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36. Nxnl2 splicing results in dual functions in neuronal cell survival and maintenance of cell integrity

52. Impact of the Usher syndrome on olfaction

54. Deletion of myosin VI causes slow retinal optic neuropathy and age-related macular degeneration (AMD)-relevant retinal phenotype

55. TALPID3 controls centrosome and cell polarity and the human ortholog KIAA0586 is mutated in Joubert syndrome (JBTS23)

59. New functions and signaling mechanisms for the class of adhesion G protein-coupled receptors

63. Mutation of POC1B in a Severe Syndromic Retinal Ciliopathy

73. MPP1 links the Usher protein network and the Crumbs protein complex in the retina

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