E. Ferda Perçin

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

E. Ferda Perçin, Horsford Dj, A.J. Rutherford et al. · Nature Genetics · 2000 · 286 citations

Ocular Disease, Developmental Biology, Retina +8

Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome

Hans van Bokhoven, Jacopo Celli, Hülya Kayserili et al. · Nature Genetics · 2000 · 270 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +7

Blood-Derived Human iPS Cells Generate Optic Vesicle–Like Structures with the Capacity to Form Retinal Laminae and Develop Synapses

M. Joseph Phillips, Kyle A. Wallace, Sarah Dickerson et al. · Investigative Ophthalmology & Visual Science · 2012 · 205 citations · Full text

LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and Kidney Malformations in Cenani-Lenz Syndrome

Yun Li, Barbara Pawlik, Nursel Elçioğlu et al. · The American Journal of Human Genetics · 2010 · 163 citations · Full text

Modeling Human Retinal Development with Patient-Specific Induced Pluripotent Stem Cells Reveals Multiple Roles for Visual System Homeobox 2

M. Joseph Phillips, Enio T. Perez, Jessica Martin et al. · Stem Cells · 2014 · 123 citations · Full text

Optogenetics, Cell Specialization, Ganglion Cell +16