Managers of genomic biobanks constantly face ethical and legal challenges ranging from issues associated with the informed consent process to procedural concerns related to access by researchers. Yet, with the availability of next-generation sequencing technologies, one topic is emerging as the focus of ongoing debate: the return of individual research results and incidental findings to participants. This article examines this topic from an international perspective, where policies and guidelines discussing the matter in the context of genomic biobanks and genomic research are analyzed and commented. This approach aims to highlight the shortcomings of these international norms, mainly the danger arising from both the therapeutic misconception and the conflation of research results with incidental findings. This article suggests some elements to consider in order to complement available guidance at the international level.
Genet Med 2012:14(4):484–489
Genomic biobanks have been identified as “vital research tools in the drive to uncover the consequences of human health and disease.”1 These organized collections of human biological material and associated data2 have even been described as one of the top 10 ideas changing the world.3 With scientists recognizing that common diseases result from a multitude of interactions between genetic variation, lifestyle behaviors, and the environment, there has been a rise in the number of biobanks in the past decades, especially in large-scale genomic studies (over 10,000 individuals), which aim to produce aggregate findings derived from the data and samples of groups of persons.4 The collection of data and samples and their analysis in the context of biobanks have traditionally led to debates about the return of individual research results (IRRs) to participants.5 Although some biobanks limit feedback to general results (sometimes called “aggregate results”),6 others that recruit through physicians may return individual findings to research participants.7 For the purposes of this text, IRRs are results discovered during the course of a research project—and within its objectives—that concern an individual participant and have potential health or reproductive importance.8
With next-generation sequencing technology producing vast amounts of data, the debate has become more complex due to the ensuing increase in incidental findings (IFs) in research.9 IFs are defined as findings concerning a research participant that have potential health or reproductive importance and are discovered during the course of research but are outside the objectives of the project.10 The rise of data-intensive science stemming from the use of high-throughput technology has led to a debate on the pertinence of returning IRRs and IFs in genomic biobanks.11,12,13 Although most of these debates are jurisdiction-specific, how is the issue of the return of IRRs and IFs reflected in international norms? What trends, if any, are discernable? The term “international” refers to laws, guidelines, and policies emanating from non-US countries and international organizations. Analyzing the issue of return of IRRs and IFs from an international perspective will serve to highlight current trends as well as the factors influencing possible future change.
Methodology and Results
The international documents retrieved and referenced in this text were collected using the PopGen Module (http://www.popgen.info) of the HumGen International Database (http://www.humgen.org), a database of international, national, and regional guidelines and policies specific to human genetic research. The PopGen module is a specialized database composed of laws, guidelines, policies, and literature addressing the legal and ethical issues in biobanks generally and population biobanks more specifically. For the purpose of our research and in order to focus only on pertinent documents, the keywords “biobanks” and “communication of results” were used. Keywords such as “research result” or “incidental findings” were not available. All organizations were selected, and no limitations were set as to jurisdiction. This provided a large selection of documents. Only English documents dating from 1985 to 2011 (the default date restriction) were queried. This search resulted in 149 results.
US documents were removed from the list of documents retrieved, which reduced the number of results to 125. A thorough analysis of the remaining documents further narrowed the number of laws, policies, and guidelines pertinent to the return of IRRs and IFs to 15. This small number was expected, given that the term “communication of results” covers a wide array of feedback procedures and communication is not limited to research results or IFs. Moreover, many of these documents mention IFs or research results but do not provide guidance. The final list ( Table 1 ) includes both laws and guidelines. Laws are binding, whereas guidelines are generally nonbinding but may be considered professional norms.14
Therapeutic misconception15 occurs when a “research subject … inaccurately attributes therapeutic intent to research procedures.”15 It has been argued that alluding to the possible future disclosure of any IRRs and IFs promotes the therapeutic misconception. Indeed, the Singapore Bioethics Advisory Committee’s 2002 Human Tissue Research Report16 maintains that “… donors should not expect any personal or direct benefit from the donation of tissue, including information of any medical condition or predisposition or likelihood of such discovered in the course of research on the sample. Likewise, researchers and tissue bankers should not be under an obligation to disclose such information to the donors, unless they have agreed to do so in advance of the donation.”16
