Cargando…
Reactions to clinical reinterpretation of a gene variant by participants in a sequencing study
INTRODUCTION: As genome science advances, people receiving personalized genetic information may receive reinterpretations of pathogenicity. Little is known about responses to adjusted results. We examined how reinterpretations might affect attitudes about genetic testing and intentions to share resu...
Autores principales: | Taber, Jennifer M., Klein, William M.P., Lewis, Katie L., Johnston, Jennifer J., Biesecker, Leslie G., Biesecker, Barbara B. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611163/ https://www.ncbi.nlm.nih.gov/pubmed/28771245 http://dx.doi.org/10.1038/gim.2017.88 |
Ejemplares similares
-
Health Behaviors Amongst Unaffected Participants Following Receipt of Variants of Uncertain Significance in Cardiomyopathy-Associated Genes
por: Miller, Ilana M., et al.
Publicado: (2018) -
Dyadic concordance and associations of beliefs with intentions to learn carrier results from genomic sequencing
por: Huelsnitz, Chloe O., et al.
Publicado: (2021) -
How do research participants perceive “uncertainty” in genomic sequencing?
por: Biesecker, Barbara B, et al.
Publicado: (2014) -
Characterizing Participants in the ClinSeq Genome Sequencing Cohort as Early Adopters of a New Health Technology
por: Lewis, Katie L., et al.
Publicado: (2015) -
Determining the prevalence of McArdle disease from gene frequency by analysis of next generation sequencing data: McArdle prevalence by NGS data
por: De Castro, Mauricio, et al.
Publicado: (2015)