Noora Andersson
Impact in
- Reproductive Medicine top 5%
- Ovarian cancer diagnosis and treatment
- Cancer Research top 10%
- Cancer-related molecular mechanisms research
- Cancer Genomics and Diagnostics
Papers in
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- Single-cell and spatial transcriptomics 5
- FOXO transcription factor regulation 3
- RNA modifications and cancer 3
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- Cancer Genomics and Diagnostics 5
- Co-authors
- Markku Heikinheimo (13 shared papers)Mikko Anttonen (9 shared papers)Leila Unkila‐Kallio (9 shared papers)Ralf Bützow (5 shared papers)Maria Alexiadis (1 shared paper)Stacey Jamieson (1 shared paper)Peter J. Fuller (1 shared paper)Olli Carpén (9 shared papers)
- Journals
- Bioinformatics (2 papers)PLoS ONE (2 papers)Cancer Research (2 papers)Journal of Clinical Medicine (1 paper)Human Molecular Genetics (1 paper)
- Partner nations
- FinlandUnited StatesUnited Kingdom
In The Last Decade
Noora Andersson
24 papers receiving 738 citations
Peers
Comparison fields: 5 of 80
- Reproductive Medicine 241
- Cancer Research 163
- Molecular Biology 368
- Geriatrics and Gerontology 20
- Pulmonary and Respiratory Medicine 159
Countries citing papers authored by Noora Andersson
This map shows the geographic impact of Noora Andersson'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 Noora Andersson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Noora Andersson more than expected).
Fields of papers citing papers by Noora Andersson
This network shows the impact of papers produced by Noora Andersson. 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 Noora Andersson. The network helps show where Noora Andersson may publish in the future.
Co-authors
The 25 scholars most cited alongside Noora Andersson, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 171 | |
| 2 | 2021 | 102 | |
| 3 | 2022 | 93 | |
| 4 | 2011 | 77 | |
| 5 | 2014 | 49 | |
| 6 | 2019 | 31 | |
| 7 | 2014 | 28 | |
| 8 | 2017 | 27 | |
| 9 | 2023 | 23 | |
| 10 | 2017 | 20 | |
| 11 | 2021 | 17 | |
| 12 | 2020 | 15 | |
| 13 | 2018 | 13 | |
| 14 | 2018 | 13 | |
| 15 | 2022 | 12 | |
| 16 | 2021 | 11 | |
| 17 | 2021 | 11 | |
| 18 | 2019 | 8 | |
| 19 | 2022 | 7 | |
| 20 | 2014 | 5 |
About Noora Andersson
Noora Andersson is a scholar working on Molecular Biology, Cancer Research, Reproductive Medicine, Surgery and Pulmonary and Respiratory Medicine, having authored 24 papers that have together received 741 indexed citations. Recurring topics across this work include Ovarian cancer diagnosis and treatment (7 papers), Single-cell and spatial transcriptomics (5 papers), Cancer Genomics and Diagnostics (5 papers), Pediatric Hepatobiliary Diseases and Treatments (4 papers), FOXO transcription factor regulation (3 papers), Congenital Anomalies and Fetal Surgery (3 papers), RNA modifications and cancer (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Reproductive Medicine (241 citations), Cancer Research (163 citations), Molecular Biology (368 citations), Geriatrics and Gerontology (20 citations) and Pulmonary and Respiratory Medicine (159 citations). Noora Andersson has collaborated with scholars based in Finland, United States and United Kingdom. Frequent co-authors include Markku Heikinheimo, Mikko Anttonen, Leila Unkila‐Kallio, Ralf Bützow, Maria Alexiadis, Stacey Jamieson, Peter J. Fuller, Olli Carpén, Anniina Färkkilä and Marjut Pihlajoki. Their work appears in journals such as Bioinformatics, PLoS ONE, Cancer Research, Journal of Clinical Medicine and Human Molecular 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.