The Singapore Bioethics Advisory Committee reiterates this stance in its 2005 document, titled Ethical, Legal and Social Issues in Genetic Testing and Genetic Research.17 It posits that since “human genetics research enhances our understanding of the genetic basis of disease and how genetic and environmental factors influence one’s health,”17 the main goal is not to offer research participants or their families “specific information about their genetic status or health.”17 This “no-return” policy is not new to the biobanking field and is largely followed by large-scale, longitudinal population biobanks that are mainly epidemiological in nature.18,19,20,21,22 Yet large-scale biobanks do provide their participants with feedback at assessment—which is provided as a matter of course and should not be confused with eventual IRRs, and more importantly, should not be considered equivalent to a medical checkup.23
That being said, it could be argued that the risk of therapeutic misconception engendered by return of results can be lessened if limited to disclosure of findings in exceptional cases where they are analytically valid, clinically significant, and medically actionable.23 It is policies that mandate broader and imprecise obligations that constitute a greater risk. Witness the 2010 Canadian Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans,24 which states that “researchers have an obligation to disclose to the participant any material incidental findings discovered in the course of research.”24 In this text, material IFs are defined as having “significant welfare implications for the participant, whether health-related, psychological or social.”24 Return of these findings is described as an ethical “obligation.” The statement does, however, encourage researchers who “are unsure of how to interpret findings or uncertain whether findings are material”24 to consult with colleagues or refer to standards in their discipline. There could be several practical limitations to such a broad approach in the biobanking field, especially with the presence of privacy and confidentiality clauses in access agreements signed by researchers wishing to use biobanks.25 Faced with an open-ended ethical obligation, researchers might be inclined in cases of doubt to systematically disclose findings. If so, rather than reflecting an exceptional situation, the disclosure of findings may well become the rule in cases of uncertainty, hence indirectly promoting the therapeutic misconception.
The Conflation of Research Results and Incidental Findings
Another visible trend in some of the international documents reviewed was the tendency to conflate various notions, such as (i) general research results with IRRs, (ii) the return of IRRs with IFs, and (iii) the return of IRRs and IFs with the legal duty to rescue.
General research results versus IRRs
General research results and individual results are distinct, as are as well the modalities and conditions for their return.23 As mentioned earlier, IRRs concern an individual participant and general research results concern a group of persons. Whereas general results are largely returned through newsletters and websites,26 IRRs are returned per the policies of the biobanks as reflected in their informed consent forms and information brochures.27
Yet, while differences between these two types of results are obvious, some international norms conflate the two. One example of such confusion can be found in the Italian Society of Human Genetics’ 2004 Guidelines for Genetic Biobanks,28 which state that the research participant “should have the possibility to take separate decisions regarding whether: to wish/not wish to be informed about the results or diagnostic possibilities deriving from continuing research.”28 It is not clear whether the term “results” refers to general or IRRs. The issues associated with the return of individual as opposed to general results are not the same, and conflating the two can lead the research participants to expect future notice of both types of results—an expectation that could sometimes turn out to be groundless. That being said, this lack of clarity could be the result of a modest translation of this document from Italian by the country’s Society of Human Genetics.
Along the same lines, the opinion of the German National Ethics Council’s 2004 Biobanks for Research29 specifies that it would involve unacceptable effort and expense to inform donors of “all results of the research.”29 Although later discussing “personal results,”29 the document is not consistent in differentiating between general and IRRs. However, the German council’s 2010 opinion on Human Biobanks for Research clearly specifies “individual research results”30 in its text, which lists the reporting of such results as an occasion “for the donor to be contacted again in the future.”30
IRRs versus IFs
The difference between IRRs and IFs ultimately relates to the objectives associated with the research project in question. Nonetheless, many international norms do not explicitly distinguish between them. An interesting example is Estonia’s 2001 Human Genes Research Act,31 which states that gene donors might not always want “data on hereditary characteristics and genetic risks obtained as a result of genetic research.”31 This Act uses the word “risks,” which could emanate from IRRs or IFs. The Norwegian University of Science and Technology’s 2004 Medical Technology: Health Surveys and Biobanking32 uses a similar term when it specifies that “some individuals could possibly benefit by being contacted when unexpected genetic risks for future disease were discovered.”32
In 2008, the Canadian College of Medical Geneticists and Canadian Association of Genetic Counsellors adopted a Joint Statement on the Process of Informed Consent for Genetic Research.33 This document states that if individual results are to be disclosed, then participants should be made aware that “unexpected results” could be obtained.33 It is unclear whether this joint statement refers to IRRs or IFs more specifically, or even both.
