-
1
-
-
84975795680
-
An integrated map of genetic variation from 1,092 human genomes
-
PID: 23128226
-
Abecasis GR, Auton A, Brooks LD, DePristo MA, Durbin RM, Handsaker RE, Kang HM, Marth GT, McVean GA (2012) An integrated map of genetic variation from 1,092 human genomes. Nature 491(7422):56–65. doi:10.1038/nature11632
-
(2012)
Nature
, vol.491
, Issue.7422
, pp. 56-65
-
-
Abecasis, G.R.1
Auton, A.2
Brooks, L.D.3
DePristo, M.A.4
Durbin, R.M.5
Handsaker, R.E.6
Kang, H.M.7
Marth, G.T.8
McVean, G.A.9
-
2
-
-
84866372949
-
Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction
-
COI: 1:CAS:528:DC%2BC38Xht1GitLrN, PID: 22584867
-
Ayalew M, Le-Niculescu H, Levey D, Jain N, Changala B, Patel S, Winiger E, Breier A, Shekhar A, Amdur R, Koller D, Nurnberger J, Corvin A, Geyer M, Tsuang M, Salomon D, Schork N, Fanous A, O’Donovan M, Niculescu A (2012) Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction. Mol Psychiatry 17(9):887–905. doi:10.1038/mp.2012.37
-
(2012)
Mol Psychiatry
, vol.17
, Issue.9
, pp. 887-905
-
-
Ayalew, M.1
Le-Niculescu, H.2
Levey, D.3
Jain, N.4
Changala, B.5
Patel, S.6
Winiger, E.7
Breier, A.8
Shekhar, A.9
Amdur, R.10
Koller, D.11
Nurnberger, J.12
Corvin, A.13
Geyer, M.14
Tsuang, M.15
Salomon, D.16
Schork, N.17
Fanous, A.18
O’Donovan, M.19
Niculescu, A.20
more..
-
3
-
-
84899717370
-
22q11. 2 deletion carriers and schizophrenia-associated novel variants
-
PID: 24482440
-
Balan S, Iwayama Y, Toyota T, Toyoshima M, Maekawa M, Yoshikawa T (2014) 22q11. 2 deletion carriers and schizophrenia-associated novel variants. Br J Psychiatry. doi:10.1192/bjp.bp.113.138420
-
(2014)
Br J Psychiatry
-
-
Balan, S.1
Iwayama, Y.2
Toyota, T.3
Toyoshima, M.4
Maekawa, M.5
Yoshikawa, T.6
-
4
-
-
78650680152
-
Characterization of the proteome, diseases and evolution of the human postsynaptic density
-
PID: 21170055
-
Bayés À, van de Lagemaat LN, Collins MO, Croning MD, Whittle IR, Choudhary JS, Grant SG (2010) Characterization of the proteome, diseases and evolution of the human postsynaptic density. Nat Neurosci 14(1):19–21. doi:10.1038/nn.2719
-
(2010)
Nat Neurosci
, vol.14
, Issue.1
, pp. 19-21
-
-
Bayés, À.1
van de Lagemaat, L.N.2
Collins, M.O.3
Croning, M.D.4
Whittle, I.R.5
Choudhary, J.S.6
Grant, S.G.7
-
5
-
-
0032714352
-
Genomic control for association studies
-
Devlin B, Roeder K (2004) Genomic control for association studies. Biometrics 55(4):997–1004. doi:10.1111/j.0006-341X.1999.00997.x
-
(2004)
Biometrics
, vol.55
, Issue.4
, pp. 997-1004
-
-
Devlin, B.1
Roeder, K.2
-
6
-
-
27944447718
-
The ubiquitously expressed Csk adaptor protein Cbp is dispensable for embryogenesis and T-cell development and function
