-
1
-
-
0029082109
-
Symptoms, signs, and diagnosis of schizophrenia
-
Andreasen, N.C. (1995) Symptoms, signs, and diagnosis of schizophrenia. Lancet 346, 477-481
-
(1995)
Lancet
, vol.346
, pp. 477-481
-
-
Andreasen, N.C.1
-
2
-
-
45749158144
-
Psychiatric genetics: Progress amid controversy
-
Burmeister, M., McInnis, M.G. and Zollner, S. (2008) Psychiatric genetics: progress amid controversy. Nat. Rev. Genet. 9, 527-540
-
(2008)
Nat. Rev. Genet.
, vol.9
, pp. 527-540
-
-
Burmeister, M.1
McInnis, M.G.2
Zollner, S.3
-
3
-
-
23644439204
-
Schizophrenia: Genes at last?
-
Owen, M.J., Craddock, N. and O'Donovan, M.C. (2005) Schizophrenia: genes at last? Trends Genet. 21, 518-525
-
(2005)
Trends Genet.
, vol.21
, pp. 518-525
-
-
Owen, M.J.1
Craddock, N.2
O'Donovan, M.C.3
-
4
-
-
77950461601
-
Origins and functional impact of copy number variation in the human genome
-
doi:10.1038/nature08516
-
Conrad, D.F., Pinto, D., Redon, R., Feuk, L., Gokcumen, O., Zhang, Y., Aerts, J., Andrews, T.D., Barnes, C., Campbell, P. et al. (2009) Origins and functional impact of copy number variation in the human genome. Nature, doi:10.1038/nature08516
-
(2009)
Nature
-
-
Conrad, D.F.1
Pinto, D.2
Redon, R.3
Feuk, L.4
Gokcumen, O.5
Zhang, Y.6
Aerts, J.7
Andrews, T.D.8
Barnes, C.9
Campbell, P.10
-
5
-
-
33751349817
-
Accurate and reliable high-throughput detection of copy number variation in the human genome
-
DOI 10.1101/gr.5630906
-
Fiegler, H., Redon, R., Andrews, D., Scott, C., Andrews, R., Carder, C., Clark, R., Dovey, O., Ellis, P., Feuk, L. et al. (2006) Accurate and reliable high-throughput detection of copy number variation in the human genome. Genome Res. 16, 1566-1574 (Pubitemid 44878495)
-
(2006)
Genome Research
, vol.16
, Issue.12
, pp. 1566-1574
-
-
Fiegler, H.1
Redon, R.2
Andrews, D.3
Scott, C.4
Andrews, R.5
Carder, C.6
Clark, R.7
Dovey, O.8
Ellis, P.9
Feuk, L.10
French, L.11
Hunt, P.12
Kalaitzopoulos, D.13
Larkin, J.14
Montgomery, L.15
Perry, G.H.16
Plumb, B.W.17
Porter, K.18
Rigby, R.E.19
Rigler, D.20
Valsesia, A.21
Langford, C.22
Humphray, S.J.23
Scherer, S.W.24
Lee, C.25
Hurles, M.E.26
Carter, N.P.27
more..
