Tim Parr

3.7k total citations
94 papers, 2.8k citations indexed

About

Tim Parr is a scholar working on Cell Biology, Animal Science and Zoology and Molecular Biology. According to data from OpenAlex, Tim Parr has authored 94 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Cell Biology, 41 papers in Animal Science and Zoology and 37 papers in Molecular Biology. Recurrent topics in Tim Parr's work include Calpain Protease Function and Regulation (36 papers), Meat and Animal Product Quality (26 papers) and Adipose Tissue and Metabolism (19 papers). Tim Parr is often cited by papers focused on Calpain Protease Function and Regulation (36 papers), Meat and Animal Product Quality (26 papers) and Adipose Tissue and Metabolism (19 papers). Tim Parr collaborates with scholars based in United Kingdom, United States and China. Tim Parr's co-authors include R.G. Bardsley, John M. Brameld, P. J. Buttery, Paul L. Sensky, Sarah J. Storr, Stewart G. Martin, Margaret C. Frame, Neil O. Carragher, P.L. Sensky and A. J. Fahey and has published in prestigious journals such as Journal of Biological Chemistry, Nature reviews. Cancer and PLoS ONE.

In The Last Decade

Tim Parr

89 papers receiving 2.7k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Tim Parr 1.2k 1.1k 1.1k 502 302 94 2.8k
Isabelle Cassar‐Malek 1.7k 1.4× 1.1k 1.0× 485 0.5× 803 1.6× 692 2.3× 101 3.2k
W.R. Dayton 1.7k 1.4× 1.2k 1.1× 1.4k 1.3× 485 1.0× 517 1.7× 77 3.4k
Brigitte Picard 1.8k 1.5× 3.0k 2.6× 798 0.7× 646 1.3× 684 2.3× 129 4.7k
A.L. Grant 1.0k 0.9× 967 0.9× 414 0.4× 517 1.0× 312 1.0× 78 2.5k
Valery F. Thompson 2.5k 2.1× 1.6k 1.4× 2.9k 2.8× 604 1.2× 443 1.5× 41 4.7k
Jinyang Cong 1.6k 1.3× 474 0.4× 1.9k 1.8× 338 0.7× 276 0.9× 9 2.7k
C. D. K. Bottema 1.9k 1.6× 734 0.7× 267 0.3× 195 0.4× 1.1k 3.5× 118 3.7k
R.G. Bardsley 1.0k 0.9× 1.1k 1.0× 704 0.7× 250 0.5× 178 0.6× 59 2.0k
Qing Zhu 1.6k 1.3× 704 0.6× 168 0.2× 215 0.4× 556 1.8× 204 3.2k
Mitsuaki Fujimoto 2.7k 2.2× 104 0.1× 850 0.8× 375 0.7× 217 0.7× 61 3.4k

Countries citing papers authored by Tim Parr

Since Specialization
Citations

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

Fields of papers citing papers by Tim Parr

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tim Parr. 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 Tim Parr. The network helps show where Tim Parr may publish in the future.

