David Brodin

1.2k total citations
30 papers, 890 citations indexed

About

David Brodin is a scholar working on Molecular Biology, Immunology and Surgery. According to data from OpenAlex, David Brodin has authored 30 papers receiving a total of 890 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 8 papers in Immunology and 5 papers in Surgery. Recurrent topics in David Brodin's work include Epigenetics and DNA Methylation (5 papers), Immune Cell Function and Interaction (3 papers) and T-cell and B-cell Immunology (3 papers). David Brodin is often cited by papers focused on Epigenetics and DNA Methylation (5 papers), Immune Cell Function and Interaction (3 papers) and T-cell and B-cell Immunology (3 papers). David Brodin collaborates with scholars based in Sweden, France and Denmark. David Brodin's co-authors include Ingrid Dahlman, Peter Arner, Karin Dahlman‐Wright, Neus Visa, Mikael Rydén, Karine Clément, Dan Grandér, Alena Maljukova, Lei Liu and Takeaki Dohda and has published in prestigious journals such as The Journal of Cell Biology, PLoS ONE and Diabetes.

In The Last Decade

David Brodin

29 papers receiving 882 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 Brodin Sweden 17 495 176 109 109 99 30 890
Hsiang‐Ying Lee Taiwan 18 728 1.5× 129 0.7× 137 1.3× 80 0.7× 143 1.4× 33 1.1k
Safak Yalcin United States 13 722 1.5× 181 1.0× 140 1.3× 95 0.9× 102 1.0× 19 1.1k
Tomoko Tsuchiya Japan 17 471 1.0× 186 1.1× 162 1.5× 110 1.0× 216 2.2× 34 882
Andreas Ritter Germany 19 341 0.7× 104 0.6× 173 1.6× 102 0.9× 107 1.1× 32 902
Jin Zheng China 13 284 0.6× 123 0.7× 151 1.4× 87 0.8× 194 2.0× 52 746
Anne Rowzee United States 13 331 0.7× 99 0.6× 182 1.7× 102 0.9× 59 0.6× 15 627
Takehiro Serikawa Japan 14 288 0.6× 87 0.5× 112 1.0× 201 1.8× 77 0.8× 30 771
Thomas E. Akie United States 12 853 1.7× 191 1.1× 58 0.5× 81 0.7× 133 1.3× 17 1.3k
Akiko Fujimura Japan 13 563 1.1× 63 0.4× 180 1.7× 66 0.6× 82 0.8× 40 842
Tohru Ikuta United States 20 680 1.4× 274 1.6× 68 0.6× 88 0.8× 104 1.1× 48 1.6k

Countries citing papers authored by David Brodin

Since Specialization
Citations

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

Fields of papers citing papers by David Brodin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Brodin