The same could be said of Taiwan’s 2010 Human Biobank Management Act,34 one of the few Asian laws on biobanks. The Act discusses the need for the research participants to be made aware of “any possible impacts of the genetic information derived from the biological specimens on the participant, and his/her relatives or an ethnic group.”34 Here again, the term “genetic information” is broad and it is unclear whether this refers to IRRs or to IFs.
Although the conditions for returning IFs and IRRs may be similar,8 an important difference lies in the expertise of the researchers handling them. In the case of research results, the researcher is usually competent to interpret them. The same cannot be said for IFs, which are not only largely clinical in nature, but could also fall outside the particular field of expertise of the researcher who discovered them. Echoing a similar concern in the Therapeutic Misconception section, a conflation between IRRs and IFs could create arduous responsibilities for researchers and prompt some of them to return potentially important health information that may be discovered—although originally unexpected—for fear of liability.14,35
Return of IRRs and IFs versus legal duty to rescue
The duty to rescue is a tradition found in many civil law jurisdictions and often carries penal sanctions. Generally, this duty is characterized as an obligation to provide assistance to an individual whose physical integrity is in peril.36 In other words, there needs to be a situation where an identifiable individual is faced with immediate danger. Although not explicitly addressing the duty to rescue, the World Health Organization’s European Partnership on Patients’ Rights and Citizens’ Empowerment’s 2004 report37 generally reflects the legal stance in Europe. It states that because “research includes matters of unknown future import, sometimes unexpected findings can be generated”;37 and when “an immediate and clear benefit to identifiable individuals can be achieved … [which] will avert or minimize significant harm to the relevant individuals,”37 such findings should be returned. Another example comes from the Spanish 2007 Law on Biomedical Research, where the participant’s right “not to know” about IFs is affirmed.38 This law allows a close family member or a representative to be informed of IFs if this will avoid a serious damage to the health of the participants or that of their biological family.38
Although some authors have reconciled the notion of return of findings with an ethical duty to rescue,39 this article posits that the legal duty to rescue is not a solid basis for a duty to return research results and IFs. Currently, five criteria for return dominate the debate on the return of IRRs and IFs:
”The findings are analytically valid;
Returning them to the donor comports with applicable law …;
The donor has been offered the option of consenting to return of individual findings … and has opted to receive them;
The findings reveal an established and substantial risk of (a) a serious health condition, or (b) a serious condition of reproductive importance …; and
The findings are actionable … .”8
It is conceivable that situations giving rise to a duty to rescue could satisfy these conditions, but that will not always be the case. One of the issues here is participants’ right not to know. Unless explicitly mentioned—as in the Spanish biomedical research law—the element of consent and the right not to know are generally not at the forefront of decisions based on a duty to rescue. As mentioned earlier, what characterizes the duty to rescue is the seriousness and urgency of the situation. Rarely is genetic information “urgent.” Moreover, what happens when participants have clearly consented not to receive IRRs or IFs? Using the concept of a duty to rescue in this case could be problematic, as it may ignore the participant’s decision not to know. In an effort to provide consistent and harmonized guidance to researchers for the return of IRRs and IFs, the concept of the duty to rescue also falls short because it is not a legal obligation in all jurisdictions.23
Finally, another potential difficulty in using the concept of duty to rescue as a basis for the return of IRRs and IFs is the practical limitations associated with the nature of some biobanks. In large-scale, longitudinal population studies—where samples and data are collected and stored for future unspecified research, for example—it will be difficult to apply the urgency criterion once the data and samples are stored, given that discovering findings that satisfy the requirement of a legal duty to rescue is hypothetical and could stretch over time.
Untying The Gordian Knot: Elements to Consider
Our comparative review of international normative guidance provides an interesting perspective that complements the analysis of issues in specific jurisdictions. As biobanking becomes more international, such a review is necessary. That being said, it is clear from the sections on Therapeutic Misconception and The Conflation of Research Results and Incidental Findings that the existing international norms pertinent to the return of IRRs and IFs are not consistent. They use ambiguous terminology and conflate different concepts. Creating a lexicon covering IRRs and IFs has been proposed.40 It is necessary, however, that such a lexicon be adopted or adapted by international organizations through a mechanism similar to the International Conference on Harmonization.41 Such a guidance document could include clear definitions of terms such as IFs, return of results, and clinical utility. This lexicon, if disseminated internationally, would provide much needed consistency in international norms and could reduce ambiguity and contradictions.
