Gregory B. Willer

Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish.

D. Hyde, B. Link, R. Gregg, 2006, Developmental biology.

Phosphatidylinositol synthase is required for lens structural integrity and photoreceptor cell survival in the zebrafish eye.

C. Watson, D. Hyde, V. Bankaitis, 2011, Experimental eye research.

Zebrafish blowout provides genetic evidence for Patched1-mediated negative regulation of Hedgehog signaling within the proximal optic vesicle of the vertebrate eye.

Jiwoon Lee, R. Gregg, J. Willer, 2008, Developmental biology.

Muscle Contractions Guide Rohon–Beard Peripheral Sensory Axons

R. Gregg, J. Willer, M. Halloran, 2009, The Journal of Neuroscience.

Mutations in Zebrafish lrp2 Result in Adult-Onset Ocular Pathogenesis That Models Myopia and Other Risk Factors for Glaucoma

Richard S. Smith, D. Wagner, S. John, 2011, PLoS genetics.

Mechanisms Underlying Metabolic and Neural Defects in Zebrafish and Human Multiple Acyl-CoA Dehydrogenase Deficiency (MADD)

R. Balice-Gordon, C. Watson, M. Selak, 2009, PloS one.

The loss of vacuolar protein sorting 11 (vps11) causes retinal pathogenesis in a vertebrate model of syndromic albinism.

D. Hyde, R. Gregg, A. denDekker, 2011, Investigative ophthalmology & visual science.

Positional cloning of the young mutation identifies an essential role for the Brahma chromatin remodeling complex in mediating retinal cell differentiation

J. Dowling, J. M. Fadool, B. Link, 2003, Proceedings of the National Academy of Sciences of the United States of America.