-
6
-
-
54049144653
-
Copy-number variations associated with neuropsychiatric conditions
-
Cook, Jr, E.H. and Scherer, S.W. (2008) Copy-number variations associated with neuropsychiatric conditions. Nature 455, 919-923
-
(2008)
Nature
, vol.455
, pp. 919-923
-
-
Cook Jr., E.H.1
Scherer, S.W.2
-
7
-
-
70350724411
-
The role of DNA copy number variation in schizophrenia
-
Tam, G.W., Redon, R., Carter, N.P. and Grant, S.G. (2009) The role of DNA copy number variation in schizophrenia. Biol. Psychiatry 66, 1005-1012
-
(2009)
Biol. Psychiatry
, vol.66
, pp. 1005-1012
-
-
Tam, G.W.1
Redon, R.2
Carter, N.P.3
Grant, S.G.4
-
8
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
International Schizophrenia Consortium
-
International Schizophrenia Consortium (2008) Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455, 237-241
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
-
9
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson, H., Rujescu, D., Cichon, S., Pietilainen, O.P., Ingason, A., Steinberg, S., Fossdal, R., Sigurdsson, E., Sigmundsson, T., Buizer-Voskamp, J.E. et al. (2008) Large recurrent microdeletions associated with schizophrenia. Nature 455, 232-236
-
(2008)
Nature
, vol.455
, pp. 232-236
-
-
Stefansson, H.1
Rujescu, D.2
Cichon, S.3
Pietilainen, O.P.4
Ingason, A.5
Steinberg, S.6
Fossdal, R.7
Sigurdsson, E.8
Sigmundsson, T.9
Buizer-Voskamp, J.E.10
-
10
-
-
42349088634
-
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
-
DOI 10.1126/science.1155174
-
Walsh, T., McClellan, J.M., McCarthy, S.E., Addington, A.M., Pierce, S.B., Cooper, G.M., Nord, A.S., Kusenda, M., Malhotra, D., Bhandari, A. et al. (2008) Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 320, 539-543 (Pubitemid 351590668)
-
(2008)
Science
, vol.320
, Issue.5875
, pp. 539-543
-
-
Walsh, T.1
McClellan, J.M.2
McCarthy, S.E.3
Addington, A.M.4
Pierce, S.B.5
Cooper, G.M.6
Nord, A.S.7
Kusenda, M.8
Malhotra, D.9
Bhandari, A.10
Stray, S.M.11
Rippey, C.F.12
Roccanova, P.13
Makarov, V.14
Lakshmi, B.15
Findling, R.L.16
Sikich, L.17
Stromberg, T.18
Merriman, B.19
Gogtay, N.20
Butler, P.21
Eckstrand, K.22
Noory, L.23
Gochman, P.24
Long, R.25
Chen, Z.26
Davis, S.27
Baker, C.28
Eichler, E.E.29
Meltzer, P.S.30
Nelson, S.F.31
Singleton, A.B.32
Lee, M.K.33
Rapoport, J.L.34
King, M.-C.35
Sebat, J.36
more..
-
11
-
-
46249093584
-
Strong association of de novo copy number mutations with sporadic schizophrenia
-
Xu, B., Roos, J.L., Levy, S., van Rensburg, E.J., Gogos, J.A. and Karayiorgou, M. (2008) Strong association of de novo copy number mutations with sporadic schizophrenia. Nat. Genet. 40, 880-885
-
(2008)
Nat. Genet.
, vol.40
, pp. 880-885
-
-
Xu, B.1
Roos, J.L.2
Levy, S.3
Van Rensburg, E.J.4
Gogos, J.A.5
Karayiorgou, M.6
-
12
-
-
1642455817
-
The impact of childhood intelligence on later life: Following up the Scottish mental surveys of 1932 and 1947
-
Deary, I.J., Whiteman, M.C., Starr, J.M., Whalley, L.J. and Fox, H.C. (2004) The impact of childhood intelligence on later life: following up the Scottish mental surveys of 1932 and 1947. J. Pers. Soc. Psychol. 86, 130-147
-
(2004)
