Thomas E. Fisher

3.1k total citations
63 papers, 2.4k citations indexed

About

Thomas E. Fisher is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Physiology. According to data from OpenAlex, Thomas E. Fisher has authored 63 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Cellular and Molecular Neuroscience, 19 papers in Molecular Biology and 13 papers in Physiology. Recurrent topics in Thomas E. Fisher's work include Ion channel regulation and function (14 papers), Neuroscience and Neuropharmacology Research (13 papers) and Asthma and respiratory diseases (11 papers). Thomas E. Fisher is often cited by papers focused on Ion channel regulation and function (14 papers), Neuroscience and Neuropharmacology Research (13 papers) and Asthma and respiratory diseases (11 papers). Thomas E. Fisher collaborates with scholars based in Canada, United States and Japan. Thomas E. Fisher's co-authors include Julio M. Fernández, Piotr E. Marszałek, Charles W. Bourque, Mariano Carrión‐Vázquez, Andrés F. Oberhauser, Hongbin Li, W. R. A. K. J. S. Rajapaksha, M. Diane Lougheed, Dinara Baimoukhametova and Grant R. Gordon and has published in prestigious journals such as Journal of Biological Chemistry, Neuron and Journal of Neuroscience.

In The Last Decade

Thomas E. Fisher

60 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas E. Fisher Canada 23 947 716 716 348 321 63 2.4k
Robert P. Erickson United States 40 819 0.9× 646 0.9× 431 0.6× 99 0.3× 288 0.9× 104 4.0k
Julian A. Barden Australia 36 1.1k 1.2× 329 0.5× 146 0.2× 135 0.4× 779 2.4× 120 3.7k
Y. Kawai Japan 32 1.3k 1.4× 2.6k 3.6× 200 0.3× 446 1.3× 868 2.7× 148 4.5k
Y. Urade Japan 34 1.1k 1.2× 675 0.9× 80 0.1× 54 0.2× 530 1.7× 85 3.8k
Marcel Egger United States 32 1.0k 1.1× 1.3k 1.8× 101 0.1× 156 0.4× 200 0.6× 90 3.4k
Toshio Ikeda Japan 34 1.9k 2.0× 1.5k 2.1× 73 0.1× 172 0.5× 181 0.6× 174 5.8k
Takayuki Yoshida Japan 35 1.8k 1.9× 1.8k 2.5× 102 0.1× 185 0.5× 230 0.7× 138 4.8k
Pierre Poulain France 25 691 0.7× 583 0.8× 75 0.1× 401 1.2× 436 1.4× 101 2.1k
Thomas Michaelis Germany 28 963 1.0× 1000 1.4× 73 0.1× 205 0.6× 69 0.2× 56 3.8k
Sung‐Yon Kim South Korea 22 1.5k 1.6× 2.3k 3.2× 57 0.1× 786 2.3× 451 1.4× 35 5.8k

Countries citing papers authored by Thomas E. Fisher

Since Specialization
Citations

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

Fields of papers citing papers by Thomas E. Fisher

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas E. Fisher. 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 Thomas E. Fisher. The network helps show where Thomas E. Fisher may publish in the future.

