Veronique Kitiratschky

Identification and Functional Characterization of Complement Regulator-Acquiring Surface Protein 1 of the Lyme Disease Spirochetes<i>Borrelia afzelii</i>and<i>Borrelia garinii</i>

Reinhard Wallich, Joseph Pattathu, Veronique Kitiratschky et al. · Infection and Immunity · 2005 · 106 citations · Full text

Microbial Pathogens, Immunology, Molecular Biology +17

Mutations in the<i>GUCA1A</i>gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase

Veronique Kitiratschky, Petra Behnen, Ulrich Kellner et al. · Human Mutation · 2009 · 81 citations · Full text

Ocular Disease, Genetics, Molecular Biology +20

Mutation Analysis Identifies<i>GUCY2D</i>as the Major Gene Responsible for Autosomal Dominant Progressive Cone Degeneration

Veronique Kitiratschky, Robert Wilke, Agnes B. Renner et al. · Investigative Ophthalmology & Visual Science · 2008 · 68 citations

ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies

Veronique Kitiratschky, Tanja Grau, Antje Bernd et al. · European Journal of Human Genetics · 2008 · 60 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Safety evaluation of “retina implant alpha IMS”—a prospective clinical trial

Veronique Kitiratschky, Katarína Štingl, Barbara Wilhelm et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 2014 · 51 citations

Retina, Ophthalmology, Eye Health +5