Sari Tuupanen

4.1k total citations
33 papers, 756 citations indexed

About

Sari Tuupanen is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Sari Tuupanen has authored 33 papers receiving a total of 756 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 15 papers in Pathology and Forensic Medicine and 10 papers in Genetics. Recurrent topics in Sari Tuupanen's work include Genetic factors in colorectal cancer (14 papers), Retinal Development and Disorders (6 papers) and Cancer Genomics and Diagnostics (6 papers). Sari Tuupanen is often cited by papers focused on Genetic factors in colorectal cancer (14 papers), Retinal Development and Disorders (6 papers) and Cancer Genomics and Diagnostics (6 papers). Sari Tuupanen collaborates with scholars based in Finland, United States and Sweden. Sari Tuupanen's co-authors include Lauri A. Aaltonen, Heikki Järvinen, Jukka‐Pekka Mecklin, Jussi Taipale, Auli Karhu, Henna Tyynismaa, Tiina Alitalo, Terho Latvala, Timo Tervo and Riku Katainen and has published in prestigious journals such as Bioinformatics, Gastroenterology and Cancer Research.

In The Last Decade

Sari Tuupanen

31 papers receiving 750 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sari Tuupanen Finland 16 361 265 164 157 147 33 756
Christopher W. Jenkins United Kingdom 5 269 0.7× 92 0.3× 282 1.7× 54 0.3× 48 0.3× 11 657
Sandra Angèle France 14 641 1.8× 154 0.6× 312 1.9× 307 2.0× 186 1.3× 17 834
Zaletaev Dv Russia 12 435 1.2× 53 0.2× 154 0.9× 201 1.3× 86 0.6× 93 674
Dagmar Arnold United States 8 403 1.1× 32 0.1× 141 0.9× 91 0.6× 46 0.3× 11 630
Yong Sam Shin South Korea 12 278 0.8× 99 0.4× 106 0.6× 69 0.4× 60 0.4× 18 501
Kimihiro Tanaka Japan 12 228 0.6× 57 0.2× 211 1.3× 154 1.0× 73 0.5× 51 530
Germaine Caldwell United Kingdom 11 779 2.2× 95 0.4× 82 0.5× 105 0.7× 310 2.1× 14 884
S. Gururangan United States 12 214 0.6× 101 0.4× 86 0.5× 54 0.3× 18 0.1× 29 537
SV Hodgson United Kingdom 13 233 0.6× 164 0.6× 225 1.4× 128 0.8× 177 1.2× 21 550

