Neeme Tõnisson
Impact in
- Cancer Research top 10%
- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
- Molecular Biology top 10%
- Epigenetics and DNA Methylation
- Retinal Development and Disorders
- Gene expression and cancer classification
- RNA modifications and cancer
- Molecular Biology Techniques and Applications
Papers in
-
- Gene expression and cancer classification 8
- Molecular Biology Techniques and Applications 5
- Genetics 12
- BRCA gene mutations in cancer 5
- Genomic variations and chromosomal abnormalities 5
- Co-authors
- Andres Metspalu (17 shared papers)Ants Kurg (11 shared papers)Raivo Kolde (3 shared papers)Jaak Vilo (2 shared papers)Marina Koltšina (4 shared papers)Andres Salumets (7 shared papers)Reedik Mägi (3 shared papers)Kaie Lokk (2 shared papers)
- Journals
- European Journal of Human Genetics (3 papers)Prenatal Diagnosis (2 papers)International Journal of Pediatric Otorhinolaryngology (2 papers)Clinical Chemistry (2 papers)Human Mutation (2 papers)
- Partner nations
- EstoniaFinlandUnited States
In The Last Decade
Neeme Tõnisson
37 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 110
- Cancer Research 206
- Molecular Biology 877
- Ophthalmology 90
- Genetics 290
- Sensory Systems 45
Countries citing papers authored by Neeme Tõnisson
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
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-authors
The 25 scholars most cited alongside Neeme Tõnisson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 299 | |
| 2 | 2003 | 214 | |
| 3 | 2000 | 159 | |
| 4 | 2011 | 115 | |
| 5 | 2002 | 75 | |
| 6 | 2002 | 55 | |
| 7 | 2012 | 54 | |
| 8 | Reliable detection of beta-thalassemia and G6PD mutations by a DNA microarray. | 2002 | 53 |
| 9 | 2000 | 44 | |
| 10 | 2019 | 29 | |
| 11 | 2017 | 27 | |
| 12 | 2011 | 22 | |
| 13 | 2019 | 21 | |
| 14 | 2020 | 21 | |
| 15 | 2005 | 21 | |
| 16 | 2013 | 18 | |
| 17 | 2010 | 16 | |
| 18 | 2015 | 15 | |
| 19 | 2005 | 14 | |
| 20 | 2010 | 12 |
About Neeme Tõnisson
Neeme Tõnisson is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Oncology and Cancer Research, having authored 39 papers that have together received 1.4k indexed citations. Recurring topics across this work include Gene expression and cancer classification (8 papers), BRCA gene mutations in cancer (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Molecular Biology Techniques and Applications (5 papers), Prenatal Screening and Diagnostics (4 papers), Cancer-related Molecular Pathways (3 papers), Hearing, Cochlea, Tinnitus, Genetics (3 papers) and Cancer Genomics and Diagnostics (2 papers). The work is most often cited by research in Cancer Research (206 citations), Molecular Biology (877 citations), Ophthalmology (90 citations), Genetics (290 citations) and Sensory Systems (45 citations). Neeme Tõnisson has collaborated with scholars based in Estonia, Finland and United States. Frequent co-authors include Andres Metspalu, Ants Kurg, Raivo Kolde, Jaak Vilo, Marina Koltšina, Andres Salumets, Reedik Mägi, Kaie Lokk, Kaspar Märtens and Ioannis Georgiou. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis, International Journal of Pediatric Otorhinolaryngology, Clinical Chemistry and Human Mutation.
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.