-
1
-
-
46249104490
-
Systematic meta-analyses and field synopsis of genetic association studies in schizophrenia: the SzGene database
-
Allen, N.C., Bagade, S., McQueen, M.B. et al. (2008) Systematic meta-analyses and fi eld synopsis of genetic association studies in schizophrenia: the SzGene database. Nature Genetics 40, 827-834.
-
(2008)
Nature Genetics
, vol.40
, pp. 827-834
-
-
Allen, N.C.1
Bagade, S.2
McQueen, M.B.3
-
2
-
-
0035985480
-
Characterisation, mutation detection, and association analysis of alternative promoters and 5 '?UTRs of the human dopamine D3 receptor gene in schizophrenia
-
Anney, R.J., Rees, M.I., Bryan, E. et al. (2002) Characterisation, mutation detection, and association analysis of alternative promoters and 5 '?UTRs of the human dopamine D3 receptor gene in schizophrenia. Molecular Psychiatry 7, 493-502.
-
(2002)
Molecular Psychiatry
, vol.7
, pp. 493-502
-
-
Anney, R.J.1
Rees, M.I.2
Bryan, E.3
-
3
-
-
0029965226
-
Further association study on dopamine D2 receptor variant S311C in schizophrenia and affective disorders
-
Arinami, T., Itokawa, M., Aoki, J. et al. (1996) Further association study on dopamine D2 receptor variant S311C in schizophrenia and affective disorders. American Journal of Medical Genetics 67, 133-138.
-
(1996)
American Journal of Medical Genetics
, vol.67
, pp. 133-138
-
-
Arinami, T.1
Itokawa, M.2
Aoki, J.3
-
4
-
-
0030933979
-
A functional polymorphism in the promoter region of the dopamine D2 receptor gene is associated with schizophrenia
-
Arinami, T., Gao, M, Hamaguchi, H. & Toru, M. (1997) A functional polymorphism in the promoter region of the dopamine D2 receptor gene is associated with schizophrenia. Human Molecular Genetics 6, 577-582.
-
(1997)
Human Molecular Genetics
, vol.6
, pp. 577-582
-
-
Arinami, T.1
Gao, M.2
Hamaguchi, H.3
Toru, M.4
-
5
-
-
33847327313
-
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
-
Autism Genome Project Consortium
-
Autism Genome Project Consortium (2007) Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature Genetics 39, 319-328.
-
(2007)
Nature Genetics
, vol.39
, pp. 319-328
-
-
-
6
-
-
45449095888
-
Meta-analysis of the cognitive effects of the catechol-O-methyltransferase gene Val158/108Met polymorphism
-
Barnett, J.H., Scoriels, L. & Munafò, M.R. (2008) Meta-analysis of the cognitive effects of the catechol-O-methyltransferase gene Val158/108Met polymorphism. Biological Psychiatry 64, 137-144.
-
(2008)
Biological Psychiatry
, vol.64
, pp. 137-144
-
-
Barnett, J.H.1
Scoriels, L.2
Munafò, M.R.3
-
7
-
-
0034927864
-
Schizophrenia and affective disorders-cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 fi ndings in a family
-
Blackwood, D.H., Fordyce, A., Walker, M.T., St Clair, D.M., Porteous, D.J. & Muir, W.J. (2001) Schizophrenia and affective disorders-cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 fi ndings in a family. American Journal of Human Genetics 69, 428-433.
-
(2001)
American Journal of Human Genetics
, vol.69
, pp. 428-433
-
-
Blackwood, D.H.1
Fordyce, A.2
Walker, M.T.3
St Clair, D.M.4
Porteous, D.J.5
Muir, W.J.6
-
8
-
-
77953226461
-
TCF4, schizophrenia, and Pitt-Hopkins Syndrome
-
Blake, D.J., Forrest, M., Chapman, R.M., Tinsley, C.L., O'Donovan, M.C. & Owen, M.J. (2010) TCF4, schizophrenia, and Pitt-Hopkins Syndrome. Schizophrenia Bulletin 36, 443-447.
-
(2010)
Schizophrenia Bulletin
, vol.36
, pp. 443-447
-
-
Blake, D.J.1
Forrest, M.2
Chapman, R.M.3
Tinsley, C.L.4
O'Donovan, M.C.5
Owen, M.J.6
-
9
-
-
0038389841
-
A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain
-
Bray, N.J., Buckland, P.R., Williams, N.M. et al. (2003) A haplotype implicated in schizophrenia susceptibility is associated with reduced COMT expression in human brain. American Journal of Human Genetics 73, 152-161.
-
(2003)
American Journal of Human Genetics
, vol.73
, pp. 152-161
-
-
Bray, N.J.1
Buckland, P.R.2
Williams, N.M.3
-
10
-
-
0842286644
-
The serotonin-2A receptor gene locus does not contain common polymorphism affecting mRNA levels in adult brain
-
Bray, N.J., Buckland, P.R., Hall, H., Owen, M.J. & O'Donovan, M.C. (2004) The serotonin-2A receptor gene locus does not contain common polymorphism affecting mRNA levels in adult brain. Molecular Psychiatry 9, 109-114.
-
(2004)
Molecular Psychiatry
, vol.9
, pp. 109-114
-
-
Bray, N.J.1
Buckland, P.R.2
Hall, H.3
Owen, M.J.4
O'Donovan, M.C.5
-
11
-
-
0033588110
-
-
141 C del/ins polymorphism of the dopamine receptor 2 gene is associated with schizophrenia in a British population
-
Breen, G., Brown, J., Maude, S. et al. (1999)-141 C del/ins polymorphism of the dopamine receptor 2 gene is associated with schizophrenia in a British population. American Journal of Medical Genetics 88, 407-410.
-
(1999)
American Journal of Medical Genetics
, vol.88
, pp. 407-410
-
-
Breen, G.1
Brown, J.2
Maude, S.3
-
12
-
-
2342625339
-
Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22
-
Brzustowicz, L.M., Simone, J., Mohseni, P. et al. (2004) Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22. American Journal of Human Genetics 74, 1057-1063.
-
(2004)
American Journal of Human Genetics
, vol.74
, pp. 1057-1063
-
-
Brzustowicz, L.M.1
Simone, J.2
Mohseni, P.3
-
13
-
-
0026612908
-
Changes in dopamine D1, D2 and D3 receptor mRNA levels in rat brain following antipsychotic treatment
-
Berlin
-
Buckland, P.R., O'Donovan, M.C. & McGuffin, P. (1992) Changes in dopamine D1, D2 and D3 receptor mRNA levels in rat brain following antipsychotic treatment. Psychopharmacology (Berlin) 106, 479-483.
-
(1992)
Psychopharmacology
, vol.106
, pp. 479-483
-
-
Buckland, P.R.1
O'Donovan, M.C.2
McGuffin, P.3
-
14
-
-
20844463251
-
Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia
-
Callicott, J.H., Straub, R.E., Pezawas, L. et al. (2005) Variation in DISC1 affects hippocampal structure and function and increases risk for schizophrenia. Proceedings of the National Academy of Science of the USA 102, 8627-8632.
