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Genes with de novo mutations are shared by four neuropsychiatric disorders discovered from NPdenovo database.
Li, Jinchen; Cai, Tao; Jiang, Yi; Chen, Huiqian; He, Xin; Chen, Chao; Li, Xianfeng; Shao, Qianzhi; Ran, Xia; Li, Zhongshan; Xia, Kun; Liu, Chunyu; Sun, Zhong Sheng; Wu, Jinyu.
Afiliação
  • Li J; Beijing Institutes of Life Science, Chinese Academy of Sciences, Beijing, China.
  • Cai T; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
  • Jiang Y; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Chen H; Experimental Medicine Section, NIDCR/NIH, Bethesda, MD, USA.
  • He X; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
  • Chen C; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
  • Li X; Department of Human Genetics, University of Chicago, Chicago, IL, USA.
  • Shao Q; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Ran X; Department of Psychiatry, University of Illinois at Chicago, Chicago, IL, USA.
  • Li Z; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
  • Xia K; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
  • Liu C; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
  • Sun ZS; Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, China.
  • Wu J; State Key Laboratory of Medical Genetics, Central South University, Changsha, China.
Mol Psychiatry ; 21(2): 290-7, 2016 Feb.
Article em En | MEDLINE | ID: mdl-25849321

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia / Transtorno do Espectro Autista / Deficiência Intelectual Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esquizofrenia / Transtorno do Espectro Autista / Deficiência Intelectual Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article