Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference22 articles.
1. Hart MR, Biesecker BB, Blout CL, Christensen KD, Amendola LM, Bergstrom KL, et al. Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study. Genet Med. 2019;21:1100–10.
2. eMERGE Clinical Annotation Working Group. Frequency of genomic secondary findings among 21,915 eMERGE network participants. Genet Med. 2020;22:1470–7.
3. The National Health and Medical Research Council, the Australian Research Council, Universities Australia. National Statement on Ethical Conduct in Human Research. Commonwealth of Australia, Canberra: National Health and Medical Research Council; 2007 (Updated 2018).
4. Forrest LE, Young MA. Clinically significant germline mutations in cancer-causing genes identified through research studies should be offered to research participants by genetic counselors. J Clin Oncol. 2016;34:898–901.
5. Henrikson NB, Scrol A, Leppig KA, Ralston JD, Larson EB, Jarvik GP. Preferences of biobank participants for receiving actionable genomic test results: results of a recontacting study. Genet Med. 2021;23:1163–6.
Cited by
9 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献