Concepedia

Margriet Verstreken

MV

Statistics

Publications

20

Citations

1.2K

H-Index

16

Active since

1996

Affiliations

University of Antwerp(Current)

Antwerp University Hospital

University of Iowa

GZA Ziekenhuizen Campus Sint-Augustinus

Radboud University Nijmegen

Margriet Verstreken is an author at University of Antwerp specializing in hearing loss, genetics, and medical genetics.

Publications per year

1996–2023

20

Publications

20

Nonsyndromic hearing impairment is associated with a mutation in DFNA5

Lut Van Laer, E. H. Huizing, Margriet Verstreken et al. · Nature Genetics · 1998 · 391 citations · Full text

, , +11

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 · 146 citations · Full text

, , +15

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 · 111 citations

, , +17

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

, , +14

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

, , +10

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