Agnes B. Renner

TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

Isabelle Audo, Susanne Kohl, Bart P. Leroy et al. · The American Journal of Human Genetics · 2009 · 262 citations · Full text

Life Sciences, Genetics, Neuroscience +10

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 · 153 citations · Full text

Health Professions, Ophthalmology, Vision Science +16

Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness

Isabelle Audo, Kinga M. Bujakowska, Elise Orhan et al. · The American Journal of Human Genetics · 2012 · 134 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

MORPHOLOGY AND FUNCTIONAL CHARACTERISTICS IN ADULT VITELLIFORM MACULAR DYSTROPHY

Agnes B. Renner, H. Tillack, Hannelore Kraus et al. · Retina · 2004 · 94 citations

Medicine, Genetics, Ophthalmology +17

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 et al. · Investigative Ophthalmology & Visual Science · 2012 · 88 citations · Full text

Medicine, Genetics, Ophthalmology +17