Rapid Deorphanization of Human Olfactory Receptors in Yeast von Yasi, Emily A, Eisen, Sara L, Wang, Hanfei, Sugianto, Widianti, Minniefield, Anita R, Hoover, Kaitlyn A, Branham, Paul J, Peralta-Yahya, Pamela

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Quantification of SARS-CoV-2 spike protein expression from mRNA vaccines using isotope dilution mass spectrometry von Sutton, William J.H., Branham, Paul J., Williamson, Yulanda M., Cooper, Hans C., Najjar, Fabio N., Pierce-Ruiz, Carrie L., Barr, John R., Williams, Tracie L.

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An antibody-free evaluation of an mRNA COVID-19 vaccine von Branham, Paul J., Cooper, Hans C., Williamson, Yulanda M., Najjar, Fabio N., Sutton, William J.H., Pierce-Ruiz, Carrie L., Barr, John R., Williams, Tracie L.

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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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Toll-like receptor 4 variant D299G is associated with susceptibility to age-related macular degeneration von Zareparsi, Sepideh, Buraczynska, Monika, Branham, Kari E.H., Shah, Sapna, Eng, Donna, Li, Mingyao, Pawar, Hemant, Yashar, Beverly M., Moroi, Sayoko E., Lichter, Paul R., Petty, Howard R., Richards, Julia E., Abecasis, Gonçalo R., Elner, Victor M., Swaroop, Anand

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Age-Related Macular Degeneration: A High-Resolution Genome Scan for Susceptibility Loci in a Population Enriched for Late-Stage Disease von Abecasis, Gonçalo R., Yashar, Beverly M., Zhao, Yu, Ghiasvand, Noor M., Zareparsi, Sepideh, Branham, Kari E.H., Reddick, Adam C., Trager, Edward H., Yoshida, Shigeo, Bahling, John, Filippova, Elena, Elner, Susan, Johnson, Mark W., Vine, Andrew K., Sieving, Paul A., Jacobson, Samuel G., Richards, Julia E., Swaroop, Anand

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Seven new loci associated with age-related macular degeneration von Fritsche, Lars G, Chen, Wei, Schu, Matthew, Yaspan, Brian L, Yu, Yi, Thorleifsson, Gudmar, Zack, Donald J, Arakawa, Satoshi, Cipriani, Valentina, Ripke, Stephan, Igo, Jr, Robert P, Buitendijk, Gabriëlle H S, Sim, Xueling, Weeks, Daniel E, Guymer, Robyn H, Merriam, Joanna E, Francis, Peter J, Hannum, Gregory, Agarwal, Anita, Armbrecht, Ana Maria, Audo, Isabelle, Aung, Tin, Barile, Gaetano R, Benchaboune, Mustapha, Bird, Alan C, Bishop, Paul N, Branham, Kari E, Brooks, Matthew, Brucker, Alexander J, Cade, William H, Cain, Melinda S, Campochiaro, Peter A, Chan, Chi-Chao, Cheng, Ching-Yu, Chew, Emily Y, Chin, Kimberly A, Chowers, Itay, Clayton, David G, Cojocaru, Radu, Conley, Yvette P, Cornes, Belinda K, Daly, Mark J, Dhillon, Baljean, Edwards, Albert O, Evangelou, Evangelos, Fagerness, Jesen, Ferreyra, Henry A, Friedman, James S, Geirsdottir, Asbjorg, George, Ronnie J, Gieger, Christian, Gupta, Neel, Hagstrom, Stephanie A, Harding, Simon P, Haritoglou, Christos, Heckenlively, John R, Holz, Frank G, Hughes, Guy, Ioannidis, John P A, Ishibashi, Tatsuro, Joseph, Peronne, Jun, Gyungah, Kamatani, Yoichiro, Katsanis, Nicholas, N Keilhauer, Claudia, Khan, Jane C, Kim, Ivana K, Kiyohara, Yutaka, Klein, Barbara E K, Klein, Ronald, Kovach, Jaclyn L, Kozak, Igor, Lee, Clara J, Lee, Kristine E, Lichtner, Peter, Lotery, Andrew J, Meitinger, Thomas, Mitchell, Paul, Mohand-Saïd, Saddek, Moore, Anthony T, Morgan, Denise J, Morrison, Margaux A, Myers, Chelsea E, Naj, Adam C, Nakamura, Yusuke, Okada, Yukinori, Orlin, Anton, Ortube, M Carolina, Othman, Mohammad I, Pappas, Chris, Park, Kyu Hyung, Pauer, Gayle J T, Peachey, Neal S, Poch, Olivier, Priya, Rinki Ratna, Reynolds, Robyn, Richardson, Andrea J, Ripp, Raymond, Rudolph, Guenther, Ryu, Euijung

