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Molecular Vision|May 6, 1999
Identifying and mapping novel retinal-expressed ESTs from humansK Malone, M M Sohocki, L S Sullivan, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 23, 2001
Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humansM M Sohocki, L S Sullivan, D L Tirpak, et al.Genomics|May 20, 1999
Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disordersM M Sohocki, K A Malone, L S Sullivan, et al.Molecular Medicine Today|September 1, 1996
Inherited retinal degeneration: exceptional genetic and clinical heterogeneityL S Sullivan, S P DaigerOphthalmic Genetics|August 1, 2000
Visual phenotype in patients with Arg41Gln and ala196+1bp mutations in the CRX geneR T Tzekov, M M Sohocki, S P Daiger, et al.Genomics|March 1, 1997
Human glutamate pyruvate transaminase (GPT): localization to 8q24.3, cDNA and genomic sequences, and polymorphic sitesM M Sohocki, L S Sullivan, W R Harrison, et al.American Journal of Human Genetics|October 30, 1998
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor geneM M Sohocki, L S Sullivan, H A Mintz-Hittner, et al.Clinical Genetics|May 25, 2013
Genes and mutations causing retinitis pigmentosaS P Daiger, L S Sullivan, S J BowneInvestigative Ophthalmology & Visual Science|May 1, 2001
Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX geneR T Tzekov, Y Liu, M M Sohocki, et al.Human Mutation|January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesM M Sohocki, S P Daiger, S J Bowne, et al.Pageof 19