-
3
-
-
0030813634
-
A turning point in schizophrenia genetics
-
Karayiorgou M, Gogos JA. A turning point in schizophrenia genetics. Neuron 1997; 19: 967-979.
-
(1997)
Neuron
, vol.19
, pp. 967-979
-
-
Karayiorgou, M.1
Gogos, J.A.2
-
4
-
-
33846642542
-
The genetics of schizophrenia
-
Sullivan PF. The genetics of schizophrenia. PLoS Med 2005; 2: e212.
-
(2005)
PLoS Med
, vol.2
-
-
Sullivan, P.F.1
-
5
-
-
45549110436
-
Genome-wide association studies in psychiatry: Lessons from early studies of non-psychiatric and psychiatric phenotypes
-
Craddock N, O'Donovan MC, Owen MJ. Genome-wide association studies in psychiatry: lessons from early studies of non-psychiatric and psychiatric phenotypes. Mol Psychiatry 2008; 13: 649-653.
-
(2008)
Mol Psychiatry
, vol.13
, pp. 649-653
-
-
Craddock, N.1
O'Donovan, M.C.2
Owen, M.J.3
-
7
-
-
46449113977
-
-
Tandon R, Keshavan MS, Nasrallah HA. Schizophrenia, 'Just the Facts' what we know in 2008. 2. Epidemiology and etiology. Schizophr Res 2008; 102: 1-18.
-
Tandon R, Keshavan MS, Nasrallah HA. Schizophrenia, 'Just the Facts' what we know in 2008. 2. Epidemiology and etiology. Schizophr Res 2008; 102: 1-18.
-
-
-
-
9
-
-
0036799545
-
The allelic architecture of human disease genes: Common disease-common variant... or not?
-
Pritchard JK, Cox NJ. The allelic architecture of human disease genes: common disease-common variant... or not? Hum Mol Genet 2002; 11: 2417-2423.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 2417-2423
-
-
Pritchard, J.K.1
Cox, N.J.2
-
10
-
-
1342332173
-
The common variants/multiple disease hypothesis of common complex genetic disorders
-
Becker KG. The common variants/multiple disease hypothesis of common complex genetic disorders. Med Hypotheses 2004; 62: 309-317.
-
(2004)
Med Hypotheses
, vol.62
, pp. 309-317
-
-
Becker, K.G.1
-
11
-
-
33744518475
-
Bipolar disorder and schizophrenia: Not so distant relatives?
-
Berrettini W. Bipolar disorder and schizophrenia: not so distant relatives? World Psychiatry 2003; 2: 68-72.
-
(2003)
World Psychiatry
, vol.2
, pp. 68-72
-
-
Berrettini, W.1
-
12
-
-
0041328892
-
Oligodendrocyte dysfunction in schizophrenia and bipolar disorder
-
Tkachev D, Mimmack ML, Ryan MM, Wayland M, Freeman T, Jones PB et al. Oligodendrocyte dysfunction in schizophrenia and bipolar disorder. Lancet 2003; 362: 798-805.
-
(2003)
Lancet
, vol.362
, pp. 798-805
-
-
Tkachev, D.1
Mimmack, M.L.2
Ryan, M.M.3
Wayland, M.4
Freeman, T.5
Jones, P.B.6
-
13
-
-
47049102295
-
Psychiatric genetics: The brains of the family
-
Abbott A. Psychiatric genetics: the brains of the family. Nature 2008; 454: 154-157.
-
(2008)
Nature
, vol.454
, pp. 154-157
-
-
Abbott, A.1
-
14
-
-
40349093482
-
The Investigators of the Consortium on the Genetics of Schizophrenia. Advances in endophenotyping schizophrenia
-
Braff DL, Greenwood TA, Swerdlow NR, Light GA, Schork NJ, The Investigators of the Consortium on the Genetics of Schizophrenia. Advances in endophenotyping schizophrenia. World Psychiatry 2008; 7: 11-18.
