B.36
Sigmundsson, T.37
Olason, P.38
Masson, G.39
Gulcher, J.R.40
Haraldsson, M.41
Fossdal, R.42
Thorgeirsson, T.E.43
Thorsteinsdottir, U.44
Ruggeri, M.45
Tosato, S.46
Franke, B.47
Strengman, E.48
Kiemeney, L.A.49
Group Melle, I.50
Djurovic, S.51
Abramova, L.52
Kaleda, V.53
Sanjuan, J.54
more..
-
63
-
-
85015449680
-
-
The International Schizophrenia Consortium, Corvin A: Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Mol Psychiatry.
-
O'Dushlaine C, Kenny E, Heron E, Donohoe G, Gill M, Morris D. The International Schizophrenia Consortium, Corvin A: Molecular pathways involved in neuronal cell adhesion and membrane scaffolding contribute to schizophrenia and bipolar disorder susceptibility. Mol Psychiatry. 2010.
-
(2010)
-
-
O'Dushlaine, C.1
Kenny, E.2
Heron, E.3
Donohoe, G.4
Gill, M.5
Morris, D.6
-
64
-
-
78149301263
-
Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2
-
21048216 3065863 1:CAS:528:DC%2BC3cXhsVahs7vE
-
Scott-Van Zeeland AA, Abrahams BS, Alvarez-Retuerto AI, Sonnenblick LI, Rudie JD, Ghahremani D, Mumford JA, Poldrack RA, Dapretto M, Geschwind DH, Bookheimer SY. Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2. Sci Transl Med. 2010;2(56):56ra80.
-
(2010)
Sci Transl Med
, vol.2
, Issue.56
, pp. 56ra80
-
-
Scott-Van Zeeland, A.A.1
Abrahams, B.S.2
Alvarez-Retuerto, A.I.3
Sonnenblick, L.I.4
Rudie, J.D.5
Ghahremani, D.6
Mumford, J.A.7
Poldrack, R.A.8
Dapretto, M.9
Geschwind, D.H.10
Bookheimer, S.Y.11
-
65
-
-
38749140677
-
Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene
-
1:CAS:528:DC%2BD1cXhsFOksL8%3D 18179893 2253955
-
Alarcon M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH. Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. Am J Hum Genet. 2008;82(1):150-9.
-
(2008)
Am J Hum Genet
, vol.82
, Issue.1
, pp. 150-159
-
-
Alarcon, M.1
Abrahams, B.S.2
Stone, J.L.3
Duvall, J.A.4
Perederiy, J.V.5
Bomar, J.M.6
Sebat, J.7
Wigler, M.8
Martin, C.L.9
Ledbetter, D.H.10
Nelson, S.F.11
Cantor, R.M.12
Geschwind, D.H.13
-
66
-
-
38749096303
-
A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism
-
1:CAS:528:DC%2BD1cXhsFOksLw%3D 18179894 2253968
-
Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. Am J Hum Genet. 2008;82(1):160-4.
-
(2008)
Am J Hum Genet
, vol.82
, Issue.1
, pp. 160-164
-
-
Arking, D.E.1
Cutler, D.J.2
Brune, C.W.3
Teslovich, T.M.4
West, K.5
Ikeda, M.6
Rea, A.7
Guy, M.8
Lin, S.9
Cook, E.H.10
Chakravarti, A.11
-
67
-
-
39449121016
-
CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy
-
1:CAS:528:DC%2BD1cXitVKnsrk%3D 17646849
-
Friedman JI, Vrijenhoek T, Markx S, Janssen IM, van der Vliet WA, Faas BH, Knoers NV, Cahn W, Kahn RS, Edelmann L, Davis KL, Silverman JM, Brunner HG, van Kessel AG, Wijmenga C, Ophoff RA, Veltman JA. CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy. Mol Psychiatry. 2008;13(3):261-6.
-
(2008)
Mol Psychiatry
, vol.13
, Issue.3
, pp. 261-266
-
-
Friedman, J.I.1
Vrijenhoek, T.2
Markx, S.3
Janssen, I.M.4
Van der Vliet, W.A.5
Faas, B.H.6
Knoers, N.V.7
Cahn, W.8
Kahn, R.S.9
Edelmann, L.10
Davis, K.L.11
Silverman, J.M.12
Brunner, H.G.13
Van Kessel, A.G.14
Wijmenga, C.15
Ophoff, R.A.16
Veltman, J.A.17
-
68
-
-
84860351742
-
Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium: Identification of common variants associated with human hippocampal and intracranial volumes
-
Alzheimer's Disease Neuroimaging Initiative, EPIGEN Consortium, IMAGEN Consortium, Saguenay Youth Study Group Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium 1:CAS:528:DC%2BC38XlsFSqu7k%3D 22504417 3635491
-
Stein JL, Medland SE, Vasquez AA, Hibar DP, Senstad RE, Winkler AM, Toro R, Appel K, Bartecek R, Bergmann O, Bernard M, Brown AA, Cannon DM, Chakravarty MM, Christoforou A, Domin M, Grimm O, Hollinshead M, Holmes AJ, Homuth G, Hottenga JJ, Langan C, Lopez LM, Hansell NK, Hwang KS, Kim S, Laje G, Lee PH, Liu X, Loth E, Lourdusamy A, Mattingsdal M, Mohnke S, Maniega SM, Nho K, Nugent AC, O'Brien C, Papmeyer M, Putz B, Ramasamy A, Rasmussen J, Rijpkema M, Risacher SL, Roddey JC, Rose EJ, Ryten M, Shen L, Sprooten E, Strengman E, Teumer A, Trabzuni D, Turner J, van Eijk K, van Erp TG, van Tol MJ, Wittfeld K, Wolf C, Woudstra S, Aleman A, Alhusaini S, Almasy L, Binder EB, Brohawn DG, Cantor RM, Carless MA, Corvin A, Czisch M, Curran JE, Davies G, de Almeida MA, Delanty N, Depondt C, Duggirala R, Dyer TD, Erk S, Fagerness J, Fox PT, Freimer NB, Gill M, Goring HH, Hagler DJ, Hoehn D, Holsboer F, Hoogman M, Hosten N, Jahanshad N, Johnson MP, Kasperaviciute D, Kent Jr JW, Kochunov P, Lancaster JL, Lawrie SM, Liewald DC, Mandl R, Matarin M, Mattheisen M, Meisenzahl E, Melle I, Moses EK, Muhleisen TW, Nauck M, Nothen MM, Olvera RL, Pandolfo M, Pike GB, Puls R, Reinvang I, Renteria ME, Rietschel M, Roffman JL, Royle NA, Rujescu D, Savitz J, Schnack HG, Schnell K, Seiferth N, Smith C, Steen VM, Valdes Hernandez MC, Van den Heuvel M, van der Wee NJ, Van Haren NE, Veltman JA, Volzke H, Walker R, Westlye LT, Whelan CD, Agartz I, Boomsma DI, Cavalleri GL, Dale AM, Djurovic S, Drevets WC, Hagoort P, Hall J, Heinz A, Jack Jr CR, Foroud TM, Le Hellard S, Macciardi F, Montgomery GW, Poline JB, Porteous DJ, Sisodiya SM, Starr JM, Sussmann J, Toga AW, Veltman DJ, Walter H, Weiner MW, Alzheimer’s Disease Neuroimaging Initiative, EPIGEN Consortium, IMAGEN Consortium, Saguenay Youth Study Group, Bis JC, Ikram MA, Smith AV, Gudnason V, Tzourio C, Vernooij MW, Launer LJ, DeCarli C, Seshadri S, Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium, Andreassen OA, Apostolova LG, Bastin ME, Blangero J, Brunner HG, Buckner RL, Cichon S, Coppola G, de Zubicaray GI, Deary IJ, Donohoe G, de Geus EJ, Espeseth T, Fernandez G, Glahn DC, Grabe HJ, Hardy J, Hulshoff Pol HE, Jenkinson M, Kahn RS, McDonald C, McIntosh AM, McMahon FJ, McMahon KL, Meyer-Lindenberg A, Morris DW, Muller-Myhsok B, Nichols TE, Ophoff RA, Paus T, Pausova Z, Penninx BW, Potkin SG, Samann PG, Saykin AJ, Schumann G, Smoller JW, Wardlaw JM, Weale ME, Martin NG, Franke B, Wright MJ, Thompson PM. Enhancing Neuro Imaging Genetics through Meta-Analysis Consortium: Identification of common variants associated with human hippocampal and intracranial volumes. Nat Genet. 2012;44(5):552-61.
-
(2012)
Nat Genet
, vol.44
, Issue.5
, pp. 552-561
-
-
Stein, J.L.1
Medland, S.E.2
Vasquez, A.A.3
Hibar, D.P.4
Senstad, R.E.5
Winkler, A.M.6
Toro, R.7
Appel, K.8
Bartecek, R.9
Bergmann, O.10
Bernard, M.11
Brown, A.A.12
Cannon, D.M.13
Chakravarty, M.M.14
Christoforou, A.15
Domin, M.16
Grimm, O.17
Hollinshead, M.18
Holmes, A.J.19
Homuth, G.20
Hottenga, J.J.21
Langan, C.22
Lopez, L.M.23
Hansell, N.K.24
Hwang, K.S.25
Kim, S.26
Laje, G.27
Lee, P.H.28
Liu, X.29
Loth, E.30
Lourdusamy, A.31
Mattingsdal, M.32
Mohnke, S.33
Maniega, S.M.34
Nho, K.35
Nugent, A.C.36
O'Brien, C.37
Papmeyer, M.38
Putz, B.39
Ramasamy, A.40
Rasmussen, J.41
Rijpkema, M.42
Risacher, S.L.43
Roddey, J.C.44
Rose, E.J.45
Ryten, M.46
Shen, L.47
Sprooten, E.48
Strengman, E.49
Teumer, A.50
Trabzuni, D.51
Turner, J.52
Van Eijk, K.53
Van Erp, T.G.54
Van Tol, M.J.55
Wittfeld, K.56
Wolf, C.57
Woudstra, S.58
Aleman, A.59
Alhusaini, S.60
Almasy, L.61
Binder, E.B.62
Brohawn, D.G.63
Cantor, R.M.64
Carless, M.A.65
Corvin, A.66
Czisch, M.67
Curran, J.E.68
Davies, G.69
De Almeida, M.A.70
Delanty, N.71
Depondt, C.72
Duggirala, R.73
Dyer, T.D.74
Erk, S.75
Fagerness, J.76
Fox, P.T.77
Freimer, N.B.78
Gill, M.79
Goring, H.H.80
Hagler, D.J.81
Hoehn, D.82
Holsboer, F.83
Hoogman, M.84
Hosten, N.85
Jahanshad, N.86
Johnson, M.P.87
Kasperaviciute, D.88
Kent, J.W.89
Kochunov, P.90
Lancaster, J.L.91
Lawrie, S.M.92
Liewald, D.C.93
Mandl, R.94
Matarin, M.95
Mattheisen, M.96
Meisenzahl, E.97
Melle, I.98
Moses, E.K.99
Muhleisen, T.W.100
Nauck, M.101
Nothen, M.M.102
Olvera, R.L.103
Pandolfo, M.104
Pike, G.B.105
Puls, R.106
Reinvang, I.107
Renteria, M.E.108
Rietschel, M.109
Roffman, J.L.110
Royle, N.A.111
Rujescu, D.112
Savitz, J.113
Schnack, H.G.114
Schnell, K.115
Seiferth, N.116
Smith, C.117
Steen, V.M.118
Valdes Hernandez, M.C.119
Van den Heuvel, M.120
Van der Wee, N.J.121
Van Haren, N.E.122
Veltman, J.A.123
Volzke, H.124
Walker, R.125
Westlye, L.T.126
Whelan, C.D.127
Agartz, I.128
Boomsma, D.I.129
Cavalleri, G.L.130
Dale, A.M.131
Djurovic, S.132
Drevets, W.C.133
Hagoort, P.134
Hall, J.135
Heinz, A.136
Jack, C.R.137
Foroud, T.M.138
Le Hellard, S.139
Macciardi, F.140
Montgomery, G.W.141
Poline, J.B.142
Porteous, D.J.143
Sisodiya, S.M.144
Starr, J.M.145
Sussmann, J.146
Toga, A.W.147
Veltman, D.J.148
Walter, H.149
Weiner, M.W.150
Bis, J.C.151
Ikram, M.A.152
Smith, A.V.153
Gudnason, V.154
Tzourio, C.155
Vernooij, M.W.156
Launer, L.J.157
DeCarli, C.158
Seshadri, S.159
Andreassen, O.A.160
Apostolova, L.G.161
Bastin, M.E.162
Blangero, J.163
Brunner, H.G.164
Buckner, R.L.165
Cichon, S.166
Coppola, G.167
De Zubicaray, G.I.168
Deary, I.J.169
Donohoe, G.170
De Geus, E.J.171
Espeseth, T.172
Fernandez, G.173
Glahn, D.C.174
Grabe, H.J.175
Hardy, J.176
Hulshoff Pol, H.E.177
Jenkinson, M.178
Kahn, R.S.179
McDonald, C.180
McIntosh, A.M.181
McMahon, F.J.182
McMahon, K.L.183
Meyer-Lindenberg, A.184
Morris, D.W.185
Muller-Myhsok, B.186
Nichols, T.E.187
Ophoff, R.A.188
Paus, T.189
Pausova, Z.190
Penninx, B.W.191
Potkin, S.G.192
Samann, P.G.193
Saykin, A.J.194
Schumann, G.195
Smoller, J.W.196
Wardlaw, J.M.197
Weale, M.E.198
Martin, N.G.199
Franke, B.200
Wright, M.J.201
Thompson, P.M.202
more..