Moreover, it is important for any international guidelines on the matter to provide recommendations on the decision-making process leading to the return of IRRs and IFs, similar to the one proposed by the Working Group recommendations in this issue8 and the 2010 National Cancer Institute Workshop on the Release of Research Results to Participants in Biospecimen Studies.27 Indeed, future guidelines should include practical considerations for establishing analytical validity, assessing the seriousness of the risk, and concretizing actionability, while recognizing the different types of studies involved, a point we will clarify in the following.
That being said, any future international guidance document should uphold the discretion of researchers, as evident in documents such as the Council for International Organizations of Medical Sciences’ 2009 International Ethical Guidelines for Epidemiological Studies,42 the 2009 Organization for Economic Co-operation and Development Guidelines on Human Biobanks and Genetic Research Databases43 and the Australian Office of Population Health Genomics’ 2010 Guidelines for Human Biobanks, Genetic Research Databases and Associated Data.44 While offering practical guidance on establishing analytical validity, and on the seriousness of risk and actionability, some discretion should be provided to researchers to determine whether findings satisfy these conditions. Due to the potential scientific uncertainty of some findings,45 such an approach would provide researchers with much needed professional leverage and avoid both stringent and open-ended obligations.
Finally, when one scrutinizes the scope of the international guidance available on the return of research results and IFs, it becomes clear that they are not homogeneous: some provide guidance for research at large; others are specific to tissue biobanking or genetic research. Differences are therefore understandable. We echo calls for distinguishing different contexts as concerns the return of findings to participants, based on the nature of the study in question.46 In fact, although it is important to remain consistent with the general provisions existing in the majority of laws, regulations, policies, and guidelines, homogeneous approaches to the micromanagement of IRRs and IFs at the international level risk harming the integrity, credibility, and transparency of research.25 For example, imposing the same modalities on the return of IRRs and IFs that are currently applicable in clinical trials on the broader infrastructure resource mission of population biobanks could undermine their longitudinal design to say nothing of the altruistic nature of the contribution of a citizen of a given country. This could inadvertently create unrealistic participant expectations and limitless, undefined duties for researchers.
We discern two trends from our analysis. In a culture of heightened attention to IRRs and IFs, lack of specificity in obligations promotes professional confusion as well as the therapeutic misconception. Second, the tendency to confuse notions, such as general versus individual results, research results versus IFs, and the return of findings versus the duty to rescue, slows progress. Three key innovations are needed to address the elements to consider identified in the section on Untying the Gordian Knot: Elements to Consider. First, it is important to encourage endeavors that aim to provide a clear set of definitions related to the return of IRRs and IFs at the international level. This will allow for much needed consistency in international norms and will reduce ambiguity and contradictions. Second, clear practical guidance establishing the principal conditions for the return of findings, such as analytical validity, seriousness of the risk, and actionability must also be offered at the international level. This will create an important and consistent approach for researchers working in international biobanking initiatives across various jurisdictions. Finally, approaches to IRRs and IFs will need to reflect the types of biobanks and their contexts as well as the nature of the participation in question. Indeed, when proposing norms for the return of IRRs and IFs, the key will be to provide simple criteria that do not cover all possible situations but instead distinguish between the different research objectives and contexts. The Public Population Project in Genomics and Society provides a recent example of this.47 At a time when it is perceived as increasingly difficult to establish the scientific certainty of genomic findings—where “distinctive cultures with respect to interpreting and reporting results” 48 exist—specificity, clarity, and transparency in policy will provide proper guidance that can bolster the trust of participants who altruistically contribute their data and samples for research.25
The authors declare no conflict of interest.
Chalmers D, Nicol D . Human genetic research databases and biobanks: towards uniform terminology and Australian best practice. J Law Med 2008;15:538–555.
P3G Lexicon—PopGen, Center of Genomics and Policy, 2011. http://www.popgen.info Accessed 9 September 2011.
Parks A . 10 ideas changing the world right now: biobanks. Time 2009. http://www.time.com/time/specials/packages/article/0,28804,1884779_1884782_1884766,00.html. Accessed 22 August 2011.
Meulenkamp TM, Gevers SK, Bovenberg JA, Koppelman GH, van Hylckama Vlieg A, Smets EM . Communication of biobanks’ research results: what do (potential) participants want? Am J Med Genet A 2010;152A:2482–2492.
