智能生物学实验室(IBLab)

复旦大学医学遗传研究院。上海市徐汇区东安路131号科研二号楼。yuanbo@ion.ac.cn · 021-54231035。

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智能生物学实验室(IBLab)

上海市徐汇区东安路131号科研二号楼

中国 上海 200032

yuanbo@ion.ac.cn · 021-54231035

袁博博士现任复旦大学医学遗传研究院青年研究员、硕士生导师。2010年本科毕业于浙江大学生物科学专业,2017年博士毕业于中国科学院大学神经生物学专业(导师:仇子龙研究员)。博士毕业后留在中国科学院神经科学研究所(现脑科学与智能技术卓越创新中心)工作,历任助理研究员、副研究员、高性能计算平台负责人。2024年10月加入复旦大学医学遗传研究院,组建智能生物学实验室。

袁博博士长期聚焦孤独症谱系障碍等神经发育疾病的遗传机理与精准干预研究,围绕“遗传发现—工具创新—在体验证”主线,在人群遗传学、分子机制、基因编辑工具开发和神经系统疾病模型等方面形成连续积累。以第一作者或共同第一作者(含排名第一)在 Molecular PsychiatryNature CommunicationsNucleic Acids ResearchNeuroscience Bulletin 等期刊发表多篇论文;主持国家自然科学基金青年项目、上海市自然科学基金面上项目,并作为骨干参与国家重点研发计划重点专项。

智能生物学实验室(IBLab)依托复旦大学医学遗传研究院,聚焦孤独症谱系障碍等神经发育疾病的遗传基础、致病机制与精准干预策略。实验室整合人群遗传学、基因组学、类脑器官与组装体、基因编辑和人工智能等前沿技术,围绕“遗传发现—工具创新—在体验证”的研究主线,致力于建立从风险基因鉴定到干预参数优化的连续证据链。

我们的研究方向包括:

  1. 中国人群神经精神疾病候选基因的致病机制与干预策略研究;
  2. 基于诱导多能干细胞(iPSC)和类脑器官/组装体的人源发育模型构建;
  3. 基于大语言模型和结构生物学的基因编辑工具(碱基编辑器)优化与开发;
  4. 高性能计算与多组学数据整合分析方法开发。

实验室依托复旦大学医学遗传研究院、医学科研数据中心和超能智算平台,具备“干湿结合”的交叉研究条件。

我们欢迎有志于神经发育疾病遗传机制与精准干预研究的学生和合作者加入。如有兴趣,请联系袁博博士:yuanbo@ion.ac.cn

news

Dec 31, 2025 Commentary “Re-examining interneuron-specific Nrp2 deletion: overlooked striatal and cortical contributions” was published in Molecular Psychiatry.
Dec 31, 2024 Collaborative paper “Effective in vivo RNA base editing via engineered cytidine deaminase APOBECs fused with PUF proteins” was published in Nature Communications.
Dec 14, 2024 The laboratory joined the National Key R&D Program key special project on reproductive health and women and children’s health as a core participant.
Nov 30, 2024 The laboratory was awarded a Shanghai Natural Science Foundation General Program grant on mitochondrial dysfunction candidate genes in the Chinese autism cohort.
Sep 30, 2024 Dr. Bo Yuan joined the Institute of Medical Genetics and Genomics, Fudan University, and established the Intelligent Biology Laboratory (IBLab).

latest posts

Mar 26, 2025 a post with plotly.js
Dec 04, 2024 a post with image galleries
May 01, 2024 a post with tabs