This figure shows the co-authorship network connecting the top 25 collaborators of David Brodin. A scholar is included among the top collaborators of David Brodin 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 Brodin. David Brodin 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.
2.
Ohshima, Makiko, David Brodin, Yu Wang, et al.. (2024). Intravenous chaperone treatment of late-stage Alzheimer´s disease (AD) mouse model affects amyloid plaque load, reactive gliosis and AD-related genes. Translational Psychiatry. 14(1). 453–453. 3 indexed citations
3.
Acevedo, Nathalie, Josefina Zakzuk, David Brodin, et al.. (2024). Cystatin from the helminth Ascaris lumbricoides upregulates mevalonate and cholesterol biosynthesis pathways and immunomodulatory genes in human monocyte-derived dendritic cells. Frontiers in Immunology. 15. 1328401–1328401. 6 indexed citations
4.
Breuer, Olof, Ola Brodin, Ali Razaghi, et al.. (2023). Intravenous Infusion of High Dose Selenite in End-Stage Cancer Patients: Analysis of Systemic Exposure to Selenite and Seleno-Metabolites. Biomedicines. 11(2). 295–295. 2 indexed citations
5.
Heiden, Marieke van der, et al.. (2022). Staphylococcus aureus ‐derived factors promote human Th9 cell polarization and enhance a transcriptional program associated with allergic inflammation. European Journal of Immunology. 53(3). e2250083–e2250083. 7 indexed citations
6.
Henriksson, Pontus, Antonio Lentini, Signe Altmäe, et al.. (2020). DNA methylation in infants with low and high body fatness. BMC Genomics. 21(1). 769–769. 2 indexed citations
7.
Sola-Carvajal, Agustín, Gwladys Revêchon, Hafdís T. Helgadóttir, et al.. (2019). Accumulation of Progerin Affects the Symmetry of Cell Division and Is Associated with Impaired Wnt Signaling and the Mislocalization of Nuclear Envelope Proteins. Journal of Investigative Dermatology. 139(11). 2272–2280.e12. 17 indexed citations
8.
Järver, Peter, Candice Poux, AnnSofi Sandberg, et al.. (2018). Single-Stranded Nucleic Acids Regulate TLR3/4/7 Activation through Interference with Clathrin-Mediated Endocytosis. Scientific Reports. 8(1). 15841–15841. 14 indexed citations
9.
Brodin, David, et al.. (2016). Study on genetic stability in human urothelial cells in vitro. Journal of Tissue Engineering and Regenerative Medicine. 12(2). e720–e726. 2 indexed citations
10.
Putnik, Goran D., David Brodin, Tomasz K. Wojdacz, et al.. (2016). The transcriptional coregulator MAML1 affects DNA methylation and gene expression patterns in human embryonic kidney cells. Molecular Biology Reports. 43(3). 141–150. 4 indexed citations
11.
Dahlman, Ingrid, Indranil Sinha, Hui Gao, et al.. (2015). The fat cell epigenetic signature in post-obese women is characterized by global hypomethylation and differential DNA methylation of adipogenesis genes. International Journal of Obesity. 39(6). 910–919. 76 indexed citations
12.
Brodin, David, et al.. (2014). A Study on Proliferation and Gene Expression in Normal Human Urothelial Cells in Culture. Tissue Engineering Part A. 21(3-4). 510–517. 7 indexed citations
13.
Jiao, Hong, Peter Arner, Johan Hoffstedt, et al.. (2011). Genome wide association study identifies KCNMA1contributing to human obesity. BMC Medical Genomics. 4(1). 51–51. 136 indexed citations
14.
Wang, Zhi, et al.. (2011). SWI/SNF regulates the alternative processing of a specific subset of pre-mRNAs in Drosophila melanogaster. BMC Molecular Biology. 12(1). 46–46. 20 indexed citations
15.
16.
Dahlman, Ingrid, Niklas Mejhert, Thorhallur Agustsson, et al.. (2010). Adipose tissue pathways involved in weight loss of cancer cachexia. British Journal of Cancer. 102(10). 1541–1548. 108 indexed citations
17.
Block, Tomas, et al.. (2010). Altered mRNA Expression due to Acute Mesenteric Ischaemia in a Porcine Model. European Journal of Vascular and Endovascular Surgery. 41(2). 281–287. 11 indexed citations
18.
Thắng, Phạm Hồng, Nicolas Ruffin, David Brodin, et al.. (2010). The role of IL‐1β in reduced IL‐7 production by stromal and epithelial cells: a model for impaired T‐cell numbers in the gut during HIV‐1 infection. Journal of Internal Medicine. 268(2). 181–193. 16 indexed citations
19.
Dohda, Takeaki, Alena Maljukova, Lei Liu, et al.. (2007). Notch signaling induces SKP2 expression and promotes reduction of p27Kip1 in T-cell acute lymphoblastic leukemia cell lines. Experimental Cell Research. 313(14). 3141–3152. 95 indexed citations
20.
Bergqvist, Michael, Daniel Brattström, David Brodin, et al.. (2005). Genes associated with telomerase activity levels in esophageal carcinoma cell lines. Diseases of the Esophagus. 19(1). 20–23. 6 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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