Ashley Crook

1.2k total citations
28 papers, 357 citations indexed

About

Ashley Crook is a scholar working on Neurology, Genetics and Genetics. According to data from OpenAlex, Ashley Crook has authored 28 papers receiving a total of 357 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Neurology, 11 papers in Genetics and 10 papers in Genetics. Recurrent topics in Ashley Crook's work include Neurogenetic and Muscular Disorders Research (10 papers), Amyotrophic Lateral Sclerosis Research (10 papers) and BRCA gene mutations in cancer (6 papers). Ashley Crook is often cited by papers focused on Neurogenetic and Muscular Disorders Research (10 papers), Amyotrophic Lateral Sclerosis Research (10 papers) and BRCA gene mutations in cancer (6 papers). Ashley Crook collaborates with scholars based in Australia, United States and United Kingdom. Ashley Crook's co-authors include Alison McEwen, Chris Jacobs, Toby Newton‐John, Ian P. Blair, Dominic B. Rowe, Kelly L. Williams, Rosie O’Shea, Ebony Richardson, Angela Chou and Stephen Clarke and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Neurology.

In The Last Decade

Ashley Crook

26 papers receiving 353 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ashley Crook Australia	11	97	93	88	86	63	28	357
Awni Musharbash Jordan	11	56 0.6×	65 0.7×	39 0.4×	23 0.3×	144 2.3×	20	341
Yassir Sbitti Morocco	10	125 1.3×	22 0.2×	52 0.6×	81 0.9×	19 0.3×	31	295
Colleen McGuire United States	10	270 2.8×	226 2.4×	45 0.5×	144 1.7×	50 0.8×	16	801
Shanna Gustafson United States	12	79 0.8×	24 0.3×	109 1.2×	290 3.4×	84 1.3×	16	636
Junko Nomoto Japan	14	211 2.2×	86 0.9×	298 3.4×	21 0.2×	106 1.7×	37	496
Yi‐Bin Chen United States	9	172 1.8×	58 0.6×	126 1.4×	14 0.2×	45 0.7×	12	308
Guenter Henze Germany	13	133 1.4×	81 0.9×	119 1.4×	12 0.1×	52 0.8×	34	525
PD Kottaridis United Kingdom	13	88 0.9×	52 0.6×	34 0.4×	15 0.2×	103 1.6×	19	428
Victor Evangelista de Faria Ferraz Brazil	11	47 0.5×	18 0.2×	45 0.5×	192 2.2×	22 0.3×	34	377
Andréa Glezer Brazil	15	47 0.5×	69 0.7×	40 0.5×	23 0.3×	105 1.7×	42	765

Countries citing papers authored by Ashley Crook

Since Specialization

Citations

This map shows the geographic impact of Ashley Crook's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ashley Crook with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ashley Crook more than expected).

Fields of papers citing papers by Ashley Crook

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ashley Crook. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ashley Crook. The network helps show where Ashley Crook may publish in the future.

Co-authorship network of co-authors of Ashley Crook

This figure shows the co-authorship network connecting the top 25 collaborators of Ashley Crook. A scholar is included among the top collaborators of Ashley Crook based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ashley Crook. Ashley Crook is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Jenny, Kim, Kristiana Salmon, Ashley Crook, et al.. (2025). The Importance of Offering Genetic Counseling and Testing to All Persons Diagnosed With Frontotemporal Degeneration Spectrum Disorders. Neurology. 105(3). e213814–e213814.

Fleming, Jane, Ashley Crook, Katrina Moore, et al.. (2025). The development and evaluation of educational resources for young women with neurofibromatosis type 1 undergoing breast cancer surveillance. Women s Health. 21. 922747806–922747806.

