Urmo Võsa
Impact in
- Cancer Research top 5%
- Cancer-related molecular mechanisms research
- MicroRNA in disease regulation
- Biological Psychiatry top 5%
Papers in
-
- RNA modifications and cancer 6
- Metabolomics and Mass Spectrometry Studies 5
- RNA Research and Splicing 4
- Epigenetics and DNA Methylation 3
- Genetics 11
- Genetic Associations and Epidemiology 10
- Co-authors
- Lude Franke (10 shared papers)Adriaan van der Graaf (2 shared papers)Sipko van Dam (1 shared paper)João Pedro de Magalhães (1 shared paper)Cisca Wijmenga (6 shared papers)Jingyuan Fu (3 shared papers)Alexandra Zhernakova (3 shared papers)Serena Sanna (4 shared papers)
- Journals
- Scientific Reports (5 papers)Nature Genetics (3 papers)European Neuropsychopharmacology (3 papers)Human Molecular Genetics (2 papers)PLoS Genetics (2 papers)
- Partner nations
- EstoniaUnited StatesNetherlands
In The Last Decade
Urmo Võsa
34 papers receiving 3.0k citations
Urmo Võsa's Hit Papers
Peers
Comparison fields: 5 of 137
- Cancer Research 624
- Biological Psychiatry 78
- Molecular Biology 2.1k
- Immunology 402
- Physiology 481
Countries citing papers authored by Urmo Võsa
This map shows the geographic impact of Urmo Võsa'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 Urmo Võsa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Urmo Võsa more than expected).
Fields of papers citing papers by Urmo Võsa
This network shows the impact of papers produced by Urmo Võsa. 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 Urmo Võsa. The network helps show where Urmo Võsa may publish in the future.
Co-authors
The 25 scholars most cited alongside Urmo Võsa, 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 37 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases Hit paper breakdown → | 2019 | 1055 |
| 2 | Gene co-expression analysis for functional classification and gene–disease predictions Hit paper breakdown → | 2016 | 666 |
| 3 | 2013 | 216 | |
| 4 | 2017 | 188 | |
| 5 | 2012 | 182 | |
| 6 | 2019 | 122 | |
| 7 | 2011 | 112 | |
| 8 | 2022 | 95 | |
| 9 | 2018 | 86 | |
| 10 | 2018 | 62 | |
| 11 | 2012 | 53 | |
| 12 | 2014 | 36 | |
| 13 | 2021 | 23 | |
| 14 | 2021 | 23 | |
| 15 | 2015 | 21 | |
| 16 | 2016 | 19 | |
| 17 | 2013 | 18 | |
| 18 | 2019 | 17 | |
| 19 | 2017 | 13 | |
| 20 | 2023 | 10 |
About Urmo Võsa
Urmo Võsa is a scholar working on Molecular Biology, Genetics, Cancer Research, Epidemiology and Immunology, having authored 37 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (10 papers), Cancer-related molecular mechanisms research (7 papers), RNA modifications and cancer (6 papers), MicroRNA in disease regulation (5 papers), Metabolomics and Mass Spectrometry Studies (5 papers), RNA Research and Splicing (4 papers), Epigenetics and DNA Methylation (3 papers) and Liver Disease Diagnosis and Treatment (3 papers). The work is most often cited by research in Cancer Research (624 citations), Biological Psychiatry (78 citations), Molecular Biology (2.1k citations), Immunology (402 citations) and Physiology (481 citations). Urmo Võsa has collaborated with scholars based in Estonia, United States and Netherlands. Frequent co-authors include Lude Franke, Adriaan van der Graaf, Sipko van Dam, João Pedro de Magalhães, Cisca Wijmenga, Jingyuan Fu, Alexandra Zhernakova, Serena Sanna, Mihai G. Netea and Andres Metspalu. Their work appears in journals such as Scientific Reports, Nature Genetics, European Neuropsychopharmacology, Human Molecular Genetics and PLoS Genetics.
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.