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Ophthalmic Genetics|September 3, 2015
Risk Factors for Second Eye Involvement in Eyes with Unilateral Polypoidal Choroidal VasculopathyYasushi Tateno, Yoichi Sakurada, Seigo Yoneyama, et al.
Ophthalmic Genetics|December 6, 2014
A distinct vitreo-retinal dystrophy with early-onset cataract from recessive KCNJ13 mutationsArif O Khan, Carsten Bergmann, Christine Neuhaus, et al.
Ophthalmic Genetics|January 14, 2020
Novel homozygous OPA3 mutation in an Afghani family with 3-methylglutaconic aciduria type III and optic atrophyEric D Gaier, Inderneel Sahai, Janey L Wiggs, et al.
Ophthalmic Genetics|February 20, 2020
The role of external beam radiation therapy for retinoblastoma after failure of combined chemoreduction and focal consolidation therapyYacoub A Yousef, Mona Mohammad, Imad Jaradat, et al.
Ophthalmic Genetics|February 11, 2020
Novel mutation in CTNNB1 causes familial exudative vitreoretinopathy (FEVR) and microcephaly: case report and review of the literatureRazek Georges Coussa, Yue Zhao, Meghan J DeBenedictis, et al.
Ophthalmic Genetics|March 7, 2020
Genetic testing for inherited ocular conditions in a developing countryMario Zanolli, Joaquín I Oporto, Juan I Verdaguer, et al.
Ophthalmic Genetics|August 19, 2017
Retinopathy and optic atrophy: Expanding the phenotypic spectrum of pathogenic variants in the AARS2 geneJason H Peragallo, Stephanie Keller, Marjo S van der Knaap, et al.
Ophthalmic Genetics|February 7, 2018
Identification of PITX3 mutations in individuals with various ocular developmental defectsCelia Zazo Seco, Julie Plaisancié, Tatiana Lupasco, et al.
Ophthalmic Genetics|January 17, 2018
Incidental neuroblastoma with bilateral retinoblastoma: what are the chances?Kelsey Roelofs, Furqan Shaikh, William Astle, et al.
Ophthalmic Genetics|February 1, 2018
The relationship between HDAC6, CXCR3, and SIRT1 genes expression levels with progression of primary open-angle glaucomaMateusz Siwak, Marcin Maślankiewicz, Alicja Nowak-Zduńczyk, et al.
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