| Year |
Citation |
Score |
| 2020 |
Tekin AM, de Ceulaer G, Govaerts P, Bayazit Y, Wuyts W, Van de Heyning P, Topsakal V. A New Pathogenic Variant in the TRIOBP Associated with Profound Deafness Is Remediable with Cochlear Implantation. Audiology & Neuro-Otology. 1-9. PMID 32877897 DOI: 10.1159/000508434 |
0.304 |
|
| 2015 |
Battmer RD, Borel S, Brendel M, Buchner A, Cooper H, Fielden C, Gazibegovic D, Goetze R, Govaerts P, Kelleher K, Lenartz T, Mosnier I, Muff J, Nunn T, Vaerenberg B, et al. Assessment of 'Fitting to Outcomes Expert' FOX™ with new cochlear implant users in a multi-centre study. Cochlear Implants International. 16: 100-9. PMID 25118042 DOI: 10.1179/1754762814Y.0000000093 |
0.322 |
|
| 2015 |
Buechner A, Vaerenberg B, Gazibegovic D, Brendel M, De Ceulaer G, Govaerts P, Lenarz T. Evaluation of the 'Fitting to Outcomes eXpert' (FOX®) with established cochlear implant users. Cochlear Implants International. 16: 39-46. PMID 24950595 DOI: 10.1179/1754762814Y.0000000085 |
0.3 |
|
| 2012 |
Schauwers K, Coene MMR, Heeren W, Bo LD, Pascu A, Vaerenberg B, Govaerts P. Perception of Pitch Changes in Hearing-Impaired Adults with Aided and Unaided Hearing Loss Journal of Hearing Science. 2012: 25-34. DOI: 10.17430/883510 |
0.333 |
|
| 2009 |
Hilgert N, Huentelman MJ, Thorburn AQ, Fransen E, Dieltjens N, Mueller-Malesinska M, Pollak A, Skorka A, Waligora J, Ploski R, Castorina P, Primignani P, Ambrosetti U, Murgia A, Orzan E, ... ... Govaerts P, et al. Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene. European Journal of Human Genetics : Ejhg. 17: 517-24. PMID 18985073 DOI: 10.1038/Ejhg.2008.201 |
0.341 |
|
| 2007 |
Declau F, Van den Bogaert K, Van De Heyning P, Offeciers E, Govaerts P, Van Camp G. Phenotype-genotype correlations in otosclerosis: clinical features of OTSC2. Advances in Oto-Rhino-Laryngology. 65: 114-8. PMID 17245031 DOI: 10.1159/000098745 |
0.551 |
|
| 2006 |
Govaerts PJ, Daemers K, Yperman M, De Beukelaer C, De Saegher G, De Ceulaer G. Auditory speech sounds evaluation (A§E®): A new test to assess detection, discrminination and identification in hearing impairment Cochlear Implants International. 7: 92-106. DOI: 10.1179/146701006807508106 |
0.307 |
|
| 2002 |
Van Den Bogaert K, Govaerts PJ, De Leenheer EM, Schatteman I, Verstreken M, Chen W, Declau F, Cremers CW, Van De Heyning PH, Offeciers FE, Somers T, Smith RJ, Van Camp G. Otosclerosis: a genetically heterogeneous disease involving at least three different genes. Bone. 30: 624-30. PMID 11934656 DOI: 10.1016/S8756-3282(02)00679-8 |
0.576 |
|
| 2001 |
Van Den Bogaert K, Govaerts PJ, Schatteman I, Brown MR, Caethoven G, Offeciers FE, Somers T, Declau F, Coucke P, Van de Heyning P, Smith RJ, Van Camp G. A second gene for otosclerosis, OTSC2, maps to chromosome 7q34-36. American Journal of Human Genetics. 68: 495-500. PMID 11170898 DOI: 10.1086/318185 |
0.587 |
|
| 1998 |
Govaerts PJ, De Ceulaer G, Daemers K, Verhoeven K, Van Camp G, Schatteman I, Verstreken M, Willems PJ, Somers T, Offeciers FE. A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss. The American Journal of Otology. 19: 718-23. PMID 9831143 |
0.383 |
|
| 1998 |
Verhoeven K, Van Laer L, Kirschhofer K, Legan PK, Hughes DC, Schatteman I, Verstreken M, Van Hauwe P, Coucke P, Chen A, Smith RJ, Somers T, Offeciers FE, Van de Heyning P, Richardson GP, ... ... Govaerts PJ, et al. Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment. Nature Genetics. 19: 60-2. PMID 9590290 DOI: 10.1038/ng0598-60 |
0.301 |
|
| 1997 |
Verhoeven K, Van Camp G, Govaerts PJ, Balemans W, Schatteman I, Verstreken M, Van Laer L, Smith RJ, Brown MR, Van de Heyning PH, Somers T, Offeciers FE, Willems PJ. A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24. American Journal of Human Genetics. 60: 1168-73. PMID 9150164 |
0.368 |
|
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