Silke Feil

Positional cloning of the gene for X-linked retinitis pigmentosa 2

Uwe Schwahn, Steffen Lenzner, Juan Dong et al. · Nature Genetics · 1998 · 382 citations

Life Sciences, Genetics, Molecular Genetics +7

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

Carsten M. Pusch, Christina Zeitz, Oliver Brandau et al. · Nature Genetics · 2000 · 260 citations

Medicine, Genetics, Molecular Genetics +13

Mutation in the Auxiliary Calcium-Channel Subunit CACNA2D4 Causes Autosomal Recessive Cone Dystrophy

Katharina Agnes Wycisk, Christina Zeitz, Silke Feil et al. · The American Journal of Human Genetics · 2006 · 166 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Role of the Norrie Disease Pseudoglioma Gene in Sprouting Angiogenesis during Development of the Retinal Vasculature

Ulrich F. O. Luhmann, Jihong Lin, Niyazi Acar et al. · Investigative Ophthalmology & Visual Science · 2005 · 155 citations

Medicine, Developmental Biology, Ophthalmology +17

RPGR Transcription Studies in Mouse and Human Tissues Reveal a Retina-Specific Isoform That Is Disrupted in a Patient With X-Linked Retinitis Pigmentosa

Thomas Rosenberg, Robert Schultz‐Heienbrok, Steffen Lenzner et al. · Human Molecular Genetics · 1999 · 146 citations

Medicine, Genetics, Molecular Genetics +12