Sari Tuupanen
- Co-authors
- Lauri A. AaltonenHeikki JärvinenJukka‐Pekka MecklinJussi TaipaleTimo TervoTerho LatvalaHenna TyynismaaAuli Karhu
- Topics
- Genetic factors in colorectal cancer (14 papers)Retinal Development and Disorders (6 papers)Cancer Genomics and Diagnostics (6 papers)
- Partner nations
- FinlandUnited StatesSweden
In The Last Decade
Sari Tuupanen
31 papers receiving 750 citations
Peers
Comparison fields: 5 of 66
- Molecular Biology 361
- Pathology and Forensic Medicine 265
- Oncology 164
- Cancer Research 157
- Genetics 147
Countries citing papers authored by Sari Tuupanen
This map shows the geographic impact of Sari Tuupanen'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 Sari Tuupanen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sari Tuupanen more than expected).
Fields of papers citing papers by Sari Tuupanen
This network shows the impact of papers produced by Sari Tuupanen. 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 Sari Tuupanen. The network helps show where Sari Tuupanen may publish in the future.
Co-authorship network of co-authors of Sari Tuupanen
This figure shows the co-authorship network connecting the top 25 collaborators of Sari Tuupanen. A scholar is included among the top collaborators of Sari Tuupanen 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 Sari Tuupanen. Sari Tuupanen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 21 | |
| 3 | 2 | |
| 4 | Multiple copies of rhodopsin as a novel cause of autosomal dominant retinitis pigmentosa | 1 |
| 5 | Prevalence and genetic characteristics of RPE65-associated retinal disease | 3 |
| 6 | A whole exome sequencing-based panel assay with boosted clinical content generates a high diagnostic yield in patients with inherited eye diseases | 1 |
| 7 | 14 | |
| 8 | 2 | |
| 9 | 17 | |
| 10 | 22 | |
| 11 | 31 | |
| 12 | 60 | |
| 13 | 13 | |
| 14 | 65 | |
| 15 | 28 | |
| 16 | 19 | |
| 17 | 9 | |
| 18 | 57 | |
| 19 | 15 | |
| 20 | A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families. | 112 |
About Sari Tuupanen
Sari Tuupanen is a scholar working on Pathology and Forensic Medicine, Ophthalmology and Cancer Research, having authored 33 papers that have together received 756 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (14 papers), Retinal Development and Disorders (6 papers) and Cancer Genomics and Diagnostics (6 papers). The work is most often cited by research in Pathology and Forensic Medicine (265 citations), Cancer Research (157 citations) and Ophthalmology (64 citations). Sari Tuupanen has collaborated with scholars based in Finland, United States and Sweden. Frequent co-authors include Lauri A. Aaltonen, Heikki Järvinen, Jukka‐Pekka Mecklin, Jussi Taipale, Timo Tervo, Terho Latvala, Henna Tyynismaa, Auli Karhu, Riku Katainen and Tiina Alitalo. Their work appears in journals such as Bioinformatics, Gastroenterology and Cancer Research.
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.