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Missing Data Imputation in the Electronic Health Record Using Deeply Learned Autoencoders., , и . PSB, стр. 207-218. (2017)Genome-Wide Genetic Interaction Analysis of Glaucoma Using Expert Knowledge Derived from Human Phenotype Networks., , , , и . Pacific Symposium on Biocomputing, стр. 207-218. (2015)Building the Next Generation of Quantitative Biologists., , , , , , и . Pacific Symposium on Biocomputing, стр. 417-421. (2014)Using the Bipartite Human Phenotype Network to Reveal Pleiotropy and Epistasis Beyond the Gene., , и . Pacific Symposium on Biocomputing, стр. 188-199. (2014)Data-driven advice for applying machine learning to bioinformatics problems., , , , и . PSB, стр. 192-203. (2018)SGP-DT: Semantic Genetic Programming Based on Dynamic Targets., , и . EuroGP, том 12101 из Lecture Notes in Computer Science, стр. 167-183. Springer, (2020)An augmented estimation procedure for EHR-based association studies accounting for differential misclassification., , , , , , и . J. Am. Medical Informatics Assoc., 27 (2): 244-253 (2020)Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors., , , , , , , , , и 5 other автор(ы). BioData Min., (2014)The influence of whole genome duplication and subsequent diversification on environmental robustness and evolutionary innovation in gene regulatory networks., , , , и . ECAL, стр. 614-621. MIT Press, (2011)Robustness, evolvability, and accessibility in the signal-integration space of gene regulatory circuits., и . ECAL, стр. 638-645. MIT Press, (2011)