-
(2005)
Proceedings of the National Academy of Science of the USA
, vol.102
, pp. 8627-8632
-
-
Callicott, J.H.1
Straub, R.E.2
Pezawas, L.3
-
15
-
-
20944446077
-
Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: longitudinal evidence of a gene ??environment interaction
-
Caspi, A., Moffi tt, T.E., Cannon, M. et al. (2005) Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: longitudinal evidence of a gene ??environment interaction. Biological Psychiatry 57, 1117-1127.
-
(2005)
Biological Psychiatry
, vol.57
, pp. 1117-1127
-
-
Caspi, A.1
Moffitt, T.E.2
Cannon, M.3
-
16
-
-
6344265879
-
Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain
-
Chen, J., Lipska, B.K., Halim, N. et al. (2004) Functional analysis of genetic variation in catechol-O-methyltransferase (COMT): effects on mRNA, protein, and enzyme activity in postmortem human brain. American Journal of Human Genetics 75, 807-821.
-
(2004)
American Journal of Human Genetics
, vol.75
, pp. 807-821
-
-
Chen, J.1
Lipska, B.K.2
Halim, N.3
-
17
-
-
71749085915
-
Association and linkage analyses of RGS4 polymorphisms in schizophrenia
-
Chowdari, K.V., Mirnics, K., Semwal, P. et al. (2002) Association and linkage analyses of RGS4 polymorphisms in schizophrenia. Human Molecular Genetics 11, 1373-1380.
-
(2002)
Human Molecular Genetics
, vol.11
, pp. 1373-1380
-
-
Chowdari, K.V.1
Mirnics, K.2
Semwal, P.3
-
18
-
-
0037108758
-
Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia
-
Chumakov, I., Blumenfeld, M., Guerassimenko, O. et al. (2002) Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia. Proceedings of the National Academy of Science of the USA 99, 13675-13680.
-
(2002)
Proceedings of the National Academy of Science of the USA
, vol.99
, pp. 13675-13680
-
-
Chumakov, I.1
Blumenfeld, M.2
Guerassimenko, O.3
-
19
-
-
35148825001
-
Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sample
-
Corvin, A., McGhee, K.A., Murphy, K. et al. (2007) Evidence for association and epistasis at the DAOA/G30 and D-amino acid oxidase loci in an Irish schizophrenia sample. American Journal of Medical Genetics Part B Neuropsychiatric Genetics 144B, 949-953.
-
(2007)
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
, vol.144 B
, pp. 949-953
-
-
Corvin, A.1
McGhee, K.A.2
Murphy, K.3
-
20
-
-
33646344731
-
The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons
-
Craddock, N., Owen, M.J. & O'Donovan, M.C. (2006) The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons. Molecular Psychiatry 11, 446-458.
-
(2006)
Molecular Psychiatry
, vol.11
, pp. 446-458
-
-
Craddock, N.1
Owen, M.J.2
O'Donovan, M.C.3
-
21
-
-
0029860139
-
Functional analysis of the human D2 dopamine receptor missense variants
-
Cravchik, A., Sibley, D.R. & Gejman, P.V. (1996) Functional analysis of the human D2 dopamine receptor missense variants. Journal of Biological Chemistry 271, 26013-26017.
-
(1996)
Journal of Biological Chemistry
, vol.271
, pp. 26013-26017
-
-
Cravchik, A.1
Sibley, D.R.2
Gejman, P.V.3
-
22
-
-
0027076725
-
Association between schizophrenia and homozygosity at the dopamine D3 receptor gene
-
Crocq, M.A., Mant, R., Asherson, P. et al. (1992) Association between schizophrenia and homozygosity at the dopamine D3 receptor gene. Journal of Medical Genetics 29, 858-860.
-
(1992)
Journal of Medical Genetics
, vol.29
, pp. 858-860
-
-
Crocq, M.A.1
Mant, R.2
Asherson, P.3
-
23
-
-
13344284664
-
No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity
-
Daniels, J.K., Williams, N.M., Williams, J. et al. (1996) No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity. American Journal of Psychiatry 153, 268-270.
-
(1996)
American Journal of Psychiatry
, vol.153
, pp. 268-270
-
-
Daniels, J.K.1
Williams, N.M.2
Williams, J.3
-
24
-
-
55949127945
-
Association of the SerCys DISC1 polymorphism with human hippocampal formation gray matter and function during memory encoding
-
Di Giorgio, A., Blasi, G., Sambataro, F. et al. (2008) Association of the SerCys DISC1 polymorphism with human hippocampal formation gray matter and function during memory encoding. European Journal of Neuroscience 28, 2129-136.
-
(2008)
European Journal of Neuroscience
, vol.28
, pp. 2129-136
-
-
Di Giorgio, A.1
Blasi, G.2
Sambataro, F.3
-
25
-
-
33846804188
-
Extensive linkage disequilibrium mapping at HTR2A and DRD3 for schizophrenia susceptibility genes in the Galician population
-
Dom í nguez, E., Loza, M.I., Pad í n, F. et al. (2007) Extensive linkage disequilibrium mapping at HTR2A and DRD3 for schizophrenia susceptibility genes in the Galician population. Schizophrenia Research 90, 123-129.
-
(2007)
Schizophrenia Research
, vol.90
, pp. 123-129
-
-
Domínguez, E.1
Loza, M.I.2
Padín, F.3
-
26
-
-
0037320652
-
Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor
-
Duan, J., Wainwright, M.S., Comeron, J.M. et al. (2003) Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor. Human Molecular Genetics 12, 205-216.
-
(2003)
Human Molecular Genetics
, vol.12
, pp. 205-216
-
-
Duan, J.1
Wainwright, M.S.2
Comeron, J.M.3
-
27
-
-
77955293516
-
The DISC1 Ser704Cys substitution affects centrosomal localisation of its binding partner PCM1 in glia in human brain
-
Eastwood, S.L., Walker, M., Hyde, T.M., Kleinman, J.E. & Harrison, P.J. (2010) The DISC1 Ser704Cys substitution affects centrosomal localisation of its binding partner PCM1 in glia in human brain. Human Molecular Genetics 19, 2487-2496.
-
(2010)
Human Molecular Genetics
, vol.19
, pp. 2487-2496
-
-
Eastwood, S.L.1
Walker, M.2
Hyde, T.M.3
Kleinman, J.E.4
Harrison, P.J.5
-
28
-
-
0035810850
-
Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia
-
Egan, M.F., Goldberg, T.E., Kolachana, B.S. et al. (2001) Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia. Proceedings of the National Academy of Sciences of the USA 98, 6917-6922.
-
(2001)
Proceedings of the National Academy of Sciences of the USA
, vol.98
, pp. 6917-6922
-
-
Egan, M.F.1
Goldberg, T.E.2
Kolachana, B.S.3
-
29
-
-
65549147665
-
Neural mechanisms of a genome-wide supported psychosis variant
-
Esslinger, C., Walter, H., Kirsch, P. et al. (2009) Neural mechanisms of a genome-wide supported psychosis variant. Science 324, 605.
