Statistics
Publications
9
Citations
799
H-Index
9
Active since
1997
Affiliations
K. Verhoeven is an author at University of Antwerp specializing in genetics, medical genetics, and human genetics.
Publications per year
1997–2009
9
9
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy
Kristl G. Claeys, Stephan Züchner, Marina Kennerson et al. · Brain · 2009 · 94 citations · Full text
Alpha-tectorin involvement in hearing disabilities: one gene - two phenotypes
Jorune Balciuniene, Niklas Dahl, Paula Jalonen et al. · Human Genetics · 1999 · 67 citations
Medicine, Genetics, Neuroscience +12
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.
K. Verhoeven, Guy Van Camp, Paul Govaerts et al. · PubMed · 1997 · 61 citations
Phenotype–genotype correlations in a CMT2B family with refined 3q13-q22 locus
Michaela Auer‐Grumbach, Peter De Jonghe, Klaus Wagner et al. · Neurology · 2000 · 48 citations
1–5 of 9