Public interest in unexpected genomic findings: a survey study identifying aspects of sequencing attitudes that influence preferences-Reference-Cited by-同舟云学术

Public interest in unexpected genomic findings: a survey study identifying aspects of sequencing attitudes that influence preferences

Published:2022-01-21 Issue:2 Volume:13 Page:235-245
ISSN:1868-310X
Container-title:Journal of Community Genetics
language:en
Short-container-title:J Community Genet

Author:

Etchegary Holly^ORCID,Pullman Daryl,Simmonds Charlene,Rahman Proton

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Public Health, Environmental and Occupational Health,Epidemiology

Link

https://link.springer.com/content/pdf/10.1007/s12687-022-00577-0.pdf

Reference38 articles.

1. Abhyankar S, Etchegary H (2019) Rolling out genomic screening: the Newfoundland and Labrador public advisory council on genomics (PACG). BMJ Partnership in Practice Series. https://blogs.bmj.com/bmj/2019/12/17/rolling-out-genomic-screening/

2. Berg J, Khoury M, Evans J (2011) Deploying whole genome sequencing in clinical practice and public health: meeting the challenge one bin at a time. Genet Med 6:499–504

3. Biesecker L, Green R (2014) Diagnostic clinical genome and exome sequencing. N Eng J Med 370:2418–2425

4. Bijlsma RM, Wessels H, Wouters RHP et al (2018) Cancer patients’ intentions towards receiving unsolicited genetic information obtained using next-generation sequencing. Fam Cancer 17(2):309–316

5. Boardman F, Hale R (2015) Responsibility, identity and genomic sequencing: a comparison of published recommendations and patient perspectives on accepting or declining incidental findings. Mol Genet Genomic Med 6:1079–1096

Cited by 1 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

1. “There should be one spot that you can go:” BRCA mutation carriers’ perspectives on cancer risk management and a hereditary cancer registry;Journal of Community Genetics;2023-10-21