Charles T. Putman

3.1k total citations · 1 hit paper
47 papers, 2.4k citations indexed

About

Charles T. Putman is a scholar working on Molecular Biology, Physiology and Cell Biology. According to data from OpenAlex, Charles T. Putman has authored 47 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 19 papers in Physiology and 12 papers in Cell Biology. Recurrent topics in Charles T. Putman's work include Muscle Physiology and Disorders (24 papers), Muscle metabolism and nutrition (11 papers) and Adipose Tissue and Metabolism (9 papers). Charles T. Putman is often cited by papers focused on Muscle Physiology and Disorders (24 papers), Muscle metabolism and nutrition (11 papers) and Adipose Tissue and Metabolism (9 papers). Charles T. Putman collaborates with scholars based in Canada, Germany and France. Charles T. Putman's co-authors include Tessa Gordon, Janka Hegedus, Walter T. Dixon, Vera C. Mazurak, Vickie E. Baracos, Nina Esfandiari, Jocelyn B. Aubrey, Jérôme Frenette, François-Alexandre Buteau and Dirk Pette and has published in prestigious journals such as PLoS ONE, The Journal of Physiology and Journal of Neurophysiology.

In The Last Decade

Charles T. Putman

47 papers receiving 2.4k citations

Hit Papers

Measurement of skeletal muscle radiation attenuation and ... 2014 2026 2018 2022 2014 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Charles T. Putman Canada 24 862 757 469 387 283 47 2.4k
Veena M. Bhopale United States 29 268 0.3× 1.0k 1.3× 336 0.7× 147 0.4× 152 0.5× 74 2.6k
Martin K. Childers United States 32 389 0.5× 1.3k 1.7× 793 1.7× 278 0.7× 551 1.9× 97 2.9k
Kazumoto Shibuya Japan 33 367 0.4× 616 0.8× 2.0k 4.3× 785 2.0× 203 0.7× 189 3.4k
C. Goddard United Kingdom 23 234 0.3× 716 0.9× 59 0.1× 123 0.3× 147 0.5× 74 1.7k
Anna Skottner Sweden 34 516 0.6× 1.3k 1.7× 161 0.3× 138 0.4× 551 1.9× 83 3.6k
Susan Hall United Kingdom 37 519 0.6× 934 1.2× 520 1.1× 125 0.3× 607 2.1× 83 3.8k
Wen‐Lang Lin United States 19 815 0.9× 1.0k 1.4× 679 1.4× 227 0.6× 109 0.4× 36 2.6k
Lan Zhou United States 30 537 0.6× 1.6k 2.1× 357 0.8× 356 0.9× 508 1.8× 66 3.0k
Julien Ochala United Kingdom 28 770 0.9× 1.9k 2.5× 125 0.3× 282 0.7× 198 0.7× 95 3.2k
Bianca Maria Scicchitano Italy 25 556 0.6× 1.1k 1.4× 186 0.4× 312 0.8× 135 0.5× 51 2.0k

Countries citing papers authored by Charles T. Putman

Since Specialization
Citations

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

Fields of papers citing papers by Charles T. Putman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Charles T. Putman

