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European Journal of Human Genetics : EJHG|May 20, 2020
Quality of life drives patients' preferences for secondary findings from genomic sequencingChloe Mighton, Lindsay Carlsson, Marc Clausen, et al.Human Genetics|September 19, 2021
Patient and public preferences for being recontacted with updated genomic results: a mixed methods studyChloe Mighton, Marc Clausen, Agnes Sebastian, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 3, 2021
The role of digital tools in the delivery of genomic medicine: enhancing patient-centered careSalma Shickh, Sara A Rafferty, Marc Clausen, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 15, 2023
How do members of the public expect to use variants of uncertain significance in their health care? A population-based surveyChloe Mighton, Marc Clausen, Salma Shickh, et al.The Oncologist|April 6, 2022
"Game Changer": Health Professionals' Views on the Clinical Utility of Circulating Tumor DNA Testing in Hereditary Cancer Syndrome ManagementSalma Shickh, Leslie E Oldfield, Marc Clausen, et al.European Journal of Human Genetics : EJHG|October 11, 2023
"I just wanted more": Hereditary cancer syndromes patients' perspectives on the utility of circulating tumour DNA testing for cancer screeningElla Adi-Wauran, Marc Clausen, Salma Shickh, et al.European Journal of Human Genetics : EJHG|March 9, 2019
Development of patient "profiles" to tailor counseling for incidental genomic sequencing resultsChloe Mighton, Lindsay Carlsson, Marc Clausen, et al.Human Genetics|June 23, 2022
A comprehensive genomic reporting structure for communicating all clinically significant primary and secondary findingsJordan Sam, Emma Reble, Rita Kodida, et al.BMJ Open|April 28, 2018
Evaluation of a decision aid for incidental genomic results, the Genomics ADvISER: protocol for a mixed methods randomised controlled trialSalma Shickh, Marc Clausen, Chloe Mighton, et al.Journal of Medical Genetics|May 22, 2023
A model for the return and referral of all clinically significant secondary findings of genomic sequencingRita Kodida, Emma Reble, Marc Clausen, et al.Pageof 4