Thomas H. Moss

2.0k total citations
44 papers, 1.6k citations indexed

About

Thomas H. Moss is a scholar working on Molecular Biology, Cell Biology and Materials Chemistry. According to data from OpenAlex, Thomas H. Moss has authored 44 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 15 papers in Cell Biology and 11 papers in Materials Chemistry. Recurrent topics in Thomas H. Moss's work include Hemoglobin structure and function (14 papers), Photosynthetic Processes and Mechanisms (11 papers) and Protein Structure and Dynamics (7 papers). Thomas H. Moss is often cited by papers focused on Hemoglobin structure and function (14 papers), Photosynthetic Processes and Mechanisms (11 papers) and Protein Structure and Dynamics (7 papers). Thomas H. Moss collaborates with scholars based in United States, Sweden and Netherlands. Thomas H. Moss's co-authors include Martin M. Maltempo, Alan J. Bearden, Michael A. Cusanovich, Winslow S. Caughey, Bernard Babior, Anders Ehrenberg, Helmut Beinert, B C Antanaitis, Howard S. Mason and William H. Orme‐Johnson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and The Journal of Chemical Physics.

In The Last Decade

Thomas H. Moss

44 papers receiving 1.4k 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 H. Moss United States 24 836 485 436 353 193 44 1.6k
A Ehrenberg Sweden 27 1.2k 1.4× 255 0.5× 328 0.8× 526 1.5× 185 1.0× 71 2.3k
Alessandro Coda Italy 32 2.1k 2.5× 896 1.8× 592 1.4× 361 1.0× 122 0.6× 80 3.2k
Marvin W. Makinen United States 27 1.1k 1.4× 518 1.1× 532 1.2× 398 1.1× 58 0.3× 80 2.2k
Hideo Kon United States 23 579 0.7× 428 0.9× 385 0.9× 219 0.6× 40 0.2× 78 1.8k
Barry D. Howes Italy 28 1.4k 1.7× 645 1.3× 340 0.8× 297 0.8× 326 1.7× 82 2.3k
W. N. Lipscomb United States 25 832 1.0× 223 0.5× 642 1.5× 217 0.6× 27 0.1× 60 1.8k
Russell LoBrutto United States 24 850 1.0× 79 0.2× 257 0.6× 547 1.5× 250 1.3× 48 1.5k
Paul K. Glasoe United States 5 1.0k 1.2× 163 0.3× 455 1.0× 244 0.7× 87 0.5× 8 2.1k
Emma Sigfridsson Sweden 10 501 0.6× 223 0.5× 290 0.7× 292 0.8× 117 0.6× 11 1.0k
Lyle H. Jensen United States 18 1.1k 1.3× 287 0.6× 623 1.4× 609 1.7× 366 1.9× 33 2.0k

Countries citing papers authored by Thomas H. Moss

Since Specialization
Citations

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

Fields of papers citing papers by Thomas H. Moss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas H. Moss

