H. Annika Siitonen

888 total citations
10 papers, 482 citations indexed

About

H. Annika Siitonen is a scholar working on Molecular Biology, Oncology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, H. Annika Siitonen has authored 10 papers receiving a total of 482 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 2 papers in Oncology and 2 papers in Public Health, Environmental and Occupational Health. Recurrent topics in H. Annika Siitonen's work include DNA Repair Mechanisms (4 papers), RNA modifications and cancer (2 papers) and Acute Lymphoblastic Leukemia research (2 papers). H. Annika Siitonen is often cited by papers focused on DNA Repair Mechanisms (4 papers), RNA modifications and cancer (2 papers) and Acute Lymphoblastic Leukemia research (2 papers). H. Annika Siitonen collaborates with scholars based in Finland, Sweden and Hungary. H. Annika Siitonen's co-authors include Marjo Kestilä, Valérie Delague, Ethylin Wang Jabs, Y. Gillerot, Outi Elomaa, Nadine Jalkh, Alain Verloès, Juha Kere, Mari Tervaniemi and LL Wang and has published in prestigious journals such as PLoS ONE, Scientific Reports and Human Molecular Genetics.

In The Last Decade

H. Annika Siitonen

10 papers receiving 473 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H. Annika Siitonen Finland 9 357 98 91 79 79 10 482
Mariana Boroni Brazil 15 340 1.0× 95 1.0× 75 0.8× 28 0.4× 93 1.2× 29 545
Masahiko Mori Japan 12 403 1.1× 89 0.9× 123 1.4× 70 0.9× 65 0.8× 22 529
Mahalakshmi Nair United States 6 261 0.7× 45 0.5× 50 0.5× 66 0.8× 22 0.3× 7 374
Parirokh Awasthi United States 11 307 0.9× 36 0.4× 51 0.6× 77 1.0× 129 1.6× 18 483
Zhongcheng Zhou China 12 350 1.0× 73 0.7× 63 0.7× 40 0.5× 46 0.6× 39 482
Misuzu Ueki Japan 13 307 0.9× 45 0.5× 34 0.4× 118 1.5× 150 1.9× 57 522
Hisayo Nishida‐Fukuda Japan 12 285 0.8× 15 0.2× 116 1.3× 77 1.0× 49 0.6× 18 444
Julia W. Skinner United Kingdom 9 315 0.9× 51 0.5× 88 1.0× 34 0.4× 44 0.6× 9 551
Kyoko Maruyama Japan 9 193 0.5× 47 0.5× 25 0.3× 55 0.7× 71 0.9× 10 405

Countries citing papers authored by H. Annika Siitonen

Since Specialization
Citations

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

Fields of papers citing papers by H. Annika Siitonen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by H. Annika Siitonen. 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 H. Annika Siitonen. The network helps show where H. Annika Siitonen may publish in the future.

Co-authorship network of co-authors of H. Annika Siitonen

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

All Works

10 of 10 papers shown
1.
Siitonen, H. Annika, Johanna Joensuu, Hanna Savolainen‐Peltonen, et al.. (2025). Update of the impact of menopausal hormone therapy on breast cancer risk. European Journal of Cancer. 220. 115340–115340. 3 indexed citations
2.
Tervaniemi, Mari, Shintaro Katayama, Tiina Skoog, et al.. (2018). Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes. BMC Genomics. 19(1). 432–432. 13 indexed citations
3.
Tervaniemi, Mari, Shintaro Katayama, Tiina Skoog, et al.. (2016). NOD-like receptor signaling and inflammasome-related pathways are highlighted in psoriatic epidermis. Scientific Reports. 6(1). 22745–22745. 75 indexed citations
4.
Katayama, Shintaro, Tiina Skoog, Eeva‐Mari Jouhilahti, et al.. (2015). Gene expression analysis of skin grafts and cultured keratinocytes using synthetic RNA normalization reveals insights into differentiation and growth control. BMC Genomics. 16(1). 476–476. 18 indexed citations
5.
Tervaniemi, Mari, H. Annika Siitonen, Cilla Söderhäll, et al.. (2012). Centrosomal Localization of the Psoriasis Candidate Gene Product, CCHCR1, Supports a Role in Cytoskeletal Organization. PLoS ONE. 7(11). e49920–e49920. 23 indexed citations
6.
Sznajer, Yves, H. Annika Siitonen, Gaia Roversi, et al.. (2007). Atypical Rothmund-Thomson syndrome in a patient with compound Heterozygous Mutations in RECQL4 Gene and phenotypic features in RECQL4 syndromes. European Journal of Pediatrics. 167(2). 175–181. 14 indexed citations
7.
Kellermayer, Richárd, H. Annika Siitonen, Kinga Hadzsiev, Marjo Kestilä, & György Kosztolányi. (2005). A Patient With Rothmund-Thomson Syndrome and All Features of RAPADILINO. Archives of Dermatology. 141(5). 617–20. 15 indexed citations
8.
Maldergem, Lionel Van, H. Annika Siitonen, Nadine Jalkh, et al.. (2005). Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene. Journal of Medical Genetics. 43(2). 148–152. 162 indexed citations
9.
Haravuori, Henna, H. Annika Siitonen, I. Mahjneh, et al.. (2004). Linkage to two separate loci in a family with a novel distal myopathy phenotype (MPD3). Neuromuscular Disorders. 14(3). 183–187. 10 indexed citations
10.
Siitonen, H. Annika. (2003). Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases. Human Molecular Genetics. 12(21). 2837–2844. 149 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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