-
(2008)
World Psychiatry
, vol.7
, pp. 11-18
-
-
Braff, D.L.1
Greenwood, T.A.2
Swerdlow, N.R.3
Light, G.A.4
Schork, N.J.5
-
16
-
-
33845904134
-
Environment and schizophrenia: Environmental factors in schizophrenia: childhood trauma - a critical review
-
Morgan C, Fisher H. Environment and schizophrenia: environmental factors in schizophrenia: childhood trauma - a critical review. Schizophr Bull 2007; 33: 3-10.
-
(2007)
Schizophr Bull
, vol.33
, pp. 3-10
-
-
Morgan, C.1
Fisher, H.2
-
17
-
-
2942750478
-
Incidental neurodevelopmental episodes in the etiology of schizophrenia: An expanded model involving epigenetics and development
-
Singh SM, McDonald P, Murphy B, O'Reilly R. Incidental neurodevelopmental episodes in the etiology of schizophrenia: an expanded model involving epigenetics and development. Clin Genet 2004; 65: 435-440.
-
(2004)
Clin Genet
, vol.65
, pp. 435-440
-
-
Singh, S.M.1
McDonald, P.2
Murphy, B.3
O'Reilly, R.4
-
18
-
-
0038825296
-
Monozygotic twins exhibit numerous epigenetic differences: Clues to twin discordance?
-
Petronis A, Gottesman II, Kan P, Kennedy JL, Basile VS, Paterson AD et al. Monozygotic twins exhibit numerous epigenetic differences: clues to twin discordance? Schizophr Bull 2003; 29: 169-178.
-
(2003)
Schizophr Bull
, vol.29
, pp. 169-178
-
-
Petronis, A.1
Gottesman, I.I.2
Kan, P.3
Kennedy, J.L.4
Basile, V.S.5
Paterson, A.D.6
-
19
-
-
35648963256
-
Aberrant epigenetic regulation could explain the relationship of paternal age to schizophrenia
-
Perrin MC, Brown AS, Malaspina D. Aberrant epigenetic regulation could explain the relationship of paternal age to schizophrenia. Schizophr Bull 2007; 33: 1270-1273.
-
(2007)
Schizophr Bull
, vol.33
, pp. 1270-1273
-
-
Perrin, M.C.1
Brown, A.S.2
Malaspina, D.3
-
20
-
-
0029962317
-
Retroviruses and schizophrenia revisited
-
O'Reilly RL, Singh SM. Retroviruses and schizophrenia revisited. Am J Med Genet 1996; 67: 19-24.
-
(1996)
Am J Med Genet
, vol.67
, pp. 19-24
-
-
O'Reilly, R.L.1
Singh, S.M.2
-
21
-
-
0033569484
-
Molecular characterization of a MSRV-like sequence identified by RDA from monozygotic twin pairs discordant for schizophrenia
-
Deb-Rinker P, Klempan TA, O'Reilly RL, Torrey EF, Singh SM. Molecular characterization of a MSRV-like sequence identified by RDA from monozygotic twin pairs discordant for schizophrenia. Genomics 1999; 61: 133-144.
-
(1999)
Genomics
, vol.61
, pp. 133-144
-
-
Deb-Rinker, P.1
Klempan, T.A.2
O'Reilly, R.L.3
Torrey, E.F.4
Singh, S.M.5
-
22
-
-
34250788651
-
Epigenetic mechanisms in the context of complex diseases
-
van Vliet J, Oates NA, Whitelaw E. Epigenetic mechanisms in the context of complex diseases. Cell Mol Life Sci 2007; 64: 1531-1538.
-
(2007)
Cell Mol Life Sci
, vol.64
, pp. 1531-1538
-
-
van Vliet, J.1
Oates, N.A.2
Whitelaw, E.3
-
23
-
-
0033023626
-
New genetic hypothesis of schizophrenia
-
Guidry J, Kent TA. New genetic hypothesis of schizophrenia. Med Hypotheses 1999; 52: 69-75.
