A. Vandenberghe

2.0k citations

55 papers · 1.3k indexed · h-index 20

Impact in

Cellular and Molecular Neuroscience top 5%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
Neurology top 5%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders
- Peripheral Neuropathies and Disorders

Papers in

Cellular and Molecular Neuroscience 29
- Hereditary Neurological Disorders 25
- Genetic Neurodegenerative Diseases 15
Neurology 10
- Neurological diseases and metabolism 9
- Botulinum Toxin and Related Neurological Disorders 4

Co-authors: Rupert De Wächter Philippe Latour Christine Van Broeckhoven Walter Fiers Erik Huysmans Stephen W. Schaeffer Françoise Chapon Willy Min Jou
Journals: International Journal of Legal Medicine (5 papers)Neurology (3 papers)FEBS Letters (3 papers)Human Molecular Genetics (2 papers)Journal of the Peripheral Nervous System (2 papers)
Partner nations: France Belgium Nigeria

In The Last Decade

A. Vandenberghe

54 papers receiving 1.2k citations

Peers

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

The 25 scholars most cited alongside A. Vandenberghe, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with A. Vandenberghe Line = papers co-authored together A. Vandenberghe links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Unveiling 14 novel 2-hydroxy acid racemization and epimerization reactions in the lactate racemase superfamily Journal of Biological Chemistry ·Bing Wang, A. Vandenberghe, Gergana Dimitrova, Benoît Desguin	2024	2
2	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 ·Pierre‐Marie Gonnaud, Franck Sturtz, V. Fourbil, Dermot McGeown, Christine Tranchant, Jean‐Marie Warter, G Chazot, B Bady, Christophe Vial, Paul Begaud, A. Vandenberghe	2009	3
3	Flemish population data and sequence structure of the hypervariable tetranucleotide repeat locus D12S1090 International Journal of Legal Medicine ·Gerhard Mertens, 王春敏, Laetitia Boutrand, Polat İ.Y., A. Vandenberghe	2001	9
4	Analysis of eight STR loci in two Hungarian populations Forensic Science International ·Balázs Egyed, S. Füredi, Andrew C. Allan, Laetitia Boutrand, A. Vandenberghe, Laboratoire Valoria, Zsolt Pádár	2000	18
5	La neuropathie héréditaire avec paralysie à la pression chez l'enfant : diagnostic clinique et biologique. À propos d'un cas Archives de Pédiatrie ·Gaëtan Lesca, 葛阳生, Azel Zine, Nathaniel A. Olinger, Philippe Latour, A. Vandenberghe	2000	8
6	Mutational analysis and genotype/phenotype correlation in Turkish Charcot–Marie–Tooth Type 1 and HNPP patients Clinical Genetics ·Nisrine Bissar‐Tadmouri, Yeşim Parman, Laetitia Boutrand, Feza Deymeer, (unknown), A. Vandenberghe, Esra Battaloğlu	2000	24
7	Analysis of eight STR loci in two Hungarian populations International Journal of Legal Medicine ·Balázs Egyed, S. Füredi, Andrew C. Allan, Laetitia Boutrand, A. Vandenberghe, Laboratoire Valoria, Zsolt Pádár	2000	19
8	Mutation of the repeat number of the HPRTB locus and structure of rare intermediate alleles International Journal of Legal Medicine ·Gerhard Mertens, Polat İ.Y., 王春敏, H. Boutchiche, Jérôme Lamartine, Yuan Zhoumi, L. Muylle, A. Vandenberghe	1999	8
9	Demyelinating X-linked Charcot-Marie-Tooth disease: Unusual electrophysiological findings Muscle & Nerve ·F Tabaraud, Dariusz Latka, Philippe Sindou, A. Vandenberghe, Nicolas Lévy, J.M. Vallat	1999	63
10	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 ·Judith Lopes, N. Ravisé, A. Vandenberghe, Francesc Palau, Victor Ionâşescu, M. Mayer, Nicolas Lévy, Nicholas Wood, Nobutada Tachi, P. Bouché, Philippe Latour, Merle Ruberg, Alexis Brice, I. Krommydas	1998	66
