Roger Pocock

5.1k total citations
66 papers, 1.8k citations indexed

About

Roger Pocock is a scholar working on Aging, Molecular Biology and Endocrine and Autonomic Systems. According to data from OpenAlex, Roger Pocock has authored 66 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Aging, 40 papers in Molecular Biology and 13 papers in Endocrine and Autonomic Systems. Recurrent topics in Roger Pocock's work include Genetics, Aging, and Longevity in Model Organisms (48 papers), Circadian rhythm and melatonin (13 papers) and Pluripotent Stem Cells Research (10 papers). Roger Pocock is often cited by papers focused on Genetics, Aging, and Longevity in Model Organisms (48 papers), Circadian rhythm and melatonin (13 papers) and Pluripotent Stem Cells Research (10 papers). Roger Pocock collaborates with scholars based in Australia, Denmark and United States. Roger Pocock's co-authors include Oliver Hobert, Charles Claudianos, Michelle Watts, Konstantinos Kagias, Sandeep Gopal, John Couchman, Hinke A.B. Multhaupt, Matilda Haas, Agnieszka Podolska and Gregory M. Davis and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Communications.

In The Last Decade

Roger Pocock

65 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roger Pocock Australia 22 900 574 262 257 248 66 1.8k
Erica D. Smith United States 24 1.1k 1.2× 677 1.2× 283 1.1× 593 2.3× 108 0.4× 35 2.9k
Elizabeth A. Pollina United States 13 1.7k 1.9× 289 0.5× 163 0.6× 457 1.8× 334 1.3× 15 2.7k
Brian D. Ackley United States 18 766 0.9× 466 0.8× 155 0.6× 115 0.4× 97 0.4× 37 1.6k
Ana Cristina Calvo Spain 26 760 0.8× 234 0.4× 186 0.7× 269 1.0× 110 0.4× 65 2.0k
Bertrand Ducos France 20 1.4k 1.6× 900 1.6× 278 1.1× 797 3.1× 143 0.6× 46 3.0k
Linda Lee United States 25 1.7k 1.9× 1.2k 2.1× 455 1.7× 804 3.1× 113 0.5× 42 3.2k
Renaud Legouis France 29 1.6k 1.8× 795 1.4× 240 0.9× 248 1.0× 71 0.3× 58 3.1k
Weiwei Zhong United States 25 908 1.0× 405 0.7× 126 0.5× 117 0.5× 79 0.3× 77 1.9k
Karl Kornacker United States 17 1.5k 1.7× 240 0.4× 850 3.2× 509 2.0× 179 0.7× 26 2.9k
Hilary Wilkinson United States 19 961 1.1× 235 0.4× 217 0.8× 160 0.6× 73 0.3× 32 2.3k

