Outi Kuismin
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- Genomics and Rare Diseases 6
- BRCA gene mutations in cancer 5
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 3
- Genetic Syndromes and Imprinting 2
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- NF-κB Signaling Pathways 3
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- Immunodeficiency and Autoimmune Disorders 3
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- DNA Repair Mechanisms 3
- Co-authors
- Jukka S. MoilanenAarno PalotieMitja KurkiJanna SaarelaBenjamin M. NealeElmo SaarentausLauri A. AaltonenAki S. Havulinna
- Cited by
- GeneticsCancer ResearchImmunology
- Journals
- PLoS ONE (1 paper)The Journal of Clinical Endocrinology & Metabolism (1 paper)International Journal of Cancer (1 paper)
- Partner nations
- FinlandUnited StatesUnited Kingdom
In The Last Decade
Outi Kuismin
32 papers receiving 251 citations
Peers
Comparison fields: 5 of 53
- Genetics 106
- Cancer Research 40
- Immunology 41
- Molecular Biology 118
- Aging 3
Countries citing papers authored by Outi Kuismin
This map shows the geographic impact of Outi Kuismin'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 Outi Kuismin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Outi Kuismin more than expected).
Fields of papers citing papers by Outi Kuismin
This network shows the impact of papers produced by Outi Kuismin. 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 Outi Kuismin. The network helps show where Outi Kuismin may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Outi Kuismin, 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 | 2025 | 0 | |
| 2 | 2024 | 1 | |
| 3 | 2024 | 4 | |
| 4 | 2024 | 0 | |
| 5 | 2024 | 2 | |
| 6 | 2024 | 1 | |
| 7 | 2023 | 16 | |
| 8 | 2023 | 5 | |
| 9 | 2023 | 3 | |
| 10 | 2022 | 3 | |
| 11 | 2022 | 4 | |
| 12 | 2022 | 3 | |
| 13 | 2022 | 10 | |
| 14 | 2020 | 4 | |
| 15 | 2019 | 7 | |
| 16 | 2019 | 10 | |
| 17 | 2018 | 26 | |
| 18 | 2018 | 54 | |
| 19 | 2012 | 3 | |
| 20 | 2010 | 9 |
About Outi Kuismin
Outi Kuismin is a scholar working on Genetics, Immunology and Cancer Research, having authored 35 papers that have together received 253 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), BRCA gene mutations in cancer (5 papers), Genetics and Neurodevelopmental Disorders (5 papers), DNA Repair Mechanisms (3 papers), Immunodeficiency and Autoimmune Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), NF-κB Signaling Pathways (3 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (106 citations), Cancer Research (40 citations) and Immunology (41 citations). Outi Kuismin has collaborated with scholars based in Finland, United States and United Kingdom. Frequent co-authors include Jukka S. Moilanen, Aarno Palotie, Mitja Kurki, Janna Saarela, Benjamin M. Neale, Elmo Saarentaus, Lauri A. Aaltonen, Aki S. Havulinna, Andrea Ganna and Samuli Ripatti. Their work appears in journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and International Journal of Cancer.
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.