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A reference panel of 64,976 haplotypes for genotype imputation von McCarthy, Shane, Das, Sayantan, Kretzschmar, Warren, Delaneau, Olivier, Wood, Andrew R, Teumer, Alexander, Kang, Hyun Min, Fuchsberger, Christian, Danecek, Petr, Sharp, Kevin, Luo, Yang, Sidore, Carlo, Kwong, Alan, Timpson, Nicholas, Koskinen, Seppo, Vrieze, Scott, Scott, Laura J, Zhang, He, Mahajan, Anubha, Veldink, Jan, Peters, Ulrike, Pato, Carlos, van Duijn, Cornelia M, Gillies, Christopher E, Gandin, Ilaria, Mezzavilla, Massimo, Gilly, Arthur, Cocca, Massimiliano, Traglia, Michela, Angius, Andrea, Barrett, Jeffrey C, Boomsma, Dorrett, Branham, Kari, Breen, Gerome, Brummett, Chad M, Busonero, Fabio, Campbell, Harry, Chan, Andrew, Chen, Sai, Chew, Emily, Collins, Francis S, Corbin, Laura J, Smith, George Davey, Dedoussis, George, Dorr, Marcus, Farmaki, Aliki-Eleni, Ferrucci, Luigi, Forer, Lukas, Fraser, Ross M, Gabriel, Stacey, Levy, Shawn, Groop, Leif, Harrison, Tabitha, Hattersley, Andrew, Holmen, Oddgeir L, Hveem, Kristian, Kretzler, Matthias, Lee, James C, McGue, Matt, Meitinger, Thomas, Melzer, David, Min, Josine L, Mohlke, Karen L, Vincent, John B, Nauck, Matthias, Nickerson, Deborah, Palotie, Aarno, Pato, Michele, Pirastu, Nicola, McInnis, Melvin, Richards, J Brent, Sala, Cinzia, Salomaa, Veikko, Schlessinger, David, Schoenherr, Sebastian, Slagboom, P Eline, Small, Kerrin, Spector, Timothy, Stambolian, Dwight, Tuke, Marcus, Tuomilehto, Jaakko, Van den Berg, Leonard H, Van Rheenen, Wouter, Volker, Uwe, Wijmenga, Cisca, Toniolo, Daniela, Zeggini, Eleftheria, Gasparini, Paolo, Sampson, Matthew G, Wilson, James F, Frayling, Timothy, de Bakker, Paul I W, Swertz, Morris A, McCarroll, Steven, Kooperberg, Charles, Dekker, Annelot, Altshuler, David, Willer, Cristen, Iacono, William, Ripatti, Samuli

