Art

J-GLOBAL ID：200902288342115700   Reference number：08A0925440

Large recurrent microdeletions associated with schizophrenia

統合失調症に関連する大規模で頻発する微小欠失

Author (40)： STEFANSSON Hreinn (deCODE genetics, Reykjavik, ISL) ,  RUJESCU Dan (Ludwig-Maximilians-Univ., Munich, DEU) ,  CICHON Sven (Univ. Bonn, Bonn, DEU) ,  PIETILAEINEN Olli P. H. (National Public Health Inst., Helsinki, FIN) ,  INGASON Andres (deCODE genetics, Reykjavik, ISL) ,  STEINBERG Stacy (deCODE genetics, Reykjavik, ISL) ,  FOSSDAL Ragnheidur (deCODE genetics, Reykjavik, ISL) ,  SIGURDSSON Engilbert (National Univ. Hospital, Reykjavik, ISL) ,  SIGMUNDSSON Thordur (National Univ. Hospital, Reykjavik, ISL) ,  BUIZER-VOSKAMP Jacobine E. (Univ. Medical Center Utrecht, Utrecht, NLD) ,  HANSEN Thomas (Mental Health Centre Sct. Hans Copenhagen Univ. Hospital, Roskilde, DNK) ,  HANSEN Thomas (Univ. Copenhagen, Copenhagen, DNK) ,  JAKOBSEN Klaus D. (Mental Health Centre Sct. Hans Copenhagen Univ. Hospital, Roskilde, DNK) ,  JAKOBSEN Klaus D. (Univ. Copenhagen, Copenhagen, DNK) ,  MUGLIA Pierandrea (GlaxoSmithKline R&D, Verona, ITA) ,  FRANCKS Clyde (GlaxoSmithKline R&D, Verona, ITA) ,  MATTHEWS Paul M. (GlaxoSmithKline, London, GBR) ,  GYLFASON Arnaldur (deCODE genetics, Reykjavik, ISL) ,  HALLDORSSON Bjarni V. (deCODE genetics, Reykjavik, ISL) ,  GUDBJARTSSON Daniel (deCODE genetics, Reykjavik, ISL) ,  THORGEIRSSON Thorgeir E. (deCODE genetics, Reykjavik, ISL) ,  SIGURDSSON Asgeir (deCODE genetics, Reykjavik, ISL) ,  JONASDOTTIR Adalbjorg (deCODE genetics, Reykjavik, ISL) ,  JONASDOTTIR Aslaug (deCODE genetics, Reykjavik, ISL) ,  BJORNSSON Asgeir (deCODE genetics, Reykjavik, ISL) ,  MATTIASDOTTIR Sigurborg (deCODE genetics, Reykjavik, ISL) ,  BLONDAL Thorarinn (deCODE genetics, Reykjavik, ISL) ,  HARALDSSON Magnus (National Univ. Hospital, Reykjavik, ISL) ,  MAGNUSDOTTIR Brynja B. (National Univ. Hospital, Reykjavik, ISL) ,  GIEGLING Ina (Ludwig-Maximilians-Univ., Munich, DEU) ,  MOELLER Hans-Juergen (Ludwig-Maximilians-Univ., Munich, DEU) ,  HARTMANN Annette (Ludwig-Maximilians-Univ., Munich, DEU) ,  SHIANNA Kevin V. (Duke Univ., North Carolina, USA) ,  GE Dongliang (Duke Univ., North Carolina, USA) ,  NEED Anna C. (Duke Univ., North Carolina, USA) ,  CROMBIE Caroline (Univ. Aberdeen, Aberdeen, GBR) ,  FRASER Gillian (Univ. Aberdeen, Aberdeen, GBR) ,  WALKER Nicholas (Ravenscraig hospital, Greenock, GBR) ,  LONNQVIST Jouko (National Public Health Inst., Helsinki, FIN) ,  SUVISAARI Jaana (National Public Health Inst., Helsinki, FIN)
Material： Nature (London)  (Nature (Lond))
Volume： 455  Issue： 7210  Page： 232-236  Publication year： Sep. 11, 2008 
JST Material Number： D0193B  ISSN： 0028-0836  Document type： Article
Article type： 原著論文  Country of issue： United Kingdom (GBR)  Language： ENGLISH (EN)

Thesaurus term： *schizophrenia ,  *deletion mutation ,  human ,  case control study ,  autosome ,  risk factor ,  genome ,  copy number

JST classification (1)： Genetic variation  (EC01030Y)

Terms in the title (3)： 統合失調症 ,  大規模 ,  微小欠失