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How to customize common data models for rare diseases: an OMOP-based implementation and lessons learned.
Ahmadi N, Zoch M, Guengoeze O, Facchinello C, Mondorf A, Stratmann K, Musleh K, Erasmus HP, Tchertov J, Gebler R, Schaaf J, Frischen LS, Nasirian A, Dai J, Henke E, Tremblay D, Srisuwananukorn A, Bornhäuser M, Röllig C, Eckardt JN, Middeke JM, Wolfien M, Sedlmayr M. Ahmadi N, et al. Among authors: facchinello c. Orphanet J Rare Dis. 2024 Aug 14;19(1):298. doi: 10.1186/s13023-024-03312-9. Orphanet J Rare Dis. 2024. PMID: 39143600 Free PMC article.