David E. Nelson

3.1k total citations · 1 hit paper
33 papers, 2.4k citations indexed

About

David E. Nelson is a scholar working on Molecular Biology, Epidemiology and Immunology. According to data from OpenAlex, David E. Nelson has authored 33 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 10 papers in Epidemiology and 10 papers in Immunology. Recurrent topics in David E. Nelson's work include Ubiquitin and proteasome pathways (5 papers), Immune Response and Inflammation (5 papers) and NF-κB Signaling Pathways (5 papers). David E. Nelson is often cited by papers focused on Ubiquitin and proteasome pathways (5 papers), Immune Response and Inflammation (5 papers) and NF-κB Signaling Pathways (5 papers). David E. Nelson collaborates with scholars based in United Kingdom, United States and Kenya. David E. Nelson's co-authors include Michael White, David G. Spiller, Douglas B. Kell, Caroline A. Horton, Violaine Sée, John Unitt, Glyn Nelson, Heike Laman, Suzanne J. Randle and James R. Johnson and has published in prestigious journals such as Science, JAMA and Journal of Biological Chemistry.

In The Last Decade

David E. Nelson

32 papers receiving 2.3k citations

Hit Papers

Oscillations in NF-κB Signaling Control the Dynamics of G... 2004 2026 2011 2018 2004 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David E. Nelson United Kingdom 17 1.3k 547 493 354 257 33 2.4k
Lingbo Kong China 30 1.2k 0.9× 316 0.6× 284 0.6× 335 0.9× 254 1.0× 101 2.5k
Jichao Chen United States 31 1.8k 1.3× 243 0.4× 432 0.9× 150 0.4× 264 1.0× 77 3.1k
Arnaud Droit Canada 36 2.1k 1.6× 428 0.8× 468 0.9× 304 0.9× 523 2.0× 183 3.8k
Philipp E. Geyer Germany 25 2.2k 1.7× 203 0.4× 236 0.5× 406 1.1× 207 0.8× 38 4.1k
Jennifer C. Boldrick United States 10 1.3k 1.0× 721 1.3× 246 0.5× 357 1.0× 452 1.8× 10 2.8k
Renaud Gaujoux Israel 12 1.8k 1.3× 654 1.2× 620 1.3× 261 0.7× 363 1.4× 16 3.1k
Xiaochen Bo China 31 2.7k 2.0× 304 0.6× 553 1.1× 306 0.9× 196 0.8× 166 4.2k
Karin Rodland United States 41 3.2k 2.4× 391 0.7× 425 0.9× 566 1.6× 437 1.7× 126 5.2k
Joshua W. Modell United States 13 3.5k 2.6× 261 0.5× 491 1.0× 209 0.6× 422 1.6× 16 4.6k

Countries citing papers authored by David E. Nelson

Since Specialization
Citations

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

Fields of papers citing papers by David E. Nelson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David E. Nelson

