Assessment of knowledge about biobanking among healthcare students and their willingness to donate biospecimens

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Last Posted: May 11, 2017

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• Assessment of knowledge about biobanking among healthcare students and their willingness to donate biospecimens.  
  Merdad Leena et al. BMC medical ethics 2017 May 18(1) 32
• Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.  
  Sanderson Saskia C et al. American journal of human genetics 2017 Mar 100(3) 414-427
• Community recommendations on biobank governance: Results from a deliberative community engagement in California.  
  Dry Sarah M et al. PloS one 2017 12(2) e0172582
• Engaging a state: Facebook comments on a large population biobank.  
  Platt Tevah et al. Journal of community genetics 2017 Apr
• A qualitative study of adolescents' understanding of biobanks and their attitudes toward participation, re-contact, and data sharing.  
  Murad Andrea M et al. American journal of medical genetics. Part A 2017 Apr 173(4) 930-937
• Genetic Testing and Molecular Biomarkers  
  Genetic Testing & Biomarkers, March 2017
• "Still Rather Hazy at Present": Citizens' and Physicians' Views on Returning Results from Biobank Research Using Broad Consent.  
  Barazzetti Gaia et al. Genetic testing and molecular biomarkers 2017 Mar 21(3) 159-165
• Regulation of genomic and biobanking research in Africa: a content analysis of ethics guidelines, policies and procedures from 22 African countries.  
  de Vries Jantina et al. BMC medical ethics 2017 Feb 18(1) 8
• Whose Biobank? Should Biobanks Serve Research Interests or the Needs for Personalized Medicine? Analysis of the Hungarian Law.  
  Sándor Judit et al. Genetic testing and molecular biomarkers 2017 Jan
• Access Governance for Biobanks: The Case of the BioSHaRE-EU Cohorts.  
  Kaye Jane et al. Biopreservation and biobanking 2016 Jun 14(3) 201-6
• Lay Attitudes Toward Trust, Uncertainty, and the Return of Pediatric Research Results in Biobanking.  
  Lynch John et al. AJOB empirical bioethics 2016 7(3) 160-166
• Access policies in biobank research: what criteria do they include and how publicly available are they? A cross-sectional study.  
  Langhof Holger et al. European journal of human genetics : EJHG 2016 Dec
• Business Planning in Biobanking: How to Implement a Tool for Sustainability.  
  Ciaburri Mirella et al. Biopreservation and biobanking 2016 Nov
• Conducting a large, multi-site survey about patients' views on broad consent: challenges and solutions.  
  Smith Maureen E et al. BMC medical research methodology 2016 Nov 16(1) 162
• The alliance between genetic biobanks and patient organisations: the experience of the telethon network of genetic biobanks.  
  Baldo Chiara et al. Orphanet journal of rare diseases 2016 Oct 11(1) 142
• "It's all about trust": reflections of researchers on the complexity and controversy surrounding biobanking in South Africa.  
  Moodley Keymanthri et al. BMC medical ethics 2016 Oct 17(1) 57

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