Marijke Bauters

2.1k total citations
25 papers, 1.3k citations indexed

About

Marijke Bauters is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Marijke Bauters has authored 25 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 14 papers in Molecular Biology and 3 papers in Plant Science. Recurrent topics in Marijke Bauters's work include Genetics and Neurodevelopmental Disorders (18 papers), Genomic variations and chromosomal abnormalities (15 papers) and Congenital heart defects research (6 papers). Marijke Bauters is often cited by papers focused on Genetics and Neurodevelopmental Disorders (18 papers), Genomic variations and chromosomal abnormalities (15 papers) and Congenital heart defects research (6 papers). Marijke Bauters collaborates with scholars based in Belgium, France and Netherlands. Marijke Bauters's co-authors include Guy Froyen, Hilde Van Esch, Peter Marynen, Jean‐Pierre Fryns, Karen Hollanders, Martine Raynaud, Jaakko Ignatius, Jozef Gécz, Claude Moraine and Lars Riff Jensen and has published in prestigious journals such as Nature Genetics, PLoS ONE and FEBS Letters.

In The Last Decade

Marijke Bauters

24 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Marijke Bauters Belgium 17 911 809 199 138 96 25 1.3k
Chiara Pescucci Italy 19 745 0.8× 692 0.9× 224 1.1× 48 0.3× 67 0.7× 37 1.3k
Fabiola Quintero‐Rivera United States 16 907 1.0× 634 0.8× 83 0.4× 57 0.4× 65 0.7× 54 1.4k
Fikret Erdogan Germany 18 951 1.0× 799 1.0× 143 0.7× 196 1.4× 25 0.3× 25 1.4k
Roberto Ciccone Italy 23 956 1.0× 681 0.8× 82 0.4× 270 2.0× 27 0.3× 51 1.4k
Ruth N. MacKinnon Australia 15 449 0.5× 523 0.6× 136 0.7× 92 0.7× 82 0.9× 31 739
Udo Trautmann Germany 23 1.1k 1.2× 930 1.1× 55 0.3× 331 2.4× 94 1.0× 65 1.7k
Gordana Raca United States 18 1.1k 1.2× 586 0.7× 88 0.4× 85 0.6× 138 1.4× 62 1.7k
M. F. Bertheas France 9 1.1k 1.2× 889 1.1× 519 2.6× 46 0.3× 90 0.9× 17 1.5k
Marloes Steehouwer Netherlands 13 740 0.8× 719 0.9× 39 0.2× 67 0.5× 138 1.4× 18 1.4k
Silvestre Oltra Spain 20 478 0.5× 626 0.8× 39 0.2× 75 0.5× 44 0.5× 69 1.1k

Countries citing papers authored by Marijke Bauters

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

20 of 20 papers shown
1.
Race, Valérie, et al.. (2019). Challenges in molecular diagnosis of X-linked Intellectual disability. British Medical Bulletin. 133(1). 36–48. 13 indexed citations
2.
Fieremans, Nathalie, Hilde Van Esch, Thomy de Ravel, et al.. (2015). Microdeletion of the escape genes KDM5C and IQSEC2 in a girl with severe intellectual disability and autistic features. European Journal of Medical Genetics. 58(5). 324–327. 25 indexed citations
3.
Fieremans, Nathalie, Marijke Bauters, Stefanie Belet, et al.. (2014). De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed X-inactivation. Human Genetics. 133(11). 1359–1367. 33 indexed citations
4.
Breckpot, Jeroen, Bernard Thienpont, Marijke Bauters, et al.. (2013). Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1. 24(1). 126–127.
5.
Vandewalle, Joke, Bonnie Nijhof, Jamie M. Kramer, et al.. (2013). Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/β-Catenin Pathway in a Drosophila Model for Intellectual Disability. PLoS ONE. 8(11). e81791–e81791. 18 indexed citations
6.
Breckpot, Jeroen, Bernard Thienpont, Marijke Bauters, et al.. (2012). Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1. American Journal of Medical Genetics Part A. 158A(3). 574–580. 32 indexed citations
7.
Dewaele, Barbara, Agnieszka Woźniak, Marijke Bauters, et al.. (2012). Promoting role of cholecystokinin 2 receptor (CCK2R) in gastrointestinal stromal tumour pathogenesis. The Journal of Pathology. 228(4). 565–574. 16 indexed citations
8.
Breckpot, Jeroen, Léon-Charles Tranchevent, Bernard Thienpont, et al.. (2011). BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome. European Journal of Medical Genetics. 55(1). 12–16. 22 indexed citations
9.
Bauters, Marijke, et al.. (2008). Detection and validation of copy number variation in X-linked mental retardation. Cytogenetic and Genome Research. 123(1-4). 44–53. 11 indexed citations
10.
Bauters, Marijke, Hilde Van Esch, Michael J. Friez, et al.. (2008). Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair. Genome Research. 18(6). 847–858. 92 indexed citations
11.
Froyen, Guy, Marijke Bauters, Suzanna G.M. Frints, et al.. (2008). Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: Important role for increased gene dosage of XLMR genes. 30(3). 256–257. 4 indexed citations
12.
Pourebrahim, Rasoul, Marijke Bauters, Ivo De Wever, et al.. (2007). ZIC1 gene expression is controlled by DNA and histone methylation in mesenchymal proliferations. FEBS Letters. 581(26). 5122–5126. 25 indexed citations
13.
Froyen, Guy, Marijke Bauters, Jackie Boyle, et al.. (2007). Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region. Human Genetics. 121(5). 539–547. 37 indexed citations
14.
Froyen, Guy, Hilde Van Esch, Marijke Bauters, et al.. (2007). Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage ofXLMRgenes. Human Mutation. 28(10). 1034–1042. 138 indexed citations
15.
Esch, Hilde Van, Anna Jansen, Marijke Bauters, Guy Froyen, & Jean‐Pierre Fryns. (2007). Encephalopathy and bilateral cataract in a boy with an interstitial deletion of Xp22 comprising the CDKL5 and NHS genes. American Journal of Medical Genetics Part A. 143A(4). 364–369. 59 indexed citations
16.
Lahortiga, Idoya, Kim De Keersmaecker, Pieter Van Vlierberghe, et al.. (2007). Duplication of the MYB oncogene in T cell acute lymphoblastic leukemia. Nature Genetics. 39(5). 593–595. 197 indexed citations
17.
Esch, Hilde Van, Marijke Bauters, Jaakko Ignatius, et al.. (2006). Duplication of the MECP2 region is a frequent cause of severe mental retardation and neurological symptoms in males. 17(1). 119–119. 1 indexed citations
18.
Froyen, Guy, Marijke Bauters, Thierry Voet, & Peter Marynen. (2006). X-linked mental retardation and epigenetics. Journal of Cellular and Molecular Medicine. 10(4). 808–825. 12 indexed citations
19.
Bauters, Marijke, Hilde Van Esch, Peter Marynen, & Guy Froyen. (2005). X chromosome array-CGH for the identification of novel X-linked mental retardation genes. European Journal of Medical Genetics. 48(3). 263–275. 39 indexed citations
20.
Esch, Hilde Van, Marijke Bauters, Jaakko Ignatius, et al.. (2005). Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males. The American Journal of Human Genetics. 77(3). 442–453. 473 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.

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