11	Allele frequencies of nine STR systems in the Flemish population and application in parentage testing International Journal of Legal Medicine ·Gerhard Mertens, 王春敏, Yuan Zhoumi, Polat İ.Y., L. Muylle, A. Vandenberghe	1997	15
12	Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French population Neurogenetics ·Philippe Latour, Nicolas Lévy, Mathews L. Paret, Françoise Chapon, G Chazot, Pierre Clavelou, Philippe Couratier, Robert Dumas, B. Sung, Jean Pouget, J. F. Torres Simental, Jean‐Michel Vallat, M. Boucherat, Michel Fontés, A. Vandenberghe	1997	11
13	Cytotoxicity towards human endothelial cells, induced by neutrophil myeloperoxidase: protection by ceftazidime Mediators of Inflammation ·M. Mathy‐Hartert, G. Deby‐Dupont, C. Deby, Agnes van der Waerden, A. Vandenberghe, Maurice Lamy	1995	19
14	Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP) Cytogenetic and Genome Research ·E. Le Guern, O. S. Sadovyi, Michel Gugenheim, Riadh Gouider, Dermot McGeown, N. Ravisé, Pierre‐Marie Gonnaud, 經州王, P. Bouché, G Chazot, Y. Agid, A. Vandenberghe, Alexis Brice	1994	37
15	Evidence for Allelic Heterogeneity in Familial Early-Onset Alzheimer's Disease The British Journal of Psychiatry ·Cornelia M. van Duijn, Christine Van Broeckhoven, John Hardy, Alison Goate, Martin N. Rossor, A. Vandenberghe, J.J. Martin, Albert Hofman, Michael Mullan	1991	18
16	An informative MspI polymorphism detected at the D21S16 locus Human Genetics ·Guy Van Camp, A. Vandenberghe, Christine Van Broeckhoven	1990	2
17	[Genetic coupling study using DNA markers in the familial form of Alzheimer's disease]. PubMed ·A. Vandenberghe, Christine Van Broeckhoven	1989	1
18	Absence of genetic linkage of Charcot‐Marie‐Tooth disease (HMSN Ia) with chromosome 1 gene markers Neurology ·Peter Raeymaekers, Peter De Jonghe, H. Backhovens, Anita Wehnert, G. De Winter, Điêu Thị Mai Hoa, J. Gheuens, J. J. Martin, A. Vandenberghe, Christine Van Broeckhoven	1989	7
19	Germline mosaicism and Duchenne muscular dystrophy mutations Nature ·Egbert Bakker, Christine Van Broeckhoven, Pedishyus Rk, Rena Firudin kızı Mamedova, H Veenema, Wim Van Hul, G.J.B. van Ommen, A. Vandenberghe, P. Pearson	1987	155
20	Studies on the bacteriophage MS2. Some nucleotide sequences from the RNA‐polymerase gene FEBS Letters ·Roland Contreras, A. Vandenberghe, G. Volckaerţ, Willy Min Jou, Walter Fiers	1972	14

About A. Vandenberghe

A. Vandenberghe is a scholar working on Cellular and Molecular Neuroscience, Neurology, Genetics, Molecular Biology and Neurology, having authored 55 papers that have together received 1.3k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (25 papers), Genetic Neurodegenerative Diseases (15 papers), Neurological diseases and metabolism (9 papers), RNA and protein synthesis mechanisms (9 papers), Bacteriophages and microbial interactions (8 papers), Molecular Biology Techniques and Applications (7 papers), Botulinum Toxin and Related Neurological Disorders (4 papers) and Forensic and Genetic Research (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (530 citations), Neurology (195 citations), Neurology (242 citations), Molecular Biology (676 citations) and Genetics (273 citations). A. Vandenberghe has collaborated with scholars based in France, Belgium and Nigeria. Frequent 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. Their work appears in journals such as International Journal of Legal Medicine, Neurology, FEBS Letters, Human Molecular Genetics and Journal of the Peripheral Nervous System.

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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