-
1
-
-
0033149175
-
Neurodevelopmental abnormalities in schizophrenia: Insights from neuropathology
-
S.E. Arnold Neurodevelopmental abnormalities in schizophrenia: insights from neuropathology Dev. Psychopathol. 11 1999 439 456
-
(1999)
Dev. Psychopathol.
, vol.11
, pp. 439-456
-
-
Arnold, S.E.1
-
3
-
-
4544386317
-
Sra-1 interacts with Kette and Wasp and is required for neuronal and bristle development in Drosophila
-
S. Bogdan, O. Grewe, M. Strunk, A. Mertens, and C. Klämbt Sra-1 interacts with Kette and Wasp and is required for neuronal and bristle development in Drosophila Development 131 2004 3981 3989
-
(2004)
Development
, vol.131
, pp. 3981-3989
-
-
Bogdan, S.1
Grewe, O.2
Strunk, M.3
Mertens, A.4
Klämbt, C.5
-
4
-
-
84865000639
-
Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice
-
O. Bozdagi, T. Sakurai, N. Dorr, M. Pilorge, N. Takahashi, and J.D. Buxbaum Haploinsufficiency of Cyfip1 produces fragile X-like phenotypes in mice PLoS ONE 7 2012 e42422
-
(2012)
PLoS ONE
, vol.7
, pp. 42422
-
-
Bozdagi, O.1
Sakurai, T.2
Dorr, N.3
Pilorge, M.4
Takahashi, N.5
Buxbaum, J.D.6
-
5
-
-
33846460770
-
Spindle regulation in neural precursors of flies and mammals
-
J.J. Buchman, and L.H. Tsai Spindle regulation in neural precursors of flies and mammals Nat. Rev. Neurosci. 8 2007 89 100
-
(2007)
Nat. Rev. Neurosci.
, vol.8
, pp. 89-100
-
-
Buchman, J.J.1
Tsai, L.H.2
-
6
-
-
79953048441
-
Integration-free induced pluripotent stem cells derived from schizophrenia patients with a DISC1 mutation
-
C.H. Chiang, Y. Su, Z. Wen, N. Yoritomo, C.A. Ross, R.L. Margolis, H. Song, and G.L. Ming Integration-free induced pluripotent stem cells derived from schizophrenia patients with a DISC1 mutation Mol. Psychiatry 16 2011 358 360
-
(2011)
Mol. Psychiatry
, vol.16
, pp. 358-360
-
-
Chiang, C.H.1
Su, Y.2
Wen, Z.3
Yoritomo, N.4
Ross, C.A.5
Margolis, R.L.6
Song, H.7
Ming, G.L.8
-
7
-
-
84861441557
-
Application of reprogrammed patient cells to investigate the etiology of neurological and psychiatric disorders
-
K. Christian, H. Song, and G. Ming Application of reprogrammed patient cells to investigate the etiology of neurological and psychiatric disorders Front. Biol. 7 2012 179 188
-
(2012)
Front. Biol.
, vol.7
, pp. 179-188
-
-
Christian, K.1
Song, H.2
Ming, G.3
-
8
-
-
80055015161
-
Temporal dynamics and genetic control of transcription in the human prefrontal cortex
-
C. Colantuoni, B.K. Lipska, T. Ye, T.M. Hyde, R. Tao, J.T. Leek, E.A. Colantuoni, A.G. Elkahloun, M.M. Herman, D.R. Weinberger, and J.E. Kleinman Temporal dynamics and genetic control of transcription in the human prefrontal cortex Nature 478 2011 519 523
-
(2011)
Nature
, vol.478
, pp. 519-523
-
-
Colantuoni, C.1
Lipska, B.K.2
Ye, T.3
Hyde, T.M.4
Tao, R.5
Leek, J.T.6
Colantuoni, E.A.7
Elkahloun, A.G.8
Herman, M.M.9
Weinberger, D.R.10
Kleinman, J.E.11
-
9
-
-
80052260252
-
A copy number variation morbidity map of developmental delay
-
G.M. Cooper, B.P. Coe, S. Girirajan, J.A. Rosenfeld, T.H. Vu, C. Baker, C. Williams, H. Stalker, R. Hamid, and V. Hannig et al. A copy number variation morbidity map of developmental delay Nat. Genet. 43 2011 838 846
-
(2011)
Nat. Genet.
