David J. Forsthoefel

1.4k total citations
18 papers, 1.0k citations indexed

About

David J. Forsthoefel is a scholar working on Molecular Biology, Global and Planetary Change and Paleontology. According to data from OpenAlex, David J. Forsthoefel has authored 18 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 10 papers in Global and Planetary Change and 5 papers in Paleontology. Recurrent topics in David J. Forsthoefel's work include Planarian Biology and Electrostimulation (11 papers), Marine Ecology and Invasive Species (10 papers) and Marine Invertebrate Physiology and Ecology (5 papers). David J. Forsthoefel is often cited by papers focused on Planarian Biology and Electrostimulation (11 papers), Marine Ecology and Invasive Species (10 papers) and Marine Invertebrate Physiology and Ecology (5 papers). David J. Forsthoefel collaborates with scholars based in United States, Japan and France. David J. Forsthoefel's co-authors include Phillip A. Newmark, Mark A. Seeger, Eric C. Liebl, Peter A. Kolodziej, Jennifer Cowger, Jon E. Hess, R. King, Jennifer Weiss, Kiyokazu Agata and Takeshi Inoue and has published in prestigious journals such as Nature Communications, Neuron and Molecular Cell.

In The Last Decade

David J. Forsthoefel

18 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David J. Forsthoefel United States 13 852 380 230 191 174 18 1.0k
Jason Pellettieri United States 11 793 0.9× 335 0.9× 57 0.2× 162 0.8× 160 0.9× 14 1.0k
Ian Henry Germany 13 1.1k 1.2× 308 0.8× 92 0.4× 99 0.5× 162 0.9× 17 1.3k
Albert Erives United States 21 1.2k 1.5× 314 0.8× 161 0.7× 120 0.6× 195 1.1× 31 1.5k
Erin L. Davies United States 8 623 0.7× 166 0.4× 97 0.4× 78 0.4× 96 0.6× 9 741
Makiko Seimiya Switzerland 15 1.1k 1.2× 102 0.3× 228 1.0× 157 0.8× 84 0.5× 24 1.3k
Weiyang Shi United States 17 960 1.1× 275 0.7× 89 0.4× 140 0.7× 62 0.4× 27 1.2k
Andreu Casali Spain 15 532 0.6× 109 0.3× 160 0.7× 114 0.6× 91 0.5× 25 849
Craig R. Magie United States 13 598 0.7× 182 0.5× 119 0.5× 427 2.2× 37 0.2× 13 970
Naharajan Lakshmanaperumal Germany 6 475 0.6× 132 0.3× 57 0.2× 77 0.4× 65 0.4× 6 629
Kevin G. Nyberg United States 7 360 0.4× 170 0.4× 58 0.3× 109 0.6× 34 0.2× 11 651

Countries citing papers authored by David J. Forsthoefel

Since Specialization
Citations

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

Fields of papers citing papers by David J. Forsthoefel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David J. Forsthoefel. 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 David J. Forsthoefel. The network helps show where David J. Forsthoefel may publish in the future.

Co-authorship network of co-authors of David J. Forsthoefel

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

All Works

18 of 18 papers shown
1.
Wong, Lily, et al.. (2025). Extracellular Vesicles Derived From Regenerating Tissue Promote Stem Cell Proliferation in the Planarian Schmidtea mediterranea. Journal of Extracellular Biology. 4(3). e70040–e70040. 1 indexed citations
2.
Wong, Lily, et al.. (2022). Intestine-enriched apolipoprotein b orthologs are required for stem cell progeny differentiation and regeneration in planarians. Nature Communications. 13(1). 3803–3803. 8 indexed citations
3.
Forsthoefel, David J., et al.. (2022). An Emerging Frontier in Intercellular Communication: Extracellular Vesicles in Regeneration. Frontiers in Cell and Developmental Biology. 10. 849905–849905. 27 indexed citations
4.
Forsthoefel, David J., et al.. (2020). Cell-type diversity and regionalized gene expression in the planarian intestine. eLife. 9. 30 indexed citations
5.
Forsthoefel, David J., Kelly G. Ross, Phillip A. Newmark, & Ricardo M. Zayas. (2018). Fixation, Processing, and Immunofluorescent Labeling of Whole Mount Planarians. Methods in molecular biology. 353–366. 9 indexed citations
6.
Forsthoefel, David J., et al.. (2014). Generation of cell type-specific monoclonal antibodies for the planarian and optimization of sample processing for immunolabeling. BMC Developmental Biology. 14(1). 45–45. 26 indexed citations
7.
Rouhana, Labib, Jennifer Weiss, David J. Forsthoefel, et al.. (2013). RNA interference by feeding in vitro–synthesized double‐stranded RNA to planarians: Methodology and dynamics. Developmental Dynamics. 242(6). 718–730. 159 indexed citations
8.
Rouhana, Labib, Jennifer Weiss, David J. Forsthoefel, et al.. (2013). RNA interference by feeding in vitro–synthesized double‐stranded RNA to planarians: Methodology and dynamics. Developmental Dynamics. 242(6). 4 indexed citations
9.
Forsthoefel, David J., et al.. (2012). An RNAi Screen Reveals Intestinal Regulators of Branching Morphogenesis, Differentiation, and Stem Cell Proliferation in Planarians. Developmental Cell. 23(4). 691–704. 105 indexed citations
10.
Vaqué, José P., Robert T. Dorsam, Xiaodong Feng, et al.. (2012). A Genome-wide RNAi Screen Reveals a Trio-Regulated Rho GTPase Circuitry Transducing Mitogenic Signals Initiated by G Protein-Coupled Receptors. Molecular Cell. 49(1). 94–108. 110 indexed citations
11.
Forsthoefel, David J., et al.. (2011). Stem cell-based growth, regeneration, and remodeling of the planarian intestine. Developmental Biology. 356(2). 445–459. 103 indexed citations
12.
Forsthoefel, David J. & Phillip A. Newmark. (2009). Emerging patterns in planarian regeneration. Current Opinion in Genetics & Development. 19(4). 412–420. 49 indexed citations
13.
Forsthoefel, David J., David Escobar, Joel M. Stary, & Phillip A. Newmark. (2008). Intestinal renewal and regeneration in the planarian Schmidtea mediterranea. Developmental Biology. 319(2). 559–559. 1 indexed citations
14.
Forsthoefel, David J., Eric C. Liebl, Peter A. Kolodziej, & Mark A. Seeger. (2005). The Abelson tyrosine kinase, the Trio GEF and Enabled interact with the Netrin receptor Frazzled in Drosophila. Development. 132(8). 1983–1994. 98 indexed citations
15.
16.
Zhao, Chen, Allen J. York, Fan Yang, et al.. (2002). The activity of theDrosophilamorphogenetic protein Bicoid is inhibited by a domain located outside its homeodomain. Development. 129(7). 1669–1680. 38 indexed citations
17.
18.
Smith, James L., Matthew Hartman, Wei Guo, et al.. (2000). ets-2 Is a Target for an Akt (Protein Kinase B)/Jun N-Terminal Kinase Signaling Pathway in Macrophages of motheaten-viable Mutant Mice. Molecular and Cellular Biology. 20(21). 8026–8034. 61 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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