Priit Palta
Impact in
- Genetics top 5%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic and phenotypic traits in livestock
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 21
- Genomic variations and chromosomal abnormalities 10
- Genetic Associations and Epidemiology 7
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- Molecular Biology Techniques and Applications 5
- Genomics and Phylogenetic Studies 4
- RNA and protein synthesis mechanisms 4
- Co-authors
- Aarno Palotie (11 shared papers)Samuli Ripatti (6 shared papers)Veikko Salomaa (5 shared papers)Aki S. Havulinna (4 shared papers)Mark J. Daly (3 shared papers)Pietari Ripatti (3 shared papers)Tuomo Kiiskinen (2 shared papers)Nina Mars (2 shared papers)
- Journals
- European Journal of Human Genetics (5 papers)BMC Biotechnology (3 papers)PLoS ONE (3 papers)Scientific Reports (2 papers)Nature Medicine (2 papers)
- Partner nations
- EstoniaFinlandUnited States
In The Last Decade
Priit Palta
37 papers receiving 939 citations
Priit Palta's Hit Papers
Peers
Comparison fields: 5 of 100
- Genetics 438
- Cancer Research 98
- Molecular Biology 381
- Obstetrics and Gynecology 40
- Reproductive Medicine 42
Countries citing papers authored by Priit Palta
This map shows the geographic impact of Priit Palta'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 Priit Palta with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Priit Palta more than expected).
Fields of papers citing papers by Priit Palta
This network shows the impact of papers produced by Priit Palta. 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 Priit Palta. The network helps show where Priit Palta may publish in the future.
Co-authors
The 25 scholars most cited alongside Priit Palta, 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 43 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers Hit paper breakdown → | 2020 | 245 |
| 2 | 2017 | 104 | |
| 3 | 2012 | 71 | |
| 4 | 2013 | 59 | |
| 5 | 2020 | 55 | |
| 6 | 2011 | 43 | |
| 7 | 2017 | 38 | |
| 8 | 2017 | 34 | |
| 9 | 2014 | 30 | |
| 10 | 2018 | 26 | |
| 11 | 2009 | 22 | |
| 12 | Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel | 2017 | 20 |
| 13 | 2023 | 17 | |
| 14 | 2009 | 16 | |
| 15 | 2021 | 15 | |
| 16 | 2020 | 15 | |
| 17 | 2012 | 14 | |
| 18 | 2018 | 12 | |
| 19 | 2011 | 11 | |
| 20 | 2019 | 10 |
About Priit Palta
Priit Palta is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cancer Research and Immunology, having authored 43 papers that have together received 951 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Prenatal Screening and Diagnostics (8 papers), Genetic Associations and Epidemiology (7 papers), Molecular Biology Techniques and Applications (5 papers), Genomics and Phylogenetic Studies (4 papers), RNA and protein synthesis mechanisms (4 papers), Reproductive System and Pregnancy (4 papers) and Fetal and Pediatric Neurological Disorders (4 papers). The work is most often cited by research in Genetics (438 citations), Cancer Research (98 citations), Molecular Biology (381 citations), Obstetrics and Gynecology (40 citations) and Reproductive Medicine (42 citations). Priit Palta has collaborated with scholars based in Estonia, Finland and United States. Frequent co-authors include Aarno Palotie, Samuli Ripatti, Veikko Salomaa, Aki S. Havulinna, Mark J. Daly, Pietari Ripatti, Tuomo Kiiskinen, Nina Mars, Andres Metspalu and Alison J. Coffey. Their work appears in journals such as European Journal of Human Genetics, BMC Biotechnology, PLoS ONE, Scientific Reports and Nature Medicine.
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.