, vol.43
, pp. 838-846
-
-
Cooper, G.M.1
Coe, B.P.2
Girirajan, S.3
Rosenfeld, J.A.4
Vu, T.H.5
Baker, C.6
Williams, C.7
Stalker, H.8
Hamid, R.9
Hannig, V.10
-
10
-
-
74249088463
-
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
-
C.G. de Kovel, H. Trucks, I. Helbig, H.C. Mefford, C. Baker, C. Leu, C. Kluck, H. Muhle, S. von Spiczak, and P. Ostertag et al. Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies Brain 133 2010 23 32
-
(2010)
Brain
, vol.133
, pp. 23-32
-
-
De Kovel, C.G.1
Trucks, H.2
Helbig, I.3
Mefford, H.C.4
Baker, C.5
Leu, C.6
Kluck, C.7
Muhle, H.8
Von Spiczak, S.9
Ostertag, P.10
-
11
-
-
84886261029
-
Genetic counseling for susceptibility loci and neurodevelopmental disorders: The del15q11.2 as an example
-
V. De Wolf, N. Brison, K. Devriendt, and H. Peeters Genetic counseling for susceptibility loci and neurodevelopmental disorders: the del15q11.2 as an example Am. J. Med. Genet. A. 161A 2013 2846 2854
-
(2013)
Am. J. Med. Genet. A.
, vol.161 A
, pp. 2846-2854
-
-
De Wolf, V.1
Brison, N.2
Devriendt, K.3
Peeters, H.4
-
12
-
-
79955563189
-
Essential role for Abi1 in embryonic survival and WAVE2 complex integrity
-
P.M. Dubielecka, K.I. Ladwein, X. Xiong, I. Migeotte, A. Chorzalska, K.V. Anderson, J.A. Sawicki, K. Rottner, T.E. Stradal, and L. Kotula Essential role for Abi1 in embryonic survival and WAVE2 complex integrity Proc. Natl. Acad. Sci. USA 108 2011 7022 7027
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, pp. 7022-7027
-
-
Dubielecka, P.M.1
Ladwein, K.I.2
Xiong, X.3
Migeotte, I.4
Chorzalska, A.5
Anderson, K.V.6
Sawicki, J.A.7
Rottner, K.8
Stradal, T.E.9
Kotula, L.10
-
13
-
-
12144266963
-
Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex
-
C. Englund, A. Fink, C. Lau, D. Pham, R.A. Daza, A. Bulfone, T. Kowalczyk, and R.F. Hevner Pax6, Tbr2, and Tbr1 are expressed sequentially by radial glia, intermediate progenitor cells, and postmitotic neurons in developing neocortex J. Neurosci. 25 2005 247 251
-
(2005)
J. Neurosci.
, vol.25
, pp. 247-251
-
-
Englund, C.1
Fink, A.2
Lau, C.3
Pham, D.4
Daza, R.A.5
Bulfone, A.6
Kowalczyk, T.7
Hevner, R.F.8
-
14
-
-
80053618318
-
CYFIP dependent actin remodeling controls specific aspects of Drosophila eye morphogenesis
-
A. Galy, A. Schenck, H.B. Sahin, A. Qurashi, J.A. Sahel, C. Diebold, and A. Giangrande CYFIP dependent actin remodeling controls specific aspects of Drosophila eye morphogenesis Dev. Biol. 359 2011 37 46
-
(2011)
Dev. Biol.
, vol.359
, pp. 37-46
-
-
Galy, A.1
Schenck, A.2
Sahin, H.B.3
Qurashi, A.4
Sahel, J.A.5
Diebold, C.6
Giangrande, A.7
-
15
-
-
67650732715
-
Advances in autism
-
D.H. Geschwind Advances in autism Annu. Rev. Med. 60 2009 367 380
-
(2009)
Annu. Rev. Med.
