Peter De Jonghe

36.7k total citations · 2 hit papers
235 papers, 13.0k citations indexed

About

Peter De Jonghe is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Peter De Jonghe has authored 235 papers receiving a total of 13.0k indexed citations (citations by other indexed papers that have themselves been cited), including 146 papers in Cellular and Molecular Neuroscience, 102 papers in Molecular Biology and 58 papers in Neurology. Recurrent topics in Peter De Jonghe's work include Hereditary Neurological Disorders (123 papers), Neurological diseases and metabolism (58 papers) and Genetic Neurodegenerative Diseases (52 papers). Peter De Jonghe is often cited by papers focused on Hereditary Neurological Disorders (123 papers), Neurological diseases and metabolism (58 papers) and Genetic Neurodegenerative Diseases (52 papers). Peter De Jonghe collaborates with scholars based in Belgium, Germany and United States. Peter De Jonghe's co-authors include Vincent Timmerman, Christine Van Broeckhoven, Lieve Claes, Eva Nelis, Jurgen Del‐Favero, Berten Ceulemans, Arvid Suls, Lieven Lagae, Michaela Auer‐Grumbach and Jonathan Baets and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Peter De Jonghe

230 papers receiving 12.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy

2001 916 citations Lieve Claes, Jurgen Del‐Favero et al. The American Journal of Human Genetics profile →
DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)

2004 602 citations Peter De Jonghe, Vincent Timmerman et al. The American Journal of Human Genetics profile →