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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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Identification of a rare coding variant in complement 3 associated with age-related macular degeneration von Zhan, Xiaowei, Larson, David E, Wang, Chaolong, Koboldt, Daniel C, Sergeev, Yuri V, Fulton, Robert S, Fulton, Lucinda L, Fronick, Catrina C, Branham, Kari E, Bragg-Gresham, Jennifer, Jun, Goo, Hu, Youna, Kang, Hyun Min, Liu, Dajiang, Othman, Mohammad, Brooks, Matthew, Ratnapriya, Rinki, Boleda, Alexis, Grassmann, Felix, von Strachwitz, Claudia, Olson, Lana M, Buitendijk, Gabriëlle H S, Hofman, Albert, van Duijn, Cornelia M, Cipriani, Valentina, Moore, Anthony T, Shahid, Humma, Jiang, Yingda, Conley, Yvette P, Morgan, Denise J, Kim, Ivana K, Johnson, Matthew P, Cantsilieris, Stuart, Richardson, Andrea J, Guymer, Robyn H, Luo, Hongrong, Ouyang, Hong, Licht, Christoph, Pluthero, Fred G, Zhang, Mindy M, Zhang, Kang, Baird, Paul N, Blangero, John, Klein, Michael L, Farrer, Lindsay A, DeAngelis, Margaret M, Weeks, Daniel E, Gorin, Michael B, Yates, John R W, Klaver, Caroline C W, Pericak-Vance, Margaret A, Haines, Jonathan L, Weber, Bernhard H F, Wilson, Richard K, Heckenlively, John R, Chew, Emily Y, Stambolian, Dwight, Mardis, Elaine R, Swaroop, Anand, Abecasis, Goncalo R

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Genome-wide association analyses identify distinct genetic architectures for age-related macular degeneration across ancestries von Gorman, Bryan R., Voloudakis, Georgios, Igo, Robert P., Kinzy, Tyler, Halladay, Christopher W., Bigdeli, Tim B., Zeng, Biao, Venkatesh, Sanan, Cooke Bailey, Jessica N., Crawford, Dana C., Markianos, Kyriacos, Dong, Frederick, Schreiner, Patrick A., Zhang, Wen, Hadi, Tamer, Anger, Matthew D., Stockwell, Amy, Melles, Ronald B., Yin, Jie, Choquet, Hélène, Kaye, Rebecca, Patasova, Karina, Patel, Praveen J., Yaspan, Brian L., Jorgenson, Eric, Hysi, Pirro G., Lotery, Andrew J., Gaziano, J. Michael, Tsao, Philip S., Fliesler, Steven J., Sullivan, Jack M., Greenberg, Paul B., Wu, Wen-Chih, Assimes, Themistocles L., Pyarajan, Saiju, Roussos, Panos, Peachey, Neal S., Iyengar, Sudha K.

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Cationic Liposome-Mediated E1A Gene Transfer to Human Breast and Ovarian Cancer Cells and Its Biologic Effects: A Phase I Clinical Trial von Hortobagyi, G N, Ueno, N T, Xia, W, Zhang, S, Wolf, J K, Putnam, J B, Weiden, P L, Willey, J S, Carey, M, Branham, D L, Payne, J Y, Tucker, S D, Bartholomeusz, C, Kilbourn, R G, De Jager, R L, Sneige, N, Katz, R L, Anklesaria, P, Ibrahim, N K, Murray, J L, Theriault, R L, Valero, V, Gershenson, D M, Bevers, M W, Huang, L, Lopez-Berestein, G, Hung, M C

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A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration von Strunz, Tobias, Lauwen, Susette, Kiel, Christina, Hollander, Anneke den, Weber, Bernhard H. F.

