C. Ceuterick

2.9k citations

58 papers · 2.1k indexed · h-index 27

Impact in

Neurology top 2%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders
Cellular and Molecular Neuroscience top 2%
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases

Papers in

Neurology 11
- Neurological diseases and metabolism 10
Cellular and Molecular Neuroscience 22
- Hereditary Neurological Disorders 14
- Genetic Neurodegenerative Diseases 11

Co-authors: Christine Van Broeckhoven Peter De Jonghe Vincent Timmerman Jean‐Jacques Martin Eva Nelis A. Löfgren J.J. Martin J. J. Martin
Journals: Neuromuscular Disorders (5 papers)Acta Neuropathologica (5 papers)Journal of the Neurological Sciences (3 papers)Neurology (3 papers)Neuropediatrics (2 papers)
Partner nations: Belgium Netherlands Italy

In The Last Decade

C. Ceuterick

58 papers receiving 2.0k citations

Peers

Countries citing papers authored by C. Ceuterick

Since Specialization

Citations

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

Fields of papers citing papers by C. Ceuterick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside C. Ceuterick, 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 C. Ceuterick Line = papers co-authored together C. Ceuterick links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Characterization of Ubiquitinated Intraneuronal Inclusions in a Novel Belgian Frontotemporal Lobar Degeneration Family Journal of Neuropathology & Experimental Neurology ·Daniel Pirici, Rik Vandenberghe, Rosa Rademakers, Bart Dermaut, Marc Cruts, Krist’l Vennekens, Ivy Cuijt, Ursula Lübke, C. Ceuterick, Jean‐Jacques Martin, Christine Van Broeckhoven, Samir Kumar‐Singh	2006	37
2	Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10 The American Journal of Human Genetics ·Kristien Verhoeven, Peter De Jonghe, Tom Van de Putte, Eva Nelis, An Zwijsen, Nathalie Verpoorten, Els De Vriendt, An Jacobs, Veerle Van Gerwen, Annick Francis, C. Ceuterick, Danny Huylebroeck, Vincent Timmerman	2003	90
3	Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease Neuromuscular Disorders ·Yiğit Özbek, Eva Nelis, Luciano Merlini, Nina Barišić, Rim Amouri, C. Ceuterick, Jean‐Jacques Martin, Vincent Timmerman, Fayçal Hentati, Peter De Jonghe	2003	37
4	Autosomal Dominant Adult Neuronal Ceroid Lipofuscinosis: a Novel Form of NCL with Granular Osmiophilic Deposits without Palmitoyl Protein Thioesterase 1 Deficiency Brain Pathology ·Peter C.G. Nijssen, C. Ceuterick, Otto P. van Diggelen, M. Elleder, Jean‐Jacques Martin, Johannes L. Teepen, Jaana Tyynelä, Raymund A.C. Roos	2003	46
5	Dense-Core Senile Plaques in the Flemish Variant of Alzheimer's Disease Are Vasocentric American Journal Of Pathology ·Samir Kumar‐Singh, Patrick Cras, Rong Wang, J. M. Kros, Xiang Guochun, Ursula Lübke, C. Ceuterick, Sally Serneels, Krist’l Vennekens, Jean‐Pierre Timmermans, Eric Van Marck, Jean‐Jacques Martin, Cornelia M. van Duijn, Christine Van Broeckhoven	2002	89
6	A novel 3′-splice site mutation in peripheral myelin protein 22 causing hereditary neuropathy with liability to pressure palsies Neuromuscular Disorders ·Jan Meuleman, A Pou-Serradell, A. Löfgren, C. Ceuterick, J. J. Martin, Vincent Timmerman, Christine Van Broeckhoven, Peter De Jonghe	2001	19
7	Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies Neuroreport ·Koen J. T. Venken, Jan Meuleman, Joy Irobi, C. Ceuterick, Rudolf Martini, Peter De Jonghe, Vincent Timmerman	2001	2
8	Infantile and juvenile presentations of Alexander's disease: a report of two cases Acta Neurologica Scandinavica ·Manuel Deprez, Marion Dhooge, Jean‐Paul Misson, Laurence de Leval, C. Ceuterick, M Reznik, J. J. Martin	1999	16
9	A Novel Type of Hereditary Motor and Sensory Neuropathy Characterized by a Mild Phenotype Archives of Neurology ·Peter De Jonghe, Vincent Timmerman, Eva Nelis, Els De Vriendt, Ann Löfgren, C. Ceuterick, N. Hayashi, Christine Van Broeckhoven	1999	7
10	The Thr124Met mutation in the peripheral myelin protein zero (MPZ) gene is associated with a clinically distinct Charcot–Marie–Tooth phenotype Brain ·Peter De Jonghe, Vincent Timmerman, C. Ceuterick, Eva Nelis, Els De Vriendt, A. Löfgren, Anina Vercruyssen, Christine Verellen, Lionel Van Maldergem, J. J. Martin, Christine Van Broeckhoven	1999	175
11	Detection of β-A4 amyloid and its precursor protein in the muscle of a patient with juvenile neuronal ceroid lipofuscinosis (Spielmeyer-Vogt-Sjögren) Acta Neuropathologica ·Marcello Villanova, C. Ceuterick, M. T. Dotti, Filippo M. Santorelli, Carlo Casali, Alex Malandrini, Nicola De Stefano, Ursula Lübke, J. J. Martin, G. C. Guazzi, Antonio Federico	1999	3
12	Presenile Alzheimer dementia characterized by amyloid angiopathy and large amyloid core type senile plaques in the APP 692Ala→Gly mutation Acta Neuropathologica ·Patrick Cras, F. van Harskamp, Lydia Hendriks, C. Ceuterick, Cornelia M. van Duijn, S Stefanko, Albert Hofman, J. M. Kros, Christine Van Broeckhoven, Jean‐Jacques Martin	1998	88
13	Carbohydrate‐deficient glycoprotein syndrome with previously unreported features Acta Paediatrica ·François Eyskens, C. Ceuterick, Fátima Caropeso, Chae-Hyeong Park, Jaak Jaeken	1994	26
14	On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family Acta Neuropathologica ·Jean‐Jacques Martin, Sherry Wityshyn, C. Ceuterick, Christine Van Broeckhoven, Nicole Van Regemorter, Burke O’Neill, J.-M. Brucher, Th. de Barsy, Claudiu Curcă, S. Chang, Marie‐José Tassignon, 紀彦上石, Patrick J. Willems	1994	76
15	Rimmed vacuoles of inclusion body myositis and oculopharyngeal muscular dystrophy contain amyloid precursor protein and lysosomal markers Brain Research ·Marcello Villanova, Mitsuru Kawai, Ursula Lübke, Shin J. Oh, George Perry, Jan Six, C. Ceuterick, Jean‐Jacques Martin, Patrick Cras	1993	39
16	Krabbe Globoid Cell Leukodystrophy Pathology - Research and Practice ·C. Ceuterick, J. J. Martin	1993	3
17	Specific monoclonal antibodies against normal microtubule-associated protein-2 (MAP2) epitopes present in Alzheimer pathological structures do not recognize paired helical filaments Acta Neuropathologica ·Jan Six, Ursula Lübke, Marc Mercken, M. Vandermeeren, C. Ceuterick, A. Van de Voorde, Jef Boons, J. Gheuens	1992	10
18	Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree Journal of the Neurological Sciences ·Vincent Timmerman, Viorel Filer, Eva Nelis, Peter De Jonghe, L. Muylle, C. Ceuterick, Jean‐Jacques Martin, Christine Van Broeckhoven	1992	26
19	Marshall-Smith Syndrome: New Aspects Neuropediatrics ·Viviane Borsato Botelho, K. Van Acker, Cainan Sun, J. J. Martin, C. Ceuterick	1988	14
20	Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal ganglia Journal of the Neurological Sciences ·Jean‐Jacques Martin, Frank L. Van de Vyver, H.R. Scholte, Viviane Borsato Botelho, C. Ceuterick, L. Martin, I. E. M. Luyt‐Houwen	1988	27

