John S. Satterlee

2.7k total citations
22 papers, 1.5k citations indexed

About

John S. Satterlee is a scholar working on Molecular Biology, Aging and Endocrine and Autonomic Systems. According to data from OpenAlex, John S. Satterlee has authored 22 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 4 papers in Aging and 3 papers in Endocrine and Autonomic Systems. Recurrent topics in John S. Satterlee's work include Epigenetics and DNA Methylation (7 papers), Genetics, Aging, and Longevity in Model Organisms (4 papers) and RNA modifications and cancer (4 papers). John S. Satterlee is often cited by papers focused on Epigenetics and DNA Methylation (7 papers), Genetics, Aging, and Longevity in Model Organisms (4 papers) and RNA modifications and cancer (4 papers). John S. Satterlee collaborates with scholars based in United States, United Kingdom and Germany. John S. Satterlee's co-authors include Piali Sengupta, Michael R. Sussman, Ikue Mori, R. Mako Saito, Sander van den Heuvel, Michael Korenjak, Rein Aasland, Olivier Nolan-Stevaux, Ulrich K. Binné and Helen White‐Cooper and has published in prestigious journals such as Nature, Cell and Neuron.

In The Last Decade

John S. Satterlee

22 papers receiving 1.5k citations

Peers

John S. Satterlee

AGING

EAS

PHYSI

Swathi Arur United States

Justine A. Melo United States

Julián Cerón Spain

Christi M. Gendron United States

David J. Reiner United States

Wesley Hung Canada

Baris Tursun Germany

Julie Secombe United States

Popi Syntichaki Greece

Kui Lin China

Swathi Arur United States

John S. Satterlee

1.1k ×1.2

760 ×1.7

AGING

182 ×0.7

EAS

135 ×0.6

146 ×0.9

PHYSI

Citations per year, relative to John S. Satterlee John S. Satterlee (= 1×) peers Swathi Arur

Countries citing papers authored by John S. Satterlee

Since Specialization

Citations

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

Fields of papers citing papers by John S. Satterlee

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John S. Satterlee. 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 John S. Satterlee. The network helps show where John S. Satterlee may publish in the future.

Co-authorship network of co-authors of John S. Satterlee

This figure shows the co-authorship network connecting the top 25 collaborators of John S. Satterlee. A scholar is included among the top collaborators of John S. Satterlee 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 John S. Satterlee. John S. Satterlee is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Ganguly, Aniruddha, T. Kevin Howcroft, Lillian S. Kuo, et al.. (2025). Extracellular RNA communication: A decade of NIH common fund support illuminates exRNA biology. Journal of Extracellular Vesicles. 14(1). e70016–e70016. 3 indexed citations

Satterlee, John S., Jonathan D. Pollock, & Nora D. Volkow. (2023). The NIDA Avenir award in genetics or epigenetics of substance use disorders. Molecular and Cellular Neuroscience. 127. 103899–103899. 1 indexed citations

Satterlee, John S., Lisa H. Chadwick, Frederick L. Tyson, et al.. (2019). The NIH Common Fund/Roadmap Epigenomics Program: Successes of a comprehensive consortium. Science Advances. 5(7). eaaw6507–eaaw6507. 31 indexed citations

Satterlee, John S., et al.. (2015). Neuroepigenomics: resources, obstacles, and opportunities. PubMed. 1. 2–13. 10 indexed citations

Satterlee, John S., Maria Basanta‐Sanchez, Sandra Blanco, et al.. (2014). Novel RNA Modifications in the Nervous System: Form and Function. Journal of Neuroscience. 34(46). 15170–15177. 52 indexed citations

Satterlee, John S., et al.. (2014). Community Resources and Technologies Developed Through the NIH Roadmap Epigenomics Program. Methods in molecular biology. 1238. 27–49. 7 indexed citations

Pollock, Jonathan D., Da-Yu Wu, & John S. Satterlee. (2014). Molecular neuroanatomy: a generation of progress. Trends in Neurosciences. 37(2). 106–123. 20 indexed citations

Satterlee, John S., Dirk Schübeler, & Huck‐Hui Ng. (2010). Tackling the epigenome: challenges and opportunities for collaboration. Nature Biotechnology. 28(10). 1039–1044. 52 indexed citations

Dimitriadi, Maria, James N. Sleigh, Amy K. Walker, et al.. (2010). Conserved Genes Act as Modifiers of Invertebrate SMN Loss of Function Defects. PLoS Genetics. 6(10). e1001172–e1001172. 76 indexed citations

10.

Satterlee, John S., Scott A. Barbee, Peng Jin, et al.. (2007). Noncoding RNAs in the Brain. Journal of Neuroscience. 27(44). 11856–11859. 35 indexed citations

11.

Yang, Fajun, Bryan W. Vought, John S. Satterlee, et al.. (2006). An ARC/Mediator subunit required for SREBP control of cholesterol and lipid homeostasis. Nature. 442(7103). 700–704. 334 indexed citations

12.

Inada, Hitoshi, Hiroko Itô, John S. Satterlee, et al.. (2006). Identification of Guanylyl Cyclases That Function in Thermosensory Neurons of Caenorhabditis elegans. Genetics. 172(4). 2239–2252. 132 indexed citations

13.

Satterlee, John S., William S. Ryu, & Piali Sengupta. (2004). The CMK-1 CaMKI and the TAX-4 Cyclic Nucleotide-Gated Channel Regulate Thermosensory Neuron Gene Expression and Function in C. elegans. Current Biology. 14(1). 62–68. 57 indexed citations

14.

Korenjak, Michael, Barbie Taylor‐Harding, Ulrich K. Binné, et al.. (2004). Native E2F/RBF Complexes Contain Myb-Interacting Proteins and Repress Transcription of Developmentally Controlled E2F Target Genes. Cell. 119(2). 181–193. 242 indexed citations

15.

Saito, R. Mako, et al.. (2004). The CDC-14 phosphatase controls developmental cell-cycle arrest in C. elegans. Nature Cell Biology. 6(8). 777–783. 75 indexed citations

16.

Satterlee, John S., et al.. (2001). Specification of Thermosensory Neuron Fate in C. elegans Requires ttx-1, a Homolog of otd/Otx. Neuron. 31(6). 943–956. 128 indexed citations

17.

Satterlee, John S. & Michael R. Sussman. (1998). Unusual Membrane-Associated Protein Kinases in Higher Plants. The Journal of Membrane Biology. 164(3). 205–213. 56 indexed citations

18.

Hrabak, Estelle M., Leslie J. Dickmann, John S. Satterlee, & Michael R. Sussman. (1996). Characterization of eight new members of the calmodulin-like domain protein kinase gene family from Arabidopsis thaliana. Plant Molecular Biology. 31(2). 405–412. 95 indexed citations

19.

Chang, Gu‐Gang, John S. Satterlee, & Robert Y. Hsu. (1993). Essential sulfhydryl group of malic enzyme fromEscherichia coli. Journal of Protein Chemistry. 12(1). 7–10. 4 indexed citations

20.

Satterlee, John S. & Robert Y. Hsu. (1991). Duck liver malic enzyme: sequence of a tryptic peptide containing the cysteine residue labeled by the substrate analog bromopyruvate. Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology. 1079(3). 247–252. 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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