Anitta Tamminen

1.5k citations
13 papers · 1.1k indexed · h-index 12
Topics
BRCA gene mutations in cancer (9 papers)DNA Repair Mechanisms (6 papers)Cancer-related Molecular Pathways (4 papers)
Partner nations
FinlandSwedenDenmark

In The Last Decade

Anitta Tamminen

13 papers receiving 1.0k citations

Peers

Anitta Tamminen
Comparison fields: 5 of 50
  • Molecular Biology 648
  • Genetics 633
  • Oncology 406
  • Cancer Research 314
  • Pathology and Forensic Medicine 267
Replace Aðalgeir Arason with:
Aðalgeir Arason Iceland
Hannaleena Eerola Finland
Tone Ikdahl Andersen Norway
Sharon N. Teraoka United States
Jón Þór Bergþorsson Iceland
Dominika Wokołorczyk Poland
Munaza Ahmed United Kingdom
Tasnim Chagtai United Kingdom
Beate Betz Germany
Manuela Pinheiro Portugal
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Citations per field
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Citations per year

Countries citing papers authored by Anitta Tamminen

Since Specialization
Citations

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

Fields of papers citing papers by Anitta Tamminen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anitta Tamminen

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

All Works

13 of 13 papers shown
#WorkIndexed citations
1 98
2 22
3 6
4 126
5 24
6 30
7 50
8 47
9 74
10 346
11 46
12 85
13
p53, CHK2, and CHK1 genes in Finnish families with Li-Fraumeni syndrome: further evidence of CHK2 in inherited cancer predisposition.
130

About Anitta Tamminen

Anitta Tamminen is a scholar working on Reproductive Medicine, Genetics and Pathology and Forensic Medicine, having authored 13 papers that have together received 1.1k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (9 papers), DNA Repair Mechanisms (6 papers) and Cancer-related Molecular Pathways (4 papers). The work is most often cited by research in Genetics (633 citations), Cancer Research (314 citations) and Oncology (406 citations). Anitta Tamminen has collaborated with scholars based in Finland, Sweden and Denmark. Frequent co-authors include Heli Nevanlinna, Carl Blomqvist, Hannaleena Eerola, Kristiina Aittomäki, Pia Vahteristo, Päivi Heikkilä, Jiřina Bártková, Jiří Bártek, Outi Kilpivaara and Kirsimari Aaltonen. Their work appears in journals such as The American Journal of Human Genetics, British Journal of Cancer and International Journal of Cancer.

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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