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Mendelian randomization highlights significant difference and genetic heterogeneity in clinically diagnosed Alzheimer's disease GWAS and self-report proxy phenotype GWAX.
Liu, Haijie; Hu, Yang; Zhang, Yan; Zhang, Haihua; Gao, Shan; Wang, Longcai; Wang, Tao; Han, Zhifa; Sun, Bao-Liang; Liu, Guiyou.
Afiliación
  • Liu H; Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, 100053, China.
  • Hu Y; School of Life Science and Technology, Harbin Institute of Technology, Harbin, 150080, China.
  • Zhang Y; Department of Pathology, The Affiliated Hospital of Weifang Medical University, Weifang, 261053, China.
  • Zhang H; Beijing Institute of Brain Disorders, Laboratory of Brain Disorders, Ministry of Science and Technology, Collaborative Innovation Center for Brain Disorders, Capital Medical University, Beijing, 100069, China.
  • Gao S; Beijing Institute of Brain Disorders, Laboratory of Brain Disorders, Ministry of Science and Technology, Collaborative Innovation Center for Brain Disorders, Capital Medical University, Beijing, 100069, China.
  • Wang L; Department of Anesthesiology, The Affiliated Hospital of Weifang Medical University, Weifang, 261053, China.
  • Wang T; Chinese Institute for Brain Research, Beijing, China.
  • Han Z; State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, Beijing, China.
  • Sun BL; Key Laboratory of Cerebral Microcirculation in Universities of Shandong, Department of Neurology, Second Affiliated Hospital, Shandong First Medical University & Shandong Academy of Medical Sciences, Taian, 271000, Shandong, China.
  • Liu G; Beijing Institute of Brain Disorders, Laboratory of Brain Disorders, Ministry of Science and Technology, Collaborative Innovation Center for Brain Disorders, Capital Medical University, Beijing, 100069, China. liuguiyou1981@163.com.
Alzheimers Res Ther ; 14(1): 17, 2022 01 28.
Article en En | MEDLINE | ID: mdl-35090530
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Estudio de Asociación del Genoma Completo / Enfermedad de Alzheimer Tipo de estudio: Clinical_trials / Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Alzheimers Res Ther Año: 2022 Tipo del documento: Article País de afiliación: China
Texto completo
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Estudio de Asociación del Genoma Completo / Enfermedad de Alzheimer Tipo de estudio: Clinical_trials / Diagnostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Alzheimers Res Ther Año: 2022 Tipo del documento: Article País de afiliación: China