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Integrating clinical decision support systems for pharmacogenomic testing into clinical routine - a scoping review of designs of user-system interactions in recent system development.
Hinderer M, Boeker M, Wagner SA, Lablans M, Newe S, Hülsemann JL, Neumaier M, Binder H, Renz H, Acker T, Prokosch HU, Sedlmayr M. Hinderer M, et al. Among authors: sedlmayr m. BMC Med Inform Decis Mak. 2017 Jun 6;17(1):81. doi: 10.1186/s12911-017-0480-y. BMC Med Inform Decis Mak. 2017. PMID: 28587608 Free PMC article. Review.
MIRACUM: Medical Informatics in Research and Care in University Medicine.
Prokosch HU, Acker T, Bernarding J, Binder H, Boeker M, Boerries M, Daumke P, Ganslandt T, Hesser J, Höning G, Neumaier M, Marquardt K, Renz H, Rothkötter HJ, Schade-Brittinger C, Schmücker P, Schüttler J, Sedlmayr M, Serve H, Sohrabi K, Storf H. Prokosch HU, et al. Among authors: sedlmayr m. Methods Inf Med. 2018 Jul;57(S 01):e82-e91. doi: 10.3414/ME17-02-0025. Epub 2018 Jul 17. Methods Inf Med. 2018. PMID: 30016814 Free PMC article.
The Status Quo of Rare Diseases Centres for the Development of a Clinical Decision Support System - A Cross-Sectional Study.
Schaaf J, Sedlmayr M, Prokosch HU, Ganslandt T, Schade-Brittinger C, von Wagner M, Kadioglu D, Schubert K, Lee-Kirsch MA, Kraemer BK, Winner B, Mueller T, Schaefer JR, Wagner TOF, Bruckner-Tuderman L, Tuescher O, Boeker M, Storf H. Schaaf J, et al. Among authors: sedlmayr m. Stud Health Technol Inform. 2020 Jun 23;271:176-183. doi: 10.3233/SHTI200094. Stud Health Technol Inform. 2020. PMID: 32578561
Adaption of the OMOP CDM for Rare Diseases.
Zoch M, Gierschner C, Peng Y, Gruhl M, Leutner LA, Sedlmayr M, Bathelt F. Zoch M, et al. Among authors: sedlmayr m. Stud Health Technol Inform. 2021 May 27;281:138-142. doi: 10.3233/SHTI210136. Stud Health Technol Inform. 2021. PMID: 34042721
83 results