Jaakko Leisti
- Molecular Biology top 10%
- Genetics top 2%
- Cellular and Molecular Neuroscience top 5%
- Pediatrics, Perinatology and Child Health top 5%
- Genetics top 5%
- Co-authors
- Pirkko SantavuoriS. KruusPerttì AulaRiitta HervaAune HirvasniemiMichael M. KabackD L RimoinPertti Kirkinen
- Topics
- Genomic variations and chromosomal abnormalities (17 papers)Genetics and Neurodevelopmental Disorders (17 papers)Prenatal Screening and Diagnostics (14 papers)
- Cited by
- Chemical Health and SafetyGenetics
- Partner nations
- FinlandSwedenUnited States
In The Last Decade
Jaakko Leisti
81 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 94
- Molecular Biology 1.1k
- Genetics 873
- Cellular and Molecular Neuroscience 338
- Pediatrics, Perinatology and Child Health 267
- Genetics 202
Countries citing papers authored by Jaakko Leisti
This map shows the geographic impact of Jaakko Leisti'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 Jaakko Leisti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jaakko Leisti more than expected).
Fields of papers citing papers by Jaakko Leisti
This network shows the impact of papers produced by Jaakko Leisti. 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 Jaakko Leisti. The network helps show where Jaakko Leisti may publish in the future.
Co-authorship network of co-authors of Jaakko Leisti
This figure shows the co-authorship network connecting the top 25 collaborators of Jaakko Leisti. A scholar is included among the top collaborators of Jaakko Leisti based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Jaakko Leisti. Jaakko Leisti is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 23 | |
| 3 | 20 | |
| 4 | 18 | |
| 5 | 30 | |
| 6 | 13 | |
| 7 | 23 | |
| 8 | 23 | |
| 9 | 12 | |
| 10 | 34 | |
| 11 | 3 | |
| 12 | 26 | |
| 13 | 26 | |
| 14 | 89 | |
| 15 | 157 | |
| 16 | 39 | |
| 17 | 18 | |
| 18 | 35 | |
| 19 | Allelic mutations in the mucopolysaccharidoses. | 4 |
| 20 | 2 |
About Jaakko Leisti
Jaakko Leisti is a scholar working on Genetics, Chemical Health and Safety and Developmental Biology, having authored 82 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (17 papers) and Prenatal Screening and Diagnostics (14 papers). The work is most often cited by research in Chemical Health and Safety (40 citations), Genetics (873 citations) and Genetics (202 citations). Jaakko Leisti has collaborated with scholars based in Finland, Sweden and United States. Frequent co-authors include Pirkko Santavuori, S. Kruus, Perttì Aula, Riitta Herva, Aune Hirvasniemi, Michael M. Kaback, D L Rimoin, Pertti Kirkinen, M. Kähkönen and Hannaleena Kokkonen. Their work appears in journals such as Proceedings of the National Academy of Sciences, The Lancet and Nature 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.