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Found 8 results
Author Title [ Type(Asc)] Year
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Journal Article
Xu Z, Mao C, Su C, Zhang H, Siempos I, Torres LK, Pan D, Luo Y, Schenck EJ, Wang F.  2022.  Sepsis subphenotyping based on organ dysfunction trajectory.. Crit Care. 26(1):197.
Adekkanattu P, Rasmussen LV, Pacheco JA, Kabariti J, Stone DJ, Yu Y, Jiang G, Luo Y, Brandt PS, Xu Z et al..  2023.  Prediction of left ventricular ejection fraction changes in heart failure patients using machine learning and electronic health records: a multi-site study.. Sci Rep. 13(1):294.
Kline A, Wang H, Li Y, Dennis S, Hutch M, Xu Z, Wang F, Cheng F, Luo Y.  2022.  Multimodal machine learning in precision health: A scoping review.. NPJ Digit Med. 5(1):171.
Xu J, Mao C, Hou Y, Luo Y, Binder JL, Zhou Y, Bekris LM, Shin J, Hu M, Wang F et al..  2022.  Interpretable deep learning translation of GWAS and multi-omics findings to identify pathobiology and drug repurposing in Alzheimer's disease.. Cell Rep. 41(9):111717.
Xu Z, Chou J, Zhang XSheryl, Luo Y, Isakova T, Adekkanattu P, Ancker JS, Jiang G, Kiefer RC, Pacheco JA et al..  2020.  Identifying sub-phenotypes of acute kidney injury using structured and unstructured electronic health record data with memory networks.. J Biomed Inform. 102:103361.
Sharma H, Mao C, Zhang Y, Vatani H, Yao L, Zhong Y, Rasmussen L, Jiang G, Pathak J, Luo Y.  2019.  Developing a portable natural language processing based phenotyping system.. BMC Med Inform Decis Mak. 19(Suppl 3):78.
Brandt PS, Pacheco JA, Adekkanattu P, Sholle ET, Abedian S, Stone DJ, Knaack DM, Xu J, Xu Z, Peng Y et al..  2022.  Design and validation of a FHIR-based EHR-driven phenotyping toolbox.. J Am Med Inform Assoc. 29(9):1449-1460.
Zeng X, Wang F, Luo Y, Kang S-G, Tang J, Lightstone FC, Fang EF, Cornell W, Nussinov R, Cheng F.  2022.  Deep generative molecular design reshapes drug discovery.. Cell Rep Med. 3(12):100794.