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Association analysis between two functional dopamine D2 receptor gene polymorphisms and schizophrenia
The dopamine D2 receptor (DRD2) gene has been listed as one of the candidate genes for susceptibility to schizophrenia. To date, a significant association between schizophrenia and two functional DRD2 gene polymorphisms, Ser311Cys and −141C Ins/Del, in Japanese samples, has been reported by Arinami...
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Published in: | American journal of medical genetics 2001-03, Vol.105 (2), p.176-178 |
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description | The dopamine D2 receptor (DRD2) gene has been listed as one of the candidate genes for susceptibility to schizophrenia. To date, a significant association between schizophrenia and two functional DRD2 gene polymorphisms, Ser311Cys and −141C Ins/Del, in Japanese samples, has been reported by Arinami et al. [1994: Lancet 343:703–704; 1997: Hum Mol Genet 6:577–582]. In the present study, we replicated the findings of Arinami et al. [1994: Lancet 343:703–704; 1997: Hum Mol Genet 6:577–582] in the same ethnic groups (Japanese samples) with the same polymorphisms (Ser311Cys and −141C Ins/Del). We genotyped these two polymorphisms for 241 patients and for 201 controls. Neither polymorphism was associated with schizophrenia. Moreover, in a haplotype analysis of the present sample, combined pairs of two polymorphisms provided no evidence for the association of either haplotype with schizophrenia. Our findings indicate that an association between the two functional DRD2 gene polymorphisms, Ser311Cys and −141C Ins/Del, and schizophrenia is unlikely. © 2001 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/ajmg.1196 |
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To date, a significant association between schizophrenia and two functional DRD2 gene polymorphisms, Ser311Cys and −141C Ins/Del, in Japanese samples, has been reported by Arinami et al. [1994: Lancet 343:703–704; 1997: Hum Mol Genet 6:577–582]. In the present study, we replicated the findings of Arinami et al. [1994: Lancet 343:703–704; 1997: Hum Mol Genet 6:577–582] in the same ethnic groups (Japanese samples) with the same polymorphisms (Ser311Cys and −141C Ins/Del). We genotyped these two polymorphisms for 241 patients and for 201 controls. Neither polymorphism was associated with schizophrenia. Moreover, in a haplotype analysis of the present sample, combined pairs of two polymorphisms provided no evidence for the association of either haplotype with schizophrenia. Our findings indicate that an association between the two functional DRD2 gene polymorphisms, Ser311Cys and −141C Ins/Del, and schizophrenia is unlikely. © 2001 Wiley‐Liss, Inc.</description><identifier>ISSN: 0148-7299</identifier><identifier>EISSN: 1096-8628</identifier><identifier>DOI: 10.1002/ajmg.1196</identifier><identifier>PMID: 11304833</identifier><identifier>CODEN: AJMGDA</identifier><language>eng</language><publisher>New York: John Wiley & Sons, Inc</publisher><subject>Adult and adolescent clinical studies ; Aged ; association study ; Biological and medical sciences ; Case-Control Studies ; dopamine D2 receptor gene ; Female ; Gene Deletion ; Genotype ; Haplotypes ; Humans ; Japan ; Male ; Medical sciences ; Middle Aged ; Models, Statistical ; polymorphism ; Polymorphism, Genetic ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Psychoses ; Receptors, Dopamine D2 - genetics ; Schizophrenia ; Schizophrenia - genetics</subject><ispartof>American journal of medical genetics, 2001-03, Vol.105 (2), p.176-178</ispartof><rights>Copyright © 2001 Wiley‐Liss, Inc.</rights><rights>2001 INIST-CNRS</rights><rights>Copyright 2001 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4536-58967fa070dab4e74bf211ef53c77d04edf78e378bae15dc3c869efeeb94f42e3</citedby><cites>FETCH-LOGICAL-c4536-58967fa070dab4e74bf211ef53c77d04edf78e378bae15dc3c869efeeb94f42e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=960853$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11304833$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hori, Hiroko</creatorcontrib><creatorcontrib>Ohmori, Osamu</creatorcontrib><creatorcontrib>Shinkai, Takahiro</creatorcontrib><creatorcontrib>Kojima, Hideki</creatorcontrib><creatorcontrib>Nakamura, Jun</creatorcontrib><title>Association analysis between two functional dopamine D2 receptor gene polymorphisms and schizophrenia</title><title>American journal of medical genetics</title><addtitle>Am. J. Med. Genet</addtitle><description>The dopamine D2 receptor (DRD2) gene has been listed as one of the candidate genes for susceptibility to schizophrenia. To date, a significant association between schizophrenia and two functional DRD2 gene polymorphisms, Ser311Cys and −141C Ins/Del, in Japanese samples, has been reported by Arinami et al. [1994: Lancet 343:703–704; 1997: Hum Mol Genet 6:577–582]. In the present study, we replicated the findings of Arinami et al. [1994: Lancet 343:703–704; 1997: Hum Mol Genet 6:577–582] in the same ethnic groups (Japanese samples) with the same polymorphisms (Ser311Cys and −141C Ins/Del). We genotyped these two polymorphisms for 241 patients and for 201 controls. Neither polymorphism was associated with schizophrenia. Moreover, in a haplotype analysis of the present sample, combined pairs of two polymorphisms provided no evidence for the association of either haplotype with schizophrenia. Our findings indicate that an association between the two functional DRD2 gene polymorphisms, Ser311Cys and −141C Ins/Del, and schizophrenia is unlikely. © 2001 Wiley‐Liss, Inc.