A. Schuster

The phenotype of early-onset retinal degeneration in persons with RDH12 mutations.

E. Zrenner, R. Wilke, G. Utermann, 2007, Investigative Ophthalmology and Visual Science.

Multifocal oscillatory potentials in CSNB1 and CSNB2 type congenital stationary night blindness.

E. Zrenner, C. Pusch, A. Kurtenbach, 2005, International journal of molecular medicine.

Mapping of retinal function in Best macular dystrophy using multifocal electroretinography

E. Zrenner, R. Vonthein, H. Scholl, 2002, Vision Research.

A Novel Homozygous WDR72 Mutation in Two Siblings with Amelogenesis Imperfecta and Mild Short Stature

J. Hentschel, D. Wieczorek, I. Kurth, 2012, Molecular Syndromology.

Mutation analysis of NR2E3 and NRL genes in Enhanced S Cone Syndrome

A. V. Cideciyan, T. Aleman, A. Cideciyan, 2004, Human mutation.

Autoimmune Retinopathy with RPE Hypersensitivity and ‘Negative ERG’ in X-Linked Hyper-IgM Syndrome

E. Zrenner, C. Pusch, C. Thirkill, 2005, Ocular immunology and inflammation.

Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa

E. Zrenner, D. Besch, H. Jägle, 2005, British Journal of Ophthalmology.