L Pylkkänen
- Pathology and Forensic Medicine top 0.5%
- Oncology top 5%
- Cancer Research top 5%
- Molecular Biology
- Genetics top 10%
- Co-authors
- Lauri A. AaltonenMinna NyströmPaïvi PeltomäkiRagnhild A. LotheGI MelingT I AndersenKetil HeimdalTO Rognum
- Topics
- Genetic factors in colorectal cancer (6 papers)Colorectal Cancer Treatments and Studies (5 papers)Cancer Genomics and Diagnostics (3 papers)
- Journals
- Proceedings of the National Academy of SciencesToxicologyPubMed
In The Last Decade
L Pylkkänen
9 papers receiving 1.6k citations
Hit Papers
Peers
Comparison fields: 5 of 95
- Pathology and Forensic Medicine 1.3k
- Oncology 844
- Cancer Research 645
- Molecular Biology 394
- Genetics 199
Countries citing papers authored by L Pylkkänen
This map shows the geographic impact of L Pylkkänen'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 L Pylkkänen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L Pylkkänen more than expected).
Fields of papers citing papers by L Pylkkänen
This network shows the impact of papers produced by L Pylkkänen. 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 L Pylkkänen. The network helps show where L Pylkkänen may publish in the future.
Co-authorship network of co-authors of L Pylkkänen
This figure shows the co-authorship network connecting the top 25 collaborators of L Pylkkänen. A scholar is included among the top collaborators of L Pylkkänen 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 L Pylkkänen. L Pylkkänen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | Nanosafety in Europe 2015-2020: Towards Safe and Sustainable Nanomaterials and Nanotechnology Innovations | 52 |
| 2 | Nanosafety in Europe 2015-2025: Towards Safe and Sustainable Nanomaterials and Nanotechnology Innovations. Finnish Institute of Occupational Health | 43 |
| 3 | 107 | |
| 4 | Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage. | 117 |
| 5 | 79 | |
| 6 | Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history.breakdown → | 673 |
| 7 | Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndrome. | 482 |
| 8 | Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinoma. | 24 |
| 9 | 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. | 36 |
About L Pylkkänen
L Pylkkänen is a scholar working on Pathology and Forensic Medicine, Developmental Neuroscience and Cancer Research, having authored 9 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (6 papers), Colorectal Cancer Treatments and Studies (5 papers) and Cancer Genomics and Diagnostics (3 papers). The work is most often cited by research in Pathology and Forensic Medicine (1.3k citations), Cancer Research (645 citations) and Oncology (844 citations). L Pylkkänen has collaborated with scholars based in Finland and Norway. Frequent co-authors include Lauri A. Aaltonen, Minna Nyström, Païvi Peltomäki, Ragnhild A. Lothe, GI Meling, T I Andersen, Ketil Heimdal, TO Rognum, Pål Møller and Raquel Seruca. Their work appears in journals such as Proceedings of the National Academy of Sciences, Toxicology and PubMed.
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.