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Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 12, 2019
Variant classification changes over time in BRCA1 and BRCA2Chloe Mighton, George S Charames, Marina Wang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 14, 2023
"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 sequencingSalma Shickh, Chloe Mighton, Marc Clausen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 27, 2026
Development and content validation of the Clinician-reported Genetic testing Utility InDEx for genomic newborn screening (C-GUIDE NBS)Salma Shickh, Stephanie Luca, Katharine Fooks, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 13, 2026
A comprehensive approach to evaluating the clinical utility of genome sequencing in rare disease: A large prospective Canadian cohortSalma Shickh, Katharine Fooks, Viji Venkataramanan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 25, 2022
"Doctors shouldn't have to cheat the system": Clinicians' real-world experiences of the utility of genomic sequencingSalma Shickh, Chloe Mighton, Marc Clausen, et al.
European Journal of Human Genetics : EJHG|March 29, 2021
Widening the lens of actionability: A qualitative study of primary care providers' views and experiences of managing secondary genomic findingsAgnes Sebastian, June C Carroll, Meredith Vanstone, et al.
Human Genetics|September 6, 2020
Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findingsEmma Reble, Mariana Gutierrez Salazar, Kathleen-Rose Zakoor, et al.
European Journal of Medical Genetics|November 12, 2021
Challenges and practical solutions for managing secondary genomic findings in primary careAgnes Sebastian, June C Carroll, Meredith Vanstone, et al.
JCO Precision Oncology|December 12, 2024
Clinical Utility of Genomic Sequencing for Hereditary Cancer Syndromes: An Observational Cohort StudySalma Shickh, Chloe Mighton, Marc Clausen, et al.
Human Genetics|March 21, 2023
Great expectations: patients' preferences for clinically significant results from genomic sequencingSalma Shickh, Agnes Sebastian, Marc Clausen, et al.
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