Astrid Schauß

5.2k total citations · 2 hit papers
53 papers, 3.8k citations indexed

About

Astrid Schauß is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Astrid Schauß has authored 53 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 10 papers in Cell Biology and 5 papers in Cellular and Molecular Neuroscience. Recurrent topics in Astrid Schauß's work include Mitochondrial Function and Pathology (21 papers), ATP Synthase and ATPases Research (10 papers) and Ubiquitin and proteasome pathways (6 papers). Astrid Schauß is often cited by papers focused on Mitochondrial Function and Pathology (21 papers), ATP Synthase and ATPases Research (10 papers) and Ubiquitin and proteasome pathways (6 papers). Astrid Schauß collaborates with scholars based in Germany, United States and Canada. Astrid Schauß's co-authors include Heidi M. McBride, Elena I. Rugarli, Peter Rippstein, Rodolfo Zunino, Thomas Langer, Miguel A. Andrade‐Navarro, Michael J. Baker, Ruchika Anand, Timothy Wai and Christian Jüngst and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Neuron.

In The Last Decade

Astrid Schauß

53 papers receiving 3.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission

2014 615 citations Michael J. Baker, Astrid Schauß et al. The Journal of Cell Biology profile →
Extracellular vesicle measurements with nanoparticle tracking analysis – An accuracy and repeatability comparison between NanoSight NS300 and ZetaView

2019 421 citations Felix Babatz, Astrid Schauß et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Astrid Schauß Germany	27	2.9k	515	503	501	437	53	3.8k
Ansgar Santel Germany	27	3.5k 1.2×	481 0.9×	534 1.1×	270 0.5×	562 1.3×	38	4.1k
Oliver Schmidt Germany	30	2.2k 0.7×	583 1.1×	255 0.5×	522 1.0×	255 0.6×	63	3.4k
Hua Yuan China	31	2.6k 0.9×	508 1.0×	600 1.2×	345 0.7×	183 0.4×	145	4.1k
Frédéric Catez France	26	2.9k 1.0×	403 0.8×	387 0.8×	194 0.4×	336 0.8×	38	3.4k
Olga Goldberger United States	23	4.0k 1.4×	359 0.7×	460 0.9×	1.1k 2.3×	807 1.8×	30	5.2k
Henrique Girão Portugal	36	2.7k 0.9×	378 0.7×	584 1.2×	416 0.8×	104 0.2×	116	3.8k
S. Patricia Becerra United States	39	2.7k 0.9×	159 0.3×	438 0.9×	542 1.1×	183 0.4×	93	4.1k
Eugene W. Krueger United States	27	2.5k 0.8×	650 1.3×	216 0.4×	1.8k 3.6×	258 0.6×	42	4.2k
Steven H. Seeholzer United States	32	2.0k 0.7×	415 0.8×	244 0.5×	286 0.6×	112 0.3×	79	3.5k

Countries citing papers authored by Astrid Schauß

Since Specialization

Citations

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

Fields of papers citing papers by Astrid Schauß

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Astrid Schauß

This figure shows the co-authorship network connecting the top 25 collaborators of Astrid Schauß. A scholar is included among the top collaborators of Astrid Schauß 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 Astrid Schauß. Astrid Schauß is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Schäffner, Iris, et al.. (2024). Enhanced mitochondrial fusion during a critical period of synaptic plasticity in adult-born neurons. Neuron. 112(12). 1997–2014.e6. 19 indexed citations

Pla‐Martín, David, Felix Babatz, & Astrid Schauß. (2023). Localization of Mitochondrial Nucleoids by Transmission Electron Microscopy Using the Transgenic Expression of the Mitochondrial Helicase Twinkle and APEX2. Methods in molecular biology. 2615. 173–188. 1 indexed citations

Pérez-Hernández, Daniel, Tânia Simões, Astrid Schauß, et al.. (2023). Docking and stability defects in mitofusin highlight the proteasome as a potential therapeutic target. iScience. 26(7). 107014–107014. 1 indexed citations

Klose, Jördis, Farina Bendt, Ulrike Hübenthal, et al.. (2022). Application of the adverse outcome pathway concept for investigating developmental neurotoxicity potential of Chinese herbal medicines by using human neural progenitor cells in vitro. Cell Biology and Toxicology. 39(1). 319–343. 5 indexed citations