-
(1999)
Med Hypotheses
, vol.52
, pp. 69-75
-
-
Guidry, J.1
Kent, T.A.2
-
24
-
-
40849109768
-
Phenotypically concordant and discordant monozygotic twins display different DNA copy number variation profiles
-
Bruder C, Piotrowski A, Gijsbers A, Andersson R, Erickson S, Diaz de Ståhl T et al. Phenotypically concordant and discordant monozygotic twins display different DNA copy number variation profiles. Am J Hum Genet 2008; 82: 1-9.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 1-9
-
-
Bruder, C.1
Piotrowski, A.2
Gijsbers, A.3
Andersson, R.4
Erickson, S.5
Diaz de Ståhl, T.6
-
25
-
-
23044514669
-
Epigenetic differences arise during the lifetime of monozygotic twins
-
Fraga MF, Ballestar E, Paz MF, Ropero S, Setien F, Ballestar ML et al. Epigenetic differences arise during the lifetime of monozygotic twins. Proc Natl Acad Sci USA 2005; 102: 10604-10609.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 10604-10609
-
-
Fraga, M.F.1
Ballestar, E.2
Paz, M.F.3
Ropero, S.4
Setien, F.5
Ballestar, M.L.6
-
26
-
-
42349088634
-
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
-
Walsh T, McClellan JM, McCarthy SE, Addington AM, Pierce SB, Cooper GM et al. Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 2008; 320: 539-543.
-
(2008)
Science
, vol.320
, 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
-
27
-
-
20444375468
-
The neurodevelopmental model of schizophrenia: What can very early onset cases tell us?
-
Rapoport JL, Addington A, Frangou S. The neurodevelopmental model of schizophrenia: what can very early onset cases tell us? Curr Psychiatry Rep 2005; 7: 81-82.
-
(2005)
Curr Psychiatry Rep
, vol.7
, pp. 81-82
-
-
Rapoport, J.L.1
Addington, A.2
Frangou, S.3
-
28
-
-
46249093584
-
Strong association of de novo copy number mutations with sporadic schizophrenia
-
Xu B, Roos JL, Levy S, van Rensburg EJ, Gogos JA, Karayiorgou M. Strong association of de novo copy number mutations with sporadic schizophrenia. Nat Genet 2008; 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
-
29
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson H, Rujescu D, Cichon S, Pietilainen OP, Ingason A, Steinberg S et al. Large recurrent microdeletions associated with schizophrenia. Nature 2008; 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
-
30
-
-
85153324430
-
-
The International Schizophrenia Consortium, manuscript preparationStone JL, O'Donovan MC, Gurling H, Kirov GK, Blackwood DH, Corvin A et al. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008; 455: 237-241.
-
The International Schizophrenia Consortium, manuscript preparationStone JL, O'Donovan MC, Gurling H, Kirov GK, Blackwood DH, Corvin A et al. Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 2008; 455: 237-241.
-
-
-
-
32
-
-
55549143682
-
Copy number variation and evolution in humans and chimpanzees
-
Perry GH, Yang F, Marques-Bonet T, Murphy C, Fitzgerald T, Lee AS et al. Copy number variation and evolution in humans and chimpanzees. Genome Res 2008; 18: 1698-1710.
-
(2008)
Genome Res
, vol.18
, pp. 1698-1710
-
-
Perry, G.H.1
Yang, F.2
Marques-Bonet, T.3
Murphy, C.4
Fitzgerald, T.5
Lee, A.S.6
-
33
-
-
41149121141
-
Aneuploid mosaicism in the developing and adult cerebellar cortex
-
Westra JW, Peterson SE, Yung YC, Mutoh T, Barral S, Chun J. Aneuploid mosaicism in the developing and adult cerebellar cortex. J Comp Neurol 2008; 507: 1944-1951.
-
(2008)
J Comp Neurol
, vol.507
, pp. 1944-1951
-
-
Westra, J.W.1
Peterson, S.E.2
Yung, Y.C.3
Mutoh, T.4
Barral, S.5
Chun, J.6
-
34
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T et al. Strong association of de novo copy number mutations with autism. Science 2007; 316: 445-449.
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
Troge, J.4
Lese-Martin, C.5
Walsh, T.6
|