Theo Peters

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

Heleen H. Arts, Dan Doherty, Sylvia E. C. van Beersum et al. · Nature Genetics · 2007 · 321 citations

Life Sciences, Genetics, Molecular Genetics +8

A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy

Marcel V. Alavi, Stefanie Bette, Simone Schimpf et al. · Brain · 2006 · 272 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Kidney failure in mice lacking the tetraspanin CD151

Norman Sachs, Maaike Kreft, Marius A. van den Bergh Weerman et al. · The Journal of Cell Biology · 2006 · 230 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

Erwin van Wijk, Bert van der Zwaag, Theo Peters et al. · Human Molecular Genetics · 2006 · 190 citations

Life Sciences, Genetics, Neuroscience +17

Antisense oligonucleotide-based treatment of retinitis pigmentosa caused by USH2A exon 13 mutations

Kalyan Dulla, Ralph Slijkerman, Hester C. van Diepen et al. · Molecular Therapy · 2021 · 142 citations · Full text

Medicine, Genetics, Molecular Genetics +14