-
COI: 1:CAS:528:DC%2BD2MXht1OnsLzO, PID: 16287865
-
Dobenecker M-W, Schmedt C, Okada M, Tarakhovsky A (2005) The ubiquitously expressed Csk adaptor protein Cbp is dispensable for embryogenesis and T-cell development and function. Mol Cell Biol 25(23):10533–10542. doi:10.1128/MCB.25.23.10533-10542.2005
-
(2005)
Mol Cell Biol
, vol.25
, Issue.23
, pp. 10533-10542
-
-
Dobenecker, M.-W.1
Schmedt, C.2
Okada, M.3
Tarakhovsky, A.4
-
7
-
-
79953308141
-
Synaptic changes in the brain of subjects with schizophrenia
-
PID: 21382468
-
Faludi G, Mirnics K (2011) Synaptic changes in the brain of subjects with schizophrenia. Int J Dev Neurosci 29(3):305–309. doi:10.1016/j.ijdevneu.2011.02.013
-
(2011)
Int J Dev Neurosci
, vol.29
, Issue.3
, pp. 305-309
-
-
Faludi, G.1
Mirnics, K.2
-
8
-
-
0037947831
-
Unbiased quantitative proteomics of lipid rafts reveals high specificity for signaling factors
-
COI: 1:CAS:528:DC%2BD3sXjvFOlsL0%3D, PID: 12724530
-
Foster LJ, de Hoog CL, Mann M (2003) Unbiased quantitative proteomics of lipid rafts reveals high specificity for signaling factors. Proc Natl Acad Sci 100(10):5813–5818. doi:10.1073/pnas.0631608100
-
(2003)
Proc Natl Acad Sci
, vol.100
, Issue.10
, pp. 5813-5818
-
-
Foster, L.J.1
de Hoog, C.L.2
Mann, M.3
-
9
-
-
84893919352
-
De novo mutations in schizophrenia implicate synaptic networks
-
COI: 1:CAS:528:DC%2BC2cXisVamurY%3D, PID: 24463507
-
Fromer M, Pocklington AJ, Kavanagh DH, Williams HJ, Dwyer S, Gormley P, Georgieva L, Rees E, Palta P, Ruderfer DM, Carrera N, Humphreys I, Johnson JS, Roussos P, Barker DD, Banks E, Milanova V, Grant SG, Hannon E, Rose SA, Chambert K, Mahajan M, Scolnick EM, Moran JL, Kirov G, Palotie A, McCarroll SA, Holmans P, Sklar P, Owen MJ, Purcell SM, O’Donovan MC (2014) De novo mutations in schizophrenia implicate synaptic networks. Nature 506(7487):179–184. doi:10.1038/nature12929
-
(2014)
Nature
, vol.506
, Issue.7487
, pp. 179-184
-
-
Fromer, M.1
Pocklington, A.J.2
Kavanagh, D.H.3
Williams, H.J.4
Dwyer, S.5
Gormley, P.6
Georgieva, L.7
Rees, E.8
Palta, P.9
Ruderfer, D.M.10
Carrera, N.11
Humphreys, I.12
Johnson, J.S.13
Roussos, P.14
Barker, D.D.15
Banks, E.16
Milanova, V.17
Grant, S.G.18
Hannon, E.19
Rose, S.A.20
Chambert, K.21
Mahajan, M.22
Scolnick, E.M.23
Moran, J.L.24
Kirov, G.25
Palotie, A.26
McCarroll, S.A.27
Holmans, P.28
Sklar, P.29
Owen, M.J.30
Purcell, S.M.31
O’Donovan, M.C.32
more..
-
10
-
-
84863434758
-
Synaptopathies: diseases of the synaptome
-
COI: 1:CAS:528:DC%2BC38Xjs1Ggtr0%3D, PID: 22409856
-
Grant SG (2012) Synaptopathies: diseases of the synaptome. Curr Opin Neurobiol 22(3):522–529. doi:10.1016/j.conb.2012.02.002
-
(2012)
