Isabelle Schatteman

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 · 341 citations

Life Sciences, Genetics, Molecular Genetics +10

Outcome of Cochlear Implantation at Different Ages from 0 to 6 Years

Paul Govaerts, Carina De Beukelaer, Kristin Daemers et al. · Otology & Neurotology · 2002 · 240 citations

Medicine, Audiology, Otolaryngology +17

Hearing in Children with Congenital Cytomegalovirus Infection: Results of a Longitudinal Study

Julie Goderis, Annelies Keymeulen, Koenraad Smets et al. · The Journal of Pediatrics · 2016 · 121 citations

Health Professions, Audiology, Pediatrics +14

A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36

Kris Van Den Bogaert, Paul Govaerts, Isabelle Schatteman et al. · The American Journal of Human Genetics · 2001 · 103 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations

Kim Cryns, Markus Pfister, Ronald J. E. Pennings et al. · Human Genetics · 2002 · 90 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11