Caregivers' role in using a personal electronic health record: a qualitative study of cancer patients and caregivers in Germany. - Aline Weis; Sabrina Pohlmann; Regina Poss-Doering; Beate Strauss; Charlotte Ullrich; Helene Hofmann; Dominik Ose; Eva C. Winkler; Joachim Szecsenyi; Michel Wensing (BMC Medical Informatics Decis. Mak., 2020)

Data protection-compliant broad consent for secondary use of health care data and human biosamples for (bio)medical research: Towards a new German national standard. - Sven Zenker; Daniel Strech; Kristina Ihrig; Roland Jahns; Gabriele Müller; Christoph Schickhardt; Georg Schmidt; Ronald Speer; Eva C. Winkler; Sebastian Graf von Kielmansegg; Johannes Drepper (J. Biomed. Informatics, 2022)

Establishing Adaptive Governance in NFDI Consortia: Lessons Learned from Deliberative Forums with Patients on their Role in the Governance of the German Human Genome-Phenome Archive (GHGA). - Eric Apondo; Andrea Züger; Andreas Bruns; Katja Mehlis; Christoph Schickhardt; Eva C. Winkler (CoRDI, 2023)

Developing Consent Tools for the Research Community at the German Human Genome-Phenome Archive (GHGA). - Andreas Bruns; Simon Parker; Fruzsina Molnár-Gábor; Eva C. Winkler (CoRDI, 2023)

Percentages and reasons: AI explainability and ultimate human responsibility within the medical field. - Markus Herrmann; Andreas Wabro; Eva C. Winkler (Ethics Inf. Technol., 2024)