Countries citing papers authored by Roger Pocock

Since Specialization
Citations

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

Fields of papers citing papers by Roger Pocock

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roger Pocock

This figure shows the co-authorship network connecting the top 25 collaborators of Roger Pocock. A scholar is included among the top collaborators of Roger Pocock 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 Roger Pocock. Roger Pocock 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.
Cao, Wei, et al.. (2024). Neuro-intestinal acetylcholine signalling regulates the mitochondrial stress response in Caenorhabditis elegans. Nature Communications. 15(1). 6594–6594. 7 indexed citations
2.
Wang, Wenyue, et al.. (2023). An intestinal sphingolipid confers intergenerational neuroprotection. Nature Cell Biology. 25(8). 1196–1207. 11 indexed citations
3.
Pocock, Roger, et al.. (2022). Characterization of the Doublesex/MAB-3 transcription factor DMD-9 in Caenorhabditis elegans. G3 Genes Genomes Genetics. 13(2). 2 indexed citations
4.
Cao, Wei, et al.. (2022). Conditional Degradation of UNC-31/CAPS Enables Spatiotemporal Analysis of Neuropeptide Function. Journal of Neuroscience. 42(46). 8599–8607. 6 indexed citations
5.
Fallahi, Hossein, et al.. (2022). The regulatory landscape of neurite development in Caenorhabditis elegans. Frontiers in Molecular Neuroscience. 15. 974208–974208. 3 indexed citations
6.
Glenwinkel, Lori, Seth R. Taylor, Laura Pereira, et al.. (2021). In silico analysis of the transcriptional regulatory logic of neuronal identity specification throughout the C. elegans nervous system. eLife. 10. 15 indexed citations
7.
Pocock, Roger, et al.. (2021). Functions of the extracellular matrix in development: Lessons from Caenorhabditis elegans. Cellular Signalling. 84. 110006–110006. 5 indexed citations
8.
Gopal, Sandeep, et al.. (2021). A somatic proteoglycan controls Notch-directed germ cell fate. Nature Communications. 12(1). 6708–6708. 16 indexed citations
9.
Gopal, Sandeep, et al.. (2019). A Protein Disulfide Isomerase Controls Neuronal Migration through Regulation of Wnt Secretion. Cell Reports. 26(12). 3183–3190.e5. 11 indexed citations
10.
Gopal, Sandeep & Roger Pocock. (2018). Computational Analysis of the <em>Caenorhabditis elegans</em> Germline to Study the Distribution of Nuclei, Proteins, and the Cytoskeleton. Journal of Visualized Experiments. 3 indexed citations
11.
Arnatkevičiūtė, Aurina, Ben Fulcher, Roger Pocock, & Alex Fornito. (2018). Hub connectivity, neuronal diversity, and gene expression in the Caenorhabditis elegans connectome. PLoS Computational Biology. 14(2). e1005989–e1005989. 44 indexed citations
12.
Watts, Michelle, Roger Pocock, & Charles Claudianos. (2018). Brain Energy and Oxygen Metabolism: Emerging Role in Normal Function and Disease. Frontiers in Molecular Neuroscience. 11. 216–216. 272 indexed citations
13.
Pocock, Roger, et al.. (2017). Control of Neuropeptide Expression by Parallel Activity-dependent Pathways in Caenorhabditis elegans. Scientific Reports. 7(1). 38734–38734. 15 indexed citations
14.
Hansen, Stine L., et al.. (2017). LIN-32/Atonal Controls Oxygen Sensing Neuron Development in Caenorhabditis elegans. Scientific Reports. 7(1). 7294–7294. 6 indexed citations
15.
Gopal, Sandeep, Hinke A.B. Multhaupt, Csilla Pataki, et al.. (2015). Transmembrane proteoglycans control stretch-activated channels to set cytosolic calcium levels. The Journal of Cell Biology. 210(7). 1199–1211. 71 indexed citations
16.
Kagias, Konstantinos, et al.. (2012). Neuronal Responses to Physiological Stress. Frontiers in Genetics. 3. 222–222. 62 indexed citations
17.
Pocock, Roger. (2011). Invited review: decoding the microRNA response to hypoxia. Pflügers Archiv - European Journal of Physiology. 461(3). 307–315. 65 indexed citations
18.
Seago, Julian, et al.. (2010). The UNC-4 homeobox protein represses mab-9 expression in DA motor neurons in Caenorhabditis elegans. Mechanisms of Development. 128(1-2). 49–58. 3 indexed citations
19.
Faumont, Serge, Jun Takayama, Andrew D. Goldsmith, et al.. (2009). Lateralized Gustatory Behavior of C. elegans Is Controlled by Specific Receptor-Type Guanylyl Cyclases. Current Biology. 19(12). 996–1004. 84 indexed citations
20.
Boulin, Thomas, Roger Pocock, & Oliver Hobert. (2006). A Novel Eph Receptor-Interacting IgSF Protein Provides C. elegans Motoneurons with Midline Guidepost Function. Current Biology. 16(19). 1871–1883. 41 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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