This figure shows the co-authorship network connecting the top 25 collaborators of David E. Nelson. A scholar is included among the top collaborators of David E. Nelson 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 E. Nelson. David E. Nelson 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.
Nelson, David E., et al.. (2024). Exploring the role of CITED transcriptional regulators in the control of macrophage polarization. Frontiers in Immunology. 15. 1365718–1365718. 6 indexed citations
2.
Jansson‐Knodell, Claire, Anita Gupta, Matthew Bohm, et al.. (2023). Clinical Presentation of Small Intestinal Bacterial Overgrowth from Aerodigestive Tract Bacteria Versus Colonic-Type Bacteria: A Comparison Study. Digestive Diseases and Sciences. 68(8). 3390–3399. 4 indexed citations
3.
Garcia, Sarah, et al.. (2022). Regulation of macrophage IFNγ-stimulated gene expression by the transcriptional coregulator CITED1. Journal of Cell Science. 136(1). 9 indexed citations
4.
Wu, Yongjun, et al.. (2021). A model of the innate immune response to SARS-CoV-2 in the alveolar epithelium. Royal Society Open Science. 8(8). 210090–210090. 6 indexed citations
5.
McClelland, Erin E., et al.. (2020). Intracellular Cryptococcus neoformans disrupts the transcriptome profile of M1- and M2-polarized host macrophages. PLoS ONE. 15(8). e0233818–e0233818. 15 indexed citations
6.
Nelson, David E., et al.. (2019). Temporal integration of mitochondrial stress signals by the PINK1:Parkin pathway. BMC Molecular and Cell Biology. 20(1). 33–33. 11 indexed citations
7.
Randle, Suzanne J., Sara Al Rawi, Benjamin M. Skinner, et al.. (2019). A Conserved Requirement for Fbxo7 During Male Germ Cell Cytoplasmic Remodeling. Frontiers in Physiology. 10. 1278–1278. 15 indexed citations
9.
Lai, Hoyin, et al.. (2018). Size Matters: Measurement of Capsule Diameter in <em>Cryptococcus neoformans</em>. Journal of Visualized Experiments. 12 indexed citations
10.
Nelson, David E., et al.. (2018). Signal Distortion: How Intracellular Pathogens Alter Host Cell Fate by Modulating NF-κB Dynamics. Frontiers in Immunology. 9. 2962–2962. 15 indexed citations
11.
Heusinkveld, Lauren E., et al.. (2016). Modulation of Macrophage Inflammatory Nuclear Factor κB (NF-κB) Signaling by Intracellular Cryptococcus neoformans. Journal of Biological Chemistry. 291(30). 15614–15627. 31 indexed citations
12.
Park, Hyo‐Sang, David E. Nelson, Brock A. Arivett, et al.. (2016). Suppression of LPS-induced NF-κB activity in macrophages by the synthetic aurone, (Z)-2-((5-(hydroxymethyl) furan-2-yl) methylene) benzofuran-3(2H)-one. International Immunopharmacology. 43. 116–128. 20 indexed citations
13.
Burchell, Victoria, David E. Nelson, Álvaro Sánchez-Martínez, et al.. (2013). The Parkinson's disease–linked proteins Fbxo7 and Parkin interact to mediate mitophagy. Nature Neuroscience. 16(9). 1257–1265. 243 indexed citations
14.
Lomonosov, Mikhail, et al.. (2011). Expression of Fbxo7 in Haematopoietic Progenitor Cells Cooperates with p53 Loss to Promote Lymphomagenesis. PLoS ONE. 6(6). e21165–e21165. 20 indexed citations
15.
Randle, Suzanne J., et al.. (2011). Knockdown of Fbxo7 reveals its regulatory role in proliferation and differentiation of haematopoietic precursor cells. Development. 138(14). e1–e1. 1 indexed citations
16.
Randle, Suzanne J., et al.. (2011). Knockdown of Fbxo7 reveals its regulatory role in proliferation and differentiation of haematopoietic precursor cells. Journal of Cell Science. 124(13). 2175–2186. 35 indexed citations
17.
Nelson, David E. & Heike Laman. (2011). A Competitive Binding Mechanism between Skp1 and Exportin 1 (CRM1) Controls the Localization of a Subset of F-box Proteins. Journal of Biological Chemistry. 286(22). 19804–19815. 22 indexed citations
18.
Nelson, David E., Violaine Sée, Glyn Nelson, & Michael White. (2004). Oscillations in transcription factor dynamics: a new way to control gene expression. Biochemical Society Transactions. 32(6). 1090–1092. 32 indexed citations
19.
Nelson, David E., Adaoha Ihekwaba, Malcolm C. Elliott, et al.. (2004). Oscillations in NF-κB Signaling Control the Dynamics of Gene Expression. Science. 306(5696). 704–708. 960 indexed citations breakdown →
20.
Nelson, David E., Steven B. Auerbach, Aldona L. Baltch, et al.. (1994). Epidemic Clostridium difficile- Associated Diarrhea: Role of Second- and Third-Generation Cephalosporins. Infection Control and Hospital Epidemiology. 15(2). 88–94. 71 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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