Peter Van den Bergh

2.1k total citations
15 papers, 1.3k citations indexed

About

Peter Van den Bergh is a scholar working on Cellular and Molecular Neuroscience, Neurology and Surgery. According to data from OpenAlex, Peter Van den Bergh has authored 15 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cellular and Molecular Neuroscience, 6 papers in Neurology and 5 papers in Surgery. Recurrent topics in Peter Van den Bergh's work include Hereditary Neurological Disorders (6 papers), Peripheral Neuropathies and Disorders (4 papers) and Peripheral Nerve Disorders (3 papers). Peter Van den Bergh is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Peripheral Neuropathies and Disorders (4 papers) and Peripheral Nerve Disorders (3 papers). Peter Van den Bergh collaborates with scholars based in Belgium, United Kingdom and Italy. Peter Van den Bergh's co-authors include Richard AC Hughes, Isabel Illa, Eduardo Nobile‐Orazio, Hugh J. Willison, Gıancarlo Comı, Martin Bojar, Marinos C. Dalakas, P. van Doorn, A V Swan and Christine Verellen and has published in prestigious journals such as Cell, Nature Genetics and Annals of Neurology.

In The Last Decade

Peter Van den Bergh

15 papers receiving 1.3k citations

Peers

Peter Van den Bergh
Camiel Verhamme Netherlands
Peter Van den Bergh
Citations per year, relative to Peter Van den Bergh Peter Van den Bergh (= 1×) peers Camiel Verhamme

Countries citing papers authored by Peter Van den Bergh

Since Specialization
Citations

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

Fields of papers citing papers by Peter Van den Bergh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter Van den Bergh. 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 Peter Van den Bergh. The network helps show where Peter Van den Bergh may publish in the future.

Co-authorship network of co-authors of Peter Van den Bergh

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Van den Bergh. A scholar is included among the top collaborators of Peter Van den Bergh 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 Peter Van den Bergh. Peter Van den Bergh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

15 of 15 papers shown
1.
Schryver, Nicolas De, Xavier Wittebole, Peter Van den Bergh, et al.. (2015). Severe Rhabdomyolysis Associated with Simvastatin and Role of Ciprofloxacin and Amlodipine Coadministration. Case Reports in Nephrology. 2015. 1–4. 20 indexed citations
2.
Hubinont, Corinne, et al.. (2013). Extreme Maternal Metabolic Acidosis Leading to Fetal Distress and Emergency Caesarean Section. Case Reports in Obstetrics and Gynecology. 2013. 1–3. 9 indexed citations
3.
Richard, Pascale, et al.. (2010). Novel LMNA Mutation Presenting as Severe Congenital Muscular Dystrophy. Pediatric Neurology. 43(4). 283–286. 9 indexed citations
4.
Omoumi, Patrick, Thibaut Leemrijse, Christine Galant, et al.. (2010). Value of computed tomography arthrography with delayed acquisitions in the work-up of ganglion cysts of the tarsal tunnel: report of three cases. Skeletal Radiology. 39(4). 381–386. 21 indexed citations
6.
Windpassinger, Christian, Michaela Auer‐Grumbach, Joy Irobi, et al.. (2004). Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome. Nature Genetics. 36(3). 271–276. 279 indexed citations
7.
Bennett, Craig L., Andrew J. Shirk, Valerie A. Street, et al.. (2004). SIMPLE mutation in demyelinating neuropathy and distribution in sciatic nerve. Annals of Neurology. 55(5). 713–720. 54 indexed citations
8.
McCrone, Paul, Daniel Chisholm, Martín Knapp, et al.. (2003). Cost–utility analysis of intravenous immunoglobulin and prednisolone for chronic inflammatory demyelinating polyradiculoneuropathy. European Journal of Neurology. 10(6). 687–694. 55 indexed citations
9.
Comı, Gıancarlo, Luisa Roveri, Antony D. Swan, et al.. (2002). A randomised controlled trial of intravenous immunoglobulin in IgM paraprotein associated demyelinating neuropathy. Journal of Neurology. 249(10). 1370–1377. 112 indexed citations
10.
Hughes, Richard AC, Hugh J. Willison, Peter Van den Bergh, et al.. (2001). Randomized controlled trial of intravenous immunoglobulin versus oral prednisolone in chronic inflammatory demyelinating polyradiculoneuropathy. Annals of Neurology. 50(2). 195–201. 483 indexed citations
11.
Thonnard, Jean‐Louis, et al.. (1999). Effects of chronic median nerve compression at the wrist on sensation and manual skills. Experimental Brain Research. 128(1-2). 61–64. 51 indexed citations
12.
Bergh, Peter Van den, et al.. (1996). Effect of muscle denervation on the expression of substance P in the ventral raphe-spinal pathway of the rat. Brain Research. 707(2). 206–212. 13 indexed citations
13.
McClatchey, Andrea I., Peter Van den Bergh, Margaret A. Pericak‐Vance, et al.. (1992). Temperature-sensitive mutations in the III–IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita. Cell. 68(4). 769–774. 173 indexed citations
14.
Lison, Dominique, et al.. (1990). Acute polyneuropathy after malathion poisoning.. PubMed. 90(4). 190–9. 6 indexed citations
15.
Bergh, Peter Van den, et al.. (1983). Wallenberg's syndrome caused by a craniopharyngioma ?en plaque?. Journal of Neurology. 229(1). 61–64. 1 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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