Read Secondary Schizophrenia Online

Authors: Perminder S. Sachdev

Secondary Schizophrenia (121 page)

Psychiatry, 1996.
153
:1534–40.

15 locus. Proc Natl Acad Sci USA,

disorder? Implications for

147. Faraone S. V., Matise T., Svrakic

1997.
94
:587–92.

psychiatric nosology. Schizophr

D.,
et al.
Genome scan of

156. Stober G., Saar K., Ruschendorf F.,

Bull, 2006.
32
:9–16.

European-American

et al.
Splitting schizophrenia:

166. Craddock N., O’Donovan M. C.,

schizophrenia pedigrees: results

periodic catatonia-susceptibility

Owen M. J. The genetics of

of the NIMH Genetics Initiative

locus on chromosome 15q15. Am

schizophrenia and bipolar

and Millennium Consortium. Am

J Hum Genet, 2000.
67
:1201–7.

disorder: dissecting psychosis.

J Med Genet, 1998.
81
:290–5.

157. Bulayeva K. B., Glatt S. J., Bulayev
J Med Genet, 2005.
42
:193–204.

148. Schwab S. G., Hallmayer J., Albus

O. A.,
et al.
Genomewide linkage

167. Straub R. E., Weinberger D. R.

M.,
et al.
Further evidence for a

scan of schizophrenia: a

Schizophrenia genes – famine to

susceptibility locus on

cross-isolate study. Genomics,

feast. Biol Psychiatry, 2006.

chromosome 10p14-p11 in 72

2007.
89
:167–77.

60
:81–3.

families with schizophrenia by

158. Coon H., Holik J., Hoff M.,
et al.

nonparametric linkage analysis.

168. Riley B., Kendler K. S. Molecular

Analysis of chromosome 22

Am J Med Genet, 1998.
81
:302–7.

genetic studies of schizophrenia.

markers in nine schizophrenia

Eur J Hum Genet, 2006.
14
:669–
149. Faraone S. V., Hwu H. G., Liu C.

pedigrees. Am J Med Genet, 1994.

80.

M.,
et al.
Genome scan of Han

15
:72–9.

Chinese schizophrenia families

169. Harrison P. J., Weinberger D. R.

159. Talkowski M. E., Chowdari K.,

from Taiwan: confirmation of

Schizophrenia genes, gene

Lewis D. A.,
et al.
Can RGS4

linkage to 10q22.3. Am J

expression, and neuropathology:

polymorphisms be viewed as

Psychiatry, 2006.
163
:1760–6.

on the matter of their

credible risk factors for

convergence. Mol Psychiatry,

150. Williams N. M., Norton N.,

schizophrenia? A critical review

2005.
10
:40–68.

Williams H.,
et al.
A systematic

of the evidence. Schizophr Bull,

genomewide linkage study in 353

2006.
32
:203–8.

170. Karayiorgou M., Gogos J. A.

sib pairs with schizophrenia. Am J

Schizophrenia genetics:

160. Williams J., Spurlock G., Holmans

Hum Genet, 2003.
73
:1355–67.

uncovering positional candidate

P.,
et al.
A meta-analysis and

151. Mowry B. J., Ewen K. R.,

genes. Eur J Hum Genet, 2006.

transmission disequilibrium study

Nancarrow D. J.,
et al.
Second

14
:512–19.

of association between the

stage of a genome scan of

dopamine D3 receptor gene and

171. Straub R. E., Jiang Y., MacLean C.

schizophrenia: study of five

schizophrenia. Mol Psychiatry,

J.,
et al.
Genetic variation in the
304

positive regions in an expanded

1998.
3
:141–9.

6p22.3 gene DTNBP1, the human

Chapter 23 – The status of genetic investigations of schizophrenia

ortholog of the mouse dysbindin

independent samples. Biol

gene. Am J Med Genet, 1992.
29
:
gene, is associated with

Psychiatry, 2006.
60
:152–62.

858–60.

schizophrenia. Am J Hum Genet,

180. Levitt P., Ebert P., Mirnics K.,

189. Inayama Y., Yoneda H., Sakai T.,

2002.
71
:337–48.

et al.
Making the case for a

et al.
Positive association between
172. Williams N. M., O’Donovan M.

candidate vulnerability gene in

a DNA sequence variant in the

C., Owen M. J. Is the dysbindin

schizophrenia: Convergent

serotonin 2A receptor gene and

gene (DTNBP1) a susceptibility

evidence for regulator of

schizophrenia. Am J Med Genet,

gene for schizophrenia? Schizophr

G-protein signaling 4 (RGS4). Biol

1996.
67
:103–5.

Bull, 2005.
31
:800–5.

Psychiatry, 2006.
60
:534–7.

190. Jacobs P. A., Brunton M.,

173. Stefansson H., Sigurdsson E.,

181. Ohmori O., Shinkai T., Kojima H.,

Frackiewicz A.,
et al.
Studies on a
Steinthorsdottir V.,
et al.

et al.
Association study of a

family with three cytogenetic

Neuregulin 1 and susceptibility to

functional catechol-

markers. Ann Hum Genet, 1970.

schizophrenia. Am J Hum Genet,

O-methyltransferase gene

33
:325–36.

2002.
71
:877–92.

polymorphism in Japanese

191. St Clair D., Blackwood D., Muir

174. Tosato S., Dazzan P., Collier D.

schizophrenics. Neurosci Lett.

