Charles N. David

7.7k total citations · 1 hit paper
96 papers, 5.2k citations indexed

About

Charles N. David is a scholar working on Paleontology, Molecular Biology and Cell Biology. According to data from OpenAlex, Charles N. David has authored 96 papers receiving a total of 5.2k indexed citations (citations by other indexed papers that have themselves been cited), including 74 papers in Paleontology, 53 papers in Molecular Biology and 30 papers in Cell Biology. Recurrent topics in Charles N. David's work include Marine Invertebrate Physiology and Ecology (74 papers), Planarian Biology and Electrostimulation (29 papers) and Hippo pathway signaling and YAP/TAZ (23 papers). Charles N. David is often cited by papers focused on Marine Invertebrate Physiology and Ecology (74 papers), Planarian Biology and Electrostimulation (29 papers) and Hippo pathway signaling and YAP/TAZ (23 papers). Charles N. David collaborates with scholars based in Germany, United States and Japan. Charles N. David's co-authors include Richard D. Campbell, Thomas C. G. Bosch, Thomas W. Holstein, Alfred Gierer, Hans R. Bode, Angelika Böttger, Engelbert Hobmayer, Stefan Berking, Hubert Schaller and Ekkhart Trenkner and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and The Journal of Cell Biology.

In The Last Decade

Charles N. David

95 papers receiving 4.9k citations

Hit Papers

A quantitative method for maceration of hydra tissue 1973 2026 1990 2008 1973 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Charles N. David Germany 41 3.6k 2.9k 1.2k 1.0k 440 96 5.2k
Thomas W. Holstein Germany 43 3.8k 1.1× 3.7k 1.3× 1.3k 1.1× 1.8k 1.7× 325 0.7× 110 6.3k
Toshitaka Fujisawa Japan 29 1.8k 0.5× 1.7k 0.6× 664 0.6× 616 0.6× 177 0.4× 72 3.0k
Richard D. Campbell United States 32 2.0k 0.6× 1.5k 0.5× 773 0.6× 452 0.4× 219 0.5× 123 3.9k
Ulrich Technau Austria 49 4.2k 1.2× 4.3k 1.5× 1.2k 1.0× 2.4k 2.4× 156 0.4× 102 7.5k
John R. Finnerty United States 38 2.2k 0.6× 4.1k 1.4× 390 0.3× 1.6k 1.5× 123 0.3× 79 7.0k
Bernd Schierwater Germany 43 2.1k 0.6× 2.7k 0.9× 333 0.3× 1.5k 1.5× 81 0.2× 119 6.3k
Nicole King United States 38 1.3k 0.4× 4.4k 1.5× 873 0.7× 706 0.7× 81 0.2× 72 6.6k
Evelyn Houliston France 34 1.1k 0.3× 2.1k 0.7× 958 0.8× 741 0.7× 46 0.1× 74 3.5k
Bernard M. Degnan Australia 61 2.1k 0.6× 6.3k 2.2× 481 0.4× 3.5k 3.4× 125 0.3× 245 13.3k
David Q. Matus United States 25 1.5k 0.4× 1.9k 0.7× 418 0.3× 996 1.0× 65 0.1× 49 3.6k

Countries citing papers authored by Charles N. David

Since Specialization
Citations

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

Fields of papers citing papers by Charles N. David

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles N. David. 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 Charles N. David. The network helps show where Charles N. David may publish in the future.