-
69
-
-
77950650039
-
Reelin regulates postnatal neurogenesis and enhances spine hypertrophy and long-term potentiation
-
1:CAS:528:DC%2BC3cXlvVansLY%3D 20357114
-
Pujadas L, Gruart A, Bosch C, Delgado L, Teixeira CM, Rossi D, de Lecea L, Martinez A, Delgado-Garcia JM, Soriano E. Reelin regulates postnatal neurogenesis and enhances spine hypertrophy and long-term potentiation. J Neurosci. 2010;30(13):4636-49.
-
(2010)
J Neurosci
, vol.30
, Issue.13
, pp. 4636-4649
-
-
Pujadas, L.1
Gruart, A.2
Bosch, C.3
Delgado, L.4
Teixeira, C.M.5
Rossi, D.6
De Lecea, L.7
Martinez, A.8
Delgado-Garcia, J.M.9
Soriano, E.10
-
70
-
-
55249114701
-
The Reelin signaling pathway promotes dendritic spine development in hippocampal neurons
-
1:CAS:528:DC%2BD1cXht1GksLfM 18842893 2572775
-
Niu S, Yabut O, D'Arcangelo G. The Reelin signaling pathway promotes dendritic spine development in hippocampal neurons. J Neurosci. 2008;28(41):10339-48.
-
(2008)
J Neurosci
, vol.28
, Issue.41
, pp. 10339-10348
-
-
Niu, S.1
Yabut, O.2
D'Arcangelo, G.3
-
71
-
-
84908260978
-
Extracellular matrix control of dendritic spine and synapse structure and plasticity in adulthood
-
25368556 4202714
-
Levy AD, Omar MH, Koleske AJ. Extracellular matrix control of dendritic spine and synapse structure and plasticity in adulthood. Front Neuroanat. 2014;8:116.
-
(2014)
Front Neuroanat
, vol.8
, pp. 116
-
-
Levy, A.D.1
Omar, M.H.2
Koleske, A.J.3
-
72
-
-
84897108444
-
Reelin, an extracellular matrix protein linked to early onset psychiatric diseases, drives postnatal development of the prefrontal cortex via GluN2B-NMDARs and the mTOR pathway
-
1:CAS:528:DC%2BC2cXkvVKjtro%3D 23752244
-
Iafrati J, Orejarena MJ, Lassalle O, Bouamrane L, Gonzalez-Campo C, Chavis P. Reelin, an extracellular matrix protein linked to early onset psychiatric diseases, drives postnatal development of the prefrontal cortex via GluN2B-NMDARs and the mTOR pathway. Mol Psychiatry. 2014;19(4):417-26.
-
(2014)
Mol Psychiatry
, vol.19
, Issue.4
, pp. 417-426
-
-
Iafrati, J.1
Orejarena, M.J.2
Lassalle, O.3
Bouamrane, L.4
Gonzalez-Campo, C.5
Chavis, P.6
-
73
-
-
84863890578
-
Decreased reelin expression in the left prefrontal cortex (BA9) in chronic schizophrenia patients
-
1:CAS:528:DC%2BC38XhtVCrsLzF 22797278
-
Habl G, Schmitt A, Zink M, von Wilmsdorff M, Yeganeh-Doost P, Jatzko A, Schneider-Axmann T, Bauer M, Falkai P. Decreased reelin expression in the left prefrontal cortex (BA9) in chronic schizophrenia patients. Neuropsychobiology. 2012;66(1):57-62.
-
(2012)
Neuropsychobiology
, vol.66
, Issue.1
, pp. 57-62
-
-
Habl, G.1
Schmitt, A.2
Zink, M.3
Von Wilmsdorff, M.4
Yeganeh-Doost, P.5
Jatzko, A.6
Schneider-Axmann, T.7
Bauer, M.8
Falkai, P.9
-
74
-
-
84875216807
-
The involvement of Reelin in neurodevelopmental disorders
-
1:CAS:528:DC%2BC38Xhs1agtbfF 22981949
-
Folsom TD, Fatemi SH. The involvement of Reelin in neurodevelopmental disorders. Neuropharmacology. 2013;68:122-35.
-
(2013)
Neuropharmacology
, vol.68
, pp. 122-135
-
-
Folsom, T.D.1
Fatemi, S.H.2
-
75
-
-
16844370707
-
Reelin signaling is impaired in autism
-
1:CAS:528:DC%2BD2MXjtV2jtr4%3D 15820235
-
Fatemi SH, Snow AV, Stary JM, Araghi-Niknam M, Reutiman TJ, Lee S, Brooks AI, Pearce DA. Reelin signaling is impaired in autism. Biol Psychiatry. 2005;57(7):777-87.
-
(2005)
Biol Psychiatry
, vol.57
, Issue.7
, pp. 777-787
-
-
Fatemi, S.H.1
Snow, A.V.2
Stary, J.M.3
Araghi-Niknam, M.4
Reutiman, T.J.5
Lee, S.6
Brooks, A.I.7
Pearce, D.A.8
-
76
-
-
84963762448
-
RELN mutations in autism spectrum disorder
-
27064498 4814460
-
Lammert DB, Howell BW. RELN mutations in autism spectrum disorder. Front Cell Neurosci. 2016;10:84.
-
(2016)
Front Cell Neurosci
, vol.10
, pp. 84
-
-
Lammert, D.B.1
Howell, B.W.2
-
77
-
-
84893510629
-
Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis
-
24453138 1:CAS:528:DC%2BC2cXit12rtrw%3D
-
Wang Z, Hong Y, Zou L, Zhong R, Zhu B, Shen N, Chen W, Lou J, Ke J, Zhang T, Wang W, Miao X. Reelin gene variants and risk of autism spectrum disorders: an integrated meta-analysis. Am J Med Genet B Neuropsychiatr Genet. 2014;165B(2):192-200.
-
(2014)
Am J Med Genet B Neuropsychiatr Genet
, vol.165 B
, Issue.2
, pp. 192-200
-
-
Wang, Z.1
Hong, Y.2
Zou, L.3
Zhong, R.4
Zhu, B.5
Shen, N.6
Chen, W.7
Lou, J.8
Ke, J.9
Zhang, T.10
Wang, W.11
Miao, X.12
-
78
-
-
84899840037
-
Deregulation of an imprinted gene network in prostate cancer
-
1:CAS:528:DC%2BC2cXhsFKrsLrF 24513574 4063830
-
Ribarska T, Goering W, Droop J, Bastian KM, Ingenwerth M, Schulz WA. Deregulation of an imprinted gene network in prostate cancer. Epigenetics. 2014;9(5):704-17.
-
(2014)
Epigenetics
, vol.9
, Issue.5
, pp. 704-717
-
-
Ribarska, T.1
Goering, W.2
Droop, J.3
Bastian, K.M.4
Ingenwerth, M.5
Schulz, W.A.6
-
79
-
-
84861156701
-
MEG3 noncoding RNA: a tumor suppressor
-
1:CAS:528:DC%2BC38XovFamtLk%3D 22393162 3738193
-
Zhou Y, Zhang X, Klibanski A. MEG3 noncoding RNA: a tumor suppressor. J Mol Endocrinol. 2012;48(3):R45-53.
-
(2012)
J Mol Endocrinol
, vol.48
, Issue.3
, pp. R45-R53
-
-
Zhou, Y.1
Zhang, X.2
Klibanski, A.3
-
80
-
-
77149157495
-
Maternally expressed gene 3 (MEG3) noncoding ribonucleic acid: isoform structure, expression, and functions
-
1:CAS:528:DC%2BC3cXjvVKqsLw%3D 20032057
-
Zhang X, Rice K, Wang Y, Chen W, Zhong Y, Nakayama Y, Zhou Y, Klibanski A. Maternally expressed gene 3 (MEG3) noncoding ribonucleic acid: isoform structure, expression, and functions. Endocrinology. 2010;151(3):939-47.
-
(2010)
Endocrinology
, vol.151
, Issue.3
, pp. 939-947
-
-
Zhang, X.1
Rice, K.2
Wang, Y.3
Chen, W.4
Zhong, Y.5
Nakayama, Y.6
Zhou, Y.7
Klibanski, A.8
-
81
-
-
84885015533
-
Long non-coding RNA MEG3 inhibits NSCLC cells proliferation and induces apoptosis by affecting p53 expression
-
24098911 3851462 1:CAS:528:DC%2BC2cXjslaku7Y%3D 2407-13-461
-
Lu KH, Li W, Liu XH, Sun M, Zhang ML, Wu WQ, Xie WP, Hou YY. Long non-coding RNA MEG3 inhibits NSCLC cells proliferation and induces apoptosis by affecting p53 expression. BMC Cancer. 2013;13:461. 2407-13-461.
-
(2013)
BMC Cancer
, vol.13
, pp. 461
-
-
Lu, K.H.1
Li, W.2
Liu, X.H.3
Sun, M.4
Zhang, M.L.5
Wu, W.Q.6
Xie, W.P.7
Hou, Y.Y.8
-
82
-
-
84948672332
-
Long noncoding RNA MEG3 interacts with p53 protein and regulates partial p53 target genes in hepatoma cells
-
26444285 4596861 1:CAS:528:DC%2BC2MXhvVeiurzF
-
Zhu J, Liu S, Ye F, Shen Y, Tie Y, Zhu J, Wei L, Jin Y, Fu H, Wu Y, Zheng X. Long noncoding RNA MEG3 interacts with p53 protein and regulates partial p53 target genes in hepatoma cells. PLoS One. 2015;10(10):e0139790.
