Hans Zischka

10.8k total citations · 3 hit papers
101 papers, 4.8k citations indexed

About

Hans Zischka is a scholar working on Molecular Biology, Nutrition and Dietetics and Oncology. According to data from OpenAlex, Hans Zischka has authored 101 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 59 papers in Molecular Biology, 18 papers in Nutrition and Dietetics and 16 papers in Oncology. Recurrent topics in Hans Zischka's work include Mitochondrial Function and Pathology (28 papers), Trace Elements in Health (17 papers) and Heavy Metal Exposure and Toxicity (12 papers). Hans Zischka is often cited by papers focused on Mitochondrial Function and Pathology (28 papers), Trace Elements in Health (17 papers) and Heavy Metal Exposure and Toxicity (12 papers). Hans Zischka collaborates with scholars based in Germany, United States and France. Hans Zischka's co-authors include Guido Kroemer, Lorenzo Galluzzi, Ilio Vitale, Maria Castedo, Maria Chiara Maiuri, Laurence Zitvogel, Sabine Schmitt, Josef Lichtmannegger, Ralf J. Braun and Marius Ueffing and has published in prestigious journals such as Nature, Journal of Biological Chemistry and Journal of Clinical Investigation.

In The Last Decade

Hans Zischka

93 papers receiving 4.7k citations

Hit Papers

Cell death modalities: classification and pathophysiologi... 2007 2026 2013 2019 2007 2020 2018 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hans Zischka Germany 37 2.8k 732 513 503 452 101 4.8k
Dominique Lagadic‐Gossmann France 42 3.1k 1.1× 453 0.6× 390 0.8× 293 0.6× 597 1.3× 130 5.7k
Alakananda Basu United States 36 3.3k 1.2× 667 0.9× 457 0.9× 368 0.7× 1.4k 3.1× 109 5.1k
Joshua L. Dunaief United States 45 3.6k 1.3× 317 0.4× 292 0.6× 1.1k 2.1× 425 0.9× 146 6.9k
Jeen‐Woo Park South Korea 42 3.1k 1.1× 451 0.6× 373 0.7× 369 0.7× 297 0.7× 180 6.0k
Yefim Manevich United States 43 4.2k 1.5× 262 0.4× 472 0.9× 504 1.0× 233 0.5× 77 5.7k
Cesare Indiveri Italy 46 4.7k 1.7× 450 0.6× 452 0.9× 271 0.5× 994 2.2× 211 7.3k
Nükhet Aykin‐Burns United States 31 3.0k 1.1× 632 0.9× 208 0.4× 322 0.6× 567 1.3× 72 5.7k
Darius J.R. Lane Australia 38 2.1k 0.8× 251 0.3× 270 0.5× 1.1k 2.2× 735 1.6× 72 4.5k
Nancy Carrasco United States 48 3.5k 1.3× 741 1.0× 182 0.4× 252 0.5× 936 2.1× 100 8.5k
Bryan C. Dickinson United States 40 3.9k 1.4× 222 0.3× 419 0.8× 253 0.5× 334 0.7× 105 7.3k

Countries citing papers authored by Hans Zischka

Since Specialization
Citations

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

Fields of papers citing papers by Hans Zischka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hans Zischka

