Christopher M. Adams

15.1k total citations
117 papers, 6.6k citations indexed

About

Christopher M. Adams is a scholar working on Molecular Biology, Cell Biology and Surgery. According to data from OpenAlex, Christopher M. Adams has authored 117 papers receiving a total of 6.6k indexed citations (citations by other indexed papers that have themselves been cited), including 77 papers in Molecular Biology, 19 papers in Cell Biology and 17 papers in Surgery. Recurrent topics in Christopher M. Adams's work include Muscle Physiology and Disorders (28 papers), Adipose Tissue and Metabolism (14 papers) and Mass Spectrometry Techniques and Applications (10 papers). Christopher M. Adams is often cited by papers focused on Muscle Physiology and Disorders (28 papers), Adipose Tissue and Metabolism (14 papers) and Mass Spectrometry Techniques and Applications (10 papers). Christopher M. Adams collaborates with scholars based in United States, Sweden and United Kingdom. Christopher M. Adams's co-authors include Scott M. Ebert, Michael J. Welsh, Roman A. Zubarev, Peter M. Snyder, Amos B. Smith, Daniel K. Fox, Kale S. Bongers, Michael C. Dyle, Steven D. Kunkel and Steven A. Bullard and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

Christopher M. Adams

114 papers receiving 6.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher M. Adams United States 44 3.8k 1.1k 1.0k 791 732 117 6.6k
Marc Baumann Finland 39 3.0k 0.8× 1.5k 1.4× 704 0.7× 344 0.4× 433 0.6× 170 6.1k
Pentti Somerharju Finland 47 5.1k 1.3× 1.5k 1.3× 1.6k 1.5× 693 0.9× 649 0.9× 145 7.3k
Jan‐Eric Månsson Sweden 43 2.8k 0.7× 2.1k 1.9× 1.1k 1.1× 451 0.6× 572 0.8× 157 5.4k
Timothy Haystead United States 58 8.5k 2.2× 979 0.9× 1.9k 1.8× 392 0.5× 397 0.5× 170 11.7k
Ryuichi Kato Japan 49 4.3k 1.1× 677 0.6× 1.1k 1.1× 518 0.7× 784 1.1× 272 7.8k
Masayuki Matsushita Japan 45 3.7k 1.0× 616 0.6× 750 0.7× 620 0.8× 283 0.4× 157 6.7k
Brett Garner Australia 48 2.8k 0.7× 2.1k 1.9× 706 0.7× 1.1k 1.4× 654 0.9× 120 6.7k
Stefan Bröer Australia 64 6.0k 1.6× 1.5k 1.4× 831 0.8× 686 0.9× 358 0.5× 179 11.7k
Pierre De Meyts United States 48 5.6k 1.5× 1.6k 1.4× 828 0.8× 2.3k 2.9× 507 0.7× 145 9.1k
Yoshio Hirabayashi Japan 56 7.0k 1.8× 1.9k 1.7× 1.7k 1.7× 1.0k 1.3× 591 0.8× 429 11.1k