, vol.60
, pp. 367-380
-
-
Geschwind, D.H.1
-
16
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia Consortium
-
International Schizophrenia Consortium Rare chromosomal deletions and duplications increase risk of schizophrenia Nature 455 2008 237 241
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
17
-
-
84875639152
-
Scratch regulates neuronal migration onset via an epithelial-mesenchymal transition-like mechanism
-
Y. Itoh, Y. Moriyama, T. Hasegawa, T.A. Endo, T. Toyoda, and Y. Gotoh Scratch regulates neuronal migration onset via an epithelial-mesenchymal transition-like mechanism Nat. Neurosci. 16 2013 416 425
-
(2013)
Nat. Neurosci.
, vol.16
, pp. 416-425
-
-
Itoh, Y.1
Moriyama, Y.2
Hasegawa, T.3
Endo, T.A.4
Toyoda, T.5
Gotoh, Y.6
-
18
-
-
84890802172
-
Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies
-
J.A. Jähn, S. von Spiczak, H. Muhle, T. Obermeier, A. Franke, H.C. Mefford, U. Stephani, and I. Helbig Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carrierFs in pediatric epilepsies Epilepsy Res. 108 2014 109 116
-
(2014)
Epilepsy Res.
, vol.108
, pp. 109-116
-
-
Jähn, J.A.1
Von Spiczak, S.2
Muhle, H.3
Obermeier, T.4
Franke, A.5
Mefford, H.C.6
Stephani, U.7
Helbig, I.8
-
19
-
-
84861203696
-
Astrocytes generated from patient induced pluripotent stem cells recapitulate features of Huntington's disease patient cells
-
T.A. Juopperi, W.R. Kim, C.H. Chiang, H. Yu, R.L. Margolis, C.A. Ross, G.L. Ming, and H. Song Astrocytes generated from patient induced pluripotent stem cells recapitulate features of Huntington's disease patient cells Mol. Brain 5 2012 17
-
(2012)
Mol. Brain
, vol.5
, pp. 17
-
-
Juopperi, T.A.1
Kim, W.R.2
Chiang, C.H.3
Yu, H.4
Margolis, R.L.5
Ross, C.A.6
Ming, G.L.7
Song, H.8
-
20
-
-
64549147485
-
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
-
International Schizophrenia Consortium Wellcome Trust Case Control Consortium
-
G. Kirov, D. Grozeva, N. Norton, D. Ivanov, K.K. Mantripragada, P. Holmans, N. Craddock, M.J. Owen, M.C. O'Donovan International Schizophrenia Consortium Wellcome Trust Case Control Consortium Support for the involvement of large copy number variants in the pathogenesis of schizophrenia Hum. Mol. Genet. 18 2009 1497 1503
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 1497-1503
-
-
Kirov, G.1
Grozeva, D.2
Norton, N.3
Ivanov, D.4
Mantripragada, K.K.5
Holmans, P.6
Craddock, N.7
Owen, M.J.8
O'Donovan, M.C.9
-
21
-
-
0031972690
-
P140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase
-
K. Kobayashi, S. Kuroda, M. Fukata, T. Nakamura, T. Nagase, N. Nomura, Y. Matsuura, N. Yoshida-Kubomura, A. Iwamatsu, and K. Kaibuchi p140Sra-1 (specifically Rac1-associated protein) is a novel specific target for Rac1 small GTPase J. Biol. Chem. 273 1998 291 295
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 291-295
-
-
Kobayashi, K.1
Kuroda, S.2
Fukata, M.3
Nakamura, T.4
Nagase, T.5
Nomura, N.6
Matsuura, Y.7
Yoshida-Kubomura, N.8
Iwamatsu, A.9
Kaibuchi, K.10
-
22
-
-
67651036549
-
The glial nature of embryonic and adult neural stem cells
-
A. Kriegstein, and A. Alvarez-Buylla The glial nature of embryonic and adult neural stem cells Annu. Rev. Neurosci. 32 2009 149 184
-
(2009)
Annu. Rev. Neurosci.
