Charles G. Sagerström

2.1k total citations
51 papers, 1.6k citations indexed

About

Charles G. Sagerström is a scholar working on Molecular Biology, Cell Biology and Immunology. According to data from OpenAlex, Charles G. Sagerström has authored 51 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 20 papers in Cell Biology and 5 papers in Immunology. Recurrent topics in Charles G. Sagerström's work include Developmental Biology and Gene Regulation (31 papers), Congenital heart defects research (22 papers) and Zebrafish Biomedical Research Applications (20 papers). Charles G. Sagerström is often cited by papers focused on Developmental Biology and Gene Regulation (31 papers), Congenital heart defects research (22 papers) and Zebrafish Biomedical Research Applications (20 papers). Charles G. Sagerström collaborates with scholars based in United States, United Kingdom and Japan. Charles G. Sagerström's co-authors include Seong‐Kyu Choe, Hazel Sive, Mark M. Davis, Franck Ladam, Alexander P. Runko, Brigitte Devaux, Yevgenya Grinblat, Mako Nakamura, John F. Elliott and Augustine Y. Lin and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Charles G. Sagerström

49 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Charles G. Sagerström United States 23 1.2k 307 305 253 119 51 1.6k
Carolina Mailhos United Kingdom 15 1.3k 1.1× 361 1.2× 199 0.7× 189 0.7× 216 1.8× 20 1.9k
Cornel Popovici France 23 1.1k 0.9× 150 0.5× 161 0.5× 331 1.3× 43 0.4× 51 1.8k
Milton A. English United States 20 1.4k 1.2× 152 0.5× 372 1.2× 346 1.4× 26 0.2× 36 1.7k
Gisèle A. Deblandre United States 11 1.1k 1.0× 181 0.6× 332 1.1× 164 0.6× 25 0.2× 12 1.4k
Christopher Seidel United States 23 1.4k 1.2× 132 0.4× 193 0.6× 169 0.7× 43 0.4× 36 1.8k
Panayiotis Zagouras United States 14 1.1k 1.0× 157 0.5× 187 0.6× 159 0.6× 38 0.3× 15 1.5k
Yevgenya Grinblat United States 19 1.0k 0.9× 169 0.6× 327 1.1× 247 1.0× 33 0.3× 29 1.3k
Lilach Gilboa Israel 17 1.0k 0.9× 179 0.6× 183 0.6× 287 1.1× 45 0.4× 23 1.3k
J. Hurst United Kingdom 14 1.3k 1.2× 272 0.9× 135 0.4× 539 2.1× 89 0.7× 21 1.8k
Richa Wilson United States 6 1.4k 1.2× 208 0.7× 273 0.9× 205 0.8× 25 0.2× 6 1.5k

Countries citing papers authored by Charles G. Sagerström

Since Specialization
Citations

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

Fields of papers citing papers by Charles G. Sagerström

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles G. Sagerström. 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 Charles G. Sagerström. The network helps show where Charles G. Sagerström may publish in the future.

