Martin Ott

7.0k total citations · 2 hit papers
73 papers, 5.4k citations indexed

About

Martin Ott is a scholar working on Molecular Biology, Cell Biology and Clinical Biochemistry. According to data from OpenAlex, Martin Ott has authored 73 papers receiving a total of 5.4k indexed citations (citations by other indexed papers that have themselves been cited), including 67 papers in Molecular Biology, 10 papers in Cell Biology and 5 papers in Clinical Biochemistry. Recurrent topics in Martin Ott's work include Mitochondrial Function and Pathology (54 papers), ATP Synthase and ATPases Research (30 papers) and RNA and protein synthesis mechanisms (23 papers). Martin Ott is often cited by papers focused on Mitochondrial Function and Pathology (54 papers), ATP Synthase and ATPases Research (30 papers) and RNA and protein synthesis mechanisms (23 papers). Martin Ott collaborates with scholars based in Sweden, Germany and Austria. Martin Ott's co-authors include Sten Orrenius, Boris Zhivotovsky, Vladimir Gogvadze, John D. Robertson, Johannes M. Herrmann, Alan Brown, Alexey Amunts, Kirsten Kehrein, Soledad Funes and Sabrina Büttner and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Martin Ott

70 papers receiving 5.3k citations

Hit Papers

Mitochondria, oxidative stress and cell death 2002 2026 2010 2018 2007 2002 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin Ott Sweden 35 4.0k 504 425 390 370 73 5.4k
Anna‐Liisa Nieminen United States 34 2.7k 0.7× 239 0.5× 323 0.8× 463 1.2× 398 1.1× 48 5.0k
Ivano Eberini Italy 36 2.6k 0.7× 213 0.4× 325 0.8× 195 0.5× 449 1.2× 151 4.4k
Icksoo Lee United States 40 3.6k 0.9× 323 0.6× 289 0.7× 430 1.1× 750 2.0× 82 5.5k
Masaru Miyagi United States 37 3.8k 1.0× 218 0.4× 339 0.8× 196 0.5× 506 1.4× 128 5.9k
Jens Knudsen Denmark 39 4.0k 1.0× 448 0.9× 772 1.8× 406 1.0× 790 2.1× 95 5.4k
Jan M. Suski Poland 19 2.7k 0.7× 178 0.4× 521 1.2× 508 1.3× 523 1.4× 29 4.2k
Boris V. Chernyak Russia 37 3.2k 0.8× 320 0.6× 172 0.4× 410 1.1× 511 1.4× 140 4.9k
Antoni Barrientos United States 53 6.5k 1.6× 1.2k 2.3× 490 1.2× 397 1.0× 721 1.9× 135 8.0k
Giovanna Musco Italy 35 3.0k 0.8× 691 1.4× 226 0.5× 247 0.6× 239 0.6× 99 5.3k
Andrea Rasola Italy 40 4.2k 1.1× 301 0.6× 503 1.2× 457 1.2× 535 1.4× 86 5.7k

