R.E. Hurd

Two mouse retinal degenerations caused by missense mutations in the β-subunit of rod cGMP phosphodiesterase gene

Bo Chang, Norman L. Hawes, Machelle T. Pardue et al. · Vision Research · 2007 · 422 citations · Full text

Medicine, Genetics, Molecular Genetics +16

In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouse

Bo Chang, Hemant Khanna, Norman L. Hawes et al. · Human Molecular Genetics · 2006 · 381 citations · Full text

Life Sciences, Cell Biology, Molecular Biology +17

A homologous genetic basis of the murine <i>cpfl1</i> mutant and human achromatopsia linked to mutations in the <i>PDE6C</i> gene

Bo Chang, Tanja Grau, Susann Dangel et al. · Proceedings of the National Academy of Sciences · 2009 · 187 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice

Karsten Boldt, Dorus A. Mans, Jungyeon Won et al. · Journal of Clinical Investigation · 2011 · 109 citations · Full text

Life Sciences, Cell Biology, Genetics +15

Survey of Common Eye Diseases in Laboratory Mouse Strains

Bo Chang, R.E. Hurd, Jieping Wang et al. · Investigative Ophthalmology & Visual Science · 2013 · 103 citations · Full text

Medicine, Genetics, Ophthalmology +15