Mark W. Sherwood

1.5k total citations
19 papers, 936 citations indexed

About

Mark W. Sherwood is a scholar working on Cellular and Molecular Neuroscience, Surgery and Molecular Biology. According to data from OpenAlex, Mark W. Sherwood has authored 19 papers receiving a total of 936 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 7 papers in Surgery and 6 papers in Molecular Biology. Recurrent topics in Mark W. Sherwood's work include Neuroscience and Neuropharmacology Research (6 papers), Pancreatic function and diabetes (6 papers) and Pancreatitis Pathology and Treatment (5 papers). Mark W. Sherwood is often cited by papers focused on Neuroscience and Neuropharmacology Research (6 papers), Pancreatic function and diabetes (6 papers) and Pancreatitis Pathology and Treatment (5 papers). Mark W. Sherwood collaborates with scholars based in United Kingdom, Japan and France. Mark W. Sherwood's co-authors include Ole H. Petersen, Alexei V. Tepikin, Oleg V. Gerasimenko, Julia V. Gerasimenko, Katsuhiko Mikoshiba, Etsuko Ebisui, Misa Arizono, Hiroko Bannai, Stéphane H. R. Oliet and Aude Panatier and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Gastroenterology.

In The Last Decade

Mark W. Sherwood

19 papers receiving 929 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark W. Sherwood United Kingdom 14 356 316 283 217 152 19 936
Kyota Aoyagi Japan 16 279 0.8× 584 1.8× 191 0.7× 58 0.3× 73 0.5× 25 1.0k
Sundeep Malik United States 22 127 0.4× 1.2k 3.9× 355 1.3× 68 0.3× 63 0.4× 35 1.6k
Tonia E. Tse United States 11 168 0.5× 657 2.1× 268 0.9× 47 0.2× 16 0.1× 12 1.2k
Carl M. Hurt United States 16 65 0.2× 539 1.7× 291 1.0× 138 0.6× 73 0.5× 27 922
Edward Kaftan United States 15 37 0.1× 790 2.5× 479 1.7× 94 0.4× 87 0.6× 24 1.2k
Adriaan Nelemans Netherlands 20 64 0.2× 526 1.7× 237 0.8× 265 1.2× 54 0.4× 37 798
María Teresa Alonso Spain 13 91 0.3× 718 2.3× 381 1.3× 86 0.4× 98 0.6× 22 912
Tomasz Węgierski Poland 15 51 0.1× 635 2.0× 145 0.5× 42 0.2× 360 2.4× 19 1.1k
Nestor X. Barrezueta United States 13 53 0.1× 614 1.9× 494 1.7× 27 0.1× 50 0.3× 14 1.3k
Maksym I. Harhun United Kingdom 15 103 0.3× 470 1.5× 162 0.6× 103 0.5× 88 0.6× 29 799

Countries citing papers authored by Mark W. Sherwood

Since Specialization
Citations

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

Fields of papers citing papers by Mark W. Sherwood

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark W. Sherwood. 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 Mark W. Sherwood. The network helps show where Mark W. Sherwood may publish in the future.

