Thomas M. Wishart

6.2k total citations
80 papers, 3.2k citations indexed

About

Thomas M. Wishart is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Physiology. According to data from OpenAlex, Thomas M. Wishart has authored 80 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 30 papers in Cellular and Molecular Neuroscience and 22 papers in Physiology. Recurrent topics in Thomas M. Wishart's work include Neurogenetic and Muscular Disorders Research (17 papers), Alzheimer's disease research and treatments (13 papers) and RNA modifications and cancer (13 papers). Thomas M. Wishart is often cited by papers focused on Neurogenetic and Muscular Disorders Research (17 papers), Alzheimer's disease research and treatments (13 papers) and RNA modifications and cancer (13 papers). Thomas M. Wishart collaborates with scholars based in United Kingdom, United States and Germany. Thomas M. Wishart's co-authors include Thomas H. Gillingwater, Samantha L. Eaton, Maica Llavero Hurtado, Simon H. Parson, Douglas J. Lamont, Karla J. Oldknow, Colin Farquharson, Sarah L. Roche, Laura C. Graham and Derek Thomson and has published in prestigious journals such as Journal of Clinical Investigation, Nature Communications and Journal of Neuroscience.

In The Last Decade

Thomas M. Wishart

76 papers receiving 3.2k 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 M. Wishart United Kingdom 31 1.9k 951 703 675 418 80 3.2k
Juan Carlos Tapia Chile 30 1.9k 1.0× 1.1k 1.1× 641 0.9× 425 0.6× 823 2.0× 70 3.5k
Brian J. Wainger United States 19 2.9k 1.5× 1.4k 1.5× 648 0.9× 947 1.4× 927 2.2× 38 4.8k
Cathleen Lutz United States 33 2.8k 1.5× 1.1k 1.2× 1.3k 1.9× 443 0.7× 861 2.1× 82 4.3k
Nicholas D. Mazarakis United Kingdom 36 2.5k 1.4× 1.0k 1.1× 675 1.0× 346 0.5× 883 2.1× 63 4.2k
John Woulfe Canada 34 1.9k 1.0× 1.2k 1.3× 562 0.8× 1.1k 1.7× 1.3k 3.2× 119 4.8k
Kathy Keyvani Germany 35 1.1k 0.6× 536 0.6× 758 1.1× 1.0k 1.5× 433 1.0× 103 3.3k
Maria Pennuto Italy 31 1.9k 1.0× 1.6k 1.7× 713 1.0× 210 0.3× 532 1.3× 81 3.0k
Philipp Koch Germany 33 2.9k 1.6× 1.2k 1.3× 391 0.6× 545 0.8× 221 0.5× 75 4.2k
Kevin D. Foust United States 31 3.0k 1.6× 825 0.9× 1.7k 2.4× 608 0.9× 1.2k 2.9× 47 5.4k
Alfred Bach Germany 20 2.0k 1.1× 1.2k 1.2× 251 0.4× 264 0.4× 382 0.9× 24 3.6k

