Daniel Chauss

2.3k total citations
24 papers, 420 citations indexed

About

Daniel Chauss is a scholar working on Molecular Biology, Immunology and Cancer Research. According to data from OpenAlex, Daniel Chauss has authored 24 papers receiving a total of 420 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 7 papers in Immunology and 4 papers in Cancer Research. Recurrent topics in Daniel Chauss's work include Connexins and lens biology (13 papers), Heme Oxygenase-1 and Carbon Monoxide (4 papers) and Autophagy in Disease and Therapy (3 papers). Daniel Chauss is often cited by papers focused on Connexins and lens biology (13 papers), Heme Oxygenase-1 and Carbon Monoxide (4 papers) and Autophagy in Disease and Therapy (3 papers). Daniel Chauss collaborates with scholars based in United States, Germany and India. Daniel Chauss's co-authors include Marc Kantorow, Lisa Brennan, A. Sue Menko, Subhasree Basu, Ashik Mohamed, Rebecca McGreal, Jianning Wei, M. Joseph Costello, Kurt O. Gilliland and Sönke Johnsen and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Journal of Virology.

In The Last Decade

Daniel Chauss

21 papers receiving 418 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel Chauss United States 11 321 89 64 61 49 24 420
Oonagh T. Lynch United Kingdom 8 129 0.4× 109 1.2× 23 0.4× 39 0.6× 29 0.6× 10 402
Haixiang Wu China 11 143 0.4× 21 0.2× 29 0.5× 93 1.5× 17 0.3× 27 341
Shahabuddin Alam United States 11 168 0.5× 40 0.4× 31 0.5× 31 0.5× 26 0.5× 19 387
Yongwu Hu China 13 481 1.5× 41 0.5× 14 0.2× 20 0.3× 130 2.7× 19 625
N. Strunnikova United States 7 313 1.0× 24 0.3× 32 0.5× 222 3.6× 17 0.3× 9 453
Yalitza Lopez Corcino United States 10 115 0.4× 99 1.1× 10 0.2× 98 1.6× 18 0.4× 12 307
Nasrollah Samiy United States 12 310 1.0× 37 0.4× 74 1.2× 239 3.9× 10 0.2× 12 609
Soon-Suk Kang South Korea 9 103 0.3× 13 0.1× 18 0.3× 40 0.7× 31 0.6× 21 374
Nina Stratmann Germany 6 154 0.5× 52 0.6× 17 0.3× 260 4.3× 15 0.3× 11 428
Sylvia Simon Sweden 10 146 0.5× 43 0.5× 9 0.1× 26 0.4× 21 0.4× 13 357

Countries citing papers authored by Daniel Chauss

Since Specialization
Citations

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

Fields of papers citing papers by Daniel Chauss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniel Chauss

