David Wilcockson

2.4k total citations · 1 hit paper
48 papers, 1.8k citations indexed

About

David Wilcockson is a scholar working on Cellular and Molecular Neuroscience, Ecology and Genetics. According to data from OpenAlex, David Wilcockson has authored 48 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Cellular and Molecular Neuroscience, 18 papers in Ecology and 11 papers in Genetics. Recurrent topics in David Wilcockson's work include Neurobiology and Insect Physiology Research (19 papers), Crustacean biology and ecology (12 papers) and Circadian rhythm and melatonin (10 papers). David Wilcockson is often cited by papers focused on Neurobiology and Insect Physiology Research (19 papers), Crustacean biology and ecology (12 papers) and Circadian rhythm and melatonin (10 papers). David Wilcockson collaborates with scholars based in United Kingdom, Germany and France. David Wilcockson's co-authors include V. Hugh Perry, Colm Cunningham, Katie Lunnon, Suzanne Campion, Simon G. Webster, Sandra J. Campbell, Daniel C. Anthony, Lin Zhang, Andrew Oliphant and Charalambos P. Kyriacou and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Neuroscience and The Science of The Total Environment.

In The Last Decade

David Wilcockson

45 papers receiving 1.8k citations

Hit Papers

Central and Systemic Endotoxin Challenges Exacerbate the ... 2005 2026 2012 2019 2005 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David Wilcockson United Kingdom 21 508 494 413 346 341 48 1.8k
Amalia Molinero Spain 29 482 0.9× 284 0.6× 165 0.4× 449 1.3× 685 2.0× 55 2.3k
Charlie S. Thompson Canada 28 198 0.4× 548 1.1× 240 0.6× 175 0.5× 1.1k 3.1× 45 2.4k
Pedro Fernández‐Llebrez Spain 30 497 1.0× 850 1.7× 200 0.5× 248 0.7× 839 2.5× 94 2.8k
Christian F. Deschepper Canada 34 119 0.2× 685 1.4× 182 0.4× 155 0.4× 1.6k 4.8× 115 4.3k
Xiujun Sun China 26 58 0.1× 190 0.4× 240 0.6× 474 1.4× 579 1.7× 105 2.2k
Bruno Cozzi Italy 26 108 0.2× 567 1.1× 479 1.2× 51 0.1× 392 1.1× 166 2.3k
Edward W. Green United States 29 46 0.1× 665 1.3× 145 0.4× 93 0.3× 733 2.1× 67 2.8k
Joseph G. Duman United States 31 79 0.2× 728 1.5× 610 1.5× 82 0.2× 905 2.7× 51 2.3k
Silvana Allodi Brazil 21 65 0.1× 380 0.8× 189 0.5× 249 0.7× 315 0.9× 91 1.4k
Leslie T. Buck Canada 35 86 0.2× 715 1.4× 1.7k 4.2× 215 0.6× 1.7k 5.0× 109 4.3k

Countries citing papers authored by David Wilcockson

Since Specialization
Citations

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

Fields of papers citing papers by David Wilcockson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Wilcockson

This figure shows the co-authorship network connecting the top 25 collaborators of David Wilcockson. A scholar is included among the top collaborators of David Wilcockson 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 David Wilcockson. David Wilcockson 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
2.
Wilcockson, David, et al.. (2025). Allatostatin-C signaling in the crab Carcinus maenas is implicated in the ecdysis program. Journal of Experimental Biology. 228(5).
3.
Payton, Laura, et al.. (2024). Revealing the profound influence of diapause on gene expression: Insights from the annual transcriptome of the copepod Calanus finmarchicus. Molecular Ecology. 33(13). e17425–e17425. 1 indexed citations
4.
Zhang, Lin, Edward W. Green, Simon G. Webster, et al.. (2023). The circadian clock gene bmal1 is necessary for co-ordinated circatidal rhythms in the marine isopod Eurydice pulchra (Leach). PLoS Genetics. 19(10). e1011011–e1011011. 5 indexed citations
5.
Ugolini, Alberto, Takahiko Hariyama, David Wilcockson, & Luca Mercatelli. (2023). The use of polarized light in the zonal orientation of the sandhopper Talitrus saltator (Montagu). Zoological Letters. 9(1). 10–10. 1 indexed citations
6.
Wilcockson, David, et al.. (2022). Towards an Understanding of Circatidal Clocks. Frontiers in Physiology. 13. 830107–830107. 8 indexed citations
7.
Tidau, Svenja, Tim Smyth, David McKee, et al.. (2021). Marine artificial light at night: An empirical and technical guide. Methods in Ecology and Evolution. 12(9). 1588–1601. 29 indexed citations
8.
Rawlinson, Kate A., Adam J. Reid, Zhigang Lu, et al.. (2021). Daily rhythms in gene expression of the human parasite Schistosoma mansoni. BMC Biology. 19(1). 255–255. 12 indexed citations
9.
Payton, Laura, Céline Noirot, Claire Hoede, et al.. (2020). Daily transcriptomes of the copepod Calanus finmarchicus during the summer solstice at high Arctic latitudes. Scientific Data. 7(1). 415–415. 7 indexed citations
10.
Oliphant, Andrew, et al.. (2020). Pigment Dispersing Factors and Their Cognate Receptors in a Crustacean Model, With New Insights Into Distinct Neurons and Their Functions. Frontiers in Neuroscience. 14. 595648–595648. 5 indexed citations
11.
Oliphant, Andrew, et al.. (2018). Transcriptomic analysis of crustacean neuropeptide signaling during the moult cycle in the green shore crab, Carcinus maenas. BMC Genomics. 19(1). 711–711. 59 indexed citations
12.
King, Nathan G., et al.. (2017). Cumulative stress restricts niche filling potential of habitat‐forming kelps in a future climate. Functional Ecology. 32(2). 288–299. 28 indexed citations
14.
Webster, Simon G., et al.. (2012). Bursicon and neuropeptide cascades during the ecdysis program of the shore crab, Carcinus maenas. General and Comparative Endocrinology. 182. 54–64. 40 indexed citations
15.
Wilcockson, David, et al.. (2010). Design and Construction of Yarra River Crossing Cofferdam for Melbourne Main Sewer Replacement Project. 412. 1 indexed citations
16.
Wilcockson, David, Lin Zhang, Michael H. Hastings, Charalambos P. Kyriacou, & Simon G. Webster. (2010). A novel form of pigment‐dispersing hormone in the central nervous system of the intertidal marine isopod, Eurydice pulchra (leach). The Journal of Comparative Neurology. 519(3). 562–575. 22 indexed citations
17.
Wilcockson, David & Lin Zhang. (2008). Circatidal clocks. Current Biology. 18(17). R753–R755. 43 indexed citations
18.
Wilcockson, David & Simon G. Webster. (2007). Identification and developmental expression of mRNAs encoding putative insect cuticle hardening hormone, bursicon in the green shore crab Carcinus maenas. General and Comparative Endocrinology. 156(1). 113–125. 39 indexed citations
19.
Wilcockson, David, et al.. (2002). Is crustacean hyperglycaemic hormone precursor-related peptide a circulating neurohormone in crabs?. Cell and Tissue Research. 307(1). 129–138. 45 indexed citations
20.
Campbell, Sandra J., David Wilcockson, Angus G. Butchart, V. Hugh Perry, & Daniel C. Anthony. (2002). Altered chemokine expression in the spinal cord and brain contributes to differential interleukin‐1β‐induced neutrophil recruitment. Journal of Neurochemistry. 83(2). 432–441. 53 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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