IL-15 induces strong but short-lived tumor-infiltrating CD8 T cell responses through the regulation of Tim-3 in breast cancer von Heon, Elise K., Wulan, Hasi, Macdonald, Loch P., Malek, Adel O., Braunstein, Glenn H., Eaves, Connie G., Schattner, Mark D., Allen, Peter M., Alexander, Michael O., Hawkins, Cynthia A., McGovern, Dermot W., Freeman, Richard L., Amir, Eitan P., Huse, Jason D., Zaltzman, Jeffrey S., Kauff, Noah P., Meyers, Paul G., Gleason, Michelle H., Overholtzer, Michael G., Wiseman, Sam S., Streutker, Catherine D., Asa, Sylvia W., McAlindon, Timothy P., Newcomb, Polly O., Sorensen, Poul M., Press, Oliver A.

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Photoreceptor function and structure in retinal degenerations caused by biallelic BEST1 mutations von Cideciyan, Artur V., Jacobson, Samuel G., Sumaroka, Alexander, Swider, Malgorzata, Krishnan, Arun K., Sheplock, Rebecca, Garafalo, Alexandra V., Guziewicz, Karina E., Aguirre, Gustavo D., Beltran, William A., Matsui, Yoshitsugu, Kondo, Mineo, Heon, Elise

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Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia von Kohl, Susanne, Zobor, Ditta, Chiang, Wei-Chieh, Weisschuh, Nicole, Staller, Jennifer, Menendez, Irene Gonzalez, Chang, Stanley, Beck, Susanne C, Garrido, Marina Garcia, Sothilingam, Vithiyanjali, Seeliger, Mathias W, Stanzial, Franco, Benedicenti, Francesco, Inzana, Francesca, Héon, Elise, Vincent, Ajoy, Beis, Jill, Strom, Tim M, Rudolph, Günther, Roosing, Susanne, Hollander, Anneke I den, Cremers, Frans P M, Lopez, Irma, Ren, Huanan, Moore, Anthony T, Webster, Andrew R, Michaelides, Michel, Koenekoop, Robert K, Zrenner, Eberhart, Kaufman, Randal J, Tsang, Stephen H, Wissinger, Bernd, Lin, Jonathan H

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VSX1: A gene for posterior polymorphous dystrophy and keratoconus von Héon, Elise, Greenberg, Alex, Kopp, Kelly K., Rootman, David, Vincent, Andrea L., Billingsley, Gail, Priston, Megan, Dorval, Kimberley M., Chow, Robert L., McInnes, Roderick R., Heathcote, Godfrey, Westall, Carol, Sutphin, John E., Semina, Elena, Bremner, Rod, Stone, Edwin M.

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Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet–Biedl syndrome patient population von Billingsley, Gail, Bin, Jenea, Fieggen, Karen J, Duncan, Jacque L, Gerth, Christina, Ogata, Koji, Wodak, Shoshana S, Traboulsi, Elias I, Fishman, Gerald A, Paterson, Andrew, Chitayat, David, Knueppel, Tanja, Millán, José M, Mitchell, Grant A, Deveault, Catherine, Héon, Elise

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Identifying Photoreceptors in Blind Eyes Caused by RPE65 Mutations: Prerequisite for Human Gene Therapy Success von Jacobson, Samuel G., Aleman, Tomas S., Cideciyan, Artur V., Sumaroka, Alexander, Schwartz, Sharon B., Elizabeth A. M. Windsor, Traboulsi, Elias I., Heon, Elise, Pittler, Steven J., Milam, Ann H., Maguire, Albert M., Palczewski, Krzysztof, Stone, Edwin M., Bennett, Jean, Nathans, Jeremy

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Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium von Thompson, Debra A, Ali, Robin R, Banin, Eyal, Branham, Kari E, Flannery, John G, Gamm, David M, Hauswirth, William W, Heckenlively, John R, Iannaccone, Alessandro, Jayasundera, K Thiran, Khan, Naheed W, Molday, Robert S, Pennesi, Mark E, Reh, Thomas A, Weleber, Richard G, Zacks, David N

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Scaling up Functional Analyses of the G Protein-Coupled Receptor Rhodopsin von Scott, Benjamin M., Chen, Steven K., Van Nynatten, Alexander, Liu, Jing, Schott, Ryan K., Heon, Elise, Peisajovich, Sergio G., Chang, Belinda S. W.

