Ashley Crook

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 13

Top Venues

European journal of human genetics : EJHG

Amyotrophic lateral sclerosis & frontotemporal degeneration

Journal of genetic counseling

Familial cancer

Royal North Shore Hospital

University of Melbourne (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Royal North Shore Hospital Apr 01 2012

Australia

Senior Genetic Counsellor :: Clinical Genetics

Education History

University of Melbourne Jan 01 2008 - Dec 01 2010

Australia

MSC

Publications

Mathilda Wilding, Jane Fleming, Katrina Moore, Ashley Crook, Ranjani Reddy, Sarah Choi, Timothy E Schlub, Michael J Field, Lavvina Thiyagarajan, Jeff Thompson, Yemima D Berman
Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1. Familial cancer (2023)
Chelsea Chambers, Lauren Lichten, Ashley Crook, Wendy R Uhlmann, Laynie Dratch
Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders. Neurology. Clinical practice 13 (5) (2023)
Ashley Crook, Chris Jacobs, Toby R O Newton-John, Alison McEwen
Toward genetic counseling practice standards for diagnostic testing in amyotrophic lateral sclerosis and frontotemporal dementia. Amyotrophic lateral sclerosis & frontotemporal degeneration 23 (7-8) (2022)
Ashley Crook, Chris Jacobs, Toby R O Newton-John, Alison McEwen
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) (2022)
Ashley Crook, Alison McEwen
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 : EJHG 30 (4) (2022)
Alisdair McNeill, Maria-Del-Mar Amador, Hilary Bekker, Angus John Clarke, Ashley Crook, Cathy Cummings, Alison McEwen, Christopher McDermott, Oliver Quarrell, Alessandra Renieri, Jennifer Roggenbuck, Kristiana Salmon, Alexander Volk, Jochen Weishaupt, null null
Predictive genetic testing for Motor neuron disease: time for a guideline? European journal of human genetics : EJHG 30 (6) (2022)
Ebony Richardson, Alison McEwen, Toby Newton-John, Ashley Crook, Chris Jacobs
Incorporating patient perspectives in the development of a core outcome set for reproductive genetic carrier screening: a sequential systematic review. European journal of human genetics : EJHG 30 (7) (2022)
Ashley Crook, Rebekah Kwa, Sarah Ephraums, Mathilda Wilding, Lavvina Thiyagarajan, Jane Fleming, Katrina Moore, Yemima D Berman
The psychological impact and experience of breast cancer screening in young women with an increased risk of breast cancer due to neurofibromatosis type 1. Familial cancer (2021)
Ashley Crook, Chris Jacobs, Toby R O Newton-John, Rosie O'Shea, Alison McEwen
Genetic counseling and testing practices for late-onset neurodegenerative disease: a systematic review. Journal of neurology (2021)
Georgina M Schlub, Ashley Crook, Kristine Barlow-Stewart, Jane Fleming, Judy Kirk, Kathy Tucker, Sian Greening
Helping young children understand inherited cancer predisposition syndromes using bibliotherapy. Journal of genetic counseling 30 (4) (2021)
Emma Tudini, Aimee L Davidson, Uwe Dressel, Lesley Andrews, Yoland Antill, Ashley Crook, Michael J Field, Michael Gattas, Rebecca Harris, Bettina Meiser, Nicholas Pachter, Lucinda Salmon, Rachel Susman, Sharron Townshend, Alison H Trainer, Katherine M Tucker, Gillian Mitchell, Paul A James, Robyn L Ward, Helen Mar Fan, Nicola K Poplawski, Amanda B Spurdle
Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility. Journal of medical genetics 58 (12) (2020)
Ashley Crook, Alison McEwen, Jennifer A Fifita, Katharine Zhang, John B J Kwok, Glenda M Halliday, Ian P Blair, Dominic B Rowe
The C9orf72 hexanucleotide repeat expansion presents a challenge for testing laboratories and genetic counseling. Amyotrophic lateral sclerosis & frontotemporal degeneration 20 (5-6) (2019)
Ashley Crook, Kelly Louise Williams, Lorel Adams, Ian Blair, Dominic B Rowe
Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations. Amyotrophic lateral sclerosis & frontotemporal degeneration 18 (7-8) (2017)

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Publication Activity (10 Years)

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Ashley Crook