selected publications

  1. Re-examining interneuron-specific Nrp2 deletion: overlooked striatal and cortical contributions
    AiHua Yuan, and Bo Yuan
    Molecular Psychiatry, 2025
    Accepted
  2. Effective in vivo RNA base editing via engineered cytidine deaminase APOBECs fused with PUF proteins
    WenJian Han, Bo Yuan, XiaoJuan Fan, and 8 more authors
    Nature Communications, 2025
    Accepted
  3. Whole-brain in vivo base editing reverses behavioral changes in Mef2c-mutant mice
    WeiKe Li, ShuQian Zhang, WanLing Peng, and 15 more authors
    Nature Neuroscience, 2025
  4. Identification of de novo mutations in the Chinese ASD cohort via whole-exome sequencing unveils brain regions implicated in autism
    Bo Yuan, MengDi Wang, XinRan Wu, and 8 more authors
    Neuroscience Bulletin, 2023
  5. Engineering of cytosine base editors with genotoxicity minimization and editing scope diversification
    Bo Yuan, ShuQian Zhang, LiTing Song, and 7 more authors
    Nucleic Acids Research, 2023
  6. TadA orthologs enable both cytosine and adenine editing of base editors
    ShuQian Zhang, Bo Yuan, JiXin Cao, and 7 more authors
    Nature Communications, 2023
  7. TadA reprogramming to generate potent miniature base editors with high precision
    ShuQian Zhang, LiTing Song, Bo Yuan, and 9 more authors
    Nature Communications, 2023
  8. Novel IL1RAP mutation associated with schizophrenia interferes with neuronal growth and related NF-κB signal pathways
    PeiPei Cheng, Ran Zhang, ShiFang Shan, and 4 more authors
    Neuroscience Letters, 2022
  9. Identification of CHMP4C as a new risk gene for inherited dilated cardiomyopathy
    NianWei Zhou, Lu Tang, YingYing Jiang, and 9 more authors
    Journal of Genetics and Genomics, 2022
  10. An intronic variant of CHD7 identified in autism patients interferes with neuronal differentiation and development
    Ran Zhang, Hui He, Bo Yuan, and 5 more authors
    Neuroscience Bulletin, 2021
  11. Visualization and correction of social abnormalities-associated neural ensembles in adult MECP2 duplication mice
    Le Sun, RuiGuo Chen, Long Li, and 11 more authors
    Science Bulletin, 2020
  12. Reversal of social recognition deficit in adult mice with MECP2 duplication via normalization of MeCP2 in the medial prefrontal cortex
    Bin Yu, Bo Yuan, Jian-Kun Dai, and 9 more authors
    Neuroscience Bulletin, 2020
  13. Docking sites inside Cas9 for adenine base editing diversification and RNA off-target elimination
    Shuo Li, Bo Yuan, JiXin Cao, and 7 more authors
    Nature Communications, 2020
  14. Expanding C-T base editing toolkit with diversified cytidine deaminases
    Tian-Lin Cheng, Shuo Li, Bo Yuan, and 3 more authors
    Nature Communications, 2019
  15. Towards the framework of understanding autism spectrum disorders
    ZiLong Qiu, and Bo Yuan
    Neuroscience Bulletin, 2019
  16. Mir505-3p regulates axonal development via inhibiting the autophagy pathway by targeting Atg12
    Kan Yang, Bin Yu, Cheng Cheng, and 6 more authors
    Autophagy, 2017
  17. Accumulated quiescent neural stem cells in adult hippocampus of the mouse model for the MECP2 duplication syndrome
    ZhiFang Che, Xiao Li, JingJing Zhou, and 12 more authors
    Scientific Reports, 2017
  18. Autism-related protein MeCP2 regulates FGF13 expression and emotional behaviors
    Bo Yuan, Tian-Lin Cheng, Kan Yang, and 2 more authors
    Journal of Genetics and Genomics, 2017
  19. Reciprocal regulation of autism-related genes MeCP2 and PTEN via microRNAs
    Jing-Wen Lyu, Bo Yuan, Tian-Lin Cheng, and 2 more authors
    Scientific Reports, 2016
  20. Tet1-mediated DNA demethylation regulates neuronal cell death induced by oxidative stress
    Yong-Juan Xin, Bo Yuan, Bin Yu, and 4 more authors
    Scientific Reports, 2015
  21. NeuroD2 regulates the development of hippocampal mossy fiber synapses
    Scott A Wilke, Benjamin J Hall, Joseph K Antonios, and 10 more authors
    Neural Development, 2012