This figure shows the co-authorship network connecting the top 25 collaborators of Hans Zischka. A scholar is included among the top collaborators of Hans Zischka 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 Hans Zischka. Hans Zischka 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
3.
Flis, Damian Józef, et al.. (2024). Amyotrophic lateral sclerosis associated disturbance of iron metabolism is blunted by swim training-role of AKT signaling pathway. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1870(4). 167014–167014. 9 indexed citations
4.
Hu, Yudong, Hans Zischka, Uli Kazmaier, et al.. (2024). Thermal Proteome Profiling Reveals Insight to Antiproliferative and Pro‐Apoptotic Effects of Lagunamide A in the Modulation of DNA Damage Repair. ChemBioChem. 25(13). e202400024–e202400024. 1 indexed citations
5.
Ebert, Franziska, Christiane Ott, Judith Nagel, et al.. (2024). Subzero project: comparing trace element profiles of enriched mitochondria fractions from frozen and fresh liver tissue. Analytical and Bioanalytical Chemistry. 416(20). 4591–4604. 1 indexed citations
6.
Gruber, Andreas, et al.. (2023). Hfe Actions in Kupffer Cells Are Dispensable for Hepatic and Systemic Iron Metabolism. International Journal of Molecular Sciences. 24(10). 8948–8948. 1 indexed citations
7.
Maares, Maria, Julian Hackler, Claudia Keil, et al.. (2023). A fluorometric assay to determine labile copper(II) ions in serum. Scientific Reports. 13(1). 12807–12807. 9 indexed citations
8.
Kabiri, Yaschar, Rachel Tang, Yu‐Kai Chao, et al.. (2022). Lysosomal TRPML1 regulates mitochondrial function in hepatocellular carcinoma cells. Journal of Cell Science. 135(6). 22 indexed citations
9.
Dudek, Michael, Sainitin Donakonda, Tobias Baumann, et al.. (2022). IL-6-induced FOXO1 activity determines the dynamics of metabolism in CD8 T cells cross-primed by liver sinusoidal endothelial cells. Cell Reports. 38(7). 110389–110389. 17 indexed citations
10.
Liang, Xujun, Wenyu Gu, Aloys Schepers, et al.. (2021). Evidence for methanobactin “Theft” and novel chalkophore production in methanotrophs: impact on methanotrophic-mediated methylmercury degradation. The ISME Journal. 16(1). 211–220. 25 indexed citations
11.
Simões, Inês C. M., Agnieszka Karkucińska‐Więckowska, Justyna Janikiewicz, et al.. (2020). Western Diet Causes Obesity-Induced Nonalcoholic Fatty Liver Disease Development by Differentially Compromising the Autophagic Response. Antioxidants. 9(10). 995–995. 34 indexed citations
12.
Baldini, Francesca, Rita Fabbri, Carola Eberhagen, et al.. (2020). Adipocyte hypertrophy parallels alterations of mitochondrial status in a cell model for adipose tissue dysfunction in obesity. Life Sciences. 265. 118812–118812. 33 indexed citations
13.
Quarles, C. Derrick, et al.. (2020). LC-ICP-MS method for the determination of “extractable copper” in serum. Metallomics. 12(9). 1348–1355. 36 indexed citations
14.
Bartel, Karin, Helmut Pein, Bastian Popper, et al.. (2019). Connecting lysosomes and mitochondria – a novel role for lipid metabolism in cancer cell death. Cell Communication and Signaling. 17(1). 87–87. 34 indexed citations
15.
Sauer, Vanessa, et al.. (2017). Downregulation of hepatic multi-drug resistance protein 1 (MDR1) after copper exposure. Metallomics. 9(9). 1279–1287. 5 indexed citations
16.
Walsh, Dietrich W. M., Christian Siebenwirth, Christoph Greubel, et al.. (2017). Live cell imaging of mitochondria following targeted irradiation in situ reveals rapid and highly localized loss of membrane potential. Scientific Reports. 7(1). 46684–46684. 46 indexed citations
17.
Schmitt, Sabine, Carola Eberhagen, Susanne Weber, Michaela Aichler, & Hans Zischka. (2015). Isolation of Mitochondria from Cultured Cells and Liver Tissue Biopsies for Molecular and Biochemical Analyses. Methods in molecular biology. 1295. 87–97. 15 indexed citations
18.
Dolga, Amalia M., Michael F. Netter, Fabiana Perocchi, et al.. (2013). Mitochondrial Small Conductance SK2 Channels Prevent Glutamate-induced Oxytosis and Mitochondrial Dysfunction. Journal of Biological Chemistry. 288(15). 10792–10804. 83 indexed citations
19.
Galluzzi, Lorenzo, Ilio Vitale, Laura Senovilla, et al.. (2012). Independent transcriptional reprogramming and apoptosis induction by cisplatin. Cell Cycle. 11(18). 3472–3480. 24 indexed citations
20.
Hense, Burkhard A., et al.. (2010). A mathematical model of mitochondrial swelling. BMC Research Notes. 3(1). 67–67. 20 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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