-
(2009)
Science
, vol.324
, pp. 605
-
-
Esslinger, C.1
Walter, H.2
Kirsch, P.3
-
30
-
-
27144517184
-
Meta-analysis reveals association between serotonin transporter gene STin2 VNTR polymorphism and schizophrenia
-
Fan, J.B. & Sklar, P. (2005) Meta-analysis reveals association between serotonin transporter gene STin2 VNTR polymorphism and schizophrenia. Molecular Psychiatry 10, 928-938.
-
(2005)
Molecular Psychiatry
, vol.10
, pp. 928-938
-
-
Fan, J.B.1
Sklar, P.2
-
31
-
-
42749089914
-
PDE4B polymorphisms and decreased PDE4B expression are associated with schizophrenia
-
Fatemi, S.H., King, D.P., Reutiman, T.J. et al. (2008) PDE4B polymorphisms and decreased PDE4B expression are associated with schizophrenia. Schizophrenia Research 101, 36-49.
-
(2008)
Schizophrenia Research
, vol.101
, pp. 36-49
-
-
Fatemi, S.H.1
King, D.P.2
Reutiman, T.J.3
-
32
-
-
48749127996
-
Support for neuregulin 1 as a susceptibility gene for bipolar disorder and schizophrenia
-
Georgieva, L., Dimitrova, A., Ivanov, D. et al. (2008) Support for neuregulin 1 as a susceptibility gene for bipolar disorder and schizophrenia. Biological Psychiatry 64, 419-427.
-
(2008)
Biological Psychiatry
, vol.64
, pp. 419-427
-
-
Georgieva, L.1
Dimitrova, A.2
Ivanov, D.3
-
33
-
-
32244447628
-
The Cys allele of the DRD2 Ser311Cys polymorphism has a dominant effect on risk for schizophrenia: evidence from fixed-and random-effects meta-analyses
-
Glatt, S.J. & Jönsson, E.G. (2006) The Cys allele of the DRD2 Ser311Cys polymorphism has a dominant effect on risk for schizophrenia: evidence from fi xed-and random-effects meta-analyses. American Journal of Medical Genetics B Neuropsychiatric Genetics 141B, 149-154.
-
(2006)
American Journal of Medical Genetics B Neuropsychiatric Genetics
, vol.141 B
, pp. 149-154
-
-
Glatt, S.J.1
Jönsson, E.G.2
-
34
-
-
0242317420
-
Schizophrenia is not associated with DRD4 48-base-pair-repeat length or individual alleles: results of a meta-analysis
-
Glatt, S.J., Faraone, S.V. & Tsuang, M.T. (2003) Schizophrenia is not associated with DRD4 48-base-pair-repeat length or individual alleles: results of a meta-analysis. Biological Psychiatry 54, 629-635.
-
(2003)
Biological Psychiatry
, vol.54
, pp. 629-635
-
-
Glatt, S.J.1
Faraone, S.V.2
Tsuang, M.T.3
-
35
-
-
3042805378
-
DRD2-141C insertion/deletion polymorphism is not associated with schizophrenia: results of a meta-analysis
-
Glatt, S.J., Faraone, S.V. & Tsuang, M.T. (2004) DRD2-141C insertion/deletion polymorphism is not associated with schizophrenia: results of a meta-analysis. American Journal of Medical Genetics B Neuropsychiatric Genetics 128B, 21-23.
-
(2004)
American Journal of Medical Genetics B Neuropsychiatric Genetics
, vol.128 B
, pp. 21-23
-
-
Glatt, S.J.1
Faraone, S.V.2
Tsuang, M.T.3
-
36
-
-
69249123764
-
Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan
-
Glatt, S.J., Faraone, S.V., Lasky-Su, J.A. et al. (2009) Family-based association testing strongly implicates DRD2 as a risk gene for schizophrenia in Han Chinese from Taiwan. Molecular Psychiatry 14, 885-893.
-
(2009)
Molecular Psychiatry
, vol.14
, pp. 885-893
-
-
Glatt, S.J.1
Faraone, S.V.2
Lasky-Su, J.A.3
-
37
-
-
0032544012
-
Catechol-O-methyltransferase-defi cient mice exhibit sexually dimorphic changes in catecholamine levels and behavior
-
Gogos, J.A., Morgan, M., Luine, V. et al. (1998) Catechol-O-methyltransferase-defi cient mice exhibit sexually dimorphic changes in catecholamine levels and behavior. Proceedings of the National Academy of Science of the USA 95, 9991-9996.
-
(1998)
Proceedings of the National Academy of Science of the USA
, vol.95
, pp. 9991-9996
-
-
Gogos, J.A.1
Morgan, M.2
Luine, V.3
-
38
-
-
33748066634
-
Evidence that a DISC1 frame-shift deletion associated with psychosis in a single family may not be a pathogenic mutation
-
Green, E.K., Norton, N., Peirce, T. et al. (2006) Evidence that a DISC1 frame-shift deletion associated with psychosis in a single family may not be a pathogenic mutation. Molecular Psychiatry 11, 798-799.
-
(2006)
Molecular Psychiatry
, vol.11
, pp. 798-799
-
-
Green, E.K.1
Norton, N.2
Peirce, T.3
-
39
-
-
25844501532
-
Genomewide linkage scan in schizoaffective disorder: signifi cant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13
-
Hamshere, M.L., Bennett, P, Williams, N. et al. (2005) Genomewide linkage scan in schizoaffective disorder: signifi cant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13. Archives of General Psychiatry 62, 1081-1088.
-
(2005)
Archives of General Psychiatry
, vol.62
, pp. 1081-1088
-
-
Hamshere, M.L.1
Bennett, P.2
Williams, N.3
-
40
-
-
0037730178
-
Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series
-
Hattori, E., Liu, C., Badner, J.A. et al. (2003) Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series. American Journal of Human Genetics 72, 1131-1140.
-
(2003)
American Journal of Human Genetics
, vol.72
, pp. 1131-1140
-
-
Hattori, E.1
Liu, C.2
Badner, J.A.3
-
41
-
-
59149096726
-
15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
-
Helbig, I., Mefford, H.C., Sharp, A.J. et al. (2009) 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy. Nature Genetics 41, 160-162.
-
(2009)
Nature Genetics
, vol.41
, pp. 160-162
-
-
Helbig, I.1
Mefford, H.C.2
Sharp, A.J.3
-
42
-
-
69249128690
-
DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder
-
Hennah, W., Thomson, P., McQuillin, A. et al. (2009) DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder. Molecular Psychiatry 14, 863-873.
