Kristien Verhoeven

Mutations in the Small GTP-ase Late Endosomal Protein RAB7 Cause Charcot-Marie-Tooth Type 2B Neuropathy

Kristien Verhoeven, Peter De Jonghe, Katrien Coen et al. · The American Journal of Human Genetics · 2003 · 452 citations · Full text

Neurodegenerative Diseases, Molecular Neuroscience, Genetic Disorder +7

Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2

Stephan Züchner, Peter De Jonghe, Albena Jordanova et al. · Annals of Neurology · 2006 · 358 citations

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

Stephan Züchner, Maher Noureddine, Marina Kennerson et al. · Nature Genetics · 2005 · 356 citations

Mendelian Disorder, Genetics, Pathogenesis +6

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Kristien Verhoeven, Lut Van Laer, Karin Kirschhofer et al. · Nature Genetics · 1998 · 335 citations

Developmental Biology, Genetic Disorder, Genetics +10

Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity

Philip Van Damme, Elke Bogaert, Maarten Dewil et al. · Proceedings of the National Academy of Sciences · 2007 · 206 citations · Full text