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Chantal Ceuterick‐de Groote

Observed names: C Ceuterick-de Groote, C. Ceuterick-De Groote, C. Ceuterick-de Groote, C. Ceuterick‐De Groote, C. Ceuterick‐de Groote, Chantal Ceuterick de Groote, Chantal Ceuterick-De Groote, Chantal Ceuterick-de Groote
Observed institutions: Université Libre de Bruxelles, Vrije Universiteit Brussel, University of Antwerp, Inserm, The University of Melbourne, The University of Western Australia, City, University of London, Charles University, Harry Perkins Institute of Medical Research, Leiden University Medical Center, Ghent University Hospital, Medical University of Sofia, Ghent University, Queen Elizabeth II Medical Centre, Assistance Publique – Hôpitaux de Paris, Antwerp University Hospital, Amsterdam Neuroscience, ZNA Middelheim Hospital, Hôpital Lariboisière, Universitair Ziekenhuis Brussel, VIB-UAntwerp Center for Molecular Neurology, Thomayer University Hospital, Austin Health, Université Paris Diderot, Institute Born-Bunge, Vrije Universiteit Amsterdam, Amsterdam UMC Location Vrije Universiteit Amsterdam, KU Leuven
OpenAlex ID: A5057641888
TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration
2010 · Hans Wils, Gernot Kleinberger, et al. · Proceedings of the National Academy of Sciences · 587
Linezolid-Induced Inhibition of Mitochondrial Protein Synthesis
2006 · A. S. De Vriese, R. Van Coster, et al. · Clinical Infectious Diseases · 323
Desmin‐related myopathy with mallory body–like inclusions is caused by mutations of the selenoprotein N gene
2004 · Ana Ferreiro, Chantal Ceuterick‐de Groote, et al. · Annals of Neurology · 196
Cathepsin A–related arteriopathy with strokes and leukoencephalopathy (CARASAL)
2016 · Marianna Bugiani, Sietske H. Kevelam, et al. · Neurology · 111
Overexpression of ALS-Associated p.M337V Human TDP-43 in Mice Worsens Disease Features Compared to Wild-type Human TDP-43 Mice
2013 · Jonathan Janssens, Hans Wils, et al. · Molecular Neurobiology · 105
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Cap disease caused by heterozygous deletion of the β-tropomyosin gene TPM2
2007 · Vilma-Lotta Lehtokari, Chantal Ceuterick-de Groote, et al. · Neuromuscular Disorders · 100
Roux-en-y gastric bypass attenuates hepatic mitochondrial dysfunction in mice with non-alcoholic steatohepatitis
2014 · Jef Verbeek, Matthias Lannoo, et al. · Gut · 76
A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8
2017 · Delphine Bouhy, Manisha Juneja, et al. · Acta Neuropathologica · 75
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Neuropathology in classical and variant ataxia‐telangiectasia
2011 · Mijke M.M. Verhagen, Jean‐Jacques Martin, et al. · Neuropathology · 67
Distal myopathy with upper limb predominance caused by filamin C haploinsufficiency
2011 · V. Guergueltcheva, K. Peeters, et al. · Neurology · 60
Myosin storage myopathy: Slow skeletal myosin ( MYH7 ) mutation in two isolated cases
2005 · N. G. Laing, C. Ceuterick-de Groote, et al. · Neurology · 55
A New Mitochondrial Point Mutation in the Transfer RNALeu Gene in a Patient With a Clinical Phenotype Resembling Kearns-Sayre Syndrome
2001 · Sara Seneca, Helene Verhelst, et al. · Archives of Neurology · 48
Compound RYR1 heterozygosity resulting in a complex phenotype of malignant hyperthermia susceptibility and a core myopathy
2015 · N. Kraeva, L. Heytens, et al. · Neuromuscular Disorders · 44
Clinical and neuropathological parameters affecting the diagnostic yield of nerve biopsy
2000 · M Deprez, C Ceuterick-de Groote, et al. · Neuromuscular Disorders · 42
Effect of an R69C Mutation in the Myelin Protein Zero Gene on Myelination and Ion Channel Subtypes
2006 · Yunhong Bai, Emilia Ianokova, et al. · Archives of Neurology · 40
Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV
2005 · Nathalie Verpoorten, Kristl G. Claeys, et al. · Neuromuscular Disorders · 37
Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the young
2012 · Isabel De Brabander, Laetitia Yperzeele, et al. · Clinical Neurology and Neurosurgery · 36
Mutant HSPB8 causes protein aggregates and a reduced mitochondrial membrane potential in dermal fibroblasts from distal hereditary motor neuropathy patients
2012 · Joy Irobi, Anne Holmgren, et al. · Neuromuscular Disorders · 36
111th ENMC International Workshop on Multi-minicore Disease. 2nd International MmD Workshop, 9–11 November 2002, Naarden, The Netherlands
2004 · Heinz Jungbluth, Alan Beggs, et al. · Neuromuscular Disorders · 31
A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13
2012 · Dominique Hervé, Hugues Chabriat, et al. · Neurology · 30
Mutated CTSF in adult-onset neuronal ceroid lipofuscinosis and FTD
2016 · Julie van der Zee, Peter Mariën, et al. · Neurology Genetics · 29
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Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene
2010 · Karen Buysse, Sarah Vergult, et al. · American Journal of Medical Genetics Part A · 22
Functional characterization of novel MFSD8 pathogenic variants anticipates neurological involvement in juvenile isolated maculopathy
2019 · Miriam Bauwens, Stephan Storch, et al. · Clinical Genetics · 21
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Peripheral neuropathy and 46XY gonadal dysgenesis: A heterogeneous entity
2009 · Jonathan Baets, Ines Dierick, et al. · Neuromuscular Disorders · 15
Infantile Demyelinating Neuropathy Associated with a de novo Point Mutation on Ser72 in PMP22 and Basal Lamina Onion Bulbs in Skin Biopsy
2001 · C. Ceuterick-de Groote, P. De Jonghe, et al. · Pathology - Research and Practice · 15
Works count: 49
Citation count: 2,327
H-index: 22
I10-index: 32
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