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Archives of Ophthalmology (Chicago, Ill. : 1960)|October 9, 2002
Electroretinographic abnormalities in parents of patients with Leber congenital amaurosis who have heterozygous GUCY2D mutationsRobert K Koenekoop, Gerald A Fishman, Alessandro Iannaccone, et al.
Ophthalmic Genetics|October 7, 2025
A novel missense TUBB4B variant outside of the canonical hotspot is associated with cone-rod dystrophy and sensorineural hearing lossLauren Y Cao, Anna Duemler, Emily H Jung, et al.
Investigative Ophthalmology & Visual Science|September 28, 2006
Elovl4 5-bp-deletion knock-in mice develop progressive photoreceptor degenerationVidyullatha Vasireddy, Monica M Jablonski, Md Nawajes A Mandal, et al.
Age and Ageing|January 18, 2014
Macular pigment optical density is related to cognitive function in older peopleRohini Vishwanathan, Alessandro Iannaccone, Tammy M Scott, et al.
Ophthalmology Science|May 27, 2026
Association of Autosomal Dominant Snowflake Vitreoretinal Degeneration with RetinoschisisBikash R Pattnaik, Ken K Nischal, Oleg Alekseev, et al.
Ophthalmology|November 4, 2022
Ophthalmic Manifestations of ROSAH (Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Headache) Syndrome, an Inherited NF κB-Mediated Autoinflammatory Disease with Retinal DystrophyLaryssa A Huryn, Christina Torres Kozycki, Jasmine Y Serpen, et al.
Plos One|April 25, 2015
Blue cone monochromacy: visual function and efficacy outcome measures for clinical trialsXunda Luo, Artur V Cideciyan, Alessandro Iannaccone, et al.
The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences|March 9, 2011
The association of cataract with leukocyte telomere length in older adults: defining a new marker of agingJason L Sanders, Alessandro Iannaccone, Robert M Boudreau, et al.
Plos One|April 2, 2011
Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degenerationKylee L Spencer, Lana M Olson, Nathalie Schnetz-Boutaud, et al.
Investigative Ophthalmology & Visual Science|June 5, 2012
Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 geneTomas R Burke, Gerald A Fishman, Jana Zernant, et al.
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