Anu Suomalainen

24.3k total citations · 4 hit papers
189 papers, 15.7k citations indexed

About

Anu Suomalainen is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Anu Suomalainen has authored 189 papers receiving a total of 15.7k indexed citations (citations by other indexed papers that have themselves been cited), including 174 papers in Molecular Biology, 75 papers in Clinical Biochemistry and 28 papers in Cellular and Molecular Neuroscience. Recurrent topics in Anu Suomalainen's work include Mitochondrial Function and Pathology (133 papers), Metabolism and Genetic Disorders (75 papers) and ATP Synthase and ATPases Research (49 papers). Anu Suomalainen is often cited by papers focused on Mitochondrial Function and Pathology (133 papers), Metabolism and Genetic Disorders (75 papers) and ATP Synthase and ATPases Research (49 papers). Anu Suomalainen collaborates with scholars based in Finland, United States and United Kingdom. Anu Suomalainen's co-authors include Jodi Nunnari, Henna Tyynismaa, Brendan J. Battersby, Massimo Zeviani, Anders Paetau, Pirjo Isohanni, Douglass M. Turnbull, Jyrki Kaukonen, Leena Peltonen and Robert McFarland and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Anu Suomalainen

182 papers receiving 15.4k citations

Hit Papers

Mitochondria: In Sickness... 2012 2026 2016 2021 2012 2016 2017 2024 500 1000 1.5k 2.0k 2.5k

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Anu Suomalainen 12.7k 5.4k 2.1k 1.5k 1.3k 189 15.7k
Michio Hirano 16.4k 1.3× 7.8k 1.5× 1.6k 0.8× 2.1k 1.4× 1.1k 0.9× 341 20.5k
Carlos T. Moraes 16.0k 1.3× 7.1k 1.3× 2.1k 1.0× 2.3k 1.5× 927 0.7× 230 19.8k
Agnès Rötig 12.7k 1.0× 6.1k 1.1× 1.2k 0.5× 1.9k 1.2× 690 0.5× 251 15.9k
Nils‐Göran Larsson 19.8k 1.6× 6.5k 1.2× 3.9k 1.9× 2.2k 1.4× 1.9k 1.4× 193 24.2k
Valério Carelli 12.4k 1.0× 3.4k 0.6× 1.2k 0.6× 1.7k 1.1× 668 0.5× 330 15.3k
Manuel Palacı́n 10.7k 0.8× 3.2k 0.6× 3.6k 1.7× 1.3k 0.9× 1.5k 1.1× 255 17.1k
S. DiMauro 12.7k 1.0× 8.0k 1.5× 1.5k 0.7× 1.8k 1.1× 565 0.4× 237 15.9k
Eric A. Schon 19.7k 1.6× 8.9k 1.7× 3.1k 1.5× 2.8k 1.8× 1.4k 1.1× 221 23.5k
Hiromi Sesaki 9.9k 0.8× 2.1k 0.4× 2.1k 1.0× 1.0k 0.7× 2.1k 1.6× 156 13.2k
Hugo W. Moser 11.0k 0.9× 4.4k 0.8× 4.0k 1.9× 621 0.4× 545 0.4× 275 14.4k

Countries citing papers authored by Anu Suomalainen

Since Specialization
Citations

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

Fields of papers citing papers by Anu Suomalainen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anu Suomalainen

