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UnknownThe Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results.
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S-EPMC6018661 | biostudies-literature
UnknownColorectal cancer cells display chaperone dependency for the unconventional prefoldin URI1.
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S-EPMC5045422 | biostudies-literature
UnknownDescription and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies.
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S-EPMC3927794 | biostudies-literature
UnknownHealth outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial.
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S-EPMC6797333 | biostudies-literature
UnknownOpportunistic genomic screening has clinical utility: An interventional cohort study.
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S-EPMC12257567 | biostudies-literature
UnknownOncology Clinic-Based Hereditary Cancer Genetic Testing in a Population-Based Health Care System.
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S-EPMC7072228 | biostudies-literature
UnknownQuality of life drives patients' preferences for secondary findings from genomic sequencing.
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S-EPMC7609335 | biostudies-literature
Unknown"I don't need any more unknowns hanging over my head": Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing.
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S-EPMC11262616 | biostudies-literature
UnknownRecommendations for the implementation of genetic testing for metastatic prostate cancer patients in Canada.
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S-EPMC9565071 | biostudies-literature
UnknownAssessment of SLX4 Mutations in Hereditary Breast Cancers.
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S-EPMC3694110 | biostudies-literature
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