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User-centered design of multi-gene sequencing panel reports for clinicians.
Cutting E, Banchero M, Beitelshees AL, Cimino JJ, Fiol GD, Gurses AP, Hoffman MA, Jeng LJ, Kawamoto K, Kelemen M, Pincus HA, Shuldiner AR, Williams MS, Pollin TI, Overby CL. Cutting E, et al. Among authors: fiol gd. J Biomed Inform. 2016 Oct;63:1-10. doi: 10.1016/j.jbi.2016.07.014. Epub 2016 Jul 14. J Biomed Inform. 2016. PMID: 27423699 Free PMC article.
Identifying Patients Who Meet Criteria for Genetic Testing of Hereditary Cancers Based on Structured and Unstructured Family Health History Data in the Electronic Health Record: Natural Language Processing Approach.
Shi J, Morgan KL, Bradshaw RL, Jung SH, Kohlmann W, Kaphingst KA, Kawamoto K, Fiol GD. Shi J, et al. Among authors: fiol gd. JMIR Med Inform. 2022 Aug 11;10(8):e37842. doi: 10.2196/37842. JMIR Med Inform. 2022. PMID: 35969459 Free PMC article.
Correction: Identifying Patients Who Meet Criteria for Genetic Testing of Hereditary Cancers Based on Structured and Unstructured Family Health History Data in the Electronic Health Record: Natural Language Processing Approach.
Shi J, Morgan KL, Bradshaw RL, Jung SH, Kohlmann W, Kaphingst KA, Kawamoto K, Fiol GD. Shi J, et al. Among authors: fiol gd. JMIR Med Inform. 2022 Sep 13;10(9):e42533. doi: 10.2196/42533. JMIR Med Inform. 2022. PMID: 36099593 Free PMC article.
Enhancing the use of EHR systems for pragmatic embedded research: lessons from the NIH Health Care Systems Research Collaboratory.
Richesson RL, Marsolo KS, Douthit BJ, Staman K, Ho PM, Dailey D, Boyd AD, McTigue KM, Ezenwa MO, Schlaeger JM, Patil CL, Faurot KR, Tuzzio L, Larson EB, O'Brien EC, Zigler CK, Lakin JR, Pressman AR, Braciszewski JM, Grudzen C, Fiol GD. Richesson RL, et al. Among authors: fiol gd. J Am Med Inform Assoc. 2021 Nov 25;28(12):2626-2640. doi: 10.1093/jamia/ocab202. J Am Med Inform Assoc. 2021. PMID: 34597383 Free PMC article.
11 results