William T. Mason

6.6k total citations
152 papers, 5.3k citations indexed

About

William T. Mason is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Social Psychology. According to data from OpenAlex, William T. Mason has authored 152 papers receiving a total of 5.3k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 52 papers in Cellular and Molecular Neuroscience and 18 papers in Social Psychology. Recurrent topics in William T. Mason's work include Ion channel regulation and function (30 papers), Neuroscience and Neuropharmacology Research (27 papers) and Neuroendocrine regulation and behavior (18 papers). William T. Mason is often cited by papers focused on Ion channel regulation and function (30 papers), Neuroscience and Neuropharmacology Research (27 papers) and Neuroendocrine regulation and behavior (18 papers). William T. Mason collaborates with scholars based in United Kingdom, United States and Slovakia. William T. Mason's co-authors include John S. Hoyland, Robert Zorec, G.I. Hatton, Sujit Kumar Sikdar, Gareth Leng, Pierre‐Marie Lledo, Peter Cobbett, R.J. Bicknell, Richard Bunting and Paul P. Yevich and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Neuron.

In The Last Decade

William T. Mason

148 papers receiving 5.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
William T. Mason United Kingdom 42 2.4k 1.6k 871 693 545 152 5.3k
James F. Battey United States 50 4.7k 1.9× 2.7k 1.6× 564 0.6× 617 0.9× 493 0.9× 144 9.7k
Kazutoshi Yamamoto Japan 36 1.5k 0.6× 1.2k 0.8× 487 0.6× 1.2k 1.7× 185 0.3× 221 5.7k
A. Oksche Germany 46 2.6k 1.1× 1.7k 1.0× 454 0.5× 846 1.2× 528 1.0× 143 5.5k
Madhabananda Sar United States 52 3.1k 1.3× 1.8k 1.1× 1.0k 1.2× 643 0.9× 312 0.6× 107 10.9k
Akira Matsumoto Japan 44 2.1k 0.9× 1.5k 0.9× 421 0.5× 1.2k 1.7× 152 0.3× 181 7.2k
M. Reinecke Switzerland 46 2.2k 0.9× 2.0k 1.2× 225 0.3× 539 0.8× 401 0.7× 137 7.4k
Bkc Chow Hong Kong 41 2.3k 0.9× 2.2k 1.4× 496 0.6× 912 1.3× 152 0.3× 204 6.0k
Allan R. Jones United States 30 4.5k 1.9× 2.2k 1.3× 239 0.3× 498 0.7× 529 1.0× 54 8.8k
Anders Ericsson Sweden 44 1.0k 0.4× 1.5k 0.9× 947 1.1× 940 1.4× 116 0.2× 206 7.8k
Yoshitaka Oka Japan 54 3.9k 1.6× 1.5k 0.9× 823 0.9× 648 0.9× 345 0.6× 341 9.8k

Countries citing papers authored by William T. Mason

Since Specialization
Citations

This map shows the geographic impact of William T. Mason'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 William T. Mason with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites William T. Mason more than expected).

Fields of papers citing papers by William T. Mason

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by William T. Mason. 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 William T. Mason. The network helps show where William T. Mason may publish in the future.

