Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases von Qian, Xinye, Wang, Jun, Wang, Meng, Igelman, Austin D., Jones, Kaylie D., Li, Yumei, Wang, Keqing, Goetz, Kerry E., Birch, David G., Yang, Paul, Pennesi, Mark E., Chen, Rui

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A Novel Dominant Mutation in SAG, the Arrestin-1 Gene, Is a Common Cause of Retinitis Pigmentosa in Hispanic Families in the Southwestern United States von Sullivan, Lori S, Bowne, Sara J, Koboldt, Daniel C, Cadena, Elizabeth L, Heckenlively, John R, Branham, Kari E, Wheaton, Dianna H, Jones, Kaylie D, Ruiz, Richard S, Pennesi, Mark E, Yang, Paul, Davis-Boozer, David, Northrup, Hope, Gurevich, Vsevold V, Chen, Rui, Xu, Mingchu, Li, Yumei, Birch, David G, Daiger, Stephen P

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Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa von Kiser, Kelly, Webb-Jones, Kaylie D., Bowne, Sara J., Sullivan, Lori S., Daiger, Stephen P., Birch, David G.

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Next-generation sequencing to solve complex inherited retinal dystrophy: A case series of multiple genes contributing to disease in extended families von Jones, Kaylie D, Wheaton, Dianna K, Bowne, Sara J, Sullivan, Lori S, Birch, David G, Chen, Rui, Daiger, Stephen P

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North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene von Bowne, Sara J, Sullivan, Lori S, Wheaton, Dianna K, Locke, Kirsten G, Jones, Kaylie D, Koboldt, Daniel C, Fulton, Robert S, Wilson, Richard K, Blanton, Susan H, Birch, David G, Daiger, Stephen P

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X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa von Fahim, Abigail T., Sullivan, Lori S., Bowne, Sara J., Jones, Kaylie D., Wheaton, Dianna K.H., Khan, Naheed W., Heckenlively, John R., Jayasundera, K. Thiran, Branham, Kari H., Andrews, Chris A., Othman, Mohammad I., Karoukis, Athanasios J., Birch, David G., Daiger, Stephen P.

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Dynamics of Daily Glioblastoma Evolution During Chemoradiation Therapy on the 0.35T Magnetic Resonance Imaging-Linear Accelerator von Cullison, Kaylie, Samimi, Kayla, Bell, Jonathan B., Maziero, Danilo, Valderrama, Alessandro, Breto, Adrian L., Jones, Kolton, De La Fuente, Macarena I., Kubicek, Gregory, Meshman, Jessica, Azzam, Gregory A., Ford, John C., Stoyanova, Radka, Mellon, Eric A.

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A Deep Learning Approach for Automatic Segmentation during Daily MRI-Linac Radiotherapy of Glioblastoma von Breto, Adrian L, Cullison, Kaylie, Zacharaki, Evangelia I, Wallaengen, Veronica, Maziero, Danilo, Jones, Kolton, Valderrama, Alessandro, de la Fuente, Macarena I, Meshman, Jessica, Azzam, Gregory A, Ford, John C, Stoyanova, Radka, Mellon, Eric A

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Disease Progression in Patients with Autosomal Dominant Retinitis Pigmentosa due to a Mutation in Inosine Monophosphate Dehydrogenase 1 (IMPDH1) von Bennett, Lea D., Klein, Martin, John, Finny T., Radojevic, Bojana, Jones, Kaylie, Birch, David G.

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Impact of intensive care unit supportive care on the physiology of Ebola virus disease in a universally lethal non-human primate model von Poliquin, Guillaume, Funk, Duane, Jones, Shane, Tran, Kaylie, Ranadheera, Charlene, Hagan, Mable, Tierney, Kevin, Grolla, Allen, Dhaliwal, Amrinder, Bello, Alexander, Leung, Anders, Nakamura, Cory, Kobasa, Darwyn, Falzarano, Darryl, Garnett, Lauren, Bovendo, Hugues Fausther, Feldmann, Heinz, Kesselman, Murray, Hansen, Gregory, Gren, Jason, Risi, George, Biondi, Mia, Mortimer, Todd, Racine, Trina, Deschambault, Yvon, Aminian, Sam, Edmonds, Jocelyn, Sourette, Ray, Allan, Mark, Rondeau, Lauren, Hadder, Sharron, Press, Christy, DeGraff, Christine, Kucas, Stephanie, Cook, Bradley W. M., Hancock, B. J., Kumar, Anand, Soni, Reeni, Schantz, Darryl, McKitrick, Jarrid, Warner, Bryce, Griffin, Bryan D., Qiu, Xiangguo, Kobinger, Gary P., Safronetz, Dave, Stein, Derek, Cutts, Todd, Kenny, James, Soule, Geoff, Kozak, Robert, Theriault, Steven, Menec, Liam, Vendramelli, Robert, Higgins, Sean, Liu, Guodong, Rahim, Niaz Md, Kasloff, Samantha, Sloan, Angela, He, Shihua, Tailor, Nikesh, Gray, Michael, Strong, James E.

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