, vol.32
, pp. 149-184
-
-
Kriegstein, A.1
Alvarez-Buylla, A.2
-
23
-
-
0242286595
-
Abi, Sra1, and Kette control the stability and localization of SCAR/WAVE to regulate the formation of actin-based protrusions
-
P. Kunda, G. Craig, V. Dominguez, and B. Baum Abi, Sra1, and Kette control the stability and localization of SCAR/WAVE to regulate the formation of actin-based protrusions Curr. Biol. 13 2003 1867 1875
-
(2003)
Curr. Biol.
, vol.13
, pp. 1867-1875
-
-
Kunda, P.1
Craig, G.2
Dominguez, V.3
Baum, B.4
-
24
-
-
46549089463
-
The determination of projection neuron identity in the developing cerebral cortex
-
D.P. Leone, K. Srinivasan, B. Chen, E. Alcamo, and S.K. McConnell The determination of projection neuron identity in the developing cerebral cortex Curr. Opin. Neurobiol. 18 2008 28 35
-
(2008)
Curr. Opin. Neurobiol.
, vol.18
, pp. 28-35
-
-
Leone, D.P.1
Srinivasan, K.2
Chen, B.3
Alcamo, E.4
McConnell, S.K.5
-
25
-
-
79957777958
-
Rapid induction and long-term self-renewal of primitive neural precursors from human embryonic stem cells by small molecule inhibitors
-
W. Li, W. Sun, Y. Zhang, W. Wei, R. Ambasudhan, P. Xia, M. Talantova, T. Lin, J. Kim, and X. Wang et al. Rapid induction and long-term self-renewal of primitive neural precursors from human embryonic stem cells by small molecule inhibitors Proc. Natl. Acad. Sci. USA 108 2011 8299 8304
-
(2011)
Proc. Natl. Acad. Sci. USA
, vol.108
, pp. 8299-8304
-
-
Li, W.1
Sun, W.2
Zhang, Y.3
Wei, W.4
Ambasudhan, R.5
Xia, P.6
Talantova, M.7
Lin, T.8
Kim, J.9
Wang, X.10
-
26
-
-
69349099442
-
Beta1 integrin maintains integrity of the embryonic neocortical stem cell niche
-
K. Loulier, J.D. Lathia, V. Marthiens, J. Relucio, M.R. Mughal, S.C. Tang, T. Coksaygan, P.E. Hall, S. Chigurupati, and B. Patton et al. beta1 integrin maintains integrity of the embryonic neocortical stem cell niche PLoS Biol. 7 2009 e1000176
-
(2009)
PLoS Biol.
, vol.7
, pp. 1000176
-
-
Loulier, K.1
Lathia, J.D.2
Marthiens, V.3
Relucio, J.4
Mughal, M.R.5
Tang, S.C.6
Coksaygan, T.7
Hall, P.E.8
Chigurupati, S.9
Patton, B.10
-
27
-
-
84858434210
-
CNVs: Harbingers of a rare variant revolution in psychiatric genetics
-
D. Malhotra, and J. Sebat CNVs: harbingers of a rare variant revolution in psychiatric genetics Cell 148 2012 1223 1241
-
(2012)
Cell
, vol.148
, pp. 1223-1241
-
-
Malhotra, D.1
Sebat, J.2
-
28
-
-
79959662116
-
Normalization of cortical gray matter deficits in nonpsychotic siblings of patients with childhood-onset schizophrenia
-
A.A. Mattai, B. Weisinger, D. Greenstein, R. Stidd, L. Clasen, R. Miller, J.W. Tossell, J.L. Rapoport, and N. Gogtay Normalization of cortical gray matter deficits in nonpsychotic siblings of patients with childhood-onset schizophrenia J. Am. Acad. Child Adolesc. Psychiatry 50 2011 697 704
-
(2011)
J. Am. Acad. Child Adolesc. Psychiatry
, vol.50
, pp. 697-704
-
-
Mattai, A.A.1
Weisinger, B.2
Greenstein, D.3
Stidd, R.4
Clasen, L.5
Miller, R.6
Tossell, J.W.7
Rapoport, J.L.8
Gogtay, N.9
-
29
-
-
84888253405
-
Copy number variants are frequent in genetic generalized epilepsy with intellectual disability
-
