Ghent University Academic Bibliography

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GRM7 variants confer susceptibility to age-related hearing impairment

RA Friedman, Lut Van Laer (UGent) , MJ Huentelman, SS Sheth, E Van Eyken, JJ Corneveaux, WD Tembe, RF Halperin, AQ Thorburn, S Thys, et al.

(2009) HUMAN MOLECULAR GENETICS. 18(4). p.785-796
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- Journal Article
- A1
Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait

JR Huyghe, Lut Van Laer (UGent) , JJ Hendrickx, E Fransen, K Demeester, V Topsakal, S Kunst, M Manninen, M Jensen, A Bonaconsa, et al.

(2008) AMERICAN JOURNAL OF HUMAN GENETICS. 83(3). p.401-407
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The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

Lut Van Laer (UGent) , E VAN EYKEN, E FRANSEN, Jeroen HUYGHE, V TOPSAKAL, JJ HENDRICKX, S HANNULA, E MAKI-TORKKO, M JENSEN, K DEMEESTER, et al.

(2008) HUMAN MOLECULAR GENETICS. 17(2). p.159-169
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Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment

E VAN EYKEN, G VAN CAMP, E FRANSEN, V TOPSAKAL, JJ HENDRICKX, K DEMEESTER, PV DE HEYNING, EM KI-TORKKO, S HANNULA, M SORRI, et al.

(2007) JOURNAL OF MEDICAL GENETICS. 44(9).
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Stickler syndrome type I and stapes ankylosis

LWJ BAIJENS, EMR DE LEENHEER, HH WEEKAMP, JRM CRUYSBERG, Geert Mortier (UGent) and CWRJ CREMERS

(2004) INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY. 68(12). p.1573-1580
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A novel mutation identified in the DFNA5 gene in a Dutch family: A clinical and genetic evaluation

AMLC Bischoff, MWJ Luijendijk, PLM Huygen, G van Duijnhoven, Els De Leenheer (UGent) , GG Oudesluijs, Lut Van Laer (UGent) , FPM Cremers, CWRJ Cremers and H Kremer

(2004) AUDIOLOGY AND NEURO-OTOLOGY. 9(1). p.34-46
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The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the Branchio-Oto-Renal syndrome. A family study.

C STINCKENS, Lien Standaert (UGent) , Jan Casselman (UGent) , PLM HUYGEN, S KUMAR, J VAN DE WALLEN and CWRJ CREMERS

(2001) INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY. 59(3). p.163-172
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Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNA(Ser(UCN)) gene

K Verhoeven, RJH Ensink, V Tiranti, PLM Huygen, DF Johnson, I Schatteman, Lut Van Laer (UGent) , M Verstreken, P Van de Heyning, N Fischel-Ghodsian, et al.

(1999) EUROPEAN JOURNAL OF HUMAN GENETICS. 7(1). p.45-51

Academic Bibliography

GRM7 variants confer susceptibility to age-related hearing impairment

Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait

The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment

Stickler syndrome type I and stapes ankylosis

A novel mutation identified in the DFNA5 gene in a Dutch family: A clinical and genetic evaluation

The presence of a widened vestibular aqueduct and progressive sensorineural hearing loss in the Branchio-Oto-Renal syndrome. A family study.

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNA(Ser(UCN)) gene

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