-
(2009)
Molecular Psychiatry
, vol.14
, pp. 863-873
-
-
Hennah, W.1
Thomson, P.2
McQuillin, A.3
-
43
-
-
6344255274
-
Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder
-
Hodgkinson, C.A., Goldman, D., Jaeger, J. et al. (2004) Disrupted in schizophrenia 1 (DISC1): association with schizophrenia, schizoaffective disorder, and bipolar disorder. American Journal of Human Genetics 75, 862-872.
-
(2004)
American Journal of Human Genetics
, vol.75
, pp. 862-872
-
-
Hodgkinson, C.A.1
Goldman, D.2
Jaeger, J.3
-
44
-
-
33745509160
-
No association of serotonin transporter gene (SLC6A4) with schizophrenia and bipolar disorder in Japanese patients: association analysis based on linkage disequilibrium
-
Ikeda, M., Iwata, N., Suzuki, T. et al. (2006) No association of serotonin transporter gene (SLC6A4) with schizophrenia and bipolar disorder in Japanese patients: association analysis based on linkage disequilibrium. Journal of Neural Transmission 113, 899-905.
-
(2006)
Journal of Neural Transmission
, vol.113
, pp. 899-905
-
-
Ikeda, M.1
Iwata, N.2
Suzuki, T.3
-
45
-
-
0029988749
-
Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia
-
Inayama, Y., Yoneda, H., Sakai, T. et al. (1996) Positive association between a DNA sequence variant in the serotonin 2A receptor gene and schizophrenia. American Journal of Medical Genetics 67, 103-105.
-
(1996)
American Journal of Medical Genetics
, vol.67
, pp. 103-105
-
-
Inayama, Y.1
Yoneda, H.2
Sakai, T.3
-
46
-
-
78650514762
-
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
-
2009 Sept 29 Epub ahead of print
-
Ingason, A., Rujescu, D., Cichon, S. et al. (2009) Copy number variations of chromosome 16p13.1 region associated with schizophrenia. M olecular Psychiatry 2009 Sept 29 [Epub ahead of print].
-
(2009)
Molecular Psychiatry
-
-
Ingason, A.1
Rujescu, D.2
Cichon, S.3
-
47
-
-
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
-
-
-
48
-
-
68449086236
-
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
-
International Schizophrenia Consortium
-
International Schizophrenia Consortium (2009) Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Nature 460, 748-752.
-
(2009)
Nature
, vol.460
, pp. 748-752
-
-
-
49
-
-
33845286875
-
RGS4 is not a susceptibility gene for schizophrenia in Japanese: association study in a large case-control population
-
Ishiguro, H., Horiuchi, Y., Koga, M. et al. (2007) RGS4 is not a susceptibility gene for schizophrenia in Japanese: association study in a large case-control population. Schizophrenia Research 89, 161-164.
-
(2007)
Schizophrenia Research
, vol.89
, pp. 161-164
-
-
Ishiguro, H.1
Horiuchi, Y.2
Koga, M.3
-
50
-
-
0037336692
-
Dopamine D3 receptor gene Ser9Gly variant and schizophrenia: association study and meta-analysis
-
Jönsson, E.G., Flyckt, L., Burgert, E. et al. (2003) Dopamine D3 receptor gene Ser9Gly variant and schizophrenia: association study and meta-analysis. Psychiatric Genetics 13, 1-12.
-
(2003)
Psychiatric Genetics
, vol.13
, pp. 1-12
-
-
Jönsson, E.G.1
Flyckt, L.2
Burgert, E.3
-
51
-
-
38349106160
-
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
-
Kirov, G., Gumus, D., Chen, W. et al. (2008) Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia. Human Molecular Genetics 17, 458-465.
-
(2008)
Human Molecular Genetics
, vol.17
, pp. 458-465
-
-
Kirov, G.1
Gumus, D.2
Chen, W.3
-
52
-
-
67651180973
-
A genome-wide association study in 574 schizophrenia trios using DNA pooling
-
Kirov, G., Zaharieva, I., Georgieva, L. et al. (2009a) A genome-wide association study in 574 schizophrenia trios using DNA pooling. Molecular Psychiatry 14, 796-803.
-
(2009)
Molecular Psychiatry
, vol.14
, pp. 796-803
-
-
Kirov, G.1
Zaharieva, I.2
Georgieva, L.3
-
53
-
-
64549147485
-
Support for the involvement of large copy number variants in the pathogenesis of schizophrenia
-
Kirov, G., Grozeva, D., Norton, N. et al. (2009b) Support for the involvement of large copy number variants in the pathogenesis of schizophrenia. Human Molecular Genetics 18, 1497-1503.
-
(2009)
Human Molecular Genetics
, vol.18
, pp. 1497-1503
-
-
Kirov, G.1
Grozeva, D.2
Norton, N.3
-
54
-
-
69249091299
-
Neurexin 1 (NRXN1) deletions in schizophrenia
-
Kirov, G., Rujescu, D., Ingason, A., Collier, D.A., O'Donovan, M.C. & Owen MJ. (2009c) Neurexin 1 (NRXN1) deletions in schizophrenia. Schizophrenia Bulletin 35, 851-854.
-
(2009)
Schizophrenia Bulletin
, vol.35
, pp. 851-854
-
-
Kirov, G.1
Rujescu, D.2
Ingason, A.3
Collier, D.A.4
O'Donovan, M.C.5
Owen, M.J.6
-
55
-
-
20244380171
-
Complement factor H polymorphism in age-related macular degeneration
-
Klein, R.J., Zeiss, C., Chew, E.Y. et al. (2005) Complement factor H polymorphism in age-related macular degeneration. Science 308, 385-389.
-
(2005)
Science
, vol.308
, pp. 385-389
-
-
Klein, R.J.1
Zeiss, C.2
Chew, E.Y.3
-
56
-
-
9644272541
-
The C/C genotype of the C957T polymorphism of the dopamine D2 receptor is associated with schizophrenia
-
Lawford, B.R., Young, R.M., Swagell, C.D. et al. (2005) The C/C genotype of the C957T polymorphism of the dopamine D2 receptor is associated with schizophrenia. Schizophrenia Research 73, 31-37.
-
(2005)
Schizophrenia Research
, vol.73
, pp. 31-37
-
-
Lawford, B.R.1
Young, R.M.2
Swagell, C.D.3
-
57
-
-
14044255978
-
Association of Ala72Ser polymorphism with COMT enzyme activity and the risk of schizophrenia in Koreans
-
Lee, S.G., Joo, Y., Kim, B. et al. (2005) Association of Ala72Ser polymorphism with COMT enzyme activity and the risk of schizophrenia in Koreans. Human Genetics 116, 319-328.
-
(2005)
Human Genetics
, vol.116
, pp. 319-328
-
-
Lee, S.G.1
Joo, Y.2
Kim, B.3
-
58
-
-
34249332776
-
Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia
-
Lencz, T., Morgan, T.V., Athanasiou, M. et al. (2007) Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia. Molecular Psychiatry 12, 572-580.
