Siim Sõber
Impact in
- Genetics top 1%
- Genetic Associations and Epidemiology
- Nutrition, Genetics, and Disease
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- Hormonal Regulation and Hypertension
Papers in
- Genetics 14
- Genetic Associations and Epidemiology 11
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- Diet, Metabolism, and Disease 4
- Hormonal Regulation and Hypertension 3
- Co-authors
- Laan Maris (11 shared papers)Kristiina Rull (4 shared papers)Tarmo Annilo (1 shared paper)Marina Grigorova (2 shared papers)Margus Punab (2 shared papers)Frank Tüttelmann (1 shared paper)Jörg Gromoll (1 shared paper)Pirkko Mattila (2 shared papers)
- Journals
- Scientific Reports (3 papers)Human Molecular Genetics (2 papers)Nature Genetics (2 papers)The American Journal of Human Genetics (2 papers)Cancers (2 papers)
- Partner nations
- EstoniaUnited KingdomUnited States
In The Last Decade
Siim Sõber
30 papers receiving 4.8k citations
Siim Sõber's Hit Papers
Peers
Comparison fields: 5 of 123
- Genetics 1.8k
- Endocrinology, Diabetes and Metabolism 749
- Cardiology and Cardiovascular Medicine 824
- Nephrology 239
- Pediatrics, Perinatology and Child Health 517
Countries citing papers authored by Siim Sõber
This map shows the geographic impact of Siim Sõber'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 Siim Sõber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Siim Sõber more than expected).
Fields of papers citing papers by Siim Sõber
This network shows the impact of papers produced by Siim Sõber. 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 Siim Sõber. The network helps show where Siim Sõber may publish in the future.
Co-authors
The 25 scholars most cited alongside Siim Sõber, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk Hit paper breakdown → | 2011 | 1677 |
| 2 | Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits Hit paper breakdown → | 2018 | 990 |
| 3 | Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function Hit paper breakdown → | 2016 | 426 |
| 4 | 2011 | 354 | |
| 5 | 2009 | 157 | |
| 6 | 2011 | 146 | |
| 7 | 2011 | 139 | |
| 8 | 2017 | 132 | |
| 9 | 2012 | 108 | |
| 10 | 2017 | 103 | |
| 11 | 2009 | 98 | |
| 12 | 2014 | 97 | |
| 13 | 2009 | 91 | |
| 14 | 2015 | 90 | |
| 15 | 2012 | 50 | |
| 16 | 2016 | 47 | |
| 17 | 2021 | 45 | |
| 18 | 2017 | 40 | |
| 19 | 2011 | 31 | |
| 20 | 2017 | 28 |
About Siim Sõber
Siim Sõber is a scholar working on Genetics, Endocrinology, Diabetes and Metabolism, Pediatrics, Perinatology and Child Health, Cancer Research and Molecular Biology, having authored 31 papers that have together received 4.9k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (11 papers), Diet, Metabolism, and Disease (4 papers), Birth, Development, and Health (3 papers), Hormonal Regulation and Hypertension (3 papers), Bioinformatics and Genomic Networks (3 papers), Prenatal Screening and Diagnostics (2 papers), Global Cancer Incidence and Screening (2 papers) and Cancer-related molecular mechanisms research (2 papers). The work is most often cited by research in Genetics (1.8k citations), Endocrinology, Diabetes and Metabolism (749 citations), Cardiology and Cardiovascular Medicine (824 citations), Nephrology (239 citations) and Pediatrics, Perinatology and Child Health (517 citations). Siim Sõber has collaborated with scholars based in Estonia, United Kingdom and United States. Frequent co-authors include Laan Maris, Kristiina Rull, Tarmo Annilo, Marina Grigorova, Margus Punab, Frank Tüttelmann, Jörg Gromoll, Pirkko Mattila, Jesús María López Martí and Pille Vaas. Their work appears in journals such as Scientific Reports, Human Molecular Genetics, Nature Genetics, The American Journal of Human Genetics and Cancers.
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.