Countries citing papers authored by Christopher M. Adams

Since Specialization
Citations

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

Fields of papers citing papers by Christopher M. Adams

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher M. Adams

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher M. Adams. A scholar is included among the top collaborators of Christopher M. Adams 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 Christopher M. Adams. Christopher M. Adams 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.
Zhang, Zengming, Tongbin Wu, Zeyu Chen, et al.. (2025). Transcriptional readthrough at Atf4 locus suppresses Rps19bp1 and impairs heart development. Cardiovascular Research. 121(18). 2909–2921.
2.
Pataky, Mark W., Carrie J. Heppelmann, Katherine A. Klaus, et al.. (2025). Aerobic and resistance exercise-regulated phosphoproteome and acetylproteome modifications in human skeletal muscle. Nature Communications. 16(1). 5700–5700. 1 indexed citations
3.
Ebert, Scott M., Céline S. Nicolas, Paul Schreiber, et al.. (2024). Ursolic Acid Induces Beneficial Changes in Skeletal Muscle mRNA Expression and Increases Exercise Participation and Performance in Dogs with Age-Related Muscle Atrophy. Animals. 14(2). 186–186. 2 indexed citations
4.
Bjorkman, Sarah H., Eric T. Weatherford, Jason Chen, et al.. (2024). ATF4 expression in thermogenic adipocytes is required for cold-induced thermogenesis in mice via FGF21-independent mechanisms. Scientific Reports. 14(1). 1563–1563. 8 indexed citations
5.
Miller, Matthew J., Kevin J. Gries, George R. Marcotte, et al.. (2024). Human myofiber‐enriched aging‐induced lncRNAFRAIL1 promotes loss of skeletal muscle function. Aging Cell. 23(4). e14097–e14097. 2 indexed citations
6.
Gnanaprakasam, JN Rashida, Bhavana Kushwaha, Lingling Liu, et al.. (2023). Asparagine restriction enhances CD8+ T cell metabolic fitness and antitumoral functionality through an NRF2-dependent stress response. Nature Metabolism. 5(8). 1423–1439. 58 indexed citations
7.
Miller, Matthew J., George R. Marcotte, Nathan Basisty, et al.. (2023). The transcription regulator ATF4 is a mediator of skeletal muscle aging. GeroScience. 45(4). 2525–2543. 18 indexed citations
8.
Ebert, Scott M., Hee‐Woong Lim, Byung Chul Jung, et al.. (2021). A necessary role of DNMT3A in endurance exercise by suppressing ALDH1L1‐mediated oxidative stress. The EMBO Journal. 40(9). e106491–e106491. 29 indexed citations
9.
Rapino, Francesca, Kevin Rouault‐Pierre, Joan Somja, et al.. (2021). Loss of tRNA-modifying enzyme Elp3 activates a p53-dependent antitumor checkpoint in hematopoiesis. The Journal of Experimental Medicine. 218(3). 17 indexed citations
10.
Ebert, Scott M., Jason M. Dierdorff, David K. Meyerholz, et al.. (2019). An investigation of p53 in skeletal muscle aging. Journal of Applied Physiology. 127(4). 1075–1084. 21 indexed citations
11.
Pereira, Renata O., Satya Murthy Tadinada, Karen Jesus Oliveira, et al.. (2017). OPA 1 deficiency promotes secretion of FGF 21 from muscle that prevents obesity and insulin resistance. The EMBO Journal. 36(14). 2126–2145. 150 indexed citations
12.
Martin, Sarah, et al.. (2016). Sexual dimorphism in obesity-related genes in the epicardial fat during aging. Journal of Physiology and Biochemistry. 73(2). 215–224. 14 indexed citations
13.
Bullard, Steven A., Seongjin Seo, Birgit Schilling, et al.. (2016). Gadd45a Protein Promotes Skeletal Muscle Atrophy by Forming a Complex with the Protein Kinase MEKK4. Journal of Biological Chemistry. 291(34). 17496–17509. 40 indexed citations
14.
Moro, Tatiana, Scott M. Ebert, Christopher M. Adams, & Blake B. Rasmussen. (2016). Amino Acid Sensing in Skeletal Muscle. Trends in Endocrinology and Metabolism. 27(11). 796–806. 70 indexed citations
15.
Wang, Dongxue, Christopher M. Adams, John Fernandes, Rachel L. Egger, & Virginia Walbot. (2012). A low molecular weight proteome comparison of fertile and male sterile 8 anthers of Zea mays. Plant Biotechnology Journal. 10(8). 925–935. 18 indexed citations
16.
Lan, Xun, Christopher M. Adams, Mark Landers, et al.. (2011). High Resolution Detection and Analysis of CpG Dinucleotides Methylation Using MBD-Seq Technology. PLoS ONE. 6(7). e22226–e22226. 65 indexed citations
17.
Ebert, Scott M., Alex Mas Monteys, Daniel K. Fox, et al.. (2010). The Transcription Factor ATF4 Promotes Skeletal Myofiber Atrophy during Fasting. Molecular Endocrinology. 24(4). 790–799. 106 indexed citations
18.
Maddalo, Gianluca, Mohammadreza Shariatgorji, Christopher M. Adams, et al.. (2010). Porcine P2 myelin protein primary structure and bound fatty acids determined by mass spectrometry. Analytical and Bioanalytical Chemistry. 397(5). 1903–1910. 3 indexed citations
19.
Adams, Christopher M., Julian Reitz, Jef K. De Brabander, et al.. (2004). Cholesterol and 25-Hydroxycholesterol Inhibit Activation of SREBPs by Different Mechanisms, Both Involving SCAP and Insigs. Journal of Biological Chemistry. 279(50). 52772–52780. 370 indexed citations
20.
Volk, Kenneth A., et al.. (1998). Inhibition of the Epithelial Na+ Channel by Interaction of Nedd4 with a PY Motif Deleted in Liddle's Syndrome. Journal of Biological Chemistry. 273(45). 30012–30017. 144 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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