Knoppers BM, Abdul-Rahman (Zawati) M . Biobanks in the literature. In: Elger B, Biller-Andorno N, Mauron A, Capron A (eds). Ethical Issues in Governing Biobanks: Global Perspectives. Ashgate: Aldershot, UK, 2008.
ALSPAC Ethics and Law Committee. Policy guidance regarding divulging biomedical information to individual participants, 2010. http://www.bristol.ac.uk/alspac/documents/divulgingbiomed.pdf. Accessed 14 April 2011.
Wallace S, Kent A . Population biobanks and returning individual research results – mission impossible or new directions?” Hum Genet 2011;130: 393–401.
Wolf SM, Crock BN, Van Ness B, et al. Managing incidental findings and research results in genomic research involving biobanks and archived datasets. Genetics in Medicine, 2012;14:361–384.
Zawati MH, Hendy M, Joly Y . Incidental findings in data-intensive postgenomics science and legal liability of clinician-researchers: ready for vaccinomics? OMICS 2011;15:615–624.
Wolf SM, Lawrenz FP, Nelson CA, et al. Managing incidental findings in human subjects research: analysis and recommendations. J Law Med Ethics 2008;36:219–248, 211.
Forsberg JS, Hansson MG, Eriksson S . Changing perspectives in biobank research: from individual rights to concerns about public health regarding the return of results. Eur J Hum Genet 2009;17:1544–1549.
Bredenoord AL, Kroes HY, Cuppen E, Parker M, van Delden JJ . Disclosure of individual genetic data to research participants: the debate reconsidered. Trends Genet 2011;27:41–47.
Miller FA, Christensen R, Giacomini M, Robert JS . Duty to disclose what? Querying the putative obligation to return research results to participants. J Med Ethics 2008;34:210–213.
Zawati MH, Van Ness B, Knoppers BM . Incidental findings in genomic research: a review of international norms. GenEdit 2011;9:1–8.
Lidz CW, Appelbaum PS . The therapeutic misconception: problems and solutions. Med Care 2002;40(suppl 9):V55–V63.
Singapore Bioethics Advisory Committee. Human tissue research, 2002. http://www.bioethics-singapore.org/uploadfile/60104%20PMHT%20Research.pdf. Accessed 8 September 2011.
Singapore Bioethics Advisory Committee. Ethical, legal and social issues in genetic testing and genetic research: a consultation paper, 2005. http://www.bioethics-singapore.org/resources/pdf/GT%20CP%20Final.pdf. Accessed 10 June 2011.
CARTaGENE. Information brochure for participants. http://www.cartagene.qc.ca/images/stories/cartagene_brochure.pdf. Accessed 9 September 2011.
UK Biobank. Ethics and governance framework, 2007. http://www.ukbiobank.ac.uk/docs/EGF20082.pdf. Accessed 9 September 2011.
Generation Scotland, FAQs website. http://www.generationscotland.org/index.php?option=com_content&view-article&id=43&itemid=50#BAP5. Accessed 15 June 2011.
ALSPAC Ethics and Law Committee. Policy guidance regarding divulging biomedical information to individual participants, 2010. http://www.bristol.ac.uk/alspac/documents/divulgingbiomed.pdf. Accessed 12 June 2011.
LifeGene Ethics Group. LifeGene ethics policy, 2010. https://www.lifegene.se/PageFiles/104/20100916_LifeGene_Ethics_Policy4.3.docx. Accessed 16 June 2011.
Zawati MH, Rioux A . Biobanks and the return of research results: out with the old and in with the new? J Law Med Ethics 2011;39:614–620.
Canadian Institutes of Health Research (CIHR). Natural Sciences and Engineering Research Council of Canada, Social Sciences and Humanities Research Council of Canada, Tri-council policy statement: ethical conduct for research involving humans (2010), Ottawa, Art. 3.4, 34.
Knoppers B, Zawati M . Population biobanks and access. In: Rodota S, Zatti P (eds) Il Governo Del Corpo: Trattato Di Biodiritto. Giuffrè Editore: Milan, 2011, 1181–1194.
Participant consent form, Ontario Health Study. https://ontariohealthstudy.ca/files/B4%20Consent%20Form%20ENG.pdf. Accessed 22 August 2011.
Office of Biorepositories and Biospecimen Research, National Cancer Institute, and National Institutes of Health NCI. Report—workshop on release of research results to participants in biospecimen studies, 2011. http://biospecimens.cancer.gov/resources/publications/workshop/rrra.asp.
