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BMJ Case Reports
|
September 25, 2025
Optineurin mutation-associated language variant frontotemporal dementia
Ashley 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 relatives
Adrienne 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 department
Maie 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 dementia
Aamira 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 perspective
Dhamidhu 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 ataxia
Haloom 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 Years
Kushani Jayasinghe, Erik Biros, Trudie Harris, et al.
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Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
BMJ Case Reports
|
September 25, 2025
Optineurin mutation-associated language variant frontotemporal dementia
Ashley 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 relatives
Adrienne 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 department
Maie 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 dementia
Aamira 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 perspective
Dhamidhu 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 ataxia
Haloom 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 Years
Kushani Jayasinghe, Erik Biros, Trudie Harris, et al.
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of 1