Co-authorship network of co-authors of Mark W. Sherwood

This figure shows the co-authorship network connecting the top 25 collaborators of Mark W. Sherwood. A scholar is included among the top collaborators of Mark W. Sherwood 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 Mark W. Sherwood. Mark W. Sherwood is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Soma, Shogo, Norihito Hayatsu, Kengo Nomura, et al.. (2025). Channel synapse mediates neurotransmission of airway protective chemoreflexes. Cell. 188(10). 2687–2704.e29. 3 indexed citations
2.
Sherwood, Mark W., Stéphane H. R. Oliet, & Aude Panatier. (2021). NMDARs, Coincidence Detectors of Astrocytic and Neuronal Activities. International Journal of Molecular Sciences. 22(14). 7258–7258. 14 indexed citations
3.
Sherwood, Mark W., Misa Arizono, Aude Panatier, Katsuhiko Mikoshiba, & Stéphane H. R. Oliet. (2021). Astrocytic IP3Rs: Beyond IP3R2. Frontiers in Cellular Neuroscience. 15. 695817–695817. 35 indexed citations
4.
Chvanov, Michael, Danielle Moore, Mark W. Sherwood, et al.. (2018). Intracellular rupture, exocytosis and actin interaction of endocytic vacuoles in pancreatic acinar cells: initiating events in acute pancreatitis. The Journal of Physiology. 596(13). 2547–2564. 23 indexed citations
5.
Sherwood, Mark W., Misa Arizono, Chihiro Hisatsune, et al.. (2017). Astrocytic IP3Rs: Contribution to Ca2+ signalling and hippocampal LTP. Glia. 65(3). 502–513. 101 indexed citations
6.
Bannai, Hiroko, Mark W. Sherwood, Amulya Nidhi Shrivastava, et al.. (2015). Bidirectional Control of Synaptic GABAAR Clustering by Glutamate and Calcium. Cell Reports. 13(12). 2768–2780. 76 indexed citations
7.
Gerasimenko, Julia V., Mark W. Sherwood, Paweł E. Ferdek, et al.. (2015). Both RyRs and TPCs are required for NAADP-induced intracellular Ca2+ release. Cell Calcium. 58(3). 237–245. 45 indexed citations
8.
Arizono, Misa, Hiroko Bannai, Kyoko Nakamura, et al.. (2012). Receptor-Selective Diffusion Barrier Enhances Sensitivity of Astrocytic Processes to Metabotropic Glutamate Receptor Stimulation. Science Signaling. 5(218). ra27–ra27. 49 indexed citations
9.
Lür, György, Mark W. Sherwood, Etsuko Ebisui, et al.. (2011). InsP3 receptors and Orai channels in pancreatic acinar cells: co-localization and its consequences. Biochemical Journal. 436(2). 231–239. 49 indexed citations
10.
Gerasimenko, Julia V., György Lür, Paweł E. Ferdek, et al.. (2011). Calmodulin protects against alcohol-induced pancreatic trypsinogen activation elicited via Ca 2+ release through IP 3 receptors. Proceedings of the National Academy of Sciences. 108(14). 5873–5878. 40 indexed citations
11.
Gerasimenko, Julia V., György Lür, Mark W. Sherwood, et al.. (2009). Pancreatic protease activation by alcohol metabolite depends on Ca 2+ release via acid store IP 3 receptors. Proceedings of the National Academy of Sciences. 106(26). 10758–10763. 85 indexed citations
12.
Murphy, John A., David N. Criddle, Mark W. Sherwood, et al.. (2008). Direct Activation of Cytosolic Ca2+ Signaling and Enzyme Secretion by Cholecystokinin in Human Pancreatic Acinar Cells. Gastroenterology. 135(2). 632–641. 106 indexed citations
13.
Voronina, Svetlana, et al.. (2008). Downstream from calcium signalling: mitochondria, vacuoles and pancreatic acinar cell damage. Acta Physiologica. 195(1). 161–169. 6 indexed citations
14.
Voronina, Svetlana, Mark W. Sherwood, Oleg V. Gerasimenko, Ole H. Petersen, & Alexei V. Tepikin. (2007). Visualizing formation and dynamics of vacuoles in living cells using contrasting dextran-bound indicator: endocytic and nonendocytic vacuoles. American Journal of Physiology-Gastrointestinal and Liver Physiology. 293(6). G1333–G1338. 7 indexed citations
15.
Haynes, Lee P., Mark W. Sherwood, Nick J. Dolman, & Robert D. Burgoyne. (2007). Specificity, Promiscuity and Localization of ARF Protein Interactions with NCS‐1 and Phosphatidylinositol‐4 Kinase‐IIIβ. Traffic. 8(8). 1080–1092. 36 indexed citations
16.
Sherwood, Mark W., Ian A. Prior, Svetlana Voronina, et al.. (2007). Activation of trypsinogen in large endocytic vacuoles of pancreatic acinar cells. Proceedings of the National Academy of Sciences. 104(13). 5674–5679. 132 indexed citations
17.
Murphy, John A., David N. Criddle, Mark W. Sherwood, et al.. (2006). HUMAN PANCREATIC ACINAR CELLS HAVE FUNCTIONAL CHOLECYSTOKININ RECEPTORS. Pancreas. 33(4). 485–485. 1 indexed citations
18.
Barrow, Stephanie L., Mark W. Sherwood, Nick J. Dolman, et al.. (2006). Movement of calcium signals and calcium-binding proteins: firewalls, traps and tunnels. Biochemical Society Transactions. 34(3). 381–384. 4 indexed citations
19.
Gerasimenko, Julia V., Mark W. Sherwood, Alexei V. Tepikin, Ole H. Petersen, & Oleg V. Gerasimenko. (2006). NAADP, cADPR and IP3 all release Ca2+ from the endoplasmic reticulum and an acidic store in the secretory granule area. Journal of Cell Science. 119(2). 226–238. 124 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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