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas H. Moss. A scholar is included among the top collaborators of Thomas H. Moss 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 H. Moss. Thomas H. Moss 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.
McCloskey, Diane E., Shridhar Bale, John A. Secrist, et al.. (2009). New Insights into the Design of Inhibitors of Human S-Adenosylmethionine Decarboxylase: Studies of Adenine C8 Substitution in Structural Analogues of S-Adenosylmethionine. Journal of Medicinal Chemistry. 52(5). 1388–1407. 24 indexed citations
2.
Lundstedt, Sven B. & Thomas H. Moss. (1989). Managing Innovation and Change. 16 indexed citations
3.
Moss, Thomas H.. (1984). The Modern Politics of Laboratory Animal Use. Science Technology & Human Values. 9(2). 51–56. 3 indexed citations
4.
Moss, Thomas H.. (1981). BACKGROUND OF THE THREE MILE ISLAND NUCLEAR ACCIDENT, I: GENERAL DISCUSSION. Annals of the New York Academy of Sciences. 365(1). 48–53. 1 indexed citations
5.
Maltempo, Martin M., Thomas H. Moss, & K. Spartalian. (1980). Mossbauer spectroscopy of the mixed-spin and high-spin states of C h r o m a t i u m ferricytochrome c′. The Journal of Chemical Physics. 73(5). 2100–2106. 26 indexed citations
6.
Moss, Thomas H.. (1978). [21] Magnetic susceptibility applied to metalloproteins. Methods in enzymology on CD-ROM/Methods in enzymology. 54. 379–396. 4 indexed citations
7.
Moss, Thomas H., E Shapiro, T E King, Helmut Beinert, & Charles R. Hartzell. (1978). The magnetic susceptibility of cytochrome oxidase in the 4.2-1.5 K range.. Journal of Biological Chemistry. 253(22). 8072–8073. 38 indexed citations
8.
Maltempo, Martin M. & Thomas H. Moss. (1976). The spin 3/2 state and quantum spin mixtures in haem proteins. Quarterly Reviews of Biophysics. 9(2). 181–215. 151 indexed citations
9.
Fee, J.A., E Shapiro, & Thomas H. Moss. (1976). Direct evidence for manganese (III) binding to the manganosuperoxide dismutase of Escherichia coli B.. Journal of Biological Chemistry. 251(19). 6157–6159. 43 indexed citations
10.
O’Keeffe, David H., Clyde H. Barlow, George A. Smythe, et al.. (1975). Magnetic and spectroscopic probes for FeOFe linkages in hemin systems. Bioinorganic Chemistry. 5(2). 125–147. 53 indexed citations
11.
Moss, Thomas H. & James A. Fee. (1975). On the magnetic properties of cobalt substituted bovine superoxide dismutase derivatives. Biochemical and Biophysical Research Communications. 66(2). 799–808. 19 indexed citations
12.
Champion, P. M., Eckard Münck, Peter G. Debrunner, et al.. (1975). The magnetic susceptibility of reduced cytochrome P-450cam. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 376(3). 579–582. 23 indexed citations
13.
Maltempo, Martin M., Thomas H. Moss, & Michael A. Cusanovich. (1974). Magnetic studies on the changes in the iron environment in Chromatium ferricytochrome c′. Biochimica et Biophysica Acta (BBA) - Protein Structure. 342(2). 290–305. 112 indexed citations
14.
Moss, Thomas H. & Tore Vänngård. (1974). Magnetic susceptibility of lacquer tree laccase. Biochimica et Biophysica Acta (BBA) - Protein Structure. 371(1). 39–43. 7 indexed citations
15.
Moss, Thomas H., et al.. (1971). Magnetic susceptibility evidence for a binuclear iron complex in hemerythrin. Biochemistry. 10(5). 840–842. 21 indexed citations
16.
Moss, Thomas H., Anders Ehrenberg, & Alan J. Bearden. (1969). Moessbauer spectroscopic evidence for the electronic configuration of iron in horseradish peroxidase and its peroxide derivatives. Biochemistry. 8(10). 4159–4162. 122 indexed citations
17.
Moss, Thomas H., Alan J. Bearden, Robert Bartsch, & Michael A. Cusanovich. (1968). Moessbauer spectroscopy of bacterial cytochromes. Biochemistry. 7(4). 1583–1590. 30 indexed citations
18.
Caughey, Winslow S., Wilfred Y. Fujimoto, Alan J. Bearden, & Thomas H. Moss. (1966). Mossbauer Spectroscopic Evidence for Low-Spin Iron in Dehydrated Metmyoglobin*. Biochemistry. 5(4). 1255–1262. 48 indexed citations
19.
Moss, Thomas H.. (1965). Moessbauer Spectroscopy of Iron Proteins.. PhDT. 1 indexed citations
20.
Bearden, Alan J., et al.. (1965). Mössbauer spectroscopy of heme and hemin compounds.. Proceedings of the National Academy of Sciences. 53(6). 1246–1253. 42 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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