Kallabis, Sebastian, Christian Jüngst, Julian Nüchel, et al.. (2022). Mitochondrial membrane proteins and VPS35 orchestrate selective removal of mtDNA. Nature Communications. 13(1). 6704–6704. 51 indexed citations

Jüngst, Christian, Markus M. Rinschen, Sybille Koehler, et al.. (2020). Injured Podocytes Are Sensitized to Angiotensin II–Induced Calcium Signaling. Journal of the American Society of Nephrology. 31(3). 532–542. 26 indexed citations

Janoschek, Ruth, Inga Bae‐Gartz, Peter Zentis, et al.. (2020). Effect of Maternal Obesity in Mice on IL-6 Levels and Placental Endothelial Cell Homeostasis. Nutrients. 12(2). 296–296. 21 indexed citations

Jüngst, Christian, Astrid Schauß, Olivier R. Baris, et al.. (2020). Mitochondrial Dysfunction Combined with High Calcium Load Leads to Impaired Antioxidant Defense Underlying the Selective Loss of Nigral Dopaminergic Neurons. Journal of Neuroscience. 40(9). 1975–1986. 34 indexed citations

Gessner, Isabel, Xiaojie Yu, Christian Jüngst, et al.. (2019). Selective Capture and Purification of MicroRNAs and Intracellular Proteins through Antisense-vectorized Magnetic Nanobeads. Scientific Reports. 9(1). 2069–2069. 23 indexed citations

10.

Wunderlich, Claudia M., Merly C. Vogt, Bengt‐Frederik Belgardt, et al.. (2019). Intestinal insulin/IGF1 signalling through FoxO1 regulates epithelial integrity and susceptibility to colon cancer. Nature Metabolism. 1(3). 371–389. 14 indexed citations

11.

Koehler, Felix C., Oliver A. Cornely, Hilmar Wisplinghoff, et al.. (2018). Candida-Reactive T Cells for the Diagnosis of Invasive Candida Infection—A Prospective Pilot Study. Frontiers in Microbiology. 9. 1381–1381. 12 indexed citations

12.

Cornely, Oliver A., et al.. (2017). Candida reactive T cells for diagnosis of invasive Candida infection. Mycoses. 1 indexed citations

13.

Schatton, Désirée, David Pla‐Martín, Arnaud Mourier, et al.. (2017). CLUH regulates mitochondrial metabolism by controlling translation and decay of target mRNAs. The Journal of Cell Biology. 216(3). 675–693. 68 indexed citations

14.

Rübsam, Matthias, Aaron F. Mertz, Akiharu Kubo, et al.. (2017). E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning. Nature Communications. 8(1). 1250–1250. 146 indexed citations

15.

Miller, Sharon, Signe Mathiasen, Nicholas A. Bright, et al.. (2015). CALM Regulates Clathrin-Coated Vesicle Size and Maturation by Directly Sensing and Driving Membrane Curvature. Developmental Cell. 33(2). 163–175. 156 indexed citations

16.

Kondadi, Arun Kumar, Shaomeng Wang, Sara Montagner, et al.. (2014). Loss of the m-AAA protease subunit AFG3L2 causes mitochondrial transport defects and tau hyperphosphorylation. The EMBO Journal. 33(9). 1011–1026. 64 indexed citations

17.

Donovan, Catriona, Astrid Schauß, Reinhard Krämer, & Marc Bramkamp. (2013). Chromosome Segregation Impacts on Cell Growth and Division Site Selection in Corynebacterium glutamicum. PLoS ONE. 8(2). e55078–e55078. 29 indexed citations

18.

Schauß, Astrid, et al.. (2013). Defining the action spectrum of potential PGC-1α activators on a mitochondrial and cellular level in vivo. Human Molecular Genetics. 23(9). 2400–2415. 39 indexed citations

19.

Schauß, Astrid, Emélie Braschi, Rodolfo Zunino, et al.. (2008). Cargo-Selected Transport from the Mitochondria to Peroxisomes Is Mediated by Vesicular Carriers. Current Biology. 18(2). 102–108. 467 indexed citations

20.

Jakobs, Stefan, Astrid Schauß, & Stefan W. Hell. (2003). Photoconversion of matrix targeted GFP enables analysis of continuity and intermixing of the mitochondrial lumen. FEBS Letters. 554(1-2). 194–200. 37 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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