Curr Opin Neurobiol
, vol.22
, Issue.3
, pp. 522-529
-
-
Grant, S.G.1
-
11
-
-
83655167387
-
The regulation of N-methyl-d-aspartate receptors by Src kinase
-
COI: 1:CAS:528:DC%2BC38Xit1SnsQ%3D%3D, PID: 22060915
-
Groveman BR, Feng S, Fang XQ, Pflueger M, Lin SX, Bienkiewicz EA, Yu X (2012) The regulation of N-methyl-d-aspartate receptors by Src kinase. FEBS J 279(1):20–28. doi:10.1111/j.1742-4658.2011.08413.x
-
(2012)
FEBS J
, vol.279
, Issue.1
, pp. 20-28
-
-
Groveman, B.R.1
Feng, S.2
Fang, X.Q.3
Pflueger, M.4
Lin, S.X.5
Bienkiewicz, E.A.6
Yu, X.7
-
12
-
-
33745912772
-
Altered neuregulin 1–erbB4 signaling contributes to NMDA> receptor hypofunction in schizophrenia
-
COI: 1:CAS:528:DC%2BD28Xms1eksL4%3D, PID: 16767099
-
Hahn C-G, Wang H-Y, Cho D-S, Talbot K, Gur RE, Berrettini WH, Bakshi K, Kamins J, Borgmann-Winter KE, Siegel SJ, Gallop RJ, Arnold SE (2006) Altered neuregulin 1–erbB4 signaling contributes to NMDA> receptor hypofunction in schizophrenia. Nat Med 12(7):824–828. doi:10.1038/nm1418
-
(2006)
Nat Med
, vol.12
, Issue.7
, pp. 824-828
-
-
Hahn, C.-G.1
Wang, H.-Y.2
Cho, D.-S.3
Talbot, K.4
Gur, R.E.5
Berrettini, W.H.6
Bakshi, K.7
Kamins, J.8
Borgmann-Winter, K.E.9
Siegel, S.J.10
Gallop, R.J.11
Arnold, S.E.12
-
13
-
-
72049127779
-
Preliminary genome-wide association study of bipolar disorder in the Japanese population
-
Hattori E, Toyota T, Ishitsuka Y, Iwayama Y, Yamada K, Ujike H, Morita Y, Kodama M, Nakata K, Minabe Y, Nakamura K, Iwata Y, Takei N, Mori N, Naitoh H, Yamanouchi Y, Iwata N, Ozaki N, Kato T, Nishikawa T, Kashiwa A, Suzuki M, Shioe K, Shinohara M, Hirano M, Nanko S, Akahane A, Ueno M, Kaneko N, Watanabe Y, Someya T, Hashimoto K, Iyo M, Itokawa M, Arai M, Nankai M, Inada T, Yoshida S, Kunugi H, Nakamura M, Iijima Y, Okazaki Y, Higuchi T, Yoshikawa T (2009) Preliminary genome-wide association study of bipolar disorder in the Japanese population. Am J Med Genet Part B: Neuropsychiatr Genet 150(8):1110–1117. doi:10.1002/ajmg.b.30941
-
(2009)
Am J Med Genet Part B: Neuropsychiatr Genet
, vol.150
, Issue.8
, pp. 1110-1117
-
-
Hattori, E.1
Toyota, T.2
Ishitsuka, Y.3
Iwayama, Y.4
Yamada, K.5
Ujike, H.6
Morita, Y.7
Kodama, M.8
Nakata, K.9
Minabe, Y.10
Nakamura, K.11
Iwata, Y.12
Takei, N.13
Mori, N.14
Naitoh, H.15
Yamanouchi, Y.16
Iwata, N.17
Ozaki, N.18
Kato, T.19
Nishikawa, T.20
Kashiwa, A.21
Suzuki, M.22
Shioe, K.23
Shinohara, M.24
Hirano, M.25
Nanko, S.26
Akahane, A.27
Ueno, M.28
Kaneko, N.29
Watanabe, Y.30
Someya, T.31
Hashimoto, K.32
Iyo, M.33
Itokawa, M.34
Arai, M.35
Nankai, M.36
Inada, T.37
Yoshida, S.38
Kunugi, H.39
Nakamura, M.40
Iijima, Y.41
Okazaki, Y.42
Higuchi, T.43
Yoshikawa, T.44
more..
