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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.
NPJ Genomic Medicine
|
February 14, 2026
Supporting decisions about genomic newborn screening at scale in the digital age: the BabyScreen+ study
Lilian Downie, Jade Caruana, Nathasha Kugenthiran, 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.
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.
Journal of Acquired Immune Deficiency Syndromes (1999)
|
January 4, 2014
Computerized counseling reduces HIV-1 viral load and sexual transmission risk: findings from a randomized controlled trial
Ann E Kurth, Freya Spielberg, Charles M Cleland, 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.
European Journal of Human Genetics : EJHG
|
April 2, 2026
Correction: The development and usability of 'The Genetics Navigator': a digital solution for adult and paediatric clinical genetics services
Saumeh Saeedi, Daena Hirjikaka, Marc Clausen, et al.
European Journal of Human Genetics : EJHG
|
May 30, 2025
The development and usability of 'The Genetics Navigator': a digital solution for adult and paediatric clinical genetics services
Saumeh Saeedi, Daena Hirijkaka, Marc Clausen, et al.
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Showing results (11-20 of 52) with videos related to
Sort By:
Page
of 6
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.
NPJ Genomic Medicine
|
February 14, 2026
Supporting decisions about genomic newborn screening at scale in the digital age: the BabyScreen+ study
Lilian Downie, Jade Caruana, Nathasha Kugenthiran, 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.
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.
Journal of Acquired Immune Deficiency Syndromes (1999)
|
January 4, 2014
Computerized counseling reduces HIV-1 viral load and sexual transmission risk: findings from a randomized controlled trial
Ann E Kurth, Freya Spielberg, Charles M Cleland, 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.
European Journal of Human Genetics : EJHG
|
April 2, 2026
Correction: The development and usability of 'The Genetics Navigator': a digital solution for adult and paediatric clinical genetics services
Saumeh Saeedi, Daena Hirjikaka, Marc Clausen, et al.
European Journal of Human Genetics : EJHG
|
May 30, 2025
The development and usability of 'The Genetics Navigator': a digital solution for adult and paediatric clinical genetics services
Saumeh Saeedi, Daena Hirijkaka, Marc Clausen, et al.
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of 6