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References
Børsting C, Morling N (2015) Next generation sequencing and its applications in forensic genetics. Forensic Sci Int Genet 18:78–89. https://doi.org/10.1016/j.fsigen.2015.02.002
Council of Europe (2014) Guidelines on the role of court-appointed experts in judicial proceedings of Council of Europe’s Member States. Document adopted by CEPEJ at its 24th Plenary meeting. https://rm.coe.int/168074827a. Accessed 10 Mar 2020
Williams R, Wienroth M (2017) Social and ethical aspects of forensic genetics: a critical review. Forensic Sci Rev 29:145–169
Wienroth M, Morling N, Williams R (2014) Technological innovations in forensic genetics: social, legal and ethical aspects. Recent Adv DNA Genet Seq 8:98–103. https://doi.org/10.2174/2352092209666150328010557
Boardman F, Hale R (2018) Responsibility, identity, and genomic sequencing: a comparison of published recommendations and patient perspectives on accepting or declining incidental findings. Mol Genet Genom Med 6:1079–1096. https://doi.org/10.1002/mgg3.485
Koplin JJ, Savulescu J, Vears DF (2020) Why genomics researchers are sometimes morally required to hunt for secondary findings. BMC Med Ethics 21:11. https://doi.org/10.1186/s12910-020-0449-8
Christenhusz GM, Devriendt K, Dierickx K (2013) To tell or not to tell? A systematic review of ethical refections on incidental findings arising in genetics contexts. Eur J Hum Genet 21:248–255. https://doi.org/10.1038/ejhg.2012.130
Perry TJ, Patton SI, Farmer MB, Hurst CB, McGwin G, Robin NH (2020) The duty to warn at-risk relatives-The experience of genetic counselors and medical geneticists. Am J Med Genet A 182:314–321. https://doi.org/10.1002/ajmg.a.61425
Middleton A, Milne R, Robarts L, Roberts J, Patch C (2019) Should doctors have a legal duty to warn relatives of their genetic risks? Lancet 394:2133–2135. https://doi.org/10.1016/S0140-6736(19)32941-1
Suter S (2019) Legal challenges in genetics, including duty to warn and genetic discrimination. Cold Spring Harb Perspect Med a036665. https://doi.org/10.1101/cshperspect.a036665
Michaud K, Fellmann F, Abriel H, Beckmann JS, Mangin P, Elger BS (2009) Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration. Swiss Med Wkly 139:712–718
Elger BS, Michaud K, Fellmann F, Mangin P (2010) Sudden death: ethical and legal problems of post-mortem forensic genetic testing for hereditary cardiac diseases. Clin Genet Mar 77:287–292. https://doi.org/10.1111/j.1399-0004.2009.01293.x
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L.C. and K.D. contributed to the study conception and design. The first draft of the manuscript was written by L.C. and P.T., and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.
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Caenazzo, L., Tozzo, P. & Dierickx, K. Incidental findings in forensics: are we sure that it is a question easy to deal with?. Int J Legal Med 135, 591–592 (2021). https://doi.org/10.1007/s00414-020-02427-5
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DOI: https://doi.org/10.1007/s00414-020-02427-5