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Seminars in Ophthalmology|December 20, 2022
Disparities in Inherited Retinal DegenerationsSarah Chorfi, Emily M Place, Rachel M Huckfeldt
Seminars in Ophthalmology|October 18, 2014
Systemic diseases associated with retinal dystrophiesXiang Q Werdich, Emily M Place, Eric A Pierce
Advances in Experimental Medicine and Biology|February 10, 2025
Novel Potentially Pathogenic Variants in TBC1D32 Cause Non-syndromic Rod-Cone DegenerationRiccardo Sangermano, Emily M Place, Eric A Pierce, et al.
American Journal of Ophthalmology Case Reports|June 14, 2019
Predictive value of genetic testing for inherited retinal diseases in patients with suspected atypical autoimmune retinopathyLynn K Stanwyck, Emily M Place, Jason Comander, et al.
Retinal Cases & Brief Reports|August 29, 2023
RP2 X-LINKED RETINITIS PIGMENTOSA CARRIER STATE PRESENTING WITH VASCULAR LEAKAGE AND UNILATERAL MACULAR ATROPHYEva Raparia, Brian G Ballios, Emily M Place, et al.
Seminars in Ophthalmology|March 10, 2016
Course of Ocular Function in PRPF31 Retinitis PigmentosaBrian P Hafler, Jason Comander, Carol Weigel DiFranco, et al.
Genes|December 24, 2021
Beyond Sector Retinitis Pigmentosa: Expanding the Phenotype and Natural History of the Rhodopsin Gene Codon 106 Mutation (Gly-to-Arg) in Autosomal Dominant Retinitis PigmentosaBrian G Ballios, Emily M Place, Luis Martinez-Velazquez, et al.
Stem Cell Research|December 22, 2023
Generation of a human induced pluripotent stem cell line (OGIi001) from peripheral blood mononuclear cells of a healthy male donorHanmeng Zhang, Laurence Daheron, Rodrigo Cerna-Chavez, et al.
Ophthalmic Genetics|July 14, 2022
Combined X-linked familial exudative vitreoretinopathy and retinopathy of prematurity phenotype in an infant with mosaic turner syndrome with ring X chromosomeSandra Hoyek, Marlene Wang, Audina M Berrocal, et al.
Cold Spring Harbor Molecular Case Studies|November 14, 2022
Identification of a novel large multigene deletion and a frameshift indel in <i>PDE6B</i> as the underlying cause of early-onset recessive rod-cone degenerationRiccardo Sangermano, Pooja Biswas, Lori S Sullivan, et al.
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