-
(2015)
PLoS One
, vol.10
, Issue.10
, pp. e0139790
-
-
Zhu, J.1
Liu, S.2
Ye, F.3
Shen, Y.4
Tie, Y.5
Zhu, J.6
Wei, L.7
Jin, Y.8
Fu, H.9
Wu, Y.10
Zheng, X.11
-
83
-
-
79951828066
-
Wnt5a is a transcriptional target of Dlx homeogenes and promotes differentiation of interneuron progenitors in vitro and in vivo
-
1:CAS:528:DC%2BC3MXisFKmurc%3D 21325536
-
Paina S, Garzotto D, DeMarchis S, Marino M, Moiana A, Conti L, Cattaneo E, Perera M, Corte G, Calautti E, Merlo GR. Wnt5a is a transcriptional target of Dlx homeogenes and promotes differentiation of interneuron progenitors in vitro and in vivo. J Neurosci. 2011;31(7):2675-87.
-
(2011)
J Neurosci
, vol.31
, Issue.7
, pp. 2675-2687
-
-
Paina, S.1
Garzotto, D.2
DeMarchis, S.3
Marino, M.4
Moiana, A.5
Conti, L.6
Cattaneo, E.7
Perera, M.8
Corte, G.9
Calautti, E.10
Merlo, G.R.11
-
84
-
-
49549096037
-
DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex
-
1:CAS:528:DC%2BD1cXhtFGhsbnO 18537997 3597349
-
Miyano M, Horike S, Cai S, Oshimura M, Kohwi-Shigematsu T. DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex. J Cell Mol Med. 2008;12(4):1188-91.
-
(2008)
J Cell Mol Med
, vol.12
, Issue.4
, pp. 1188-1191
-
-
Miyano, M.1
Horike, S.2
Cai, S.3
Oshimura, M.4
Kohwi-Shigematsu, T.5
-
85
-
-
84875302751
-
Loss of Gsx1 and Gsx2 function rescues distinct phenotypes in Dlx1/2 mutants
-
1:CAS:528:DC%2BC3sXksVKrs7s%3D 23042297
-
Wang B, Long JE, Flandin P, Pla R, Waclaw RR, Campbell K, Rubenstein JL. Loss of Gsx1 and Gsx2 function rescues distinct phenotypes in Dlx1/2 mutants. J Comp Neurol. 2013;521(7):1561-84.
-
(2013)
J Comp Neurol
, vol.521
, Issue.7
, pp. 1561-1584
-
-
Wang, B.1
Long, J.E.2
Flandin, P.3
Pla, R.4
Waclaw, R.R.5
Campbell, K.6
Rubenstein, J.L.7
-
86
-
-
77956601621
-
An SNP in an ultraconserved regulatory element affects Dlx5/Dlx6 regulation in the forebrain
-
1:CAS:528:DC%2BC3cXhsVWgtLvO 20702565 3188590
-
Poitras L, Yu M, Lesage-Pelletier C, Macdonald RB, Gagne JP, Hatch G, Kelly I, Hamilton SP, Rubenstein JL, Poirier GG, Ekker M. An SNP in an ultraconserved regulatory element affects Dlx5/Dlx6 regulation in the forebrain. Development. 2010;137(18):3089-97.
-
(2010)
Development
, vol.137
, Issue.18
, pp. 3089-3097
-
-
Poitras, L.1
Yu, M.2
Lesage-Pelletier, C.3
Macdonald, R.B.4
Gagne, J.P.5
Hatch, G.6
Kelly, I.7
Hamilton, S.P.8
Rubenstein, J.L.9
Poirier, G.G.10
Ekker, M.11
-
87
-
-
84989865627
-
Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling
-
1:CAS:528:DC%2BC28Xhs1SltLrK 27694995
-
Durak O, Gao F, Kaeser-Woo YJ, Rueda R, Martorell AJ, Nott A, Liu CY, Watson LA, Tsai LH. Chd8 mediates cortical neurogenesis via transcriptional regulation of cell cycle and Wnt signaling. Nat Neurosci. 2016;19(11):1477-88.
-
(2016)
Nat Neurosci
, vol.19
, Issue.11
, pp. 1477-1488
-
-
Durak, O.1
Gao, F.2
Kaeser-Woo, Y.J.3
Rueda, R.4
Martorell, A.J.5
Nott, A.6
Liu, C.Y.7
Watson, L.A.8
Tsai, L.H.9
-
88
-
-
78649351382
-
Beta-catenin promoter ChIP-chip reveals potential schizophrenia and bipolar disorder gene network
-
Pedrosa E, Shah A, Tenore C, Capogna M, Villa C, Guo X, Zheng D, Lachman HM. Beta-catenin promoter ChIP-chip reveals potential schizophrenia and bipolar disorder gene network. J Neurogenet. 2010;24(4):182-93.
-
(2010)
J Neurogenet
, vol.24
, Issue.4
, pp. 182-193
-
-
Pedrosa, E.1
Shah, A.2
Tenore, C.3
Capogna, M.4
Villa, C.5
Guo, X.6
Zheng, D.7
Lachman, H.M.8
-
89
-
-
68449104276
-
Lithium pharmacodynamics and pharmacogenetics: focus on inositol mono phosphatase (IMPase), inositol poliphosphatase (IPPase) and glycogen sinthase kinase 3 beta (GSK-3 beta)
-
1:CAS:528:DC%2BD1MXnt1Ggsrs%3D 19442155
-
Serretti A, Drago A, De Ronchi D. Lithium pharmacodynamics and pharmacogenetics: focus on inositol mono phosphatase (IMPase), inositol poliphosphatase (IPPase) and glycogen sinthase kinase 3 beta (GSK-3 beta). Curr Med Chem. 2009;16(15):1917-48.
-
(2009)
Curr Med Chem
, vol.16
, Issue.15
, pp. 1917-1948
-
-
Serretti, A.1
Drago, A.2
De Ronchi, D.3
-
90
-
-
84929948919
-
Lithium in the treatment of bipolar disorder: pharmacology and pharmacogenetics
-
1:CAS:528:DC%2BC2MXivFWkur0%3D 25687772 5125816
-
Alda M. Lithium in the treatment of bipolar disorder: pharmacology and pharmacogenetics. Mol Psychiatry. 2015;20(6):661-70.
-
(2015)
Mol Psychiatry
, vol.20
, Issue.6
, pp. 661-670
-
-
Alda, M.1
-
91
-
-
84925510733
-
Lithium and GSK-3beta promoter gene variants influence cortical gray matter volumes in bipolar disorder
-
1:CAS:528:DC%2BC2cXhvVGksLrK
-
Benedetti F, Poletti S, Radaelli D, Locatelli C, Pirovano A, Lorenzi C, Vai B, Bollettini I, Falini A, Smeraldi E, Colombo C. Lithium and GSK-3beta promoter gene variants influence cortical gray matter volumes in bipolar disorder. Psychopharmacology (Berl). 2015;232(7):1325-36.
-
(2015)
Psychopharmacology (Berl)
, vol.232
, Issue.7
, pp. 1325-1336
-
-
Benedetti, F.1
Poletti, S.2
Radaelli, D.3
Locatelli, C.4
Pirovano, A.5
Lorenzi, C.6
Vai, B.7
Bollettini, I.8
Falini, A.9
Smeraldi, E.10
Colombo, C.11
-
92
-
-
84886096735
-
Glycogen synthase kinase 3 substrates in mood disorders and schizophrenia
-
1:CAS:528:DC%2BC3sXhs1Wnsr3M 23796137
-
Cole AR. Glycogen synthase kinase 3 substrates in mood disorders and schizophrenia. FEBS J. 2013;280(21):5213-27.
-
(2013)
FEBS J
, vol.280
, Issue.21
, pp. 5213-5227
-
-
Cole, A.R.1
-
93
-
-
58149230875
-
Adjunctive lithium and anticonvulsants for the treatment of schizophrenia: what is the evidence?
-
1:CAS:528:DC%2BD1cXhsFCisrvI 19102669
-
Citrome L. Adjunctive lithium and anticonvulsants for the treatment of schizophrenia: what is the evidence? Expert Rev Neurother. 2009;9(1):55-71.
-
(2009)
Expert Rev Neurother
, vol.9
, Issue.1
, pp. 55-71
-
-
Citrome, L.1
-
95
-
-
84979851541
-
Lithium for schizophrenia
-
Leucht S, Helfer B, Dold M, Kissling W, McGrath JJ. Lithium for schizophrenia. Cochrane Database Syst Rev. 2015;10:CD003834.
-
(2015)
Cochrane Database Syst Rev
, vol.10
, pp. CD003834
-
-
Leucht, S.1
Helfer, B.2
Dold, M.3
Kissling, W.4
McGrath, J.J.5
-
96
-
-
84941919695
-
Mood stabilizers in children and adolescents with autism spectrum disorders
-
1:CAS:528:DC%2BC2MXhsFCrtbvO 26366961
-
Canitano R. Mood stabilizers in children and adolescents with autism spectrum disorders. Clin Neuropharmacol. 2015;38(5):177-82.
-
(2015)
Clin Neuropharmacol
, vol.38
, Issue.5
, pp. 177-182
-
-
Canitano, R.1
-
97
-
-
84907029014
-
Preliminary investigation of lithium for mood disorder symptoms in children and adolescents with autism spectrum disorder
-
1:CAS:528:DC%2BC2cXhsFamsrvF 25093602
-
Siegel M, Beresford CA, Bunker M, Verdi M, Vishnevetsky D, Karlsson C, Teer O, Stedman A, Smith KA. Preliminary investigation of lithium for mood disorder symptoms in children and adolescents with autism spectrum disorder. J Child Adolesc Psychopharmacol. 2014;24(7):399-402.
-
(2014)
J Child Adolesc Psychopharmacol
, vol.24
, Issue.7
, pp. 399-402
-
-
Siegel, M.1
Beresford, C.A.2
Bunker, M.3
Verdi, M.4
Vishnevetsky, D.5
Karlsson, C.6
Teer, O.7
Stedman, A.8
Smith, K.A.9
-
98
-
-
84937810710
-
Skating on thin ice: pragmatic prescribing for medication refractory schizophrenia
-
26205327 4513623 1:CAS:528:DC%2BC28XlslGrtLw%3D 015-0559-x
-
Tracy DK, Joyce DW, Sarkar SN, Mateos Fernandez MJ, Shergill SS. Skating on thin ice: pragmatic prescribing for medication refractory schizophrenia. BMC Psychiatry. 2015;15:174. 015-0559-x.
