German funders' data sharing policies-A qualitative interview study von Anger, Michael, Wendelborn, Christian, Schickhardt, Christoph

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Neither carrots nor sticks? Challenges surrounding data sharing from the perspective of research funding agencies-A qualitative expert interview study von Anger, Michael, Wendelborn, Christian, Winkler, Eva C, Schickhardt, Christoph

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Physicians' attitudes towards secondary use of clinical data for biomedical research purposes in Germany. Results of a quantitative survey von Köngeter, Anja, Schickhardt, Christoph, Jungkunz, Martin, Mehlis, Katja, Winkler, Eva C

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Patients’ Willingness to Provide Their Clinical Data for Research Purposes and Acceptance of Different Consent Models: Findings From a Representative Survey of Patients With Cancer... von Köngeter, Anja, Schickhardt, Christoph, Jungkunz, Martin, Bergbold, Susanne, Mehlis, Katja, Winkler, Eva C

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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 von Zenker, Sven, Strech, Daniel, Ihrig, Kristina, Jahns, Roland, Müller, Gabriele, Schickhardt, Christoph, Schmidt, Georg, Speer, Ronald, Winkler, Eva, von Kielmansegg, Sebastian Graf, Drepper, Johannes

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Do patients and research subjects have a right to receive their genomic raw data? An ethical and legal analysis von Schickhardt, Christoph, Fleischer, Henrike, Winkler, Eva C

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Applying systems biology to biomedical research and health care: a précising definition of systems medicine von Schleidgen, Sebastian, Fernau, Sandra, Fleischer, Henrike, Schickhardt, Christoph, Oßa, Ann-Kristin, Winkler, Eva C

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'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods von Middleton, Anna, Niemiec, Emilia, Prainsack, Barbara, Bobe, Jason, Farley, Lauren, Steed, Claire, Smith, James, Bevan, Paul, Bonhomme, Natasha, Kleiderman, Erika, Thorogood, Adrian, Schickhardt, Christoph, Garattini, Chiara, Vears, Danya, Littler, Katherine, Banner, Natalie, Scott, Erick, Kovalevskaya, Nadezda V, Levin, Elissa, Morley, Katherine I, Howard, Heidi Carmen

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National standardisierter Broad Consent in der Praxis: erste Erfahrungen, aktuelle Entwicklungen und kritische Betrachtungen von Zenker, Sven, Strech, Daniel, Jahns, Roland, Müller, Gabriele, Prasser, Fabian, Schickhardt, Christoph, Schmidt, Georg, Semler, Sebastian C., Winkler, Eva, Drepper, Johannes

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What is data stewardship? Towards a comprehensive understanding von Wendelborn, Christian, Anger, Michael, Schickhardt, Christoph

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Promoting Data Sharing: The Moral Obligations of Public Funding Agencies von Wendelborn, Christian, Anger, Michael, Schickhardt, Christoph

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Secondary Use of Clinical Data in Data-Gathering, Non-Interventional Research or Learning Activities: Definition, Types, and a Framework for Risk Assessment von Jungkunz, Martin, Köngeter, Anja, Mehlis, Katja, Winkler, Eva C, Schickhardt, Christoph

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German funders' data sharing policies-A qualitative interview study von Michael Anger, Christian Wendelborn, Christoph Schickhardt

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Data infrastructures for health research : Ethical framework and legal implementation von Schickhardt, Christoph, Winkler, Eva, Sax, Ulrich, Buchner, Benedikt

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Do Physicians Have a Duty to Support Secondary Use of Clinical Data in Biomedical Research? An Inquiry into the Professional Ethics of Physicians von Jungkunz, Martin, Köngeter, Anja, Winkler, Eva C, Schickhardt, Christoph

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Kinder im Wahlrecht und in Demokratien. Für eine elterliche Stellvertreterwahlpflicht von Schickhardt, Christoph

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Stakeholders' perspectives on biobank-based genomic research: systematic review of the literature von Husedzinovic, Alma, Ose, Dominik, Schickhardt, Christoph, Fröhling, Stefan, Winkler, Eva C

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Nationally standardized broad consent in practice: initial experiences, current developments, and critical assessment von Zenker, Sven, Strech, Daniel, Jahns, Roland, Müller, Gabriele, Prasser, Fabian, Schickhardt, Christoph, Schmidt, Georg, Semler, Sebastian C, Winkler, Eva, Drepper, Johannes

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National standardisierter Broad Consent in der Praxis: erste Erfahrungen, aktuelle Entwicklungen und kritische Betrachtungen von Zenker, Sven, Strech, Daniel, Jahns, Roland, Müller, Gabriele, Prasser, Fabian, Schickhardt, Christoph, Schmidt, Georg, Semler, Sebastian C., Winkler, Eva, Drepper, Johannes

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Haben Krankenhäuser die Pflicht, die sekundäre Forschungsnutzung von Behandlungsdaten zu unterstützen? von Jungkunz, Martin, Winkler, Eva C., Schickhardt, Christoph

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