This figure shows the co-authorship network connecting the top 25 collaborators of Anu Suomalainen. A scholar is included among the top collaborators of Anu Suomalainen 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 Anu Suomalainen. Anu Suomalainen 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.
Vasilescu, Catalina, Tiina Ojala, Tuula Manninen, et al.. (2024). Recessive TMOD1 mutation causes childhood cardiomyopathy. Communications Biology. 7(1). 7–7. 3 indexed citations
2.
Kang, Yilin, Jussi Hepojoki, Takayuki Mito, et al.. (2024). Ancestral allele of DNA polymerase gamma modifies antiviral tolerance. Nature. 628(8009). 844–853. 11 indexed citations
3.
Brilhante, Virginia, et al.. (2023). Genetic etiology of progressive pediatric neurological disorders. Pediatric Research. 95(1). 102–111. 5 indexed citations
4.
Dollet, Lucile, Steffen H. Raun, Lisbeth L. V. Møller, et al.. (2023). TNIK is a conserved regulator of glucose and lipid metabolism in obesity. Science Advances. 9(32). 15 indexed citations
5.
Pirnes-Karhu, Sini, et al.. (2023). Alternative oxidase causes cell type- and tissue-specific responses in mutator mice. Life Science Alliance. 6(11). e202302036–e202302036. 4 indexed citations
6.
Vihinen, Helena, Joni Nikkanen, Alexander Kononov, et al.. (2022). Mitochondrial dysfunction compromises ciliary homeostasis in astrocytes. The Journal of Cell Biology. 222(1). 30 indexed citations
7.
Chakrabarti, Rajarshi, et al.. (2022). Mitochondrial dysfunction triggers actin polymerization necessary for rapid glycolytic activation. The Journal of Cell Biology. 221(11). 20 indexed citations
8.
Korkalo, Liisa, Riitta Freese, Essi Skaffari, et al.. (2021). Vegan diet in young children remodels metabolism and challenges the statuses of essential nutrients. EMBO Molecular Medicine. 13(2). e13492–e13492. 65 indexed citations
9.
Hytönen, Marjo K., Christopher B. Jackson, Pernilla Syrjä, et al.. (2021). In-frame deletion in canine PITRM1 is associated with a severe early-onset epilepsy, mitochondrial dysfunction and neurodegeneration. Human Genetics. 140(11). 1593–1609. 11 indexed citations
10.
Nikkanen, Joni, et al.. (2020). Mitochondrial spongiotic brain disease: astrocytic stress and harmful rapamycin and ketosis effect. Life Science Alliance. 3(9). e202000797–e202000797. 15 indexed citations
11.
Richter, Uwe, Fumi Suomi, Paula Marttinen, et al.. (2019). Mitochondrial stress response triggered by defects in protein synthesis quality control. Life Science Alliance. 2(1). e201800219–e201800219. 33 indexed citations
12.
Wang, Liya, et al.. (2018). Quantitative solid-phase assay to measure deoxynucleoside triphosphate pools. Biology Methods and Protocols. 3(1). bpy011–bpy011. 3 indexed citations
13.
Jackson, Christopher B., Martina Huemer, Franck Martin, et al.. (2018). A variant inMRPS14(uS14m) causes perinatal hypertrophic cardiomyopathy with neonatal lactic acidosis, growth retardation, dysmorphic features and neurological involvement. Human Molecular Genetics. 28(4). 639–649. 33 indexed citations
14.
Trokovic, Ras, Jere Weltner, Tuula Manninen, et al.. (2012). Small Molecule Inhibitors Promote Efficient Generation of Induced Pluripotent Stem Cells From Human Skeletal Myoblasts. Stem Cells and Development. 22(1). 114–123. 34 indexed citations
15.
Nunnari, Jodi & Anu Suomalainen. (2012). Mitochondria: In Sickness and in Health. Cell. 148(6). 1145–1159. 2573 indexed citations breakdown →
16.
Sulonen, Anna-Maija, Pekka Ellonen, Henrikki Almusa, et al.. (2011). Comparison of solution-based exome capture methods for next generation sequencing. STM:n Hallinnonalan avoin julkaisuarkisto (Julkari). 1 indexed citations
17.
Pietiläinen, Kirsi H., Jussi Naukkarinen, Aila Rissanen, et al.. (2008). Global Transcript Profiles of Fat in Monozygotic Twins Discordant for BMI: Pathways behind Acquired Obesity. PLoS Medicine. 5(3). e51–e51. 230 indexed citations
18.
Inoue, Takahiro, Tomomi Ide, Henna Tyynismaa, et al.. (2008). Abstract 1370: Overexpression of Mitochondria DNA Helicase, Twinkle, Ameliorates Cardiac Remodeling and Failure in Mice. Circulation. 118.
19.
Hakonen, Anna H., Pirjo Isohanni, Anders Paetau, et al.. (2007). Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion. Brain. 130(11). 3032–3040. 145 indexed citations
20.
Suomalainen, Anu, Anna Majander, Matti Haltia, et al.. (1992). Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia.. Journal of Clinical Investigation. 90(1). 61–66. 191 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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