Catherine J. Spellicy

Prevalence of Disease-Causing Mutations in Families with Autosomal Dominant Retinitis Pigmentosa: A Screen of Known Genes in 200 Families

Lori S. Sullivan, Sara J. Bowne, David G. Birch et al. · Investigative Ophthalmology & Visual Science · 2006 · 287 citations · Full text

Life Sciences, Genetics, Ophthalmology +16

Spectrum and Frequency of Mutations in IMPDH1 Associated with Autosomal Dominant Retinitis Pigmentosa and Leber Congenital Amaurosis

Sara J. Bowne, Lori S. Sullivan, Sarah Mortimer et al. · Investigative Ophthalmology & Visual Science · 2005 · 166 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Why Do Mutations in the Ubiquitously Expressed Housekeeping Gene<i>IMPDH1</i>Cause Retina-Specific Photoreceptor Degeneration?

Sara J. Bowne, Qin Liu, Lori S. Sullivan et al. · Investigative Ophthalmology & Visual Science · 2006 · 71 citations · Full text

Medicine, Genetics, Molecular Genetics +17

ANKK1 and DRD2 pharmacogenetics of disulfiram treatment for cocaine abuse

Catherine J. Spellicy, Thomas R. Kosten, Sara Hamon et al. · Pharmacogenetics and Genomics · 2013 · 31 citations

Medicine, Pharmacology, Pharmacotherapy +17

Characterization of retinal inosine monophosphate dehydrogenase 1 in several mammalian species.

Catherine J. Spellicy, Stephen P. Daiger, Lori S. Sullivan et al. · PubMed · 2007 · 27 citations

Life Sciences, Biochemistry, Molecular Biology +11