Co-authorship network of co-authors of Tim Parr

This figure shows the co-authorship network connecting the top 25 collaborators of Tim Parr. A scholar is included among the top collaborators of Tim Parr 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 Tim Parr. Tim Parr 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.
Salter, Andrew M., et al.. (2025). Effects of feed nutrients on growth, development and the deposition of protein and fat in Tenebrio molitor larvae. Journal of Insects as Food and Feed. 11(9). 1619–1632. 1 indexed citations
2.
González-Carranza, Zinnia H., Arturo Castro‐Castro, M. Socorro González‐Elizondo, et al.. (2024). Comparative analyses of the nutritional and antinutritional composition of pod flours from Neltuma spp. (Fabaceae, Caesalpinioideae) species from drylands of Mexico, Kenya and Tanzania. Future Foods. 10. 100434–100434. 1 indexed citations
3.
4.
Brameld, John M., et al.. (2024). The juvenile hormone analogue, pyriproxifen, alters protein and fat composition of Tenebrio molitor larvae. Journal of Insects as Food and Feed. 10(9). 1633–1644. 3 indexed citations
5.
6.
Brameld, John M., et al.. (2020). Leucine and mTORc1 act independently to regulate 2-deoxyglucose uptake in L6 myotubes. Amino Acids. 52(3). 477–486. 9 indexed citations
7.
Jones, Sarah, et al.. (2019). Effect of adeno-associated virus (AAV)-mediated overexpression of PEPCK-M (Pck2) on Clenbuterol-induced muscle growth. PLoS ONE. 14(6). e0218970–e0218970. 5 indexed citations
8.
Stewart, A. H., Z. Daniel, H.V. Masey O’Neill, et al.. (2019). The association between faecal host DNA or faecal calprotectin and feed efficiency in pigs fed yeast-enriched protein concentrate. animal. 13(11). 2483–2491. 5 indexed citations
9.
Brown, David M., Sarah Jones, Jo E. Lewis, et al.. (2018). Effect of sodium 4-phenylbutyrate on Clenbuterol-mediated muscle growth. PLoS ONE. 13(7). e0201481–e0201481. 12 indexed citations
10.
Brown, David M., Kevin J. Ryan, Thomas L. Wilson, et al.. (2016). Mitochondrial phosphoenolpyruvate carboxykinase (PEPCK-M) and serine biosynthetic pathway genes are co-ordinately increased during anabolic agent-induced skeletal muscle growth. Scientific Reports. 6(1). 28693–28693. 31 indexed citations
11.
Storr, Sarah J., Caroline M. Woolston, Sabreena Safuan, et al.. (2012). Calpain system protein expression in basal-like and triple-negative invasive breast cancer. Annals of Oncology. 23(9). 2289–2296. 54 indexed citations
12.
Stephens, Francis B., Luke Norton, Kirsty Jewell, et al.. (2010). Basal and insulin‐stimulated pyruvate dehydrogenase complex activation, glycogen synthesis and metabolic gene expression in human skeletal muscle the day after a single bout of exercise. Experimental Physiology. 95(7). 808–818. 12 indexed citations
13.
Stock, Nicholas, Deborah L. Volkots, Karin J. Stebbins, et al.. (2010). Sodium [2′-[(cyclopropanecarbonyl-ethyl-amino)-methyl]-4′-(6-ethoxy-pyridin-3-yl)-6-methoxy-biphenyl-3-yl]-acetate (AM432): A potent, selective prostaglandin D2 receptor antagonist. Bioorganic & Medicinal Chemistry Letters. 21(3). 1036–1040. 9 indexed citations
14.
Feng, Shengnan, Andrew M. Salter, Tim Parr, & P. C. Garnsworthy. (2007). Extraction and Quantitative Analysis of Stearoyl-Coenzyme A Desaturase mRNA from Dairy Cow Milk Somatic Cells. Journal of Dairy Science. 90(9). 4128–4136. 31 indexed citations
15.
Parr, Tim, Kirsty Jewell, Paul L. Sensky, et al.. (2004). Expression of calpastatin isoforms in muscle and functionality of multiple calpastatin promoters. Archives of Biochemistry and Biophysics. 427(1). 8–15. 35 indexed citations
16.
Sazili, Awis Qurni, Tim Parr, P.L. Sensky, et al.. (2004). The relationship between slow and fast myosin heavy chain content, calpastatin and meat tenderness in different ovine skeletal muscles. Meat Science. 69(1). 17–25. 79 indexed citations
17.
Sazili, Awis Qurni, et al.. (2003). The effect of altered growth rates on the calpain proteolytic system and meat tenderness in cattle. Meat Science. 66(1). 195–201. 28 indexed citations
18.
Greenhaff, Paul L., et al.. (2002). Resistance training induces the expression of calpain protease and its inhibitor calpastatin in human. Proceedings of The Physiological Society. 1 indexed citations
19.
Sazili, Awis Qurni, Tim Parr, P.L. Sensky, et al.. (2002). Comparison of immunochemical and histochemical analysis of fibre type distribution in ovine skeletal muscles. Proceedings of the British Society of Animal Science. 2002. 175–175. 1 indexed citations
20.
Bardsley, R.G., et al.. (1992). Effect of β-agonists on expression of calpain and calpastatin activity in skeletal muscle. Biochimie. 74(3). 267–273. 65 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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