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel Chauss. A scholar is included among the top collaborators of Daniel Chauss 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 Daniel Chauss. Daniel Chauss 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.
Sabapathy, Vikram, Daniel Chauss, Shuqiu Zheng, et al.. (2025). Spatial transcriptomics maps complement-driven cell-to-cell interactions during acute kidney injury. Immunobiology. 230(4). 153071–153071.
2.
Chauss, Daniel, et al.. (2025). Transcriptional cross-talk regulates complement C3 expression during CD4+ T-cell activation. Immunobiology. 230(4). 152973–152973.
3.
Freiwald, Tilo, Md Tajmul, Daniel Chauss, et al.. (2025). Inflammatory cytokines drive local C3 transcription to regulate metabolic reprogramming in kidney epithelial cells and subsequent fibrosis. Immunobiology. 230(4). 153070–153070.
4.
Portilla, Didier, Vikram Sabapathy, & Daniel Chauss. (2025). Role of local complement activation in kidney fibrosis and repair. Journal of Clinical Investigation. 135(12). 1 indexed citations
5.
Sabapathy, Vikram, Daniel Chauss, Shuqiu Zheng, et al.. (2024). Spatial Transcriptomics Enables Generation of a Complement Atlas of Mouse AKI. Journal of the American Society of Nephrology. 35(10S). 1 indexed citations
6.
Kumar, Dhaneshwar, Subhransu S. Sahoo, Daniel Chauss, Majid Kazemian, & Behdad Afzali. (2022). Non-coding RNAs in immunoregulation and autoimmunity: Technological advances and critical limitations. Journal of Autoimmunity. 134. 102982–102982. 22 indexed citations
7.
Chauss, Daniel, et al.. (2022). Suppression of PI3K signaling is linked to autophagy activation and the spatiotemporal induction of the lens organelle free zone. Experimental Cell Research. 412(2). 113043–113043. 21 indexed citations
8.
Bishop, Emma L., Nancy Gudgeon, Daniel Chauss, et al.. (2022). 1,25‐Dihydroxyvitamin D3 suppresses CD4+ T‐cell effector functionality by inhibition of glycolysis. Immunology. 166(3). 299–309. 10 indexed citations
9.
Brennan, Lisa, et al.. (2021). A functional map of genomic HIF1α-DNA complexes in the eye lens revealed through multiomics analysis. BMC Genomics. 22(1). 497–497. 7 indexed citations
10.
Yan, Bingyu, Carmen Mirabelli, Luopin Wang, et al.. (2021). Host-Virus Chimeric Events in SARS-CoV-2-Infected Cells Are Infrequent and Artifactual. Journal of Virology. 95(15). e0029421–e0029421. 19 indexed citations
11.
12.
Kantorow, Marc, et al.. (2015). Parkin-directed mitophagy is required for lens cell survival upon exposure to cataract-associated environmental insults.. Investigative Ophthalmology & Visual Science. 56(7). 2654–2654. 1 indexed citations
13.
Brennan, Lisa, Rebecca McGreal, Daniel Chauss, et al.. (2015). BNIP3L/Nix is required for mitochondrial elimination through mitophagy and the subsequent elimination of endoplasmic reticulum during the lens fiber cell differentiation program.. Investigative Ophthalmology & Visual Science. 56(7). 4838–4838. 1 indexed citations
14.
Chauss, Daniel, Lisa Brennan, О. В. Бакина, & Marc Kantorow. (2015). Integrin αVβ5-mediated Removal of Apoptotic Cell Debris by the Eye Lens and Its Inhibition by UV Light Exposure. Journal of Biological Chemistry. 290(51). 30253–30266. 14 indexed citations
15.
Chauss, Daniel, et al.. (2014). Lens epithelial cells use phagocytosis as a mechanism to remove apoptotic cellular debris. Investigative Ophthalmology & Visual Science. 55(13). 3568–3568. 1 indexed citations
16.
Costello, M. Joseph, Lisa Brennan, Subhasree Basu, et al.. (2013). Autophagy and mitophagy participate in ocular lens organelle degradation. Experimental Eye Research. 116. 141–150. 120 indexed citations
17.
McGreal, Rebecca, et al.. (2013). Chaperone-independent mitochondrial translocation and protection by αB-crystallin in RPE cells. Experimental Eye Research. 110. 10–17. 9 indexed citations
18.
McGreal, Rebecca, et al.. (2012). αB-crystallin/sHSP protects cytochrome c and mitochondrial function against oxidative stress in lens and retinal cells. Biochimica et Biophysica Acta (BBA) - General Subjects. 1820(7). 921–930. 48 indexed citations
19.
Brennan, Lisa, Daniel Chauss, Rebecca McGreal, et al.. (2012). Spatial expression patterns of autophagy genes in the eye lens and induction of autophagy in lens cells.. PubMed. 18. 1773–86. 41 indexed citations
20.
Kantorow, Marc, et al.. (2010). Focus on Molecules: Methionine sulfoxide reductase A. Experimental Eye Research. 100. 110–111. 10 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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