Catherine D. Nobes

12.5k total citations · 3 hit papers
48 papers, 10.3k citations indexed

About

Catherine D. Nobes is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Catherine D. Nobes has authored 48 papers receiving a total of 10.3k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 25 papers in Cell Biology and 20 papers in Cellular and Molecular Neuroscience. Recurrent topics in Catherine D. Nobes's work include Axon Guidance and Neuronal Signaling (17 papers), Hippo pathway signaling and YAP/TAZ (14 papers) and Cellular Mechanics and Interactions (11 papers). Catherine D. Nobes is often cited by papers focused on Axon Guidance and Neuronal Signaling (17 papers), Hippo pathway signaling and YAP/TAZ (14 papers) and Cellular Mechanics and Interactions (11 papers). Catherine D. Nobes collaborates with scholars based in United Kingdom, United States and Germany. Catherine D. Nobes's co-authors include Alan Hall, A Hall, Martin D. Brand, Phillip T. Hawkins, Len Stephens, Sarah E. Moorey, Ralf H. Adams, Daniel J. Marston, Magdalena L. Bochenek and Mara E. Pitulescu and has published in prestigious journals such as Nature, Cell and Journal of Biological Chemistry.

In The Last Decade

Catherine D. Nobes

48 papers receiving 10.2k citations

Hit Papers

Rho, Rac, and Cdc42 GTPases regulate the assembly of mult... 1995 2026 2005 2015 1995 1999 2010 1000 2.0k 3.0k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Catherine D. Nobes United Kingdom 35 6.7k 4.6k 1.9k 1.6k 1.1k 48 10.3k
Louis Lim Singapore 56 9.8k 1.5× 6.1k 1.3× 2.1k 1.1× 1.4k 0.9× 1.6k 1.5× 147 13.5k
Toshimasa Ishizaki Japan 44 9.6k 1.4× 7.3k 1.6× 1.7k 0.9× 1.7k 1.0× 1.4k 1.3× 76 15.4k
Akira Nagafuchi Japan 53 11.8k 1.8× 5.2k 1.1× 1.2k 0.7× 1.8k 1.1× 1.4k 1.3× 78 16.1k
Hugh F. Paterson United Kingdom 35 8.0k 1.2× 3.8k 0.8× 854 0.4× 1.2k 0.7× 1.8k 1.6× 41 10.6k
Edward Manser Singapore 40 7.3k 1.1× 3.9k 0.9× 890 0.5× 968 0.6× 1.3k 1.2× 71 9.2k
Johan de Rooij Netherlands 38 5.7k 0.9× 3.1k 0.7× 967 0.5× 1.1k 0.7× 943 0.9× 63 8.8k
Takuya Sasaki Japan 51 6.8k 1.0× 5.4k 1.2× 1.1k 0.6× 963 0.6× 690 0.6× 110 9.9k
Kazumasa Ohashi Japan 45 4.2k 0.6× 3.6k 0.8× 1.5k 0.8× 1.2k 0.7× 645 0.6× 130 8.7k
Sheila Μ. Thomas United States 35 6.2k 0.9× 3.0k 0.6× 879 0.5× 2.3k 1.4× 1.4k 1.3× 50 9.7k
Sandrine Etienne‐Manneville France 47 7.6k 1.1× 6.2k 1.4× 1.3k 0.7× 1.6k 0.9× 1.8k 1.6× 102 13.2k

Countries citing papers authored by Catherine D. Nobes

Since Specialization
Citations

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

Fields of papers citing papers by Catherine D. Nobes

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Catherine D. Nobes. 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 Catherine D. Nobes. The network helps show where Catherine D. Nobes may publish in the future.