-
(2015)
BMC Psychiatry
, vol.15
, pp. 174
-
-
Tracy, D.K.1
Joyce, D.W.2
Sarkar, S.N.3
Mateos Fernandez, M.J.4
Shergill, S.S.5
-
99
-
-
84926395609
-
Common genetic variants influence human subcortical brain structures
-
Alzheimer’s Disease Neuroimaging Initiative, CHARGE Consortium, EPIGEN, IMAGEN, SYS 1:CAS:528:DC%2BC2MXht1Omsbc%3D 25607358 4393366
-
Hibar DP, Stein JL, Renteria ME, Arias-Vasquez A, Desrivieres S, Jahanshad N, Toro R, Wittfeld K, Abramovic L, Andersson M, Aribisala BS, Armstrong NJ, Bernard M, Bohlken MM, Boks MP, Bralten J, Brown AA, Chakravarty MM, Chen Q, Ching CR, Cuellar-Partida G, den Braber A, Giddaluru S, Goldman AL, Grimm O, Guadalupe T, Hass J, Woldehawariat G, Holmes AJ, Hoogman M, Janowitz D, Jia T, Kim S, Klein M, Kraemer B, Lee PH, Olde Loohuis LM, Luciano M, Macare C, Mather KA, Mattheisen M, Milaneschi Y, Nho K, Papmeyer M, Ramasamy A, Risacher SL, Roiz-Santianez R, Rose EJ, Salami A, Samann PG, Schmaal L, Schork AJ, Shin J, Strike LT, Teumer A, van Donkelaar MM, van Eijk KR, Walters RK, Westlye LT, Whelan CD, Winkler AM, Zwiers MP, Alhusaini S, Athanasiu L, Ehrlich S, Hakobjan MM, Hartberg CB, Haukvik UK, Heister AJ, Hoehn D, Kasperaviciute D, Liewald DC, Lopez LM, Makkinje RR, Matarin M, Naber MA, McKay DR, Needham M, Nugent AC, Putz B, Royle NA, Shen L, Sprooten E, Trabzuni D, van der Marel SS, van Hulzen KJ, Walton E, Wolf C, Almasy L, Ames D, Arepalli S, Assareh AA, Bastin ME, Brodaty H, Bulayeva KB, Carless MA, Cichon S, Corvin A, Curran JE, Czisch M, de Zubicaray GI, Dillman A, Duggirala R, Dyer TD, Erk S, Fedko IO, Ferrucci L, Foroud TM, Fox PT, Fukunaga M, Gibbs JR, Goring HH, Green RC, Guelfi S, Hansell NK, Hartman CA, Hegenscheid K, Heinz A, Hernandez DG, Heslenfeld DJ, Hoekstra PJ, Holsboer F, Homuth G, Hottenga JJ, Ikeda M, Jack Jr CR, Jenkinson M, Johnson R, Kanai R, Keil M, Kent Jr JW, Kochunov P, Kwok JB, Lawrie SM, Liu X, Longo DL, McMahon KL, Meisenzahl E, Melle I, Mohnke S, Montgomery GW, Mostert JC, Muhleisen TW, Nalls MA, Nichols TE, Nilsson LG, Nothen MM, Ohi K, Olvera RL, Perez-Iglesias R, Pike GB, Potkin SG, Reinvang I, Reppermund S, Rietschel M, Romanczuk-Seiferth N, Rosen GD, Rujescu D, Schnell K, Schofield PR, Smith C, Steen VM, Sussmann JE, Thalamuthu A, Toga AW, Traynor BJ, Troncoso J, Turner JA, Valdes Hernandez MC, van’t Ent D, van der Brug M, van der Wee NJ, van Tol MJ, Veltman DJ, Wassink TH, Westman E, Zielke RH, Zonderman AB, Ashbrook DG, Hager R, Lu L, McMahon FJ, Morris DW, Williams RW, Brunner HG, Buckner RL, Buitelaar JK, Cahn W, Calhoun VD, Cavalleri GL, Crespo-Facorro B, Dale AM, Davies GE, Delanty N, Depondt C, Djurovic S, Drevets WC, Espeseth T, Gollub RL, Ho BC, Hoffmann W, Hosten N, Kahn RS, Le Hellard S, Meyer-Lindenberg A, Muller-Myhsok B, Nauck M, Nyberg L, Pandolfo M, Penninx BW, Roffman JL, Sisodiya SM, Smoller JW, van Bokhoven H, van Haren NE, Volzke H, Walter H, Weiner MW, Wen W, White T, Agartz I, Andreassen OA, Blangero J, Boomsma DI, Brouwer RM, Cannon DM, Cookson MR, de Geus EJ, Deary IJ, Donohoe G, Fernandez G, Fisher SE, Francks C, Glahn DC, Grabe HJ, Gruber O, Hardy J, Hashimoto R, Hulshoff Pol HE, Jonsson EG, Kloszewska I, Lovestone S, Mattay VS, Mecocci P, McDonald C, McIntosh AM, Ophoff RA, Paus T, Pausova Z, Ryten M, Sachdev PS, Saykin AJ, Simmons A, Singleton A, Soininen H, Wardlaw JM, Weale ME, Weinberger DR, Adams HH, Launer LJ, Seiler S, Schmidt R, Chauhan G, Satizabal CL, Becker JT, Yanek L, van der Lee SJ, Ebling M, Fischl B, Longstreth Jr WT, Greve D, Schmidt H, Nyquist P, Vinke LN, van Duijn CM, Xue L, Mazoyer B, Bis JC, Gudnason V, Seshadri S, Ikram MA, Alzheimer’s Disease Neuroimaging Initiative, CHARGE Consortium, EPIGEN, IMAGEN, SYS, Martin NG, Wright MJ, Schumann G, Franke B, Thompson PM, Medland SE. Common genetic variants influence human subcortical brain structures. Nature. 2015;520(7546):224-9.
-
(2015)
Nature
, vol.520
, Issue.7546
, pp. 224-229
-
-
Hibar, D.P.1
Stein, J.L.2
Renteria, M.E.3
Arias-Vasquez, A.4
Desrivieres, S.5
Jahanshad, N.6
Toro, R.7
Wittfeld, K.8
Abramovic, L.9
Andersson, M.10
Aribisala, B.S.11
Armstrong, N.J.12
Bernard, M.13
Bohlken, M.M.14
Boks, M.P.15
Bralten, J.16
Brown, A.A.17
Chakravarty, M.M.18
Chen, Q.19
Ching, C.R.20
Cuellar-Partida, G.21
Den Braber, A.22
Giddaluru, S.23
Goldman, A.L.24
Grimm, O.25
Guadalupe, T.26
Hass, J.27
Woldehawariat, G.28
Holmes, A.J.29
Hoogman, M.30
Janowitz, D.31
Jia, T.32
Kim, S.33
Klein, M.34
Kraemer, B.35
Lee, P.H.36
Olde Loohuis, L.M.37
Luciano, M.38
Macare, C.39
Mather, K.A.40
Mattheisen, M.41
Milaneschi, Y.42
Nho, K.43
Papmeyer, M.44
Ramasamy, A.45
Risacher, S.L.46
Roiz-Santianez, R.47
Rose, E.J.48
Salami, A.49
Samann, P.G.50
Schmaal, L.51
Schork, A.J.52
Shin, J.53
Strike, L.T.54
Teumer, A.55
Van Donkelaar, M.M.56
Van Eijk, K.R.57
Walters, R.K.58
Westlye, L.T.59
Whelan, C.D.60
Winkler, A.M.61
Zwiers, M.P.62
Alhusaini, S.63
Athanasiu, L.64
Ehrlich, S.65
Hakobjan, M.M.66
Hartberg, C.B.67
Haukvik, U.K.68
Heister, A.J.69
Hoehn, D.70
Kasperaviciute, D.71
Liewald, D.C.72
Lopez, L.M.73
Makkinje, R.R.74
Matarin, M.75
Naber, M.A.76
McKay, D.R.77
Needham, M.78
Nugent, A.C.79
Putz, B.80
Royle, N.A.81
Shen, L.82
Sprooten, E.83
Trabzuni, D.84
Van der Marel, S.S.85
Van Hulzen, K.J.86
Walton, E.87
Wolf, C.88
Almasy, L.89
Ames, D.90
Arepalli, S.91
Assareh, A.A.92
Bastin, M.E.93
Brodaty, H.94
Bulayeva, K.B.95
Carless, M.A.96
Cichon, S.97
Corvin, A.98
Curran, J.E.99
Czisch, M.100
De Zubicaray, G.I.101
Dillman, A.102
Duggirala, R.103
Dyer, T.D.104
Erk, S.105
Fedko, I.O.106
Ferrucci, L.107
Foroud, T.M.108
Fox, P.T.109
Fukunaga, M.110
Gibbs, J.R.111
Goring, H.H.112
Green, R.C.113
Guelfi, S.114
Hansell, N.K.115
Hartman, C.A.116
Hegenscheid, K.117
Heinz, A.118
Hernandez, D.G.119
Heslenfeld, D.J.120
Hoekstra, P.J.121
Holsboer, F.122
Homuth, G.123
Hottenga, J.J.124
Ikeda, M.125
Jack, C.R.126
Jenkinson, M.127
Johnson, R.128
Kanai, R.129
Keil, M.130
Kent, J.W.131
Kochunov, P.132
Kwok, J.B.133
Lawrie, S.M.134
Liu, X.135
Longo, D.L.136
McMahon, K.L.137
Meisenzahl, E.138
Melle, I.139
Mohnke, S.140
Montgomery, G.W.141
Mostert, J.C.142
Muhleisen, T.W.143
Nalls, M.A.144
Nichols, T.E.145
Nilsson, L.G.146
Nothen, M.M.147
Ohi, K.148
Olvera, R.L.149
Perez-Iglesias, R.150
Pike, G.B.151
Potkin, S.G.152
Reinvang, I.153
Reppermund, S.154
Rietschel, M.155
Romanczuk-Seiferth, N.156
Rosen, G.D.157
Rujescu, D.158
Schnell, K.159
Schofield, P.R.160
Smith, C.161
Steen, V.M.162
Sussmann, J.E.163
Thalamuthu, A.164
Toga, A.W.165
Traynor, B.J.166
Troncoso, J.167
Turner, J.A.168
Valdes Hernandez, M.C.169
Van’t Ent, D.170
Van der Brug, M.171
Van der Wee, N.J.172
Van Tol, M.J.173
Veltman, D.J.174
Wassink, T.H.175
Westman, E.176
Zielke, R.H.177
Zonderman, A.B.178
Ashbrook, D.G.179
Hager, R.180
Lu, L.181
McMahon, F.J.182
Morris, D.W.183
Williams, R.W.184
Brunner, H.G.185
Buckner, R.L.186
Buitelaar, J.K.187
Cahn, W.188
Calhoun, V.D.189
Cavalleri, G.L.190
Crespo-Facorro, B.191
Dale, A.M.192
Davies, G.E.193
Delanty, N.194
Depondt, C.195
Djurovic, S.196
Drevets, W.C.197
Espeseth, T.198
Gollub, R.L.199
Ho, B.C.200
Hoffmann, W.201
Hosten, N.202
Kahn, R.S.203
Le Hellard, S.204
Meyer-Lindenberg, A.205
Muller-Myhsok, B.206
Nauck, M.207
Nyberg, L.208
Pandolfo, M.209
Penninx, B.W.210
Roffman, J.L.211
Sisodiya, S.M.212
Smoller, J.W.213
Van Bokhoven, H.214
Van Haren, N.E.215
Volzke, H.216
Walter, H.217
Weiner, M.W.218
Wen, W.219
White, T.220
Agartz, I.221
Andreassen, O.A.222
Blangero, J.223
Boomsma, D.I.224
Brouwer, R.M.225
Cannon, D.M.226
Cookson, M.R.227
De Geus, E.J.228
Deary, I.J.229
Donohoe, G.230
Fernandez, G.231
Fisher, S.E.232
Francks, C.233
Glahn, D.C.234
Grabe, H.J.235
Gruber, O.236
Hardy, J.237
Hashimoto, R.238
Hulshoff Pol, H.E.239
Jonsson, E.G.240
Kloszewska, I.241
Lovestone, S.242
Mattay, V.S.243
Mecocci, P.244
McDonald, C.245
McIntosh, A.M.246
Ophoff, R.A.247
Paus, T.248
Pausova, Z.249
Ryten, M.250
Sachdev, P.S.251
Saykin, A.J.252
Simmons, A.253
Singleton, A.254
Soininen, H.255
Wardlaw, J.M.256
Weale, M.E.257
Weinberger, D.R.258
Adams, H.H.259
Launer, L.J.260
Seiler, S.261
Schmidt, R.262
Chauhan, G.263
Satizabal, C.L.264
Becker, J.T.265
Yanek, L.266
Van der Lee, S.J.267
Ebling, M.268
Fischl, B.269
Longstreth, W.T.270
Greve, D.271
Schmidt, H.272
Nyquist, P.273
Vinke, L.N.274
Van Duijn, C.M.275
Xue, L.276
Mazoyer, B.277
Bis, J.C.278
Gudnason, V.279
Seshadri, S.280
Ikram, M.A.281
Martin, N.G.282
Wright, M.J.283
Schumann, G.284
Franke, B.285
Thompson, P.M.286
Medland, S.E.287
more..
