Jane B. Clarke

2.3k total citations · 1 hit paper
24 papers, 2.0k citations indexed

About

Jane B. Clarke is a scholar working on Molecular Biology, Endocrinology, Diabetes and Metabolism and Cancer Research. According to data from OpenAlex, Jane B. Clarke has authored 24 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Endocrinology, Diabetes and Metabolism and 8 papers in Cancer Research. Recurrent topics in Jane B. Clarke's work include Growth Hormone and Insulin-like Growth Factors (12 papers), Cancer, Hypoxia, and Metabolism (7 papers) and Metabolism, Diabetes, and Cancer (5 papers). Jane B. Clarke is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (12 papers), Cancer, Hypoxia, and Metabolism (7 papers) and Metabolism, Diabetes, and Cancer (5 papers). Jane B. Clarke collaborates with scholars based in United States, United Kingdom and Russia. Jane B. Clarke's co-authors include Adrian L. Harris, Michael J. Greenall, Russell Leek, R Whitehouse, Claire E. Lewis, David R. Clemmons, Walker H. Busby, Yumi Imai, Catherine Rees and T L Moore and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and The EMBO Journal.

In The Last Decade

Jane B. Clarke

22 papers receiving 1.9k citations

Hit Papers

Association of macrophage infiltration with angiogenesis ... 1996 2026 2006 2016 1996 250 500 750 1000

Peers

Jane B. Clarke
Suzanne Jordan United Kingdom
Gary Elliott United States
Regina Raz United States
Suzanne Jordan United Kingdom
Jane B. Clarke
Citations per year, relative to Jane B. Clarke Jane B. Clarke (= 1×) peers Suzanne Jordan

Countries citing papers authored by Jane B. Clarke

Since Specialization
Citations

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

Fields of papers citing papers by Jane B. Clarke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jane B. Clarke. 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 Jane B. Clarke. The network helps show where Jane B. Clarke may publish in the future.

Co-authorship network of co-authors of Jane B. Clarke

This figure shows the co-authorship network connecting the top 25 collaborators of Jane B. Clarke. A scholar is included among the top collaborators of Jane B. Clarke 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 Jane B. Clarke. Jane B. Clarke 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.
Maile, Laura A., et al.. (2005). Insulin‐like growth factor binding protein‐5 (IGFBP‐5) interacts with thrombospondin‐1 to induce negative regulatory effects on IGF‐I actions. Journal of Cellular Physiology. 203(2). 328–334. 12 indexed citations
2.
Perks, Claire M., Catherine McCaig, Jane B. Clarke, David R. Clemmons, & Jeffrey M P Holly. (2002). A non-IGF binding mutant of IGFBP-3 modulates cell function in breast epithelial cells. Biochemical and Biophysical Research Communications. 294(5). 988–994. 26 indexed citations
3.
Maile, Laura A., Yumi Imai, Jane B. Clarke, & David R. Clemmons. (2002). Insulin-like Growth Factor I Increases αVβ3 Affinity by Increasing the Amount of Integrin-associated Protein That Is Associated with Non-raft Domains of the Cellular Membrane. Journal of Biological Chemistry. 277(3). 1800–1805. 38 indexed citations
4.
Perks, Claire M., Catherine McCaig, Jane B. Clarke, David R. Clemmons, & Jeff M.P. Holly. (2002). Effects of a non-IGF binding mutant of IGFBP-5 on cell death in human breast cancer cells. Biochemical and Biophysical Research Communications. 294(5). 995–1000. 19 indexed citations
5.
Sakai, Keiji, Walker H. Busby, Jane B. Clarke, & David R. Clemmons. (2001). Tissue Transglutaminase Facilitates the Polymerization of Insulin-like Growth Factor-binding Protein-1 (IGFBP-1) and Leads to Loss of IGFBP-1's Ability to Inhibit Insulin-like Growth Factor-I-stimulated Protein Synthesis. Journal of Biological Chemistry. 276(12). 8740–8745. 40 indexed citations
6.
Imai, Yumi, et al.. (2000). Substitutions for Hydrophobic Amino Acids in the N-terminal Domains of IGFBP-3 and -5 Markedly Reduce IGF-I Binding and Alter Their Biologic Actions. Journal of Biological Chemistry. 275(24). 18188–18194. 98 indexed citations
7.
Badinga, L., et al.. (1999). Complex mediation of uterine endometrial epithelial cell growth by insulin-like growth factor-II (IGF-II) and IGF-binding protein-2. Journal of Molecular Endocrinology. 23(3). 277–285. 35 indexed citations
8.
Smith, Kelly J., Stephen B. Fox, M Taylor, et al.. (1999). Upregulation of basic fibroblast growth factor in breast carcinoma and its relationship to vascular density, oestrogen receptor, epidermal growth factor receptor and survival. Annals of Oncology. 10(6). 707–713. 76 indexed citations
9.
10.
Rees, Catherine, et al.. (1998). A Protease-Resistant Form of Insulin-Like Growth Factor (IGF) Binding Protein 4 Inhibits IGF-1 Actions1. Endocrinology. 139(10). 4182–4188. 39 indexed citations
11.
Zheng, Bo, Jane B. Clarke, Walker H. Busby, Cunming Duan, & David R. Clemmons. (1998). Insulin-Like Growth Factor-Binding Protein-5 Is Cleaved by Physiological Concentrations of Thrombin*. Endocrinology. 139(4). 1708–1714. 51 indexed citations
14.
Leek, Russell, Claire E. Lewis, R Whitehouse, et al.. (1996). Association of macrophage infiltration with angiogenesis and prognosis in invasive breast carcinoma.. PubMed. 56(20). 4625–9. 1001 indexed citations breakdown →
15.
Clemmons, David R., Walker H. Busby, T Arai, et al.. (1995). Role of insulin-like growth factor binding proteins in the control of IGF actions. PubMed. 6(2-4). 357–366. 65 indexed citations
16.
Wright, Kenneth L., T L Moore, Gang Li, et al.. (1994). CCAAT box binding protein NF-Y facilitates in vivo recruitment of upstream DNA binding transcription factors.. The EMBO Journal. 13(17). 4042–4053. 134 indexed citations
17.
Zeleznik‐Le, Nancy J., Yoshie Itoh-Lindstrom, Jane B. Clarke, T L Moore, & Jenny P.‐Y. Ting. (1992). The B cell-specific nuclear factor OTF-2 positively regulates transcription of the human class II transplantation gene, DRA.. Journal of Biological Chemistry. 267(11). 7677–7682. 14 indexed citations
18.
Clarke, Jane B., Elias Eliopoulos, J. B. C. Findlay, & P.F. Zagalsky. (1990). Alternative ligands as probes for the carotenoid-binding site of lobster carapace crustacyanin. Biochemical Journal. 265(3). 919–921. 9 indexed citations
19.
Crane, Mark St. J., Jane B. Clarke, & D. B. Thomas. (1977). Cell cycle dependent changes in morphology. Experimental Cell Research. 107(1). 89–94. 4 indexed citations
20.
Bird, O. D., et al.. (1970). 2-Amino-4-hydroxyquinazolines as Inhibitors of Thymidylate Synthetase. Molecular Pharmacology. 6(5). 573–575. 27 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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