-
14
-
-
84921815877
-
PAG-a multipurpose transmembrane adaptor protein
-
PID: 24213579
-
Hrdinka M, Horejsi V (2013) PAG-a multipurpose transmembrane adaptor protein. Oncogene. doi:10.1038/onc.2013.485
-
(2013)
Oncogene
-
-
Hrdinka, M.1
Horejsi, V.2
-
15
-
-
0034720166
-
Transmembrane phosphoprotein Cbp regulates the activities of Src-family tyrosine kinases
-
COI: 1:CAS:528:DC%2BD3cXjtFynt7w%3D, PID: 10801129
-
Kawabuchi M, Satomi Y, Takao T, Shimonishi Y, Nada S, Nagai K, Tarakhovsky A, Okada M (2000) Transmembrane phosphoprotein Cbp regulates the activities of Src-family tyrosine kinases. Nature 404(6781):999–1003. doi:10.1038/35010121
-
(2000)
Nature
, vol.404
, Issue.6781
, pp. 999-1003
-
-
Kawabuchi, M.1
Satomi, Y.2
Takao, T.3
Shimonishi, Y.4
Nada, S.5
Nagai, K.6
Tarakhovsky, A.7
Okada, M.8
-
16
-
-
80052440338
-
Phosphoprotein associated with glycosphingolipid-enriched microdomains differentially modulates Src kinase activity in brain maturation
-
COI: 1:CAS:528:DC%2BC3MXht1ent7fN, PID: 21915273
-
Lindquist S, Karitkina D, Langnaese K, Posevitz-Fejfar A, Schraven B, Xavier R, Seed B, Lindquist JA (2011) Phosphoprotein associated with glycosphingolipid-enriched microdomains differentially modulates Src kinase activity in brain maturation. PLoS One 6(9):e23978. doi:10.1371/journal.pone.0023978
-
(2011)
PLoS One
, vol.6
, Issue.9
, pp. 23978
-
-
Lindquist, S.1
Karitkina, D.2
Langnaese, K.3
Posevitz-Fejfar, A.4
Schraven, B.5
Xavier, R.6
Seed, B.7
Lindquist, J.A.8
-
17
-
-
84866736529
-
Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia
-
PID: 21931320
-
Lips ES, Cornelisse LN, Toonen RF, Min JL, Hultman C, Holmans P, O’Donovan M, Purcell S, Smit A, Verhage M, Sullivan PF, Visscher P, Posthuma D (2011) Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia. Mol Psychiatry 17(10):996–1006. doi:10.1038/mp.2011.117
-
(2011)
Mol Psychiatry
, vol.17
, Issue.10
, pp. 996-1006
-
-
Lips, E.S.1
Cornelisse, L.N.2
Toonen, R.F.3
Min, J.L.4
Hultman, C.5
Holmans, P.6
O’Donovan, M.7
Purcell, S.8
Smit, A.9
Verhage, M.10
Sullivan, P.F.11
Visscher, P.12
Posthuma, D.13
-
18
-
-
84863116742
-
A systematic survey of loss-of-function variants in human protein-coding genes
-
COI: 1:CAS:528:DC%2BC38XitFGqur0%3D, PID: 22344438
-
MacArthur DG, Balasubramanian S, Frankish A, Huang N, Morris J, Walter K, Jostins L, Habegger L, Pickrell JK, Montgomery SB, Albers CA, Zhang ZD, Conrad DF, Lunter G, Zheng H, Ayub Q, DePristo MA, Banks E, Hu M, Handsaker RE, Rosenfeld JA, Fromer M, Jin M, Mu XJ, Khurana E, Ye K, Kay M, Saunders GI, Suner M-M, Hunt T, Barnes IHA, Amid C, Carvalho-Silva, Bignell AH, Snow C, Yngvadottir B, Bumpstead S, Cooper DN, Xue Y, Romero IG, Consortium GP, Wang J, Li Y, Gibbs RA, McCarroll SA, Dermitzakis ET, Pritchard JK, Barrett JC, Harrow J, Hurles ME, Gerstein MB, Tyler-Smith C (2012) A systematic survey of loss-of-function variants in human protein-coding genes. Science 335(6070):823–828. doi:10.1126/science.1215040
-
(2012)
Science
, vol.335
, Issue.6070
, pp. 823-828
-
-
MacArthur, D.G.1
Balasubramanian, S.2
Frankish, A.3
Huang, N.4
Morris, J.5
Walter, K.6
Jostins, L.7
Habegger, L.8
Pickrell, J.K.9
Montgomery, S.B.10
Albers, C.A.11
Zhang, Z.D.12
Conrad, D.F.13
Lunter, G.14
Zheng, H.15
Ayub, Q.16
DePristo, M.A.17
Banks, E.18
Hu, M.19
Handsaker, R.E.20
Rosenfeld, J.A.21
Fromer, M.22
Jin, M.23
Mu, X.J.24
Khurana, E.25
Ye, K.26
Kay, M.27
Saunders, G.I.28
Suner, M.-M.29
Hunt, T.30
Barnes, I.H.A.31
Amid, C.32
Carvalho-Silva, D.R.33
Bignell, A.H.34
Snow, C.35
Yngvadottir, B.36
Bumpstead, S.37
Cooper, D.N.38
Xue, Y.39
Romero, I.G.40
Consortium, G.P.41
Wang, J.42
Li, Y.43
Gibbs, R.A.44
McCarroll, S.A.45
Dermitzakis, E.T.46
Pritchard, J.K.47
Barrett, J.C.48
Harrow, J.49
Hurles, M.E.50
Gerstein, M.B.51
Tyler-Smith, C.52
more..
