David E. Sanin

6.8k total citations · 4 hit papers
36 papers, 3.5k citations indexed

About

David E. Sanin is a scholar working on Immunology, Molecular Biology and Parasitology. According to data from OpenAlex, David E. Sanin has authored 36 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Immunology, 8 papers in Molecular Biology and 8 papers in Parasitology. Recurrent topics in David E. Sanin's work include Immune cells in cancer (8 papers), Parasites and Host Interactions (7 papers) and Immune Cell Function and Interaction (6 papers). David E. Sanin is often cited by papers focused on Immune cells in cancer (8 papers), Parasites and Host Interactions (7 papers) and Immune Cell Function and Interaction (6 papers). David E. Sanin collaborates with scholars based in Germany, United States and United Kingdom. David E. Sanin's co-authors include Adrian P. Mountford, Edward J. Pearce, Erika L. Pearce, David O’Sullivan, Ramon I. Klein Geltink, Michael D. Buck, Qiongyu Chen, Jing Qiu, Chih‐Hao Chang and Jonathan D. Curtis and has published in prestigious journals such as Nature, Cell and Nature Communications.

In The Last Decade

David E. Sanin

35 papers receiving 3.5k citations

Hit Papers

Mitochondrial Dynamics Controls T Cell Fate through Metab... 2015 2026 2018 2022 2016 2015 2019 2021 250 500 750 1000

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. Sanin Germany 21 1.7k 1.2k 536 497 376 36 3.5k
Pablo Fuentes‐Prior Spain 37 1.1k 0.7× 2.5k 2.1× 370 0.7× 420 0.8× 440 1.2× 77 5.0k
Hitoshi Hasegawa Japan 42 2.3k 1.4× 1.1k 0.9× 1.0k 1.9× 187 0.4× 419 1.1× 190 5.1k
Xing Liu China 28 1.1k 0.7× 1.4k 1.1× 262 0.5× 622 1.3× 323 0.9× 100 2.5k
Zvi Fishelson Israel 36 1.9k 1.2× 1.2k 1.0× 298 0.6× 241 0.5× 324 0.9× 118 3.9k
Geert Raes Belgium 44 3.5k 2.1× 1.8k 1.5× 1.6k 2.9× 298 0.6× 802 2.1× 106 6.3k
Youichi Suzuki Japan 25 1.2k 0.7× 2.4k 1.9× 897 1.7× 441 0.9× 696 1.9× 78 5.9k
Lea Brys Belgium 34 2.0k 1.2× 918 0.8× 459 0.9× 258 0.5× 928 2.5× 58 3.6k
Laurie S. Davis United States 47 3.3k 2.0× 1.3k 1.0× 903 1.7× 284 0.6× 250 0.7× 91 5.9k
Takashi Imai Japan 32 801 0.5× 1.7k 1.4× 360 0.7× 237 0.5× 267 0.7× 134 3.3k
Paul Eggleton United Kingdom 43 2.9k 1.7× 1.5k 1.2× 293 0.5× 165 0.3× 758 2.0× 107 5.4k

Countries citing papers authored by David E. Sanin

Since Specialization
Citations

This map shows the geographic impact of David E. Sanin'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. Sanin 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. Sanin more than expected).