Italian Society of Human Genetics. Guidelines for genetic biobanks, 2004. http://www.biobanknetwork.org/documents/GUIDELINES.pdf.
German National Ethics Council. Biobanks for research, 2004. http://www.ethikrat.org/_english/publications/Opinion_Biobanks-for-research.pdf. Accessed 9 September 2011.
German National Ethics Council. Human biobanks for research, 2010. http://www.ethikrat.org/files/der_opinion_human-biobanks.pdf. Accessed 9 September 2011.
Estonia Government. Human Genes Research Act, 2000. http://www.legaltext.ee/text/en/X50010.htm. Accessed 9 September 2011.
Norwegian University of Science and Technology. Medical Technology: Health surveys and biobanking, a foresight analysis towards 2020, 2004. http://www.bioethics.ntnu.no/biobanks/documents/Foresightrapport.pdf. Accessed 9 September 2011.
Canadian College of Medical Geneticists & Canadian Association of Genetic Counsellors. Joint statement on the process of informed consent for genetic research, 2008. http://www.ccmg-ccgm.org/pdf/policy/2010/%2822%29%20CCMG_PosStmt_EPP_CAGCInformedConsent_16Jul2008.pdf. Accessed 9 September 2011.
Government of Taiwan. Human Biobank Management Act, 2010. dohlaw.doh.gov.tw/Chi/EngDownLoad.asp?msgid=252&file=cfile1. Accessed 9 September 2011.
Illes J, Chin VN . Bridging philosophical and practical implications of incidental findings in brain research. J Law Med Ethics 2008;36:298–304, 212.
Quebec. Charter of Human Rights and Freedoms, RSQ, c C-12, Article 2. http://www2.publicationsduquebec.gouv.qc.ca/dynamicSearch/telecharge.php?type=2&file=/C_12/C12_A.HTM.
WHO. World Health Organization: European Partnership on Patients’ Rights and Citizens’ Empowerment (EEPRCE), Genetic databases: assessing the benefits and the impact on human & patient rights, 2004.
Spain Parliament: Law 14/2007, of 3 July, on biomedical research. Madrid, s.58(2).
Richardson HS . Incidental findings and ancillary-care obligations. J Law Med Ethics 2008;36:256–70, 211.
Knoppers BM, Dam A . Return of results: towards a lexicon? J Law Med Ethics 2011;39:577–582.
The International Conference on Harmonization. http://www.ich.org. Accessed 11 November 2011.
Council for International Organizations of Medical Science (CIOMS) and World Health Organization (WHO). International ethical guidelines for epidemiological studies, 2009.
Organization for Economic Co-operation and Development. Guidelines for human biobanks and genetic research databases (HBGRD), 2009.
Australia: Western Australia Department of Health, Office of Population Health Genomics – Public Health Division. Guidelines for human biobanks, genetic research databases and associated data, 2010.
Hayeems RZ, Miller FA, Li L, Bytautas JP . Not so simple: a quasi-experimental study of how researchers adjudicate genetic research results. Eur J Hum Genet 2011;19:740–747.
Beskow LM, Burke W . Offering individual genetic research results: context matters. Sci Transl Med 2010;2:38cm20.
Population studies: return of results and incidental findings. Policy Statement, Public Population Project in Genomics and Society, Montreal, 2011. http://www.p3g.org/secretariat/news/P3G%20Return%20of%20Results.pdf
Miller FA, Hayeems RZ, Bytautas JP . What is a meaningful result? Disclosing the results of genomic research in autism to research participants. Eur J Hum Genet 2010;18:867–871.
The authors acknowledge the financial support of the National Institutes of Health, National Human Genome Research Institute grant no. 2-R01HG003178, and the Canadian Partnership Against Cancer. The authors also thank Adrian Thorogood and Supriya Dwivedi for their assistance.
About this article
Cite this article
Zawati, M., Knoppers, B. International normative perspectives on the return of individual research results and incidental findings in genomic biobanks. Genet Med 14, 484–489 (2012). https://doi.org/10.1038/gim.2012.13
- general research results
- genomic research
- incidental findings
- individual research results
- international norms
This article is cited by
Implementation of genomics in medical practice to deliver precision medicine for an Asian population
npj Genomic Medicine (2019)
Ethical frameworks for obtaining informed consent in tumour profiling: an evidence-based case for Singapore
Human Genomics (2017)
Life Sciences, Society and Policy (2015)
Genome Medicine (2015)
Nature Reviews Genetics (2015)