• Publications
  • Influence

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  • Carsten Matthias Pusch, Christina Zeitz, +12 authors Alfons Meindl
  • Medicine, Biology
  • Nature Genetics
  • 2000 (First Publication: 1 November 2000)
  • X-linked congenital stationary night blindness (XLCSNB) is characterized by impaired scotopic vision with associated ocular symptoms such as myopia, hyperopia, nystagmus and reduced visual acuity.Expand
  • Francesca Donaudy, Rik L Snoeckx, +16 authors Anna Savoia
  • Biology, Medicine
  • American journal of human genetics
  • 2004 (First Publication: 1 April 2004)
  • Myosins have been implicated in various motile processes, including organelle translocation, ion-channel gating, and cytoskeleton reorganization. Different members of the myosin superfamily areExpand
  • Carsten Matthias Pusch, Lutz Bachmann
  • Medicine, Biology
  • Molecular biology and evolution
  • 2004 (First Publication: 22 January 2004)
  • Proof of authenticity is the greatest challenge in palaeogenetic research, and many safeguards have become standard routine in laboratories specialized on ancient DNA research. Here we describe anExpand
  • Carsten Matthias Pusch, Martina Broghammer, Bernhard Jurklies, Dorothea Besch, Felix Jacobi
  • Medicine, Biology
  • Human mutation
  • 2002 (First Publication: 1 November 2002)
  • RGPR was the first gene found to be mutated in XLRP, the subtype of RP displaying the most severe form of retinal degeneration with partial or complete blindness in the third or fourth decade ofExpand