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Elisabeth F. Nyoungui

Observed names: E. Nyoungui, Elisabeth Nyoungui, Nyoungui E, Nyoungui, E., Nyoungui, Elisabeth, Nyoungui, Elisabeth F., Nyoungui, Elisabeth Felicite, Nyoungui, Elisabeth Félicité
ORCID: 0000-0003-4263-4629
Observed ORCID: 0000-0003-4263-4629
OpenAlex ID: A5017524618
An ontology-based rare disease common data model harmonising international registries, FHIR, and Phenopackets
2025 · Adam S. L. Graefe, Miriam R. Hübner, et al. · Scientific Data · 12
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Genetic Screening in Europe
2010 · P. Javaher, E. Nyoungui, et al. · Public Health Genomics · 9
OPTINOFA – Intelligenter Assistenzdienst zur strukturierten Ersteinschätzung in der Notaufnahme
2024 · Elisabeth Nyoungui, Marina V. Karg, et al. · Medizinische Klinik - Intensivmedizin und Notfallmedizin · 5
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RareLink: scalable REDCap-based framework for rare disease interoperability linking international registries to FHIR and Phenopackets
2025 · Adam S. L. Graefe, Filip Rehburg, et al. · npj Genomic Medicine · 4
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Se-atlas-cartographic representation of experts for rare diseases
2014 · Holger Storf, Tobias Hartz, et al. · Orphanet Journal of Rare Diseases · 4
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Strukturierte Ersteinschätzung in der Notaufnahme mittels des intelligenten Assistenzdienstes OPTINOFA
2024 · Sabine Blaschke, Harald Dormann, et al. · Medizinische Klinik - Intensivmedizin und Notfallmedizin · 2
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Linking international registries to FHIR and Phenopackets with RareLink: a scalable REDCap-based framework for rare disease data interoperability
2025 · Adam S.L. Graefe, Filip Rehburg, et al. · medRxiv · 1
Improving Clinical Documentation of Rare Neuromuscular Diseases: Development of a Standardised Information Model
2024 · Miriam Hübner, Elisabeth Nyoungui, et al. · Studies in health technology and informatics · 1
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Orphanet – das europäische Portal für seltene Krankheiten
2010 · K. Rommel, E. Nyoungui, et al. · Medizinische Genetik · 1
Patients’ and Providers’ Attitudes Toward Artificial Intelligence and Electronic Health Record Use in Deep Phenotyping and Rare-Disease Screening: An Empty Systematic Review
2026 · Sylvia Martin, Åsa Grauman, et al. · Healthcare
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Utilizing Routine Care Data of Rare Diseases: Challenges, Chances and Call for Collaboration
2026 · Miriam Hübner, Marco Schaarschmidt, et al. · Studies in health technology and informatics
HEG-TKG: Hierarchical Evidence-Grounded Temporal Knowledge Graphs for Rare Disease Reasoning - Paper 1 Reproducibility Bundle (v1.0.0)
2026 · Ahmed, Md Shamim, Dusanic, Maja, et al. · Zenodo (CERN European Organization for Nuclear Research)
HEG-TKG: Hierarchical Evidence-Grounded Temporal Knowledge Graphs for Rare Disease Reasoning - Paper 1 Reproducibility Bundle (v1.0.0)
2026 · Ahmed, Md Shamim, Dusanic, Maja, et al. · Zenodo (CERN European Organization for Nuclear Research)
The Provenance Gap in Clinical AI: Evidence-Traceable Temporal Knowledge Graphs for Rare Disease Reasoning
2026 · Ahmed, Md Shamim, Dusanic, Maja, et al. · arXiv (Cornell University)
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Patients' and Providers' Attitudes Toward Artificial Intelligence and Electronic Health Record Use in Deep Phenotyping and Rare Disease Screening: An Empty Systematic Review
2026 · Martin, Sylvia Isabelle Amélia, Grauman, Åsa, et al.
Classifying polyneuropathy and myopathy patients on Electronic Health Records
2025 · Md Shamim Ahmed, Nicolai Dinh Khang Truong, et al. · medRxiv
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548PAttitudes towards the use of AI on electronic health records for phenotyping and screening of rare diseases: a systematic review
2025 · S. Martin, A. Grauman, et al. · Neuromuscular Disorders
RareLink: scalable REDCap-based framework for rare disease interoperability linking international registries to FHIR and Phenopackets
2025 · Graefe, Adam S.L., Rehburg, Filip, et al. · Fraunhofer-Publica (Fraunhofer-Gesellschaft)
222P Development of a standardized information model for rare neuromuscular diseases
2024 · E. Gazzerro, M. Hübner, et al. · Neuromuscular Disorders
Subject Index Vol. 13, No. 7–8, 2010
2010 · K.D. Christensen, T.E. Jayaratne, et al. · Public Health Genomics
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Author Index Vol. 13, No. 7–8, 2010
2010 · K.D. Christensen, T.E. Jayaratne, et al. · Public Health Genomics
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Supplementary Material for: Genetic Screening in Europe
2010 · Javaher, P., Nyoungui, E., et al. · Figshare
Works count: 32
Citation count: 40
H-index: 4
I10-index: 1
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