S.A. Mullen, G.L. Carvill, S. Bellows, M.A. Bayly, H. Trucks, D. Lal, T. Sander, S.F. Berkovic, L.M. Dibbens, I.E. Scheffer, and H.C. Mefford Copy number variants are frequent in genetic generalized epilepsy with intellectual disability Neurology 81 2013 1507 1514
-
(2013)
Neurology
, vol.81
, pp. 1507-1514
-
-
Mullen, S.A.1
Carvill, G.L.2
Bellows, S.3
Bayly, M.A.4
Trucks, H.5
Lal, D.6
Sander, T.7
Berkovic, S.F.8
Dibbens, L.M.9
Scheffer, I.E.10
Mefford, H.C.11
-
30
-
-
51549108502
-
The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP
-
I. Napoli, V. Mercaldo, P.P. Boyl, B. Eleuteri, F. Zalfa, S. De Rubeis, D. Di Marino, E. Mohr, M. Massimi, and M. Falconi et al. The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP Cell 134 2008 1042 1054
-
(2008)
Cell
, vol.134
, pp. 1042-1054
-
-
Napoli, I.1
Mercaldo, V.2
Boyl, P.P.3
Eleuteri, B.4
Zalfa, F.5
De Rubeis, S.6
Di Marino, D.7
Mohr, E.8
Massimi, M.9
Falconi, M.10
-
31
-
-
34547731978
-
Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways
-
Y. Nishimura, C.L. Martin, A. Vazquez-Lopez, S.J. Spence, A.I. Alvarez-Retuerto, M. Sigman, C. Steindler, S. Pellegrini, N.C. Schanen, S.T. Warren, and D.H. Geschwind Genome-wide expression profiling of lymphoblastoid cell lines distinguishes different forms of autism and reveals shared pathways Hum. Mol. Genet. 16 2007 1682 1698
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 1682-1698
-
-
Nishimura, Y.1
Martin, C.L.2
Vazquez-Lopez, A.3
Spence, S.J.4
Alvarez-Retuerto, A.I.5
Sigman, M.6
Steindler, C.7
Pellegrini, S.8
Schanen, N.C.9
Warren, S.T.10
Geschwind, D.H.11
-
32
-
-
34347359603
-
Numb and Numbl are required for maintenance of cadherin-based adhesion and polarity of neural progenitors
-
M.R. Rasin, V.R. Gazula, J.J. Breunig, K.Y. Kwan, M.B. Johnson, S. Liu-Chen, H.S. Li, L.Y. Jan, Y.N. Jan, P. Rakic, and N. Sestan Numb and Numbl are required for maintenance of cadherin-based adhesion and polarity of neural progenitors Nat. Neurosci. 10 2007 819 827
-
(2007)
Nat. Neurosci.
, vol.10
, pp. 819-827
-
-
Rasin, M.R.1
Gazula, V.R.2
Breunig, J.J.3
Kwan, K.Y.4
Johnson, M.B.5
Liu-Chen, S.6
Li, H.S.7
Jan, L.Y.8
Jan, Y.N.9
Rakic, P.10
Sestan, N.11
-
33
-
-
0034940174
-
Human brain malformations and their lessons for neuronal migration
-
M.E. Ross, and C.A. Walsh Human brain malformations and their lessons for neuronal migration Annu. Rev. Neurosci. 24 2001 1041 1070
-
(2001)
Annu. Rev. Neurosci.
, vol.24
, pp. 1041-1070
-
-
Ross, M.E.1
Walsh, C.A.2
-
34
-
-
84860310017
-
Foxp-mediated suppression of N-cadherin regulates neuroepithelial character and progenitor maintenance in the CNS
-
D.L. Rousso, C.A. Pearson, Z.B. Gaber, A. Miquelajauregui, S. Li, C. Portera-Cailliau, E.E. Morrisey, and B.G. Novitch Foxp-mediated suppression of N-cadherin regulates neuroepithelial character and progenitor maintenance in the CNS Neuron 74 2012 314 330
-
(2012)
Neuron
, vol.74
, pp. 314-330
-
-
Rousso, D.L.1
Pearson, C.A.2
Gaber, Z.B.3
Miquelajauregui, A.4
Li, S.5
Portera-Cailliau, C.6
Morrisey, E.E.7
Novitch, B.G.8
-
35
-
-
34347210350
-
In vivo electroporation in the embryonic mouse central nervous system
-
T. Saito In vivo electroporation in the embryonic mouse central nervous system Nat. Protoc. 1 2006 1552 1558
-
(2006)
Nat. Protoc.