J. Pers. Soc. Psychol.
, vol.86
, pp. 130-147
-
-
Deary, I.J.1
Whiteman, M.C.2
Starr, J.M.3
Whalley, L.J.4
Fox, H.C.5
-
13
-
-
33751329250
-
Global variation in copy number in the human genome
-
DOI 10.1038/nature05329, PII NATURE05329
-
Redon, R., Ishikawa, S., Fitch, K.R., Feuk, L., Perry, G.H., Andrews, T.D., Fiegler, H., Shapero, M.H., Carson, A.R., Chen, W. et al. (2006) Global variation in copy number in the human genome. Nature 444, 444-454 (Pubitemid 44809057)
-
(2006)
Nature
, vol.444
, Issue.7118
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
Fiegler, H.7
Shapero, M.H.8
Carson, A.R.9
Chen, W.10
Cho, E.K.11
Dallaire, S.12
Freeman, J.L.13
Gonzalez, J.R.14
Gratacos, M.15
Huang, J.16
Kalaitzopoulos, D.17
Komura, D.18
MacDonald, J.R.19
Marshall, C.R.20
Mei, R.21
Montgomery, L.22
Nishimura, K.23
Okamura, K.24
Shen, F.25
Somerville, M.J.26
Tchinda, J.27
Valsesia, A.28
Woodwark, C.29
Yang, F.30
Zhang, J.31
Zerjal, T.32
Zhang, J.33
Armengol, L.34
Conrad, D.F.35
Estivill, X.36
Tyler-Smith, C.37
Carter, N.P.38
Aburatani, H.39
Lee, C.40
Jones, K.W.41
Scherer, S.W.42
Hurles, M.E.43
more..
-
15
-
-
51549108502
-
The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP
-
Napoli, I., Mercaldo, V., Boyl, P.P., Eleuteri, B., Zalfa, F., De Rubeis, S., Di Marino, D., Mohr, E., Massimi, M., Falconi, M. et al. (2008) The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP. Cell. 134, 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
-
16
-
-
12644303225
-
Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus
-
Freedman, R., Coon, H., Myles-Worsley, M., Orr-Urtreger, A., Olincy, A., Davis, A., Polymeropoulos, M., Holik, J., Hopkins, J., Hoff, M. et al. (1997) Linkage of a neurophysiological deficit in schizophrenia to a chromosome 15 locus. Proc. Natl. Acad. Sci. U.S.A. 94, 587-592
-
(1997)
Proc. Natl. Acad. Sci. U.S.A.
, vol.94
, pp. 587-592
-
-
Freedman, R.1
Coon, H.2
Myles-Worsley, M.3
Orr-Urtreger, A.4
Olincy, A.5
Davis, A.6
Polymeropoulos, M.7
Holik, J.8
Hopkins, J.9
Hoff, M.10
-
17
-
-
0035825230
-
7-nicotinic acetylcholine receptor subunit gene (CHRNA7)
-
7-nicotinic acetylcholine receptor subunit gene (CHRNA7). Am. J. Med. Genet. 105, 20-22
-
(2001)
Am. J. Med. Genet.
, vol.105
, pp. 20-22
-
-
Freedman, R.1
Leonard, S.2
Gault, J.M.3
Hopkins, J.4
Cloninger, C.R.5
Kaufmann, C.A.6
Tsuang, M.T.7
Farone, S.V.8
Malaspina, D.9
Svrakic, D.M.10
-
18
-
-
36849005006
-
The Down syndrome critical region protein RCAN1 regulates long-term potentiation and memory via inhibition of phosphatase signaling
-
DOI 10.1523/JNEUROSCI.3974-07.2007
-
Hoeffer, C.A., Dey, A., Sachan, N., Wong, H., Patterson, R.J., Shelton, J.M., Richardson, J.A., Klann, E. and Rothermel, B.A. (2007) The Down syndrome critical region protein RCAN1 regulates long-term potentiation and memory via inhibition of phosphatase signaling. J. Neurosci. 27, 13161-13172 (Pubitemid 350220501)
-
(2007)
Journal of Neuroscience
, vol.27
, Issue.48
, pp. 13161-13172
-
-
Hoeffer, C.A.1
Dey, A.2
Sachan, N.3
Wong, H.4
Patterson, R.J.5
Shelton, J.M.6
Richardson, J.A.7
Klann, E.8
Rothermel, B.A.9
-
19
-
-
41149154002
-
