Pertti Sistonen
Impact in
- Pathology and Forensic Medicine top 0.5%
- Genetic factors in colorectal cancer
- Reproductive Medicine top 1%
- Ovarian function and disorders
Papers in
-
- RNA Research and Splicing 3
- Genetics 17
- Forensic and Genetic Research 7
- Genetic Associations and Epidemiology 5
- Genetic diversity and population structure 4
- Co-authors
- Lauri A. Aaltonen (8 shared papers)Stina Roth (3 shared papers)Heikki Järvinen (5 shared papers)Markku Koskenvuo (1 shared paper)Seppo Sarna (1 shared paper)Jaakko Kaprio (1 shared paper)Virpi Launonen (4 shared papers)Kristiina Aittomäki (2 shared papers)
- Journals
- European Journal of Human Genetics (7 papers)Genomics (6 papers)Vox Sanguinis (4 papers)Human Genetics (3 papers)Nature Genetics (3 papers)
- Partner nations
- FinlandUnited StatesSweden
In The Last Decade
Pertti Sistonen
50 papers receiving 4.9k citations
Pertti Sistonen's Hit Papers
Peers
Comparison fields: 5 of 140
- Pathology and Forensic Medicine 1.4k
- Reproductive Medicine 499
- Genetics 1.2k
- Oncology 986
- Cancer Research 540
Countries citing papers authored by Pertti Sistonen
This map shows the geographic impact of Pertti Sistonen'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 Pertti Sistonen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pertti Sistonen more than expected).
Fields of papers citing papers by Pertti Sistonen
This network shows the impact of papers produced by Pertti Sistonen. 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 Pertti Sistonen. The network helps show where Pertti Sistonen may publish in the future.
Co-authors
The 25 scholars most cited alongside Pertti Sistonen, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure Hit paper breakdown → | 1995 | 815 |
| 2 | Mutations in the SMAD4/DPC4 Gene in Juvenile Polyposis Hit paper breakdown → | 1998 | 724 |
| 3 | Allelic Loss of Chromosome 18q and Prognosis in Colorectal Cancer Hit paper breakdown → | 1994 | 573 |
| 4 | Inherited susceptibility to uterine leiomyomas and renal cell cancer Hit paper breakdown → | 2001 | 502 |
| 5 | 1978 | 404 | |
| 6 | 1997 | 395 | |
| 7 | Low-level microsatellite instability in most colorectal carcinomas. | 2002 | 162 |
| 8 | 2001 | 154 | |
| 9 | A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families. | 2002 | 118 |
| 10 | 2008 | 104 | |
| 11 | 2002 | 90 | |
| 12 | 1993 | 79 | |
| 13 | 1999 | 69 | |
| 14 | 1994 | 67 | |
| 15 | 2001 | 65 | |
| 16 | 2006 | 63 | |
| 17 | 1999 | 55 | |
| 18 | 2000 | 52 | |
| 19 | mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy. | 1998 | 50 |
| 20 | 2000 | 49 |
About Pertti Sistonen
Pertti Sistonen is a scholar working on Molecular Biology, Genetics, Immunology, Hematology and Pathology and Forensic Medicine, having authored 51 papers that have together received 5.2k indexed citations. Recurring topics across this work include Forensic and Genetic Research (7 papers), Genetic factors in colorectal cancer (6 papers), Erythrocyte Function and Pathophysiology (5 papers), Genetic Associations and Epidemiology (5 papers), Blood groups and transfusion (5 papers), Genetic diversity and population structure (4 papers), interferon and immune responses (3 papers) and RNA Research and Splicing (3 papers). The work is most often cited by research in Pathology and Forensic Medicine (1.4k citations), Reproductive Medicine (499 citations), Genetics (1.2k citations), Oncology (986 citations) and Cancer Research (540 citations). Pertti Sistonen has collaborated with scholars based in Finland, United States and Sweden. Frequent co-authors include Lauri A. Aaltonen, Stina Roth, Heikki Järvinen, Markku Koskenvuo, Seppo Sarna, Jaakko Kaprio, Virpi Launonen, Kristiina Aittomäki, Richard S. Houlston and Outi Vierimaa. Their work appears in journals such as European Journal of Human Genetics, Genomics, Vox Sanguinis, Human Genetics 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.