, vol.1
, pp. 1552-1558
-
-
Saito, T.1
-
36
-
-
0035902466
-
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P
-
A. Schenck, B. Bardoni, A. Moro, C. Bagni, and J.L. Mandel A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P Proc. Natl. Acad. Sci. USA 98 2001 8844 8849
-
(2001)
Proc. Natl. Acad. Sci. USA
, vol.98
, pp. 8844-8849
-
-
Schenck, A.1
Bardoni, B.2
Moro, A.3
Bagni, C.4
Mandel, J.L.5
-
37
-
-
0037523396
-
CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein
-
A. Schenck, B. Bardoni, C. Langmann, N. Harden, J.L. Mandel, and A. Giangrande CYFIP/Sra-1 controls neuronal connectivity in Drosophila and links the Rac1 GTPase pathway to the fragile X protein Neuron 38 2003 887 898
-
(2003)
Neuron
, vol.38
, pp. 887-898
-
-
Schenck, A.1
Bardoni, B.2
Langmann, C.3
Harden, N.4
Mandel, J.L.5
Giangrande, A.6
-
38
-
-
84862778046
-
Human cerebral cortex development from pluripotent stem cells to functional excitatory synapses
-
Y. Shi, P. Kirwan, J. Smith, H.P.C. Robinson, and F.J. Livesey Human cerebral cortex development from pluripotent stem cells to functional excitatory synapses Nat. Neurosci. 15 2012 477 486
-
(2012)
Nat. Neurosci.
, vol.15
, pp. 477-486
-
-
Shi, Y.1
Kirwan, P.2
Smith, J.3
Robinson, H.P.C.4
Livesey, F.J.5
-
39
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
GROUP
-
H. Stefansson, D. Rujescu, S. Cichon, O.P. Pietiläinen, A. Ingason, S. Steinberg, R. Fossdal, E. Sigurdsson, T. Sigmundsson, J.E. Buizer-Voskamp GROUP Large recurrent microdeletions associated with schizophrenia Nature 455 2008 232 236
-
(2008)
Nature
, vol.455
, pp. 232-236
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
Pietiläinen, O.P.4
Ingason, A.5
Steinberg, S.6
Fossdal, R.7
Sigurdsson, E.8
Sigmundsson, T.9
Buizer-Voskamp, J.E.10
-
40
-
-
84892620880
-
CNVs conferring risk of autism or schizophrenia affect cognition in controls
-
H. Stefansson, A. Meyer-Lindenberg, S. Steinberg, B.B. Magnusdottir, K. Morgen, S. Arnarsdottir, and K. Stefansson CNVs conferring risk of autism or schizophrenia affect cognition in controls Nature 505 2014 361 366
-
(2014)
Nature
, vol.505
, pp. 361-366
-
-
Stefansson, H.1
Meyer-Lindenberg, A.2
Steinberg, S.3
Magnusdottir, B.B.4
Morgen, K.5
Arnarsdottir, S.6
Stefansson, K.7
-
41
-
-
1842562381
-
Sra-1 and Nap1 link Rac to actin assembly driving lamellipodia formation
-
A. Steffen, K. Rottner, J. Ehinger, M. Innocenti, G. Scita, J. Wehland, and T.E. Stradal Sra-1 and Nap1 link Rac to actin assembly driving lamellipodia formation EMBO J. 23 2004 749 759
-
(2004)
EMBO J.
