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Christoph Schickhardt

Showing results (11-20 of 20) with videos related to

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Journal of Medical Ethics|May 25, 2023
Patient data for commercial companies? An ethical framework for sharing patients' data with for-profit companies for researchEva C Winkler, Martin Jungkunz, Adrian Thorogood, et al.
European Journal of Human Genetics : EJHG|March 5, 2015
Stakeholders' perspectives on biobank-based genomic research: systematic review of the literatureAlma Husedzinovic, Dominik Ose, Christoph Schickhardt, et al.
Public Health Genomics|May 28, 2025
Toward Patient Involvement and Representation in the Governance of Genomic Data Archives: Deliberative Forums with Patients in GermanyEric Apondo, Katja Mehlis, Andreas Bruns, et al.
Journal of Medical Internet Research|August 25, 2022
Patients' Willingness to Provide Their Clinical Data for Research Purposes and Acceptance of Different Consent Models: Findings From a Representative Survey of Patients With CancerAnja Köngeter, Christoph Schickhardt, Martin Jungkunz, et al.
BMC Health Services Research|November 23, 2017
Applying systems biology to biomedical research and health care: a précising definition of systems medicineSebastian Schleidgen, Sandra Fernau, Henrike Fleischer, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|April 19, 2024
[Nationally standardized broad consent in practice: initial experiences, current developments, and critical assessment]Sven Zenker, Daniel Strech, Roland Jahns, et al.
Genome Medicine|August 1, 2015
So rare we need to hunt for them: reframing the ethical debate on incidental findingsSebastian Schuol, Christoph Schickhardt, Stefan Wiemann, et al.
Journal of Biomedical Informatics|June 1, 2022
Data protection-compliant broad consent for secondary use of health care data and human biosamples for (bio)medical research: Towards a new German national standardSven Zenker, Daniel Strech, Kristina Ihrig, et al.
JAMA Pediatrics|March 20, 2018
Key Implications of Data Sharing in Pediatric GenomicsVasiliki Rahimzadeh, Christoph Schickhardt, Bartha M Knoppers, et al.
Personalized Medicine|June 2, 2018
'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methodsAnna Middleton, Emilia Niemiec, Barbara Prainsack, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Journal of Medical Ethics|May 25, 2023
Patient data for commercial companies? An ethical framework for sharing patients' data with for-profit companies for researchEva C Winkler, Martin Jungkunz, Adrian Thorogood, et al.
European Journal of Human Genetics : EJHG|March 5, 2015
Stakeholders' perspectives on biobank-based genomic research: systematic review of the literatureAlma Husedzinovic, Dominik Ose, Christoph Schickhardt, et al.
Public Health Genomics|May 28, 2025
Toward Patient Involvement and Representation in the Governance of Genomic Data Archives: Deliberative Forums with Patients in GermanyEric Apondo, Katja Mehlis, Andreas Bruns, et al.
Journal of Medical Internet Research|August 25, 2022
Patients' Willingness to Provide Their Clinical Data for Research Purposes and Acceptance of Different Consent Models: Findings From a Representative Survey of Patients With CancerAnja Köngeter, Christoph Schickhardt, Martin Jungkunz, et al.
BMC Health Services Research|November 23, 2017
Applying systems biology to biomedical research and health care: a précising definition of systems medicineSebastian Schleidgen, Sandra Fernau, Henrike Fleischer, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|April 19, 2024
[Nationally standardized broad consent in practice: initial experiences, current developments, and critical assessment]Sven Zenker, Daniel Strech, Roland Jahns, et al.
Genome Medicine|August 1, 2015
So rare we need to hunt for them: reframing the ethical debate on incidental findingsSebastian Schuol, Christoph Schickhardt, Stefan Wiemann, et al.
Journal of Biomedical Informatics|June 1, 2022
Data protection-compliant broad consent for secondary use of health care data and human biosamples for (bio)medical research: Towards a new German national standardSven Zenker, Daniel Strech, Kristina Ihrig, et al.
JAMA Pediatrics|March 20, 2018
Key Implications of Data Sharing in Pediatric GenomicsVasiliki Rahimzadeh, Christoph Schickhardt, Bartha M Knoppers, et al.
Personalized Medicine|June 2, 2018
'Your DNA, Your Say': global survey gathering attitudes toward genomics: design, delivery and methodsAnna Middleton, Emilia Niemiec, Barbara Prainsack, et al.
Pageof 2