Last Posted: Apr 04, 2019
- Managing the Unimaginable: Biobank Participant Views on Reconsent for Whole Genome Sequencing of Stored Biospecimens.
Sutton Erica J et al. Biopreservation and biobanking 2019 Mar - Linking pre-existing biorepositories for medical research: the PopGen 2.0 Network.
Lieb Wolfgang et al. Journal of community genetics 2019 Mar - Personalized Medicine and the Power of Electronic Health Records.
Abul-Husn Noura S et al. Cell 2019 Mar 177(1) 58-69 - Anticipatory Waivers of Consent for Pediatric Biobanking.
Hartsock Jane A et al. Ethics & human research 2019 Mar 41(2) 14-21 - National Rare Diseases Registry System of China and Related Cohort Studies: Vision and Roadmap.
Feng Shi et al. Human gene therapy 2018 29(2) 128-135 - Outlier detection for questionnaire data in biobanks.
Sakurai Rieko et al. International journal of epidemiology 2019 Mar - New genetic data on 50,000 UK Biobank participants made available to the global health research community
UK Biobank, March 10, 2019 - Best Practices for Obtaining Genomic Consent in Pediatric Traumatic Brain Injury Research.
Schnur Kaylee C et al. Nursing research 68(2) E11-E20 - Ethical implications of using biobanks and population databases for genetic suicide research.
Shade Jess et al. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2019 Feb - Next Chapter of the Taiwan Biobank: Sustainability and Perspectives.
Lin Jui-Chu et al. Biopreservation and biobanking 2019 Feb
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