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Implementation considerations for offering personal genomic risk information to the public

A qualitative study

Bibliographic Data

ID15382058
AuthorsAmelia K Smit (0000-0001-5712-220X, The University of Sydney, corresponding author), Gillian Reyes-Marcelino (0000-0002-3250-0961, The University of Sydney), Louise Keogh (0000-0003-2963-6451, The University of Melbourne), Kate Dunlop (0000-0001-9544-9764, The University of Sydney), Ainsley J Newson (0000-0002-3460-772X, The University of Sydney), Anne E Cust (0000-0002-5331-6370, The University of Sydney)
Year2020
Volume20
Issue1
Pages1028-1028
Publication date2020-06-29
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueBMC Public Health (JOURNAL)
Journal identifiersISSN: 1471-2458 • E-ISSN: 1471-2458
PublisherBioMed Central (PUBLISHER • GB)
DOI10.1186/s12889-020-09143-0
PMID32600382
OpenAlexW3039609740
LanguageEN
Citations received2
References cited39

Participants felt that offering personal genomic risk information to the general population to inform prevention and early detection recommendations is acceptable, particularly for common, complex conditions such as cancer. Understanding participants' preferences for receiving genomic risk information will assist with communication strategies and health workforce planning. We anticipate that these findings will contribute to the development of implementation strategies for incorporating genomic risk information into routine clinical practice

Biostatistics · Environmental health · Genomic information · Population · Public health · Qualitative research · BRCA gene mutations in cancer · Ethics in Clinical Research · Health Systems, Economic Evaluations, Quality of Life · Medicine · Nursing · Health Informatics

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Unique citing works2
Citations per year0,4
Citation span2021 - 2024 (4)
Citation velocityrecent
Highly citedNo
Citation typesNeutral: 2
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