Reetta Kariola
Impact in
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- Genetic factors in colorectal cancer
- Cancer Research top 10%
- Cancer Genomics and Diagnostics
Papers in
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- Genetic factors in colorectal cancer 15
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- Cancer Genomics and Diagnostics 12
- Co-authors
- Minna Nyström (13 shared papers)Païvi Peltomäki (7 shared papers)Wael M. Abdel‐Rahman (5 shared papers)Miina Ollikainen (3 shared papers)Tiina Raevaara (5 shared papers)Ralf Bützow (2 shared papers)Heather Hampel (3 shared papers)Minna Pöyhönen (1 shared paper)
- Journals
- Familial Cancer (3 papers)Human Mutation (2 papers)British Journal of Cancer (2 papers)Gastroenterology (2 papers)Journal of Clinical Oncology (1 paper)
- Partner nations
- FinlandUnited StatesDenmark
In The Last Decade
Reetta Kariola
15 papers receiving 510 citations
Peers
Comparison fields: 5 of 29
- Pathology and Forensic Medicine 473
- Cancer Research 291
- Oncology 235
- Genetics 102
- Obstetrics and Gynecology 19
Countries citing papers authored by Reetta Kariola
This map shows the geographic impact of Reetta Kariola'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 Reetta Kariola with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Reetta Kariola more than expected).
Fields of papers citing papers by Reetta Kariola
This network shows the impact of papers produced by Reetta Kariola. 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 Reetta Kariola. The network helps show where Reetta Kariola may publish in the future.
Co-authors
The 25 scholars most cited alongside Reetta Kariola, 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 | 2005 | 98 | |
| 2 | 2005 | 71 | |
| 3 | 2002 | 61 | |
| 4 | 2006 | 54 | |
| 5 | 2004 | 43 | |
| 6 | 2004 | 37 | |
| 7 | 2003 | 32 | |
| 8 | 2010 | 29 | |
| 9 | 2003 | 28 | |
| 10 | 2010 | 19 | |
| 11 | 2006 | 16 | |
| 12 | 2005 | 12 | |
| 13 | 2012 | 12 | |
| 14 | 2009 | 6 | |
| 15 | 2011 | 2 |
About Reetta Kariola
Reetta Kariola is a scholar working on Pathology and Forensic Medicine, Cancer Research, Oncology, Molecular Biology and Genetics, having authored 15 papers that have together received 520 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (15 papers), Cancer Genomics and Diagnostics (12 papers), Colorectal Cancer Screening and Detection (5 papers), DNA Repair Mechanisms (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Cancer-related gene regulation (1 paper), Colorectal Cancer Treatments and Studies (1 paper) and RNA Research and Splicing (1 paper). The work is most often cited by research in Pathology and Forensic Medicine (473 citations), Cancer Research (291 citations), Oncology (235 citations), Genetics (102 citations) and Obstetrics and Gynecology (19 citations). Reetta Kariola has collaborated with scholars based in Finland, United States and Denmark. Frequent co-authors include Minna Nyström, Païvi Peltomäki, Wael M. Abdel‐Rahman, Miina Ollikainen, Tiina Raevaara, Ralf Bützow, Heather Hampel, Minna Pöyhönen, Anne‐Marie Gerdes and Irma Järvelä. Their work appears in journals such as Familial Cancer, Human Mutation, British Journal of Cancer, Gastroenterology and Journal of Clinical Oncology.
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.