Judith Simcox

3.5k total citations · 2 hit papers
39 papers, 2.3k citations indexed

About

Judith Simcox is a scholar working on Molecular Biology, Physiology and Biochemistry. According to data from OpenAlex, Judith Simcox has authored 39 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 20 papers in Physiology and 7 papers in Biochemistry. Recurrent topics in Judith Simcox's work include Adipose Tissue and Metabolism (17 papers), Lipid metabolism and biosynthesis (7 papers) and Metabolomics and Mass Spectrometry Studies (5 papers). Judith Simcox is often cited by papers focused on Adipose Tissue and Metabolism (17 papers), Lipid metabolism and biosynthesis (7 papers) and Metabolomics and Mass Spectrometry Studies (5 papers). Judith Simcox collaborates with scholars based in United States, United Kingdom and Switzerland. Judith Simcox's co-authors include Donald A. McClain, Dudley W. Lamming, Jingyu Huang, Robert C. Cooksey, Deborah L. Jones, Claudio J. Villanueva, William L. Holland, Stephen B. Spurgin, Jiyoung Park and Ying Lin and has published in prestigious journals such as Nature, Cell and Journal of Clinical Investigation.

In The Last Decade

Judith Simcox

34 papers receiving 2.3k citations

Hit Papers

Iron and Diabetes Risk 2013 2026 2017 2021 2013 2024 100 200 300 400

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Judith Simcox United States 21 872 733 555 532 320 39 2.3k
Tomáš Mráček Czechia 28 744 0.9× 1.3k 1.7× 172 0.3× 324 0.6× 83 0.3× 73 2.3k
Wangsen Cao China 36 410 0.5× 2.1k 2.8× 233 0.4× 232 0.4× 122 0.4× 70 3.4k
Yonghan He China 31 683 0.8× 1.4k 1.9× 161 0.3× 240 0.5× 70 0.2× 91 2.4k
Yanyan Zhang China 29 278 0.3× 907 1.2× 507 0.9× 174 0.3× 263 0.8× 126 2.4k
Giorgio Biasiotto Italy 28 166 0.2× 752 1.0× 903 1.6× 207 0.4× 454 1.4× 75 2.4k
Marie‐Jeanne Richard France 30 263 0.3× 986 1.3× 190 0.3× 132 0.2× 330 1.0× 65 2.9k
Mariarosaria Santillo Italy 27 413 0.5× 1.1k 1.4× 78 0.1× 228 0.4× 123 0.4× 73 2.7k
Saranya Ravi United States 20 419 0.5× 1.0k 1.4× 131 0.2× 453 0.9× 50 0.2× 27 2.3k
Louise Dunn Australia 20 162 0.2× 729 1.0× 237 0.4× 98 0.2× 156 0.5× 44 1.7k
Kimihiko Sano Japan 24 231 0.3× 1.3k 1.8× 321 0.6× 145 0.3× 144 0.5× 60 2.7k

