C. Ceuterick

2.9k citations

58 papers · 2.1k · h-index 27

Impact in

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

Papers in

Molecular Biology 33
- Mitochondrial Function and Pathology 10
Cellular and Molecular Neuroscience 21
- Hereditary Neurological Disorders 13
- Genetic Neurodegenerative Diseases 9

Co-authors: Christine Van Broeckhoven (19 shared papers)Peter De Jonghe (13 shared papers)Vincent Timmerman (13 shared papers)Jean‐Jacques Martin (11 shared papers)Eva Nelis (8 shared papers)J.J. Martin (10 shared papers)A. Löfgren (6 shared papers)J. J. Martin (8 shared papers)
Journals: Neuromuscular Disorders (5 papers)Acta Neuropathologica (5 papers)Neurology (3 papers)Journal of the Neurological Sciences (3 papers)American Journal Of Pathology (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-authors

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

Showing the 20 most-cited of 58 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia Neuromuscular Disorders ·G. Van Goethem, J.J. Martin, Bart Dermaut, Ann Löfgren, Alain Wibail, D Ververken, Peter I. Tack, I. Dehaene, Michel Van Zandijcke, M Moonen, C. Ceuterick, Peter De Jonghe, Christine Van Broeckhoven	2003	182
2	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
3	Dense-Core Plaques in Tg2576 and PSAPP Mouse Models of Alzheimer's Disease Are Centered on Vessel Walls American Journal Of Pathology ·Samir Kumar‐Singh, Daniel Pirici, Eileen McGowan, Sally Serneels, C. Ceuterick, John Hardy, Karen Duff, Dennis W. Dickson, Christine Van Broeckhoven	2005	152
4	Novel missense mutation in the early growth response 2 gene associated with Dejerine–Sottas syndrome phenotype Neurology ·Vincent Timmerman, Peter De Jonghe, C. Ceuterick, Els De Vriendt, A. Löfgren, Eva Nelis, Laura E. Warner, James R. Lupski, J. J. Martin, Christine Van Broeckhoven	1999	121
5	Mutations in GDAP1 Neurology ·Eva Nelis, Sevim Erdem‐Özdamar, Peter Van den Bergh, Marie‐Claude Belpaire‐Dethiou, C. Ceuterick, Veerle Van Gerwen, Ana Cuesta, Laia Pedrola, Francesc Palau, A.A.W.M. Gabreëls‐Festen, Christine Verellen, Ersin Tan, Mehmet Demirci, Christine Van Broeckhoven, Peter De Jonghe, Haluk Topaloğlu, Vincent Timmerman	2002	111
6	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	91
7	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, Johan van Swieten, 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
8	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
9	Behavioral Disturbances without Amyloid Deposits in Mice Overexpressing Human Amyloid Precursor Protein with Flemish (A692G) or Dutch (E693Q) Mutation Neurobiology of Disease ·Samir Kumar‐Singh, Ilse Dewachter, Dieder Moechars, Ursula Lübke, Chris De Jonghe, C. Ceuterick, Frédéric Checler, Asha Naidu, Barbara Cordell, Patrick Cras, Christine Van Broeckhoven, Fred Van Leuven	2000	84
10	On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family Acta Neuropathologica ·Jean‐Jacques Martin, Luc Krols, C. Ceuterick, Christine Van Broeckhoven, Nicole Van Regemorter, F. Hayer-Delatte, J.-M. Brucher, Th. de Barsy, H. Szliwowski, P. Evrard, Marie‐José Tassignon, H. Smet-Dieleman, Patrick J. Willems	1994	77
11	Periaxin mutations cause a broad spectrum of demyelinating neuropathies Annals of Neurology ·Hiroshi Takashima, Cornelius F. Boerkoel, Peter De Jonghe, C. Ceuterick, Jean‐Jacques Martin, Thomas Voit, J. M. Schröder, Anna Williams, Peter J. Brophy, Vincent Timmerman, James R. Lupski	2002	74
12	Patient homozygous for a recessive POLG mutation presents with features of MERRF Neurology ·G. Van Goethem, R. Mercelis, A. Löfgren, Sara Seneca, C. Ceuterick, Jean‐Jacques Martin, Christine Van Broeckhoven	2003	63
13	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
14	Identification and localization of ataxin-7 in brain and retina of a patient with cerebellar ataxia type II using anti-peptide antibody Molecular Brain Research ·C. Mauger, Jurgen Del‐Favero, C. Ceuterick, Ursula Lübke, Christine Van Broeckhoven, Jean‐Jacques Martin	1999	43
15	In Vitro Studies of Flemish, Dutch, and Wild-Type β-Amyloid Provide Evidence for Two-Staged Neurotoxicity Neurobiology of Disease ·Samir Kumar‐Singh, Ann Julliams, Rony Nuydens, C. Ceuterick, Christine Labeur, (unknown), Krist’l Vennekens, Peter Van Osta, Hugo Geerts, Bart De Strooper, Christine Van Broeckhoven	2002	42
16	Nuclear inclusions in oculopharyngeal muscular dystrophy Muscle & Nerve ·Jean‐Jacques R. Martin, C. Ceuterick, R. Mercelis	1982	39
17	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
18	Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease Neuromuscular Disorders ·Nadia Ammar, Eva Nelis, Luciano Merlini, Nina Barišić, Rim Amouri, C. Ceuterick, Jean‐Jacques Martin, Vincent Timmerman, Fayçal Hentati, Peter De Jonghe	2003	38
19	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
20	Type I Sialidosis: A Clinical, Biochemical and Neuroradiological Study European Neurology ·Silvia Palmeri, Marcello Villanova, Alessandro Malandrini, Otto P. van Diggelen, Jean G.M. Huijmans, C. Ceuterick, Alessandra Rufa, Danilo DeFalco, G. Ciacci, J. J. Martin, Giancarlo Guazzi	2000	34

About C. Ceuterick

C. Ceuterick is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Physiology, Neurology and Cell Biology, having authored 58 papers that have together received 2.1k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (13 papers), Mitochondrial Function and Pathology (10 papers), Neurological diseases and metabolism (9 papers), Alzheimer's disease research and treatments (9 papers), Genetic Neurodegenerative Diseases (9 papers), Lysosomal Storage Disorders Research (8 papers), Metabolism and Genetic Disorders (6 papers) and Neurogenetic and Muscular Disorders Research (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (907 citations), Neurology (391 citations), Clinical Biochemistry (247 citations), Neurology (373 citations) and Physiology (557 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, J.J. Martin, A. Löfgren, J. J. Martin, Samir Kumar‐Singh and Els De Vriendt. Their work appears in journals such as Neuromuscular Disorders, Acta Neuropathologica, Neurology, Journal of the Neurological Sciences and American Journal Of Pathology.

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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C. Ceuterick

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