Karin Kirschhofer

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Kristien Verhoeven, Lut Van Laer, Karin Kirschhofer et al. · Nature Genetics · 1998 · 335 citations

Developmental Biology, Genetic Disorder, Genetics +10

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

Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family

Karin Kirschhofer, Judith B. Kenyon, D.M. Hoover et al. · Cytogenetic and Genome Research · 1998 · 43 citations

Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria

Klemens Frei, Reinhard Ramsebner, Trevor Lucas et al. · Hearing Research · 2004 · 26 citations

Developmental Biology, Genetic Disorder, Genetics +8

Emergence of Myogenic and Endothelial Cell Lineages in Avian Embryos

Karin Kirschhofer, Miloš Grim, Bodo Christ et al. · Developmental Biology · 1994 · 24 citations

Biology, Embryonic Stem Cell, Cell Lineage +9