DSCR1/RCAN1 regulates vesicle exocytosis and fusion pore kinetics: Implications for Down syndrome and Alzheimer's disease
-
Keating, D.J., Dubach, D., Zanin, M.P., Yu, Y., Martin, K., Zhao, Y.F., Chen, C., Porta, S., Arbones, M.L., Mittaz, L. and Pritchard, M.A. (2008) DSCR1/RCAN1 regulates vesicle exocytosis and fusion pore kinetics: implications for Down syndrome and Alzheimer's disease. Hum. Mol. Genet. 17, 1020-1030
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 1020-1030
-
-
Keating, D.J.1
Dubach, D.2
Zanin, M.P.3
Yu, Y.4
Martin, K.5
Zhao, Y.F.6
Chen, C.7
Porta, S.8
Arbones, M.L.9
Mittaz, L.10
Pritchard, M.A.11
-
20
-
-
34447306022
-
RCAN1 (DSCR1) increases neuronal susceptibility to oxidative stress: A potential pathogenic process in neurodegeneration
-
Porta, S., Serra, S.A., Huch, M., Valverde, M.A., Llorens, F., Estivill, X., Arbones, M.L. and Marti, E. (2007) RCAN1 (DSCR1) increases neuronal susceptibility to oxidative stress: a potential pathogenic process in neurodegeneration. Hum. Mol. Genet. 16, 1039-1050
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 1039-1050
-
-
Porta, S.1
Serra, S.A.2
Huch, M.3
Valverde, M.A.4
Llorens, F.5
Estivill, X.6
Arbones, M.L.7
Marti, E.8
-
21
-
-
33646258512
-
RCAN1 (DSCR1 or Adapt78) stimulates expression of GSK-3β
-
Ermak, G., Harris, C.D., Battocchio, D. and Davies, K.J. (2006) RCAN1 (DSCR1 or Adapt78) stimulates expression of GSK-3β. FEBS J. 273, 2100-2109
-
(2006)
FEBS J.
, vol.273
, pp. 2100-2109
-
-
Ermak, G.1
Harris, C.D.2
Battocchio, D.3
Davies, K.J.4
-
22
-
-
36849078297
-
The role of glycogen synthase kinase-3β in schizophrenia
-
DOI 10.1358/dnp.2007.20.7.1149632
-
Koros, E. and Dorner-Ciossek, C. (2007) The role of glycogen synthase kinase-3β in schizophrenia. Drug News Perspect. 20, 437-445 (Pubitemid 350232812)
-
(2007)
Drug News and Perspectives
, vol.20
, Issue.7
, pp. 437-445
-
-
Koros, E.1
Dorner-Ciossek, C.2
-
23
-
-
16844371331
-
Reduced expression of the Sp4 gene in mice causes deficits in sensorimotor gating and memory associated with hippocampal vacuolization
-
DOI 10.1038/sj.mp.4001621
-
Zhou, X., Long, J.M., Geyer, M.A., Masliah, E., Kelsoe, J.R., Wynshaw-Boris, A. and Chien, K.R. (2005) Reduced expression of the Sp4 gene in mice causes deficits in sensorimotor gating and memory associated with hippocampal vacuolization. Mol. Psychiatry 10, 393-406 (Pubitemid 40490807)
-
(2005)
Molecular Psychiatry
, vol.10
, Issue.4
, pp. 393-406
-
-
Zhou, X.1
Long, J.M.2
Geyer, M.A.3
Masliah, E.4
Kelsoe, J.R.5
Wynshaw-Boris, A.6
Chien, K.R.7
-
24
-
-
65249124607
-
Transcription factor SP4 is a susceptibility gene for bipolar disorder
-
Zhou, X., Tang, W., Greenwood, T.A., Guo, S., He, L., Geyer, M.A. and Kelsoe, J.R. (2009) Transcription factor SP4 is a susceptibility gene for bipolar disorder. PLoS ONE 4, e5196
-
(2009)
PLoS ONE
, vol.4
-
-
Zhou, X.1
Tang, W.2
Greenwood, T.A.3
Guo, S.4
He, L.5
Geyer, M.A.6
Kelsoe, J.R.7
-
25
-
-
68349113702
-
Sp4-dependent repression of neurotrophin-3 limits dendritic branching
-
Ramos, B., Valin, A., Sun, X. and Gill, G. (2009) Sp4-dependent repression of neurotrophin-3 limits dendritic branching. Mol. Cell. Neurosci. 42, 152-159
-
(2009)
Mol. Cell. Neurosci.