-
19
-
-
0035183947
-
Neural development, cell-cell signaling, and the “two-hit” hypothesis of schizophrenia
-
COI: 1:STN:280:DC%2BD3MrltVantg%3D%3D, PID: 11596847
-
Maynard TM, Sikich L, Lieberman JA, LaMantia A-S (2001) Neural development, cell-cell signaling, and the “two-hit” hypothesis of schizophrenia. Schizophr Bull 27(3):457–476
-
(2001)
Schizophr Bull
, vol.27
, Issue.3
, pp. 457-476
-
-
Maynard, T.M.1
Sikich, L.2
Lieberman, J.A.3
LaMantia, A.-S.4
-
20
-
-
0031457622
-
Signaling through scaffold, anchoring, and adaptor proteins
-
COI: 1:CAS:528:DyaK1cXhvVKh, PID: 9405336
-
Pawson T, Scott JD (1997) Signaling through scaffold, anchoring, and adaptor proteins. Science 278(5346):2075–2080. doi:10.1126/science.278.5346.2075
-
(1997)
Science
, vol.278
, Issue.5346
, pp. 2075-2080
-
-
Pawson, T.1
Scott, J.D.2
-
21
-
-
0034118493
-
Inference of population structure using multilocus genotype data
-
COI: 1:STN:280:DC%2BD3cvislKrtA%3D%3D, PID: 10835412
-
Pritchard JK, Stephens M, Donnelly P (2000) Inference of population structure using multilocus genotype data. Genetics 155(2):945–959
-
(2000)
Genetics
, vol.155
, Issue.2
, pp. 945-959
-
-
Pritchard, J.K.1
Stephens, M.2
Donnelly, P.3
-
22
-
-
84893904007
-
A polygenic burden of rare disruptive mutations in schizophrenia
-
COI: 1:CAS:528:DC%2BC2cXisVamurc%3D, PID: 24463508
-
Purcell SM, Moran JL, Fromer M, Ruderfer D, Solovieff N, Roussos P, O/’Dushlaine C, Chambert K, Bergen SE, Kahler A, Duncan L, Stahl E, Genovese G, Fernandez E, Collins MO, Komiyama NH, Choudhary JS, Magnusson PKE, Banks E, Shakir K, Garimella K, Fennell T, DePristo M, Grant SGN, Haggarty SJ, Gabriel S, Scolnick EM, Lander ES, Hultman CM, Sullivan PF, McCarroll SA, Sklar P (2014) A polygenic burden of rare disruptive mutations in schizophrenia. Nature 506(7487):185–190. doi:10.1038/nature12975
-
(2014)
Nature
, vol.506
, Issue.7487
, pp. 185-190
-
-
Purcell, S.M.1
Moran, J.L.2
Fromer, M.3
Ruderfer, D.4
Solovieff, N.5
Roussos, P.6
Dushlaine, C.7
Chambert, K.8
Bergen, S.E.9
Kahler, A.10
Duncan, L.11
Stahl, E.12
Genovese, G.13
Fernandez, E.14
Collins, M.O.15
Komiyama, N.H.16
Choudhary, J.S.17
Magnusson, P.K.E.18
Banks, E.19
Shakir, K.20
Garimella, K.21
Fennell, T.22
DePristo, M.23
Grant, S.G.N.24
Haggarty, S.J.25
Gabriel, S.26
Scolnick, E.M.27
Lander, E.S.28
Hultman, C.M.29
Sullivan, P.F.30
McCarroll, S.A.31
Sklar, P.32
more..
