The interactions of genes, age, and environment in glaucoma pathogenesis by Doucette, Lance P., PhD, Rasnitsyn, Alexandra, BSc, Seifi, Morteza, MSc, Walter, Michael A., PhD

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Prostaglandins in the eye: Function, expression, and roles in glaucoma by Doucette, Lance P., Walter, Michael A.

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Disrupting the Repeat Domain of Premelanosome Protein (PMEL) Produces Dysamyloidosis and Dystrophic Ocular Pigment Reflective of Pigmentary Glaucoma by Hodges, Elizabeth D., Chrystal, Paul W., Footz, Tim, Doucette, Lance P., Noel, Nicole C. L., Li, Zixuan, Walter, Michael A., Allison, W. Ted

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FOXC1 Regulates Expression of Prostaglandin Receptors Leading to an Attenuated Response to Latanoprost by Doucette, Lance P, Footz, Tim, Walter, Michael A

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Autosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene by Pater, Justin A., Penney, Cindy, O’Rielly, Darren D., Griffin, Anne, Kamal, Lara, Brownstein, Zippora, Vona, Barbara, Vinkler, Chana, Shohat, Mordechai, Barel, Ortal, French, Curtis R., Singh, Sushma, Werdyani, Salem, Burt, Taylor, Abdelfatah, Nelly, Houston, Jim, Doucette, Lance P., Squires, Jessica, Glaser, Fabian, Roslin, Nicole M., Vincent, Daniel, Marquis, Pascale, Woodland, Geoffrey, Benoukraf, Touati, Hawkey-Noble, Alexia, Avraham, Karen B., Stanton, Susan G., Young, Terry-Lynn

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Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation by Doucette, Lance P, Noel, Nicole C L, Zhai, Yi, Xu, Manlong, Caluseriu, Oana, Hoang, Stephanie C, Radziwon, Alina J, MacDonald, Ian M

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A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene by Abdelfatah, Nelly, Mostafa, Ahmed A., French, Curtis R., Doucette, Lance P., Penney, Cindy, Lucas, Matthew B., Griffin, Anne, Booth, Valerie, Rowley, Christopher, Besaw, Jessica E., Tranebjærg, Lisbeth, Rendtorff, Nanna Dahl, Hodgkinson, Kathy A., Little, Leichelle A., Agrawal, Sumit, Parnes, Lorne, Batten, Tony, Moore, Susan, Hu, Pingzhao, Pater, Justin A., Houston, Jim, Galutira, Dante, Benteau, Tammy, MacDonald, Courtney, French, Danielle, O’Rielly, Darren D., Stanton, Susan G., Young, Terry-Lynn

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PEX6 Mutations in Peroxisomal Biogenesis Disorders: An Usher Syndrome Mimic by Benson, Matthew D, Papp, Kimberly M, Casey, Geoffrey A, Radziwon, Alina, St Laurent, Chris D, Doucette, Lance P, MacDonald, Ian M

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PEX6 Mutations in Peroxisomal Biogenesis Disorders by Benson, Matthew D., Papp, Kimberly M., Casey, Geoffrey A., Radziwon, Alina, St Laurent, Chris D., Doucette, Lance P., MacDonald, Ian M.

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A pathogenic deletion in Forkhead Box L1 gene by Abdelfatah, Nelly, Mostafa, Ahmed A, French, Cu, Doucette, Lance P, Penney, Cindy, Lucas, Matthew B, Griffin, Anne

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