, vol.42
, pp. 152-159
-
-
Ramos, B.1
Valin, A.2
Sun, X.3
Gill, G.4
-
26
-
-
0035845539
-
Cloning and characterization of a histone deacetylase, HDAC9
-
Zhou, X., Marks, P.A., Rifkind, R.A. and Richon, V.M. (2001) Cloning and characterization of a histone deacetylase, HDAC9. Proc. Natl. Acad. Sci. U.S.A. 98, 10572-10577
-
(2001)
Proc. Natl. Acad. Sci. U.S.A.
, vol.98
, pp. 10572-10577
-
-
Zhou, X.1
Marks, P.A.2
Rifkind, R.A.3
Richon, V.M.4
-
27
-
-
33646265796
-
Neuroprotection by histone deacetylase-related protein
-
Morrison, B.E., Majdzadeh, N., Zhang, X., Lyles, A., Bassel-Duby, R., Olson, E.N. and D'Mello, S.R. (2006) Neuroprotection by histone deacetylase-related protein. Mol. Cell. Biol. 26, 3550-3564
-
(2006)
Mol. Cell. Biol.
, vol.26
, pp. 3550-3564
-
-
Morrison, B.E.1
Majdzadeh, N.2
Zhang, X.3
Lyles, A.4
Bassel-Duby, R.5
Olson, E.N.6
D'Mello, S.R.7
-
28
-
-
0029739225
-
Structural features of a close homologue of L1 (CHL1) in the mouse: A new member of the L1 family of neural recognition molecules
-
Holm, J., Hillenbrand, R., Steuber, V., Bartsch, U., Moos, M., Lubbert, H., Montag, D. and Schachner, M. (1996) Structural features of a close homologue of L1 (CHL1) in the mouse: a new member of the L1 family of neural recognition molecules. Eur. J. Neurosci. 8, 1613-1629
-
(1996)
Eur. J. Neurosci.
, vol.8
, pp. 1613-1629
-
-
Holm, J.1
Hillenbrand, R.2
Steuber, V.3
Bartsch, U.4
Moos, M.5
Lubbert, H.6
Montag, D.7
Schachner, M.8
-
29
-
-
0036841466
-
Misguided axonal projections, neural cell adhesion molecule 180 mRNA upregulation, and altered behavior in mice deficient for the close homolog of L1
-
Montag-Sallaz, M., Schachner, M. and Montag, D. (2002) Misguided axonal projections, neural cell adhesion molecule 180 mRNA upregulation, and altered behavior in mice deficient for the close homolog of L1. Mol. Cell. Biol. 22, 7967-7981
-
(2002)
Mol. Cell. Biol.
, vol.22
, pp. 7967-7981
-
-
Montag-Sallaz, M.1
Schachner, M.2
Montag, D.3
-
30
-
-
33645452924
-
Enhanced perisomatic inhibition and impaired long-term potentiation in the CA1 region of juvenile CHL1-deficient mice
-
Nikonenko, A.G., Sun, M., Lepsveridze, E., Apostolova, I., Petrova, I., Irintchev, A., Dityatev, A. and Schachner, M. (2006) Enhanced perisomatic inhibition and impaired long-term potentiation in the CA1 region of juvenile CHL1-deficient mice. Eur. J. Neurosci. 23, 1839-1852
-
(2006)
Eur. J. Neurosci.
