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Genomics

Genetic testing for amyotrophic lateral sclerosis in Canada – an assessment of current practices

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Pages 305-312 | Received 28 Jul 2021, Accepted 12 Sep 2021, Published online: 27 Sep 2021

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Allison A. Dilliott, Ahmad Al Nasser, Marwa Elnagheeb, Jennifer Fifita, Lyndal Henden, Ingrid M. Keseler, Steven Lenz, Heather Marriott, Emily Mccann, Maysen Mesaros, Sarah Opie-Martin, Emma Owens, Brooke Palus, Justyne Ross, Zhanjun Wang, Hannah White, Ammar Al-Chalabi, Peter M. Andersen, Michael Benatar, Ian Blair, Johnathan Cooper-Knock, Elizabeth A. Harrington, Jeannine Heckmann, John Landers, Cristiane Moreno, Melissa Nel, Evadnie Rampersaud, Jennifer Roggenbuck, Guy Rouleau, Bryan Traynor, Marka Van Blitterswijk, Wouter Van Rheenen, Jan Veldink, Jochen Weishaupt, Luke Drury, Matthew B. Harms & Sali M. K. Farhan. (2023) Clinical testing panels for ALS: global distribution, consistency, and challenges. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:5-6, pages 420-435.
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Hugo M. De Oliveira, Arunachalam Soma, Mark R. Baker, Martin R. Turner, Kevin Talbot & Timothy L. Williams. (2023) A survey of current practice in genetic testing in amyotrophic lateral sclerosis in the UK and Republic of Ireland: implications for future planning. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 24:5-6, pages 405-413.
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Ashley Crook, Chris Jacobs, Toby Newton-John & Alison McEwen. (2022) Toward genetic counseling practice standards for diagnostic testing in amyotrophic lateral sclerosis and frontotemporal dementia. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 23:7-8, pages 562-574.
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Articles from other publishers (2)

Ashley Crook, Chris Jacobs, Toby Newton‐John & Alison McEwen. (2022) Genetic counseling and diagnostic genetic testing for familial amyotrophic lateral sclerosis and/or frontotemporal dementia: A qualitative study of client experiences. Journal of Genetic Counseling 31:5, pages 1206-1218.
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Ashley Crook & Alison McEwen. (2022) Genetic counselling and testing for neurodegenerative disorders using a proposed standard of practice for ALS/MND: diagnostic testing comes first. European Journal of Human Genetics 30:4, pages 394-395.
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