Author

Sophie Anne Inès Klopfenstein

Berlin Institute of Health at Charité - Universitätsmedizin BerlinORCID 0000-0002-8470-2258Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Approach:benchmark study· 1 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Assay:electronic health records· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Adam S L GraefeiD· 1 shared Alexander BartschkeiD· 1 shared Ana GrönkeiD· 1 shared Beáta DérfalviiD· 1 shared Chris MungalliD· 1 shared Daniel DanišiD· 1 shared Elisabeth F. NyounguiiD· 1 shared Filip RehburgiD· 1 shared

Activity by Year

2025-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Adam S L GraefeORCID

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1 paper

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintMay 9, 2025

Linking international registries to FHIR and Phenopackets with RareLink: a scalable REDCap-based framework for rare disease data interoperability

Adam S L Graefe, Filip Rehburg, Samer Alkarkoukly…·Oya Beyan

RareLink enables interoperability between REDCap and global health standards by exporting data to Phenopackets and FHIR, improving rare disease research scalability and data reuse.

1 citation

humanelectronic health records

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