Sonja Lagström

2.9k total citations
22 papers, 791 citations indexed

About

Sonja Lagström is a scholar working on Molecular Biology, Immunology and Epidemiology. According to data from OpenAlex, Sonja Lagström has authored 22 papers receiving a total of 791 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Immunology and 6 papers in Epidemiology. Recurrent topics in Sonja Lagström's work include Cervical Cancer and HPV Research (6 papers), Chronic Lymphocytic Leukemia Research (4 papers) and Molecular Biology Techniques and Applications (4 papers). Sonja Lagström is often cited by papers focused on Cervical Cancer and HPV Research (6 papers), Chronic Lymphocytic Leukemia Research (4 papers) and Molecular Biology Techniques and Applications (4 papers). Sonja Lagström collaborates with scholars based in Finland, Norway and United States. Sonja Lagström's co-authors include Pekka Ellonen, Satu Mustjoki, Trine B. Rounge, Emma Andersson, Kimmo Porkka, Hanna Rajala, Samuli Eldfors, Michael J. Clemente, Sakari Knuutila and Virinder Kaur Sarhadi and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and Blood.

In The Last Decade

Sonja Lagström

22 papers receiving 774 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sonja Lagström Finland 13 274 262 226 187 162 22 791
Shafinaz Hussein United States 9 489 1.8× 428 1.6× 347 1.5× 158 0.8× 419 2.6× 31 1.1k
Roberta Guglielmino Italy 13 316 1.2× 178 0.7× 166 0.7× 108 0.6× 174 1.1× 23 687
Sven Kracker France 22 858 3.1× 375 1.4× 155 0.7× 212 1.1× 282 1.7× 40 1.3k
Jamie P. Nourse Australia 16 286 1.0× 274 1.0× 334 1.5× 68 0.4× 479 3.0× 36 959
Masakatsu Hishizawa Japan 20 758 2.8× 413 1.6× 294 1.3× 138 0.7× 542 3.3× 70 1.6k
Kandasamy Hariharan United States 17 467 1.7× 286 1.1× 353 1.6× 253 1.4× 292 1.8× 36 1.1k
Naotaka Shibagaki Japan 16 372 1.4× 362 1.4× 103 0.5× 44 0.2× 278 1.7× 42 920
Likun Du Sweden 21 495 1.8× 524 2.0× 63 0.3× 58 0.3× 227 1.4× 35 1.0k
Pauline Crooks Australia 18 389 1.4× 128 0.5× 350 1.5× 95 0.5× 578 3.6× 37 950
Juliane S. Walz Germany 16 453 1.7× 349 1.3× 67 0.3× 67 0.4× 385 2.4× 70 923