</description><subject>Adult and adolescent clinical studies</subject><subject>Aged</subject><subject>association study</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>dopamine D2 receptor gene</subject><subject>Female</subject><subject>Gene Deletion</subject><subject>Genotype</subject><subject>Haplotypes</subject><subject>Humans</subject><subject>Japan</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Models, Statistical</subject><subject>polymorphism</subject><subject>Polymorphism, Genetic</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Psychoses</subject><subject>Receptors, Dopamine D2 - genetics</subject><subject>Schizophrenia</subject><subject>Schizophrenia - genetics</subject><issn>0148-7299</issn><issn>1096-8628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNp10E1v1DAQBmALgehSOPAHkCUkJA5p7TixneOqwAJd4MKXuFiOM-66JHHwZLUsv55EG5UTJ0vjZ96RXkKecnbBGcsv7W13c8F5Je-RFWeVzLTM9X2yYrzQmcqr6ow8QrxljE-D_CE541ywQguxIrBGjC7YMcSe2t62RwxIaxgPAD0dD5H6fe_mX9vSJg62Cz3QVzlN4GAYY6I3MA2G2B67mIZdwA6nnIai24U_cdgl6IN9TB542yI8Wd5z8uXN689Xb7Ptp827q_U2c0UpZFbqSipvmWKNrQtQRe1zzsGXwinVsAIarzQIpWsLvGyccFpW4AHqqvBFDuKcvDjlDin-2gOOpgvooG1tD3GPRikmWanEBF-eoEsRMYE3QwqdTUfDmZk7NXOnZu50ss-W0H3dQfNPLiVO4PkCLDrb-mR7F_DOVZLpclaXJ3UILRz_f8-s33_YLIez00bAEX7fbdj000glVGm-fdwYfV382Iqv1-a7-AtYKZ93</recordid><startdate>20010308</startdate><enddate>20010308</enddate><creator>Hori, Hiroko</creator><creator>Ohmori, Osamu</creator><creator>Shinkai, Takahiro</creator><creator>Kojima, Hideki</creator><creator>Nakamura, Jun</creator><general>John Wiley & Sons, Inc</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20010308</creationdate><title>Association analysis between two functional dopamine D2 receptor gene polymorphisms and schizophrenia</title><author>Hori, Hiroko ; Ohmori, Osamu ; Shinkai, Takahiro ; Kojima, Hideki ; Nakamura, Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4536-58967fa070dab4e74bf211ef53c77d04edf78e378bae15dc3c869efeeb94f42e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Adult and adolescent clinical studies</topic><topic>Aged</topic><topic>association study</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>dopamine D2 receptor gene</topic><topic>Female</topic><topic>Gene Deletion</topic><topic>Genotype</topic><topic>Haplotypes</topic><topic>Humans</topic><topic>Japan</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Models, Statistical</topic><topic>polymorphism</topic><topic>Polymorphism, Genetic</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Psychoses</topic><topic>Receptors, Dopamine D2 - genetics</topic><topic>Schizophrenia</topic><topic>Schizophrenia - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hori, Hiroko</creatorcontrib><creatorcontrib>Ohmori, Osamu</creatorcontrib><creatorcontrib>Shinkai, Takahiro</creatorcontrib><creatorcontrib>Kojima, Hideki</creatorcontrib><creatorcontrib>Nakamura, Jun</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of medical genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hori, Hiroko</au><au>Ohmori, Osamu</au><au>Shinkai, Takahiro</au><au>Kojima, Hideki</au><au>Nakamura, Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association analysis between two functional dopamine D2 receptor gene polymorphisms and schizophrenia</atitle><jtitle>American journal of medical genetics</jtitle><addtitle>Am. J. Med. Genet</addtitle><date>2001-03-08</date><risdate>2001</risdate><volume>105</volume><issue>2</issue><spage>176</spage><epage>178</epage><pages>176-178</pages><issn>0148-7299</issn><eissn>1096-8628</eissn><coden>AJMGDA</coden><abstract>The dopamine D2 receptor (DRD2) gene has been listed as one of the candidate genes for susceptibility to schizophrenia. To date, a significant association between schizophrenia and two functional DRD2 gene polymorphisms, Ser311Cys and −141C Ins/Del, in Japanese samples, has been reported by Arinami et al. [1994: Lancet 343:703–704; 1997: Hum Mol Genet 6:577–582]. In the present study, we replicated the findings of Arinami et al. [1994: Lancet 343:703–704; 1997: Hum Mol Genet 6:577–582] in the same ethnic groups (Japanese samples) with the same polymorphisms (Ser311Cys and −141C Ins/Del). We genotyped these two polymorphisms for 241 patients and for 201 controls. Neither polymorphism was associated with schizophrenia. Moreover, in a haplotype analysis of the present sample, combined pairs of two polymorphisms provided no evidence for the association of either haplotype with schizophrenia. Our findings indicate that an association between the two functional DRD2 gene polymorphisms, Ser311Cys and −141C Ins/Del, and schizophrenia is unlikely. © 2001 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>John Wiley & Sons, Inc</pub><pmid>11304833</pmid><doi>10.1002/ajmg.1196</doi><tpages>3</tpages></addata></record> |
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subjects | Adult and adolescent clinical studies Aged association study Biological and medical sciences Case-Control Studies dopamine D2 receptor gene Female Gene Deletion Genotype Haplotypes Humans Japan Male Medical sciences Middle Aged Models, Statistical polymorphism Polymorphism, Genetic Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses Receptors, Dopamine D2 - genetics Schizophrenia Schizophrenia - genetics |
title | Association analysis between two functional dopamine D2 receptor gene polymorphisms and schizophrenia |
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