Fields of papers citing papers by David E. Sanin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of David E. Sanin. A scholar is included among the top collaborators of David E. Sanin 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. Sanin. David E. Sanin 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.
Sanin, David E., Christopher R. Bailey, Emmanuel S. Antonarakis, et al.. (2024). Intratumoral heterogeneity drives acquired therapy resistance in a patient with metastatic prostate cancer. npj Precision Oncology. 8(1). 275–275. 3 indexed citations
2.
Mennuni, Mara, David Alsina, Roberta Filograna, et al.. (2024). High mitochondrial DNA levels accelerate lung adenocarcinoma progression. Science Advances. 10(44). eadp3481–eadp3481. 7 indexed citations
3.
Willenborg, Sebastian, et al.. (2023). FADD- and RIPK3-Mediated Cell Death Ensures Clearance of Ly6Chigh Wound Macrophages from Damaged Tissue. Journal of Investigative Dermatology. 144(1). 152–164.e7. 4 indexed citations
4.
Sanin, David E., Yan Ge, Emilija Marinković, et al.. (2022). A common framework of monocyte-derived macrophage activation. Science Immunology. 7(70). eabl7482–eabl7482. 86 indexed citations
5.
Zahalka, Sophie, Philipp Starkl, Martin L. Watzenboeck, et al.. (2022). Trained immunity of alveolar macrophages requires metabolic rewiring and type 1 interferon signaling. Mucosal Immunology. 15(5). 896–907. 59 indexed citations
6.
Willenborg, Sebastian, David E. Sanin, Alexander Jaïs, et al.. (2021). Mitochondrial metabolism coordinates stage-specific repair processes in macrophages during wound healing. Cell Metabolism. 33(12). 2398–2414.e9. 183 indexed citations breakdown →
7.
Grzes, Katarzyna M., David E. Sanin, Agnieszka M. Kabat, et al.. (2021). Plasmacytoid dendritic cell activation is dependent on coordinated expression of distinct amino acid transporters. Immunity. 54(11). 2514–2530.e7. 46 indexed citations
8.
Castoldi, Ângela, Lauar de Brito Monteiro, Nikki van Teijlingen Bakker, et al.. (2020). Triacylglycerol synthesis enhances macrophage inflammatory function. Nature Communications. 11(1). 4107–4107. 212 indexed citations
9.
Geltink, Ramon I. Klein, Joy Edwards-Hicks, Petya Apostolova, et al.. (2020). Metabolic conditioning of CD8+ effector T cells for adoptive cell therapy. Nature Metabolism. 2(8). 703–716. 95 indexed citations
10.
Sanin, David E., et al.. (2019). Angiospermas no arbóreas de un bosque húmedo tropical en el piedemonte Andino-Amazónico colombiano.. Boletín Científico Centro de Museos Museo de Historia Natural. 23(2). 62–94. 4 indexed citations
11.
Field, Cameron S., Francesc Baixauli, Ryan Kyle, et al.. (2019). Mitochondrial Integrity Regulated by Lipid Metabolism Is a Cell-Intrinsic Checkpoint for Treg Suppressive Function. Cell Metabolism. 31(2). 422–437.e5. 301 indexed citations breakdown →
12.
O’Sullivan, David, David E. Sanin, Edward J. Pearce, & Erika L. Pearce. (2019). Metabolic interventions in the immune response to cancer. Nature reviews. Immunology. 19(5). 324–335. 218 indexed citations
13.
Buck, Michael D., David O’Sullivan, Ramon I. Klein Geltink, et al.. (2016). Mitochondrial Dynamics Controls T Cell Fate through Metabolic Programming. Cell. 166(1). 63–76. 1041 indexed citations breakdown →
14.
Wu, Duojiao, David E. Sanin, Bart Everts, et al.. (2016). Type 1 Interferons Induce Changes in Core Metabolism that Are Critical for Immune Function. Immunity. 44(6). 1325–1336. 254 indexed citations
15.
Prendergast, Catriona T., David E. Sanin, & Adrian P. Mountford. (2016). Alternatively Activated Mononuclear Phagocytes from the Skin Site of Infection and the Impact of IL-4Rα Signalling on CD4+T Cell Survival in Draining Lymph Nodes after Repeated Exposure to Schistosoma mansoni Cercariae. PLoS neglected tropical diseases. 10(8). e0004911–e0004911. 5 indexed citations
16.
Sanin, David E., et al.. (2016). Catálogo comentado de las especies de melastomataceae de un bosque húmedo a orillas del río Cauca (Chinchiná, Caldas, Colombia). Boletín Científico Centro de Museos Museo de Historia Natural. 20(1). 17–26. 1 indexed citations
17.
Sanin, David E. & Adrian P. Mountford. (2015). Sm16, a major component of Schistosoma mansoni cercarial excretory/secretory products, prevents macrophage classical activation and delays antigen processing. Parasites & Vectors. 8(1). 1–1. 356 indexed citations breakdown →
18.
Sanin, David E., et al.. (2013). Araceae in a High Andean Forest of the Colombian Occidental Cordillera (Natural National Park Tatam. 76–91. 2 indexed citations
19.
Ward, Jonathan S., Jason M. Lynam, James Moir, et al.. (2012). A therapeutically viable photo-activated manganese-based CO-releasing molecule (photo-CO-RM). Dalton Transactions. 41(35). 10514–10514. 43 indexed citations
20.
Ferret‐Bernard, Stéphanie, William Castro‐Borges, Adam Dowle, et al.. (2011). Plasma membrane proteomes of differentially matured dendritic cells identified by LC–MS/MS combined with iTRAQ labelling. Journal of Proteomics. 75(3). 938–948. 17 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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