Jonathon Gray

1.2k total citations
41 papers, 897 citations indexed

About

Jonathon Gray is a scholar working on Genetics, Oncology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Jonathon Gray has authored 41 papers receiving a total of 897 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Genetics, 8 papers in Oncology and 7 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Jonathon Gray's work include BRCA gene mutations in cancer (28 papers), Genomics and Rare Diseases (6 papers) and Global Cancer Incidence and Screening (6 papers). Jonathon Gray is often cited by papers focused on BRCA gene mutations in cancer (28 papers), Genomics and Rare Diseases (6 papers) and Global Cancer Incidence and Screening (6 papers). Jonathon Gray collaborates with scholars based in United Kingdom, United States and Singapore. Jonathon Gray's co-authors include Kate Brain, Rachel Iredale, Robert E. Mansel, Paul Norman, Paul Bennett, Andrew Hill, Marinus D. J. Stowers, Jacob T. Munro, Brendan Coleman and Lindsay Prior and has published in prestigious journals such as Journal of the American College of Cardiology, Cochrane Database of Systematic Reviews and The British Journal of Psychiatry.

In The Last Decade

Jonathon Gray

40 papers receiving 861 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jonathon Gray United Kingdom 18 439 145 139 133 126 41 897
Juan Acuña United States 15 449 1.0× 37 0.3× 202 1.5× 112 0.8× 102 0.8× 52 1.2k
Iman K. Martin United States 14 174 0.4× 76 0.5× 330 2.4× 204 1.5× 71 0.6× 21 1.1k
Leigh Jackson United Kingdom 20 549 1.3× 83 0.6× 55 0.4× 270 2.0× 70 0.6× 47 1.2k
Heather Zierhut United States 20 635 1.4× 113 0.8× 174 1.3× 269 2.0× 131 1.0× 74 1.4k
Laura Forrest Australia 17 438 1.0× 160 1.1× 102 0.7× 177 1.3× 23 0.2× 66 989
Angela Trepanier United States 12 550 1.3× 84 0.6× 77 0.6× 114 0.9× 51 0.4× 35 841
Stephanie A. Cohen United States 17 735 1.7× 98 0.7× 206 1.5× 183 1.4× 29 0.2× 42 1.1k
Rebecca Nash United States 17 131 0.3× 234 1.6× 204 1.5× 219 1.6× 63 0.5× 37 1.5k
Susan Fleming United States 17 126 0.3× 72 0.5× 51 0.4× 242 1.8× 90 0.7× 38 1.1k
Alison Metcalfe United Kingdom 23 595 1.4× 244 1.7× 83 0.6× 322 2.4× 71 0.6× 62 1.5k

Countries citing papers authored by Jonathon Gray

Since Specialization
Citations

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

Fields of papers citing papers by Jonathon Gray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jonathon Gray

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

All Works

20 of 20 papers shown
1.
Gray, Jonathon & Donald M. Berwick. (2009). Peering into the chasm: Improving the quality of clinical genetic services. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 151C(3). 173–174. 3 indexed citations
2.
McCann, Emma, et al.. (2009). Improving service delivery by evaluation of the referral pattern and capacity in a clinical genetics setting. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 151C(3). 200–206. 6 indexed citations
3.
Gray, Jonathon, et al.. (2009). Identification and prioritization of quality indicators in clinical genetics: An international survey. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 151C(3). 179–190. 11 indexed citations
4.
Bennett, Paul, Clare Wilkinson, Jim Turner, et al.. (2008). Psychological Factors Associated with Emotional Responses to Receiving Genetic Risk Information. Journal of Genetic Counseling. 17(3). 234–241. 36 indexed citations
5.
Iredale, Rachel, Frances Rapport, Stephanie Sivell, et al.. (2008). Exploring the requirements for a decision aid on familial breast cancer in the UK context: a qualitative study with patients referred to a cancer genetics service. Journal of Evaluation in Clinical Practice. 14(1). 110–115. 8 indexed citations
6.
Edwards, Rhiannon Tudor, James Williams, Jonathon Gray, et al.. (2008). Patient preferences and National Health Service costs: a cost-consequences analysis of cancer genetic services. Familial Cancer. 8(4). 265–275. 10 indexed citations
7.
Bennett, Paul, Ceri Phelps, Kate Brain, Kerenza Hood, & Jonathon Gray. (2007). A randomized controlled trial of a brief self-help coping intervention designed to reduce distress when awaiting genetic risk information. Journal of Psychosomatic Research. 63(1). 59–64. 40 indexed citations
8.
Rapport, Frances, Rachel Iredale, Wendy Jones, et al.. (2006). Decision aids for familial breast cancer: exploring women's views using focus groups. Health Expectations. 9(3). 232–244. 20 indexed citations
9.
Iredale, Rachel, Glyn Elwyn, Adrian Edwards, & Jonathon Gray. (2006). Attitudes of genetic clinicians in Wales to the future development of cancer genetics services. Journal of Evaluation in Clinical Practice. 13(1). 86–89. 9 indexed citations
10.
Tempest, Vanessa, et al.. (2005). Pedigree construction and disease confirmation: a pilot study in Wales exploring the role of nonclinical personnel. European Journal of Human Genetics. 13(9). 1063–1070. 4 indexed citations
11.
Elwyn, Glyn, Adrian Edwards, Rachel Iredale, Peter Davies, & Jonathon Gray. (2005). Identifying future models for delivering genetic services: a nominal group study in primary care. BMC Family Practice. 6(1). 14–14. 18 indexed citations
12.
Tempest, Vanessa, et al.. (2005). A Pilot Study of Spatial Patterns in Referrals to a Multicentre Cancer Genetics Service. Public Health Genomics. 8(2). 73–79. 3 indexed citations
13.
14.
Cohen, David, Garry Barton, Jonathon Gray, & Kate Brain. (2004). Health economics and genetic service development: a familial cancer genetic example. Familial Cancer. 3(1). 61–67. 10 indexed citations
15.
Watts, Patrick, Mark I. Rees, Angus Clarke, et al.. (2000). Linkage analysis in an autosomal dominant ‘zonular nuclear pulverulent’ congenital cataract, mapped to chromosome 13q11-13. Eye. 14(2). 172–175. 3 indexed citations
16.
Broadstock, Marita, Susan Michie, Jonathon Gray, James Mackay, & Theresa M. Marteau. (2000). The psychological consequences of offering mutation searching in the family for those at risk of hereditary breast and ovarian cancer?a pilot study. Psycho-Oncology. 9(6). 537–548. 32 indexed citations
17.
Brain, Kate, Paul Norman, Jonathon Gray, & Robert E. Mansel. (1999). Anxiety and Adherence to Breast Self-Examination in Women With a Family History of Breast Cancer. Psychosomatic Medicine. 61(2). 181–187. 97 indexed citations
18.
Cardno, Alastair G., Kieran C. Murphy, Lisa Jones, et al.. (1998). Polydactyly and psychosis. The British Journal of Psychiatry. 172(2). 184–185. 2 indexed citations
19.
Black, Cheryl, et al.. (1998). Correlation of a recurrent FBN1 mutation (R122C) with an atypical familial marfan syndrome phenotype. Human Mutation. 11(S1). S198–S200. 16 indexed citations
20.
Scourfield, Jane, et al.. (1997). Huntington's disease: Psychiatric practice in molecular genetic prediction and diagnosis. The British Journal of Psychiatry. 170(2). 146–149. 10 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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