Countries citing papers authored by Sonja Lagström

Since Specialization
Citations

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

Fields of papers citing papers by Sonja Lagström

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sonja Lagström

This figure shows the co-authorship network connecting the top 25 collaborators of Sonja Lagström. A scholar is included among the top collaborators of Sonja Lagström 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 Sonja Lagström. Sonja Lagström 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.
Lagström, Sonja, Ewoud Ewing, Klementy Shchetynsky, et al.. (2023). Simultaneous detection of DNA variation and methylation at HLA class II locus and immune gene promoters using targeted SureSelect Methyl-Sequencing. Frontiers in Immunology. 14. 1251772–1251772. 2 indexed citations
2.
Lagström, Sonja, et al.. (2022). Differences in integration frequencies and APOBEC3 profiles of five high-risk HPV types adheres to phylogeny. SHILAP Revista de lepidopterología. 14. 200247–200247. 7 indexed citations
3.
Lagström, Sonja, Sinan U. Umu, Ole Herman Ambur, et al.. (2021). HPV16 and HPV18 type-specific APOBEC3 and integration profiles in different diagnostic categories of cervical samples. SHILAP Revista de lepidopterología. 12. 200221–200221. 17 indexed citations
4.
Mandishora, Racheal S. Dube, Trine B. Rounge, Megan B. Fitzpatrick, et al.. (2021). Self-collected and clinician-collected anal swabs show modest agreement for HPV genotyping. PLoS ONE. 16(4). e0250426–e0250426. 10 indexed citations
5.
Lagström, Sonja, Sinan U. Umu, Maija Lepistö, et al.. (2019). TaME-seq: An efficient sequencing approach for characterisation of HPV genomic variability and chromosomal integration. Scientific Reports. 9(1). 524–524. 23 indexed citations
6.
Lagström, Sonja, et al.. (2019). HPV16 whole genome minority variants in persistent infections from young Dutch women. Journal of Clinical Virology. 119. 24–30. 9 indexed citations
7.
Raju, Sajan C., Sonja Lagström, Pekka Ellonen, et al.. (2019). Gender-Specific Associations Between Saliva Microbiota and Body Size. Frontiers in Microbiology. 10. 767–767. 55 indexed citations
8.
Keskitalo, Salla, Emma Haapaniemi, Elísabet Einarsdóttir, et al.. (2019). Novel TMEM173 Mutation and the Role of Disease Modifying Alleles. Frontiers in Immunology. 10. 2770–2770. 43 indexed citations
9.
Mandishora, Racheal S. Dube, Sonja Lagström, Babill Stray‐Pedersen, et al.. (2018). Intra-host sequence variability in human papillomavirus. Papillomavirus Research. 5. 180–191. 27 indexed citations
10.
Raju, Sajan C., Sonja Lagström, Pekka Ellonen, et al.. (2018). Reproducibility and repeatability of six high-throughput 16S rDNA sequencing protocols for microbiota profiling. Journal of Microbiological Methods. 147. 76–86. 24 indexed citations
11.
Savola, Paula, Tiina Kelkka, Hanna Rajala, et al.. (2017). Somatic mutations in clonally expanded cytotoxic T lymphocytes in patients with newly diagnosed rheumatoid arthritis. Nature Communications. 8(1). 15869–15869. 78 indexed citations
12.
Kontro, Mika, Henrik Edgren, Pekka Ellonen, et al.. (2016). Monitoring therapy responses at the leukemic subclone level by ultra-deep amplicon resequencing in acute myeloid leukemia. Leukemia. 31(5). 1048–1058. 6 indexed citations
13.
Kontro, Mika, Henrik Edgren, Pekka Ellonen, et al.. (2016). Abstract 2378: Responses of AML patients to tailored drug regimens: monitoring cancer subclones by ultra-deep resequencing. Cancer Research. 76(14_Supplement). 2378–2378. 2 indexed citations
14.
Sarhadi, Virinder Kaur, Aija Knuuttila, Ilari Scheinin, et al.. (2015). Driver Gene and Novel Mutations in Asbestos-Exposed Lung Adenocarcinoma and Malignant Mesothelioma Detected by Exome Sequencing. Lung. 194(1). 125–135. 32 indexed citations
15.
Rajala, Hanna, Thomas L. Olson, Michael J. Clemente, et al.. (2014). The analysis of clonal diversity and therapy responses using STAT3 mutations as a molecular marker in large granular lymphocytic leukemia. Haematologica. 100(1). 91–99. 68 indexed citations
16.
17.
Rajala, Hanna, Samuli Eldfors, Heikki Kuusanmäki, et al.. (2013). Discovery of somatic STAT5b mutations in large granular lymphocytic leukemia. Blood. 121(22). 4541–4550. 195 indexed citations
18.
Kontro, Mika, Heikki Kuusanmäki, Samuli Eldfors, et al.. (2013). Novel Activating STAT5B Mutations As Drivers Of T-ALL. Blood. 122(21). 3863–3863. 2 indexed citations
19.
Rajala, Hanna, Samuli Eldfors, Heikki Kuusanmäki, et al.. (2012). Discovery of STAT5b Mutations and Small Subclones of STAT3 Mutations in Large Granular Lymphocytic (LGL) Leukemia. Blood. 120(21). 871–871. 3 indexed citations
20.
Pöyhönen, Minna, Aarno Palotie, Pekka Ellonen, et al.. (2012). A balanced translocation truncates Neurotrimin in a family with intracranial and thoracic aortic aneurysm. Journal of Medical Genetics. 49(10). 621–629. 29 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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