-
(2007)
Molecular Psychiatry
, vol.12
, pp. 572-580
-
-
Lencz, T.1
Morgan, T.V.2
Athanasiou, M.3
-
59
-
-
0006463359
-
Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region
-
Lesch, K.P., Bengel, D., Heils, A. et al. (1996) Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region. Science 274, 1527-1531.
-
(1996)
Science
, vol.274
, pp. 1527-1531
-
-
Lesch, K.P.1
Bengel, D.2
Heils, A.3
-
60
-
-
33847230623
-
No gene is an island: the fl ip-fl op phenomenon
-
Lin, P.I., Vance, J.M. Pericak-Vance, M.A. & Martin, E.R. (2007) No gene is an island: the fl ip-fl op phenomenon. American Journal of Human Genetics 80, 531-538.
-
(2007)
American Journal of Human Genetics
, vol.80
, pp. 531-538
-
-
Lin, P.I.1
Vance, J.M.2
Pericak-Vance, M.A.3
Martin, E.R.4
-
61
-
-
0029052146
-
Schizophrenia and chromosomal deletions within 22q11.2
-
Lindsay, E.A., Morris, M.A., Gos, A. et al. (1995) Schizophrenia and chromosomal deletions within 22q11.2. American Journal of Human Genetics 56, 1502-1503.
-
(1995)
American Journal of Human Genetics
, vol.56
, pp. 1502-1503
-
-
Lindsay, E.A.1
Morris, M.A.2
Gos, A.3
-
62
-
-
42749095256
-
The Ser9Gly polymorphism of the dopamine D3 receptor gene and risk of schizophrenia: an association study and a large meta-analysis
-
Ma, G., et al. (2008) The Ser9Gly polymorphism of the dopamine D3 receptor gene and risk of schizophrenia: an association study and a large meta-analysis. Schizophrenia Research 101, 26-35.
-
(2008)
Schizophrenia Research
, vol.101
, pp. 26-35
-
-
Ma, G.1
-
63
-
-
0037947438
-
Catechol O-methyltransferase val158-met genotype and individual variation in the brain response to amphetamine
-
Mattay, V.S., Goldberg, T.E., Fera, F. et al. (2003) Catechol O-methyltransferase val158-met genotype and individual variation in the brain response to amphetamine. Proceedings of the National Academy of Science of the USA 100, 6186-6191.
-
(2003)
Proceedings of the National Academy of Science of the USA
, vol.100
, pp. 6186-6191
-
-
Mattay, V.S.1
Goldberg, T.E.2
Fera, F.3
-
64
-
-
70350626873
-
Microduplications of 16p11.2 are associated with schizophrenia
-
McCarthy, S.E., Makarov, V., Kirov, G. et al. (2009) Microduplications of 16p11.2 are associated with schizophrenia. Nature Genetics 41, 1223-1227.
-
(2009)
Nature Genetics
, vol.41
, pp. 1223-1227
-
-
McCarthy, S.E.1
Makarov, V.2
Kirov, G.3
-
65
-
-
54049094444
-
Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes
-
Mefford, H.C., Sharp, R.J., Baker, C. et al. (2008) Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes. New England Journal of Medicine 359, 1685-1699.
-
(2008)
New England Journal of Medicine
, vol.359
, pp. 1685-1699
-
-
Mefford, H.C.1
Sharp, R.J.2
Baker, C.3
-
66
-
-
0034702026
-
Disruption of two novel genes by a translocation co-segregating with schizophrenia
-
Millar, J.K., Wilson-Annan, J.C., Anderson, S. et al. (2000) Disruption of two novel genes by a translocation co-segregating with schizophrenia. Human Molecular Genetics 9, 1415-1423.
-
(2000)
Human Molecular Genetics
, vol.9
, pp. 1415-1423
-
-
Millar, J.K.1
Wilson-Annan, J.C.2
Anderson, S.3
-
67
-
-
27944502874
-
DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling
-
Millar, J.K., Pickard, B.S., Mackie, S. et al. (2005) DISC1 and PDE4B are interacting genetic factors in schizophrenia that regulate cAMP signaling. Science 310, 1187-1191.
-
(2005)
Science
, vol.310
, pp. 1187-1191
-
-
Millar, J.K.1
Pickard, B.S.2
Mackie, S.3
-
68
-
-
39949084676
-
Association study of three polymorphisms in the dopamine D2 receptor gene and schizophrenia in the Russian population
-
Monakhov, M., Golimbet, V., Abramson, L., Kaleda, V. & Karpov, V. (2008) Association study of three polymorphisms in the dopamine D2 receptor gene and schizophrenia in the Russian population. Schizophrenia Research 100, 302-307.
-
(2008)
Schizophrenia Research
, vol.100
, pp. 302-307
-
-
Monakhov, M.1
Golimbet, V.2
Abramson, L.3
Kaleda, V.4
Karpov, V.5
-
69
-
-
0942268965
-
Confirming RGS4 as a susceptibility gene for schizophrenia
-
Morris, D.W., Rodgers, A., McGhee, K.A. et al. (2004) Confi rming RGS4 as a susceptibility gene for schizophrenia. American Journal of Medical Genetics 125B, 50-53.
-
(2004)
American Journal of Medical Genetics
, vol.125 B
, pp. 50-53
-
-
Morris, D.W.1
Rodgers, A.2
McGhee, K.A.3
-
70
-
-
34247576159
-
Detailed analysis of the relative power of direct and indirect association studies and the implications for their interpretation
-
Moskvina, V. & O'Donovan, M.C. (2007) Detailed analysis of the relative power of direct and indirect association studies and the implications for their interpretation. Human Heredity 64, 63-73.
-
(2007)
Human Heredity
, vol.64
, pp. 63-73
-
-
Moskvina, V.1
O'Donovan, M.C.2
-
71
-
-
33744481021
-
Effects of differential genotyping error rate on the type I error probability of case-control studies
-
Moskvina, V., Craddock, N., Holmans, P., Owen, M.J. & O'Donovan, M.C. (2006) Effects of differential genotyping error rate on the type I error probability of case-control studies. Human Heredity 61, 55-64.
-
(2006)
Human Heredity
, vol.61
, pp. 55-64
-
-
Moskvina, V.1
Craddock, N.2
Holmans, P.3
Owen, M.J.4
O'Donovan, M.C.5
-
72
-
-
0032882849
-
High rates of schizophrenia in adults with velo-cardio-facial syndrome
-
Murphy, K.C., Jones, L.A. & Owen, M.J. (1999) High rates of schizophrenia in adults with velo-cardio-facial syndrome. Archives of General Psychiatry 56, 940-945.
-
(1999)
Archives of General Psychiatry
, vol.56
, pp. 940-945
-
-
Murphy, K.C.1
Jones, L.A.2
Owen, M.J.3
-
73
-
-
33845899137
-
Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure
-
Nackley, A.G., Shabalina, S.A., Tchivileva, I.E. et al. (2006) Human catechol-O-methyltransferase haplotypes modulate protein expression by altering mRNA secondary structure. Science 314, 1930-1933.