Co-authorship network of co-authors of Catherine D. Nobes

This figure shows the co-authorship network connecting the top 25 collaborators of Catherine D. Nobes. A scholar is included among the top collaborators of Catherine D. Nobes 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 Catherine D. Nobes. Catherine D. Nobes 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.
Severn, Charlotte E., et al.. (2019). Ephrin/Eph receptor interaction facilitates macrophage recognition of differentiating human erythroblasts. Haematologica. 105(4). 914–924. 12 indexed citations
2.
Taylor, Hannah, et al.. (2017). Ephs and ephrins. Current Biology. 27(3). R90–R95. 76 indexed citations
3.
Batson, Jennifer, Jonathan W. Astin, & Catherine D. Nobes. (2013). Regulation of contact inhibition of locomotion by Eph–ephrin signalling. Journal of Microscopy. 251(3). 232–241. 21 indexed citations
4.
Astin, Jonathan W., Jennifer Batson, Shereen Kadir, et al.. (2010). Competition amongst Eph receptors regulates contact inhibition of locomotion and invasiveness in prostate cancer cells. Nature Cell Biology. 12(12). 1194–1204. 201 indexed citations
5.
Marston, Daniel J., Sarah E. Moorey, & Catherine D. Nobes. (2003). Rac-dependent trans-endocytosis of ephrinBs regulates Eph–ephrin contact repulsion. Nature Cell Biology. 5(10). 879–888. 236 indexed citations
6.
Harmey, Dympna, Gudrun Stenbeck, Catherine D. Nobes, Alistair J. Lax, & Agamemnon E. Grigoriadis. (2001). The effects of Pasteurella multocida toxin (PMT) on osteoblast differentiation: A role for Rho GTPases.. Journal of Bone and Mineral Research. 16. 1 indexed citations
7.
Driessens, M.H.E., Hailan Hu, Catherine D. Nobes, et al.. (2001). Plexin-B semaphorin receptors interact directly with active Rac and regulate the actin cytoskeleton by activating Rho. Current Biology. 11(5). 339–344. 164 indexed citations
8.
Nobes, Catherine D. & Mark Marsh. (2000). Dendritic cells: New roles for Cdc42 and Rac in antigen uptake?. Current Biology. 10(20). R739–R741. 60 indexed citations
9.
Flynn, Peter F., et al.. (1998). PRK1 Is Targeted to Endosomes by the Small GTPase, RhoB. Journal of Biological Chemistry. 273(9). 4811–4814. 100 indexed citations
10.
Suidan, Hana S., Catherine D. Nobes, Alan Hall, & Denis Monard. (1997). Astrocyte spreading in response to thrombin and lysophosphatidic acid is dependent on the Rho GTPase. Glia. 21(2). 244–252. 85 indexed citations
11.
Nobes, Catherine D., et al.. (1996). Phosphatidylinositol 3-kinase signals activate a selective subset of Rac/Rho-dependent effector pathways. Current Biology. 6(11). 1445–1455. 249 indexed citations
12.
Nobes, Catherine D., J.B. Reppas, Annette Markus, & A M Tolkovsky. (1996). Active p21Ras is sufficient for rescue of NGF-dependent rat sympathetic neurons. Neuroscience. 70(4). 1067–1079. 41 indexed citations
13.
Nobes, Catherine D. & Alan Hall. (1995). Rho, Rac, and Cdc42 GTPases regulate the assembly of multimolecular focal complexes associated with actin stress fibers, lamellipodia, and filopodia. Cell. 81(1). 53–62. 3738 indexed citations breakdown →
14.
Nobes, Catherine D., et al.. (1995). Neutralizing Anti‐p21ras Fabs Suppress Rat Sympathetic Neuron Survival Induced by NGF, LIF, CNTF and cAMP. European Journal of Neuroscience. 7(2). 344–350. 72 indexed citations
15.
Martin, Paul, Catherine D. Nobes, Jane T. McCluskey, & Julian Lewis. (1994). Repair of excisional wounds in the embryo. Eye. 8(2). 155–160. 20 indexed citations
16.
Martin, Paul & Catherine D. Nobes. (1992). An early molecular component of the wound healing response in rat embryos—induction of c-fos protein in cells at the epidermal wound margin. Mechanisms of Development. 38(3). 209–215. 69 indexed citations
17.
Nobes, Catherine D., A. Buckmaster, & Aviva M. Tolkovsky. (1991). Mediators of nerve growth factor action in cultured rat superior cervical ganglion neurones. Journal of the Autonomic Nervous System. 33(2). 213–214. 9 indexed citations
18.
Nobes, Catherine D., et al.. (1990). Non-ohmic proton conductance of the mitochondrial inner membrane in hepatocytes.. Journal of Biological Chemistry. 265(22). 12903–12909. 148 indexed citations
19.
Nobes, Catherine D., Patricia L. Lakin‐Thomas, & Martin D. Brand. (1989). The contribution of ATP turnover by the Na+/K+-ATPase to the rate of respiration of hepatocytes. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 976(2-3). 241–245. 45 indexed citations
20.
Berry, Michael N., Roland B. GREGORY, Anthony R. Grivell, et al.. (1988). Intracellular mitochondrial membrane potential as an indicator of hepatocyte energy metabolism: Further evidence for thermodynamic control of metabolism. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 936(3). 294–306. 30 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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