Co-authorship network of co-authors of Charles G. Sagerström

This figure shows the co-authorship network connecting the top 25 collaborators of Charles G. Sagerström. A scholar is included among the top collaborators of Charles G. Sagerström 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 Charles G. Sagerström. Charles G. Sagerström 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.
Dale, Emily C., et al.. (2025). Epigenetic priming of neural progenitors by Notch enhances Sonic hedgehog signaling and establishes gliogenic competence. Genes & Development. 39(13-14). 886–906. 1 indexed citations
2.
Kim, Yong‐Il, Rebecca O’Rourke, & Charles G. Sagerström. (2023). scMultiome analysis identifies embryonic hindbrain progenitors with mixed rhombomere identities. eLife. 12. 2 indexed citations
3.
Bridoux, Laure, Víctor Latorre, Syed Murtuza Baker, et al.. (2020). HOX paralogs selectively convert binding of ubiquitous transcription factors into tissue-specific patterns of enhancer activation. PLoS Genetics. 16(12). e1009162–e1009162. 21 indexed citations
4.
5.
Sagerström, Charles G., et al.. (2018). Developing roles for Hox proteins in hindbrain gene regulatory networks. The International Journal of Developmental Biology. 62(11-12). 767–774. 8 indexed citations
6.
Sagerström, Charles G., et al.. (2018). Analysis of novel caudal hindbrain genes reveals different regulatory logic for gene expression in rhombomere 4 versus 5/6 in embryonic zebrafish. Neural Development. 13(1). 13–13. 8 indexed citations
7.
Amin, Shilu, Ian J. Donaldson, James Hensman, et al.. (2015). Hoxa2 Selectively Enhances Meis Binding to Change a Branchial Arch Ground State. Developmental Cell. 32(3). 265–277. 63 indexed citations
8.
Choe, Seong‐Kyu, Franck Ladam, & Charles G. Sagerström. (2014). TALE Factors Poise Promoters for Activation by Hox Proteins. Developmental Cell. 28(2). 203–211. 45 indexed citations
9.
Gupta, Ankit, et al.. (2014). Targeted germ line disruptions reveal general and species-specific roles for paralog group 1 hox genes in zebrafish. BMC Developmental Biology. 14(1). 25–25. 9 indexed citations
10.
Sagerström, Charles G., et al.. (2011). olig2‐expressing hindbrain cells are required for migrating facial motor neurons. Developmental Dynamics. 241(2). 315–326. 9 indexed citations
11.
Choe, Seong‐Kyu, Xiaolan Zhang, Nicolas Hirsch, Juerg Straubhaar, & Charles G. Sagerström. (2011). A screen for hoxb1-regulated genes identifies ppp1r14al as a regulator of the rhombomere 4 Fgf-signaling center. Developmental Biology. 358(2). 356–367. 21 indexed citations
12.
Lu, Peiyuan, et al.. (2009). Meis Cofactors Control HDAC and CBP Accessibility at Hox-Regulated Promoters during Zebrafish Embryogenesis. Developmental Cell. 17(4). 561–567. 77 indexed citations
13.
Choe, Seong‐Kyu, Nicolas Hirsch, Xiaolan Zhang, & Charles G. Sagerström. (2008). hnf1b Genes in Zebrafish Hindbrain Development. Zebrafish. 5(3). 179–187. 14 indexed citations
14.
Choe, Seong‐Kyu & Charles G. Sagerström. (2004). Paralog group 1 hox genes regulate rhombomere 5/6 expression of vhnf1, a repressor of rostral hindbrain fates, in a meis-dependent manner. Developmental Biology. 271(2). 350–361. 22 indexed citations
15.
Nakamura, Mako, Alexander P. Runko, & Charles G. Sagerström. (2004). A novel subfamily of zinc finger genes involved in embryonic development. Journal of Cellular Biochemistry. 93(5). 887–895. 38 indexed citations
16.
Runko, Alexander P. & Charles G. Sagerström. (2004). Isolation of nlz2 and Characterization of Essential Domains in Nlz Family Proteins. Journal of Biological Chemistry. 279(12). 11917–11925. 27 indexed citations
17.
Sagerström, Charles G., et al.. (2004). Specification of the enveloping layer and lack of autoneuralization in zebrafish embryonic explants. Developmental Dynamics. 232(1). 85–97. 33 indexed citations
18.
Runko, Alexander P. & Charles G. Sagerström. (2003). Nlz belongs to a family of zinc-finger-containing repressors and controls segmental gene expression in the zebrafish hindbrain. Developmental Biology. 262(2). 254–267. 35 indexed citations
19.
diIorio, Philip, et al.. (2002). A zebrafish unc‐45–related gene expressed during muscle development. Developmental Dynamics. 224(4). 457–460. 25 indexed citations
20.
Sagerström, Charles G., et al.. (2001). Isolation and characterization of posteriorly restricted genes in the zebrafish gastrula. Developmental Dynamics. 220(4). 402–408. 37 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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2026