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 · 250 citations · Full text

Ophthalmology, Genetic Disorder, Genetics +2

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 citations · Full text

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 · 132 citations · Full text

Ocular Disease, Developmental Biology, Mendelian Disorder +6

MORPHOLOGY AND FUNCTIONAL CHARACTERISTICS IN ADULT VITELLIFORM MACULAR DYSTROPHY

Agnes B. Renner, H. Tillack, Hannelore Kraus et al. · Retina · 2004 · 91 citations

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 · 86 citations · Full text

Ocular Disease, Genetics, Genetic Epidemiology +17