This figure shows the co-authorship network connecting the top 25 collaborators of Charles T. Putman. A scholar is included among the top collaborators of Charles T. Putman 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 Charles T. Putman. Charles T. Putman 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.
Miklavcic, John, Karen J. B. Martins, Vickie E. Baracos, et al.. (2017). Fish oil mitigates myosteatosis and improves chemotherapy efficacy in a preclinical model of colon cancer. PLoS ONE. 12(8). e0183576–e0183576. 23 indexed citations
2.
Martins, Karen J. B., Gordon K. Murdoch, Ian M. MacLean, et al.. (2012). Nitric oxide synthase inhibition prevents activity‐induced calcineurin–NFATc1 signalling and fast‐to‐slow skeletal muscle fibre type conversions. The Journal of Physiology. 590(6). 1427–1442. 46 indexed citations
3.
Bamford, Jeremy Andrew, Charles T. Putman, & Vivian K. Mushahwar. (2010). Muscle Plasticity in Rat Following Spinal Transection and Chronic Intraspinal Microstimulation. IEEE Transactions on Neural Systems and Rehabilitation Engineering. 19(1). 79–83. 13 indexed citations
4.
Bernreuther, Christian, Nicole Grabinski, Charles T. Putman, et al.. (2009). Plasminogen Activator Inhibitor Type 1 Up-Regulation Is Associated with Skeletal Muscle Atrophy and Associated Fibrosis. American Journal Of Pathology. 175(2). 763–771. 27 indexed citations
5.
Hegedus, Janka, Charles T. Putman, & Tessa Gordon. (2009). Progressive motor unit loss in the G93A mouse model of amyotrophic lateral sclerosis is unaffected by gender. Muscle & Nerve. 39(3). 318–327. 34 indexed citations
6.
Gordon, Tessa, et al.. (2009). Functional over-load saves motor units in the SOD1-G93A transgenic mouse model of amyotrophic lateral sclerosis. Neurobiology of Disease. 37(2). 412–422. 35 indexed citations
7.
Gallo, Maria Eugênia Noviski, Ian M. MacLean, Neil Tyreman, et al.. (2008). Adaptive responses to creatine loading and exercise in fast-twitch rat skeletal muscle. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 294(4). R1319–R1328. 15 indexed citations
8.
Hegedus, Janka, Charles T. Putman, Neil Tyreman, & Tessa Gordon. (2008). Preferential motor unit loss in the SOD1G93A transgenic mouse model of amyotrophic lateral sclerosis. The Journal of Physiology. 586(14). 3337–3351. 195 indexed citations
9.
Putman, Charles T., Karen J. B. Martins, Maria Eugênia Noviski Gallo, et al.. (2007). α-Catalytic subunits of 5′AMP-activated protein kinase display fiber-specific expression and are upregulated by chronic low-frequency stimulation in rat muscle. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 293(3). R1325–R1334. 20 indexed citations
10.
Foxcroft, G. R., Michael Vinsky, Francois Paradis, et al.. (2007). Macroenvironment effects on oocytes and embryos in swine. Theriogenology. 68. S30–S39. 28 indexed citations
11.
Harris, R. Luke, Charles T. Putman, Michelle M. Rank, Leo Sanelli, & David J. Bennett. (2006). Spastic Tail Muscles Recover From Myofiber Atrophy and Myosin Heavy Chain Transformations in Chronic Spinal Rats. Journal of Neurophysiology. 97(2). 1040–1051. 16 indexed citations
12.
Martins, Karen J. B., Tessa Gordon, Dirk Pette, et al.. (2006). Effect of satellite cell ablation on low‐frequency‐stimulated fast‐to‐slow fibre‐type transitions in rat skeletal muscle. The Journal of Physiology. 572(1). 281–294. 22 indexed citations
13.
Putman, Charles T., et al.. (2006). The effect of varying the time of concentric and eccentric muscle actions during resistance training on skeletal muscle adaptations in women. European Journal of Applied Physiology. 97(4). 443–453. 29 indexed citations
14.
Bamford, Jeremy Andrew, Charles T. Putman, & Vivian K. Mushahwar. (2005). Intraspinal microstimulation preferentially recruits fatigue‐resistant muscle fibres and generates gradual force in rat. The Journal of Physiology. 569(3). 873–884. 65 indexed citations
15.
Putman, Charles T., Walter T. Dixon, J. Pearcey, et al.. (2004). Chronic low-frequency stimulation upregulates uncoupling protein-3 in transforming rat fast-twitch skeletal muscle. American Journal of Physiology-Regulatory, Integrative and Comparative Physiology. 287(6). R1419–R1426. 21 indexed citations
16.
MacLean, Ian M., et al.. (2004). Effects of spaceflight on myosin heavy-chain content, fibre morphology and succinate dehydrogenase activity in rat diaphragm. Pflügers Archiv - European Journal of Physiology. 448(2). 239–247. 12 indexed citations
17.
Gallo, Maria Eugênia Noviski, Tessa Gordon, Neil Tyreman, Yang Shu, & Charles T. Putman. (2004). Reliability of isolated isometric function measures in rat muscles composed of different fibre types. Experimental Physiology. 89(5). 583–592. 17 indexed citations
18.
Putman, Charles T., Mónika Kiricsi, J. Pearcey, et al.. (2003). AMPK activation increases uncoupling protein-3 expression and mitochondrial enzyme activities in rat muscle without fibre type transitions. The Journal of Physiology. 551(1). 169–178. 70 indexed citations
19.
Peuker, Heidemarie, Agnès Conjard, Charles T. Putman, & Dirk Pette. (1999). Transient expression of myosin heavy chain MHCIα in rabbit muscle during fast-to-slow transition. Journal of Muscle Research and Cell Motility. 20(2). 147–154. 25 indexed citations
20.
Putman, Charles T., Agnès Conjard, Heidemarie Peuker, & Dirk Pette. (1999). α-cardiac-like myosin heavy chain MHCIα is not upregulated in transforming rat muscle. Journal of Muscle Research and Cell Motility. 20(2). 155–162. 23 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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