Countries citing papers authored by Sari Tuupanen

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

20 of 20 papers shown
1.
Tuupanen, Sari, et al.. (2022). A novel frameshift variant inCEP78associated with nonsyndromic retinitis pigmentosa, and a review ofCEP78-related phenotypes. Ophthalmic Genetics. 43(2). 152–158. 2 indexed citations
2.
Tuominen, Hannu, et al.. (2020). X-linked myotubular myopathy mimics hereditary spastic paraplegia in two female manifesting carriers of pathogenic MTM1 variant. European Journal of Medical Genetics. 63(11). 104040–104040. 3 indexed citations
3.
Helle, Emmi, Jaana Pihkala, Riitta Turunen, et al.. (2020). Rare Variants in Genes Associated With Cardiomyopathy Are Not Common in Hypoplastic Left Heart Syndrome Patients With Myocardial Dysfunction. Frontiers in Pediatrics. 8. 596840–596840. 2 indexed citations
4.
Mendelsohn, Bryce A., Klaus Mayer, Amit Malhotra, et al.. (2020). Diphthamide-deficiency syndrome: a novel human developmental disorder and ribosomopathy. European Journal of Human Genetics. 28(11). 1497–1508. 21 indexed citations
5.
Kämpjärvi, Kati, Miika Mehine, Johanna Känsäkoski, et al.. (2019). A whole exome sequencing-based panel assay with boosted clinical content generates a high diagnostic yield in patients with inherited eye diseases. Investigative Ophthalmology & Visual Science. 60(9). 421–421. 1 indexed citations
6.
Alastalo, Tero‐Pekka, Kati Kämpjärvi, Lucia Guidugli, et al.. (2019). Prevalence and genetic characteristics of RPE65-associated retinal disease. Investigative Ophthalmology & Visual Science. 60(9). 400–400. 3 indexed citations
7.
Duncan, Jacque L., Karmen M Trzupek, Sari Tuupanen, et al.. (2019). Multiple copies of rhodopsin as a novel cause of autosomal dominant retinitis pigmentosa. Investigative Ophthalmology & Visual Science. 60(9). 2943–2943. 1 indexed citations
8.
Kondelin, Johanna, Alexandra E. Gylfe, Tomas Tanskanen, et al.. (2017). Comprehensive Evaluation of Protein Coding Mononucleotide Microsatellites in Microsatellite-Unstable Colorectal Cancer. Cancer Research. 77(15). 4078–4088. 14 indexed citations
9.
Kondelin, Johanna, Sari Tuupanen, Alexandra E. Gylfe, et al.. (2015). 3′-UTR poly(T/U) repeat of EWSR1 is altered in microsatellite unstable colorectal cancer with nearly perfect sensitivity. Familial Cancer. 14(3). 449–453. 2 indexed citations
10.
Mehine, Miika, Hanna-Riikka Heinonen, Nanna Sarvilinna, et al.. (2015). Clonally related uterine leiomyomas are common and display branched tumor evolution. Human Molecular Genetics. 24(15). 4407–4416. 17 indexed citations
11.
Tanskanen, Tomas, Alexandra E. Gylfe, Riku Katainen, et al.. (2014). Systematic search for rare variants in Finnish early-onset colorectal cancer patients. Cancer Genetics. 208(1-2). 35–40. 22 indexed citations
12.
Tuupanen, Sari, Ulrika A. Hänninen, Johanna Kondelin, et al.. (2014). Identification of 33 candidate oncogenes by screening for base-specific mutations. British Journal of Cancer. 111(8). 1657–1662. 31 indexed citations
13.
Gylfe, Alexandra E., Sari Tuupanen, Ulrika A. Hänninen, et al.. (2014). Abstract 5193: Novel candidate oncogenes with mutation hot spots in microsatellite unstable colorectal cancer. Cancer Research. 74(19_Supplement). 5193–5193. 1 indexed citations
14.
Gylfe, Alexandra E., Riku Katainen, Johanna Kondelin, et al.. (2013). Eleven Candidate Susceptibility Genes for Common Familial Colorectal Cancer. PLoS Genetics. 9(10). e1003876–e1003876. 60 indexed citations
15.
Lehtonen, Heli, Taina Sipponen, Sari Tojkander, et al.. (2012). Segregation of a Missense Variant in Enteric Smooth Muscle Actin γ-2 With Autosomal Dominant Familial Visceral Myopathy. Gastroenterology. 143(6). 1482–1491.e3. 65 indexed citations
16.
Coissieux, Marie‐May, Jerneja Tomšič, Marie Castets, et al.. (2011). Variants in the Netrin-1 Receptor UNC5C Prevent Apoptosis and Increase Risk of Familial Colorectal Cancer. Gastroenterology. 141(6). 2039–2046. 28 indexed citations
17.
Niittymäki, Iina, Eevi Kaasinen, Sari Tuupanen, et al.. (2010). Low-Penetrance Susceptibility Variants in Familial Colorectal Cancer. Cancer Epidemiology Biomarkers & Prevention. 19(6). 1478–1483. 19 indexed citations
18.
Heliövaara, Elina, Sari Tuupanen, Shirley Hodgson, et al.. (2010). No evidence of RET germline mutations in familial pituitary adenoma. Journal of Molecular Endocrinology. 46(1). 1–8. 9 indexed citations
19.
Tuupanen, Sari, Auli Karhu, Heikki Järvinen, et al.. (2006). No evidence for dual role of loss of heterozygosity in hereditary non-polyposis colorectal cancer. Oncogene. 26(17). 2513–2517. 15 indexed citations
20.
Tyynismaa, Henna, Pertti Sistonen, Sari Tuupanen, et al.. (2002). A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families.. PubMed. 43(10). 3160–4. 112 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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