Sanna Marjavaara

933 total citations
10 papers, 382 citations indexed

About

Sanna Marjavaara is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Sanna Marjavaara has authored 10 papers receiving a total of 382 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Sanna Marjavaara's work include Mitochondrial Function and Pathology (10 papers), Metabolism and Genetic Disorders (5 papers) and RNA modifications and cancer (3 papers). Sanna Marjavaara is often cited by papers focused on Mitochondrial Function and Pathology (10 papers), Metabolism and Genetic Disorders (5 papers) and RNA modifications and cancer (3 papers). Sanna Marjavaara collaborates with scholars based in Finland, Sweden and United Kingdom. Sanna Marjavaara's co-authors include Anu Suomalainen, Anders Paetau, Pirjo Isohanni, Tuula Lönnqvist, Leena Valanne, Helena Pihko, Milla Lampinen, Keijo Mattila, Anna H. Hakonen and Johannes N. Spelbrink and has published in prestigious journals such as Brain, Biochemical and Biophysical Research Communications and Human Molecular Genetics.

In The Last Decade

Sanna Marjavaara

10 papers receiving 378 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sanna Marjavaara Finland 10 337 149 47 42 24 10 382
Nancy G. Slate United States 5 258 0.8× 126 0.8× 20 0.4× 35 0.8× 19 0.8× 5 301
Magalie Barth France 12 274 0.8× 171 1.1× 25 0.5× 92 2.2× 29 1.2× 32 378
Jack J. Collier United Kingdom 5 248 0.7× 93 0.6× 30 0.6× 37 0.9× 23 1.0× 6 344
Jorge Asin-Cayuela Sweden 11 669 2.0× 157 1.1× 28 0.6× 77 1.8× 27 1.1× 16 764
Malavika Hebbar India 9 207 0.6× 39 0.3× 28 0.6× 67 1.6× 22 0.9× 19 290
Matteo Granatiero Italy 6 420 1.2× 206 1.4× 34 0.7× 111 2.6× 31 1.3× 8 541
Tim M. Strom Germany 3 224 0.7× 89 0.6× 33 0.7× 21 0.5× 45 1.9× 3 293
Osamu Hashizume Japan 11 295 0.9× 75 0.5× 15 0.3× 32 0.8× 24 1.0× 17 364
Nastassja Himmelreich Germany 11 244 0.7× 211 1.4× 33 0.7× 70 1.7× 36 1.5× 25 365
Maja Di Rocco Italy 12 212 0.6× 122 0.8× 32 0.7× 131 3.1× 71 3.0× 20 459

Countries citing papers authored by Sanna Marjavaara

Since Specialization
Citations

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

Fields of papers citing papers by Sanna Marjavaara

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sanna Marjavaara

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

All Works

10 of 10 papers shown
1.
Davoudi, Mina, Jukka Kallijärvi, Sanna Marjavaara, et al.. (2014). A mouse model of mitochondrial complex III dysfunction induced by myxothiazol. Biochemical and Biophysical Research Communications. 446(4). 1079–1084. 9 indexed citations
2.
Götz, Alexandra, Pirjo Isohanni, Jaana Rummukainen, et al.. (2012). Fatal neonatal lactic acidosis caused by a novel de novo mitochondrial G7453A tRNA-Serine (UCN) mutation. Pediatric Research. 72(1). 90–94. 12 indexed citations
3.
Marjavaara, Sanna, et al.. (2010). Effects on mitochondrial transcription of manipulating mTERF protein levels in cultured human HEK293 cells. BMC Molecular Biology. 11(1). 72–72. 15 indexed citations
4.
Kotarsky, Heike, Riitta Karikoski, Matthias Mörgelin, et al.. (2010). Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation. Mitochondrion. 10(5). 497–509. 30 indexed citations
5.
Isohanni, Pirjo, Tarja Linnankivi, Jana Buzková, et al.. (2009). DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis. Journal of Medical Genetics. 47(1). 66–70. 48 indexed citations
6.
Lyly, Annina, Sanna Marjavaara, Aija Kyttälä, et al.. (2008). Deficiency of the INCL protein Ppt1 results in changes in ectopic F1-ATP synthase and altered cholesterol metabolism. Human Molecular Genetics. 17(10). 1406–1417. 53 indexed citations
7.
Götz, Alexandra, Pirjo Isohanni, Helena Pihko, et al.. (2008). Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome. Brain. 131(11). 2841–2850. 61 indexed citations
8.
Pérez-Martı́nez, Xochitl, et al.. (2008). Protein Synthesis and Assembly in Mitochondrial Disorders. Current Topics in Medicinal Chemistry. 8(15). 1335–1350. 29 indexed citations
9.
Hakonen, Anna H., Steffi Goffart, Sanna Marjavaara, et al.. (2008). Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion. Human Molecular Genetics. 17(23). 3822–3835. 94 indexed citations
10.
Kirino, Yohei, Takehiro Yasukawa, Sanna Marjavaara, et al.. (2006). Acquisition of the wobble modification in mitochondrial tRNALeu(CUN) bearing the G12300A mutation suppresses the MELAS molecular defect. Human Molecular Genetics. 15(6). 897–904. 31 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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