Irma Järvelä
About
In The Last Decade
Irma Järvelä
146 papers receiving 5.4k citations
Hit Papers
Peers
Comparison fields: 5 of 150
- Genetics 2.3k
- Molecular Biology 1.7k
- Physiology 1.5k
- Cognitive Neuroscience 972
- Cell Biology 680
Countries citing papers authored by Irma Järvelä
This map shows the geographic impact of Irma Järvelä'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 Irma Järvelä with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Irma Järvelä more than expected).
Fields of papers citing papers by Irma Järvelä
This network shows the impact of papers produced by Irma Järvelä. 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 Irma Järvelä. The network helps show where Irma Järvelä may publish in the future.
Co-authorship network of co-authors of Irma Järvelä
This figure shows the co-authorship network connecting the top 25 collaborators of Irma Järvelä. A scholar is included among the top collaborators of Irma Järvelä 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 Irma Järvelä. Irma Järvelä is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 1 | |
| 3 | 12 | |
| 4 | Novel changes in the SLC16A2 gene identified by X-exome sequencing in two Finnish families with Allan-Herndon Dudley syndrome | 1 |
| 5 | 64 | |
| 6 | Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds. | 12 |
| 7 | Y402H Polymorphism of Complement Factor H Affects Binding Affinity to C-Reactive Protein | 2 |
| 8 | 210 | |
| 9 | 12 | |
| 10 | 46 | |
| 11 | 114 | |
| 12 | Exclusion of 14 candidate loci for primary open angle glaucoma in Finnish families. | 10 |
| 13 | The role of TIGR and OPTN in Finnish glaucoma families: a clinical and molecular genetic study. | 32 |
| 14 | Identification of a variant associated with adult-type hypolactasia breakdown → | 674 |
| 15 | 22 | |
| 16 | 17 | |
| 17 | 50 | |
| 18 | 5 | |
| 19 | 23 | |
| 20 | 4 |
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.