Richard C. Strange

498 total citations
7 papers, 405 citations indexed

About

Richard C. Strange is a scholar working on Molecular Biology, Epidemiology and Dermatology. According to data from OpenAlex, Richard C. Strange has authored 7 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Epidemiology and 3 papers in Dermatology. Recurrent topics in Richard C. Strange's work include Glutathione Transferases and Polymorphisms (5 papers), Nonmelanoma Skin Cancer Studies (4 papers) and Genomics, phytochemicals, and oxidative stress (2 papers). Richard C. Strange is often cited by papers focused on Glutathione Transferases and Polymorphisms (5 papers), Nonmelanoma Skin Cancer Studies (4 papers) and Genomics, phytochemicals, and oxidative stress (2 papers). Richard C. Strange collaborates with scholars based in United Kingdom and United States. Richard C. Strange's co-authors include Anthony A. Fryer, Peter M. Jones, Michael Hepple, Monica Spiteri, Andrea Bianco, Peter W. Jones, Janice Gilford, John T. Lear, Bill Bowers and Helen Ramsay and has published in prestigious journals such as American Journal of Respiratory and Critical Care Medicine, Journal of Investigative Dermatology and Carcinogenesis.

In The Last Decade

Richard C. Strange

7 papers receiving 388 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Richard C. Strange United Kingdom 6 244 104 81 70 47 7 405
Eiko Matsui Japan 10 88 0.4× 103 1.0× 23 0.3× 40 0.6× 23 0.5× 37 327
Yasue Suzaki Japan 8 89 0.4× 168 1.6× 35 0.4× 13 0.2× 63 1.3× 10 406
Hironori Masuko Japan 13 144 0.6× 238 2.3× 33 0.4× 26 0.4× 22 0.5× 36 483
Philippe Marquillies France 10 97 0.4× 224 2.2× 36 0.4× 33 0.5× 7 0.1× 14 459
C.‐S. Park South Korea 11 104 0.4× 228 2.2× 16 0.2× 36 0.5× 22 0.5× 13 424
Astrid Doerner United States 5 96 0.4× 116 1.1× 57 0.7× 8 0.1× 14 0.3× 8 363
Renate Effner Germany 6 36 0.1× 93 0.9× 19 0.2× 40 0.6× 35 0.7× 9 253
Vivek Gandhi Canada 9 42 0.2× 165 1.6× 17 0.2× 30 0.4× 25 0.5× 15 342
M.T. Guinnepain France 11 51 0.2× 122 1.2× 54 0.7× 227 3.2× 10 0.2× 34 776
Jessica S. Siegle Australia 8 98 0.4× 257 2.5× 48 0.6× 17 0.2× 27 0.6× 9 451

Countries citing papers authored by Richard C. Strange

Since Specialization
Citations

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

Fields of papers citing papers by Richard C. Strange

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard C. Strange. 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 Richard C. Strange. The network helps show where Richard C. Strange may publish in the future.

Co-authorship network of co-authors of Richard C. Strange

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

All Works

7 of 7 papers shown
1.
Ramsay, Helen, et al.. (2001). Polymorphisms in Glutathione S-Transferases are Associated with Altered Risk of Nonmelanoma Skin Cancer in Renal Transplant Recipients: A Preliminary Analysis. Journal of Investigative Dermatology. 117(2). 251–255. 46 indexed citations
2.
Ramachandran, Sudarshan, Anthony A. Fryer, & Richard C. Strange. (2001). Genetic factors determining cutaneous basal cell carcinoma phenotype*. Medical and Pediatric Oncology. 36(5). 559–563. 4 indexed citations
3.
Fryer, Anthony A., Andrea Bianco, Michael Hepple, et al.. (2000). Polymorphism at the Glutathione S -transferase GSTP1 Locus: A New Marker for Bronchial Hyperresponsiveness and Asthma. American Journal of Respiratory and Critical Care Medicine. 161(5). 1437–1442. 229 indexed citations
4.
Ramachandran, Sudarshan, Paul R. Hoban, Francis Ali‐Osman, et al.. (2000). Glutathione S-transferase GSTP1 and cyclin D1 genotypes: association with numbers of basal cell carcinomas in a patient subgroup at high-risk of multiple tumours. Pharmacogenetics. 10(6). 545–556. 27 indexed citations
5.
Lear, John T., Andrew G. Smith, Bill Bowers, et al.. (1997). Truncal Tumor Site Is Associated with high Risk of Multiple Basal Cell Carcinoma and Is Influenced by Glutathione S-Transferase, GSTT1, and Cytochrome P450, CYP1A1 Genotypes, and Their Interaction. Journal of Investigative Dermatology. 108(4). 519–522. 49 indexed citations
6.
Hand, Philip, Janice Gilford, Julie Alldersea, et al.. (1996). Allelism at the glutathione S-transferase GSTM3 locus: interactionswith GSTM1 and GSTT1 as risk factors for astrocytoma. Carcinogenesis. 17(9). 1919–1922. 45 indexed citations
7.
Otter, Mark W., et al.. (1994). Immunocytochemical Studies of the Distribution of Alpha and PI Isoforms of Glutathione S-Transferase in Cystic Renal Diseases. Pediatric Pathology. 14(3). 497–504. 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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