, vol.23
, pp. 1839-1852
-
-
Nikonenko, A.G.1
Sun, M.2
Lepsveridze, E.3
Apostolova, I.4
Petrova, I.5
Irintchev, A.6
Dityatev, A.7
Schachner, M.8
-
31
-
-
0344514780
-
Mice deficient for the close homologue of the neural adhesion cell L1 (CHL1) display alterations in emotional reactivity and motor coordination
-
Pratte, M., Rougon, G., Schachner, M. and Jamon, M. (2003) Mice deficient for the close homologue of the neural adhesion cell L1 (CHL1) display alterations in emotional reactivity and motor coordination. Behav. Brain Res. 147, 31-39
-
(2003)
Behav. Brain Res.
, vol.147
, pp. 31-39
-
-
Pratte, M.1
Rougon, G.2
Schachner, M.3
Jamon, M.4
-
32
-
-
10744233700
-
CALL interrupted in a patient with non-specific mental retardation: Gene dosage-dependent alteration of murine brain development and behavior
-
Frints, S.G., Marynen, P., Hartmann, D., Fryns, J.P., Steyaert, J., Schachner, M., Rolf, B., Craessaerts, K., Snellinx, A., Hollanders, K. et al. (2003) CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior. Hum. Mol. Genet. 12, 1463-1474
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 1463-1474
-
-
Frints, S.G.1
Marynen, P.2
Hartmann, D.3
Fryns, J.P.4
Steyaert, J.5
Schachner, M.6
Rolf, B.7
Craessaerts, K.8
Snellinx, A.9
Hollanders, K.10
-
33
-
-
0037221589
-
Association of neuregulin 1 with schizophrenia confirmed in a Scottish population
-
Stefansson, H., Sarginson, J., Kong, A., Yates, P., Steinthorsdottir, V., Gudfinnsson, E., Gunnarsdottir, S., Walker, N., Petursson, H., Crombie, C. et al. (2003) Association of neuregulin 1 with schizophrenia confirmed in a Scottish population. Am. J. Hum. Genet. 72, 83-87
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 83-87
-
-
Stefansson, H.1
Sarginson, J.2
Kong, A.3
Yates, P.4
Steinthorsdottir, V.5
Gudfinnsson, E.6
Gunnarsdottir, S.7
Walker, N.8
Petursson, H.9
Crombie, C.10
-
34
-
-
0031006852
-
The vibrator mutation causes neurodegeneration via reduced expression of PITPα: Positional complementation cloning and extragenic suppression
-
Hamilton, B.A., Smith, D.J., Mueller, K.L., Kerrebrock, A.W., Bronson, R.T., van Berkel, V., Daly, M.J., Kruglyak, L., Reeve, M.P., Nemhauser, J.L. et al. (1997) The vibrator mutation causes neurodegeneration via reduced expression of PITPα: positional complementation cloning and extragenic suppression. Neuron 18, 711-722
-
(1997)
Neuron
, vol.18
, pp. 711-722
-
-
Hamilton, B.A.1
Smith, D.J.2
Mueller, K.L.3
Kerrebrock, A.W.4
Bronson, R.T.5
Van Berkel, V.6
Daly, M.J.7
Kruglyak, L.8
Reeve, M.P.9
Nemhauser, J.L.10
-
35
-
-
18344376169
-
Decreased synaptic vesicle recycling efficiency and cognitive deficits in amphiphysin 1 knockout mice
-
DOI 10.1016/S0896-6273(02)00601-3, PII S0896627302006013
-
Di Paolo, G., Sankaranarayanan, S., Wenk, M.R., Daniell, L., Perucco, E., Caldarone, B.J., Flavell, R., Picciotto, M.R., Ryan, T.A., Cremona, O. and De Camilli, P. (2002) Decreased synaptic vesicle recycling efficiency and cognitive deficits in amphiphysin 1 knockout mice. Neuron 33, 789-804 (Pubitemid 34219249)
-
(2002)
Neuron
, vol.33
, Issue.5
, pp. 789-804
-
-
Di Paolo, G.1
Sankaranarayanan, S.2
Wenk, M.R.3
Daniell, L.4
Perucco, E.5
Caldarone, B.J.6
Flavell, R.7
Picciotto, M.R.8
Ryan, T.A.9
Cremona, O.10
De Camilli, P.11
-
36
-
-
0033615674
-
CALL gene is haploinsufficient in a 3p- Syndrome patient
-
Angeloni, D., Lindor, N.M., Pack, S., Latif, F., Wei, M.H. and Lerman, M.I. (1999) CALL gene is haploinsufficient in a 3p- syndrome patient. Am. J. Med. Genet. 86, 482-485
-
(1999)
Am. J. Med. Genet.
