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Ophthalmic Genetics|April 13, 2016
Prostaglandins in the eye: Function, expression, and roles in glaucomaLance P Doucette, Michael A Walter
Investigative Ophthalmology & Visual Science|May 31, 2018
FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to LatanoprostLance P Doucette, Tim Footz, Michael A Walter
Survey of Ophthalmology|April 25, 2015
The interactions of genes, age, and environment in glaucoma pathogenesisLance P Doucette, Alexandra Rasnitsyn, Morteza Seifi, et al.
Ophthalmology Science|October 17, 2022
<i>PEX6</i> Mutations in Peroxisomal Biogenesis Disorders: An Usher Syndrome MimicMatthew D Benson, Kimberly M Papp, Geoffrey A Casey, et al.
European Journal of Human Genetics : EJHG|March 29, 2021
Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formationLance P Doucette, Nicole C L Noel, Yi Zhai, et al.
International Journal of Molecular Sciences|October 14, 2023
Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary GlaucomaElizabeth D Hodges, Paul W Chrystal, Tim Footz, et al.
Human Genetics|March 12, 2022
Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase geneJustin A Pater, Cindy Penney, Darren D O'Rielly, et al.
Human Genetics|October 11, 2021
A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) geneNelly Abdelfatah, Ahmed A Mostafa, Curtis R French, et al.
Nature Communications|November 4, 2022
The inner junction protein CFAP20 functions in motile and non-motile cilia and is critical for visionPaul W Chrystal, Nils J Lambacher, Lance P Doucette, et al.
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