Heli Nevanlinna
- Cancer Research top 1%
- Cancer Genomics and Diagnostics 24
- Genetics top 0.5%
- BRCA gene mutations in cancer 65
- Genomic variations and chromosomal abnormalities 21
- Genetic Associations and Epidemiology 9
- Oncology top 1%
- Cancer-related Molecular Pathways 20
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- Genetic factors in colorectal cancer 27
- Molecular Biology top 2%
- DNA Repair Mechanisms 36
- Epigenetics and DNA Methylation 10
- Co-authors
- Carl BlomqvistKristiina AittomäkiPäivi HeikkiläJiří BártekHannaleena EerolaAnitta TamminenPia VahteristoJiřina Bártková
- Cited by
- Cancer ResearchGeneticsOncology
- Journals
- Proceedings of the National Academy of Sciences (1 paper)Nature Communications (1 paper)Nature Genetics (1 paper)
- Partner nations
- FinlandSwedenUnited States
In The Last Decade
Heli Nevanlinna
123 papers receiving 5.0k citations
Peers
Comparison fields: 5 of 117
- Cancer Research 1.5k
- Genetics 2.3k
- Oncology 1.7k
- Pathology and Forensic Medicine 908
- Molecular Biology 3.1k
Countries citing papers authored by Heli Nevanlinna
This map shows the geographic impact of Heli Nevanlinna'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 Heli Nevanlinna with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Heli Nevanlinna more than expected).
Fields of papers citing papers by Heli Nevanlinna
This network shows the impact of papers produced by Heli Nevanlinna. 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 Heli Nevanlinna. The network helps show where Heli Nevanlinna may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Heli Nevanlinna, 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 | 2020 | 11 | |
| 2 | 2020 | 13 | |
| 3 | 2017 | 28 | |
| 4 | 2016 | 16 | |
| 5 | 2015 | 11 | |
| 6 | 2014 | 9 | |
| 7 | 2014 | 24 | |
| 8 | 2014 | 0 | |
| 9 | 2013 | 28 | |
| 10 | 2013 | 65 | |
| 11 | 2013 | 27 | |
| 12 | 2011 | 67 | |
| 13 | 2011 | 36 | |
| 14 | 2009 | 94 | |
| 15 | 2009 | 98 | |
| 16 | 2007 | 92 | |
| 17 | 2006 | 22 | |
| 18 | 2005 | 50 | |
| 19 | 2002 | 346 | |
| 20 | 1997 | 2 |
About Heli Nevanlinna
Heli Nevanlinna is a scholar working on Genetics, Cancer Research and Pathology and Forensic Medicine, having authored 124 papers that have together received 5.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (65 papers), DNA Repair Mechanisms (36 papers), Genetic factors in colorectal cancer (27 papers), Cancer Genomics and Diagnostics (24 papers), Genomic variations and chromosomal abnormalities (21 papers), Cancer-related Molecular Pathways (20 papers), Epigenetics and DNA Methylation (10 papers) and Genetic Associations and Epidemiology (9 papers). The work is most often cited by research in Cancer Research (1.5k citations), Genetics (2.3k citations) and Oncology (1.7k citations). Heli Nevanlinna has collaborated with scholars based in Finland, Sweden and United States. Frequent co-authors include Carl Blomqvist, Kristiina Aittomäki, Päivi Heikkilä, Jiří Bártek, Hannaleena Eerola, Anitta Tamminen, Pia Vahteristo, Jiřina Bártková, Johanna Tommiska and Kirsimari Aaltonen. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nature Communications 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.