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Isabelle Schatteman

Observed names: I Schatteman, I. Schatteman, Schatteman, Isabelle
Observed institutions: University of Antwerp, St James's University Hospital, GZA Ziekenhuizen Campus Sint-Augustinus, Saint John's Hospital, AZ Sint-Jan, GZA Ziekenhuizen
ORCID: 0000-0003-2887-5485
Observed ORCID: 0000-0003-2887-5485
OpenAlex ID: A5073394161
Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment
1998 · Kristien Verhoeven, Lut Van Laer, et al. · Nature Genetics · 348
Outcome of Cochlear Implantation at Different Ages from 0 to 6 Years
2002 · Paul J. Govaerts, Carina De Beukelaer, et al. · Otology & Neurotology · 245
Hearing in Children with Congenital Cytomegalovirus Infection: Results of a Longitudinal Study
2016 · Julie Goderis, Annelies Keymeulen, et al. · The Journal of Pediatrics · 133
A Second Gene for Otosclerosis, OTSC2, Maps to Chromosome 7q34-36
2001 · Kris Van Den Bogaert, Paul J. Govaerts, et al. · The American Journal of Human Genetics · 98
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Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations
2002 · Kim Cryns, Markus Pfister, et al. · Human Genetics · 86
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene
1999 · Kristien Verhoeven, Robbert JH Ensink, et al. · European Journal of Human Genetics · 86
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.
1997 · K Verhoeven, G Van Camp, et al. · Europe PMC (PubMed Central) · 59
Otosclerosis: a genetically heterogeneous disease involving at least three different genes
2002 · K Van Den Bogaert, P.J Govaerts, et al. · Bone · 50
Linkage Analysis of Progressive Hearing Loss in Five Extended Families Maps the DFNA2 Gene to a 1.25-Mb Region on Chromosome 1p
1997 · Guy Van Camp, Paul J. Coucke, et al. · Genomics · 48
Autosomal Dominantly Inherited GREB1L Variants in Individuals with Profound Sensorineural Hearing Impairment
2020 · Isabelle Schrauwen, Khurram Liaqat, et al. · Genes · 38
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A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).
1998 · N J Lench, A F Markham, et al. · Journal of Medical Genetics · 37
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Risk Factors for Hearing Loss at Birth in Newborns With Congenital Cytomegalovirus Infection
2022 · Elise De Cuyper, Frederic Acke, et al. · JAMA Otolaryngology–Head & Neck Surgery · 32
Congenital CMV-Associated Hearing Loss: Can Brain Imaging Predict Hearing Outcome?
2020 · Laura Craeghs, Julie Goderis, et al. · Ear and Hearing · 29
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss.
1998 · P J Govaerts, G De Ceulaer, et al. · PubMed · 29
Refined Mapping of a Gene for Autosomal Dominant Progressive Sensorineural Hearing Loss (DFNA5) to a 2-cM Region, and Exclusion of a Candidate Gene That Is Expressed in the Cochlea
1997 · L. Van Laer, G. Van Camp, et al. · European Journal of Human Genetics · 24
Risk Factors for Natural Hearing Evolution in Newborns With Congenital Cytomegalovirus Infection
2023 · Elise De Cuyper, Frederic Acke, et al. · JAMA Otolaryngology–Head & Neck Surgery · 22
Middle and inner ear malformations in velocardiofacial syndrome
2004 · Koenraad Devriendt, Ann Swillen, et al. · American Journal of Medical Genetics Part A · 21
Involvement of T-cell receptor-β alterations in the development of otosclerosis linked to OTSC2
2010 · I Schrauwen, K Venken, et al. · Genes and Immunity · 18
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Audiometric analysis of a Belgian family linked to the DFNA10 locus.
2000 · M Verstreken, F Declau, et al. · PubMed · 18
Selective vestibular neurectomy in Menière's disease: a review.
1997 · P H Van de Heyning, J Verlooy, et al. · PubMed · 18
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment
2000 · Kristien Verhoeven, Toril Fagerheim, et al. · Human Genetics · 13
Insufficient evidence for a role of SERPINF1 in otosclerosis
2019 · Hanne Valgaeren, Manou Sommen, et al. · Molecular Genetics and Genomics · 12
Results of 100 vestibular schwannoma operations.
2003 · Th Somers, F E Offeciers, et al. · PubMed · 12
Transient Depression of Inner Ear Function after Stapedotomy: Skeeter versus CO2 Laser Technique
2007 · T. Somers, J.P. Vercruysse, et al. · KARGER eBooks · 11
The Use of Malleus Allografts in Ossiculoplasty
2002 · Jean‐Philippe Vercruysse, F. Erwin Offeciers, et al. · The Laryngoscope · 10
Works count: 36
Citation count: 1,518
H-index: 18
I10-index: 25
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