Neeme Tõnisson

3.3k total citations
38 papers, 1.3k citations indexed

About

Neeme Tõnisson is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Neeme Tõnisson has authored 38 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 14 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Neeme Tõnisson's work include Gene expression and cancer classification (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and BRCA gene mutations in cancer (5 papers). Neeme Tõnisson is often cited by papers focused on Gene expression and cancer classification (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and BRCA gene mutations in cancer (5 papers). Neeme Tõnisson collaborates with scholars based in Estonia, Finland and United States. Neeme Tõnisson's co-authors include Andres Metspalu, Ants Kurg, Raivo Kolde, Jaak Vilo, Marina Koltšina, Andres Salumets, Kaie Lokk, Reedik Mägi, Vijayachitra Modhukur and Kaspar Märtens and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and PLoS ONE.

In The Last Decade

Neeme Tõnisson

36 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Neeme Tõnisson Estonia 16 937 305 241 167 108 38 1.3k
Koichiro Higasa Japan 20 794 0.8× 229 0.8× 175 0.7× 120 0.7× 162 1.5× 72 1.4k
Renate Kirschner‐Schwabe Germany 19 937 1.0× 213 0.7× 163 0.7× 139 0.8× 226 2.1× 38 1.7k
Liesbeth Spruijt Netherlands 23 1.0k 1.1× 620 2.0× 222 0.9× 98 0.6× 195 1.8× 43 1.6k
Hanan E. Shamseldin Saudi Arabia 24 981 1.0× 590 1.9× 100 0.4× 56 0.3× 82 0.8× 55 1.5k
Shagufta Khaliq Pakistan 23 920 1.0× 504 1.7× 69 0.3× 309 1.9× 111 1.0× 64 1.6k
Isabel Barragán Spain 21 990 1.1× 203 0.7× 198 0.8× 238 1.4× 166 1.5× 49 1.3k
Mais Hashem Saudi Arabia 23 1.1k 1.1× 544 1.8× 107 0.4× 192 1.1× 75 0.7× 51 1.8k
Simon Ramsden United Kingdom 26 1.4k 1.5× 871 2.9× 134 0.6× 547 3.3× 50 0.5× 67 2.0k
Tristan Shaffer United States 4 748 0.8× 744 2.4× 271 1.1× 24 0.1× 93 0.9× 12 1.4k
Metka Ravnik‐Glavač Slovenia 21 1.0k 1.1× 110 0.4× 558 2.3× 210 1.3× 136 1.3× 50 1.5k

Countries citing papers authored by Neeme Tõnisson

Since Specialization
Citations

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

Fields of papers citing papers by Neeme Tõnisson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neeme Tõnisson