-
(2006)
Science
, vol.314
, pp. 1930-1933
-
-
Nackley, A.G.1
Shabalina, S.A.2
Tchivileva, I.E.3
-
74
-
-
33846363929
-
Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: infl uence on risk of schizophrenia
-
Nicodemus, K.K., Callicott, J.H., Higier, R.G. et al. (2007) Evidence for statistical epistasis between catechol-O-methyltransferase (COMT) and polymorphisms in RGS4, G72 (DAOA), GRM3, and DISC1: infl uence on risk of schizophrenia. Human Genetics 120, 889-906.
-
(2007)
Human Genetics
, vol.120
, pp. 889-906
-
-
Nicodemus, K.K.1
Callicott, J.H.2
Higier, R.G.3
-
75
-
-
50449100461
-
Identifi cation of novel schizophrenia loci by genome-wide association and follow-up
-
O'Donovan, M.C., Craddock, N., Norton, N. et al. (2008) Identifi cation of novel schizophrenia loci by genome-wide association and follow-up. Nature Genetics 40, 1053-1055.
-
(2008)
Nature Genetics
, vol.40
, pp. 1053-1055
-
-
O'Donovan, M.C.1
Craddock, N.2
Norton, N.3
-
76
-
-
52049116298
-
Genetic dissection of the role of catechol-O-Methyltransferase in cognition and stress reactivity in mice
-
Papaleo, F., Crawley, J.N., Song, J. et al. (2008) Genetic dissection of the role of catechol-O-Methyltransferase in cognition and stress reactivity in mice. The Journal of Neuroscience 28, 8709-8723.
-
(2008)
The Journal of Neuroscience
, vol.28
, pp. 8709-8723
-
-
Papaleo, F.1
Crawley, J.N.2
Song, J.3
-
77
-
-
0037086178
-
Differential expression of the C and T alleles of the 5-HT2A receptor gene in the temporal cortex of normal individuals and schizophrenics
-
Polesskaya, O.O. & Sokolov, B.P. (2002) Differential expression of the C and T alleles of the 5-HT2A receptor gene in the temporal cortex of normal individuals and schizophrenics. Journal of Neuroscience Research 67, 812-822.
-
(2002)
Journal of Neuroscience Research
, vol.67
, pp. 812-822
-
-
Polesskaya, O.O.1
Sokolov, B.P.2
-
78
-
-
33847096690
-
Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene
-
Puri, V., McQuillin, A, Choudhury, K. et al. (2007) Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene. Biological Psychiatry 61, 873-879.
-
(2007)
Biological Psychiatry
, vol.61
, pp. 873-879
-
-
Puri, V.1
McQuillin, A.2
Choudhury, K.3
-
79
-
-
53249115258
-
Confi rmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3
-
Puri, V., McQuillan, A., Datta, S. et al. (2008) Confi rmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3. European Journal of Human Genetics 16, 1275-1282.
-
(2008)
European Journal of Human Genetics
, vol.16
, pp. 1275-1282
-
-
Puri, V.1
McQuillan, A.2
Datta, S.3
-
80
-
-
44949136624
-
G72 and its association with major depression and neuroticism in large population-based groups from Germany
-
Rietschel, M., Beckmann, L., Strohmaier, J. et al. (2008) G72 and its association with major depression and neuroticism in large population-based groups from Germany. American Journal of Psychiatry 165, 753-762.
-
(2008)
American Journal of Psychiatry
, vol.165
, pp. 753-762
-
-
Rietschel, M.1
Beckmann, L.2
Strohmaier, J.3
-
81
-
-
33749041047
-
Neurobiology of schizophrenia
-
Ross, C.A., Margolis, R.L., Reading, S.A., Pletnikov, M. & Coyle, J. T. (2006) Neurobiology of schizophrenia. Neuron 52, 139-153.
-
(2006)
Neuron
, vol.52
, pp. 139-153
-
-
Ross, C.A.1
Margolis, R.L.2
Reading, S.A.3
Pletnikov, M.4
Coyle, J.T.5
-
82
-
-
43349097737
-
No signifi cant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics
-
Sanders, A.R., Duan, J., Levinson, D.F. et al. (2008) No signifi cant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics. American Journal of Psychiatry 165, 497-506.
-
(2008)
American Journal of Psychiatry
, vol.165
, pp. 497-506
-
-
Sanders, A.R.1
Duan, J.2
Levinson, D.F.3
-
83
-
-
10744232028
-
Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder
-
Schumacher, J., Jamra, R.A., Freudenberg, J. et al. (2004) Examination of G72 and D-amino-acid oxidase as genetic risk factors for schizophrenia and bipolar affective disorder. Molecular Psychiatry 9, 203-207.
-
(2004)
Molecular Psychiatry
, vol.9
, pp. 203-207
-
-
Schumacher, J.1
Jamra, R.A.2
Freudenberg, J.3
-
84
-
-
67649832375
-
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations
-
Schumacher, J., Laje, G., Abou Jamra, R. et al. (2009) The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations. Human Molecular Genetics 18, 2719-2727.
-
(2009)
Human Molecular Genetics
, vol.18
, pp. 2719-2727
-
-
Schumacher, J.1
Laje, G.2
Abou Jamra, R.3
-
85
-
-
34247481814
-
Strong association of d e novo copy number mutations with autism
-
Sebat, J., Lakshmi, B., Malhotra, D. et al. (2007) Strong association of d e novo copy number mutations with autism. Science 316, 445-449.
-
(2007)
Science
, vol.316
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
-
86
-
-
36849031756
-
Allelic association of G72/G30 with schizophrenia and bipolar disorder: a comprehensive meta-analysis
-
Shi, J., Badner, J.A., Gershon, E.S. & Liu, C. (2008) Allelic association of G72/G30 with schizophrenia and bipolar disorder: a comprehensive meta-analysis. Schizophrenia Research 98, 89-97.
-
(2008)
Schizophrenia Research
, vol.98
, pp. 89-97
-
-
Shi, J.1
Badner, J.A.2
Gershon, E.S.3
Liu, C.4
-
87
-
-
58249088728
-
Further evidence for an association of G72/G30 with schizophrenia in Chinese
-
Shi, J., Badner, J.A., Gershon, E.S. et al. (2009a) Further evidence for an association of G72/G30 with schizophrenia in Chinese. Schizophrenia Research 107, 324-326.
-
(2009)
Schizophrenia Research
, vol.107
, pp. 324-326
-
-
Shi, J.1
Badner, J.A.2
Gershon, E.S.3
-
88
-
-
68449096727
-
Common variants on chromosome 6p22.1 are associated with schizophrenia
-
Shi, J., Levinson, DF., Duan, J. et al. (2009b) Common variants on chromosome 6p22.1 are associated with schizophrenia. Nature 460, 753-757.
-
(2009)
Nature
, vol.460
, pp. 753-757
-
-
Shi, J.1
Levinson, D.F.2
Duan, J.3
-
89
-
-
0036913209
-
A highly signifi cant association between a COMT haplotype and schizophrenia
-
Shifman, S., Bronstein, M., Sternfeld, M. et al. (2002) A highly signifi cant association between a COMT haplotype and schizophrenia. American Journal of Human Genetics 71, 1296-1302.