, vol.86
, pp. 482-485
-
-
Angeloni, D.1
Lindor, N.M.2
Pack, S.3
Latif, F.4
Wei, M.H.5
Lerman, M.I.6
-
37
-
-
19944428476
-
Case-control association study of the close homologue of L1 (CHL1) gene and schizophrenia in the Chinese population
-
Chen, Q.Y., Chen, Q., Feng, G.Y., Lindpaintner, K., Chen, Y., Sun, X., Chen, Z., Gao, Z., Tang, J. and He, L. (2005) Case-control association study of the close homologue of L1 (CHL1) gene and schizophrenia in the Chinese population. Schizophr. Res. 73, 269-274
-
(2005)
Schizophr. Res.
, vol.73
, pp. 269-274
-
-
Chen, Q.Y.1
Chen, Q.2
Feng, G.Y.3
Lindpaintner, K.4
Chen, Y.5
Sun, X.6
Chen, Z.7
Gao, Z.8
Tang, J.9
He, L.10
-
38
-
-
67149141899
-
Targeted tandem affinity purification of PSD-95 recovers core postsynaptic complexes and schizophrenia susceptibility proteins
-
Fernandez, E., Collins, M.O., Uren, R.T., Kopanitsa, M.V., Komiyama, N.H., Croning, M.D., Zografos, L., Armstrong, J.D., Choudhary, J.S. and Grant, S.G. (2009) Targeted tandem affinity purification of PSD-95 recovers core postsynaptic complexes and schizophrenia susceptibility proteins. Mol. Syst. Biol. 5, 269
-
(2009)
Mol. Syst. Biol.
, vol.5
, pp. 269
-
-
Fernandez, E.1
Collins, M.O.2
Uren, R.T.3
Kopanitsa, M.V.4
Komiyama, N.H.5
Croning, M.D.6
Zografos, L.7
Armstrong, J.D.8
Choudhary, J.S.9
Grant, S.G.10
-
39
-
-
27744545297
-
Synapse proteomics of multiprotein complexes: En route from genes to nervous system diseases
-
Grant, S.G., Marshall, M.C., Page, K.L., Cumiskey, M.A. and Armstrong, J.D. (2005) Synapse proteomics of multiprotein complexes: en route from genes to nervous system diseases. Hum. Mol. Genet. 14, R225-R234
-
(2005)
Hum. Mol. Genet.
, vol.14
-
-
Grant, S.G.1
Marshall, M.C.2
Page, K.L.3
Cumiskey, M.A.4
Armstrong, J.D.5
-
40
-
-
77955498689
-
Proteomic analysis of the human cortical postsynaptic density reveals a molecular structure key to human mental and neurological disease
-
Abstract 302.4
-
Bayes, A., van de Lagemaat, L.N., Collins, M.O., Whittle, I.R., Choudhary, J.S. and Grant, S.G.N. (2009) Proteomic analysis of the human cortical postsynaptic density reveals a molecular structure key to human mental and neurological disease, Neuroscience 2009 Meeting, Chicago, IL, U.S.A., 17-21 October 2009, Abstract 302.4
-
(2009)
Neuroscience 2009 Meeting, Chicago, IL, U.S.A., 17-21 October 2009
-
-
Bayes, A.1
Van De Lagemaat, L.N.2
Collins, M.O.3
Whittle, I.R.4
Choudhary, J.S.5
Grant, S.G.N.6
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