Peers

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Vitamin D3 deficiency and osteopenia in spastic paraplegia type 5 indicate impaired bone homeostasis 2024 ·Scientific Reports ·Sabrina Ehnert, Stefan Hauser, Holger Hengel, (unknown), Rebecca Schüle, Tobias Lindig, Jonathan Baets, Tine Deconinck, Peter De Jonghe, Tina Histing, Andreas K. Nüssler, Lüdger Schöls, Tim W. Rattay	1
2	Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48) 2016 ·Neurology Genetics ·Jennifer Hirst, Marianna Madeo, Katrien Smets, James R. Edgar, Lüdger Schöls, Jun Li, (unknown), Tine Deconinck, Jonathan Baets, Elisabeth Van Aken, Jan De Bleecker, Manuel B. Datiles, Ricardo H. Roda, Joachim Liepert, Stephan Züchner, Caterina Mariotti, Peter De Jonghe, Craig Blackstone, Michael C. Kruer	24
3	STXBP1 promotes Weibel-Palade body exocytosis through its interaction with the Rab27A effector Slp4-a 2014 ·Blood ·(unknown), Ambrosius P. Snijders, Nicola Hellen, Sarah Weckhuysen, (unknown), Jeroen Eikenboom, Karine M. Valentijn, Mar Fernandez‐Borja, Berten Ceulemans, Peter De Jonghe, Jan Voorberg, Matthew J. Hannah, Tom Carter, Ruben Bierings	43
4	Molecular genetics of Dravet syndrome 2011 ·Developmental Medicine & Child Neurology ·Peter De Jonghe	61
5	Absence epilepsies with widely variable onset are a key feature of familial GLUT1 deficiency 2010 ·Neurology ·Saul A. Mullen, Arvid Suls, Peter De Jonghe, Samuel F. Berkovic, Ingrid E. Scheffer	120
6	Autosomal-Dominant Striatal Degeneration Is Caused by a Mutation in the Phosphodiesterase 8B Gene 2010 ·The American Journal of Human Genetics ·Silke Appenzeller, Anja Schirmacher, Hartmut Halfter, Sebastian Bäumer, Manuela Pendziwiat, Vincent Timmerman, Peter De Jonghe, Klára Fekete, Florian Stögbauer, Peter Lüdemann, (unknown), Elgar Susanne Quabius, E. Bernd Ringelstein, Gregor Kuhlenbäumer	23
7	A Functional Null Mutation ofSCN1Bin a Patient with Dravet Syndrome 2009 ·Journal of Neuroscience ·Gustavo A. Patiño, Lieve Claes, Luis F. Lopez‐Santiago, Emily A. Slat, (unknown), Chunling Chen, Heather A. O’Malley, Charles B.B. Gray, Haruko Miyazaki, Nobuyuki Nukina, Fumitaka Oyama, Peter De Jonghe, Lori L. Isom	203
8	Early‐onset absence epilepsy caused by mutations in the glucose transporter GLUT1 2009 ·Annals of Neurology ·Arvid Suls, Saul A. Mullen, Yvonne Weber, Kristien Verhaert, Berten Ceulemans, Renzo Guerrini, Thomas V. Wuttke, (unknown), Liesbet Deprez, Lieve Claes, Albena Jordanova, Samuel F. Berkovic, Holger Lerche, Peter De Jonghe, Ingrid E. Scheffer	187
9	Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T>C 2009 ·Journal of Neurology Neurosurgery & Psychiatry ·Bart Dermaut, Sara Seneca, Lina Dom, Kaat Smets, (unknown), Joél Smet, Boél De Paepe, Simon Tousseyn, Sarah Weckhuysen, Marc Gewillig, P. Pals, Paul M. Parizel, Jan De Bleecker, Paul Boon, Linda De Meırleır, Peter De Jonghe, Rudy Van Coster, Wim Van Paesschen, Patrick Santens	27
10	TheSCN1Avariant database: a novel research and diagnostic tool 2009 ·Human Mutation ·Lieve Claes, Liesbet Deprez, Arvid Suls, Jonathan Baets, Katrien Smets, Tine Van Dyck, Tine Deconinck, Albena Jordanova, Peter De Jonghe	103
11	Epilepsy as part of the phenotype associated with ATP1A2 mutations 2007 ·Epilepsia ·Liesbet Deprez, Sarah Weckhuysen, (unknown), Tine Deconinck, Kristl G. Claeys, Lieve Claes, Arvid Suls, Tine Van Dyck, André Palmini, Gert Matthijs, Wim Van Paesschen, Peter De Jonghe	80
12	Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS 2007 ·Ghent University Academic Bibliography (Ghent University) ·Ilse Gijselinck, Kristel Sleegers, Sebastiaan Engelborghs, Wim Robberecht, Jean‐Jacques Martin, Rik Vandenberghe, Raf Sciot, Bart Dermaut, D. Goossens, Julie van der Zee, Tim De Pooter, Jurgen Del‐Favero, Patrick Santens, Peter De Jonghe, Peter P. De Deyn, Christine Van Broeckhoven, Marc Cruts	3
13	Epilepsy and migraine in a patient with Urbach–Wiethe disease 2007 ·Seizure ·Kristl G. Claeys, Lieve Claes, Johan Van Goethem, (unknown), J. Merregaert, Julien Lambert, Eric A. Van Marck, Paul M. Parizel, Peter De Jonghe	15
14	Mutations in Mitofusin 2 are a major cause for autosomal dominant axonal Charcot-Marie-Tooth neuropathy 2005 ·Journal of the Peripheral Nervous System ·Vincent Timmerman, Kristl G. Claeys, K. Verhoeven, Stephan Züchner, (unknown), (unknown), Peter De Jonghe	1
15	Mutation analysis of the LGI1/Epitempin gene in 48 patients with distinct epilepsy syndromes 2005 ·Epilepsia ·Arvid Suls, (unknown), Dominique Audenaert, Liesbet Deprez, (unknown), Berten Ceulemans, Kristl G. Claeys, Christine Van Broeckhoven, Peter De Jonghe	1
16	novoSNP, a novel computational tool for sequence variation discovery 2005 ·Genome Research ·Stefan Weckx, Jurgen Del‐Favero, Rosa Rademakers, Lieve Claes, Marc Cruts, Peter De Jonghe, Christine Van Broeckhoven, Peter De Rijk	214
17	A novel connexin 32 missense mutation (E208G) causing Charcot-Marie-Tooth disease 2001 ·Human Mutation ·Andrzej Kochański, A. Löfgren, H Jedrzejowska, Barbara Ryniewicz, Malwina Czarny‐Ratajczak, Anna‐Maria Barciszewska, (unknown), I Hausmanowa-Pétrusewicz, Peter De Jonghe, Vincent Timmerman, Anna Latos‐Bieleńska	2
18	De Novo Mutations in the Sodium-Channel Gene SCN1A Cause Severe Myoclonic Epilepsy of Infancy breakdown → 2001 ·The American Journal of Human Genetics ·Lieve Claes, Jurgen Del‐Favero, Berten Ceulemans, Lieven Lagae, Christine Van Broeckhoven, Peter De Jonghe	916
19	The natural history of hereditary neuralgic amyotrophy in the Dutch population. 2000 ·Neuromuscular Disorders ·(unknown), Peter De Jonghe, (unknown), Johan A. K. Suykens, A.A.W.M. Gabreëls‐Festen, (unknown), (unknown), Gregor Kuhlenbäumer, (unknown), Jan Meuleman, A Pou-Serradell, (unknown), Andrea Schenone, Florian Stögbauer, Vincent Timmerman, Nens van Alfen, Baziel G.M. van Engelen, Christine Van Broeckhoven	3
20	Linkage analysis of the Duffy blood group marker with several chromosome 1 genes in an extended pedigree with Charcot-Marie-Tooth disease 1989 ·Human Genetics ·Peter Raeymaekers, Christine Van Broeckhoven, Hubert Backhovens, Anita Wehnert, L. Muylle, Peter De Jonghe, (unknown), Jean‐Jacques Martin, Antoon Vandenberghe	1

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