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Visual Acuity in Patients with Leber's Congenital Amaurosis and Early Childhood-Onset Retinitis Pigmentosa von Walia, Saloni, MD, Fishman, Gerald A., MD, Jacobson, Samuel G., MD, PhD, Aleman, Tomas S., MD, Koenekoop, Robert K., MD, PhD, Traboulsi, Elias I., MD, Weleber, Richard G., MD, Pennesi, Mark E., MD, PhD, Heon, Elise, MD, Drack, Arlene, MD, Lam, Byron L., MD, Allikmets, Rando, PhD, Stone, Edwin M., MD, PhD

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Baseline Visual Field Findings in the RUSH2A Study: Associated Factors and Correlation With Other Measures of Disease Severity von Duncan, Jacque L., Liang, Wendi, Maguire, Maureen G., Audo, Isabelle, Ayala, Allison R., Birch, David G., Carroll, Joseph, Cheetham, Janet K., Esposti, Simona Degli, Durham, Todd A., Erker, Laura, Farsiu, Sina, Ferris, Frederick L., Heon, Elise, Hufnagel, Robert B., Iannaccone, Alessandro, Jaffe, Glenn J., Kay, Christine N., Michaelides, Michel, Pennesi, Mark E., Sahel, José-Alain

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Comparative Natural History of Visual Function From Patients With Biallelic Variants in BBS1 and BBS10 von Pechhacker, Monika K. Grudzinska, Jacobson, Samuel G., Drack, Arlene, Di Scipio, Matteo, Strubbe, Ine, Pfeifer, Wanda, Duncan, Jacque L., Dollfus, Helene, Goetz, Nathalie, Muller, Jean, Vincent, Andrea L., Aleman, Tomas S., Tumber, Anupreet, Van Cauwenbergh, Caroline, De Baere, Elfride, Bedoukian, Emma, Leroy, Bart P., Maynes, Jason T., Munier, Francis L., Tavares, Erika, Saleh, Eman, Vincent, Ajoy, Heon, Elise

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Transient pupillary light reflex in CEP290- or NPHP5-associated Leber congenital amaurosis: Latency as a potential outcome measure of cone function von Krishnan, Arun K., Jacobson, Samuel G., Roman, Alejandro J., Iyer, Bhavya S., Garafalo, Alexandra V., Héon, Elise, Cideciyan, Artur V.

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Functional Vision in Patients With Biallelic USH2A Variants von Heon, Elise, Melia, Michele, Bocchino, Laura E., Samarakoon, Lassana, Duncan, Jacque L., Ayala, Allison R., Audo, Isabelle, Bradley, Chris, Cheetham, Janet K., Dagnelie, Gislin, Durham, Todd A., Hoyng, Carel B., Jain, Nieraj, Jayasundera, Kanishka T., Pennesi, Mark E., Weng, Christina Y.

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Baseline Microperimetry and OCT in the RUSH2A Study: Structure−Function Association and Correlation With Disease Severity von Lad, Eleonora M., Duncan, Jacque L., Liang, Wendi, Maguire, Maureen G., Ayala, Allison R., Audo, Isabelle, Birch, David G., Carroll, Joseph, Cheetham, Janet K., Durham, Todd A., Fahim, Abigail T., Loo, Jessica, Deng, Zengtian, Mukherjee, Dibyendu, Heon, Elise, Hufnagel, Robert B., Guan, Bin, Iannaccone, Alessandro, Jaffe, Glenn J., Kay, Christine N., Michaelides, Michel, Pennesi, Mark E., Vincent, Ajoy, Weng, Christina Y., Farsiu, Sina

