Wanda L. Hicks

Alms1-disrupted mice recapitulate human Alström syndrome

Gayle B. Collin, E. Cyr, Roderick T. Bronson et al. · Human Molecular Genetics · 2005 · 185 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

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

Mutations in Lama1 Disrupt Retinal Vascular Development and Inner Limiting Membrane Formation

Malia M. Edwards, Elmina Mammadova‐Bach, Fabien Alpy et al. · Journal of Biological Chemistry · 2010 · 91 citations · Full text

Medicine, Genetics, Ophthalmology +17

NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development

Jungyeon Won, Caralina Marín de Evsikova, Richard S. Smith et al. · Human Molecular Genetics · 2010 · 82 citations

Life Sciences, Genetics, Molecular Genetics +15

Elevation of 20-carbon long chain bases due to a mutation in serine palmitoyltransferase small subunit b results in neurodegeneration

Lihong Zhao, Stefka D. Spassieva, Kenneth Gable et al. · Proceedings of the National Academy of Sciences · 2015 · 81 citations

Life Sciences, Biochemistry, Neuroscience +15