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Archives of Ophthalmology (Chicago, Ill. : 1960)|February 14, 2007
Perspective on genes and mutations causing retinitis pigmentosaStephen P Daiger, Sara J Bowne, Lori S SullivanCold Spring Harbor Perspectives in Medicine|October 12, 2014
Genes and Mutations Causing Autosomal Dominant Retinitis PigmentosaStephen P Daiger, Sara J Bowne, Lori S SullivanCold Spring Harbor Perspectives in Medicine|October 3, 2023
History of Finding Genes and Mutations Causing Inherited Retinal DiseasesStephen P Daiger, Lori S Sullivan, Elizabeth L Cadena, et al.Advances in Experimental Medicine and Biology|March 19, 2010
Investigating the mechanism of disease in the RP10 form of retinitis pigmentosaCatherine J Spellicy, Dong Xu, Garrett Cobb, et al.Investigative Ophthalmology & Visual Science|January 7, 2018
Molecular Defects of the Disease-Causing Human Arrestin-1 C147F MutantSergey A Vishnivetskiy, Lori S Sullivan, Sara J Bowne, et al.American Journal of Ophthalmology|December 25, 2018
Time Course of Disease Progression of PRPF31-mediated Retinitis PigmentosaKelly Kiser, Kaylie D Webb-Jones, Sara J Bowne, et al.Ophthalmic Genetics|July 2, 2010
PITPNM3 is an uncommon cause of cone and cone-rod dystrophiesLinda Köhn, Susanne Kohl, Sara J Bowne, et al.Molecular Vision|October 26, 2007
Characterization of retinal inosine monophosphate dehydrogenase 1 in several mammalian speciesCatherine J Spellicy, Stephen P Daiger, Lori S Sullivan, et al.Current Eye Research|October 17, 2003
Exclusion of the human collagen type XVII (COL17A1) gene as the cause of Thiel-Behnke corneal dystrophy (CDB2) on chromosome 10q23-q25Lori S Sullivan, Xinping Zhao, Sara J Bowne, et al.Advances in Experimental Medicine and Biology|December 30, 2019
Detection of Large Structural Variants Causing Inherited Retinal DiseasesStephen P Daiger, Lori S Sullivan, Sara J Bowne, et al.Pageof 6