P Sistonen
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- Genetic factors in colorectal cancer 4
- Genetics top 5%
- Genomics and Rare Diseases 1
- Oncology top 10%
- Colorectal Cancer Screening and Detection 3
- Colorectal Cancer Treatments and Studies 3
- Cancer Research top 10%
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- RNA modifications and cancer 1
- DNA Repair Mechanisms 1
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- Cystic Fibrosis Research Advances 2
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- Corneal Surgery and Treatments 1
- Co-authors
- Jukka‐Pekka MecklinJohanna HästbackaIlkka KaitilaAlbert de la ChapelleEric S. LanderAlix WeaverL PylkkänenMinna Nyström
- Journals
- Proceedings of the National Academy of Sciences (3 papers)Nature Genetics (1 paper)Gastroenterology (1 paper)
- Partner nations
- FinlandUnited States
In The Last Decade
P Sistonen
9 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 72
- Pathology and Forensic Medicine 531
- Genetics 493
- Oncology 447
- Cancer Research 170
- Molecular Biology 328
Countries citing papers authored by P Sistonen
This map shows the geographic impact of P 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 P Sistonen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P Sistonen more than expected).
Fields of papers citing papers by P Sistonen
This network shows the impact of papers produced by P 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 P Sistonen. The network helps show where P Sistonen may publish in the future.
Co-authorship network
The 25 scholars most cited alongside P 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
| # | Work | ||
|---|---|---|---|
| 1 | Genome scan in Finnish families with keratoconus. | 1999 | 1 |
| 2 | 1996 | 37 | |
| 3 | 1995 | 364 | |
| 4 | Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage. | 1994 | 117 |
| 5 | 1994 | 79 | |
| 6 | 1993 | 32 | |
| 7 | 1992 | 450 | |
| 8 | Evidence supporting exclusion of the DCC gene and a portion of chromosome 18q as the locus for susceptibility to hereditary nonpolyposis colorectal carcinoma in five kindreds. | 1991 | 36 |
| 9 | 1990 | 51 |
About P Sistonen
P Sistonen is a scholar working on Pathology and Forensic Medicine, Oncology and Hematology, having authored 9 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (4 papers), Colorectal Cancer Screening and Detection (3 papers), Colorectal Cancer Treatments and Studies (3 papers), Cystic Fibrosis Research Advances (2 papers), Genomics and Rare Diseases (1 paper), RNA modifications and cancer (1 paper), Corneal Surgery and Treatments (1 paper) and DNA Repair Mechanisms (1 paper). The work is most often cited by research in Pathology and Forensic Medicine (531 citations), Genetics (493 citations) and Oncology (447 citations). P Sistonen has collaborated with scholars based in Finland and United States. Frequent co-authors include Jukka‐Pekka Mecklin, Johanna Hästbacka, Ilkka Kaitila, Albert de la Chapelle, Eric S. Lander, Alix Weaver, Albert de la Chapelle, L Pylkkänen, Minna Nyström and Lauri A. Aaltonen. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Gastroenterology.
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.