Chambers, Chelsea, et al.. (2023). Incorporating Genetic Testing Into the Care of Patients With Amyotrophic Lateral Sclerosis/Frontotemporal Degeneration Spectrum Disorders. Neurology Clinical Practice. 13(5). e200201–e200201. 7 indexed citations

Fleming, Jane, K. Moore, Ashley Crook, et al.. (2023). Clinical and imaging modality factors impacting radiological interpretation of breast screening in young women with neurofibromatosis type 1. Familial Cancer. 22(4). 499–511. 1 indexed citations

O’Shea, Rosie, Ashley Crook, Chris Jacobs, et al.. (2023). A mainstreaming oncogenomics model: improving the identification of Lynch syndrome. Frontiers in Oncology. 13. 1140135–1140135. 4 indexed citations

Berlowitz, David J., Susan Mathers, Karen Hutchinson, et al.. (2023). The complexity of multidisciplinary respiratory care in amyotrophic lateral sclerosis. Breathe. 19(3). 220269–220269. 9 indexed citations

Crook, Ashley & 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). 394–395. 4 indexed citations

McNeill, Alisdair, Maria del Mar Amador, Hilary Bekker, et al.. (2022). Predictive genetic testing for Motor neuron disease: time for a guideline?. European Journal of Human Genetics. 30(6). 635–636. 3 indexed citations

Richardson, Ebony, Alison McEwen, Toby Newton‐John, Ashley Crook, & Chris Jacobs. (2022). 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. 30(7). 756–765. 7 indexed citations

10.

Crook, Ashley, 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). 562–574. 4 indexed citations

11.

Crook, Ashley, Chris Jacobs, Toby Newton‐John, Rosie O’Shea, & Alison McEwen. (2021). Genetic counseling and testing practices for late-onset neurodegenerative disease: a systematic review. Journal of Neurology. 269(2). 676–692. 11 indexed citations

12.

Crook, Ashley, et al.. (2021). 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. 21(2). 241–253. 8 indexed citations

13.

Richardson, Ebony, Alison McEwen, Toby Newton‐John, Ashley Crook, & Chris Jacobs. (2021). Systematic review of outcomes in studies of reproductive genetic carrier screening: Towards development of a core outcome set. Genetics in Medicine. 24(1). 1–14. 6 indexed citations

14.

O’Shea, Rosie, Natalie Taylor, Ashley Crook, et al.. (2021). Health system interventions to integrate genetic testing in routine oncology services: A systematic review. PLoS ONE. 16(5). e0250379–e0250379. 21 indexed citations

15.

Crook, Ashley, Chris Jacobs, Toby Newton‐John, Ebony Richardson, & Alison McEwen. (2021). Patient and Relative Experiences and Decision-making About Genetic Testing and Counseling for Familial ALS and FTD. Alzheimer Disease & Associated Disorders. 35(4). 374–385. 16 indexed citations

16.

Hogden, Anne & Ashley Crook. (2017). Patient-centered Decision Making in Amyotrophic Lateral Sclerosis: Where are we?. Neurodegenerative Disease Management. 7(6). 377–386. 5 indexed citations

17.

Crook, Ashley, Laura Forrest, Nina Hallowell, et al.. (2014). Connecting patients, researchers and clinical genetics services: the experiences of participants in the Australian Ovarian Cancer Study (AOCS). European Journal of Human Genetics. 23(2). 152–158. 13 indexed citations

18.

Toon, Christopher W., Michael D. Walsh, Angela Chou, et al.. (2013). BRAFV600E Immunohistochemistry Facilitates Universal Screening of Colorectal Cancers for Lynch Syndrome. The American Journal of Surgical Pathology. 37(10). 1592–1602. 104 indexed citations

19.

Hallowell, Nina, Kathryn Alsop, Margaret Gleeson, et al.. (2013). The responses of research participants and their next of kin to receiving feedback of genetic test results following participation in the Australian Ovarian Cancer Study. Genetics in Medicine. 15(6). 458–465. 23 indexed citations

20.

Pacey, Allan, Hannah Merrick, Emily Arden‐Close, et al.. (2012). Monitoring fertility (semen analysis) by cancer survivors who banked sperm prior to cancer treatment. Human Reproduction. 27(11). 3132–3139. 28 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact