558 total citations 5 papers, 445 citations indexed
About
van Ommen Gj is a scholar working on Molecular Biology, Genetics and Immunology.
According to data from OpenAlex, van Ommen Gj has authored 5 papers receiving a total of 445 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Immunology. Recurrent topics in van Ommen Gj's work include Neurogenetic and Muscular Disorders Research (2 papers), RNA Research and Splicing (2 papers) and Muscle Physiology and Disorders (2 papers) van Ommen Gj is often cited by papers focused on Neurogenetic and Muscular Disorders Research (2 papers), RNA Research and Splicing (2 papers) and Muscle Physiology and Disorders (2 papers) van Ommen Gj collaborates with scholars based in Netherlands, United Kingdom and United States van Ommen Gj's co-authors include Joseph C. Giacalone, Uta Francke, Pagon Ra, Lindgren, HD Ochs, Christine M. Distèche, Pearson Pl, Annemieke Aartsma‐Rus, A Hagemeijer and Johan T. den Dunnen and has published in prestigious journals such as PubMed.
Citations per year, relative to van Ommen Gj van Ommen Gj (= 1×)
peers
Fédor Svinartchouk
Countries citing papers authored by van Ommen Gj
Since
Specialization
Citations
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).
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
5 of 5 papers shown
1.
Gj, van Ommen, et al.. (2008). The therapeutic potential of antisense-mediated exon skipping.. PubMed. 10(2). 140–9.64 indexed citations
2.
Gj, van Ommen, et al.. (1996). Acute myelogenous leukemia: a disorder of gene splicing?. PubMed. 10(2). 204–6.6 indexed citations
3.
Martinet, Danielle, Rachel H. Giles, Bep Smit, et al.. (1996). Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia.. PubMed. 10(9). 1459–62.7 indexed citations
4.
Bakker, Egbert, et al.. (1989). Carrier detection and prenatal diagnosis of Duchenne/Becker muscular dystrophy (D/BMD) by DNA-analysis.. PubMed. 306. 51–67.1 indexed citations
5.
Francke, Uta, HD Ochs, Joseph C. Giacalone, et al.. (1985). Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.. PubMed. 37(2). 250–67.367 indexed citations
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.