Ashley Crook

41 George Street
Brisbane, QLD 4000, Australia

Last Updated: 09/26/2026

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Found 34 publications

The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders.

The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders.

Journal: Neurology

Published: September 30, 2025

The use of genetic testing in amyotrophic lateral sclerosis (ALS): a practical approach.

The use of genetic testing in amyotrophic lateral sclerosis (ALS): a practical approach.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: August 08, 2025

The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders.

The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders.

Journal: Neurology

Published: July 18, 2025

The development and evaluation of educational resources for young women with neurofibromatosis type 1 undergoing breast cancer surveillance.

The development and evaluation of educational resources for young women with neurofibromatosis type 1 undergoing breast cancer surveillance.

Journal: Women's health (London, England)

Published: June 29, 2025

The complexity of multidisciplinary respiratory care in amyotrophic lateral sclerosis.

The complexity of multidisciplinary respiratory care in amyotrophic lateral sclerosis.

Journal: Breathe (Sheffield, England)

Published: April 24, 2023

Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders.

Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders.

Journal: Neurology. Clinical practice

Published: March 13, 2023

A mainstreaming oncogenomics model: improving the identification of Lynch syndrome.

A mainstreaming oncogenomics model: improving the identification of Lynch syndrome.

Journal: Frontiers in oncology

Published: January 08, 2023

Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1.

Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1.

Journal: Familial cancer

Published: November 20, 2022

Outcomes of Importance to Patients in Reproductive Genetic Carrier Screening: A Qualitative Study to Inform a Core Outcome Set.

Outcomes of Importance to Patients in Reproductive Genetic Carrier Screening: A Qualitative Study to Inform a Core Outcome Set.

Journal: Journal of personalized medicine

Published: June 09, 2022

Correction: Incorporating patient perspectives in the development of a core outcome set for reproductive genetic carrier screening: a sequential systematic review.

Correction: Incorporating patient perspectives in the development of a core outcome set for reproductive genetic carrier screening: a sequential systematic review.

Journal: European journal of human genetics : EJHG

Published: April 15, 2022

Toward genetic counseling practice standards for diagnostic testing in amyotrophic lateral sclerosis and frontotemporal dementia.

Toward genetic counseling practice standards for diagnostic testing in amyotrophic lateral sclerosis and frontotemporal dementia.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: March 28, 2022

Predictive genetic testing for Motor neuron disease: time for a guideline?

Predictive genetic testing for Motor neuron disease: time for a guideline?

Journal: European journal of human genetics : EJHG

Published: March 15, 2022

Showing 1-12 of 34

Last Updated: 09/26/2026