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Ophthalmic Genetics|June 1, 2026
Gillespie syndrome caused by a novel ITPR1 gene variant: a phenotype-genotype correlationMeghal Gagrani, Kelly Schooping Tripi, Hannah L Scanga, et al.
Ophthalmic Genetics|April 25, 2007
Attitudes regarding predictive testing for retinitis pigmentosaEedy Mezer, Riyana Babul-Hirji, Richard Wise, et al.
Ophthalmic Genetics|June 3, 2026
Two Turkish families with type 1 Stickler syndrome carrying novel COL2A1 truncating variants: a case seriesEsra Kızıldağ Özbay, Aysel Tekmenuray-Ünal, Şenol Sabancı, et al.
Ophthalmic Genetics|March 30, 2021
Did Edgar Degas have Stargardt disease?Z A Karcioglu, E M Stone, M F Marmor
Ophthalmic Genetics|June 16, 2026
Pediatric hereditary optic neuropathies in the United Arab EmiratesArif O Khan
Ophthalmic Genetics|September 1, 2026
PCARE-associated inherited retinal diseases: clinical and molecular insights from a Portuguese populationPatrícia Barros da Silva, Maria Filipa Madeira, Rita Anjos, et al.
Ophthalmic Genetics|September 1, 2026
Intrafamilial phenotypic variability in CRX-associated retinopathy due to a frameshift variant (c.661del)Serra Luigi, Gallo Biancamaria, Karali Marianthi, et al.
Ophthalmic Genetics|September 10, 2026
Novel mutations of PIKFYVE identified in 322 sporadic cataract patientsJinglan Ni, Yubo Cui, Shaoyi Mei, et al.
Ophthalmic Genetics|October 14, 2022
Readability, Content, and Accountability Assessment of Online Health Information for Retinitis Pigmentosa & Retinitis Pigmentosa Treatment OptionsStacy Partin, Eleanor Westfall, Gregory Sanda, et al.
Ophthalmic Genetics|October 13, 2022
Multimodal imaging in Schubert-Bornschein congenital stationary night blindnessMaurizio Battaglia Parodi, Alessandro Arrigo, Firuzeh Rajabian, et al.
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