A. Vandenberghe

2.0k total citations
55 papers, 1.3k citations indexed

About

A. Vandenberghe is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, A. Vandenberghe has authored 55 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 29 papers in Cellular and Molecular Neuroscience and 13 papers in Genetics. Recurrent topics in A. Vandenberghe's work include Hereditary Neurological Disorders (25 papers), Genetic Neurodegenerative Diseases (15 papers) and Neurological diseases and metabolism (9 papers). A. Vandenberghe is often cited by papers focused on Hereditary Neurological Disorders (25 papers), Genetic Neurodegenerative Diseases (15 papers) and Neurological diseases and metabolism (9 papers). A. Vandenberghe collaborates with scholars based in France, Belgium and Nigeria. A. Vandenberghe's co-authors include Rupert De Wächter, Philippe Latour, Christine Van Broeckhoven, Walter Fiers, Erik Huysmans, Stephen W. Schaeffer, Françoise Chapon, Willy Min Jou, P. Pearson and Egbert Bakker and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

A. Vandenberghe

54 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
A. Vandenberghe France 20 676 530 273 242 195 55 1.3k
Gabriele Dekomien Germany 21 586 0.9× 186 0.4× 301 1.1× 119 0.5× 96 0.5× 65 1.1k
Aı̈da Metzenberg United States 16 660 1.0× 230 0.4× 225 0.8× 41 0.2× 87 0.4× 19 1.2k
Yevgenya Kraytsberg United States 18 1.5k 2.3× 364 0.7× 155 0.6× 264 1.1× 91 0.5× 27 1.9k
Hiroomi Keino Japan 18 586 0.9× 276 0.5× 123 0.5× 69 0.3× 72 0.4× 62 1.2k
Sarah Baxendale United Kingdom 22 834 1.2× 307 0.6× 273 1.0× 52 0.2× 51 0.3× 38 1.3k
Jayne Leggo United Kingdom 19 798 1.2× 596 1.1× 399 1.5× 264 1.1× 39 0.2× 31 1.6k
Andrea Tarlton United Kingdom 10 453 0.7× 415 0.8× 82 0.3× 143 0.6× 151 0.8× 12 1.2k
Peter O'Connell United States 14 808 1.2× 356 0.7× 295 1.1× 265 1.1× 44 0.2× 17 1.4k
P. D. Kushner United States 12 340 0.5× 338 0.6× 25 0.1× 305 1.3× 144 0.7× 18 938
Julio A. Barbas Spain 20 1.1k 1.7× 446 0.8× 195 0.7× 38 0.2× 42 0.2× 27 1.5k

Countries citing papers authored by A. Vandenberghe

Since Specialization
Citations

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

Fields of papers citing papers by A. Vandenberghe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of A. Vandenberghe

