Development of a consent resource for genomic data sharing in the clinical setting-Reference-Cited by-同舟云学术

Development of a consent resource for genomic data sharing in the clinical setting

Published:2019-01 Issue:1 Volume:21 Page:81-88
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Riggs Erin Rooney,Azzariti Danielle R.,Niehaus Annie,Goehringer Scott R.,Ramos Erin M.,Rodriguez Laura Lyman,Knoppers Bartha,Rehm Heidi L.,Martin Christa Lese

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

https://www.nature.com/articles/s41436-018-0017-5.pdf

Reference21 articles.

1. National Institutes of Health. Genomic Data Sharing [2014-20385]. Federal Register. 2014;79(167). https://federalregister.gov/a/2014-20385

2. American Medical Association. Genome Analysis and Variant Identification; 2013. http://www.ama-assn.org. Accessed May 2, 2014.

3. National Society of Genetic Counselors. Clinical Data Sharing; 2015. https://www.nsgc.org/p/bl/et/blogaid=330. Accessed August 1, 2017.

Cited by 22 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. Health data sharing attitudes towards primary and secondary use of data: a systematic review;eClinicalMedicine;2024-05

2. Secondary use of genomic data: patients’ decisions at point of testing and perspectives to inform international data sharing;European Journal of Human Genetics;2024-03-25

3. Publics’ knowledge of, attitude to and motivation towards health-related genomics: a scoping review;European Journal of Human Genetics;2024-02-06

4. Utilisations secondaires des données de santé : impacts de la transparence;Canadian Journal of Bioethics;2024

5. Technology-Enhanced Learning, Data Sharing, and Machine Learning Challenges in South African Education;Education Sciences;2023-04-24