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Modeling prior information of common genetic variants improves gene discovery for neuroticism.
Lo, Min-Tzu; Wang, Yunpeng; Kauppi, Karolina; Sanyal, Nilotpal; Fan, Chun-Chieh; Smeland, Olav B; Schork, Andrew; Holland, Dominic; Hinds, David A; Tung, Joyce Y; Andreassen, Ole A; Dale, Anders M; Chen, Chi-Hua.
Afiliação
  • Lo MT; Department of Radiology, Center for Multimodal Imaging and Genetics, University of California, San Diego, La Jolla, CA 92037, USA.
  • Wang Y; NORMENT, KG Jebsen Centre for Psychosis Research, Institute of Clinical Medicine, University of Oslo, Oslo 0407, Norway.
  • Kauppi K; Department of Neurosciences, University of California, San Diego, La Jolla, CA 92037, USA.
  • Sanyal N; Department of Radiology, Center for Multimodal Imaging and Genetics, University of California, San Diego, La Jolla, CA 92037, USA.
  • Fan CC; Department of Radiation Sciences, Umea University, Umea 90187, Sweden.
  • Smeland OB; Department of Radiology, Center for Multimodal Imaging and Genetics, University of California, San Diego, La Jolla, CA 92037, USA.
  • Schork A; Department of Radiology, Center for Multimodal Imaging and Genetics, University of California, San Diego, La Jolla, CA 92037, USA.
  • Holland D; Department of Cognitive Science, University of California, San Diego, La Jolla, CA 92037, USA.
  • Hinds DA; NORMENT, KG Jebsen Centre for Psychosis Research, Institute of Clinical Medicine, University of Oslo, Oslo 0407, Norway.
  • Tung JY; Division of Mental Health and Addiction, Oslo University Hospital, Oslo 0407, Norway.
  • Andreassen OA; Department of Cognitive Science, University of California, San Diego, La Jolla, CA 92037, USA.
  • Dale AM; Institute of Biological Psychiatry, Medical Health Center, Sct. Hans, Roskilde, 4000, Denmark.
  • Chen CH; Department of Neurosciences, University of California, San Diego, La Jolla, CA 92037, USA.
Hum Mol Genet ; 26(22): 4530-4539, 2017 11 15.
Article em En | MEDLINE | ID: mdl-28973307
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Estudo de Associação Genômica Ampla / Modelos Genéticos / Transtornos Neuróticos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência de DNA / Estudo de Associação Genômica Ampla / Modelos Genéticos / Transtornos Neuróticos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2017 Tipo de documento: Article