-
23
-
-
84885020424
-
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
-
COI: 1:CAS:528:DC%2BC3sXhtlWkur3N, PID: 23974872
-
Ripke S, O’Dushlaine C, Chambert K, Moran JL, Kahler AK, Akterin S, Bergen SE, Collins AL, Crowley JJ, Fromer M, Kim Y, Lee SH, Magnusson PKE, Sanchez N, Stahl EA, Williams S, Wray NR, Xia K, Bettella F, Borglum AD, Bulik-Sullivan BK, Cormican P, Craddock N, de Leeuw C, Durmishi N, Gill M, Golimbet V, Hamshere ML, Holmans P, Hougaard DM, Kendler KS, Lin K, Morris DW, Mors O, Mortensen PB, Neale BM, O’Neill FA, Owen MJ, Milovancevic MP, Posthuma D, Powell J, Richards AL, Riley BP, Ruderfer D, Rujescu D, Sigurdsson E, Silagadze T, Smit AB, Stefansson H, Steinberg S, Suvisaari J, Tosato S, Verhage M, Walters JT, Multicenter Genetic Studies of Schizophrenia C, Psychosis Endophenotypes International C, Wellcome Trust Case Control C, Bramon E, Corvin AP, O’Donovan MC, Stefansson K, Scolnick E, Purcell S, McCarroll SA, Sklar P, Hultman CM, Sullivan PF (2013) Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Nat Genet 45(10):1150–1159. doi:10.1038/ng.2742
-
(2013)
Nat Genet
, vol.45
, Issue.10
, pp. 1150-1159
-
-
Ripke, S.1
O’Dushlaine, C.2
Chambert, K.3
Moran, J.L.4
Kahler, A.K.5
Akterin, S.6
Bergen, S.E.7
Collins, A.L.8
Crowley, J.J.9
Fromer, M.10
Kim, Y.11
Lee, S.H.12
Magnusson, P.K.E.13
Sanchez, N.14
Stahl, E.A.15
Williams, S.16
Wray, N.R.17
Xia, K.18
Bettella, F.19
Borglum, A.D.20
Bulik-Sullivan, B.K.21
Cormican, P.22
Craddock, N.23
de Leeuw, C.24
Durmishi, N.25
Gill, M.26
Golimbet, V.27
Hamshere, M.L.28
Holmans, P.29
Hougaard, D.M.30
Kendler, K.S.31
Lin, K.32
Morris, D.W.33
Mors, O.34
Mortensen, P.B.35
Neale, B.M.36
O’Neill, F.A.37
Owen, M.J.38
Milovancevic, M.P.39
Posthuma, D.40
Powell, J.41
Richards, A.L.42
Riley, B.P.43
Ruderfer, D.44
Rujescu, D.45
Sigurdsson, E.46
Silagadze, T.47
Smit, A.B.48
Stefansson, H.49
Steinberg, S.50
Suvisaari, J.51
Tosato, S.52
Verhage, M.53
Walters, J.T.54
Multicenter Genetic Studies of Schizophrenia, C.55
Psychosis Endophenotypes International, C.56
Wellcome Trust Case Control, C.57
Bramon, E.58
Corvin, A.P.59
O’Donovan, M.C.60
Stefansson, K.61
Scolnick, E.62
Purcell, S.63
McCarroll, S.A.64
Sklar, P.65
Hultman, C.M.66
Sullivan, P.F.67
more..
-
24
-
-
1842731881
-
Src kinases: a hub for NMDA receptor regulation
-
COI: 1:CAS:528:DC%2BD2cXit12nu7k%3D, PID: 15034556
-
Salter MW, Kalia LV (2004) Src kinases: a hub for NMDA receptor regulation. Nat Rev Neurosci 5(4):317–328. doi:10.1038/nrn1368
-
(2004)
Nat Rev Neurosci
, vol.5
, Issue.4
, pp. 317-328
-
-
Salter, M.W.1
Kalia, L.V.2
-
25
-
-
84866384152
-
Lipid rafts, synaptic transmission and plasticity: impact in age-related neurodegenerative diseases
-
