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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.Public Health Genomics|October 24, 2024
"Should I Let Them Know I Have This?": Multifaceted Genetic Discrimination and Limited Awareness of Legal Protections among Individuals with Hereditary Cancer SyndromesRidhi Gopalakrishnan, Jordan Sam, Carly Butkowsky, et al.European Journal of Human Genetics : EJHG|March 3, 2026
"Where do I go from here?" Navigating a lifelong road without a map: the care experiences of hereditary cancer patientsCarly Butkowsky, June C Carroll, Melyssa Aronson, 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.BMJ Open|April 29, 2022
Genetics Adviser: a protocol for a mixed-methods randomised controlled trial evaluating a digital platform for genetics service deliverySalma Shickh, Daena Hirjikaka, Marc Clausen, et al.Journal of Medical Genetics|July 3, 2015
Improving diagnostic precision, care and syndrome definitions using comprehensive next-generation sequencing for the inherited bone marrow failure syndromesIbrahim Ghemlas, Hongbing Li, Bozana Zlateska, et al.Genetics in Medicine Open|December 13, 2024
Genetics Adviser: The development and usability testing of a new patient digital health application to support clinical genomic testingMarc Clausen, Suvetha Krishnapillai, Daena Hirjikaka, et al.BMJ Open|October 10, 2019
Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trialSalma Shickh, Marc Clausen, Chloe Mighton, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 12, 2024
Opportunistic genomic screening has clinical utility: An interventional cohort studyChloe Mighton, Rita Kodida, Salma Shickh, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 17, 2025
Opportunistic screening for broad range of medically relevant secondary findings: Laboratory benefits and burdensChloe Mighton, Emma Reble, Jordan Sam, et al.Pageof 3