-
100
-
-
84860324077
-
Early Growth Genetics Consortium: Common variants at 12q15 and 12q24 are associated with infant head circumference
-
Cohorts for Heart and Aging Research in Genetic Epidemiology Consortium Early Genetics & Lifecourse Epidemiology Consortium 1:CAS:528:DC%2BC38XlsFSqu7g%3D 22504419 3773913
-
Taal HR, St Pourcain B, Thiering E, Das S, Mook-Kanamori DO, Warrington NM, Kaakinen M, Kreiner-Moller E, Bradfield JP, Freathy RM, Geller F, Guxens M, Cousminer DL, Kerkhof M, Timpson NJ, Ikram MA, Beilin LJ, Bonnelykke K, Buxton JL, Charoen P, Chawes BL, Eriksson J, Evans DM, Hofman A, Kemp JP, Kim CE, Klopp N, Lahti J, Lye SJ, McMahon G, Mentch FD, Muller-Nurasyid M, O'Reilly PF, Prokopenko I, Rivadeneira F, Steegers EA, Sunyer J, Tiesler C, Yaghootkar H, Cohorts for Heart and Aging Research in Genetic Epidemiology Consortium, Breteler MM, Decarli C, Breteler MM, Debette S, Fornage M, Gudnason V, Launer LJ, van der Lugt A, Mosley Jr TH, Seshadri S, Smith AV, Vernooij MW, Early Genetics & Lifecourse Epidemiology Consortium, Blakemore AI, Chiavacci RM, Feenstra B, Fernandez-Banet J, Grant SF, Hartikainen AL, van der Heijden AJ, Iniguez C, Lathrop M, McArdle WL, Molgaard A, Newnham JP, Palmer LJ, Palotie A, Pouta A, Ring SM, Sovio U, Standl M, Uitterlinden AG, Wichmann HE, Vissing NH, DeCarli C, van Duijn CM, McCarthy MI, Koppelman GH, Estivill X, Hattersley AT, Melbye M, Bisgaard H, Pennell CE, Widen E, Hakonarson H, Smith GD, Heinrich J, Jarvelin MR, Jaddoe VW. Early Growth Genetics Consortium: Common variants at 12q15 and 12q24 are associated with infant head circumference. Nat Genet. 2012;44(5):532-8.
-
(2012)
Nat Genet
, vol.44
, Issue.5
, pp. 532-538
-
-
Taal, H.R.1
St Pourcain, B.2
Thiering, E.3
Das, S.4
Mook-Kanamori, D.O.5
Warrington, N.M.6
Kaakinen, M.7
Kreiner-Moller, E.8
Bradfield, J.P.9
Freathy, R.M.10
Geller, F.11
Guxens, M.12
Cousminer, D.L.13
Kerkhof, M.14
Timpson, N.J.15
Ikram, M.A.16
Beilin, L.J.17
Bonnelykke, K.18
Buxton, J.L.19
Charoen, P.20
Chawes, B.L.21
Eriksson, J.22
Evans, D.M.23
Hofman, A.24
Kemp, J.P.25
Kim, C.E.26
Klopp, N.27
Lahti, J.28
Lye, S.J.29
McMahon, G.30
Mentch, F.D.31
Muller-Nurasyid, M.32
O'Reilly, P.F.33
Prokopenko, I.34
Rivadeneira, F.35
Steegers, E.A.36
Sunyer, J.37
Tiesler, C.38
Yaghootkar, H.39
Breteler, M.M.40
Decarli, C.41
Breteler, M.M.42
Debette, S.43
Fornage, M.44
Gudnason, V.45
Launer, L.J.46
Van der Lugt, A.47
Mosley, T.H.48
Seshadri, S.49
Smith, A.V.50
Vernooij, M.W.51
Blakemore, A.I.52
Chiavacci, R.M.53
Feenstra, B.54
Fernandez-Banet, J.55
Grant, S.F.56
Hartikainen, A.L.57
Van der Heijden, A.J.58
Iniguez, C.59
Lathrop, M.60
McArdle, W.L.61
Molgaard, A.62
Newnham, J.P.63
Palmer, L.J.64
Palotie, A.65
Pouta, A.66
Ring, S.M.67
Sovio, U.68
Standl, M.69
Uitterlinden, A.G.70
Wichmann, H.E.71
Vissing, N.H.72
Decarli, C.73
Van Duijn, C.M.74
McCarthy, M.I.75
Koppelman, G.H.76
Estivill, X.77
Hattersley, A.T.78
Melbye, M.79
Bisgaard, H.80
Pennell, C.E.81
Widen, E.82
Hakonarson, H.83
Smith, G.D.84
Heinrich, J.85
Jarvelin, M.R.86
Jaddoe, V.W.87
more..
-
101
-
-
84881487023
-
The long noncoding RNA RMST interacts with SOX2 to regulate neurogenesis
-
1:CAS:528:DC%2BC3sXht1Gms7fJ 23932716
-
Ng SY, Bogu GK, Soh BS, Stanton LW. The long noncoding RNA RMST interacts with SOX2 to regulate neurogenesis. Mol Cell. 2013;51(3):349-59.
-
(2013)
Mol Cell
, vol.51
, Issue.3
, pp. 349-359
-
-
Ng, S.Y.1
Bogu, G.K.2
Soh, B.S.3
Stanton, L.W.4
-
102
-
-
84954305428
-
Dysregulated ErbB4 splicing in schizophrenia: selective effects on parvalbumin expression
-
26337038
-
Chung DW, Volk DW, Arion D, Zhang Y, Sampson AR, Lewis DA. Dysregulated ErbB4 splicing in schizophrenia: selective effects on parvalbumin expression. Am J Psychiatry. 2016;173(1):60-8.
-
(2016)
Am J Psychiatry
, vol.173
, Issue.1
, pp. 60-68
-
-
Chung, D.W.1
Volk, D.W.2
Arion, D.3
Zhang, Y.4
Sampson, A.R.5
Lewis, D.A.6
-
103
-
-
84946474781
-
Long noncoding RNA-directed epigenetic regulation of gene expression is associated with anxiety-like behavior in mice
-
1:CAS:528:DC%2BC2MXksFWlsb8%3D 25792222 4532653
-
Spadaro PA, Flavell CR, Widagdo J, Ratnu VS, Troup M, Ragan C, Mattick JS, Bredy TW. Long noncoding RNA-directed epigenetic regulation of gene expression is associated with anxiety-like behavior in mice. Biol Psychiatry. 2015;78(12):848-59.
-
(2015)
Biol Psychiatry
, vol.78
, Issue.12
, pp. 848-859
-
-
Spadaro, P.A.1
Flavell, C.R.2
Widagdo, J.3
Ratnu, V.S.4
Troup, M.5
Ragan, C.6
Mattick, J.S.7
Bredy, T.W.8
-
104
-
-
84897108067
-
The long non-coding RNA Gomafu is acutely regulated in response to neuronal activation and involved in schizophrenia-associated alternative splicing
-
1:CAS:528:DC%2BC2cXkvVGqtLo%3D 23628989
-
Barry G, Briggs JA, Vanichkina DP, Poth EM, Beveridge NJ, Ratnu VS, Nayler SP, Nones K, Hu J, Bredy TW, Nakagawa S, Rigo F, Taft RJ, Cairns MJ, Blackshaw S, Wolvetang EJ, Mattick JS. The long non-coding RNA Gomafu is acutely regulated in response to neuronal activation and involved in schizophrenia-associated alternative splicing. Mol Psychiatry. 2014;19(4):486-94.
-
(2014)
Mol Psychiatry
, vol.19
, Issue.4
, pp. 486-494
-
-
Barry, G.1
Briggs, J.A.2
Vanichkina, D.P.3
Poth, E.M.4
Beveridge, N.J.5
Ratnu, V.S.6
Nayler, S.P.7
Nones, K.8
Hu, J.9
Bredy, T.W.10
Nakagawa, S.11
Rigo, F.12
Taft, R.J.13
Cairns, M.J.14
Blackshaw, S.15
Wolvetang, E.J.16
Mattick, J.S.17
-
105
-
-
84999098100
-
Integrative transcriptome network analysis of iPSC-derived neurons from schizophrenia and schizoaffective disorder patients with 22q11.2 deletion
-
27846841 5111260
-
Lin M, Pedrosa E, Hrabovsky A, Chen J, Puliafito BR, Gilbert SR, Zheng D, Lachman HM. Integrative transcriptome network analysis of iPSC-derived neurons from schizophrenia and schizoaffective disorder patients with 22q11.2 deletion. BMC Syst Biol. 2016;10(1):105.
-
(2016)
BMC Syst Biol
, vol.10
, Issue.1
, pp. 105
-
-
Lin, M.1
Pedrosa, E.2
Hrabovsky, A.3
Chen, J.4
Puliafito, B.R.5
Gilbert, S.R.6
Zheng, D.7
Lachman, H.M.8
-
106
-
-
84938633164
-
Evf2 lncRNA/BRG1/DLX1 interactions reveal RNA-dependent inhibition of chromatin remodeling
-
1:CAS:528:DC%2BC28XmtlGgsQ%3D%3D 26138476 4529037
-
Cajigas I, Leib DE, Cochrane J, Luo H, Swyter KR, Chen S, Clark BS, Thompson J, Yates 3rd JR, Kingston RE, Kohtz JD. Evf2 lncRNA/BRG1/DLX1 interactions reveal RNA-dependent inhibition of chromatin remodeling. Development. 2015;142(15):2641-52.
-
(2015)
Development
, vol.142
, Issue.15
, pp. 2641-2652
-
-
Cajigas, I.1
Leib, D.E.2
Cochrane, J.3
Luo, H.4
Swyter, K.R.5
Chen, S.6
Clark, B.S.7
Thompson, J.8
Yates, J.R.9
Kingston, R.E.10
Kohtz, J.D.11
-
107
-
-
84929379665
-
The novel gene CRNDE encodes a nuclear peptide (CRNDEP) which is overexpressed in highly proliferating tissues
-
25978564 4433331 1:CAS:528:DC%2BC2MXhslKqsbvM
-
Szafron LM, Balcerak A, Grzybowska EA, Pienkowska-Grela B, Felisiak-Golabek A, Podgorska A, Kulesza M, Nowak N, Pomorski P, Wysocki J, Rubel T, Dansonka-Mieszkowska A, Konopka B, Lukasik M, Kupryjanczyk J. The novel gene CRNDE encodes a nuclear peptide (CRNDEP) which is overexpressed in highly proliferating tissues. PLoS One. 2015;10(5):e0127475.