Sebastião AM, Colino-Oliveira M, Assaife-Lopes N, Dias RA, Ribeiro JA (2012) Lipid rafts, synaptic transmission and plasticity: impact in age-related neurodegenerative diseases. Neuropharmacology. doi:10.1016/j.neuropharm.2012.06.053
-
(2012)
Neuropharmacology
-
-
Sebastião, A.M.1
Colino-Oliveira, M.2
Assaife-Lopes, N.3
Dias, R.A.4
Ribeiro, J.A.5
-
26
-
-
84873295237
-
Involvement of gangliosides in the process of Cbp/PAG phosphorylation by Lyn in developing cerebellar growth cones
-
COI: 1:CAS:528:DC%2BC3sXhsVOms7o%3D, PID: 23035659
-
Sekino-Suzuki N, Yuyama K, Miki T, Kaneda M, Suzuki H, Yamamoto N, Yamamoto T, Oneyama C, Okada M, Kasahara K (2013) Involvement of gangliosides in the process of Cbp/PAG phosphorylation by Lyn in developing cerebellar growth cones. J Neurochem 124(4):514–522. doi:10.1111/jnc.12040
-
(2013)
J Neurochem
, vol.124
, Issue.4
, pp. 514-522
-
-
Sekino-Suzuki, N.1
Yuyama, K.2
Miki, T.3
Kaneda, M.4
Suzuki, H.5
Yamamoto, N.6
Yamamoto, T.7
Oneyama, C.8
Okada, M.9
Kasahara, K.10
-
27
-
-
0034304851
-
Lipid rafts and signal transduction
-
COI: 1:CAS:528:DC%2BD3MXivVGjtbo%3D, PID: 11413487
-
Simons K, Toomre D (2000) Lipid rafts and signal transduction. Nat Rev Mol Cell Biol 1(1):31–39. doi:10.1038/35036052
-
(2000)
Nat Rev Mol Cell Biol
, vol.1
, Issue.1
, pp. 31-39
-
-
Simons, K.1
Toomre, D.2
-
28
-
-
33746654582
-
Synaptic plasticity and dysconnection in schizophrenia
-
COI: 1:CAS:528:DC%2BD28XksVOnurg%3D, PID: 16427028
-
Stephan KE, Baldeweg T, Friston KJ (2006) Synaptic plasticity and dysconnection in schizophrenia. Biol Psychiatry 59(10):929–939. doi:10.1016/j.biopsych.2005.10.005
-
(2006)
Biol Psychiatry
, vol.59
, Issue.10
, pp. 929-939
-
-
Stephan, K.E.1
Baldeweg, T.2
Friston, K.J.3
-
29
-
-
84856706805
-
Puzzling over schizophrenia: schizophrenia as a pathway disease
-
COI: 1:CAS:528:DC%2BC38XhvVSitLk%3D, PID: 22310687
-
Sullivan PF (2012) Puzzling over schizophrenia: schizophrenia as a pathway disease. Nat Med 18(2):210–211. doi:10.1038/nm.2670
-
(2012)
Nat Med
, vol.18
, Issue.2
, pp. 210-211
-
-
Sullivan, P.F.1
-
30
-
-
84874529521
-
A population-specific uncommon variant in< i> GRIN3A associated with schizophrenia
-
PID: 23237318
-
Takata A, Iwayama Y, Fukuo Y, Ikeda M, Okochi T, Maekawa M, Toyota T, Yamada K, Hattori E, Ohnishi T, Toyoshima M, Ujike H, Inada T, Kunugi H, Ozaki N, Nanko S, Nakamura K, Mori N, Kanba S, Iwata N, Kato T, Yoshikawa T (2012) A population-specific uncommon variant in GRIN3A associated with schizophrenia. Biol Psychiatry. doi:10.1016/j.biopsych.2012.10.024
-
(2012)
Biol Psychiatry
-
-
Takata, A.1
Iwayama, Y.2
Fukuo, Y.3
Ikeda, M.4
Okochi, T.5
Maekawa, M.6
Toyota, T.7
Yamada, K.8
Hattori, E.9
Ohnishi, T.10
Toyoshima, M.11
Ujike, H.12
Inada, T.13
Kunugi, H.14
Ozaki, N.15
Nanko, S.16
Nakamura, K.17
Mori, N.18
Kanba, S.19
Iwata, N.20
Kato, T.21
Yoshikawa, T.22
more..
