Search Results - "Schickhardt, Christoph"
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German funders' data sharing policies-A qualitative interview study
Published in PloS one (08-02-2024)“…Data sharing is commonly seen as beneficial for science but is not yet common practice. Research funding agencies are known to play a key role in promoting…”
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Neither carrots nor sticks? Challenges surrounding data sharing from the perspective of research funding agencies-A qualitative expert interview study
Published in PloS one (07-09-2022)“…Data Sharing is widely recognised as crucial for accelerating scientific research and improving its quality. However, data sharing is still not a common…”
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Physicians' attitudes towards secondary use of clinical data for biomedical research purposes in Germany. Results of a quantitative survey
Published in PloS one (13-02-2024)“…For biomedical data-driven research purposes, secondary use of clinical data carries great but largely untapped potential. Physicians' attitudes and their…”
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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
Published in Journal of medical Internet research (25-08-2022)“…Background Secondary use of clinical data for biomedical research purposes holds great potential for various types of noninterventional, data-driven studies…”
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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
Published in Journal of biomedical informatics (01-07-2022)“…[Display omitted] •A nationally standardized broad consent for long-term secondary use of health data and biosamples was developed.•This consent has been…”
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Do patients and research subjects have a right to receive their genomic raw data? An ethical and legal analysis
Published in BMC medical ethics (16-01-2020)“…As Next Generation Sequencing technologies are increasingly implemented in biomedical research and (translational) care, the number of study participants and…”
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Applying systems biology to biomedical research and health care: a précising definition of systems medicine
Published in BMC health services research (21-11-2017)“…Systems medicine has become a key word in biomedical research. Although it is often referred to as P4-(predictive, preventive, personalized and…”
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'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methods
Published in Personalized medicine (01-07-2018)“…Our international study, 'Your DNA, Your Say', uses film and an online cross-sectional survey to gather public attitudes toward the donation, access and…”
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National standardisierter Broad Consent in der Praxis: erste Erfahrungen, aktuelle Entwicklungen und kritische Betrachtungen
Published in Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz (2024)“…Zusammenfassung Hintergrund Die Digitalisierung im Gesundheitswesen verspricht eine Sekundärnutzung von Patientendaten im Sinne eines lernenden…”
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What is data stewardship? Towards a comprehensive understanding
Published in Journal of biomedical informatics (01-04-2023)“…[Display omitted] Data stewardship is a term that is understood in heterogenous ways. In recent organisational developments and efforts to build…”
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Promoting Data Sharing: The Moral Obligations of Public Funding Agencies
Published in Science and engineering ethics (06-08-2024)“…Sharing research data has great potential to benefit science and society. However, data sharing is still not common practice. Since public research funding…”
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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
Published in Journal of medical Internet research (08-06-2021)“…Background The secondary use of clinical data in data-gathering, non-interventional research or learning activities (SeConts) has great potential for…”
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German funders' data sharing policies-A qualitative interview study
Published in PloS one (01-01-2024)“…BackgroundData sharing is commonly seen as beneficial for science but is not yet common practice. Research funding agencies are known to play a key role in…”
Get full text
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Data infrastructures for health research : Ethical framework and legal implementation
Published in Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz (01-02-2023)“…The role of data infrastructures for health research is not limited to acting as a service or interface for data exchange between data producers and data…”
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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
Published in The Journal of law, medicine & ethics (01-01-2024)“…Secondary use of clinical data in research or learning activities ( ) has the potential to improve patient care and biomedical knowledge. Given this potential,…”
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Kinder im Wahlrecht und in Demokratien. Für eine elterliche Stellvertreterwahlpflicht
Published in Zeitschrift für Praktische Philosophie (01-07-2015)Get full text
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Stakeholders' perspectives on biobank-based genomic research: systematic review of the literature
Published in European journal of human genetics : EJHG (01-12-2015)“…The success of biobank-based genomic research is widely dependent on people's willingness to donate their tissue. Thus, stakeholders' opinions should be…”
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Nationally standardized broad consent in practice: initial experiences, current developments, and critical assessment
Published in Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz (01-06-2024)“…The digitalization in the healthcare sector promises a secondary use of patient data in the sense of a learning healthcare system. For this, the Medical…”
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Haben Krankenhäuser die Pflicht, die sekundäre Forschungsnutzung von Behandlungsdaten zu unterstützen?
Published in Ethik in der Medizin (01-12-2024)“…Zusammenfassung Die sekundäre Forschungsnutzung von Behandlungsdaten hat Potenzial, medizinisches Wissen zu erweitern und die Patientenbehandlung zu…”
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