W.,
et al.
Association within a

Association between the

1998.
243
:109–12.

family of a balanced autosomal

neuregulin 1 gene and

182. Chumakov I., Blumenfeld M.,

translocation with major mental

schizophrenia: a systematic

Guerassimenko O.,
et al.
Genetic

illness. Lancet, 1990.
336
:13–16.

review. Schizophr Bull, 2005.

and physiological data implicating

192. Millar J. K., Christie S., Anderson

31
:613–17.

the new human gene G72 and the

S.,
et al.
Genomic structure and

175. Millar J. K., Christie S., Semple

gene for D-amino acid oxidase in

localization within a linkage

C. A.,
et al.
Chromosomal

schizophrenia. Proc Natl Acad Sci

hotspot of Disrupted in

location and genomic structure of

USA, 2002.
99
:13675–80.

Schizophrenia 1, a gene disrupted

the human translin-associated

183. Detera-Wadleigh S. D., McMahon

by a translocation segregating

factor X gene (TRAX; TSNAX)

F. J. G72/G30 in schizophrenia

with schizophrenia. Mol

revealed by intergenic splicing to

and bipolar disorder: review and

Psychiatry, 2001.
6
:173–8.

DISC1, a gene disrupted by a

meta-analysis. Biol Psychiatry,

193. Taylor M. S., Devon R. S., Millar J.

translocation segregating with

2006.
60
:106–14.

K.,
et al.
Evolutionary constraints
schizophrenia. Genomics, 2000.

184. Li D., He L. G72/G30 genes and

on the Disrupted in Schizophrenia

67
:69–77.

schizophrenia: a systematic

locus. Genomics, 2003.
81
:67–77.

176. Porteous D. J., Millar J. K.

meta-analysis of association

194. Sachs N. A., Sawa A., Holmes S.

Disrupted in schizophrenia 1:

studies. Genetics, 2007.

E.,
et al.
A frameshift mutation in
building brains and memories.

175
:917–922.

Disrupted in Schizophrenia 1 in

Trends Mol Med, 2006.
12
:
185. Gerber D. J., Hall D., Miyakawa

an American family with

255–61.

T.,
et al.
Evidence for association
schizophrenia and schizoaffective

177. Mirnics K., Middleton F. A.,

of schizophrenia with genetic

disorder. Mol Psychiatry, 2005.

Stanwood G. D.,
et al.

variation in the 8p21.3 gene,

10
:758–64.

Disease-specific changes in

PPP3CC, encoding the

195. Jang Y. L., Kim J. W., Lee Y. S.,

regulator of G-protein signaling 4

calcineurin gamma subunit.

et al.
Linkage of schizophrenia

(RGS4) expression in

Proc Natl Acad Sci USA, 2003.

with chromosome 1q32 in Korean

schizophrenia. Mol Psychiatry,

100
:8993–8.

multiplex families. Am J Med

2001.
6
:293–301.

186. Liu Y. L., Fann C. S., Liu C. M.,

Genet B Neuropsychiatr Genet,

178. Chowdari K. V., Mirnics K.,

et al.
More evidence supports the

2007.
144
:279–84.

Semwal P.,
et al.
Association and

association of PPP3CC with

196. Ekelund J., Lichtermann D.,

linkage analyses of RGS4

schizophrenia. Mol Psychiatry,

Hovatta I.,
et al.
Genomewide

polymorphisms in schizophrenia.

2007.
12
:966–74.

scan for schizophrenia in the

Hum Mol Genet, 2002.
11
:1373–
187. Norton N., Williams H. J., Owen

Finnish population: evidence for a

80.

M. J. An update on the genetics of

locus on chromosome 7q22. Hum

179. Talkowski M. E., Seltman H.,

schizophrenia. Curr Opin

Mol Genet, 2000.
9
:1049–57.

Bassett A. S.,
et al.
Evaluation of a
Psychiatry. 2006.
19
:158–64.

197. Gasperoni T. L., Ekelund J.,

susceptibility gene for

188. Crocq M.-A., Mant R., Asherson

Huttunen M.,
et al.
Genetic

schizophrenia: genotype based

P.
et al.
Association between

linkage and association between

meta-analysis of RGS4

schizophrenia and homozygosity

chromosome 1q and working

305

polymorphisms from thirteen

at the dopamine D3 receptor

memory function in

Organic Syndromes of Schizophrenia – Section 3

schizophrenia. Am J Med Genet,

206. Cannon T. D., Hennah W., van

schizophrenia 1 genotype and

2003.
116B
:8–16.

Erp T. G.,
et al.
Association of

positive symptoms in

198. Macgregor S., Visscher P. M.,

DISC1/TRAX haplotypes with

schizophrenia. Biol Psychiatry,

Knott S. A.,
et al.
A genome scan

schizophrenia, reduced prefrontal

2007.
61
:1208–10.

and follow-up study identify a

gray matter, and impaired short-

214. Pickard B. S., Millar J. K.,

bipolar disorder susceptibility

and long-term memory. Arch Gen

Porteous D. J.,
et al.
Cytogenetics
locus on chromosome 1q42.

Psychiatry, 2005.
62
:1205–13.

and gene discovery in psychiatric

Mol Psychiatry, 2004.
9
:1083–
207. Hennah W., Tuulio-Henriksson

disorders. Pharmacogenomics J,

90.

A., Paunio T.,
et al.
A haplotype

2005.
5
:81–8.

199. Gejman P. V., Martinez M., Cao

within the DISC1 gene is

215. Curtis D., Kalsi G., Brynjolfsson

Q.,
et al.
Linkage analysis of

associated with visual memory

J.,
et al.
Genome scan of pedigrees
fifty-seven microsatellite loci to

functions in families with a high

Other books

Black Diamond by Dixon, Ja'Nese
Loose Lips by Rae Davies
The Dark Duet by KaSonndra Leigh
REAPER'S KISS by Jaxson Kidman
One Last Dance by Stephens, Angela
Too Close to Home by Linwood Barclay