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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 3, 2019
Correction: Variant classification changes over time in BRCA1 and BRCA2
Chloe Mighton, George S Charames, Marina Wang, et al.
HGG Advances
|
May 1, 2025
Pathogenic germline variants in small cell lung cancer: A systematic review and meta-analysis
Sami Ul Haq, Aleem Aamir, Chloe Mighton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 12, 2019
Variant classification changes over time in BRCA1 and BRCA2
Chloe Mighton, George S Charames, Marina Wang, et al.
CMAJ Open
|
November 25, 2020
Use of real-world evidence in cancer drug funding decisions in Canada: a qualitative study of stakeholders' perspectives
Marc Clausen, Chloe Mighton, Ruhi Kiflen, 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 sequencing
Salma Shickh, Chloe Mighton, Marc Clausen, 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 sequencing
Salma 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 findings
Agnes 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 findings
Emma 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 care
Agnes Sebastian, June C Carroll, Meredith Vanstone, et al.
European Journal of Human Genetics : EJHG
|
April 29, 2018
The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results
Yvonne Bombard, Marc Clausen, Chloe Mighton, et al.
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of 7
Search research articles
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Showing results (21-30 of 68) with videos related to
Sort By:
Page
of 7
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 3, 2019
Correction: Variant classification changes over time in BRCA1 and BRCA2
Chloe Mighton, George S Charames, Marina Wang, et al.
HGG Advances
|
May 1, 2025
Pathogenic germline variants in small cell lung cancer: A systematic review and meta-analysis
Sami Ul Haq, Aleem Aamir, Chloe Mighton, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 12, 2019
Variant classification changes over time in BRCA1 and BRCA2
Chloe Mighton, George S Charames, Marina Wang, et al.
CMAJ Open
|
November 25, 2020
Use of real-world evidence in cancer drug funding decisions in Canada: a qualitative study of stakeholders' perspectives
Marc Clausen, Chloe Mighton, Ruhi Kiflen, 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 sequencing
Salma Shickh, Chloe Mighton, Marc Clausen, 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 sequencing
Salma 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 findings
Agnes 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 findings
Emma 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 care
Agnes Sebastian, June C Carroll, Meredith Vanstone, et al.
European Journal of Human Genetics : EJHG
|
April 29, 2018
The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results
Yvonne Bombard, Marc Clausen, Chloe Mighton, et al.
Page
of 7