This figure shows the co-authorship network connecting the top 25 collaborators of A. Vandenberghe. A scholar is included among the top collaborators of A. 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 A. Vandenberghe. A. 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.
Vandenberghe, A., et al.. (2024). Unveiling 14 novel 2-hydroxy acid racemization and epimerization reactions in the lactate racemase superfamily. Journal of Biological Chemistry. 301(1). 108069–108069. 2 indexed citations
2.
Gonnaud, Pierre‐Marie, Franck Sturtz, Christine Tranchant, et al.. (2009). DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations. Acta Neurologica Scandinavica. 92(4). 313–318. 3 indexed citations
3.
Mertens, Gerhard, et al.. (2001). Flemish population data and sequence structure of the hypervariable tetranucleotide repeat locus D12S1090. International Journal of Legal Medicine. 115(1). 40–44. 9 indexed citations
4.
Egyed, Balázs, et al.. (2000). Analysis of eight STR loci in two Hungarian populations. Forensic Science International. 113(1-3). 25–27. 18 indexed citations
5.
Lesca, Gaëtan, et al.. (2000). La neuropathie héréditaire avec paralysie à la pression chez l'enfant : diagnostic clinique et biologique. À propos d'un cas. Archives de Pédiatrie. 7(3). 271–273. 8 indexed citations
6.
Bissar‐Tadmouri, Nisrine, Yeşim Parman, Laetitia Boutrand, et al.. (2000). Mutational analysis and genotype/phenotype correlation in Turkish Charcot–Marie–Tooth Type 1 and HNPP patients. Clinical Genetics. 58(5). 396–402. 24 indexed citations
7.
Egyed, Balázs, et al.. (2000). Analysis of eight STR loci in two Hungarian populations. International Journal of Legal Medicine. 113(5). 272–275. 19 indexed citations
8.
Mertens, Gerhard, et al.. (1999). Mutation of the repeat number of the HPRTB locus and structure of rare intermediate alleles. International Journal of Legal Medicine. 112(3). 192–194. 8 indexed citations
9.
Tabaraud, F, et al.. (1999). Demyelinating X-linked Charcot-Marie-Tooth disease: Unusual electrophysiological findings. Muscle & Nerve. 22(10). 1442–1447. 63 indexed citations
10.
Lopes, Judith, N. Ravisé, A. Vandenberghe, et al.. (1998). Fine mapping of de novo CMT1A and HNPP rearrangements within CMTIA-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination. Human Molecular Genetics. 7(1). 141–148. 66 indexed citations
11.
Mertens, Gerhard, et al.. (1997). Allele frequencies of nine STR systems in the Flemish population and application in parentage testing. International Journal of Legal Medicine. 110(4). 177–180. 15 indexed citations
12.
Latour, Philippe, Nicolas Lévy, Mathews L. Paret, et al.. (1997). Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French population. Neurogenetics. 1(2). 117–123. 11 indexed citations
13.
Mathy‐Hartert, M., et al.. (1995). Cytotoxicity towards human endothelial cells, induced by neutrophil myeloperoxidase: protection by ceftazidime. Mediators of Inflammation. 4(6). 437–443. 19 indexed citations
14.
Guern, E. Le, Michel Gugenheim, Riadh Gouider, et al.. (1994). Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP). Cytogenetic and Genome Research. 65(4). 261–264. 37 indexed citations
15.
Duijn, Cornelia M. van, Christine Van Broeckhoven, John Hardy, et al.. (1991). Evidence for Allelic Heterogeneity in Familial Early-Onset Alzheimer's Disease. The British Journal of Psychiatry. 158(4). 471–474. 18 indexed citations
16.
Camp, Guy Van, A. Vandenberghe, & Christine Van Broeckhoven. (1990). An informative MspI polymorphism detected at the D21S16 locus. Human Genetics. 85(1). 140–140. 2 indexed citations
17.
Vandenberghe, A. & Christine Van Broeckhoven. (1989). [Genetic coupling study using DNA markers in the familial form of Alzheimer's disease].. PubMed. 89(3-4). 300–1. 1 indexed citations
18.
Raeymaekers, Peter, Peter De Jonghe, H. Backhovens, et al.. (1989). Absence of genetic linkage of Charcot‐Marie‐Tooth disease (HMSN Ia) with chromosome 1 gene markers. Neurology. 39(6). 844–844. 7 indexed citations
19.
Bakker, Egbert, Christine Van Broeckhoven, H Veenema, et al.. (1987). Germline mosaicism and Duchenne muscular dystrophy mutations. Nature. 329(6139). 554–556. 155 indexed citations
20.
Contreras, Roland, A. Vandenberghe, G. Volckaerţ, Willy Min Jou, & Walter Fiers. (1972). Studies on the bacteriophage MS2. Some nucleotide sequences from the RNA‐polymerase gene. FEBS Letters. 24(3). 339–342. 14 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Gabriele Dekomien Breakdown of academic impact, for papers by Aı̈da Metzenberg Breakdown of academic impact, for papers by Yevgenya Kraytsberg Breakdown of academic impact, for papers by Hiroomi Keino Breakdown of academic impact, for papers by Sarah Baxendale Breakdown of academic impact, for papers by Jayne Leggo Breakdown of academic impact, for papers by Andrea Tarlton Breakdown of academic impact, for papers by Peter O'Connell Breakdown of academic impact, for papers by P. D. Kushner Breakdown of academic impact, for papers by Julio A. Barbas
Rankless by CCL
2026