Co-authorship network of co-authors of Thomas E. Fisher

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas E. Fisher. A scholar is included among the top collaborators of Thomas E. Fisher 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 Thomas E. Fisher. Thomas E. Fisher 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.
2.
Nakamura, Yoshikazu, et al.. (2023). Osmotically evoked PLCδ1-dependent translocation of ΔN-TRPV1 channels in rat supraoptic neurons. iScience. 26(3). 106258–106258. 2 indexed citations
3.
Day, Andrew G., et al.. (2020). Methacholine-Induced Cough in the Absence of Asthma: Insights From Impulse Oscillometry. Frontiers in Physiology. 11. 554679–554679. 3 indexed citations
4.
Fisher, Thomas E., et al.. (2017). Bronchoprotective effect of deep inspirations in cough variant asthma: A distinguishing feature in the spectrum of airway disease?. Respiratory Physiology & Neurobiology. 257. 55–64. 7 indexed citations
5.
Davis, Joseph, Thomas E. Fisher, Thalia R. Segal, et al.. (2016). Maternal Vitamin D Deficiency Programs Reproductive Dysfunction in Female Mice Offspring Through Adverse Effects on the Neuroendocrine Axis. Endocrinology. 157(4). 1535–1545. 20 indexed citations
6.
Xu, Jing, Min Xu, Marcelo Picinin Bernuci, et al.. (2013). Primate Follicular Development and Oocyte Maturation In Vitro. Advances in experimental medicine and biology. 761. 43–67. 43 indexed citations
7.
8.
Deesomchok, Athavudh, Thomas E. Fisher, Katherine A. Webb, et al.. (2009). Effects of Obesity on Perceptual and Mechanical Responses to Bronchoconstriction in Asthma. American Journal of Respiratory and Critical Care Medicine. 181(2). 125–133. 43 indexed citations
9.
Liu, Xiaohong, et al.. (2009). An osmosensitive voltage‐gated K+current in rat supraoptic neurons. European Journal of Neuroscience. 29(12). 2335–2346. 12 indexed citations
10.
Rajapaksha, W. R. A. K. J. S., et al.. (2008). Novel Splice Variants of Rat CaV2.1 That Lack Much of the Synaptic Protein Interaction Site Are Expressed in Neuroendocrine Cells. Journal of Biological Chemistry. 283(23). 15997–16003. 18 indexed citations
11.
Lougheed, M. Diane, Thomas E. Fisher, & Denis E. O’Donnell. (2006). Dynamic Hyperinflation During Bronchoconstriction in Asthma. CHEST Journal. 130(4). 1072–1081. 78 indexed citations
12.
Gordon, Grant R., Dinara Baimoukhametova, Sarah Hewitt, et al.. (2005). Norepinephrine triggers release of glial ATP to increase postsynaptic efficacy. Nature Neuroscience. 8(8). 1078–1086. 271 indexed citations
13.
Fisher, Thomas E. & Charles W. Bourque. (2001). The function of Ca2+ channel subtypes in exocytotic secretion: new perspectives from synaptic and non-synaptic release. Progress in Biophysics and Molecular Biology. 77(3). 269–303. 67 indexed citations
14.
Fisher, Thomas E., Mariano Carrión‐Vázquez, & Julio M. Fernández. (2000). Intracellular Ca2+ channel immunoreactivity in neuroendocrine axon terminals. FEBS Letters. 482(1-2). 131–138. 13 indexed citations
15.
Fisher, Thomas E., Mariano Carrión‐Vázquez, Andrés F. Oberhauser, et al.. (2000). Single Molecule Force Spectroscopy of Modular Proteins in the Nervous System. Neuron. 27(3). 435–446. 37 indexed citations
16.
Fernández, Julio M., Thomas E. Fisher, & Piotr E. Marszałek. (2000). Stretching single molecules into novel conformations using the atomic force microscope.. Nature Structural Biology. 7(9). 719–724. 248 indexed citations
17.
Carrión‐Vázquez, Mariano, Andrés F. Oberhauser, Thomas E. Fisher, et al.. (2000). Mechanical design of proteins studied by single-molecule force spectroscopy and protein engineering. Progress in Biophysics and Molecular Biology. 74(1-2). 63–91. 344 indexed citations
18.
Fisher, Thomas E., et al.. (1999). The micro‐mechanics of single molecules studied with atomic force microscopy. The Journal of Physiology. 520(1). 5–14. 49 indexed citations
19.
Fisher, Thomas E. & Charles W. Bourque. (1998). Properties of the Transient K+ Current in Acutely Isolated Supraoptic Neurons from Adult Rat. Advances in experimental medicine and biology. 449. 97–106. 20 indexed citations
20.
Fisher, Thomas E.. (1996). Calcium-channel subtypes in the somata and axon terminals of magnocellular neurosecretory cells. Trends in Neurosciences. 19(10). 440–444. 75 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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