Co-authorship network of co-authors of Charles N. David

This figure shows the co-authorship network connecting the top 25 collaborators of Charles N. David. A scholar is included among the top collaborators of Charles N. David 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 Charles N. David. Charles N. David 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.
Primack, Abby S., Ben D. Cox, Jack F. Cazet, et al.. (2025). A molecular, spatial and regulatory atlas of the Hydra vulgaris nervous system. Development. 152(20).
2.
Hunter, Donald A., Huaibi Zhang, P. Pidakala, et al.. (2024). On-tree ripening block of avocado fruit involves changes in ethylene sensitivity linked to gibberellin and auxin pathways. Postharvest Biology and Technology. 216. 113031–113031. 2 indexed citations
3.
Laue, Christoph Cramer von, Bianca Bertulat, Willi Salvenmoser, et al.. (2024). A new look at the architecture and dynamics of the Hydra nerve net. eLife. 12. 9 indexed citations
4.
Laue, Christoph Cramer von, Bianca Bertulat, Willi Salvenmoser, et al.. (2023). A new look at the architecture and dynamics of the Hydra nerve net. eLife. 12. 1 indexed citations
5.
Noro, Yukihiko, Seungshic Yum, Chiemi Nishimiya‐Fujisawa, et al.. (2019). Regionalized nervous system in Hydra and the mechanism of its development. Gene Expression Patterns. 31. 42–59. 20 indexed citations
6.
Takaku, Yasuharu, Jung Shan Hwang, Alexander Wolf, et al.. (2014). Innexin gap junctions in nerve cells coordinate spontaneous contractile behavior in Hydra polyps. Scientific Reports. 4(1). 3573–3573. 39 indexed citations
7.
Stadler, Sonja C., C. Vincent, V D Fedorov, et al.. (2013). Correction for Stadler et al., Dysregulation of PAD4-mediated citrullination of nuclear GSK3β activates TGF-β signaling and induces epithelial-to-mesenchymal transition in breast cancer cells. Proceedings of the National Academy of Sciences. 110(40). 16283–16283. 3 indexed citations
8.
David, Charles N.. (2012). Interstitial stem cells in Hydra: multipotency and decision-making. The International Journal of Developmental Biology. 56(6-7-8). 489–497. 74 indexed citations
9.
Hwang, Jung Shan, Yasuharu Takaku, Jarrod Chapman, et al.. (2008). Cilium Evolution: Identification of a Novel Protein, Nematocilin, in the Mechanosensory Cilium of Hydra Nematocytes. Molecular Biology and Evolution. 25(9). 2009–2017. 24 indexed citations
10.
Towb, Par, et al.. (2006). The Notch signaling pathway in the cnidarian Hydra. Developmental Biology. 303(1). 376–390. 72 indexed citations
11.
Alexandrova, Olga, et al.. (2005). Oogenesis in Hydra: Nurse cells transfer cytoplasm directly to the growing oocyte. Developmental Biology. 281(1). 91–101. 48 indexed citations
12.
David, Charles N.. (2005). Hydra and the Evolution of Apoptosis. Integrative and Comparative Biology. 45(4). 631–638. 34 indexed citations
13.
14.
Wilm, Bettina, et al.. (1999). Identification of caspases and apoptosis in the simple metazoan Hydra. Current Biology. 9(17). 959–S2. 135 indexed citations
15.
Hobmayer, Bert, Thomas W. Holstein, & Charles N. David. (1997). Stimulation of Tentacle and Bud Formation by the Neuropeptide Head Activator inHydra magnipapillata. Developmental Biology. 183(1). 1–8. 26 indexed citations
16.
David, Charles N., et al.. (1992). A quantitative method for separation of livingHydra cells. Development Genes and Evolution. 201(5). 296–300. 23 indexed citations
17.
Bosch, Thomas C. G., et al.. (1991). Role of the cellular environment in interstitial stem cell proliferation in Hydra. Development Genes and Evolution. 200(5). 269–276. 20 indexed citations
18.
Fujisawa, Toshitaka, Charles N. David, & Thomas C. G. Bosch. (1990). Transplantation stimulates interstitial cell migration in hydra. Developmental Biology. 138(2). 509–512. 18 indexed citations
19.
David, Charles N. & Richard D. Campbell. (1974). CELL CYCLE KINETICS AND DEVELOPMENT OF HYDRA ATTENUATA. Journal of Cell Science. 11(2). 349–358. 163 indexed citations
20.
David, Charles N.. (1964). UV inactivation and thymine dimerization in bacteriophageΦX. Molecular Genetics and Genomics. 1 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026