Klemens Frei

A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (<i>OTOF</i>) in subjects with nonsyndromic hearing impairment and auditory neuropathy

Montserrat Rodríguez-Ballesteros, Raúl Reynoso, M. A. Gil Olarte et al. · Human Mutation · 2008 · 178 citations

The antioxidant activity of caroverine

Natalia Udilova, Andrey V. Kozlov, Werner Bieberschulte et al. · Biochemical Pharmacology · 2002 · 101 citations

Biochemistry, Medicine, Lipid Peroxidation +5

Connexin 26 mutations in cases of sensorineural deafness in eastern Austria

Klemens Frei, Károly Szuhai, Trevor Lucas et al. · European Journal of Human Genetics · 2002 · 74 citations · Full text

Audiology, Sensorineural Deafness, Cochlear Development +4

A homozygous deletion of a normal variation locus in a patient with hearing loss from non-consanguineous parents

Jeroen Knijnenburg, Saskia A.J. Lesnik Oberstein, Klemens Frei et al. · Journal of Medical Genetics · 2009 · 62 citations

Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene

Nele Hilgert, Matthew J. Huentelman, Ashley Q. Thorburn et al. · European Journal of Human Genetics · 2008 · 53 citations · Full text

Genetic Analysis, Allelic Variant, Phenotypic Variation +8