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Improving the phenotype risk score as a scalable approach to identifying patients with Mendelian disease., , , , , , , , , and . J. Am. Medical Informatics Assoc., 26 (12): 1437-1447 (2019)The All of Us Research Program Researcher Workbench Phenotype Library: Five Disease Implementations., , , , , , , , , and 4 other author(s). AMIA, AMIA, (2020)An analytical approach to characterize morbidity profile dissimilarity between distinct cohorts using electronic medical records., , , , , , , , , and 2 other author(s). J. Biomed. Informatics, 43 (6): 914-923 (2010)Interactive network-based clustering and investigation of multimorbidity association matrices with associationSubgraphs., , , , , , , , , and 10 other author(s). Bioinform., (January 2023)Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomics., , , , , , , , , and 16 other author(s). Bioinform., (October 2023)Evaluating statistical approaches to leverage large clinical datasets for uncovering therapeutic and adverse medication effects., , , , , , and . Bioinform., 34 (17): 2988-2996 (2018)A case study evaluating the portability of an executable computable phenotype algorithm across multiple institutions and electronic health record environments., , , , , , , , , and 14 other author(s). J. Am. Medical Informatics Assoc., 25 (11): 1540-1546 (2018)Visual Integration of Results from a Large Dna Biobank (Biovu) Using Synthesis-View., , , , and . Pacific Symposium on Biocomputing, page 265-275. World Scientific Publishing, (2011)Real-time Clinical Note Monitoring to Detect Conditions for Follow-up: a Case Study of Clinical Trial Enrollment in Drug-induced Torsades de Pointes and Stevens-Johnson Syndrome., , , , , , , , , and 3 other author(s). AMIA, AMIA, (2020)The All of Us Research Program Researcher Workbench: Cloud based access and analytics to advance precision medicine., , , , , , , , and . AMIA, AMIA, (2020)