Co-authorship network of co-authors of William T. Mason

This figure shows the co-authorship network connecting the top 25 collaborators of William T. Mason. A scholar is included among the top collaborators of William T. Mason 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 William T. Mason. William T. Mason 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
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Yagodin, Sergey, Roger Hardie, Stuart J. Lansdell, et al.. (1998). Thapsigargin and receptor-mediated activation of Drosophila TRPL channels stably expressed in a Drosophila S2 cell line. Cell Calcium. 23(4). 219–228. 18 indexed citations
3.
Bolsover, Stephen R., et al.. (1998). Nuclear and cytosolic calcium changes in osteoclasts stimulated with ATP and integrin-binding peptide. Cell Calcium. 24(3). 213–221. 10 indexed citations
4.
Rupnik, Marjan Slak, Matthew Law, William T. Mason, & Robert Zorec. (1997). Mastoparan and Rab3AL peptide potentiation of calcium‐independent secretory activity in rat melanotrophs is inhibited by GDPβS. FEBS Letters. 411(2-3). 356–358. 4 indexed citations
5.
Freestone, Nicholas, Samo Ribarič, & William T. Mason. (1996). The effect of insulin-like growth factor-1 on adult rat cardiac contractility. Molecular and Cellular Biochemistry. 163-164(1). 223–229. 98 indexed citations
6.
McDonald, Fraser, et al.. (1996). Calcium Waves in Fluid Flow Stimulated Osteoblasts Are G Protein Mediated. Archives of Biochemistry and Biophysics. 326(1). 31–38. 17 indexed citations
7.
Rupnik, Marjan Slak, et al.. (1995). Brefeldin A and a synthetic peptide to ADP-ribosylation factor (ARF) inhibit regulated exocytosis in melanotrophs. Neuroreport. 6(6). 853–856. 14 indexed citations
8.
Lledo, Pierre‐Marie, Ludger Johannes, Philippe Vernier, et al.. (1994). Rab3 proteins: key players in the control of exocytosis. Trends in Neurosciences. 17(10). 426–432. 56 indexed citations
9.
Wojnowski, Leszek, et al.. (1994). Cell transformation induces a cytoplasmic Ca2+ oscillator in Madin-Darby canine kidney cells. Pflügers Archiv - European Journal of Physiology. 426(1-2). 89–94. 17 indexed citations
10.
Carew, Mark A., et al.. (1994). Extracellular ATP activates calcium entry and mobilization via P2U-purinoceptors in rat lactotrophs. Cell Calcium. 16(3). 227–235. 30 indexed citations
11.
Mason, William T.. (1993). Fluorescent and luminescent probes for biological activity : a practical guide to technology for quantitative real-time analysis. Academic Press eBooks. 97 indexed citations
12.
Boersma, C.J.C., et al.. (1993). Dynorphin 1–17 Delays the Vasopressin Induced Mobilization of Intracellular Calcium in Cultured Astrocytes from the Rat Neural Lobe. Journal of Neuroendocrinology. 5(5). 583–590. 15 indexed citations
13.
McArdle, Craig A., Richard Bunting, & William T. Mason. (1992). Dynamic video imaging of cystolic Ca2+ in the αT3-1, gonadotrope-derived cell line. Molecular and Cellular Neuroscience. 3(2). 124–132. 36 indexed citations
14.
Neylon, Craig B., William T. Mason, & R.F. Irvine. (1991). HISTAMINE‐INDUCED CALCIUM OSCILLATIONS IN HUMAN VASCULAR SMOOTH MUSCLE: TEMPORAL SEQUENCE AND SPATIAL ORGANIZATION IN SINGLE CELLS. Clinical and Experimental Pharmacology and Physiology. 18(5). 299–302. 7 indexed citations
15.
Levy, Andrew, Stafford L. Lightman, John S. Hoyland, & William T. Mason. (1990). INOSITOL PHOSPHOLIPID TURNOVER AND INTRACELLULAR Ca2+ RESPONSES TO THYROTROPHIN‐RELEASING HORMONE, GONADOTROPHIN‐RELEASING HORMONE AND ARGININE VASOPRESSIN IN PITUITARY CORTICOTROPH AND SOMATOTROPH ADENOMAS. Clinical Endocrinology. 33(1). 73–79. 13 indexed citations
16.
Cobbett, Peter, C.D. Ingram, & William T. Mason. (1987). Voltage-activated currents through calcium channels in normal bovine lactotrophs. Neuroscience. 23(2). 661–677. 18 indexed citations
17.
18.
Olson, Randall J., et al.. (1981). Atlas of coal/minerals and important resource problem areas for fish and wildlife in the conterminous United States. University of North Texas Digital Library (University of North Texas).
19.
Stauffer, Jay R., et al.. (1978). Surface mining and fish/wildlife needs in the eastern United States: proceedings of a symposium. FWS/OBS. 2 indexed citations
20.
Mason, William T., et al.. (1978). Methods for the assessment and prediction of mineral mining impacts on aquatic communities : a review and analysis : workshop proceedings, December 6-7, 1977, Harpers Ferry, West Virginia. FWS/OBS. 3 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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