全部发表信息（Publications）：https://www.researchgate.net/profile/Jingqi_Chen

代表性论文（Selected papers）:

* corresponding author(s)

(a) Computational genomics of brain disorders:

(a1) An, Z., ..., Chen, J.* & Zhao, X. M.* Characterizing schizophrenia-relevant structural variants and tandem repeats through long-read sequencing. Science Bulletin, doi:10.1016/j.scib.2025.11.004 (2026).

(a2) Cao, J., Zhang, C., ..., Cheng, T. L.*, Chen, J.*, Zhao, X. M.* & for the Alzheimer's Disease Neuroimaging Initiative. Integrating rare pathogenic variant prioritization with gene-based association analysis to identify novel genes and relevant multimodal traits for Alzheimer's disease. Alzheimer's & Dementia. doi:10.1002/alz.14444 (2025).

(a3) Chen, J.*, ... ,& Zhao, X. M.* Disrupted long-range gene regulations elucidate shared tissue-specific mechanisms of neuropsychiatric disorders. Molecular Psychiatry, doi:10.1038/s41380-022-01529-3 (2022).

(a4) Chen, J. & Tian, W. Explaining the disease phenotype of intergenic SNP through predicted long range regulation. Nucleic Acids Research. doi:10.1093/nar/gkw519 (2016).

(b) Computational models to facilitate molecular diagnosis and genome editing systems

(b1) Zhang, C., Chen, Z., Cao, J., Zhang, Z., Li, W. K.,..., Zhao, X. M.*, Chen, J.*, Zhan, C.* & Cheng, T. L.* RNA inosine sensor-guided TadA mutational scanning for toxicity minimization of adenine base editors. Molecular Therapy, doi:10.1016/j.ymthe.2025.10.011 (2025).

(b2) Yuan, B., Zhang, S., Song, L., ..., Chen, J.*, Zhao, X. M.* & Cheng, T. L.* Engineering of cytosine base editors with DNA damage minimization and editing scope diversification. Nucleic Acids Res 51, e105, doi:10.1093/nar/gkad855 (2023).

(b3) Chen, J.* A fully-automated event-based variant prioritizing solution to the CAGI5 intellectual disability gene panel challenge. Human Mutation. doi:10.1002/humu.23781 (2019).