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A missing link in the bench-to-bedside paradigm: engaging regulatory stakeholders in clinical genomics research

For genomic medicine research to be fully translated into clinical care, it is critical for researchers to engage stakeholders who ultimately regulate the use of genomic technologies and therapeutics within healthcare practice. Herein, we describe an example of how this might work.

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Pubblicato in:Genome Med
Autori principali: O’Daniel, Julianne M., Berg, Jonathan S.
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2016
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5031300/
https://ncbi.nlm.nih.gov/pubmed/27655359
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-016-0351-7
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