-
(2015)
PLoS One
, vol.10
, Issue.5
, pp. e0127475
-
-
Szafron, L.M.1
Balcerak, A.2
Grzybowska, E.A.3
Pienkowska-Grela, B.4
Felisiak-Golabek, A.5
Podgorska, A.6
Kulesza, M.7
Nowak, N.8
Pomorski, P.9
Wysocki, J.10
Rubel, T.11
Dansonka-Mieszkowska, A.12
Konopka, B.13
Lukasik, M.14
Kupryjanczyk, J.15
-
108
-
-
84875417100
-
Long non-coding RNAs function annotation: a global prediction method based on bi-colored networks
-
1:CAS:528:DC%2BC3sXhtFyjtbY%3D 23132350
-
Guo X, Gao L, Liao Q, Xiao H, Ma X, Yang X, Luo H, Zhao G, Bu D, Jiao F, Shao Q, Chen R, Zhao Y. Long non-coding RNAs function annotation: a global prediction method based on bi-colored networks. Nucleic Acids Res. 2013;41(2):e35.
-
(2013)
Nucleic Acids Res
, vol.41
, Issue.2
, pp. e35
-
-
Guo, X.1
Gao, L.2
Liao, Q.3
Xiao, H.4
Ma, X.5
Yang, X.6
Luo, H.7
Zhao, G.8
Bu, D.9
Jiao, F.10
Shao, Q.11
Chen, R.12
Zhao, Y.13
-
109
-
-
84892571529
-
Long non-coding RNAs in neurodevelopmental disorders
-
van de Devondervoort II, Gordebeke PM, Khoshab N, Tiesinga PH, Buitelaar JK, Kozicz T, Aschrafi A, Glennon JC. Long non-coding RNAs in neurodevelopmental disorders. Front Mol Neurosci. 2013;6:53.
-
(2013)
Front Mol Neurosci
, vol.6
, pp. 53
-
-
II1
Gordebeke, P.M.2
Khoshab, N.3
Tiesinga, P.H.4
Buitelaar, J.K.5
Kozicz, T.6
Aschrafi, A.7
Glennon, J.C.8
-
110
-
-
78651325932
-
lncRNAdb: a reference database for long noncoding RNAs
-
1:CAS:528:DC%2BC3sXivF2mtLk%3D 21112873
-
Amaral PP, Clark MB, Gascoigne DK, Dinger ME, Mattick JS. lncRNAdb: a reference database for long noncoding RNAs. Nucleic Acids Res. 2011;39(Database issue):D146-51.
-
(2011)
Nucleic Acids Res
, vol.39
, Issue.Database issue
, pp. D146-D151
-
-
Amaral, P.P.1
Clark, M.B.2
Gascoigne, D.K.3
Dinger, M.E.4
Mattick, J.S.5
-
111
-
-
80052978224
-
Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses
-
1:CAS:528:DC%2BC3MXht1Oju7zI 21890647 3185964
-
Cabili MN, Trapnell C, Goff L, Koziol M, Tazon-Vega B, Regev A, Rinn JL. Integrative annotation of human large intergenic noncoding RNAs reveals global properties and specific subclasses. Genes Dev. 2011;25(18):1915-27.
-
(2011)
Genes Dev
, vol.25
, Issue.18
, pp. 1915-1927
-
-
Cabili, M.N.1
Trapnell, C.2
Goff, L.3
Koziol, M.4
Tazon-Vega, B.5
Regev, A.6
Rinn, J.L.7
-
112
-
-
84958769217
-
Autism and cancer share risk genes, pathways, and drug targets
-
1:CAS:528:DC%2BC28XhtVejt7w%3D 26830258 4769654
-
Crawley JN, Heyer WD, LaSalle JM. Autism and cancer share risk genes, pathways, and drug targets. Trends Genet. 2016;32(3):139-46.
-
(2016)
Trends Genet
, vol.32
, Issue.3
, pp. 139-146
-
-
Crawley, J.N.1
Heyer, W.D.2
LaSalle, J.M.3
-
113
-
-
84929963400
-
Autism spectrum disorder profile in neurofibromatosis type I
-
25475362
-
Garg S, Plasschaert E, Descheemaeker MJ, Huson S, Borghgraef M, Vogels A, Evans DG, Legius E, Green J. Autism spectrum disorder profile in neurofibromatosis type I. J Autism Dev Disord. 2015;45(6):1649-57.
-
(2015)
J Autism Dev Disord
, vol.45
, Issue.6
, pp. 1649-1657
-
-
Garg, S.1
Plasschaert, E.2
Descheemaeker, M.J.3
Huson, S.4
Borghgraef, M.5
Vogels, A.6
Evans, D.G.7
Legius, E.8
Green, J.9
-
114
-
-
84919459048
-
Prevalence of autism spectrum disorder symptoms in children with neurofibromatosis type 1
-
25388972 1:CAS:528:DC%2BC2cXitFSqtrjL
-
Plasschaert E, Descheemaeker MJ, Van Eylen L, Noens I, Steyaert J, Legius E. Prevalence of autism spectrum disorder symptoms in children with neurofibromatosis type 1. Am J Med Genet B Neuropsychiatr Genet. 2015;168B(1):72-80.
-
(2015)
Am J Med Genet B Neuropsychiatr Genet
, vol.168 B
, Issue.1
, pp. 72-80
-
-
Plasschaert, E.1
Descheemaeker, M.J.2
Van Eylen, L.3
Noens, I.4
Steyaert, J.5
Legius, E.6
-
115
-
-
84958811524
-
Epigenetic treatment of neuropsychiatric disorders: autism and schizophrenia
-
1:CAS:528:DC%2BC28XivVWnsr8%3D 26899191
-
Moos WH, Maneta E, Pinkert CA, Irwin MH, Hoffman ME, Faller DV, Steliou K. Epigenetic treatment of neuropsychiatric disorders: autism and schizophrenia. Drug Dev Res. 2016;77(2):53-72.
-
(2016)
Drug Dev Res
, vol.77
, Issue.2
, pp. 53-72
-
-
Moos, W.H.1
Maneta, E.2
Pinkert, C.A.3
Irwin, M.H.4
Hoffman, M.E.5
Faller, D.V.6
Steliou, K.7
-
116
-
-
83955165956
-
Downregulation of zinc finger protein 132 in prostate cancer is associated with aberrant promoter hypermethylation and poor prognosis
-
1:CAS:528:DC%2BC3MXhs1egs7nM 21445975
-
Abildgaard MO, Borre M, Mortensen MM, Ulhoi BP, Torring N, Wild P, Kristensen H, Mansilla F, Ottosen PD, Dyrskjot L, Orntoft TF, Sorensen KD. Downregulation of zinc finger protein 132 in prostate cancer is associated with aberrant promoter hypermethylation and poor prognosis. Int J Cancer. 2012;130(4):885-95.
-
(2012)
Int J Cancer
, vol.130
, Issue.4
, pp. 885-895
-
-
Abildgaard, M.O.1
Borre, M.2
Mortensen, M.M.3
Ulhoi, B.P.4
Torring, N.5
Wild, P.6
Kristensen, H.7
Mansilla, F.8
Ottosen, P.D.9
Dyrskjot, L.10
Orntoft, T.F.11
Sorensen, K.D.12
-
117
-
-
0029010375
-
Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders
-
1:CAS:528:DyaK2MXmsVSnurc%3D 7557990
-
Tommerup N, Vissing H. Isolation and fine mapping of 16 novel human zinc finger-encoding cDNAs identify putative candidate genes for developmental and malignant disorders. Genomics. 1995;27(2):259-64.
-
(1995)
Genomics
, vol.27
, Issue.2
, pp. 259-264
-
-
Tommerup, N.1
Vissing, H.2
-
118
-
-
84863309750
-
ALEX1 suppresses colony formation ability of human colorectal carcinoma cell lines
-
1:CAS:528:DC%2BC38XpsFKmtr8%3D 22494058
-
Iseki H, Takeda A, Andoh T, Kuwabara K, Takahashi N, Kurochkin IV, Ishida H, Okazaki Y, Koyama I. ALEX1 suppresses colony formation ability of human colorectal carcinoma cell lines. Cancer Sci. 2012;103(7):1267-71.
-
(2012)
Cancer Sci
, vol.103
, Issue.7
, pp. 1267-1271
-
-
Iseki, H.1
Takeda, A.2
Andoh, T.3
Kuwabara, K.4
Takahashi, N.5
Kurochkin, I.V.6
Ishida, H.7
Okazaki, Y.8
Koyama, I.9
-
119
-
-
84969752477
-
The role of telomeres and telomerase reverse transcriptase isoforms in pluripotency induction and maintenance
-
Teichroeb JH, Kim J, Betts DH. The role of telomeres and telomerase reverse transcriptase isoforms in pluripotency induction and maintenance. RNA Biol. 2016;13(8):707-19.
-
(2016)
RNA Biol
, vol.13
, Issue.8
, pp. 707-719
-
-
Teichroeb, J.H.1
Kim, J.2
Betts, D.H.3
-
120
-
-
80955135601
-
Molecular regulation of telomerase activity in aging
-
1:CAS:528:DC%2BC3MXht1ymtLvN 21976062 4875265
-
Nicholls C, Li H, Wang JQ, Liu JP. Molecular regulation of telomerase activity in aging. Protein Cell. 2011;2(9):726-38.
-
(2011)
Protein Cell
, vol.2
, Issue.9
, pp. 726-738
-
-
Nicholls, C.1
Li, H.2
Wang, J.Q.3
Liu, J.P.4
-
121
-
-
84939254208
-
CRNDE, a long-noncoding RNA, promotes glioma cell growth and invasion through mTOR signaling
-
1:CAS:528:DC%2BC2MXlsVWiu7w%3D 25813405
-
Wang Y, Wang Y, Li J, Zhang Y, Yin H, Han B. CRNDE, a long-noncoding RNA, promotes glioma cell growth and invasion through mTOR signaling. Cancer Lett. 2015;367(2):122-8.
-
(2015)
Cancer Lett
, vol.367
, Issue.2
, pp. 122-128
-
-
Wang, Y.1
Wang, Y.2
Li, J.3
Zhang, Y.4
Yin, H.5
Han, B.6
-
122
-
-
84879580092
-
Epigenome-wide ovarian cancer analysis identifies a methylation profile differentiating clear-cell histology with epigenetic silencing of the HERG K+ channel
-
1:CAS:528:DC%2BC3sXhtVKiu7rK 23571109 3699065
-
Cicek MS, Koestler DC, Fridley BL, Kalli KR, Armasu SM, Larson MC, Wang C, Winham SJ, Vierkant RA, Rider DN, Block MS, Klotzle B, Konecny G, Winterhoff BJ, Hamidi H, Shridhar V, Fan JB, Visscher DW, Olson JE, Hartmann LC, Bibikova M, Chien J, Cunningham JM, Goode EL. Epigenome-wide ovarian cancer analysis identifies a methylation profile differentiating clear-cell histology with epigenetic silencing of the HERG K+ channel. Hum Mol Genet. 2013;22(15):3038-47.
