A. Vandenberghe

UCLouvain — Belgium

Neuroscience · Life Sciences

23h-index2.0kcitations82works6.02yr avg
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Research Topics

Hereditary Neurological Disorders(28), Genetic Neurodegenerative Diseases(17), RNA and protein synthesis mechanisms(11), Bacteriophages and microbial interactions(10), Neurological diseases and metabolism(10)

Publications81 total

Unveiling 14 novel 2-hydroxy acid racemization and epimerization reactions in the lactate racemase superfamily
Journal of Biological Chemistry·2024· 6 citedOpen Access
Biodiversiteitsmisdrijven in eigen land : in Vlaamse savannes en Waalse regenwouden = La criminalité en matière de biodiversité chez nous : des savanes flamandes et forêts pluviales wallonnes
Ghent University Academic Bibliography (Ghent University)·2018· 2 citedOpen Access
DNA analysis as a tool to confirm the diagnosis of asymptomatic hereditary neuropathy with liability to pressure palsies (HNPP) with further evidence for the occurrence of de novo mutations
Acta Neurologica Scandinavica·2009· 9 cited
Polyradiculonévrite aiguë inflammatoire révélant une neuropathie héréditaire avec hypersensibilité à la pression
Revue Neurologique·2004· 7 cited
Use of STRs in paternity testing in the Flemish population
International Congress Series·2003· 1 cited
Homozygous Defects In Lmna, Encoding Lamin A/C Nuclear‐Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy In Human (Charcot‐Marie‐Tooth Disorder Type 2) And Mouse
Journal of the Peripheral Nervous System·2002· 17 cited
Flemish population data and sequence structure of the hypervariable tetranucleotide repeat locus D12S1090
International Journal of Legal Medicine·2001· 9 cited
Histopathological features of X-linked Charcot-Marie-Tooth disease in 8 patients from 6 families with different connexin32 mutations
Journal of the Peripheral Nervous System·2001· 21 cited
Variations in primer sequences are the origin of allele drop-out at loci D13S317 and CD4
International Journal of Legal Medicine·2001· 31 cited
Mutational analysis and genotype/phenotype correlation in Turkish Charcot–Marie–Tooth Type 1 and HNPP patients
Clinical Genetics·2000· 32 cited
Analysis of eight STR loci in two Hungarian populations
Forensic Science International·2000· 22 cited
Analysis of eight STR loci in two Hungarian populations
International Journal of Legal Medicine·2000· 24 cited
La neuropathie héréditaire avec paralysie à la pression chez l'enfant : diagnostic clinique et biologique. À propos d'un cas
Archives de Pédiatrie·2000· 8 cited
Homologous DNA Exchanges in Humans Can Be Explained by the Yeast Double-Strand Break Repair Model: A Study of 17p11.2 Rearrangements Associated with CMT1A and HNPP
Human Molecular Genetics·1999· 57 citedOpen Access
Peripheral myelin modification in CMT1B correlates with MPZ gene mutations
Neuromuscular Disorders·1999· 31 cited
Demyelinating X-linked Charcot-Marie-Tooth disease: Unusual electrophysiological findings
Muscle & Nerve·1999· 91 cited
Alternative exon 3 splicing of the human major protein zero gene in white blood cells and peripheral nerve tissue
FEBS Letters·1999· 10 citedOpen Access
Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene
Journal of Neurology Neurosurgery & Psychiatry·1999· 122 citedOpen Access
Mutation of the repeat number of the HPRTB locus and structure of rare intermediate alleles
International Journal of Legal Medicine·1999· 13 cited
Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q)
Neurology·1999· 91 cited
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Frequent Co-authors

Christine Van Broeckhoven(12), Philippe Latour(11), Rupert De Wächter(9), J. Gheuens(7), G Chazot(7), Walter Fiers(7), Peter Raeymaekers(6), G. De Winter(6), Laetitia Boutrand(6), H. Backhovens(5), Anita Wehnert(5), Willy Min Jou(5), Wim Van Hul(4), Nicolas Lévy(4), Roland Contreras(4), N. Mommers(4), Gerhard Mertens(4), M. Bruyland(3), Jean‐Jacques Martin(3), Konrad Beyreuther(3)