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J-GLOBAL ID：200902222337389087   Reference number：06A1044546

Analyses of the associations between the genes of 22q11 deletion syndrome and schizophrenia

22q11欠損症候群遺伝子と統合失調症の間の相関分析

Author (2)： ARINAMI Tadao (Univ. Tsukuba, Ibaraki, JPN) ,  ARINAMI Tadao (JST-CREST, Saitama, JPN)
Material： Journal of Human Genetics  (J Hum Genet)
Volume： 51  Issue： 12  Page： 1037-1045  Publication year： 2006 
JST Material Number： Z0756A  ISSN： 1434-5161  Document type： Article
Article type： 文献レビュー  Country of issue： United Kingdom (GBR)  Language： ENGLISH (EN)

Thesaurus term： *gene ,...
Semi thesaurus term： *schizophrenia ,...

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JST classification (3)： Basic psychiatry  (GR01020I) ,  Congenital diseases,deformities in general.  (GD03010V) ,  Molecular genetics in general  (EC02010J)

Reference (88)：

• ANTTILA, S. Interaction between NOTCH4 and catechol-O-methyltransferase genotypes in schizophrenia patients with poor response to typical neuroleptics. Pharmacogenetics. 2004, 14, 303-307
• ARINAMI, T. Screening for 22q11 deletions in a schizophrenia population. Schizophr Res. 2001, 52, 167-170
• ARNOLD, PD. Velo-cardio-facial syndrome : implications of microdeletion 22q11 for schizophrenia and mood disorders. Am J Med Genet. 2001, 105, 354-362
• BARNEA-GORALY, N. Investigation of white matter structure in velocardiofacial syndrome : a diffusion tensor imaging study. Am J Psychiatry. 2003, 160, 1863-1869
• BASSETT, AS. 22q11 deletion syndrome : a genetic subtype of schizophrenia. Biol Psychiatry. 1999, 46, 882-891

Terms in the title (4)： 22q11欠損症候群 ,  遺伝子 ,  統合失調症 ,  相関分析