Countries citing papers authored by Thomas M. Wishart

Since Specialization
Citations

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

Fields of papers citing papers by Thomas M. Wishart

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas M. Wishart

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas M. Wishart. A scholar is included among the top collaborators of Thomas M. Wishart 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 M. Wishart. Thomas M. Wishart 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.
Kline, Rachel, Adrian Thomson, Douglas J. Lamont, et al.. (2025). Alterations in cardiac function correlate with a disruption in fatty acid metabolism in a mouse model of SMA. Human Molecular Genetics. 34(6). 547–562. 2 indexed citations
2.
Richard, Éric, Érika Hue, Anne Couroucé, et al.. (2024). Distinct Molecular Profiles Underpin Mild-To-Moderate Equine Asthma Cytological Profiles. Cells. 13(22). 1926–1926.
3.
Villalobos, Elisa, Ruth Morgan, Joanna Simpson, et al.. (2024). ATP-binding cassette family C member 1 constrains metabolic responses to high-fat diet in male mice. Journal of Endocrinology. 262(2). 1 indexed citations
4.
Arrázola, Macarena S., Matías Lira, Samantha L. Eaton, et al.. (2023). Necroptosis inhibition counteracts neurodegeneration, memory decline, and key hallmarks of aging, promoting brain rejuvenation. Aging Cell. 22(5). e13814–e13814. 19 indexed citations
5.
Edwards, Ruairidh, Rachel Kline, Laura C. Graham, et al.. (2022). The mitochondrial protein Sideroflexin 3 (SFXN3) influences neurodegeneration pathways in vivo. FEBS Journal. 289(13). 3894–3914. 10 indexed citations
6.
László, Zsófia I., Rachel Kline, Samantha L. Eaton, et al.. (2022). Synaptic proteomics reveal distinct molecular signatures of cognitive change and C9ORF72 repeat expansion in the human ALS cortex. Acta Neuropathologica Communications. 10(1). 156–156. 24 indexed citations
7.
Kline, Rachel, Dominic Kurian, Samantha L. Eaton, et al.. (2022). An Optimized Comparative Proteomic Approach as a Tool in Neurodegenerative Disease Research. Cells. 11(17). 2653–2653. 2 indexed citations
8.
Brown, Sharon J., Rachel Kline, Silvia A. Synowsky, et al.. (2022). The Proteome Signatures of Fibroblasts from Patients with Severe, Intermediate and Mild Spinal Muscular Atrophy Show Limited Overlap. Cells. 11(17). 2624–2624. 6 indexed citations
9.
Eaton, Samantha L., Nina M. Rzechorzek, Gerard Thompson, et al.. (2022). Modelling Neurological Diseases in Large Animals: Criteria for Model Selection and Clinical Assessment. Cells. 11(17). 2641–2641. 4 indexed citations
10.
Kurian, Dominic, et al.. (2022). Training associated alterations in equine respiratory immunity using a multiomics comparative approach. Scientific Reports. 12(1). 427–427. 9 indexed citations
11.
King, Declan, Paul Skehel, Owen Dando, et al.. (2021). Microarray profiling emphasizes transcriptomic differences between hippocampal in vivo tissue and in vitro cultures. Brain Communications. 3(3). fcab152–fcab152. 1 indexed citations
12.
Hurtado, Maica Llavero, Rosemary J. Jackson, Samantha L. Eaton, et al.. (2019). Comparative profiling of the synaptic proteome from Alzheimer’s disease patients with focus on the APOE genotype. Acta Neuropathologica Communications. 7(1). 214–214. 59 indexed citations
13.
Eaton, Samantha L., Chris Proudfoot, Simon Lillico, et al.. (2019). CRISPR/Cas9 mediated generation of an ovine model for infantile neuronal ceroid lipofuscinosis (CLN1 disease). Scientific Reports. 9(1). 9891–9891. 41 indexed citations
14.
Boyd, Penelope J, Hannah K. Shorrock, Ewout J. N. Groen, et al.. (2017). Bioenergetic status modulates motor neuron vulnerability and pathogenesis in a zebrafish model of spinal muscular atrophy. PLoS Genetics. 13(4). e1006744–e1006744. 72 indexed citations
15.
Fuller, Heidi R., Laura C. Graham, Maica Llavero Hurtado, & Thomas M. Wishart. (2016). Understanding the molecular consequences of inherited muscular dystrophies: advancements through proteomic experimentation. Expert Review of Proteomics. 13(7). 659–671. 17 indexed citations
16.
Comley, Laura H., Heidi R. Fuller, Thomas M. Wishart, et al.. (2011). ApoE isoform-specific regulation of regeneration in the peripheral nervous system. Human Molecular Genetics. 20(12). 2406–2421. 29 indexed citations
17.
Wright, Ann K., Thomas M. Wishart, C.A. Ingham, & Thomas H. Gillingwater. (2010). Synaptic Protection in the Brain of WldS Mice Occurs Independently of Age but Is Sensitive to Gene-Dose. PLoS ONE. 5(11). e15108–e15108. 13 indexed citations
18.
Benedict, Jared W., et al.. (2009). Protein product of CLN6 gene responsible for variant late‐onset infantile neuronal ceroid lipofuscinosis interacts with CRMP‐2. Journal of Neuroscience Research. 87(9). 2157–2166. 29 indexed citations
19.
Wishart, Thomas M., Helen N. Pemberton, Sally James, Chris J. McCabe, & Thomas H. Gillingwater. (2008). Modified cell cycle status in a mouse model of altered neuronal vulnerability (slow Wallerian degeneration; Wld s ). Genome biology. 9(6). R101–R101. 22 indexed citations
20.
Gillingwater, Thomas H., Thomas M. Wishart, Philip E. Chen, et al.. (2006). The neuroprotective WldS gene regulates expression of PTTG1 and erythroid differentiation regulator 1-like gene in mice and human cells. Human Molecular Genetics. 15(4). 625–635. 43 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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