Inga Ebermann

PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome

Inga Ebermann, Jennifer B. Phillips, Max C. Liebau et al. · Journal of Clinical Investigation · 2010 · 245 citations · Full text

Medicine, Immunology, Ophthalmology +13

A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss

Inga Ebermann, Hendrik P. N. Scholl, Peter Charbel Issa et al. · Human Genetics · 2006 · 233 citations

Life Sciences, Genetics, Molecular Genetics +11

Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics

Claudia Dafinger, Max C. Liebau, Solaf M. Elsayed et al. · Journal of Clinical Investigation · 2011 · 214 citations

Life Sciences, Cell Biology, Genetics +17

Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice

Iman Sahly, Éric Dufour, Cataldo Schietroma et al. · The Journal of Cell Biology · 2012 · 191 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

Truncating mutation of the<i>DFNB59</i>gene causes cochlear hearing impairment and central vestibular dysfunction

Inga Ebermann, Martin Walger, Hendrik P. N. Scholl et al. · Human Mutation · 2007 · 90 citations

Life Sciences, Genetics, Molecular Genetics +17