Urmo Võsa
Impact in
- Biological Psychiatry top 2%
- Genetics top 1%
- Genetic Associations and Epidemiology
Papers in
- Genetics 22
- Genetic Associations and Epidemiology 19
- Genomics and Rare Diseases 4
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- RNA modifications and cancer 6
- Epigenetics and DNA Methylation 6
- RNA Research and Splicing 5
- Bioinformatics and Genomic Networks 5
- Gene expression and cancer classification 4
- 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
- Nature Communications (8 papers)Nature Genetics (6 papers)Scientific Reports (5 papers)European Neuropsychopharmacology (3 papers)Nature Immunology (2 papers)
- Partner nations
- EstoniaNetherlandsUnited States
In The Last Decade
Urmo Võsa
59 papers receiving 9.5k citations
Urmo Võsa's Hit Papers
Peers
Comparison fields: 5 of 159
- Biological Psychiatry 217
- Genetics 2.1k
- Molecular Biology 4.4k
- Cancer Research 777
- Aging 83
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 60 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Large-scale association analyses identify host factors influencing human gut microbiome composition Hit paper breakdown → | 2021 | 1299 |
| 2 | Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression Hit paper breakdown → | 2021 | 1270 |
| 3 | Causal relationships among the gut microbiome, short-chain fatty acids and metabolic diseases Hit paper breakdown → | 2019 | 1192 |
| 4 | Gene co-expression analysis for functional classification and gene–disease predictions Hit paper breakdown → | 2016 | 723 |
| 5 | Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes Hit paper breakdown → | 2018 | 602 |
| 6 | Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis Hit paper breakdown → | 2016 | 453 |
| 7 | Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals Hit paper breakdown → | 2020 | 452 |
| 8 | Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets Hit paper breakdown → | 2023 | 432 |
| 9 | 2018 | 316 | |
| 10 | 2018 | 281 | |
| 11 | 2017 | 248 | |
| 12 | 2013 | 241 | |
| 13 | 2019 | 211 | |
| 14 | 2017 | 209 | |
| 15 | A cross-disorder dosage sensitivity map of the human genome Hit paper breakdown → | 2022 | 197 |
| 16 | 2012 | 191 | |
| 17 | 2019 | 189 | |
| 18 | 2019 | 131 | |
| 19 | 2022 | 120 | |
| 20 | 2011 | 113 |
About Urmo Võsa
Urmo Võsa is a scholar working on Genetics, Molecular Biology, Cancer Research, Immunology and Psychiatry and Mental health, having authored 60 papers that have together received 9.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (19 papers), Cancer-related molecular mechanisms research (8 papers), RNA modifications and cancer (6 papers), Epigenetics and DNA Methylation (6 papers), RNA Research and Splicing (5 papers), Bioinformatics and Genomic Networks (5 papers), Genomics and Rare Diseases (4 papers) and Gene expression and cancer classification (4 papers). The work is most often cited by research in Biological Psychiatry (217 citations), Genetics (2.1k citations), Molecular Biology (4.4k citations), Cancer Research (777 citations) and Aging (83 citations). Urmo Võsa has collaborated with scholars based in Estonia, Netherlands and United States. 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 Gheorghe Netea and Andres Metspalu. Their work appears in journals such as Nature Communications, Nature Genetics, Scientific Reports, European Neuropsychopharmacology and Nature Immunology.
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.