Parents’ attitudes towards research involving genome sequencing of their healthy children: a qualitative study
Author:
Funder
Project funded by the McLaughlin Centre (provided to Y.B.). Y.B. was supported by a New Investigator Award from the Canadian Institutes of Health Research.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://www.nature.com/articles/s41431-023-01476-9.pdf
Reference40 articles.
1. Kalia SS, Adelman K, Bale SJ, Chung WK, Eng C, Evans JP, et al. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. Genet Med. 2017;19:249–55.
2. Van El CG, Cornel MC, Borry P, Hastings RJ, Fellmann F, Hodgson SV, et al. Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics. Eur J Hum Genet. 2013;21:580–4.
3. Boycott K, Hartley T, Adam S, Bernier F, Chong K, Fernandez BA, et al. The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists. J Med Genet. 2015;52:431–7.
4. Jarvik GP, Amendola LM, Berg JS, Brothers K, Clayton EW, Chung W, et al. Return of genomic results to research participants: The floor, the ceiling, and the choices in between. Am J Hum Genet. 2014;94:818–26.
5. Lewis ACF, Knoppers BM, Green RC. An international policy on returning genomic research results. Genome Med. 2021;13:1–3.
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