J. Gray

3.5k total citations
36 papers, 1.7k citations indexed

About

J. Gray is a scholar working on Genetics, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, J. Gray has authored 36 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Genetics, 8 papers in Pathology and Forensic Medicine and 7 papers in Molecular Biology. Recurrent topics in J. Gray's work include BRCA gene mutations in cancer (19 papers), Connective tissue disorders research (8 papers) and Genetic factors in colorectal cancer (7 papers). J. Gray is often cited by papers focused on BRCA gene mutations in cancer (19 papers), Connective tissue disorders research (8 papers) and Genetic factors in colorectal cancer (7 papers). J. Gray collaborates with scholars based in United Kingdom, United States and Singapore. J. Gray's co-authors include Petros Tsipouras, Nicholas T. Kouchoukos, Kevin J. Burton, Mary J. Roman, Kate Brain, Steve Davies, C. Cirrincione, Beryl McCormick, Jeanne A. Petrek and Joachim Yahalom and has published in prestigious journals such as Neurology, Radiology and Social Science & Medicine.

In The Last Decade

J. Gray

36 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. Gray United Kingdom 19 891 410 339 314 282 36 1.7k
Alasdair G. W. Hunter Canada 36 2.0k 2.2× 471 1.1× 271 0.8× 1.5k 4.8× 170 0.6× 139 4.1k
Laurie E. Cohen United States 31 629 0.7× 105 0.3× 200 0.6× 739 2.4× 136 0.5× 78 2.9k
Dawna Gilchrist Canada 15 552 0.6× 357 0.9× 108 0.3× 221 0.7× 91 0.3× 31 1.0k
Donald W. Hadley United States 27 1.4k 1.6× 173 0.4× 63 0.2× 754 2.4× 530 1.9× 65 2.7k
Sally Ann Lynch Ireland 34 1.4k 1.6× 125 0.3× 177 0.5× 1.6k 5.2× 216 0.8× 146 3.7k
Helga V. Toriello United States 32 1.4k 1.6× 159 0.4× 154 0.5× 1.3k 4.2× 85 0.3× 97 3.1k
Yves Alembik France 36 1.2k 1.4× 429 1.0× 130 0.4× 980 3.1× 92 0.3× 128 3.8k
Bonnie Jeanne Baty United States 24 1.3k 1.5× 166 0.4× 49 0.1× 319 1.0× 207 0.7× 43 2.4k
Philippe Backeljauw United States 28 1.4k 1.6× 292 0.7× 416 1.2× 1.2k 3.8× 98 0.3× 118 3.2k
Catherine S. Choong Australia 21 385 0.4× 379 0.9× 74 0.2× 844 2.7× 109 0.4× 61 1.6k

Countries citing papers authored by J. Gray

Since Specialization
Citations

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

Fields of papers citing papers by J. Gray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. Gray

This figure shows the co-authorship network connecting the top 25 collaborators of J. Gray. A scholar is included among the top collaborators of J. 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 J. Gray. J. 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.
2.
Rieck, G, Kevin Boon Leong Lim, Mark T. Rogers, et al.. (2006). Screening for familial ovarian cancer-management and outcome of women with moderate to high risk of developing ovarian cancer. International Journal of Gynecological Cancer. 16(S1). 86–91. 1 indexed citations
3.
Brain, Kate, Stephanie Sivell, Kristina Bennert, et al.. (2005). An exploratory comparison of genetic counselling protocols for HNPCC predictive testing. Clinical Genetics. 68(3). 255–261. 16 indexed citations
4.
Hopwood, Penelope, David Wonderling, Maggie Watson, et al.. (2004). A randomised comparison of UK genetic risk counselling services for familial cancer: psychosocial outcomes. British Journal of Cancer. 91(5). 884–892. 20 indexed citations
5.
Griffith, Gary L., Rhiannon Tudor Edwards, J. Gray, et al.. (2004). A micro costing of NHS cancer genetic services. British Journal of Cancer. 92(1). 60–71. 16 indexed citations
6.
Griffith, Gary L., Rhiannon Tudor Edwards, & J. Gray. (2004). Cancer genetics services: a systematic review of the economic evidence and issues. British Journal of Cancer. 90(9). 1697–1703. 27 indexed citations
7.
8.
Scott, Susie, Lindsay Prior, Fiona Wood, & J. Gray. (2004). Repositioning the patient: the implications of being ‘at risk’. Social Science & Medicine. 60(8). 1869–1879. 83 indexed citations
9.
Griffith, Gary L., Rhiannon Tudor Edwards, J. Gray, et al.. (2004). Estimating the survival benefits gained from providing national cancer genetic services to women with a family history of breast cancer. British Journal of Cancer. 90(10). 1912–1919. 11 indexed citations
10.
Brain, Kate, et al.. (2003). Genetic counselling protocols for hereditary non‐polyposis colorectal cancer: a survey of UK regional genetics centres. Clinical Genetics. 63(3). 198–204. 16 indexed citations
11.
Iredale, Rachel, et al.. (2003). Experiences of men with breast cancer: an exploratory focus group study. British Journal of Cancer. 89(10). 1834–1836. 40 indexed citations
12.
Brain, Kate, et al.. (2002). A randomized trial of specialist genetic assessment: psychological impact on women at different levels of familial breast cancer risk. British Journal of Cancer. 86(2). 233–238. 65 indexed citations
13.
Leeson, Simon, et al.. (2001). Developing a cancer genetics service in Wales: opinions of gynaecologists on the management of women at risk of familial ovarian cancer. European Journal of Cancer Care. 10(3). 172–178. 5 indexed citations
14.
Tischkowitz, Marc, C J Chapman, Anneke Lucassen, et al.. (2000). A comparison of methods currently used in clinical practice to estimate familial breast cancer risks. Annals of Oncology. 11(4). 451–454. 15 indexed citations
15.
France, Lydéric, Susan Michie, Peter Barrett‐Lee, et al.. (2000). Male cancer: a qualitative study of male breast cancer. The Breast. 9(6). 343–348. 67 indexed citations
16.
Gray, J., et al.. (2000). A model protocol evaluating the introduction of genetic assessment for women with a family history of breast cancer: Figure 1. Journal of Medical Genetics. 37(3). 192–196. 11 indexed citations
17.
Crolla, John A., et al.. (1997). A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.. Journal of Medical Genetics. 34(3). 207–212. 30 indexed citations
18.
Gray, J. & Steve Davies. (1996). Marfan syndrome.. Journal of Medical Genetics. 33(5). 403–408. 30 indexed citations
19.
Burton, Kevin J., et al.. (1995). Life expectancy in the Marfan syndrome. The American Journal of Cardiology. 75(2). 157–160. 365 indexed citations
20.
Gray, J.. (1995). Medical Genetics: Principles and Practice. Journal of Medical Genetics. 32(2). 159–159. 5 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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