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PhenoApt leverages clinical expertise to prioritize candidate genes via machine learning.
Chen, Zefu; Zheng, Yu; Yang, Yongxin; Huang, Yingzhao; Zhao, Sen; Zhao, Hengqiang; Yu, Chenxi; Dong, Xiying; Zhang, Yuanqiang; Wang, Lianlei; Zhao, Zhengye; Wang, Shengru; Yang, Yang; Ming, Yue; Su, Jianzhong; Qiu, Guixing; Wu, Zhihong; Zhang, Terry Jianguo; Wu, Nan.
Afiliación
  • Chen Z; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; State Key Laboratory of Complex Severe and Rare Diseases, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skelet
  • Zheng Y; Financial Innovation Center, Southwestern University of Finance and Economics, Chengdu 611130, China.
  • Yang Y; Beijing Ekitech Co. Ltd., Beijing 100043, China; University of Edinburgh, 10 Crichton Street, Edinburgh, EH8 9AB, United Kindom.
  • Huang Y; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deform
  • Zhao S; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deform
  • Zhao H; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deform
  • Yu C; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deform
  • Dong X; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deform
  • Zhang Y; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deform
  • Wang L; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deform
  • Zhao Z; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deform
  • Wang S; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deform
  • Yang Y; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deform
  • Ming Y; PET-CT Center, National Cancer Center, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
  • Su J; Institute of Biomedical Big Data, Wenzhou Medical University, Wenzhou 325027, China.
  • Qiu G; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; State Key Laboratory of Complex Severe and Rare Diseases, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skelet
  • Wu Z; State Key Laboratory of Complex Severe and Rare Diseases, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Beijing 100730, China; Key Laboratory of Big Data for Spinal Deformities, Chinese Academy of Medical Sciences, Beijing 100730, China; Medical Research C
  • Zhang TJ; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; State Key Laboratory of Complex Severe and Rare Diseases, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skelet
  • Wu N; Department of Orthopedic Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China; State Key Laboratory of Complex Severe and Rare Diseases, Beijing 100730, China; Beijing Key Laboratory for Genetic Research of Skelet
Am J Hum Genet ; 109(2): 270-281, 2022 02 03.
Article en En | MEDLINE | ID: mdl-35063063
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Escoliosis / Nistagmo Congénito / Aprendizaje Automático / Pérdida Auditiva Sensorineural / Enfermedades Genéticas Congénitas / Discapacidad Intelectual / Microcefalia Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2022 Tipo del documento: Article
Texto completo
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Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Escoliosis / Nistagmo Congénito / Aprendizaje Automático / Pérdida Auditiva Sensorineural / Enfermedades Genéticas Congénitas / Discapacidad Intelectual / Microcefalia Tipo de estudio: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Am J Hum Genet Año: 2022 Tipo del documento: Article