-
(2002)
American Journal of Human Genetics
, vol.71
, pp. 1296-1302
-
-
Shifman, S.1
Bronstein, M.2
Sternfeld, M.3
-
90
-
-
40149105889
-
Genome-wide association identifi es a common variant in the reelin gene that increases the risk of schizophrenia only in women
-
Shifman, S., Johannesson, M., Bronstein, M. et al. (2008) Genome-wide association identifi es a common variant in the reelin gene that increases the risk of schizophrenia only in women. Public Library of Science Genetics 4, e28.
-
(2008)
Public Library of Science Genetics
, vol.4
-
-
Shifman, S.1
Johannesson, M.2
Bronstein, M.3
-
91
-
-
47749122607
-
COMT genotype predicts cortical-limbic D1 receptor availability measured with [11C]NNC112 and PET
-
Slifstein, M., Kolachana, B., Simpson, E.H. et al. (2008) COMT genotype predicts cortical-limbic D1 receptor availability measured with [11C]NNC112 and PET. Molecular Psychiatry 13, 821-827.
-
(2008)
Molecular Psychiatry
, vol.13
, pp. 821-827
-
-
Slifstein, M.1
Kolachana, B.2
Simpson, E.H.3
-
92
-
-
37849016892
-
Sham PC. An association study of RGS4 polymorphisms with clinical phenotypes of schizophrenia in a Chinese population
-
So, H.C., Chen, R.Y., Chen, E.Y., Cheung, E.F. & Li, T. (2008) Sham PC. An association study of RGS4 polymorphisms with clinical phenotypes of schizophrenia in a Chinese population. American Journal of Medical Genetics B Neuropsychiatric Genetics 147B, 77-85.
-
(2008)
American Journal of Medical Genetics B Neuropsychiatric Genetics
, vol.147 B
, pp. 77-85
-
-
So, H.C.1
Chen, R.Y.2
Chen, E.Y.3
Cheung, E.F.4
Li, T.5
-
93
-
-
0025277392
-
Association within a family of a balanced autosomal translocation with major mental illness
-
St Clair, D., Blackwood, D., Muir, W. et al. (1990) Association within a family of a balanced autosomal translocation with major mental illness. Lancet 336, 13-16.
-
(1990)
Lancet
, vol.336
, pp. 13-16
-
-
St Clair, D.1
Blackwood, D.2
Muir, W.3
-
94
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson, H., Rujescu, D., Cichon, S. 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
-
95
-
-
68449090594
-
Common variants conferring risk of schizophrenia
-
Stefansson, H., Ophoff, R.A., Steinberg, S. et al. (2009) Common variants conferring risk of schizophrenia. Nature 460, 744-747.
-
(2009)
Nature
, vol.460
, pp. 744-747
-
-
Stefansson, H.1
Ophoff, R.A.2
Steinberg, S.3
-
96
-
-
43949122950
-
Genomewide association for schizophrenia in the CATIE study: results of stage 1
-
Sullivan, P.F., de Guess, E.J., Willemsen, G. et al. (2008) Genomewide association for schizophrenia in the CATIE study: results of stage 1. Molecular Psychiatry 13, 570-584.
-
(2008)
Molecular Psychiatry
, vol.13
, pp. 570-584
-
-
Sullivan, P.F.1
de Guess, E.J.2
Willemsen, G.3
-
97
-
-
33745885945
-
Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples
-
Talkowski, M.E., Seltman, H., Bassett, A.S. et al. (2006) Evaluation of a susceptibility gene for schizophrenia: genotype based meta-analysis of RGS4 polymorphisms from thirteen independent samples. Biological Psychiatry 60, 152-162.
-
(2006)
Biological Psychiatry
, vol.60
, pp. 152-162
-
-
Talkowski, M.E.1
Seltman, H.2
Bassett, A.S.3
-
98
-
-
39749200988
-
A network of dopaminergic gene variations implicated as risk factors for schizophrenia
-
Talkowski, M.E., Kirov, G., Bamne, M. et al. (2008) A network of dopaminergic gene variations implicated as risk factors for schizophrenia. Human Molecular Genetics 17, 747-758.
-
(2008)
Human Molecular Genetics
, vol.17
, pp. 747-758
-
-
Talkowski, M.E.1
Kirov, G.2
Bamne, M.3
-
99
-
-
27744455936
-
The genetics of attention defi cit hyperactivity disorder
-
Thapar, A., O'Donovan, M. & Owen, M. J. (2005) The genetics of attention defi cit hyperactivity disorder. Human Molecular Genetics 14 (Spec No. 2), R275-282.
-
(2005)
Human Molecular Genetics
, vol.14
, Issue.2
-
-
Thapar, A.1
O'Donovan, M.2
Owen, M.J.3
-
100
-
-
59649120666
-
Association of variants in DISC1 with psychosis-related traits in a large population cohort
-
Tomppo, L., Hennah, W., Miettunen, J. et al. (2009) Association of variants in DISC1 with psychosis-related traits in a large population cohort. Archives of General Psychiatry 66, 134-141.
-
(2009)
Archives of General Psychiatry
, vol.66
, pp. 134-141
-
-
Tomppo, L.1
Hennah, W.2
Miettunen, J.3
-
101
-
-
2942614921
-
Catechol-o-methyltransferase inhibition improves set-shifting performance and elevates stimulated dopamine release in the rat prefrontal cortex
-
Tunbridge, E.M., Bannerman, D.M., Sharp, T. & Harrison, P.J. (2004) Catechol-o-methyltransferase inhibition improves set-shifting performance and elevates stimulated dopamine release in the rat prefrontal cortex. Journal of Neuroscience 24, 5331-5335.
-
(2004)
Journal of Neuroscience
, vol.24
, pp. 5331-5335
-
-
Tunbridge, E.M.1
Bannerman, D.M.2
Sharp, T.3
Harrison, P.J.4
-
102
-
-
38949090696
-
Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction
-
Vilella, E., Costas, J., Sanjuan, J. et al. (2008) Association of schizophrenia with DTNBP1 but not with DAO, DAOA, NRG1 and RGS4 nor their genetic interaction. Journal of Psychiatric Research 42, 278-288.
-
(2008)
Journal of Psychiatric Research
, vol.42
, pp. 278-288
-
-
Vilella, E.1
Costas, J.2
Sanjuan, J.3
-
103
-
-
42349088634
-
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia
-
Walsh, T., McClellan, J.M., McCarthy, S.E. et al. (2008) Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia. Science 320, 539-543.
-
(2008)
Science
, vol.320
, pp. 539-543
-
-
Walsh, T.1
McClellan, J.M.2
McCarthy, S.E.3
-
104
-
-
2942521644
-
Association of G72/G30 with schizophrenia in the Chinese population
-
Wang, X., He, G., Gu, N. et al. (2004) Association of G72/G30 with schizophrenia in the Chinese population. Biochemistry and Biophysics Research Communications 319, 1281-1286.
