Stina Roth

3.7k total citations · 1 hit paper
11 papers, 1.5k citations indexed

About

Stina Roth is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Cancer Research. According to data from OpenAlex, Stina Roth has authored 11 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Pathology and Forensic Medicine and 5 papers in Cancer Research. Recurrent topics in Stina Roth's work include Genetic factors in colorectal cancer (6 papers), Carcinogens and Genotoxicity Assessment (3 papers) and TGF-β signaling in diseases (3 papers). Stina Roth is often cited by papers focused on Genetic factors in colorectal cancer (6 papers), Carcinogens and Genotoxicity Assessment (3 papers) and TGF-β signaling in diseases (3 papers). Stina Roth collaborates with scholars based in Finland, United States and Sweden. Stina Roth's co-authors include Lauri A. Aaltonen, Pertti Sistonen, Heikki Järvinen, Steve Bevan, Edwin M. Stone, John C. Ringold, Frank A. Mitros, Richard S. Houlston, James R. Howe and Robert W. Summers and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and FEBS Letters.

In The Last Decade

Stina Roth

10 papers receiving 1.4k citations

Hit Papers

Mutations in the SMAD4/DPC4 Gene in Juvenile Polyposis 1998 2026 2007 2016 1998 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stina Roth Finland 8 847 601 507 412 304 11 1.5k
Ginesa García‐Rostán Spain 20 765 0.9× 328 0.5× 636 1.3× 147 0.4× 189 0.6× 27 1.9k
Ella Barclay United Kingdom 13 400 0.5× 408 0.7× 288 0.6× 200 0.5× 204 0.7× 18 800
Sara González Spain 18 1.2k 1.4× 865 1.4× 714 1.4× 162 0.4× 538 1.8× 47 1.9k
Sumiko Ohnami Japan 20 734 0.9× 221 0.4× 352 0.7× 211 0.5× 402 1.3× 54 1.3k
Hongying Zhang China 20 402 0.5× 209 0.3× 368 0.7× 751 1.8× 285 0.9× 83 1.3k
Reiko Ogawa Japan 19 380 0.4× 412 0.7× 428 0.8× 252 0.6× 345 1.1× 28 1.3k
Debra Saxe United States 20 578 0.7× 170 0.3× 300 0.6× 226 0.5× 106 0.3× 45 1.4k
Cristina Pons Spain 17 478 0.6× 257 0.4× 299 0.6× 109 0.3× 303 1.0× 24 1.2k
Fabiola Minoletti Italy 15 403 0.5× 360 0.6× 466 0.9× 832 2.0× 182 0.6× 22 1.4k
Masamichi Yasuno Japan 18 499 0.6× 416 0.7× 812 1.6× 230 0.6× 188 0.6× 65 1.4k

Countries citing papers authored by Stina Roth

Since Specialization
Citations

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

Fields of papers citing papers by Stina Roth

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stina Roth

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

All Works

11 of 11 papers shown
1.
Aaltonen, Lauri A., Stina Roth, & Charis Eng. (2003). Direct Sequencing for Cowden Syndrome Gene PTEN ( MMAC1) Mutations. PubMed. 50. 185–199.
2.
Aaltonen, Lauri A. & Stina Roth. (2003). Direct Sequencing for Juvenile Polyposis Gene SMAD4/DPC4 Mutations. PubMed. 50. 167–174. 1 indexed citations
3.
Zhang, Fan, et al.. (2002). Proteasomal activity modulates TGF‐ß signaling in a gene‐specific manner. FEBS Letters. 527(1-3). 58–62. 13 indexed citations
4.
Launonen, Virpi, Outi Vierimaa, Maija Kiuru, et al.. (2001). Inherited susceptibility to uterine leiomyomas and renal cell cancer. Proceedings of the National Academy of Sciences. 98(6). 3387–3392. 454 indexed citations
5.
Roth, Stina, Pertti Sistonen, Reijo Salovaara, et al.. (1999). SMAD genes in juvenile polyposis. Genes Chromosomes and Cancer. 26(1). 54–61. 60 indexed citations
6.
Avizienyte, Egle, Anu Loukola, Stina Roth, et al.. (1999). LKB1 Somatic Mutations in Sporadic Tumors. American Journal Of Pathology. 154(3). 677–681. 107 indexed citations
7.
Howe, James R., Stina Roth, John C. Ringold, et al.. (1998). Mutations in the SMAD4/DPC4 Gene in Juvenile Polyposis. Science. 280(5366). 1086–1088. 668 indexed citations breakdown →
8.
Avizienyte, Egle, Stina Roth, Anu Loukola, et al.. (1998). Somatic mutations in LKB1 are rare in sporadic colorectal and testicular tumors.. PubMed. 58(10). 2087–90. 92 indexed citations
9.
Roth, Stina, et al.. (1997). Molecular analysis of occupational cancer: infrequentp53 andras mutations in renal-cell cancer in workers exposed to gasoline. International Journal of Cancer. 73(4). 492–496. 4 indexed citations
11.
Norppa, Hannu, et al.. (1993). Micronucleus Assay in Lymphocytes as a Tool to Biomonitor Human Exposure to Aneuploidogens and Clastogens. Environmental Health Perspectives. 101. 139–139. 36 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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