- An empirical survey on biobanking of human genetic material and data in six EU countries.Isabelle Hirtzlin, Christine Dubreuil, Nathalie Préaubert, Jenny Duchier, Brigitte Jansen, Jürgen Simon, Paula Lobatao De Faria, Anna Perez-Lezaun, Bert Visser, Garrath D. Williams, Anne Cambon-Thomsen & The Eurogenbank Consortium - 2003 - European Journal of Human Genetics 11:475–488.details
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Collection, storage and use of blood samples for future research: views of Egyptian patients expressed in a cross-sectional survey.A. Abou-Zeid, H. Silverman, M. Shehata, M. Shams, M. Elshabrawy, T. Hifnawy, S. A. Rahman, B. Galal, H. Sleem, N. Mikhail & N. Moharram - 2010 - Journal of Medical Ethics 36 (9):539-547.details
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Attitudes towards transfers of human tissue samples across borders: An international survey of researchers and policy makers in five countries.Xinqing Zhang, Kenji Matsui, Benjamin Krohmal, Alaa Abou Zeid, Vasantha Muthuswamy, Young Mo Koo, Yoshikuni Kita & Reidar K. Lie - 2010 - BMC Medical Ethics 11 (1):16-.details
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Research on stored biological samples: the views of Ugandans.David Wendler, Christine Pace, Ambrose O. Talisuna, Faustine Maiso, Christine Grady & Ezekiel Emanuel - 2005 - IRB: Ethics & Human Research 27 (2):1.details
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"It's for a good cause, isn't it?" - Exploring views of South African TB research participants on sample storage and re-use.Gerrit van Schalkwyk, Jantina de Vries & Keymanthri Moodley - 2012 - BMC Medical Ethics 13 (1):19-.details
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Seeking consent to genetic and genomic research in a rural Ghanaian setting: a qualitative study of the MalariaGEN experience. [REVIEW]P. Tindana, S. Bull, L. Amenga-Etego, J. Vries, R. Aborigo, K. Koram, D. Kwiatkowski & M. Parker - 2012 - BMC Medical Ethics 13 (1):15-15.details
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Researchers' preferences and attitudes on ethical aspects of genomics research: a comparative study between the USA and Spain.M. Ruiz-Canela, J. I. Valle-Mansilla & D. P. Sulmasy - 2009 - Journal of Medical Ethics 35 (4):251-257.details
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Health Research Ethics Committees in South Africa 12 years into democracy.Myer Landon & Moodley Keymanthri - 2007 - BMC Medical Ethics 8 (1):1-8.details
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Examining the public refusal to consent to DNA biobanking: empirical data from a Swedish population-based study.P. A. Melas, L. K. Sjoholm, T. Forsner, M. Edhborg, N. Juth, Y. Forsell & C. Lavebratt - 2010 - Journal of Medical Ethics 36 (2):93-98.details
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Seeking consent to genetic and genomic research in a rural Ghanaian setting: A qualitative study of the MalariaGEN experience. [REVIEW]Paulina Tindana, Susan Bull, Lucas Amenga-Etego, Jantina de Vries, Raymond Aborigo, Kwadwo Koram, Dominic Kwiatkowski & Michael Parker - 2012 - BMC Medical Ethics 13 (1):15-.details
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Qualitative study of knowledge and attitudes to biobanking among lay persons in Nigeria.Michael A. Igbe & Clement A. Adebamowo - 2012 - BMC Medical Ethics 13 (1):27-.details
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Who's minding the shop? The role of Canadian research ethics boards in the creation and uses of registries and biobanks.Elaine Gibson, Kevin Brazil, Michael D. Coughlin, Claudia Emerson, Francois Fournier, Lisa Schwartz, Karen V. Szala-Meneok, Karen M. Weisbaum & Donald J. Willison - 2008 - BMC Medical Ethics 9 (1):17-.details
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