Antoon Vandenberghe

2.5k total citations
61 papers, 2.0k citations indexed

About

Antoon Vandenberghe is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ecology. According to data from OpenAlex, Antoon Vandenberghe has authored 61 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 25 papers in Cellular and Molecular Neuroscience and 12 papers in Ecology. Recurrent topics in Antoon Vandenberghe's work include Hereditary Neurological Disorders (25 papers), Genomics and Phylogenetic Studies (17 papers) and RNA and protein synthesis mechanisms (15 papers). Antoon Vandenberghe is often cited by papers focused on Hereditary Neurological Disorders (25 papers), Genomics and Phylogenetic Studies (17 papers) and RNA and protein synthesis mechanisms (15 papers). Antoon Vandenberghe collaborates with scholars based in Belgium, France and United States. Antoon Vandenberghe's co-authors include Rupert De Wächter, Erik Huysmans, Christine Van Broeckhoven, Nicolas Lévy, Jean-Michel Vallat, Erna Dams, Mériem Tazir, Colin L. Stewart, Djamel Grid and Malika Chaouch and has published in prestigious journals such as Nucleic Acids Research, Annals of Neurology and FEBS Letters.

In The Last Decade

Antoon Vandenberghe

59 papers receiving 1.9k citations

Peers

Antoon Vandenberghe
John H. Henson United States
Richard C. Moore United States
Paolo Edomi Italy
J. L. Weber United States
Sara L.F. Sunden United States
Vittorio Gremigni Italy
Toshiaki Miyadai Japan
Robert Steen United States
Laurence Ettwiller United States
Michael Finney United States
John H. Henson United States
Antoon Vandenberghe
Citations per year, relative to Antoon Vandenberghe Antoon Vandenberghe (= 1×) peers John H. Henson

Countries citing papers authored by Antoon Vandenberghe

Since Specialization
Citations

This map shows the geographic impact of Antoon Vandenberghe'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 Antoon Vandenberghe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Antoon Vandenberghe more than expected).

Fields of papers citing papers by Antoon Vandenberghe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Antoon Vandenberghe. 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 Antoon Vandenberghe. The network helps show where Antoon Vandenberghe may publish in the future.

Co-authorship network of co-authors of Antoon Vandenberghe

This figure shows the co-authorship network connecting the top 25 collaborators of Antoon Vandenberghe. A scholar is included among the top collaborators of Antoon Vandenberghe 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 Antoon Vandenberghe. Antoon Vandenberghe 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.
Zhang, Feng, Pavel Seeman, Pengfei Liu, et al.. (2010). Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability. The American Journal of Human Genetics. 86(6). 892–903. 98 indexed citations
2.
Latour, Philippe, Pierre‐Marie Gonnaud, Elisabeth Ollagnon, et al.. (2006). SIMPLE mutation analysis in dominant demyelinating Charcot‐Marie‐Tooth disease: three novel mutations. Journal of the Peripheral Nervous System. 11(2). 148–155. 43 indexed citations
3.
Stinissen, Piet, Bernadette Van Roy, Guy Van Camp, et al.. (2005). Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms. American Journal of Medical Genetics. 37(S7). 133–136. 1 indexed citations
4.
Stojkovic, Tanya, Philippe Latour, J. de Sèze, et al.. (2004). Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene. Neuromuscular Disorders. 14(4). 261–264. 34 indexed citations
5.
Bernard, Rafaëlle, Amandine Boyer, Perrine Malzac, et al.. (2002). Prenatal detection of the 17p11.2 duplication in Charcot-Marie-Tooth disease type 1A: necessity of a multidisciplinary approach for heterogeneous disorders. European Journal of Human Genetics. 10(5). 297–302. 7 indexed citations
6.
Bouhouche, Ahmed, Ali Benomar, Nazha Birouk, et al.. (1999). A Locus for an Axonal Form of Autosomal Recessive Charcot-Marie-Tooth Disease Maps to Chromosome 1q21.2-q21.3. The American Journal of Human Genetics. 65(3). 722–727. 68 indexed citations
7.
Sindou, Philippe, Jean‐Michel Vallat, F Tabaraud, et al.. (1999). Ultrastructural protein zero expression in Charcot-Marie-Tooth type 1B Disease. Muscle & Nerve. 22(1). 99–104. 9 indexed citations
8.
Latour, Philippe, Catherine Ressot, J.‐C. Antoine, et al.. (1997). New Mutations in the X-Linked Form of Charcot-Marie-Tooth Disease. European Neurology. 37(1). 38–42. 13 indexed citations
9.
Ressot, Catherine, Philippe Latour, Franck Sturtz, et al.. (1996). X-linked dominant Charcot-Marie-Tooth neuropathy (CMTX): new mutations in the connexin32 gene. Human Genetics. 98(2). 172–175. 19 indexed citations
10.
Latour, Philippe, Eva Nelis, André Dautigny, et al.. (1995). Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1B. Human Mutation. 6(1). 50–54. 31 indexed citations
11.
Bost, Muriel, Pierre‐Marie Gonnaud, Pierre Cochat, et al.. (1994). New allele of probe D17S61 present in the Charcot‐Marie‐Tooth 1A duplication. Clinical Genetics. 46(5). 380–381. 1 indexed citations
12.
Pham-Dinh, Danielle, Nathalie Roëckel, Philippe Latour, et al.. (1993). The major peripheral myelin protein zero gene: structure and localization in the cluster of Fcγ receptor genes on human chromosome 1q21.3 – q23. Human Molecular Genetics. 2(12). 2051–2054. 27 indexed citations
13.
Stinissen, Piet, Wim Van Hul, Guy Van Camp, et al.. (1990). The pericentromeric 21 DNA marker pGSM21 (D21S13) contains an expressed HTF island. Genomics. 7(1). 119–122. 4 indexed citations
14.
Stinissen, Piet, Antoon Vandenberghe, & Christine Van Broeckhoven. (1990). A high frequency EcoRI RFLP detected at the D21S13 locus. Nucleic Acids Research. 18(5). 1319–1319. 3 indexed citations
15.
Stinissen, Piet, Antoon Vandenberghe, & Christine Van Broeckhoven. (1990). PCR detection of two RFLP's at the D21S13 locus. Nucleic Acids Research. 18(12). 3672–3672. 11 indexed citations
16.
Raeymaekers, Peter, Christine Van Broeckhoven, Hubert Backhovens, et al.. (1989). Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease. Human Genetics. 81(3). 231–233. 1 indexed citations
17.
Jonghe, Peter De, L. Muylle, J. Gheuens, et al.. (1988). Absence of linkage with the Duffy blood group in a family with Charcot-Marie-Tooth neuropathy. Journal of the Neurological Sciences. 88(1-3). 145–150. 9 indexed citations
18.
Raeymaekers, Peter, Christine Van Broeckhoven, & Antoon Vandenberghe. (1988). A highly polymorphic locus is detected by probe CARLP II6.3 [D5S88]. Nucleic Acids Research. 16(16). 8196–8196. 1 indexed citations
19.
Hendriks, Lydia, Christine Van Broeckhoven, Antoon Vandenberghe, Yves Van de Peer, & Rupert De Wächter. (1988). Primary and secondary structure of the 18S ribosomal RNA of the bird spider Eurypelma californica and evolutionary relationships among eukaryotic phyla. European Journal of Biochemistry. 177(1). 15–20. 42 indexed citations
20.
Erdmann, Volker A., Erik Huysmans, Antoon Vandenberghe, & Rupert De Wächter. (1983). Collection of published 5S and 5.8S ribosomal RNA sequences. Nucleic Acids Research. 11(1). 235–235. 27 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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