Countries citing papers authored by Judith Simcox

Since Specialization
Citations

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

Fields of papers citing papers by Judith Simcox

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Judith Simcox

This figure shows the co-authorship network connecting the top 25 collaborators of Judith Simcox. A scholar is included among the top collaborators of Judith Simcox 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 Judith Simcox. Judith Simcox 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.
Burhans, Maggie S., et al.. (2025). Stearoyl-CoA desaturase 1 deficiency drives saturated lipid accumulation and increases liver and plasma acylcarnitines. Journal of Lipid Research. 66(6). 100824–100824. 2 indexed citations
2.
Zhang, Jingying, Gina Wade, Luciano A. Abriata, et al.. (2025). ACAD10 and ACAD11 enable mammalian 4-hydroxy acid lipid catabolism. Nature Structural & Molecular Biology. 32(9). 1622–1632.
3.
Green, Cara L., Michael R. MacArthur, Reji Babygirija, et al.. (2025). Dietary isoleucine content modulates the metabolic and molecular response to a Western diet in mice. Molecular Metabolism. 101. 102248–102248.
5.
Garcia, Gonzalo G., Mariah F. Calubag, Allison C. Rodgers, et al.. (2024). Late-life protein or isoleucine restriction impacts physiological and molecular signatures of aging. Nature Aging. 4(12). 1760–1771. 6 indexed citations
6.
Schneider, Andrew J., Eric A. Armstrong, R. Rivera, et al.. (2024). The role of ATP citrate lyase in myelin formation and maintenance. Glia. 73(1). 105–121. 3 indexed citations
7.
Sulaiman, Jordy Evan, Jaron Thompson, Yili Qian, et al.. (2024). Phocaeicola vulgatus shapes the long-term growth dynamics and evolutionary adaptations of Clostridioides difficile. Cell Host & Microbe. 33(1). 42–58.e10. 4 indexed citations
8.
Yu, Qing, Xinyue Liu, Mark P. Keller, et al.. (2023). Sample multiplexing-based targeted pathway proteomics with real-time analytics reveals the impact of genetic variation on protein expression. Nature Communications. 14(1). 555–555. 20 indexed citations
9.
Green, Cara L., Reji Babygirija, Heidi H. Pak, et al.. (2023). Dietary restriction of isoleucine increases healthspan and lifespan of genetically heterogeneous mice. Cell Metabolism. 35(11). 1976–1995.e6. 58 indexed citations
10.
Simcox, Judith & Dudley W. Lamming. (2022). The central moTOR of metabolism. Developmental Cell. 57(6). 691–706. 84 indexed citations
11.
Green, Cara L., Heidi H. Pak, Nicole E. Richardson, et al.. (2022). Sex and genetic background define the metabolic, physiologic, and molecular response to protein restriction. Cell Metabolism. 34(2). 209–226.e5. 60 indexed citations
12.
Wade, Gina, et al.. (2022). Determination of tissue contributions to the circulating lipid pool in cold exposure via systematic assessment of lipid profiles. Journal of Lipid Research. 63(7). 100197–100197. 16 indexed citations
13.
González, Paula, Judith Simcox, Hershel Raff, et al.. (2022). Lipid signatures of chronic pain in female adolescents with and without obesity. Lipids in Health and Disease. 21(1). 80–80. 8 indexed citations
14.
Simcox, Judith, et al.. (2021). Mitochondrial Lipid Signaling and Adaptive Thermogenesis. Metabolites. 11(2). 124–124. 23 indexed citations
15.
Panic, Vanja, Stephanie Pearson, Trevor S. Tippetts, et al.. (2020). Mitochondrial pyruvate carrier is required for optimal brown fat thermogenesis. eLife. 9. 47 indexed citations
16.
Simcox, Judith, Natalia S. Torres, Mi-Young Jeong, et al.. (2017). Mitochondrial cardiomyopathies feature increased uptake and diminished efflux of mitochondrial calcium. Journal of Molecular and Cellular Cardiology. 113. 22–32. 39 indexed citations
17.
Simcox, Judith, Gisela Geoghegan, J. Alan Maschek, et al.. (2017). Global Analysis of Plasma Lipids Identifies Liver-Derived Acylcarnitines as a Fuel Source for Brown Fat Thermogenesis. Cell Metabolism. 26(3). 509–522.e6. 188 indexed citations
18.
Simcox, Judith & Donald A. McClain. (2013). Iron and Diabetes Risk. Cell Metabolism. 17(3). 329–341. 408 indexed citations breakdown →
19.
Kusminski, Christine M., William L. Holland, Kai Sun, et al.. (2012). MitoNEET-driven alterations in adipocyte mitochondrial activity reveal a crucial adaptive process that preserves insulin sensitivity in obesity. Nature Medicine. 18(10). 1539–1549. 372 indexed citations
20.
Cooksey, Robert C., Deborah L. Jones, Jingyu Huang, et al.. (2010). Dietary iron restriction or iron chelation protects from diabetes and loss of β-cell function in the obese (ob/ob lep−/−) mouse. American Journal of Physiology-Endocrinology and Metabolism. 298(6). E1236–E1243. 141 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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