Alexandra Murray

574 total citations
18 papers, 375 citations indexed

About

Alexandra Murray is a scholar working on Genetics, Sociology and Political Science and Neurology. According to data from OpenAlex, Alexandra Murray has authored 18 papers receiving a total of 375 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Sociology and Political Science and 3 papers in Neurology. Recurrent topics in Alexandra Murray's work include BRCA gene mutations in cancer (8 papers), Family Support in Illness (5 papers) and Dental Anxiety and Anesthesia Techniques (2 papers). Alexandra Murray is often cited by papers focused on BRCA gene mutations in cancer (8 papers), Family Support in Illness (5 papers) and Dental Anxiety and Anesthesia Techniques (2 papers). Alexandra Murray collaborates with scholars based in United Kingdom, United States and Australia. Alexandra Murray's co-authors include Jenny Douglas, Sally Davies, Susan Tomkins, Helen E. Hughes, Sandra Hanks, Meena Upadhyaya, I. Karen Temple, Nazneen Rahman, Ceri Phelps and Marion McAllister and has published in prestigious journals such as The American Journal of Human Genetics, BMJ and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Alexandra Murray

18 papers receiving 367 citations

Peers

Alexandra Murray
Moniek Zoeteweij Netherlands
Lisa Bowdler Australia
Peter Heinz United Kingdom
Eliza Courtney Singapore
Michael Eleff United States
Victor Evangelista de Faria Ferraz Brazil
JC Oosterwijk Netherlands
Whitney Neufeld‐Kaiser United States
H.F.J. ten Kroode Netherlands
Emily Edelman United States
Moniek Zoeteweij Netherlands
Alexandra Murray
Citations per year, relative to Alexandra Murray Alexandra Murray (= 1×) peers Moniek Zoeteweij

Countries citing papers authored by Alexandra Murray

Since Specialization
Citations

This map shows the geographic impact of Alexandra Murray'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 Alexandra Murray with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexandra Murray more than expected).

Fields of papers citing papers by Alexandra Murray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexandra Murray. 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 Alexandra Murray. The network helps show where Alexandra Murray may publish in the future.

Co-authorship network of co-authors of Alexandra Murray

This figure shows the co-authorship network connecting the top 25 collaborators of Alexandra Murray. A scholar is included among the top collaborators of Alexandra Murray 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 Alexandra Murray. Alexandra Murray is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

18 of 18 papers shown
1.
Evans, D. Gareth, Ludwine Messiaen, William D. Foulkes, et al.. (2021). Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma. Genetics in Medicine. 23(9). 1779–1782. 3 indexed citations
2.
Morgan, Sue, Alexandra Murray, Robin L. Jones, et al.. (2021). The detection of germline and somatic BRCA1/2 genetic variants through parallel testing of patients with high‐grade serous ovarian cancer: a national retrospective audit. BJOG An International Journal of Obstetrics & Gynaecology. 129(3). 433–442. 11 indexed citations
3.
Murray, Alexandra, et al.. (2020). The Use of Point-of-Care Ultrasound to Accurately Measure Cardiac Output in Flight. Air Medical Journal. 39(3). 218–220. 1 indexed citations
4.
Murray, Alexandra & Michael C. Plewa. (2019). Case Study: 26-Year-Old Male Presenting With New Onset Seizure and History of PTSD. StatPearls. 1 indexed citations
5.
McVeigh, Terri, Deirdre Donnelly, Elizabeth A. Jones, et al.. (2019). Towards establishing consistency in triage in a tertiary specialty. European Journal of Human Genetics. 27(4). 547–555. 8 indexed citations
6.
Murray, Alexandra, et al.. (2015). Clinical genetics: a guide to a career in the specialty. BMJ. h2532–h2532. 1 indexed citations
7.
Brunstrom, Kate, Alexandra Murray, & Marion McAllister. (2015). Experiences of Women Who Underwent Predictive BRCA 1/2 Mutation Testing Before the Age of 30. Journal of Genetic Counseling. 25(1). 90–100. 34 indexed citations
8.
Evans, Tom, et al.. (2015). A review of BRCA gene carrier demographics in Wales. Breast Cancer Research. 17(S1). 1 indexed citations
9.
Phelps, Ceri, Paul Bennett, Kerenza Hood, Kate Brain, & Alexandra Murray. (2012). A self‐help coping intervention can reduce anxiety and avoidant health behaviours whilst waiting for cancer genetic risk information: results of a phase III randomised trial. Psycho-Oncology. 22(4). 837–844. 13 indexed citations
10.
Bennett, Paul, Ceri Phelps, Jennifer Hilgart, et al.. (2011). Concerns and coping during cancer genetic risk assessment. Psycho-Oncology. 21(6). 611–617. 18 indexed citations
11.
12.
Phelps, Ceri, Paul Bennett, Hywel Jones, et al.. (2009). The development of a cancer genetic‐specific measure of coping: the GRACE. Psycho-Oncology. 19(8). 847–854. 15 indexed citations
13.
14.
Murray, Alexandra. (2006). A case of multiple cutaneous schwannomas; schwannomatosis or neurofibromatosis type 2?. Journal of Neurology Neurosurgery & Psychiatry. 77(2). 269–271. 21 indexed citations
15.
Douglas, Jenny, Sandra Hanks, I. Karen Temple, et al.. (2003). NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes. The American Journal of Human Genetics. 72(1). 132–143. 210 indexed citations
16.
File, Sandra E., E. M. Goodall, Fiona Sanders, et al.. (1993). Contrasting effects of midazolam and nitrous oxide on memory and cognitive bias in dentally phobic patients. Human Psychopharmacology Clinical and Experimental. 8(3). 195–202. 3 indexed citations
17.
Murray, Alexandra. (1992). An orthodontic tour of Australia. BDJ. 172(4). 161–161. 1 indexed citations
18.
Balakrishnan, Jayaraj Mymbilly, et al.. (1992). Effects of nitrous oxide on memory for instructions in dental patients. Human Psychopharmacology Clinical and Experimental. 7(1). 37–44. 8 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.

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