, vol.23
, pp. 749-759
-
-
Steffen, A.1
Rottner, K.2
Ehinger, J.3
Innocenti, M.4
Scita, G.5
Wehland, J.6
Stradal, T.E.7
-
42
-
-
84896918827
-
Patches of disorganization in the neocortex of children with autism
-
R. Stoner, M.L. Chow, M.P. Boyle, S.M. Sunkin, P.R. Mouton, S. Roy, A. Wynshaw-Boris, S.A. Colamarino, E.S. Lein, and E. Courchesne Patches of disorganization in the neocortex of children with autism N. Engl. J. Med. 370 2014 1209 1219
-
(2014)
N. Engl. J. Med.
, vol.370
, pp. 1209-1219
-
-
Stoner, R.1
Chow, M.L.2
Boyle, M.P.3
Sunkin, S.M.4
Mouton, P.R.5
Roy, S.6
Wynshaw-Boris, A.7
Colamarino, S.A.8
Lein, E.S.9
Courchesne, E.10
-
43
-
-
77953260190
-
Confirmed rare copy number variants implicate novel genes in schizophrenia
-
G.W. Tam, L.N. van de Lagemaat, R. Redon, K.E. Strathdee, M.D. Croning, M.P. Malloy, W.J. Muir, B.S. Pickard, I.J. Deary, and D.H. Blackwood et al. Confirmed rare copy number variants implicate novel genes in schizophrenia Biochem. Soc. Trans. 38 2010 445 451
-
(2010)
Biochem. Soc. Trans.
, vol.38
, pp. 445-451
-
-
Tam, G.W.1
Van De Lagemaat, L.N.2
Redon, R.3
Strathdee, K.E.4
Croning, M.D.5
Malloy, M.P.6
Muir, W.J.7
Pickard, B.S.8
Deary, I.J.9
Blackwood, D.H.10
-
44
-
-
84873104903
-
DISC1 genetics, biology and psychiatric illness
-
P.A. Thomson, E.L. Malavasi, E. Grünewald, D.C. Soares, M. Borkowska, and J.K. Millar DISC1 genetics, biology and psychiatric illness Front. Biol. (Beijing) 8 2013 1 31
-
(2013)
Front. Biol. (Beijing)
, vol.8
, pp. 1-31
-
-
Thomson, P.A.1
Malavasi, E.L.2
Grünewald, E.3
Soares, D.C.4
Borkowska, M.5
Millar, J.K.6
-
45
-
-
77952686118
-
A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder
-
B. van der Zwaag, W.G. Staal, R. Hochstenbach, M. Poot, H.A. Spierenburg, M.V. de Jonge, N.E. Verbeek, R. van 't Slot, M.A. van Es, and F.J. Staal et al. A co-segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder Am. J. Med. Genet. B. Neuropsychiatr. Genet. 153B 2010 960 966
-
(2010)
Am. J. Med. Genet. B. Neuropsychiatr. Genet.
, vol.153 B
, pp. 960-966
-
-
Van Der Zwaag, B.1
Staal, W.G.2
Hochstenbach, R.3
Poot, M.4
Spierenburg, H.A.5
De Jonge, M.V.6
Verbeek, N.E.7
Van 'T Slot, R.8
Van Es, M.A.9
Staal, F.J.10
-
46
-
-
36549003606
-
Arp3 is required during preimplantation development of the mouse embryo
-
F. Vauti, B.R. Prochnow, E. Freese, S.K. Ramasamy, P. Ruiz, and H.H. Arnold Arp3 is required during preimplantation development of the mouse embryo FEBS Lett. 581 2007 5691 5697
-
(2007)
FEBS Lett.
, vol.581
, pp. 5691-5697
-
-
Vauti, F.1
Prochnow, B.R.2
Freese, E.3
Ramasamy, S.K.4
Ruiz, P.5
Arnold, H.H.6
-
47
-
-
84860475483
-
Abnormal intracellular accumulation and extracellular Aβ deposition in idiopathic and Dup15q11.2-q13 autism spectrum disorders
-
J. Wegiel, J. Frackowiak, B. Mazur-Kolecka, N.C. Schanen, E.H. Cook Jr., M. Sigman, W.T. Brown, I. Kuchna, J. Wegiel, and K. Nowicki et al. Abnormal intracellular accumulation and extracellular Aβ deposition in idiopathic and Dup15q11.2-q13 autism spectrum disorders PLoS ONE 7 2012 e35414
-
(2012)
PLoS ONE
, vol.7
, pp. 35414
-
-
Wegiel, J.1
Frackowiak, J.2
Mazur-Kolecka, B.3
Schanen, N.C.4
Cook, Jr.E.H.5
Sigman, M.6
Brown, W.T.7
Kuchna, I.8
Wegiel, J.9
Nowicki, K.10
-
48
-
-
0023215296
-
Implications of normal brain development for the pathogenesis of schizophrenia
-
D.R. Weinberger Implications of normal brain development for the pathogenesis of schizophrenia Arch. Gen. Psychiatry 44 1987 660 669
-
(1987)
Arch. Gen. Psychiatry
, vol.44
, pp. 660-669
-
-
Weinberger, D.R.1
-
49
-
-
0043267980
-
WAVE2 is required for directed cell migration and cardiovascular development
-
D. Yamazaki, S. Suetsugu, H. Miki, Y. Kataoka, S. Nishikawa, T. Fujiwara, N. Yoshida, and T. Takenawa WAVE2 is required for directed cell migration and cardiovascular development Nature 424 2003 452 456
-
(2003)
Nature
, vol.424
, pp. 452-456
-
-
Yamazaki, D.1
Suetsugu, S.2
Miki, H.3
Kataoka, Y.4
Nishikawa, S.5
Fujiwara, T.6
Yoshida, N.7
Takenawa, T.8
-
50
-
-
0042815094
-
WAVE2 deficiency reveals distinct roles in embryogenesis and Rac-mediated actin-based motility
-
C. Yan, N. Martinez-Quiles, S. Eden, T. Shibata, F. Takeshima, R. Shinkura, Y. Fujiwara, R. Bronson, S.B. Snapper, and M.W. Kirschner et al. WAVE2 deficiency reveals distinct roles in embryogenesis and Rac-mediated actin-based motility EMBO J. 22 2003 3602 3612
-
(2003)
EMBO J.
, vol.22
, pp. 3602-3612
-
-
Yan, C.1
Martinez-Quiles, N.2
Eden, S.3
Shibata, T.4
Takeshima, F.5
Shinkura, R.6
Fujiwara, Y.7
Bronson, R.8
Snapper, S.B.9
Kirschner, M.W.10
-
51
-
-
79955471241
-
Evidence of sex-modulated association of ZNF804A with schizophrenia
-
F. Zhang, Q. Chen, T. Ye, B.K. Lipska, R.E. Straub, R. Vakkalanka, D. Rujescu, D. St. Clair, T.M. Hyde, and L. Bigelow et al. Evidence of sex-modulated association of ZNF804A with schizophrenia Biol. Psychiatry 69 2011 914 917
-
(2011)
Biol. Psychiatry
, vol.69
, pp. 914-917
-
-
Zhang, F.1
Chen, Q.2
Ye, T.3
Lipska, B.K.4
Straub, R.E.5
Vakkalanka, R.6
Rujescu, D.7
St. Clair, D.8
Hyde, T.M.9
Bigelow, L.10
-
52
-
-
84876826922
-
Drosophila CYFIP regulates synaptic development and endocytosis by suppressing filamentous actin assembly
-
L. Zhao, D. Wang, Q. Wang, A.A. Rodal, and Y.Q. Zhang Drosophila CYFIP regulates synaptic development and endocytosis by suppressing filamentous actin assembly PLoS Genet. 9 2013 e1003450
-
(2013)
PLoS Genet.
, vol.9
, pp. 1003450
-
-
Zhao, L.1
Wang, D.2
Wang, Q.3
Rodal, A.A.4
Zhang, Y.Q.5
-
53
-
-
84876585949
-
Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population
-
Q. Zhao, T. Li, X. Zhao, K. Huang, T. Wang, Z. Li, J. Ji, Z. Zeng, Z. Zhang, and K. Li et al. Rare CNVs and tag SNPs at 15q11.2 are associated with schizophrenia in the Han Chinese population Schizophr. Bull. 39 2013 712 719
-
(2013)
Schizophr. Bull.
, vol.39
, pp. 712-719
-
-
Zhao, Q.1
Li, T.2
Zhao, X.3
Huang, K.4
Wang, T.5
Li, Z.6
Ji, J.7
Zeng, Z.8
Zhang, Z.9
Li, K.10
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