Veronique Kitiratschky

Author

Also Known As

Kitiratschky, Veronique, V B D Kitiratschky, V KITIRATSCHKY, V. Kitiratschky, Veronique B D Kitiratschky, Veronique B. D. Kitiratschky, Veronique B.D. Kitiratschky, Veronique Kitiratschky

Publications

534

Citations

H-Index

Concepts

All Affiliations

University of Tübingen STZ eyetrial Heidelberg University Goethe University Frankfurt Max Planck Institute of Immunobiology and Epigenetics

About

Veronique Kitiratschky is an author at University of Tübingen specializing in medicine, molecular genetics, and immunology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	371
2	Natural Sciences	2	2	133
3	Biomedical Engineering	1	1	51
4	Cell Biology	1	1	81
5	Cellular Physiology	1	1	81

Veronique Kitiratschky

Publications

524

Citations

H-Index

Page 1

	Year	Citations
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, Infection and Immunity Microbial PathogensImmunologyMolecular BiologyHost SpecificityTick-borne Disease	2005	106
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, Human Mutation Ocular DiseaseGeneticsMolecular BiologyMolecular GeneticsOptogenetics	2009	81
Mutation Analysis Identifies<i>GUCY2D</i>as the Major Gene Responsible for Autosomal Dominant Progressive Cone Degeneration Veronique Kitiratschky, Robert Wilke, Agnes B. Renner, Investigative Ophthalmology & Visual Science	2008	68
ABCA4 gene analysis in patients with autosomal recessive cone and cone rod dystrophies Veronique Kitiratschky, Tanja Grau, Antje Bernd, European Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyDegenerative Disease	2008	60
Safety evaluation of “retina implant alpha IMS”—a prospective clinical trial Veronique Kitiratschky, Katarína Štingl, Barbara Wilhelm, Graefe s Archive for Clinical and Experimental Ophthalmology RetinaOphthalmologyEye HealthGlaucomaBiomedical Engineering	2014	51
Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation Veronique Kitiratschky, D. Nagy, T Zabel, British Journal of Ophthalmology	2008	29
Mutational analyses of the BbCRASP-1 protein of Borrelia burgdorferi identify residues relevant for the architecture and binding of host complement regulators FHL-1 and factor H Peter Kraiczy, Christa Hanssen-Hübner, Veronique Kitiratschky, International Journal of Medical Microbiology Complement SystemFactor HMutational AnalysesPathogenesisImmunology	2009	27
<i>Borrelia burgdorferi</i>Complement Regulator-Acquiring Surface Protein 1 of the Lyme Disease Spirochetes Is Expressed in Humans and Induces Antibody Responses Restricted to Nondenatured Structural Determinants Evelyn Rossmann, Veronique Kitiratschky, Heidelore Hofmann, Infection and Immunity Microbial PathogensPathogen PersistenceHumoral ResponseImmunologyImmune System	2006	25
Genes and Mutations in Autosomal Dominant Cone and Cone-Rod Dystrophy Susanne Kohl, Veronique Kitiratschky, Monika Papke, Advances in experimental medicine and biology Mendelian DisorderGenetic DisorderGeneticsAutosomal Dominant ConePathology	2011	21
Associating the magnitude of relative afferent pupillary defect (RAPD) with visual field indices in glaucoma patients Ulrich Schiefer, Janko Dietzsch, Klaus Dietz, British Journal of Ophthalmology	2012	19

Page 1