Pertti Sistonen
Impact in
- Pathology and Forensic Medicine top 0.1%
- Genetic factors in colorectal cancer
- Cancer Research top 0.5%
- Cancer Genomics and Diagnostics
- Cancer, Hypoxia, and Metabolism
Papers in
- Genetics 16
- Forensic and Genetic Research 6
- Genetic Associations and Epidemiology 5
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- Genetic factors in colorectal cancer 10
- Co-authors
- Lauri A. Aaltonen (10 shared papers)Albert de la Chapelle (12 shared papers)Heikki Järvinen (6 shared papers)Stanley R. Hamilton (3 shared papers)Bert Vogelstein (3 shared papers)Jukka‐Pekka Mecklin (6 shared papers)Kenneth W. Kinzler (2 shared papers)Jin Jen (2 shared papers)
- Journals
- European Journal of Human Genetics (7 papers)Genomics (6 papers)Nature Genetics (4 papers)Vox Sanguinis (4 papers)Human Genetics (3 papers)
- Partner nations
- FinlandUnited StatesUnited Kingdom
In The Last Decade
Pertti Sistonen
55 papers receiving 11.1k citations
Pertti Sistonen's Hit Papers
Peers
Comparison fields: 5 of 155
- Pathology and Forensic Medicine 5.6k
- Cancer Research 2.9k
- Oncology 3.3k
- Reproductive Medicine 646
- Genetics 2.1k
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 56 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Clues to the Pathogenesis of Familial Colorectal Cancer Hit paper breakdown → | 1993 | 2339 |
| 2 | Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer Hit paper breakdown → | 1993 | 1955 |
| 3 | Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer Hit paper breakdown → | 2002 | 1297 |
| 4 | Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure Hit paper breakdown → | 1995 | 820 |
| 5 | Genetic Mapping of a Locus Predisposing to Human Colorectal Cancer Hit paper breakdown → | 1993 | 742 |
| 6 | Mutations in the SMAD4/DPC4 Gene in Juvenile Polyposis Hit paper breakdown → | 1998 | 740 |
| 7 | Allelic Loss of Chromosome 18q and Prognosis in Colorectal Cancer Hit paper breakdown → | 1994 | 591 |
| 8 | 2001 | 532 | |
| 9 | 1997 | 401 | |
| 10 | 1978 | 392 | |
| 11 | 2001 | 165 | |
| 12 | Low-level microsatellite instability in most colorectal carcinomas. | 2002 | 161 |
| 13 | A locus for autosomal dominant keratoconus: linkage to 16q22.3-q23.1 in Finnish families. | 2002 | 129 |
| 14 | 2008 | 110 | |
| 15 | 2002 | 92 | |
| 16 | 1999 | 82 | |
| 17 | 1993 | 82 | |
| 18 | Exclusion of PTEN and 10q22-24 as the susceptibility locus for juvenile polyposis syndrome. | 1997 | 75 |
| 19 | 1994 | 68 | |
| 20 | 2006 | 61 |
About Pertti Sistonen
Pertti Sistonen is a scholar working on Genetics, Pathology and Forensic Medicine, Hematology, Immunology and Molecular Biology, having authored 56 papers that have together received 11.7k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (10 papers), Forensic and Genetic Research (6 papers), Cancer Genomics and Diagnostics (5 papers), Blood groups and transfusion (5 papers), Erythrocyte Function and Pathophysiology (5 papers), Genetic Associations and Epidemiology (5 papers), DNA Repair Mechanisms (4 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). The work is most often cited by research in Pathology and Forensic Medicine (5.6k citations), Cancer Research (2.9k citations), Oncology (3.3k citations), Reproductive Medicine (646 citations) and Genetics (2.1k citations). Pertti Sistonen has collaborated with scholars based in Finland, United States and United Kingdom. Frequent co-authors include Lauri A. Aaltonen, Albert de la Chapelle, Heikki Järvinen, Stanley R. Hamilton, Bert Vogelstein, Jukka‐Pekka Mecklin, Kenneth W. Kinzler, Jin Jen, Païvi Peltomäki and Lea Pylkkänen. Their work appears in journals such as European Journal of Human Genetics, Genomics, Nature Genetics, Vox Sanguinis and Human 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.