Genomic medicine and data sharing
Author:
Affiliation:
1. PHG Foundation, 2 Worts Causeway, Cambridge, CB1 8RN, UK
Publisher
Oxford University Press (OUP)
Subject
General Medicine
Link
http://academic.oup.com/bmb/article-pdf/123/1/35/24331768/ldx024.pdf
Reference39 articles.
1. Evolving health care through personal genomics;Rehm;Nat Rev Genet,2017
2. Rare-disease genetics in the era of next-generation sequencing: discovery to translation;Boycott;Nat Rev Genet,2013
3. Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data;Wright;Lancet,2015
4. A 26-hour system of highly sensitive whole genome sequencing for emergency management of genetic diseases;Miller;Genome Med,2015
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3. Data sharing practices in collaborative human genomic research in low- and middle-income countries: A systematic review protocol;PLOS ONE;2023-11-02
4. Public attitudes towards genomic data sharing: results from a provincial online survey in Canada;BMC Medical Ethics;2023-10-07
5. Australian public perspectives on genomic data governance: responsibility, regulation, and logistical considerations;European Journal of Human Genetics;2023-05-10
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