H Kääriäinen
- Molecular Biology top 10%
- Genetics top 2%
- Surgery
- Pediatrics, Perinatology and Child Health top 5%
- Cancer Research top 10%
- Co-authors
- Albert de la ChapelleS. KarjalainenMikael LindlöfEeva‐Marja SankilaRisto SankilaOlli KoskimiesKristiina AittomäkiLeenamaija Pakarinen
- Topics
- BRCA gene mutations in cancer (9 papers)Renal and related cancers (7 papers)Genetic and Kidney Cyst Diseases (7 papers)
In The Last Decade
H Kääriäinen
46 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 85
- Molecular Biology 876
- Genetics 742
- Surgery 215
- Pediatrics, Perinatology and Child Health 190
- Cancer Research 174
Countries citing papers authored by H Kääriäinen
This map shows the geographic impact of H Kääriäinen'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 H Kääriäinen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites H Kääriäinen more than expected).
Fields of papers citing papers by H Kääriäinen
This network shows the impact of papers produced by H Kääriäinen. 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 H Kääriäinen. The network helps show where H Kääriäinen may publish in the future.
Co-authorship network of co-authors of H Kääriäinen
This figure shows the co-authorship network connecting the top 25 collaborators of H Kääriäinen. A scholar is included among the top collaborators of H Kääriäinen 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 H Kääriäinen. H Kääriäinen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 8 | |
| 2 | Predicting willingness to receive four different types of genetic risk information - A population based study | 0 |
| 3 | Novel changes in the SLC16A2 gene identified by X-exome sequencing in two Finnish families with Allan-Herndon Dudley syndrome | 1 |
| 4 | 5 | |
| 5 | 16 | |
| 6 | 23 | |
| 7 | 31 | |
| 8 | 4 | |
| 9 | 25 | |
| 10 | 169 | |
| 11 | 20 | |
| 12 | 16 | |
| 13 | 12 | |
| 14 | 60 | |
| 15 | 16 | |
| 16 | 25 | |
| 17 | 2 | |
| 18 | 119 | |
| 19 | 142 | |
| 20 | 17 |
About H Kääriäinen
H Kääriäinen is a scholar working on Genetics, Immunology and Allergy and Sensory Systems, having authored 47 papers that have together received 1.6k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (9 papers), Renal and related cancers (7 papers) and Genetic and Kidney Cyst Diseases (7 papers). The work is most often cited by research in Genetics (742 citations), Sensory Systems (112 citations) and Molecular Biology (876 citations). H Kääriäinen has collaborated with scholars based in Finland, Sweden and Italy. Frequent co-authors include Albert de la Chapelle, S. Karjalainen, Mikael Lindlöf, Eeva‐Marja Sankila, Risto Sankila, Olli Koskimies, Kristiina Aittomäki, Leenamaija Pakarinen, P. Sistonen and Margaret A. Tucker. Their work appears in journals such as Nature Genetics, Neurology and JNCI Journal of the National Cancer Institute.
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.