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
Papers in
- Genetics 20
- Genomic variations and chromosomal abnormalities 9
- Genetic Associations and Epidemiology 7
- Genomics and Rare Diseases 4
- Genetic and phenotypic traits in livestock 3
- Co-authors
- Aarno Palotie (11 shared papers)Samuli Ripatti (6 shared papers)Veikko Salomaa (5 shared papers)Mark J. Daly (3 shared papers)Nina Mars (2 shared papers)Tuomo Kiiskinen (2 shared papers)Aki S. Havulinna (4 shared papers)Pietari Ripatti (3 shared papers)
- Journals
- European Journal of Human Genetics (5 papers)PLoS ONE (3 papers)BMC Biotechnology (3 papers)European Journal of Medical Genetics (2 papers)Prenatal Diagnosis (2 papers)
- Partner nations
- EstoniaFinlandUnited States
In The Last Decade
Priit Palta
38 papers receiving 968 citations
Priit Palta's Hit Papers
Peers
Comparison fields: 5 of 97
- Genetics 393
- Cancer Research 73
- Molecular Biology 325
- Pediatrics, Perinatology and Child Health 77
- Immunology 82
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 | 254 |
| 2 | 2017 | 106 | |
| 3 | 2012 | 71 | |
| 4 | 2013 | 59 | |
| 5 | 2020 | 56 | |
| 6 | 2011 | 42 | |
| 7 | 2017 | 39 | |
| 8 | 2017 | 35 | |
| 9 | 2014 | 30 | |
| 10 | 2018 | 26 | |
| 11 | 2009 | 23 | |
| 12 | Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel | 2017 | 20 |
| 13 | 2023 | 18 | |
| 14 | 2009 | 16 | |
| 15 | 2020 | 16 | |
| 16 | 2021 | 15 | |
| 17 | 2012 | 14 | |
| 18 | 2018 | 12 | |
| 19 | 2019 | 11 | |
| 20 | 2023 | 11 |
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 980 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (7 papers), Genetic Associations and Epidemiology (7 papers), Fetal and Pediatric Neurological Disorders (4 papers), Genomics and Rare Diseases (4 papers), Cancer, Lipids, and Metabolism (3 papers), Reproductive System and Pregnancy (3 papers) and Genetic and phenotypic traits in livestock (3 papers). The work is most often cited by research in Genetics (393 citations), Cancer Research (73 citations), Molecular Biology (325 citations), Pediatrics, Perinatology and Child Health (77 citations) and Immunology (82 citations). Priit Palta has collaborated with scholars based in Estonia, Finland and United States. Frequent co-authors include Aarno Palotie, Samuli Ripatti, Veikko Salomaa, Mark J. Daly, Nina Mars, Tuomo Kiiskinen, Aki S. Havulinna, Pietari Ripatti, Alison J. Coffey and Andres Metspalu. Their work appears in journals such as European Journal of Human Genetics, PLoS ONE, BMC Biotechnology, European Journal of Medical Genetics and Prenatal Diagnosis.
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.