Robert Wilke - Concepedia

Author

Robert Wilke

University of Tübingen

Also Known As

R G H Wilke, R WILKE, R Wilke, R. Wilke, Robert G. H. Wilke, Robert G.H. Wilke, Robert Wilke, Wilke, Robert

104

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

University of Tübingen STZ eyetrial UNSW Sydney Natural and Medical Sciences Institute Steinbeis Foundation

About

Robert Wilke is an author at University of Tübingen specializing in ophthalmology, neuroscience, and social sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Social Sciences	9	9	280
2	Medicine	8	8	294
3	Biomedical Engineering	7	7	230
4	Engineering	5	5	203
5	Public Health	1	1	13

Robert Wilke

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Subretinal electronic chips allow blind patients to read letters and combine them to words Eberhart Zrenner, Karl Ulrich Bartz‐Schmidt, Heval Benav, Proceedings of the Royal Society B Biological Sciences	2010	819
Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy Katharina Agnes Wycisk, Christina Zeitz, Silke Feil, The American Journal of Human Genetics ChannelopathiesMolecular NeuroscienceGenetic DisorderGeneticsDegenerative Disease	2006	163
Spatial Resolution and Perception of Patterns Mediated by a Subretinal 16-Electrode Array in Patients Blinded by Hereditary Retinal Dystrophies Robert Wilke, Veit‐Peter Gabel, Helmut Sachs, Investigative Ophthalmology & Visual Science	2011	154
Extraocular surgery for implantation of an active subretinal visual prosthesis with external connections: feasibility and outcome in seven patients Dorothea Besch, H. Sachs, Peter Szurman, British Journal of Ophthalmology	2008	113
Electric crosstalk impairs spatial resolution of multi-electrode arrays in retinal implants Robert Wilke, Gita Khalili Moghaddam, Nigel H. Lovell, Journal of Neural Engineering Electrical EngineeringGanglion CellEngineeringRetinal ImplantsOphthalmology	2011	113
Structure-Function Correlation of the Human Central Retina Peter Charbel Issa, Eric Troeger, Robert P. Finger, Minerva Access (University of Melbourne)	2010	88
Mutation Screening of 299 Spanish Families with Retinal Dystrophies by Leber Congenital Amaurosis Genotyping Microarray Elena Vallespín, Diego Cantalapiedra, Rosa Riveiro-Álvarez, Investigative Ophthalmology & Visual Science	2007	85
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
Basic Quantitative Assessment of Visual Performance in Patients with Very Low Vision Michael Bach, Michaela Wilke, Barbara Wilhelm, Investigative Ophthalmology & Visual Science	2010	68
The Phenotype of Early-Onset Retinal Degeneration in Persons with<i>RDH12</i>Mutations Andreas Schuster, Andreas Janecke, Robert Wilke, Investigative Ophthalmology & Visual Science	2007	55

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