-
(2013)
Hum Mol Genet
, vol.22
, Issue.15
, pp. 3038-3047
-
-
Cicek, M.S.1
Koestler, D.C.2
Fridley, B.L.3
Kalli, K.R.4
Armasu, S.M.5
Larson, M.C.6
Wang, C.7
Winham, S.J.8
Vierkant, R.A.9
Rider, D.N.10
Block, M.S.11
Klotzle, B.12
Konecny, G.13
Winterhoff, B.J.14
Hamidi, H.15
Shridhar, V.16
Fan, J.B.17
Visscher, D.W.18
Olson, J.E.19
Hartmann, L.C.20
Bibikova, M.21
Chien, J.22
Cunningham, J.M.23
Goode, E.L.24
more..
-
123
-
-
84874789453
-
Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility
-
1:CAS:528:DC%2BC3sXjtlGntro%3D 23222812
-
Capasso M, Diskin SJ, Totaro F, Longo L, De Mariano M, Russo R, Cimmino F, Hakonarson H, Tonini GP, Devoto M, Maris JM, Iolascon A. Replication of GWAS-identified neuroblastoma risk loci strengthens the role of BARD1 and affirms the cumulative effect of genetic variations on disease susceptibility. Carcinogenesis. 2013;34(3):605-11.
-
(2013)
Carcinogenesis
, vol.34
, Issue.3
, pp. 605-611
-
-
Capasso, M.1
Diskin, S.J.2
Totaro, F.3
Longo, L.4
De Mariano, M.5
Russo, R.6
Cimmino, F.7
Hakonarson, H.8
Tonini, G.P.9
Devoto, M.10
Maris, J.M.11
Iolascon, A.12
-
124
-
-
85047696885
-
Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between rhabdomyosarcoma subtypes
-
1:CAS:528:DC%2BD38XjvFejurc%3D 12082533
-
Chan AS, Thorner PS, Squire JA, Zielenska M. Identification of a novel gene NCRMS on chromosome 12q21 with differential expression between rhabdomyosarcoma subtypes. Oncogene. 2002;21(19):3029-37.
-
(2002)
Oncogene
, vol.21
, Issue.19
, pp. 3029-3037
-
-
Chan, A.S.1
Thorner, P.S.2
Squire, J.A.3
Zielenska, M.4
-
125
-
-
78650565096
-
Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries
-
1:CAS:528:DC%2BC3cXhs1WgtbrJ 21037240
-
Williams HJ, Craddock N, Russo G, Hamshere ML, Moskvina V, Dwyer S, Smith RL, Green E, Grozeva D, Holmans P, Owen MJ, O'Donovan MC. Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries. Hum Mol Genet. 2011;20(2):387-91.
-
(2011)
Hum Mol Genet
, vol.20
, Issue.2
, pp. 387-391
-
-
Williams, H.J.1
Craddock, N.2
Russo, G.3
Hamshere, M.L.4
Moskvina, V.5
Dwyer, S.6
Smith, R.L.7
Green, E.8
Grozeva, D.9
Holmans, P.10
Owen, M.J.11
O'Donovan, M.C.12
-
126
-
-
84870064101
-
Modeling psychiatric disorders at the cellular and network levels
-
1:STN:280:DC%2BC38ritVSisw%3D%3D 22472874 3465628
-
Brennand KJ, Simone A, Tran N, Gage FH. Modeling psychiatric disorders at the cellular and network levels. Mol Psychiatry. 2012;17(12):1239-53.
-
(2012)
Mol Psychiatry
, vol.17
, Issue.12
, pp. 1239-1253
-
-
Brennand, K.J.1
Simone, A.2
Tran, N.3
Gage, F.H.4
-
127
-
-
84922680190
-
Altered gene expression in schizophrenia: findings from transcriptional signatures in fibroblasts and blood
-
25658856 4319917 1:CAS:528:DC%2BC2MXhs1Whu7zN
-
Cattane N, Minelli A, Milanesi E, Maj C, Bignotti S, Bortolomasi M, Bocchio Chiavetto L, Gennarelli M. Altered gene expression in schizophrenia: findings from transcriptional signatures in fibroblasts and blood. PLoS One. 2015;10(2):e0116686.
-
(2015)
PLoS One
, vol.10
, Issue.2
, pp. e0116686
-
-
Cattane, N.1
Minelli, A.2
Milanesi, E.3
Maj, C.4
Bignotti, S.5
Bortolomasi, M.6
Bocchio Chiavetto, L.7
Gennarelli, M.8
-
128
-
-
84880134983
-
Analysis of miR-137 expression and rs1625579 in dorsolateral prefrontal cortex
-
23786914 3753093
-
Guella I, Sequeira A, Rollins B, Morgan L, Torri F, van Erp TG, Myers RM, Barchas JD, Schatzberg AF, Watson SJ, Akil H, Bunney WE, Potkin SG, Macciardi F, Vawter MP. Analysis of miR-137 expression and rs1625579 in dorsolateral prefrontal cortex. J Psychiatr Res. 2013;47(9):1215-21.
-
(2013)
J Psychiatr Res
, vol.47
, Issue.9
, pp. 1215-1221
-
-
Guella, I.1
Sequeira, A.2
Rollins, B.3
Morgan, L.4
Torri, F.5
Van Erp, T.G.6
Myers, R.M.7
Barchas, J.D.8
Schatzberg, A.F.9
Watson, S.J.10
Akil, H.11
Bunney, W.E.12
Potkin, S.G.13
Macciardi, F.14
Vawter, M.P.15
-
129
-
-
80053384370
-
Genome-wide association study identifies five new schizophrenia loci
-
Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium 1:CAS:528:DC%2BC3MXhtFylsrfM
-
Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium. Genome-wide association study identifies five new schizophrenia loci. Nat Genet. 2011;43(10):969-76.
-
(2011)
Nat Genet
, vol.43
, Issue.10
, pp. 969-976
-
-
-
130
-
-
84879410405
-
Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia
-
Green MJ, Cairns MJ, Wu J, Dragovic M, Jablensky A, Tooney PA, Scott RJ, Carr VJ. Genome-wide supported variant MIR137 and severe negative symptoms predict membership of an impaired cognitive subtype of schizophrenia. Mol Psychiatry. 2013;18(7):774-80.
-
(2013)
Mol Psychiatry
, vol.18
, Issue.7
, pp. 774-780
-
-
Green, M.J.1
Cairns, M.J.2
Wu, J.3
Dragovic, M.4
Jablensky, A.5
Tooney, P.A.6
Scott, R.J.7
Carr, V.J.8
-
131
-
-
77953613107
-
Cognitive and sensorimotor gating impairments in transgenic mice overexpressing the schizophrenia susceptibility gene Tcf4 in the brain
-
1:CAS:528:DC%2BC3cXnvVensL8%3D 20434134
-
Brzozka MM, Radyushkin K, Wichert SP, Ehrenreich H, Rossner MJ. Cognitive and sensorimotor gating impairments in transgenic mice overexpressing the schizophrenia susceptibility gene Tcf4 in the brain. Biol Psychiatry. 2010;68(1):33-40.
-
(2010)
Biol Psychiatry
, vol.68
, Issue.1
, pp. 33-40
-
-
Brzozka, M.M.1
Radyushkin, K.2
Wichert, S.P.3
Ehrenreich, H.4
Rossner, M.J.5
-
132
-
-
84901625426
-
The emerging roles of TCF4 in disease and development
-
1:CAS:528:DC%2BC2cXjsF2itLk%3D 24594265
-
Forrest MP, Hill MJ, Quantock AJ, Martin-Rendon E, Blake DJ. The emerging roles of TCF4 in disease and development. Trends Mol Med. 2014;20(6):322-31.
-
(2014)
Trends Mol Med
, vol.20
, Issue.6
, pp. 322-331
-
-
Forrest, M.P.1
Hill, M.J.2
Quantock, A.J.3
Martin-Rendon, E.4
Blake, D.J.5
-
133
-
-
84960130448
-
Identification of novel genetic causes of Rett syndrome-like phenotypes
-
26740508
-
Lopes F, Barbosa M, Ameur A, Soares G, de Sa J, Dias AI, Oliveira G, Cabral P, Temudo T, Calado E, Cruz IF, Vieira JP, Oliveira R, Esteves S, Sauer S, Jonasson I, Syvanen AC, Gyllensten U, Pinto D, Maciel P. Identification of novel genetic causes of Rett syndrome-like phenotypes. J Med Genet. 2016;53(3):190-9.
-
(2016)
J Med Genet
, vol.53
, Issue.3
, pp. 190-199
-
-
Lopes, F.1
Barbosa, M.2
Ameur, A.3
Soares, G.4
De Sa, J.5
Dias, A.I.6
Oliveira, G.7
Cabral, P.8
Temudo, T.9
Calado, E.10
Cruz, I.F.11
Vieira, J.P.12
Oliveira, R.13
Esteves, S.14
Sauer, S.15
Jonasson, I.16
Syvanen, A.C.17
Gyllensten, U.18
Pinto, D.19
Maciel, P.20
more..
-
134
-
-
84925934363
-
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing
-
Redin C, Gerard B, Lauer J, Herenger Y, Muller J, Quartier A, Masurel-Paulet A, Willems M, Lesca G, El-Chehadeh S, Le Gras S, Vicaire S, Philipps M, Dumas M, Geoffroy V, Feger C, Haumesser N, Alembik Y, Barth M, Bonneau D, Colin E, Dollfus H, Doray B, Delrue MA, Drouin-Garraud V, Flori E, Fradin M, Francannet C, Goldenberg A, Lumbroso S, Mathieu-Dramard M, Martin-Coignard D, Lacombe D, Morin G, Polge A, Sukno S, Thauvin-Robinet C, Thevenon J, Doco-Fenzy M, Genevieve D, Sarda P, Edery P, Isidor B, Jost B, Olivier-Faivre L, Mandel JL, Piton A. Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing. J Med Genet. 2014;51(11):724-36.
-
(2014)
J Med Genet
, vol.51
, Issue.11
, pp. 724-736
-
-
Redin, C.1
Gerard, B.2
Lauer, J.3
Herenger, Y.4
Muller, J.5
Quartier, A.6
Masurel-Paulet, A.7
Willems, M.8
Lesca, G.9
El-Chehadeh, S.10
Le Gras, S.11
Vicaire, S.12
Philipps, M.13
Dumas, M.14
Geoffroy, V.15
Feger, C.16
Haumesser, N.17
Alembik, Y.18
Barth, M.19
Bonneau, D.20
Colin, E.21
Dollfus, H.22
Doray, B.23
Delrue, M.A.24
Drouin-Garraud, V.25
Flori, E.26
Fradin, M.27
Francannet, C.28
Goldenberg, A.29
Lumbroso, S.30
Mathieu-Dramard, M.31
Martin-Coignard, D.32
Lacombe, D.33
Morin, G.34
Polge, A.35
Sukno, S.36
Thauvin-Robinet, C.37
Thevenon, J.38
Doco-Fenzy, M.39
Genevieve, D.40
Sarda, P.41
Edery, P.42
Isidor, B.43
Jost, B.44
Olivier-Faivre, L.45
Mandel, J.L.46
Piton, A.47
more..