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Photoreceptor Function and Structure in Autosomal Dominant Vitelliform Macular Dystrophy Caused by BEST1 Mutations von Cideciyan, Artur V, Jacobson, Samuel G, Swider, Malgorzata, Sumaroka, Alexander, Sheplock, Rebecca, Krishnan, Arun K, Garafalo, Alexandra V, Guziewicz, Karina E, Aguirre, Gustavo D, Beltran, William A, Heon, Elise

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Deep intronic variant in MVK as a cause for mevalonic aciduria initially presenting as non‐syndromic retinitis pigmentosa von Dvaladze, Anna, Tavares, Erika, Di Scipio, Matteo, Nimmo, Graeme, Grudzinska‐Pechhacker, Monika K., Paton, Tara, Tumber, Anupreet, Li, Shuning, Eileen, Christabel, Ertl‐Wagner, Birgit, Mamak, Eva, Hoffmann, Georg, Marshall, Christian R., Haas, Dorothea, Mayatepek, Ertan, Schulze, Andreas, Heon, Elise, Vincent, Ajoy

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Tissue‐specific genotype–phenotype correlations among USH2A‐related disorders in the RUSH2A study von Hufnagel, Robert B., Liang, Wendi, Duncan, Jacque L., Brewer, Carmen C., Audo, Isabelle, Ayala, Allison R., Branham, Kari, Cheetham, Janet K., Daiger, Stephen P., Durham, Todd A., Guan, Bin, Heon, Elise, Hoyng, Carel B., Iannaccone, Alessandro, Kay, Christine N., Michaelides, Michel, Pennesi, Mark E., Singh, Mandeep S., Ullah, Ehsan

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Coupling of Human Rhodopsin to a Yeast Signaling Pathway Enables Characterization of Mutations Associated with Retinal Disease von Scott, Benjamin M, Chen, Steven K, Bhattacharyya, Nihar, Moalim, Abdiwahab Y, Plotnikov, Sergey V, Heon, Elise, Peisajovich, Sergio G, Chang, Belinda S W

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Retinal Dystrophies Associated With Peripherin-2: Genetic Spectrum and Novel Clinical Observations in 241 Patients von Heath Jeffery, Rachael C, Thompson, Jennifer A, Lo, Johnny, Chelva, Enid S, Armstrong, Sean, Pulido, Jose S, Procopio, Rebecca, Vincent, Andrea L, Bianco, Lorenzo, Battaglia Parodi, Maurizio, Ziccardi, Lucia, Antonelli, Giulio, Barbano, Lucilla, Marques, João P, Geada, Sara, Carvalho, Ana L, Tang, Wei C, Chan, Choi M, Boon, Camiel J F, Hensman, Jonathan, Chen, Ta-Ching, Lin, Chien-Yu, Chen, Pei-Lung, Vincent, Ajoy, Tumber, Anupreet, Heon, Elise, Grigg, John R, Jamieson, Robyn V, Cornish, Elisa E, Nash, Benjamin M, Borooah, Shyamanga, Ayton, Lauren N, Britten-Jones, Alexis Ceecee, Edwards, Thomas L, Ruddle, Jonathan B, Sharma, Abhishek, Porter, Rowan G, Lamey, Tina M, McLaren, Terri L, McLenachan, Samuel, Roshandel, Danial, Chen, Fred K

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Analysis of Myocilin Mutations in 1703 Glaucoma Patients From Five Different Populations von Fingert, John H., Héon, Elise, Liebmann, Jeffrey M., Yamamoto, Tetsuya, Craig, Jamie E., Rait, Julian, Kawase, Kazuhide, Hoh, Sek-Tien, Buys, Yvonne M., Dickinson, Joanne, Hockey, Robin R., Williams-Lyn, Donna, Trope, Graham, Kitazawa, Yoshiaki, Ritch, Robert, Mackey, David A., Alward, Wallace L. M., Sheffield, Val C., Stoned, Edwin M.

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