-
31
-
-
80052396769
-
Schizophrenia with the 22q11. 2 deletion and additional genetic defects: case history. The
-
COI: 1:STN:280:DC%2BC3Mfgt1Ghuw%3D%3D, PID: 21881099
-
Toyosima M, Maekawa M, Toyota T, Iwayama Y, Arai M, Ichikawa T, Miyashita M, Arinami T, Itokawa M, Yoshikawa T (2011) Schizophrenia with the 22q11. 2 deletion and additional genetic defects: case history. The. Br J Psychiatry 199(3):245–246. doi:10.1192/bjp.bp.111.093849
-
(2011)
Br J Psychiatry
, vol.199
, Issue.3
, pp. 245-246
-
-
Toyosima, M.1
Maekawa, M.2
Toyota, T.3
Iwayama, Y.4
Arai, M.5
Ichikawa, T.6
Miyashita, M.7
Arinami, T.8
Itokawa, M.9
Yoshikawa, T.10
-
32
-
-
25444448196
-
Cbp deficiency alters Csk localization in lipid rafts but does not affect T-cell development
-
COI: 1:CAS:528:DC%2BD2MXhtVKqsLbP, PID: 16166631
-
Xu S, Huo J, Tan JE-L, Lam K-P (2005) Cbp deficiency alters Csk localization in lipid rafts but does not affect T-cell development. Mol cell Biol 25(19):8486–8495. doi:10.1128/MCB.25.19.8486-8495.2005
-
(2005)
Mol cell Biol
, vol.25
, Issue.19
, pp. 8486-8495
-
-
Xu, S.1
Huo, J.2
Tan, J.E.-L.3
Lam, K.-P.4
-
33
-
-
80052273655
-
Exome sequencing supports a de novo mutational paradigm for schizophrenia
-
COI: 1:CAS:528:DC%2BC3MXpvVOlu7w%3D, PID: 21822266
-
Xu B, Roos JL, Dexheimer P, Boone B, Plummer B, Levy S, Gogos JA, Karayiorgou M (2011) Exome sequencing supports a de novo mutational paradigm for schizophrenia. Nat Genet 43(9):864–868. doi:10.1038/ng.902
-
(2011)
Nat Genet
, vol.43
, Issue.9
, pp. 864-868
-
-
Xu, B.1
Roos, J.L.2
Dexheimer, P.3
Boone, B.4
Plummer, B.5
Levy, S.6
Gogos, J.A.7
Karayiorgou, M.8
-
34
-
-
7444263014
-
Association analysis of FEZ1 variants with schizophrenia in Japanese cohorts
-
COI: 1:CAS:528:DC%2BD2cXptFOmt70%3D, PID: 15522253
-
Yamada K, Nakamura K, Minabe Y, Iwayama-Shigeno Y, Takao H, Toyota T, Hattori E, Takei N, Sekine Y, Suzuki K, Iwata Y, Miyoshi K, Honda A, Baba K, Katayama T, Tohyama M, Mori N, Yoshikawa T (2004) Association analysis of FEZ1 variants with schizophrenia in Japanese cohorts. Biol Psychiatry 56(9):683–690. doi:10.1016/j.biopsych.2004.08.015
-
(2004)
Biol Psychiatry
, vol.56
, Issue.9
, pp. 683-690
-
-
Yamada, K.1
Nakamura, K.2
Minabe, Y.3
Iwayama-Shigeno, Y.4
Takao, H.5
Toyota, T.6
Hattori, E.7
Takei, N.8
Sekine, Y.9
Suzuki, K.10
Iwata, Y.11
Miyoshi, K.12
Honda, A.13
Baba, K.14
Katayama, T.15
Tohyama, M.16
Mori, N.17
Yoshikawa, T.18
-
35
-
-
33745698343
-
Distinguishable haplotype blocks in the HTR3A and HTR3B region in the japanese reveal evidence of association of HTR3B with female major depression
-
COI: 1:CAS:528:DC%2BD28Xmsl2jurY%3D, PID: 16487942
-
Yamada K, Hattori E, Iwayama Y, Ohnishi T, Ohba H, Toyota T, Takao H, Minabe Y, Nakatani N, Higuchi T, Detera-Wadleigh SD, Yoshikawa T (2006) Distinguishable haplotype blocks in the HTR3A and HTR3B region in the japanese reveal evidence of association of HTR3B with female major depression. Biol Psychiatry 60(2):192–201. doi:10.1016/j.biopsych.2005.11.008
-
(2006)
Biol Psychiatry
, vol.60
, Issue.2
, pp. 192-201
-
-
Yamada, K.1
Hattori, E.2
Iwayama, Y.3
Ohnishi, T.4
Ohba, H.5
Toyota, T.6
Takao, H.7
Minabe, Y.8
Nakatani, N.9
Higuchi, T.10
Detera-Wadleigh, S.D.11
Yoshikawa, T.12
-
36
-
-
53049090475
-
Japanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studies
-
COI: 1:CAS:528:DC%2BD1cXht1Omtb3O, PID: 18817904
-
Yamaguchi-Kabata Y, Nakazono K, Takahashi A, Saito S, Hosono N, Kubo M, Nakamura Y, Kamatani N (2008) Japanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studies. Am J Hum Genet 83(4):445–456. doi:10.1016/j.ajhg.2008.08.019
-
(2008)
Am J Hum Genet
, vol.83
, Issue.4
, pp. 445-456
-
-
Yamaguchi-Kabata, Y.1
Nakazono, K.2
Takahashi, A.3
Saito, S.4
Hosono, N.5
Kubo, M.6
Nakamura, Y.7
Kamatani, N.8
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