Maria Rantamäki
- Molecular Biology
- Clinical Biochemistry top 1%
- Cellular and Molecular Neuroscience top 10%
- Genetics
- Neurology
- Co-authors
- Bjarne UddSeppo KaakkolaAnu SuomalainenPetri LuomaPeter HackmanAnders PaetauRalf KraheKari Majamaa
- Topics
- Mitochondrial Function and Pathology (8 papers)Genetic Neurodegenerative Diseases (7 papers)Metabolism and Genetic Disorders (3 papers)
- Partner nations
- FinlandBelgiumUnited States
In The Last Decade
Maria Rantamäki
9 papers receiving 562 citations
Peers
Comparison fields: 5 of 38
- Molecular Biology 512
- Clinical Biochemistry 294
- Cellular and Molecular Neuroscience 238
- Genetics 62
- Neurology 60
Countries citing papers authored by Maria Rantamäki
This map shows the geographic impact of Maria Rantamäki'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 Maria Rantamäki with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maria Rantamäki more than expected).
Fields of papers citing papers by Maria Rantamäki
This network shows the impact of papers produced by Maria Rantamäki. 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 Maria Rantamäki. The network helps show where Maria Rantamäki may publish in the future.
Co-authorship network of co-authors of Maria Rantamäki
This figure shows the co-authorship network connecting the top 25 collaborators of Maria Rantamäki. A scholar is included among the top collaborators of Maria Rantamäki 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 Maria Rantamäki. Maria Rantamäki is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | [Mitochondrial recessive ataxia syndrome (MIRAS) and valproate toxicity]. | 11 |
| 2 | Mitokondriaalinen resessiivinen ataksiasyndrooma ja valproaattihoidon toksisuus | 9 |
| 3 | 8 | |
| 4 | 31 | |
| 5 | 227 | |
| 6 | 205 | |
| 7 | 31 | |
| 8 | 56 | |
| 9 | 3 |
About Maria Rantamäki
Maria Rantamäki is a scholar working on Clinical Biochemistry, Cellular and Molecular Neuroscience and Psychiatry and Mental health, having authored 9 papers that have together received 581 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (8 papers), Genetic Neurodegenerative Diseases (7 papers) and Metabolism and Genetic Disorders (3 papers). The work is most often cited by research in Clinical Biochemistry (294 citations), Cellular and Molecular Neuroscience (238 citations) and Molecular Biology (512 citations). Maria Rantamäki has collaborated with scholars based in Finland, Belgium and United States. Frequent co-authors include Bjarne Udd, Seppo Kaakkola, Anu Suomalainen, Petri Luoma, Peter Hackman, Anders Paetau, Ralf Krahe, Kari Majamaa, Vesa Juvonen and J.J. Martin. Their work appears in journals such as Neurology, Annals of Neurology and The American Journal of Human Genetics.
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.