Peter De Jonghe

499 total citations
10 papers, 271 citations indexed

About

Peter De Jonghe is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Molecular Biology. According to data from OpenAlex, Peter De Jonghe has authored 10 papers receiving a total of 271 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 3 papers in Cell Biology and 2 papers in Molecular Biology. Recurrent topics in Peter De Jonghe's work include Hereditary Neurological Disorders (8 papers), Genetic Neurodegenerative Diseases (5 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Peter De Jonghe is often cited by papers focused on Hereditary Neurological Disorders (8 papers), Genetic Neurodegenerative Diseases (5 papers) and Neurogenetic and Muscular Disorders Research (2 papers). Peter De Jonghe collaborates with scholars based in Belgium, Russia and Italy. Peter De Jonghe's co-authors include Vincent Timmerman, Christine Van Broeckhoven, Eva Nelis, J. J. Martin, Kristien Verhoeven, Marcello Villanova, Alessandro Malandrini, Alessandro Rossi, Е. Л. Дадали and Oleg V. Evgrafov and has published in prestigious journals such as The American Journal of Human Genetics, Movement Disorders and Journal of the Neurological Sciences.

In The Last Decade

Peter De Jonghe

8 papers receiving 259 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Peter De Jonghe Belgium	7	232	95	77	73	54	10	271
S Bort Spain	6	217 0.9×	85 0.9×	89 1.2×	91 1.2×	44 0.8×	8	282
H.M.E. Bienfait Netherlands	9	187 0.8×	57 0.6×	77 1.0×	105 1.4×	102 1.9×	10	306
Tomoya Nishimura Japan	8	111 0.5×	50 0.5×	62 0.8×	109 1.5×	33 0.6×	17	246
Lindsey J. Miller United States	5	396 1.7×	146 1.5×	194 2.5×	99 1.4×	55 1.0×	6	445
Simona Capponi Italy	12	222 1.0×	74 0.8×	92 1.2×	211 2.9×	76 1.4×	16	405
Katherine Berry United States	7	174 0.8×	73 0.8×	89 1.2×	74 1.0×	29 0.5×	8	288
Helle Høyer Norway	8	243 1.0×	105 1.1×	96 1.2×	97 1.3×	50 0.9×	17	329
Sonia Nouioua Algeria	11	298 1.3×	124 1.3×	105 1.4×	164 2.2×	136 2.5×	18	441
Ana Cuesta Spain	6	373 1.6×	153 1.6×	110 1.4×	162 2.2×	61 1.1×	10	439
Menelaos Pipis United Kingdom	7	214 0.9×	79 0.8×	74 1.0×	90 1.2×	41 0.8×	10	289

Countries citing papers authored by Peter De Jonghe

Since Specialization

Citations

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

Fields of papers citing papers by Peter De Jonghe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter De Jonghe. 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 De Jonghe. The network helps show where Peter De Jonghe may publish in the future.

Co-authorship network of co-authors of Peter De Jonghe

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

All Works

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10 of 10 papers shown

Schil, Kristof Van, Tine Deconinck, Katrien Storm, et al.. (2025). TBP Repeat Expansion Analysis in Patients Carrying Heterozygous STUB1 Variants. Movement Disorders. 40(5). 980–985.

Дадали, Е. Л., et al.. (2001). A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2F) maps to chromosome 7q11-q21. European Journal of Human Genetics. 9(8). 646–650. 49 indexed citations

Verhoeven, Kristien, Marcello Villanova, Alessandro Rossi, et al.. (2001). Localization of the Gene for the Intermediate Form of Charcot-Marie-Tooth to Chromosome 10q24.1-q25.1. The American Journal of Human Genetics. 69(4). 889–894. 42 indexed citations

Kuhlenbäumer, Gregor, Jan Meuleman, Peter De Jonghe, et al.. (2001). Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous. Journal of Neurology. 248(10). 861–865. 15 indexed citations

Jonghe, Peter De, et al.. (2000). A CLONE CONTIG OF 12Q24.3 ENCOMPASSING THE DISTAL HEREDITARY MOTOR NEUROPATHY TYPE II GENE. Journal of the Peripheral Nervous System. 5(4). 242–242.

Beuten, Joke, Els De Vriendt, Peter De Jonghe, et al.. (1997). Mutation analysis of the human pancreatic phospholipase A2 gene in a family with distal hereditary motor neuropathy type II linked to 12q24. Neuroscience Letters. 223(1). 69–71. 4 indexed citations

Nelis, Eva, Vincent Timmerman, Ann Löfgren, et al.. (1997). Mutation analysis of the connexin 32 (Cx32) gene in charcot-marie-tooth neuropathy type 1: Identification of five new mutations. Human Mutation. 9(1). 47–52. 30 indexed citations

Jonghe, Peter De, Vincent Timmerman, Eva Nelis, J. J. Martin, & Christine Van Broeckhoven. (1997). Charcot-Marie-Tooth disease and related peripheral neuropathies.. PubMed. 2(4). 370–87. 96 indexed citations

Timmerman, Vincent, Eva Nelis, Peter De Jonghe, et al.. (1992). Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree. Journal of the Neurological Sciences. 109(1). 41–48. 26 indexed citations

10.

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

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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