Onderzoeker
Lut Van Laer
- Disciplines:Pediatrie en neonatologie, Moleculaire en celbiologie, Systeembiologie, Verpleegkunde, Genetica
Affiliaties
- Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf16 jan 2009 → 30 nov 2010
Publicaties
21 - 27 van 27
- Candidate Gene Association Study for Noise-induced Hearing Loss in Two Independent Noise-exposed Populations
Auteurs: A Konings, Lut Van Laer, A Wiktorek-Smagur, E Rajkowska, M Pawelczyk, PI Carlsson, ML Bondeson, A Dudarewicz, A Vandevelde, E Fransen, et al.
Pagina's: 215 - 224 - Analysis of Gene Polymorphisms Associated with K+ Ion Circulation in the Inner Ear of Patients Susceptible and Resistant to Noise-induced Hearing Loss
Auteurs: M Pawelczyk, Lut Van Laer, E Fransen, E Rajkowska, A Konings, PI Carlsson, E Borg, G Van Camp, M Sliwinska-Kowalska
Pagina's: 411 - 421 - Characterization of the murine Dfna5 promoter and regulatory regions
Auteurs: K Vrijens, G Van Camp, Lut Van Laer
Pagina's: 82 - 90 - Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene
Auteurs: Nele Hilgert, Matthew Huentelman, AQ Thorburn, Erik Fransen, Nele Dieltjens, M Meuller-Malesinska, A Pollak, A Skorka, J Waligora, R Ploski, et al.
Pagina's: 517 - 524 - Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait
Auteurs: JR Huyghe, Lut Van Laer, JJ Hendrickx, E Fransen, K Demeester, V Topsakal, S Kunst, M Manninen, M Jensen, A Bonaconsa, et al.
Pagina's: 401 - 407 - Applications in Audiological Medicine
Auteurs: Lut Van Laer, Guy Van Camp, Dhavendra Kumar
Pagina's: 467 - 484 - GRM7 variants confer susceptibility to age-related hearing impairment
Auteurs: RA Friedman, Lut Van Laer, MJ Huentelman, SS Sheth, E Van Eyken, JJ Corneveaux, WD Tembe, RF Halperin, AQ Thorburn, S Thys, et al.
Pagina's: 785 - 796