{ "items": [ "\n\n
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\n Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.\n

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\n \n Journal article\n \n

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Quinlan-Jones E. et al, (2016), Prenat Diagn, 36, 935 - 941

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\n Development of drugs for severe malaria in children.\n

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\n \n Journal article\n \n

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Cheah PY. et al, (2016), Int Health, 8, 313 - 316

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\n The genetic assessment of looked after children: common reasons for referral and recent advances.\n

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\n \n Journal article\n \n

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Parker MJ. et al, (2016), Arch Dis Child, 101, 581 - 584

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\n Ethical challenges in designing and conducting medicine quality surveys.\n

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\n \n Journal article\n \n

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Tabernero P. et al, (2016), Trop Med Int Health, 21, 799 - 806

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\n Public/community engagement in health research with men who have sex with men in sub-Saharan Africa: challenges and opportunities.\n

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\n \n Journal article\n \n

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Molyneux S. et al, (2016), Health Res Policy Syst, 14

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\n The ethics of sustainable genomic research in Africa.\n

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\n \n Journal article\n \n

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Parker M. and Kwiatkowski DP., (2016), Genome Biol, 17

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\n What is the role of individual accountability in patient safety? A multi-site ethnographic study.\n

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\n \n Journal article\n \n

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Aveling E-L. et al, (2016), Sociol Health Illn, 38, 216 - 232

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\n Good and Bad Research Collaborations: Researchers' Views on Science and Ethics in Global Health Research.\n

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\n \n Journal article\n \n

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Parker M. and Kingori P., (2016), PLoS One, 11

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\n Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.\n

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\n \n Journal article\n \n

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Middleton A. et al, (2016), Eur J Hum Genet, 24, 21 - 29

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\n A global reference for human genetic variation.\n

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\n \n Journal article\n \n

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1000 Genomes Project Consortium None. et al, (2015), Nature, 526, 68 - 74

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\n Potential research participants support the return of raw sequence data.\n

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\n \n Journal article\n \n

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Middleton A. et al, (2015), J Med Genet, 52, 571 - 574

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\n Sharing Public Health Research Data: Toward the Development of Ethical Data-Sharing Practice in Low- and Middle-Income Settings.\n

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\n \n Journal article\n \n

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Parker M. and Bull S., (2015), J Empir Res Hum Res Ethics, 10, 217 - 224

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\n Views of Ethical Best Practices in Sharing Individual-Level Data From Medical and Public Health Research: A Systematic Scoping Review.\n

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\n \n Journal article\n \n

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Bull S. et al, (2015), J Empir Res Hum Res Ethics, 10, 225 - 238

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\n Sweat, Skepticism, and Uncharted Territory: A Qualitative Study of Opinions on Data Sharing Among Public Health Researchers and Research Participants in Mumbai, India.\n

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\n \n Journal article\n \n

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Hate K. et al, (2015), J Empir Res Hum Res Ethics, 10, 239 - 250

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\n Trust, Respect, and Reciprocity: Informing Culturally Appropriate Data-Sharing Practice in Vietnam.\n

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\n \n Journal article\n \n

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Merson L. et al, (2015), J Empir Res Hum Res Ethics, 10, 251 - 263

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\n Developing Ethical Practices for Public Health Research Data Sharing in South Africa: The Views and Experiences From a Diverse Sample of Research Stakeholders.\n

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\n \n Journal article\n \n

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Denny SG. et al, (2015), J Empir Res Hum Res Ethics, 10, 290 - 301

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\n Involving Research Stakeholders in Developing Policy on Sharing Public Health Research Data in Kenya: Views on Fair Process for Informed Consent, Access Oversight, and Community Engagement.\n

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\n \n Journal article\n \n

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Jao I. et al, (2015), J Empir Res Hum Res Ethics, 10, 264 - 277

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\n Perceived Benefits, Harms, and Views About How to Share Data Responsibly: A Qualitative Study of Experiences With and Attitudes Toward Data Sharing Among Research Staff and Community Representatives in Thailand.\n

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\n \n Journal article\n \n

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Cheah PY. et al, (2015), J Empir Res Hum Res Ethics, 10, 278 - 289

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\n Best Practices for Ethical Sharing of Individual-Level Health Research Data From Low- and Middle-Income Settings.\n

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\n \n Journal article\n \n

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Bull S. et al, (2015), J Empir Res Hum Res Ethics, 10, 302 - 313

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\n Understandings of genomic research in developing countries: a qualitative study of the views of MalariaGEN participants in Mali.\n

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\n \n Journal article\n \n

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Traore K. et al, (2015), BMC Med Ethics, 16

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