All Stories

  1. Phenotypic Progression of Stargardt Disease in a Large Consanguineous Tunisian Family Harboring New ABCA4 Mutations

    Article • Journal of Ophthalmology, January 2018, Hindawi Publishing Corporation

    Professor Daniel F Schorderet

  2. Shaken, Not Stirred Collagen in Corneal Dystrophy

    Article • Human Mutation, March 2015, Wiley

    Professor Daniel F Schorderet

  3. Abrogation of HMX1 Function Causes Rare Oculoauricular Syndrome Associated With Congenital Cataract, Anterior Segment Dysgenesis, and Retinal Dystrophy

    Article • Investigative Ophthalmology & Visual Science, January 2015, Association for Research in Vision and Ophthalmology (ARVO)

    Professor Daniel F Schorderet

  4. A Dimerized HMX1 Inhibits EPHA6/epha4b in Mouse and Zebrafish Retinas

    Article • PLoS ONE, June 2014, PLOS

    Professor Daniel F Schorderet

  5. Zebrafish hmx1 promotes retinogenesis

    Article • Experimental Eye Research, December 2012, Elsevier

    Professor Daniel F Schorderet

  6. Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome

    Article • The American Journal of Human Genetics, May 2008, Elsevier

    Professor Daniel F Schorderet

  7. Identification of the minimal promoter region of the mouse NKX5-3, a transcription factor implicated in eye development

    Article • Gene, March 2008, Elsevier

    Professor Daniel F Schorderet