-
135
-
-
55549108087
-
TCF4 deletions in Pitt-Hopkins syndrome
-
18781613
-
Giurgea I, Missirian C, Cacciagli P, Whalen S, Fredriksen T, Gaillon T, Rankin J, Mathieu-Dramard M, Morin G, Martin-Coignard D, Dubourg C, Chabrol B, Arfi J, Giuliano F, Claude Lambert J, Philip N, Sarda P, Villard L, Goossens M, Moncla A. TCF4 deletions in Pitt-Hopkins syndrome. Hum Mutat. 2008;29(11):E242-51.
-
(2008)
Hum Mutat
, vol.29
, Issue.11
, pp. E242-E251
-
-
Giurgea, I.1
Missirian, C.2
Cacciagli, P.3
Whalen, S.4
Fredriksen, T.5
Gaillon, T.6
Rankin, J.7
Mathieu-Dramard, M.8
Morin, G.9
Martin-Coignard, D.10
Dubourg, C.11
Chabrol, B.12
Arfi, J.13
Giuliano, F.14
Claude Lambert, J.15
Philip, N.16
Sarda, P.17
Villard, L.18
Goossens, M.19
Moncla, A.20
more..
-
136
-
-
84896374339
-
Genome-wide association study reveals two new risk loci for bipolar disorder
-
24618891 1:CAS:528:DC%2BC2cXmtlensLc%3D
-
Muhleisen TW, Leber M, Schulze TG, Strohmaier J, Degenhardt F, Treutlein J, Mattheisen M, Forstner AJ, Schumacher J, Breuer R, Meier S, Herms S, Hoffmann P, Lacour A, Witt SH, Reif A, Muller-Myhsok B, Lucae S, Maier W, Schwarz M, Vedder H, Kammerer-Ciernioch J, Pfennig A, Bauer M, Hautzinger M, Moebus S, Priebe L, Czerski PM, Hauser J, Lissowska J, Szeszenia-Dabrowska N, Brennan P, McKay JD, Wright A, Mitchell PB, Fullerton JM, Schofield PR, Montgomery GW, Medland SE, Gordon SD, Martin NG, Krasnow V, Chuchalin A, Babadjanova G, Pantelejeva G, Abramova LI, Tiganov AS, Polonikov A, Khusnutdinova E, Alda M, Grof P, Rouleau GA, Turecki G, Laprise C, Rivas F, Mayoral F, Kogevinas M, Grigoroiu-Serbanescu M, Propping P, Becker T, Rietschel M, Nothen MM, Cichon S. Genome-wide association study reveals two new risk loci for bipolar disorder. Nat Commun. 2014;5:3339.
-
(2014)
Nat Commun
, vol.5
, pp. 3339
-
-
Muhleisen, T.W.1
Leber, M.2
Schulze, T.G.3
Strohmaier, J.4
Degenhardt, F.5
Treutlein, J.6
Mattheisen, M.7
Forstner, A.J.8
Schumacher, J.9
Breuer, R.10
Meier, S.11
Herms, S.12
Hoffmann, P.13
Lacour, A.14
Witt, S.H.15
Reif, A.16
Muller-Myhsok, B.17
Lucae, S.18
Maier, W.19
Schwarz, M.20
Vedder, H.21
Kammerer-Ciernioch, J.22
Pfennig, A.23
Bauer, M.24
Hautzinger, M.25
Moebus, S.26
Priebe, L.27
Czerski, P.M.28
Hauser, J.29
Lissowska, J.30
Szeszenia-Dabrowska, N.31
Brennan, P.32
McKay, J.D.33
Wright, A.34
Mitchell, P.B.35
Fullerton, J.M.36
Schofield, P.R.37
Montgomery, G.W.38
Medland, S.E.39
Gordon, S.D.40
Martin, N.G.41
Krasnow, V.42
Chuchalin, A.43
Babadjanova, G.44
Pantelejeva, G.45
Abramova, L.I.46
Tiganov, A.S.47
Polonikov, A.48
Khusnutdinova, E.49
Alda, M.50
Grof, P.51
Rouleau, G.A.52
Turecki, G.53
Laprise, C.54
Rivas, F.55
Mayoral, F.56
Kogevinas, M.57
Grigoroiu-Serbanescu, M.58
Propping, P.59
Becker, T.60
Rietschel, M.61
Nothen, M.M.62
Cichon, S.63
more..
-
137
-
-
57749203394
-
FBIRN: a genome-wide association study of schizophrenia using brain activation as a quantitative phenotype
-
19023125
-
Potkin SG, Turner JA, Guffanti G, Lakatos A, Fallon JH, Nguyen DD, Mathalon D, Ford J, Lauriello J, Macciardi F. FBIRN: a genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. Schizophr Bull. 2009;35(1):96-108.
-
(2009)
Schizophr Bull
, vol.35
, Issue.1
, pp. 96-108
-
-
Potkin, S.G.1
Turner, J.A.2
Guffanti, G.3
Lakatos, A.4
Fallon, J.H.5
Nguyen, D.D.6
Mathalon, D.7
Ford, J.8
Lauriello, J.9
Macciardi, F.10
-
138
-
-
77649162059
-
Direct conversion of fibroblasts to functional neurons by defined factors
-
1:CAS:528:DC%2BC3cXhtFCgsr0%3D 20107439 2829121
-
Vierbuchen T, Ostermeier A, Pang ZP, Kokubu Y, Sudhof TC, Wernig M. Direct conversion of fibroblasts to functional neurons by defined factors. Nature. 2010;463(7284):1035-41.
-
(2010)
Nature
, vol.463
, Issue.7284
, pp. 1035-1041
-
-
Vierbuchen, T.1
Ostermeier, A.2
Pang, Z.P.3
Kokubu, Y.4
Sudhof, T.C.5
Wernig, M.6
-
139
-
-
84922217833
-
An AUTS2-Polycomb complex activates gene expression in the CNS
-
1:CAS:528:DC%2BC2cXitFCqsrjL 25519132 4323097
-
Gao Z, Lee P, Stafford JM, von Schimmelmann M, Schaefer A, Reinberg D. An AUTS2-Polycomb complex activates gene expression in the CNS. Nature. 2014;516(7531):349-54.
-
(2014)
Nature
, vol.516
, Issue.7531
, pp. 349-354
-
-
Gao, Z.1
Lee, P.2
Stafford, J.M.3
Von Schimmelmann, M.4
Schaefer, A.5
Reinberg, D.6
-
140
-
-
84956829022
-
Exonic deletions of AUTS2 in Chinese patients with developmental delay and intellectual disability
-
1:CAS:528:DC%2BC28Xhs1KhsbY%3D
-
Fan Y, Qiu W, Wang L, Gu X, Yu Y. Exonic deletions of AUTS2 in Chinese patients with developmental delay and intellectual disability. Am J Med Genet A. 2016;170(2):515-22.
-
(2016)
Am J Med Genet A
, vol.170
, Issue.2
, pp. 515-522
-
-
Fan, Y.1
Qiu, W.2
Wang, L.3
Gu, X.4
Yu, Y.5
-
141
-
-
84929943707
-
De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature review
-
1:CAS:528:DC%2BC2MXpt1yitLY%3D 25851617
-
Liu Y, Zhao D, Dong R, Yang X, Zhang Y, Tammimies K, Uddin M, Scherer SW, Gai Z. De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: a case report and a brief literature review. Am J Med Genet A. 2015;167(6):1381-5.
-
(2015)
Am J Med Genet A
, vol.167
, Issue.6
, pp. 1381-1385
-
-
Liu, Y.1
Zhao, D.2
Dong, R.3
Yang, X.4
Zhang, Y.5
Tammimies, K.6
Uddin, M.7
Scherer, S.W.8
Gai, Z.9
-
142
-
-
84862541658
-
PAX5-AUTS2: a recurrent fusion gene in childhood B-cell precursor acute lymphoblastic leukemia
-
1:CAS:528:DC%2BC38XntFahtLw%3D 22578776 3389344
-
Denk D, Nebral K, Bradtke J, Pass G, Moricke A, Attarbaschi A, Strehl S. PAX5-AUTS2: a recurrent fusion gene in childhood B-cell precursor acute lymphoblastic leukemia. Leuk Res. 2012;36(8):e178-81.
-
(2012)
Leuk Res
, vol.36
, Issue.8
, pp. e178-e181
-
-
Denk, D.1
Nebral, K.2
Bradtke, J.3
Pass, G.4
Moricke, A.5
Attarbaschi, A.6
Strehl, S.7
-
143
-
-
33744804277
-
The Evf-2 noncoding RNA is transcribed from the Dlx-5/6 ultraconserved region and functions as a Dlx-2 transcriptional coactivator
-
1:CAS:528:DC%2BD28XlsF2ktLY%3D 16705037 1475760
-
Feng J, Bi C, Clark BS, Mady R, Shah P, Kohtz JD. The Evf-2 noncoding RNA is transcribed from the Dlx-5/6 ultraconserved region and functions as a Dlx-2 transcriptional coactivator. Genes Dev. 2006;20(11):1470-84.
-
(2006)
Genes Dev
, vol.20
, Issue.11
, pp. 1470-1484
-
-
Feng, J.1
Bi, C.2
Clark, B.S.3
Mady, R.4
Shah, P.5
Kohtz, J.D.6
-
144
-
-
0030331175
-
Up-regulation of GABAA receptor binding on neurons of the prefrontal cortex in schizophrenic subjects
-
1:CAS:528:DyaK28Xnt1Sksrc%3D 8938738
-
Benes FM, Vincent SL, Marie A, Khan Y. Up-regulation of GABAA receptor binding on neurons of the prefrontal cortex in schizophrenic subjects. Neuroscience. 1996;75(4):1021-31.
-
(1996)
Neuroscience
, vol.75
, Issue.4
, pp. 1021-1031
-
-
Benes, F.M.1
Vincent, S.L.2
Marie, A.3
Khan, Y.4
-
145
-
-
84929697246
-
Alterations in cortical network oscillations and parvalbumin neurons in schizophrenia
-
1:CAS:528:DC%2BC2MXmt1Sku7c%3D 25863358 4444373
-
Gonzalez-Burgos G, Cho RY, Lewis DA. Alterations in cortical network oscillations and parvalbumin neurons in schizophrenia. Biol Psychiatry. 2015;77(12):1031-40.
-
(2015)
Biol Psychiatry
, vol.77
, Issue.12
, pp. 1031-1040
-
-
Gonzalez-Burgos, G.1
Cho, R.Y.2
Lewis, D.A.3
-
146
-
-
85021271358
-
The number of parvalbumin-expressing interneurons is decreased in the medial prefrontal cortex in autism
-
Epub ahead of print
-
Hashemi E, Ariza J, Rogers H, Noctor SC, Martinez-Cerdeno V. The number of parvalbumin-expressing interneurons is decreased in the medial prefrontal cortex in autism. Cereb Cortex. 2016, [Epub ahead of print].
-
(2016)
Cereb Cortex
-
-
Hashemi, E.1
Ariza, J.2
Rogers, H.3
Noctor, S.C.4
Martinez-Cerdeno, V.5
-
147
-
-
0025066941
-
More powerful procedures for multiple significance testing
-
1:STN:280:DyaK3M%2FhvFSgsA%3D%3D 2218183
-
Hochberg Y, Benjamini Y. More powerful procedures for multiple significance testing. Stat Med. 1990;9(7):811-8.
-
(1990)
Stat Med
, vol.9
, Issue.7
, pp. 811-818
-
-
Hochberg, Y.1
Benjamini, Y.2
|