Wolfgang Voos

6.8k total citations · 1 hit paper
74 papers, 5.4k citations indexed

About

Wolfgang Voos is a scholar working on Molecular Biology, Cell Biology and Physical and Theoretical Chemistry. According to data from OpenAlex, Wolfgang Voos has authored 74 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Molecular Biology, 17 papers in Cell Biology and 6 papers in Physical and Theoretical Chemistry. Recurrent topics in Wolfgang Voos's work include Mitochondrial Function and Pathology (53 papers), Heat shock proteins research (36 papers) and ATP Synthase and ATPases Research (28 papers). Wolfgang Voos is often cited by papers focused on Mitochondrial Function and Pathology (53 papers), Heat shock proteins research (36 papers) and ATP Synthase and ATPases Research (28 papers). Wolfgang Voos collaborates with scholars based in Germany, United States and France. Wolfgang Voos's co-authors include Nikolaus Pfanner, Giovanna Cenini, Bernard Guiard, Elizabeth A. Craig, Dorothea Becker, Joachim Rassow, Cornelia Rüb, B. Diane Gambill, Oliver von Ahsen and Serge Przedborski and has published in prestigious journals such as Science, Cell and Nucleic Acids Research.

In The Last Decade

Wolfgang Voos

73 papers receiving 5.3k citations

Hit Papers

α-Synuclein Is Localized to Mitochondria-Associated ER Me... 2013 2026 2017 2021 2013 100 200 300 400
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.

  1. α-Synuclein Is Localized to Mitochondria-Associated ER Membranes
    2013 430 citations Cornelia Rüb, Dorothea Becker et al. profile →

Peers

Wolfgang Voos
Е. А. Смирнова Russia
Laura L. Lackner United States
Agnieszka Chacińska Poland
J. Samuel Zigler United States
Peter Bross Denmark
Liza A. Pon United States
Vito De Pinto Italy
Nils Wiedemann Germany
Michael P. Yaffe United States
Miriam L. Greenberg United States
Е. А. Смирнова Russia
Wolfgang Voos
Citations per year, relative to Wolfgang Voos Wolfgang Voos (= 1×) peers Е. А. Смирнова

Countries citing papers authored by Wolfgang Voos

Since Specialization
Citations

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

Fields of papers citing papers by Wolfgang Voos

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wolfgang Voos

This figure shows the co-authorship network connecting the top 25 collaborators of Wolfgang Voos. A scholar is included among the top collaborators of Wolfgang Voos 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 Wolfgang Voos. Wolfgang Voos 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.
Sylvester, Marc, et al.. (2022). Elucidation of the interaction proteome of mitochondrial chaperone Hsp78 highlights its role in protein aggregation during heat stress. Journal of Biological Chemistry. 298(10). 102494–102494. 7 indexed citations
2.
Sylvester, Marc, et al.. (2021). Proteomic analysis demonstrates the role of the quality control protease LONP1 in mitochondrial protein aggregation. Journal of Biological Chemistry. 297(4). 101134–101134. 19 indexed citations
3.
Cenini, Giovanna & Wolfgang Voos. (2019). Mitochondria as Potential Targets in Alzheimer Disease Therapy: An Update. Frontiers in Pharmacology. 10. 902–902. 186 indexed citations
4.
Rüb, Cornelia, et al.. (2017). IMiQ: a novel protein quality control compartment protecting mitochondrial functional integrity. Molecular Biology of the Cell. 29(3). 256–269. 23 indexed citations
5.
6.
Bender, Tom, et al.. (2011). Mitochondrial enzymes are protected from stress-induced aggregation by mitochondrial chaperones and the Pim1/LON protease. Molecular Biology of the Cell. 22(5). 541–554. 120 indexed citations
7.
Voos, Wolfgang. (2009). Mitochondrial protein homeostasis: the cooperative roles of chaperones and proteases. Research in Microbiology. 160(9). 718–725. 61 indexed citations
8.
Voos, Wolfgang, et al.. (2007). Chaperones and Proteases—Guardians of Protein Integrity in Eukaryotic Organelles. Annals of the New York Academy of Sciences. 1113(1). 72–86. 34 indexed citations
9.
Lim, Joo Hyun, et al.. (2006). A Cooperative Action of the ATP-Dependent Import Motor Complex and the Inner Membrane Potential Drives Mitochondrial Preprotein Import. Molecular and Cellular Biology. 27(2). 411–425. 44 indexed citations
10.
Major, Tamara, et al.. (2006). The Disaggregation Activity of the Mitochondrial ClpB Homolog Hsp78 Maintains Hsp70 Function during Heat Stress. Journal of Molecular Biology. 357(3). 793–807. 41 indexed citations
11.
Becker, Dorothea, et al.. (2006). Structure and function of Hsp78, the mitochondrial ClpB homolog. Journal of Structural Biology. 156(1). 149–164. 19 indexed citations
12.
Voos, Wolfgang. (2003). A New Connection: Chaperones Meet a Mitochondrial Receptor.: Chaperones Meet a Mitochondrial Receptor.. Molecular Cell. 12(1). 1. 1 indexed citations
13.
Strub, Andreas, Nicole Zufall, & Wolfgang Voos. (2003). The Putative Helical Lid of the Hsp70 Peptide-binding Domain is Required for Efficient Preprotein Translocation into Mitochondria. Journal of Molecular Biology. 334(5). 1087–1099. 15 indexed citations
14.
Voos, Wolfgang. (2003). A New Connection. Molecular Cell. 11(1). 1–3. 39 indexed citations
15.
Voos, Wolfgang, et al.. (2002). Molecular chaperones as essential mediators of mitochondrial biogenesis. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1592(1). 51–62. 247 indexed citations
16.
Ryan, Michael T., Wolfgang Voos, & Nikolaus Pfanner. (2001). Chapter 11 Assaying protein import into mitochondria. Methods in cell biology. 65. 189–215. 113 indexed citations
17.
Strub, Andreas, et al.. (2001). Protein Translocation into Mitochondria. Neurosignals. 10(1-2). 14–25. 8 indexed citations
18.
Strub, Andreas, et al.. (2001). The two mitochondrial heat shock proteins 70, Ssc1 and Ssq1, compete for the cochaperone Mge1 1 1Edited by M. Yaniv. Journal of Molecular Biology. 313(1). 13–26. 32 indexed citations
19.
Laloraya, Shikha, P. Dekker, Wolfgang Voos, Elizabeth A. Craig, & Nikolaus Pfanner. (1995). Mitochondrial GrpE Modulates the Function of Matrix Hsp70 in Translocation and Maturation of Preproteins. Molecular and Cellular Biology. 15(12). 7098–7105. 64 indexed citations
20.
Moczko, Martin, Birgit Schönfisch, Wolfgang Voos, Nikolaus Pfanner, & Joachim Rassow. (1995). The Mitochondrial ClpB Homolog Hsp78 Cooperates with Matrix Hsp70 in Maintenance of Mitochondrial Function. Journal of Molecular Biology. 254(4). 538–543. 47 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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