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Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1.
Du J, Hu YC, Tang BS, Chen C, Luo YY, Zhan ZX, Zhao GH, Jiang H, Xia K, Shen L. Du J, et al. Among authors: chen c. Clin Neurol Neurosurg. 2011 Jul;113(6):480-2. doi: 10.1016/j.clineuro.2011.02.011. Epub 2011 Mar 17. Clin Neurol Neurosurg. 2011. PMID: 21419568
A diagnostic gene chip for hereditary spastic paraplegias.
Luo Y, Du J, Zhan Z, Chen C, Wang J, Hu Y, Hu Z, Xia K, Tang B, Shen L. Luo Y, et al. Among authors: chen c. Brain Res Bull. 2013 Aug;97:112-8. doi: 10.1016/j.brainresbull.2013.07.002. Epub 2013 Jul 10. Brain Res Bull. 2013. PMID: 23850684
Integrating predictive coding and a user-centric interface for enhanced auditing and quality in cancer registry data.
Dai HJ, Chen CC, Mir TH, Wang TY, Wang CK, Chang YC, Yu SJ, Shen YW, Huang CJ, Tsai CH, Wang CY, Chen HJ, Weng PS, Lin YX, Chen SW, Tsai MJ, Juang SF, Wu SY, Tsai WT, Huang MY, Huang CJ, Yang CJ, Liu PZ, Huang CW, Huang CY, Wang WYC, Chong IW, Yang YH. Dai HJ, et al. Among authors: chen cc. Comput Struct Biotechnol J. 2024 Apr 7;24:322-333. doi: 10.1016/j.csbj.2024.04.007. eCollection 2024 Dec. Comput Struct Biotechnol J. 2024. PMID: 38690549 Free PMC article.
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