Martin D. Rayner

1.2k total citations
37 papers, 1.0k citations indexed

About

Martin D. Rayner is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Environmental Chemistry. According to data from OpenAlex, Martin D. Rayner has authored 37 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Cellular and Molecular Neuroscience, 21 papers in Molecular Biology and 8 papers in Environmental Chemistry. Recurrent topics in Martin D. Rayner's work include Ion channel regulation and function (19 papers), Neuroscience and Neural Engineering (15 papers) and Photoreceptor and optogenetics research (10 papers). Martin D. Rayner is often cited by papers focused on Ion channel regulation and function (19 papers), Neuroscience and Neural Engineering (15 papers) and Photoreceptor and optogenetics research (10 papers). Martin D. Rayner collaborates with scholars based in United States, Germany and Austria. Martin D. Rayner's co-authors include John G. Starkus, Stefan H. Heinemann, Peter C. Ruben, Daniel Alicata, Cedomir Todorovic, Tessi Sherrin, Joachim Spiess, Thomas Blank, Andrea Fleig and Matthew W. Pitts and has published in prestigious journals such as Nature, Science and Journal of Neuroscience.

In The Last Decade

Martin D. Rayner

37 papers receiving 947 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin D. Rayner United States 17 621 487 275 88 83 37 1.0k
Gerald Audesirk United States 25 431 0.7× 722 1.5× 29 0.1× 144 1.6× 104 1.3× 48 1.4k
Shigehiro Nakajima United States 21 1.1k 1.8× 1.2k 2.4× 346 1.3× 131 1.5× 82 1.0× 47 1.7k
W F Gilly United States 19 754 1.2× 826 1.7× 196 0.7× 91 1.0× 55 0.7× 24 1.2k
William S. Redfern United Kingdom 19 399 0.6× 344 0.7× 144 0.5× 68 0.8× 41 0.5× 35 1.1k
Vincent E. Dionne United States 25 1.3k 2.1× 1.6k 3.2× 162 0.6× 96 1.1× 25 0.3× 43 2.3k
Jordan E. Warnick United States 24 1.1k 1.7× 731 1.5× 109 0.4× 34 0.4× 18 0.2× 69 1.7k
Michael Madeja Germany 18 569 0.9× 558 1.1× 229 0.8× 103 1.2× 14 0.2× 52 1.0k
Betty M. Twarog United States 26 579 0.9× 973 2.0× 304 1.1× 52 0.6× 229 2.8× 44 2.0k
Toshio Narahashi United States 27 1.4k 2.2× 1.1k 2.3× 177 0.6× 82 0.9× 43 0.5× 60 2.2k
William Van der Kloot United States 20 788 1.3× 859 1.8× 60 0.2× 139 1.6× 53 0.6× 66 1.2k

Countries citing papers authored by Martin D. Rayner

Since Specialization
Citations

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

Fields of papers citing papers by Martin D. Rayner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martin D. Rayner. 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 Martin D. Rayner. The network helps show where Martin D. Rayner may publish in the future.

Co-authorship network of co-authors of Martin D. Rayner

This figure shows the co-authorship network connecting the top 25 collaborators of Martin D. Rayner. A scholar is included among the top collaborators of Martin D. Rayner 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 Martin D. Rayner. Martin D. Rayner 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.
Yang, Lizhen, Philip Tovote, Martin D. Rayner, et al.. (2010). Corticotropin-releasing factor receptors and urocortins, links between the brain and the heart. European Journal of Pharmacology. 632(1-3). 1–6. 34 indexed citations
2.
Sherrin, Tessi, et al.. (2010). Hippocampal c-Jun-N-Terminal Kinases Serve as Negative Regulators of Associative Learning. Journal of Neuroscience. 30(40). 13348–13361. 57 indexed citations
4.
Todorovic, Cedomir, et al.. (2008). Suppression of the MEK/ERK Signaling Pathway Reverses Depression-like Behaviors of CRF2-Deficient Mice. Neuropsychopharmacology. 34(6). 1416–1426. 68 indexed citations
5.
Starkus, John G., Stefan H. Heinemann, & Martin D. Rayner. (2000). Voltage Dependence of Slow Inactivation in Shaker Potassium Channels Results from Changes in Relative K+ and Na+ Permeabilities. The Journal of General Physiology. 115(2). 107–122. 14 indexed citations
6.
Starkus, John G., et al.. (1998). Macroscopic Na+ Currents in the “Nonconducting” Shaker Potassium Channel Mutant W434F. The Journal of General Physiology. 112(1). 85–93. 58 indexed citations
7.
Starkus, John G., et al.. (1997). Ion Conduction through C-Type Inactivated Shaker Channels. The Journal of General Physiology. 110(5). 539–550. 168 indexed citations
8.
Starkus, John G., et al.. (1995). Unilateral exposure of Shaker B potassium channels to hyperosmolar solutions. Biophysical Journal. 69(3). 860–872. 20 indexed citations
9.
Fleig, Andrea, et al.. (1994). Point mutations in IIS4 alter activation and inactivation of rat brain IIA Na channels in Xenopus oocyte macropatches. Pflügers Archiv - European Journal of Physiology. 427(5-6). 406–413. 14 indexed citations
10.
Fleig, Andrea, Peter C. Ruben, & Martin D. Rayner. (1994). Kinetic mode switch of rat brain IIA Na channels in Xenopus oocytes excised macropatches. Pflügers Archiv - European Journal of Physiology. 427(5-6). 399–405. 15 indexed citations
11.
Starkus, John G., Martin D. Rayner, Andrea Fleig, & Peter C. Ruben. (1993). Fast and slow inactivation of sodium channels: effects of photodynamic modification by methylene blue. Biophysical Journal. 65(2). 715–726. 12 indexed citations
12.
Rayner, Martin D., John G. Starkus, Peter C. Ruben, & Daniel Alicata. (1992). Voltage-sensitive and solvent-sensitive processes in ion channel gating. Kinetic effects of hyperosmolar media on activation and deactivation of sodium channels. Biophysical Journal. 61(1). 96–108. 38 indexed citations
13.
Ruben, Peter C., John G. Starkus, & Martin D. Rayner. (1992). Steady-state availability of sodium channels. Interactions between activation and slow inactivation. Biophysical Journal. 61(4). 941–955. 63 indexed citations
14.
Starkus, John G. & Martin D. Rayner. (1991). Gating current "fractionation" in crayfish giant axons. Biophysical Journal. 60(5). 1101–1119. 16 indexed citations
15.
Ruben, Peter C., John G. Starkus, & Martin D. Rayner. (1990). Holding potential affects the apparent voltage-sensitivity of sodium channel activation in crayfish giant axons. Biophysical Journal. 58(5). 1169–1181. 17 indexed citations
16.
Alicata, Daniel, Martin D. Rayner, & John G. Starkus. (1990). Sodium channel activation mechanisms. Insights from deuterium oxide substitution. Biophysical Journal. 57(4). 745–758. 30 indexed citations
17.
Alicata, Daniel, Martin D. Rayner, & John G. Starkus. (1989). Osmotic and pharmacological effects of formamide on capacity current, gating current, and sodium current in crayfish giant axons. Biophysical Journal. 55(2). 347–353. 13 indexed citations
18.
Morton, Brian, et al.. (1982). Potent inhibition of sperm motility by palytoxin. Experimental Cell Research. 140(2). 261–265. 11 indexed citations
19.
Rayner, Martin D. & C. A. G. Wiersma. (1967). Mechanisms of the Crayfish Tail Flick. Nature. 213(5082). 1231–1233. 11 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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