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Ebiomedicine|January 9, 2021
Childhood-onset genetic cone-rod photoreceptor diseases and underlying pathobiologyAlexandra V Garafalo, Rebecca Sheplock, Alexander Sumaroka, et al.Journal of Sleep Research|May 19, 2024
Sleep health among US Navy afloat versus ashore personnel in the Millennium Cohort StudyIsabel G Jacobson, Judith Harbertson, Neika Sharifian, et al.Investigative Ophthalmology & Visual Science|July 29, 2003
De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosaSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophySamuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.Investigative Ophthalmology & Visual Science|April 1, 1994
Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosaS G Jacobson, C M Kemp, A V Cideciyan, et al.Primary Care Companion to the Journal of Clinical Psychiatry|July 4, 2007
The 3-year clinical and functional course of schizophrenia among individuals with and without diabetes at study entryHaya Ascher-Svanum, Baojin Zhu, Frank R Ernst, et al.Journal of Diabetes|September 29, 2018
Concentrated insulins: History and critical reappraisalLutz Heinemann, John M Beals, James Malone, et al.American Journal of Human Genetics|June 22, 2002
Mutations in the cone photoreceptor G-protein alpha-subunit gene GNAT2 in patients with achromatopsiaSusanne Kohl, Britta Baumann, Thomas Rosenberg, et al.Investigative Ophthalmology & Visual Science|January 24, 2013
Intervisit variability of visual parameters in Leber congenital amaurosis caused by RPE65 mutationsAlejandro J Roman, Artur V Cideciyan, Sharon B Schwartz, et al.Ophthalmic Genetics|March 1, 1996
Analysis of phosducin as a candidate gene for retinopathiesF Ara-Iwata, S G Jacobson, J D Gass, et al.Pageof 57