Margriet Verstreken

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

Lut Van Laer, E. H. Huizing, Margriet Verstreken et al. · Nature Genetics · 1998 · 382 citations

Developmental Biology, Mendelian Disorder, Nonsyndromic Hearing Impairment +12

High Prevalence of Symptoms of Meniere's Disease in three Families With a Mutation in the COCH Gene

Erik Fransén, Margriet Verstreken, W. I. M. Verhagen et al. · Human Molecular Genetics · 1999 · 145 citations · Full text

DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System

Manou Sommen, Isabelle Schrauwen, Geert Vandeweyer et al. · Human Mutation · 2016 · 108 citations

Cnv Analysis, Syndromic Hearing Loss, Genetics +21

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene

Kristien Verhoeven, Robbert JH Ensink, Valeria Tiranti et al. · European Journal of Human Genetics · 1999 · 88 citations

Mitochondrial Function, Genetic Disorder, Genetics +10

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