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A Generic Data Model for Precision Medicine Applied to Rare Genetic Epilepsy

Year: 2026

Type: conference-paper

Abstract: Introduction: Understanding disease development increasingly relies on integrating diverse data sources, such as care records, cohort data, and genetic information. This integration reveals complex links between disease onset and progression, making the digital representation of multimodal data essential. [for full text, please go to the a.m. URL]

Source: German Medical Science (German Research Foundation)

DOI: 10.3205/25gmds190

Authors: Pérez Garriga, Ariadna, Honrath, Philipp, Wolking, Stefan, Coldewey, Beatrice, Bozkir, Susann, Freyer, Nils, May, Patrick, Weber, Yvonne, Röhrig, Rainer, Lipprandt, Myriam

Institutions: Universitätsklinikum Aachen, RWTH Aachen University, University of Luxembourg

Language: English

Topic: Epilepsy research and treatment

Subfield: Psychiatry and Mental health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: green

OpenAlex ID: W7147690044

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