Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trial

INTRODUCTION: Genome sequencing, a novel genetic diagnostic technology that analyses the billions of base pairs of DNA, promises to optimise healthcare through personalised diagnosis and treatment. However, implementation of genome sequencing faces challenges including the lack of consensus on discl...

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Bibliografiska uppgifter
I publikationen:BMJ Open
Huvudupphovsmän: Shickh, Salma, Clausen, Marc, Mighton, Chloe, Casalino, Selina, Joshi, Esha, Glogowski, Emily, Schrader, Kasmintan A, Scheer, Adena, Elser, Christine, Panchal, Seema, Eisen, Andrea, Graham, Tracy, Aronson, Melyssa, Semotiuk, Kara M, Winter-Paquette, Laura, Evans, Michael, Lerner-Ellis, Jordan, Carroll, June C, Hamilton, Jada G, Offit, Kenneth, Robson, Mark, Thorpe, Kevin E, Laupacis, Andreas, Bombard, Yvonne
Materialtyp: Artigo
Språk:Inglês
Publicerad: BMJ Publishing Group 2018
Ämnen:
Genetics and Genomics
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5922516/
https://ncbi.nlm.nih.gov/pubmed/29700101
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bmjopen-2018-021876
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