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IEEE Transactions on Biomedical Circuits and Systems|October 18, 2023
Human Eye Activity Monitoring Using Continuous Wave Doppler Radar: A Feasibility StudyZhijun Xiao, Chenxi Yang, Yumin Li, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|December 11, 2021
An atrial fibrillation detection system based on machine learning algorithm with mix-domain features and hardware accelerationChao Chen, Caiyun Ma, Yantao Xing, et al.
Critical Care Medicine|October 19, 2023
The International Cardiac Arrest Research Consortium Electroencephalography DatabaseEdilberto Amorim, Wei-Long Zheng, Mohammad M Ghassemi, et al.
Scientific Data|February 25, 2026
The Harvard-Emory ECG DatabaseZuzana Koscova, Qiao Li, Chad Robichaux, et al.
Medrxiv : the Preprint Server for Health Sciences|September 11, 2023
The International Cardiac Arrest Research (I-CARE) Consortium Electroencephalography DatabaseEdilberto Amorim, Wei-Long Zheng, Mohammad M Ghassemi, et al.
Plos Genetics|March 2, 2016
A RUNX2-Mediated Epigenetic Regulation of the Survival of p53 Defective Cancer CellsMin Hwa Shin, Yunlong He, Eryney Marrogi, et al.
The Journal of Clinical Investigation|May 11, 2011
Growth hormone receptor regulates β cell hyperplasia and glucose-stimulated insulin secretion in obese miceYingjie Wu, Chengyu Liu, Hui Sun, et al.
Nature Communications|September 6, 2017
The cytoplasmic nuclear receptor RARγ controls RIP1 initiated cell death when cIAP activity is inhibitedQing Xu, Siriporn Jitkaew, Swati Choksi, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 29, 2017
Cutting Edge: β-Catenin-Interacting Tcf1 Isoforms Are Essential for Thymocyte Survival but Dispensable for Thymic Maturation TransitionsZhe Xu, Shaojun Xing, Qiang Shan, et al.
Stem Cell Research|March 2, 2020
An induced pluripotent stem cell line (TRNDi001-D) from a Niemann-Pick disease type C1 (NPC1) patient carrying a homozygous p. I1061T (c. 3182T>C) mutation in the NPC1 geneRong Li, Manisha Pradhan, Miao Xu, et al.
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