Tiina Tyni
- Molecular Biology top 10%
- Clinical Biochemistry top 0.5%
- Physiology top 10%
- Pediatrics, Perinatology and Child Health top 10%
- Genetics
- Co-authors
- Helena PihkoTero KiveläAnu SuomalainenTiina OjalaAnders PaetauRiitta KarikoskiMatti K. SaloLeena Valanne
- Topics
- Metabolism and Genetic Disorders (24 papers)Mitochondrial Function and Pathology (12 papers)Neonatal Health and Biochemistry (6 papers)
- Partner nations
- FinlandUnited KingdomSweden
In The Last Decade
Tiina Tyni
34 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 68
- Molecular Biology 796
- Clinical Biochemistry 645
- Physiology 208
- Pediatrics, Perinatology and Child Health 158
- Genetics 130
Countries citing papers authored by Tiina Tyni
This map shows the geographic impact of Tiina Tyni'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 Tiina Tyni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tiina Tyni more than expected).
Fields of papers citing papers by Tiina Tyni
This network shows the impact of papers produced by Tiina Tyni. 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 Tiina Tyni. The network helps show where Tiina Tyni may publish in the future.
Co-authorship network of co-authors of Tiina Tyni
This figure shows the co-authorship network connecting the top 25 collaborators of Tiina Tyni. A scholar is included among the top collaborators of Tiina Tyni 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 Tiina Tyni. Tiina Tyni is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 6 | |
| 2 | 13 | |
| 3 | 100 | |
| 4 | 22 | |
| 5 | 12 | |
| 6 | 30 | |
| 7 | 15 | |
| 8 | 17 | |
| 9 | 8 | |
| 10 | 22 | |
| 11 | 47 | |
| 12 | 26 | |
| 13 | 59 | |
| 14 | 42 | |
| 15 | 65 | |
| 16 | Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation - A new type of hereditary metabolic chorioretinopathy | 1 |
| 17 | 71 | |
| 18 | 114 | |
| 19 | 110 | |
| 20 | 21 |
About Tiina Tyni
Tiina Tyni is a scholar working on Clinical Biochemistry, Rheumatology and Pediatrics, Perinatology and Child Health, having authored 34 papers that have together received 1.3k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (24 papers), Mitochondrial Function and Pathology (12 papers) and Neonatal Health and Biochemistry (6 papers). The work is most often cited by research in Clinical Biochemistry (645 citations), Molecular Biology (796 citations) and Ophthalmology (85 citations). Tiina Tyni has collaborated with scholars based in Finland, United Kingdom and Sweden. Frequent co-authors include Helena Pihko, Tero Kivelä, Anu Suomalainen, Tiina Ojala, Anders Paetau, Riitta Karikoski, Matti K. Salo, Leena Valanne, Anita Hiippala and Aarno Palotie. Their work appears in journals such as Journal of the American College of Cardiology, Neurology and Ophthalmology.
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.