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Kirsty West

Showing results (1-10 of 8) with videos related to

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BMJ Case Reports|September 25, 2025
Optineurin mutation-associated language variant frontotemporal dementiaAshley Park, Kirsty West, David Darby, et al.
Psychology & Health|November 24, 2020
Suicide in frontotemporal dementia and Huntington disease: analysis of family-reported pedigree data and implications for genetic healthcare for asymptomatic relativesAdrienne Sexton, Kirsty West, Gulvir Gill, et al.
Journal of Genetic Counseling|January 26, 2018
Genetic Counseling in the Era of Genomics: What's all the Fuss about?Gemma R Brett, Ella J Wilkins, Emma T Creed, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 13, 2022
Real world outcomes and implementation pathways of exome sequencing in an adult genetic departmentMaie Walsh, Kirsty West, Jessica A Taylor, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 29, 2022
Clinical impact of whole-genome sequencing in patients with early-onset dementiaAamira J Huq, Bryony Thompson, Mark F Bennett, et al.
Journal of the Neurological Sciences|December 14, 2020
The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspectiveDhamidhu Eratne, Amy Schneider, Ella Lynch, et al.
Genome Research|February 27, 2025
A prospective trial comparing programmable targeted long-read sequencing and short-read genome sequencing for genetic diagnosis of cerebellar ataxiaHaloom Rafehi, Liam G Fearnley, Justin Read, et al.
Kidney International Reports|August 19, 2024
Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 YearsKushani Jayasinghe, Erik Biros, Trudie Harris, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
BMJ Case Reports|September 25, 2025
Optineurin mutation-associated language variant frontotemporal dementiaAshley Park, Kirsty West, David Darby, et al.
Psychology & Health|November 24, 2020
Suicide in frontotemporal dementia and Huntington disease: analysis of family-reported pedigree data and implications for genetic healthcare for asymptomatic relativesAdrienne Sexton, Kirsty West, Gulvir Gill, et al.
Journal of Genetic Counseling|January 26, 2018
Genetic Counseling in the Era of Genomics: What's all the Fuss about?Gemma R Brett, Ella J Wilkins, Emma T Creed, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 13, 2022
Real world outcomes and implementation pathways of exome sequencing in an adult genetic departmentMaie Walsh, Kirsty West, Jessica A Taylor, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 29, 2022
Clinical impact of whole-genome sequencing in patients with early-onset dementiaAamira J Huq, Bryony Thompson, Mark F Bennett, et al.
Journal of the Neurological Sciences|December 14, 2020
The clinical utility of exome sequencing and extended bioinformatic analyses in adolescents and adults with a broad range of neurological phenotypes: an Australian perspectiveDhamidhu Eratne, Amy Schneider, Ella Lynch, et al.
Genome Research|February 27, 2025
A prospective trial comparing programmable targeted long-read sequencing and short-read genome sequencing for genetic diagnosis of cerebellar ataxiaHaloom Rafehi, Liam G Fearnley, Justin Read, et al.
Kidney International Reports|August 19, 2024
Implementation and Evaluation of a National Multidisciplinary Kidney Genetics Clinic Network Over 10 YearsKushani Jayasinghe, Erik Biros, Trudie Harris, et al.
Pageof 1