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Journal of Community Genetics
|
September 19, 2017
Legal issues in governing genetic biobanks: the Italian framework as a case study for the implications for citizen's health through public-private initiatives
Cinzia Piciocchi, Rossana Ducato, Lucia Martinelli, et al.
Journal of Community Genetics
|
September 27, 2017
How to responsibly acknowledge research work in the era of big data and biobanks: ethical aspects of the Bioresource Research Impact Factor (BRIF)
Heidi Carmen Howard, Deborah Mascalzoni, Laurence Mabile, et al.
Biopreservation and Biobanking
|
December 6, 2021
Governance of Access in Biobanking: The Case of Telethon Network of Genetic Biobanks
Sofia Iacomussi, Lorena Casareto, Manuela Locatelli, et al.
Journal of Community Genetics
|
September 26, 2024
How to communicate and what to disclose to participants in a recall-by-genotype research approach: a multistep empirical study
Katharina Tschigg, Luca Consoli, Norbert Brüggemann, et al.
Nature Reviews. Genetics
|
July 4, 2013
Rare diseases and now rare data?
Deborah Mascalzoni, Bartha Maria Knoppers, Ségolène Aymé, et al.
European Journal of Human Genetics : EJHG
|
September 6, 2022
Ten years of dynamic consent in the CHRIS study: informed consent as a dynamic process
Deborah Mascalzoni, Roberto Melotti, Cristian Pattaro, et al.
International Journal of Environmental Research and Public Health
|
September 26, 2018
Meeting Patients' Right to the Correct Diagnosis: Ongoing International Initiatives on Undiagnosed Rare Diseases and Ethical and Social Issues
Sabina Gainotti, Deborah Mascalzoni, Virginie Bros-Facer, et al.
Cell
|
May 16, 2025
Human mitochondrial DNA in public metagenomes: Opportunity or privacy threat?
Mohamed S Sarhan, Giacomo Antonello, Hansi Weissensteiner, et al.
JMIR Medical Informatics
|
October 19, 2022
Preferences of the Public for Sharing Health Data: Discrete Choice Experiment
Jennifer Viberg Johansson, Heidi Beate Bentzen, Nisha Shah, et al.
European Journal of Human Genetics : EJHG
|
January 4, 2023
Participant perspective on the recall-by-genotype research approach: a mixed-method embedded study with participants of the CHRIS study
Roberta Biasiotto, Maria Kösters, Katharina Tschigg, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 71) with videos related to
Sort By:
Page
of 8
Journal of Community Genetics
|
September 19, 2017
Legal issues in governing genetic biobanks: the Italian framework as a case study for the implications for citizen's health through public-private initiatives
Cinzia Piciocchi, Rossana Ducato, Lucia Martinelli, et al.
Journal of Community Genetics
|
September 27, 2017
How to responsibly acknowledge research work in the era of big data and biobanks: ethical aspects of the Bioresource Research Impact Factor (BRIF)
Heidi Carmen Howard, Deborah Mascalzoni, Laurence Mabile, et al.
Biopreservation and Biobanking
|
December 6, 2021
Governance of Access in Biobanking: The Case of Telethon Network of Genetic Biobanks
Sofia Iacomussi, Lorena Casareto, Manuela Locatelli, et al.
Journal of Community Genetics
|
September 26, 2024
How to communicate and what to disclose to participants in a recall-by-genotype research approach: a multistep empirical study
Katharina Tschigg, Luca Consoli, Norbert Brüggemann, et al.
Nature Reviews. Genetics
|
July 4, 2013
Rare diseases and now rare data?
Deborah Mascalzoni, Bartha Maria Knoppers, Ségolène Aymé, et al.
European Journal of Human Genetics : EJHG
|
September 6, 2022
Ten years of dynamic consent in the CHRIS study: informed consent as a dynamic process
Deborah Mascalzoni, Roberto Melotti, Cristian Pattaro, et al.
International Journal of Environmental Research and Public Health
|
September 26, 2018
Meeting Patients' Right to the Correct Diagnosis: Ongoing International Initiatives on Undiagnosed Rare Diseases and Ethical and Social Issues
Sabina Gainotti, Deborah Mascalzoni, Virginie Bros-Facer, et al.
Cell
|
May 16, 2025
Human mitochondrial DNA in public metagenomes: Opportunity or privacy threat?
Mohamed S Sarhan, Giacomo Antonello, Hansi Weissensteiner, et al.
JMIR Medical Informatics
|
October 19, 2022
Preferences of the Public for Sharing Health Data: Discrete Choice Experiment
Jennifer Viberg Johansson, Heidi Beate Bentzen, Nisha Shah, et al.
European Journal of Human Genetics : EJHG
|
January 4, 2023
Participant perspective on the recall-by-genotype research approach: a mixed-method embedded study with participants of the CHRIS study
Roberta Biasiotto, Maria Kösters, Katharina Tschigg, et al.
Page
of 8