Marijke Bauters
- Genetics top 2%
- Molecular Biology top 10%
- Cognitive Neuroscience top 10%
- Plant Science
- Hematology top 10%
- Co-authors
- Guy FroyenHilde Van EschPeter MarynenJean‐Pierre FrynsKaren HollandersJaakko IgnatiusMartine RaynaudClaude Moraine
- Topics
- Genetics and Neurodevelopmental Disorders (18 papers)Genomic variations and chromosomal abnormalities (15 papers)Congenital heart defects research (6 papers)
- Journals
- Nature GeneticsPLoS ONEFEBS Letters
- Partner nations
- BelgiumNetherlandsFrance
In The Last Decade
Marijke Bauters
24 papers receiving 1.3k citations
Peers
Comparison fields: 5 of 76
- Genetics 911
- Molecular Biology 809
- Cognitive Neuroscience 199
- Plant Science 138
- Hematology 96
Countries citing papers authored by Marijke Bauters
This map shows the geographic impact of Marijke Bauters'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 Marijke Bauters with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marijke Bauters more than expected).
Fields of papers citing papers by Marijke Bauters
This network shows the impact of papers produced by Marijke Bauters. 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 Marijke Bauters. The network helps show where Marijke Bauters may publish in the future.
Co-authorship network of co-authors of Marijke Bauters
This figure shows the co-authorship network connecting the top 25 collaborators of Marijke Bauters. A scholar is included among the top collaborators of Marijke Bauters 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 Marijke Bauters. Marijke Bauters is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 13 | |
| 2 | 25 | |
| 3 | 33 | |
| 4 | Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1 | 0 |
| 5 | 18 | |
| 6 | 22 | |
| 7 | 16 | |
| 8 | 32 | |
| 9 | 22 | |
| 10 | 92 | |
| 11 | 11 | |
| 12 | 25 | |
| 13 | 138 | |
| 14 | 37 | |
| 15 | 59 | |
| 16 | 197 | |
| 17 | Duplication of the MECP2 region is a frequent cause of severe mental retardation and neurological symptoms in males | 1 |
| 18 | 12 | |
| 19 | 39 | |
| 20 | 473 |
About Marijke Bauters
Marijke Bauters is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 25 papers that have together received 1.3k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (18 papers), Genomic variations and chromosomal abnormalities (15 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Genetics (911 citations), Molecular Biology (809 citations) and Cognitive Neuroscience (199 citations). Marijke Bauters has collaborated with scholars based in Belgium, Netherlands and France. Frequent co-authors include Guy Froyen, Hilde Van Esch, Peter Marynen, Jean‐Pierre Fryns, Karen Hollanders, Jaakko Ignatius, Martine Raynaud, Claude Moraine, Jozef Gécz and Thierry Bienvenu. Their work appears in journals such as Nature Genetics, PLoS ONE and FEBS Letters.
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.