This figure shows the co-authorship network connecting the top 25 collaborators of Neeme Tõnisson. A scholar is included among the top collaborators of Neeme Tõnisson 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 Neeme Tõnisson. Neeme Tõnisson 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.
Nikopensius, Tiit, Triin Jagomägi, Toomas Haller, et al.. (2024). Genetic susceptibility to temporomandibular joint involvement in juvenile idiopathic arthritis. Journal of Oral Rehabilitation. 51(11). 2445–2451. 1 indexed citations
2.
Reigo, Anu, Tarmo Annilo, Toomas Toomsoo, et al.. (2024). Use of Estonian Biobank data and participant recall to improve Wilson’s disease management. European Journal of Human Genetics. 33(11). 1499–1508.
3.
Tõnisson, Neeme, Margit Nõukas, Sander Pajusalu, et al.. (2023). The Prevalence and Molecular Landscape of Lynch Syndrome in the Affected and General Population. Cancers. 15(14). 3663–3663. 3 indexed citations
4.
Irmejs, Arvīds, Margit Nõukas, Mart Kals, et al.. (2022). Spectrum and frequency of CHEK2 variants in breast cancer affected and general population in the Baltic states region, initial results and literature review. European Journal of Medical Genetics. 65(5). 104477–104477. 5 indexed citations
5.
Reigo, Anu, Margit Nõukas, Liis Leitsalu, et al.. (2022). Do Biobank Recall Studies Matter? Long-Term Follow-Up of Research Participants With Familial Hypercholesterolemia. Frontiers in Genetics. 13. 936131–936131. 2 indexed citations
6.
Vrijenhoek, Terry, Neeme Tõnisson, H Kääriäinen, Liis Leitsalu, & Tessel Rigter. (2021). Clinical genetics in transition—a comparison of genetic services in Estonia, Finland, and the Netherlands. Journal of Community Genetics. 12(2). 277–290. 8 indexed citations
7.
Nikopensius, Tiit, Toomas Haller, Triin Jagomägi, et al.. (2021). Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients. Clinical Rheumatology. 40(10). 4157–4165. 6 indexed citations
8.
Fest, Jesse, Lisanne S. Vijfhuizen, Jelle J. Goeman, et al.. (2019). Search for Early Pancreatic Cancer Blood Biomarkers in Five European Prospective Population Biobanks Using Metabolomics. Endocrinology. 160(7). 1731–1742. 20 indexed citations
9.
Žilina, Olga, Marina Koltšina, Raivo Raid, et al.. (2015). Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome. BMC Genomics. 16(1). 703–703. 15 indexed citations
10.
Lokk, Kaie, Vijayachitra Modhukur, Balaji Rajashekar, et al.. (2014). DNA methylome profiling of human tissues identifies global and tissue-specific methylation patterns. Genome biology. 15(4). 224–224. 286 indexed citations
11.
Krjutškov, Kaarel, et al.. (2013). Tissue-specific mitochondrial heteroplasmy at position 16,093 within the same individual. Current Genetics. 60(1). 11–16. 18 indexed citations
12.
Lokk, Kaie, Tõnu Vooder, Raivo Kolde, et al.. (2012). Methylation Markers of Early-Stage Non-Small Cell Lung Cancer. PLoS ONE. 7(6). e39813–e39813. 53 indexed citations
13.
Võsa, Urmo, Tõnu Vooder, Raivo Kolde, et al.. (2011). Identification of miR‐374a as a prognostic marker for survival in patients with early‐stage nonsmall cell lung cancer. Genes Chromosomes and Cancer. 50(10). 812–822. 112 indexed citations
14.
Putku, Margus, Elin Org, Siim Sõber, et al.. (2011). Novel polymorphic AluYb8 insertion in the WNK1 gene is associated with blood pressure variation in Europeans. Human Mutation. 32(7). 806–814. 22 indexed citations
15.
Teek, Rita, Riina Žordania, Kairit Joost, et al.. (2010). Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia. International Journal of Pediatric Otorhinolaryngology. 74(9). 1007–1012. 15 indexed citations
16.
Org, Elin, Siim Sõber, Piret Kelgo, et al.. (2010). Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits. BMC Medical Genetics. 11(1). 15–15. 12 indexed citations
17.
Teek, Rita, Eneli Oitmaa, Riina Žordania, et al.. (2008). Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss. International Journal of Pediatric Otorhinolaryngology. 73(1). 103–107. 8 indexed citations
18.
Zernant, Jana, Maigi Külm, Amy Hutchinson, et al.. (2003). Genotyping microarray (gene chip) for theABCR(ABCA4) gene. Human Mutation. 22(5). 395–403. 202 indexed citations
19.
Kurg, Ants, et al.. (2000). Arrayed Primer Extension: Solid-Phase Four-Color DNA Resequencing and Mutation Detection Technology. Genetic Testing. 4(1). 1–7. 143 indexed citations
20.
Tõnisson, Neeme, Ants Kurg, Krista Kaasik, Elin Lõhmussaar, & Andres Metspalu. (2000). Unravelling Genetic Data by Arrayed Primer Extension. Clinical Chemistry and Laboratory Medicine (CCLM). 38(2). 165–170. 39 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Koichiro Higasa Breakdown of academic impact, for papers by Renate Kirschner‐Schwabe Breakdown of academic impact, for papers by Liesbeth Spruijt Breakdown of academic impact, for papers by Hanan E. Shamseldin Breakdown of academic impact, for papers by Shagufta Khaliq Breakdown of academic impact, for papers by Isabel Barragán Breakdown of academic impact, for papers by Mais Hashem Breakdown of academic impact, for papers by Simon Ramsden Breakdown of academic impact, for papers by Tristan Shaffer Breakdown of academic impact, for papers by Metka Ravnik‐Glavač
Rankless by CCL
2026