About C. Ceuterick

C. Ceuterick is a scholar working on Neurology, Cellular and Molecular Neuroscience, Clinical Biochemistry, Physiology and Cell Biology, having authored 58 papers that have together received 2.1k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (14 papers), Genetic Neurodegenerative Diseases (11 papers), Neurological diseases and metabolism (10 papers), Mitochondrial Function and Pathology (10 papers), Alzheimer's disease research and treatments (9 papers), Lysosomal Storage Disorders Research (8 papers), Metabolism and Genetic Disorders (6 papers) and Neurogenetic and Muscular Disorders Research (5 papers). The work is most often cited by research in Neurology (444 citations), Cellular and Molecular Neuroscience (935 citations), Clinical Biochemistry (277 citations), Neurology (435 citations) and Physiology (584 citations). C. Ceuterick has collaborated with scholars based in Belgium, Netherlands and Italy. Frequent co-authors include Christine Van Broeckhoven, Peter De Jonghe, Vincent Timmerman, Jean‐Jacques Martin, Eva Nelis, A. Löfgren, J.J. Martin, J. J. Martin, Samir Kumar‐Singh and Els De Vriendt. Their work appears in journals such as Neuromuscular Disorders, Acta Neuropathologica, Journal of the Neurological Sciences, Neurology and Neuropediatrics.

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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