A. Vandenberghe - Concepedia

Author

A. Vandenberghe

Also Known As

A Vandenberghe, A. VANDENBERGHE, A. Vandenberghe, A.J.C. Vandenberghe, Amandine Vandenberghe, Anton Vandenberghe, Antoon Vandenberghe

Publications

Citations

H-Index

Concepts

All Affiliations

Hôpital de l'Antiquaille University of Antwerp Université Claude Bernard Lyon 1 Ghent University Hospices Civils de Lyon

About

A. Vandenberghe is an author at Hôpital de l'Antiquaille specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	17	25	1.2K
2	Natural Sciences	9	9	325
3	Health Sciences	2	2	28
4	Public Health	2	2	45
5	Anatomy	1	1	11

A. Vandenberghe

Publications

1.9K

Citations

H-Index

Page 1

	Year	Citations
Failure of familial Alzheimer's disease to segregate with the A4-amyloid gene in several European families Christine Van Broeckhoven, A. M. Genthe, A. Vandenberghe, Nature Neurodegenerative DiseasesAlzheimer's DiseaseGeneticsGenetic EpidemiologyPathology	1987	274
Germline mosaicism and Duchenne muscular dystrophy mutations Egbert Bakker, Christine Van Broeckhoven, E. J. Bonten, Nature Mendelian DisorderGenetic DisorderGeneticsGermline MosaicismMolecular Genetics	1987	203
Axonal phenotype of Charcot-Marie-Tooth disease associated with a mutation in the myelin protein zero gene Françoise Chapon, Philippe Latour, P Diraison, Journal of Neurology Neurosurgery & Psychiatry Neurological DisorderGeneticsPathologyDisease Gene IdentificationPeripheral Nerves	1999	122
Fine mapping of de novo CMT1A and HNPP rearrangements within CMTIA-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination Judith Lopes, N. Ravisé, A. Vandenberghe, Human Molecular Genetics	1998	118
Collection of published 5S and 5.8S ribosomal RNA sequences V. A. Erdmann, J. Wolters, Erik Huysmans, Nucleic Acids Research BiologyNatural SciencesGeneticsRna Structure PredictionRna Biology	1984	110
Demyelinating X-linked Charcot-Marie-Tooth disease: Unusual electrophysiological findings F Tabaraud, E. Lagrange, Philippe Sindou, Muscle & Nerve	1999	91
Sensorineural deafness in X-linked Charcot-Marie-Tooth disease with connexin 32 mutation (R142Q) Tanya Stojkovic, Philippe Latour, A. Vandenberghe, Neurology	1999	91
Early‐onset Alzheimer's disease in 2 large Belgian families J.J. Martin, J. Gheuens, M. Bruyland, Neurology	1991	83
Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I). Peter Raeymaekers, Vincent Timmerman, Peter De Jonghe, PubMed	1989	67
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 Judith Lopes, Sandrine Tardieu, Kaisa Silander, Human Molecular Genetics Genome InstabilityDna DamageGenetic DisorderNatural SciencesGenetics	1999	57

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