Agnes B. Renner - Concepedia

Concepedia

Author

Agnes B. Renner

Charité - Universitätsmedizin Berlin

Also Known As

AGNES B. RENNER, AGNES RENNER, Agnes B Renner, Agnes B. Renner, Agnes Renner, Agnes B. Renner, Carsten Framme

41

Publications

1.6K

Citations

19

H-Index

30

Concepts

All Affiliations

Charité - Universitätsmedizin Berlin University of Regensburg University Hospital Regensburg Helios Hospital Siegburg Franklin University

AB

About

Agnes B. Renner is an author at Charité - Universitätsmedizin Berlin specializing in medicine, ophthalmology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	13	914
2	Public Health	1	1	86
3	Social Sciences	1	1	18
4	Allergy	1	1	18
5	Gastroenterology	1	1	14

Agnes B. Renner

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25

Publications

1.6K

Citations

18

H-Index

	Year	Citations
TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness Isabelle Audo, Susanne Kohl, Bart P. Leroy, The American Journal of Human Genetics OphthalmologyGenetic DisorderGeneticsTrpm1 Is MutatedMedicine	2009	250
Fundus Autofluorescence and mfERG for Early Detection of Retinal Alterations in Patients Using Chloroquine/Hydroxychloroquine Ulrich Kellner, Agnes B. Renner, H. Tillack Investigative Ophthalmology & Visual Science	2006	152
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness Isabelle Audo, Kinga M. Bujakowska, Elise Orhan, The American Journal of Human Genetics Ocular DiseaseDevelopmental BiologyMendelian DisorderOphthalmologyGenetic Disorder	2012	132
MORPHOLOGY AND FUNCTIONAL CHARACTERISTICS IN ADULT VITELLIFORM MACULAR DYSTROPHY Agnes B. Renner, H. Tillack, Hannelore Kraus, Retina	2004	91
A Subgroup of Age-Related Macular Degeneration is Associated With Mono-Allelic Sequence Variants in the<i>ABCA4</i>Gene Lars G. Fritsche, Monika Fleckenstein, Britta Fiebig, Investigative Ophthalmology & Visual Science Ocular DiseaseGeneticsGenetic EpidemiologyAge-related Macular DegenerationMolecular Genetics	2012	86
Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis Pigmentosa Thomas Langmann, Silvio Alessandro Di Gioia, Isabella Rau, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsMolecular Genetics	2010	83
Phenotypic Variability and Long-term Follow-up of Patients With Known and Novel PRPH2/RDS Gene Mutations Agnes B. Renner, Britta Fiebig, Bernhard H. F. Weber, American Journal of Ophthalmology Somatic VariantGenetic DisorderMedicineGeneticsPhenotypic Variability	2008	78
Choroideremia: Variability of Clinical and Electrophysiological Characteristics and First Report of a Negative Electroretinogram Agnes B. Renner, Ulrich Kellner, Elke Cropp, Ophthalmology Electrolyte DisorderPhysiologyElectrolyte DisturbanceElectrophysiological CharacteristicsElectrophysiology	2006	76
Variety of genotypes in males diagnosed as dichromatic on a conventional clinical anomaloscope Maureen Neitz, Joseph Carroll, Agnes B. Renner, Visual Neuroscience	2004	74
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

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