van Ommen Gj
About
In The Last Decade
van Ommen Gj
5 papers receiving 426 citations
Peers
Comparison fields: 5 of 54
- Molecular Biology 327
- Genetics 134
- Genetics 61
- Immunology 60
- Physiology 56
Countries citing papers authored by van Ommen Gj
This map shows the geographic impact of van Ommen Gj'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 van Ommen Gj with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites van Ommen Gj more than expected).
Fields of papers citing papers by van Ommen Gj
This network shows the impact of papers produced by van Ommen Gj. 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 van Ommen Gj. The network helps show where van Ommen Gj may publish in the future.
Co-authorship network of co-authors of van Ommen Gj
This figure shows the co-authorship network connecting the top 25 collaborators of van Ommen Gj. A scholar is included among the top collaborators of van Ommen Gj 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 van Ommen Gj. van Ommen Gj is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | The therapeutic potential of antisense-mediated exon skipping. | 64 |
| 2 | Acute myelogenous leukemia: a disorder of gene splicing? | 6 |
| 3 | Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia. | 7 |
| 4 | Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysis. | 1 |
| 5 | Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome. | 367 |
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.