-
(2004)
Biochemistry and Biophysics Research Communications
, vol.319
, pp. 1281-1286
-
-
Wang, X.1
He, G.2
Gu, N.3
-
105
-
-
34848925487
-
The tryptophan hydroxylase 1 (TPH1) gene and risk of schizophrenia: a moderate-scale case-control study and meta-analysis
-
Watanabe, Y., Nunokawa, A., Kaneko, N. & Someya, T. (2007) The tryptophan hydroxylase 1 (TPH1) gene and risk of schizophrenia: a moderate-scale case-control study and meta-analysis. Neuroscience Research 59, 322-326.
-
(2007)
Neuroscience Research
, vol.59
, pp. 322-326
-
-
Watanabe, Y.1
Nunokawa, A.2
Kaneko, N.3
Someya, T.4
-
106
-
-
84969213492
-
Genome-wide association study of 14000 cases of seven common diseases and 3,000 shared controls
-
Wellcome Trust Case Control Consortium
-
Wellcome Trust Case Control Consortium (2007) Genome-wide association study of 14000 cases of seven common diseases and 3,000 shared controls. Nature 447, 661-678.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
107
-
-
0029873266
-
Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene
-
Williams, J., et al. (1996) Association between schizophrenia and T102C polymorphism of the 5-hydroxytryptamine type 2a-receptor gene. European Multicentre Association Study of Schizophrenia (EMASS) Group. Lancet 347, 1294-1296.
-
(1996)
European Multicentre Association Study of Schizophrenia (EMASS) Group. Lancet
, vol.347
, pp. 1294-1296
-
-
Williams, J.1
-
108
-
-
12144286093
-
Support for RGS4 as a susceptibility gene for schizophrenia
-
Williams, N.M., Preece, A., Spurlock, G. et al. (2004) Support for RGS4 as a susceptibility gene for schizophrenia. Biological Psychiatry 55, 192-195.
-
(2004)
Biological Psychiatry
, vol.55
, pp. 192-195
-
-
Williams, N.M.1
Preece, A.2
Spurlock, G.3
-
109
-
-
33645513633
-
Variation at the DAOA/G30 locus infl uences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder
-
Williams, N.M., Green, E.K., Macgregor, S. et al. (2006) Variation at the DAOA/G30 locus infl uences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder. Archives of General Psychiatry 63, 366-373.
-
(2006)
Archives of General Psychiatry
, vol.63
, pp. 366-373
-
-
Williams, N.M.1
Green, E.K.2
Macgregor, S.3
-
110
-
-
34548021470
-
Is C OMT a susceptibility gene for schizophrenia?
-
Williams, H.J., Owen, M.J. & O'Donovan, M.C. (2007) Is C OMT a susceptibility gene for schizophrenia? Schizophrenia Bulletin 33, 635-641.
-
(2007)
Schizophrenia Bulletin
, vol.33
, pp. 635-641
-
-
Williams, H.J.1
Owen, M.J.2
O'Donovan, M.C.3
-
111
-
-
38849191674
-
Strong evidence that GNB1L is associated with schizophrenia
-
Williams, N.M., Glaser, B., Norton, N. et al. (2008) Strong evidence that GNB1L is associated with schizophrenia. Human Molecular Genetics 17, 555-566.
-
(2008)
Human Molecular Genetics
, vol.17
, pp. 555-566
-
-
Williams, N.M.1
Glaser, B.2
Norton, N.3
-
112
-
-
77955956142
-
Fine mapping of ZNF804A and genome-wide signifi cant evidence for its involvement in schizophrenia and bipolar disorder
-
Apr 6 [Epub ahead of print]
-
Williams, H.J., Norton, N., Dwyer, S. et al. (2010) Fine mapping of ZNF804A and genome-wide signifi cant evidence for its involvement in schizophrenia and bipolar disorder. Molecular Psychiatry Apr 6 [Epub ahead of print].
-
(2010)
Molecular Psychiatry
-
-
Williams, H.J.1
Norton, N.2
Dwyer, S.3
-
113
-
-
46249093584
-
Strong association of d e novo copy number mutations with sporadic schizophrenia
-
Xu, B., Roos, J.L., Levy, S., van Rensburg, E.J., Gogos, J.A. & Karayiorgou, M. (2008) Strong association of d e novo copy number mutations with sporadic schizophrenia. Nature Genetics 40, 880-885.
-
(2008)
Nature Genetics
, 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
-
114
-
-
33748748127
-
Tryptophan hydroxylase-1 gene variants associated with schizophrenia
-
Zaboli, G., J ö nsson, E.G., Gizatullin, R. et al. (2006) Tryptophan hydroxylase-1 gene variants associated with schizophrenia. Biological Psychiatry 60, 563-569.
-
(2006)
Biological Psychiatry
, vol.60
, pp. 563-569
-
-
Zaboli G.Jönsson, E.G.1
Gizatullin, R.2
-
115
-
-
35948986314
-
Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use
-
Zammit, S., Spurlock, G., Williams, H. et al. (2007) Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use. British Journal of Psychiatry 191, 402-407.
-
(2007)
British Journal of Psychiatry
, vol.191
, pp. 402-407
-
-
Zammit, S.1
Spurlock, G.2
Williams, H.3
-
116
-
-
34249895023
-
Replication of genome-wide association signals in U.K
-
Zeggini, E., Weedon, M.N., Lindgren, C.M. et al. (2007) Replication of genome-wide association signals in U.K. samples reveals risk loci for type 2 diabetes. Science 316, 1336-1341.
-
(2007)
samples reveals risk loci for type 2 diabetes. Science
, vol.316
, pp. 1336-1341
-
-
Zeggini, E.1
Weedon, M.N.2
Lindgren, C.M.3
-
117
-
-
42349106044
-
Meta-analysis of genome-wide association data and large-scale replication identifi es additional susceptibility loci for type 2 diabetes
-
Zeggini, E., Scott, L.J., Saxena, R. et al. (2008) Meta-analysis of genome-wide association data and large-scale replication identifi es additional susceptibility loci for type 2 diabetes. Nature Genetics 40, 638-645.
-
(2008)
Nature Genetics
, vol.40
, pp. 638-645
-
-
Zeggini, E.1
Scott, L.J.2
Saxena, R.3
-
118
-
-
70350515361
-
Neurogranin enhances synaptic strength through its interaction with calmodulin
-
Zhong, L., Cherry, T., Bies, C.E., Florence, M.A. & Gerges, N.Z. (2009) Neurogranin enhances synaptic strength through its interaction with calmodulin. EMBO Journal 28, 3027-3039.
-
(2009)
EMBO Journal
, vol.28
, pp. 3027-3039
-
-
Zhong, L.1
Cherry, T.2
Bies, C.E.3
Florence, M.A.4
Gerges, N.Z.5
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