Countries citing papers authored by Martin Ott

Since Specialization
Citations

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

Fields of papers citing papers by Martin Ott

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin Ott

This figure shows the co-authorship network connecting the top 25 collaborators of Martin Ott. A scholar is included among the top collaborators of Martin Ott 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 Martin Ott. Martin Ott 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.
Bridgers, Joseph B., Mary Couvillion, Abeer Prakash Singh, et al.. (2025). A molecular switch at the yeast mitoribosomal tunnel exit controls cytochrome b synthesis. Nucleic Acids Research. 53(13). 2 indexed citations
2.
Kohler, Verena, Xinxin Hao, Axel Imhof, et al.. (2024). Nuclear Hsp104 safeguards the dormant translation machinery during quiescence. Nature Communications. 15(1). 315–315. 5 indexed citations
3.
Kohler, Verena, et al.. (2023). Newly imported proteins in mitochondria are particularly sensitive to aggregation. Acta Physiologica. 238(3). e13985–e13985. 9 indexed citations
4.
Sridhara, S., et al.. (2023). Early steps in the biogenesis of mitochondrially encoded oxidative phosphorylation subunits. IUBMB Life. 76(3). 125–139. 3 indexed citations
5.
Ott, Martin, et al.. (2022). Multi-omic integration by machine learning (MIMaL). Bioinformatics. 38(21). 4908–4918. 8 indexed citations
6.
Berndtsson, Jens, Sorbhi Rathore, Lorena Marín-Buera, et al.. (2020). Respiratory supercomplexes enhance electron transport by decreasing cytochrome c diffusion distance. EMBO Reports. 21(12). e51015–e51015. 81 indexed citations
7.
Aftab, Wasim, et al.. (2020). Mapping protein networks in yeast mitochondria using proximity-dependent biotin identification coupled to proteomics. STAR Protocols. 1(3). 100219–100219. 4 indexed citations
8.
Schäfer, Jacob, et al.. (2020). Rcf1 Modulates Cytochrome c Oxidase Activity Especially Under Energy-Demanding Conditions. Frontiers in Physiology. 10. 1555–1555. 19 indexed citations
9.
Bareth, Bettina, Miroslav Nikolov, Isotta Lorenzi, et al.. (2016). Oms1 associates with cytochromecoxidase assembly intermediates to stabilize newly synthesized Cox1. Molecular Biology of the Cell. 27(10). 1570–1580. 3 indexed citations
10.
Kuzmenko, Anton, Stoyan Tankov, Gemma C. Atkinson, et al.. (2016). Aim-less translation: loss of Saccharomyces cerevisiae mitochondrial translation initiation factor mIF3/Aim23 leads to unbalanced protein synthesis. Scientific Reports. 6(1). 18749–18749. 22 indexed citations
11.
Ott, Martin, Martin Blaimer, David Grodzki, et al.. (2015). Acoustic-noise-optimized diffusion-weighted imaging. Magnetic Resonance Materials in Physics Biology and Medicine. 28(6). 511–521. 11 indexed citations
12.
Kehrein, Kirsten, Christian A. Wurm, Stefan Jakobs, et al.. (2015). Organization of Mitochondrial Gene Expression in Two Distinct Ribosome-Containing Assemblies. Cell Reports. 10(6). 843–853. 87 indexed citations
13.
Burguillos, Miguel Ángel, F.‐Nora Vögtle, Pedro Filipe Teixeira, et al.. (2014). The novel component Kgd4 recruits the E3 subunit to the mitochondrial α-ketoglutarate dehydrogenase. Molecular Biology of the Cell. 25(21). 3342–3349. 45 indexed citations
14.
Bauerschmitt, Heike, David U. Mick, Markus Deckers, et al.. (2010). Ribosome-binding Proteins Mdm38 and Mba1 Display Overlapping Functions for Regulation of Mitochondrial Translation. Molecular Biology of the Cell. 21(12). 1937–1944. 49 indexed citations
15.
Ott, Martin, Erik Norberg, Boris Zhivotovsky, & Sten Orrenius. (2009). Mitochondrial targeting of tBid/Bax: a role for the TOM complex?. Cell Death and Differentiation. 16(8). 1075–1082. 79 indexed citations
16.
Ott, Martin & Johannes M. Herrmann. (2009). Co-translational membrane insertion of mitochondrially encoded proteins. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1803(6). 767–775. 122 indexed citations
17.
Vogel, Frank, et al.. (2009). Mrpl36 Is Important for Generation of Assembly Competent Proteins during Mitochondrial Translation. Molecular Biology of the Cell. 20(10). 2615–2625. 41 indexed citations
18.
Ott, Martin, Vladimir Gogvadze, Sten Orrenius, & Boris Zhivotovsky. (2007). Mitochondria, oxidative stress and cell death. APOPTOSIS. 12(5). 913–922. 1630 indexed citations breakdown →
19.
Preuss, Marc, Martin Ott, Soledad Funes, Joen Luirink, & Johannes M. Herrmann. (2005). Evolution of Mitochondrial Oxa Proteins from Bacterial YidC. Journal of Biological Chemistry. 280(13). 13004–13011. 82 indexed citations
20.
Iverson, Suzanne L., Mari Enoksson, Vladimir Gogvadze, Martin Ott, & Sten Orrenius. (2004). Cardiolipin Is Not Required for Bax-mediated Cytochrome c Release from Yeast Mitochondria. Journal of Biological Chemistry. 279(2). 1100–1107. 65 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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