Ghent University Academic Bibliography

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Visual prognosis in USH2A-associated retinitis pigmentosa is worse for patients with Usher syndrome type IIa than for those with nonsyndromic retinitis pigmentosa

Laurence HM Pierrache, Bas P Hartel, Erwin van Wijk, Magda A Meester-Smoor, Frans PM Cremers, Elfride De Baere (UGent) , Julie De Zaeytijd (UGent) , Mary J van Schooneveld, Cor WRJ Cremers, Gislin Dagnelie, et al.

(2016) OPHTHALMOLOGY. 123(5). p.1151-1160
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Temporal bone imaging in osteogenesis imperfecta patients with hearing loss

Freya Swinnen (UGent) , Jan Casselman (UGent) , Els De Leenheer (UGent) , Cor WRJ Cremers and Ingeborg Dhooge (UGent)

(2013) LARYNGOSCOPE. 123(8). p.1988-1995
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Familial aggregation of pure tone hearing thresholds in an aging European population

Jan-Jaap Hendrickx, Jeroen R Huyghe, Vedat Topsakal, Kelly Demeester, Thomas R Wienker, Lut Van Laer (UGent) , Els Van Eyken, Erik Fransen, Elina Mäki-Torkko, Samuli Hannula, et al.

(2013) OTOLOGY & NEUROTOLOGY. 34(5). p.838-844
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Stapes surgery in osteogenesis imperfecta: retrospective analysis of 34 operated ears

Freya Swinnen (UGent) , Els De Leenheer (UGent) , Paul Coucke (UGent) , Cor WRJ Cremers and Ingeborg Dhooge (UGent)

(2012) AUDIOLOGY AND NEURO-OTOLOGY. 17(3). p.198-206
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Association between bone mineral density and hearing loss in osteogenesis imperfecta

Freya Swinnen (UGent) , Els De Leenheer (UGent) , Stefan Goemaere (UGent) , Cor WRJ Cremers, Paul Coucke (UGent) and Ingeborg Dhooge (UGent)

(2012) LARYNGOSCOPE. 122(2). p.401-408
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- Journal Article
- A1
- open access
Audiologic phenotype of osteogenesis imperfecta: use in clinical differentiation

Freya Swinnen (UGent) , Ingeborg Dhooge (UGent) , Paul Coucke (UGent) , Patrizia D'Eufemia, Francesco Zardo, Ton JTM Garretsen, Cor WRJ Cremers and Els De Leenheer (UGent)

(2012) OTOLOGY & NEUROTOLOGY. 33(2). p.115-122
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- Journal Article
- A1
- open access
Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype

Freya Swinnen (UGent) , Paul Coucke (UGent) , Anne De Paepe (UGent) , Sofie Symoens (UGent) , Fransiska Malfait (UGent) , Filomena V Gentile, Luca Sangiorgi, Patrizia D'Eufemia, Mauro Celli, Ton JTM Garretsen, et al.

(2011) ORPHANET JOURNAL OF RARE DISEASES. 6.
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Audiometric, surgical, and genetic findings in 15 ears of patients with osteogenesis imperfecta

Freya Swinnen (UGent) , Els De Leenheer (UGent) , Paul Coucke (UGent) , Cor WRJ Cremers and Ingeborg Dhooge (UGent)

(2009) LARYNGOSCOPE. 119(6). p.1171-1179
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- Journal Article
- A1
No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch population

Isabelle Schrauwen, Melissa Thys, Kathleen Vanderstraeten, Erik Fransen, Megan Ealy, Cor WRJ Cremers, Ingeborg Dhooge (UGent) , Paul Van de Heyning, Erwin Offeciers, Richard JH Smith, et al.

(2009) OTOLOGY & NEUROTOLOGY. 30(8). p.1079-1083
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A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis

Isabelle Schrauwen, Megan Ealy, Matthew J Huentelman, Melissa Thys, Nils Homer, Kathleen Vanderstraeten, Erik Fransen, Jason J. Corneveaux, David W. Craig, Mireille Claustres, et al.

(2009) AMERICAN JOURNAL OF HUMAN GENETICS. 84(3). p.328-338

Academic Bibliography

Visual prognosis in USH2A-associated retinitis pigmentosa is worse for patients with Usher syndrome type IIa than for those with nonsyndromic retinitis pigmentosa

Temporal bone imaging in osteogenesis imperfecta patients with hearing loss

Familial aggregation of pure tone hearing thresholds in an aging European population

Stapes surgery in osteogenesis imperfecta: retrospective analysis of 34 operated ears

Association between bone mineral density and hearing loss in osteogenesis imperfecta

Audiologic phenotype of osteogenesis imperfecta: use in clinical differentiation

Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype

Audiometric, surgical, and genetic findings in 15 ears of patients with osteogenesis imperfecta

No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch population

A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis

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