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Comprehensive variant spectrum of the CNGA3 gene in patients affected by achromatopsia von Solaki, Maria, Baumann, Britta, Reuter, Peggy, Andreasson, Sten, Audo, Isabelle, Ayuso, Carmen, Balousha, Ghassan, Benedicenti, Francesco, Birch, David, Bitoun, Pierre, Blain, Delphine, Bocquet, Beatrice, Branham, Kari, Català‐Mora, Jaume, De Baere, Elfride, Dollfus, Helene, Falana, Mohammed, Giorda, Roberto, Golovleva, Irina, Gottlob, Irene, Heckenlively, John R., Jacobson, Samuel G., Jones, Kaylie, Jägle, Herbert, Janecke, Andreas R., Kellner, Ulrich, Liskova, Petra, Lorenz, Birgit, Martorell‐Sampol, Loreto, Messias, André, Meunier, Isabelle, Belga Ottoni Porto, Fernanda, Papageorgiou, Eleni, Plomp, Astrid S., Ravel, Thomy J. L., Reiff, Charlotte M., Renner, Agnes B., Rosenberg, Thomas, Rudolph, Günther, Salati, Roberto, Sener, E. Cumhur, Sieving, Paul A., Stanzial, Franco, Traboulsi, Elias I., Tsang, Stephen H., Varsanyi, Balázs, Weleber, Richard G., Zobor, Ditta, Stingl, Katarina, Wissinger, Bernd, Kohl, Susanne

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Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease von Branham, Kari, Othman, Mohammad, Brumm, Matthew, Karoukis, Athanasios J, Atmaca-Sonmez, Pelin, Yashar, Beverly M, Schwartz, Sharon B, Stover, Niamh B, Trzupek, Karmen, Wheaton, Dianna, Jennings, Barbara, Ciccarelli, Maria Laura, Jayasundera, K Thiran, Lewis, Richard A, Birch, David, Bennett, Jean, Sieving, Paul A, Andreasson, Sten, Duncan, Jacque L, Fishman, Gerald A, Iannaccone, Alessandro, Weleber, Richard G, Jacobson, Samuel G, Heckenlively, John R, Swaroop, Anand

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Knowns, uncertainties, and challenges in agrivoltaics to sustainably intensify energy and food production von Gomez-Casanovas, Nuria, Mwebaze, Paul, Khanna, Madhu, Branham, Bruce, Time, Alson, DeLucia, Evan H., Bernacchi, Carl J., Knapp, Alan K., Hoque, Muhammad J., Du, Xuzhi, Blanc-Betes, Elena, Barron-Gafford, Greg A., Peng, Bin, Guan, Kaiyu, Macknick, Jordan, Miao, Ruiqing, Miljkovic, Nenad

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Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencing von Branham, Kari, Matsui, Hiroko, Biswas, Pooja, Guru, Aditya A, Hicks, Michael, Suk, John J, Li, He, Jakubosky, David, Long, Tao, Telenti, Amalio, Nariai, Naoki, Heckenlively, John R, Frazer, Kelly A, Sieving, Paul A, Ayyagari, Radha

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Mutations in the small nuclear riboprotein 200 kDa gene (SNRNP200) cause 1.6% of autosomal dominant retinitis pigmentosa von Bowne, Sara J, Sullivan, Lori S, Avery, Cheryl E, Sasser, Elizabeth M, Roorda, Austin, Duncan, Jacque L, Wheaton, Dianna H, Birch, David G, Branham, Kari E, Heckenlively, John R, Sieving, Paul A, Daiger, Stephen P

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Genome-wide association study and meta-analysis of intraocular pressure von Ozel, A. Bilge, Moroi, Sayoko E., Reed, David M., Nika, Melisa, Schmidt, Caroline M., Akbari, Sara, Scott, Kathleen, Rozsa, Frank, Pawar, Hemant, Musch, David C., Lichter, Paul R., Gaasterland, Doug, Branham, Kari, Gilbert, Jesse, Garnai, Sarah J., Chen, Wei, Othman, Mohammad, Heckenlively, John, Swaroop, Anand, Abecasis, Gonçalo, Friedman, David S., Zack, Don, Ashley-Koch, Allison, Ulmer, Megan, Kang, Jae H., Liu, Yutao, Yaspan, Brian L., Haines, Jonathan, Allingham, R. Rand, Hauser, Michael A., Pasquale, Louis, Wiggs, Janey, Richards, Julia E., Li, Jun Z.

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Phenotypic Conservation in Patients With X-Linked Retinitis Pigmentosa Caused by RPGR Mutations von Zahid, Sarwar, Khan, Naheed, Branham, Kari, Othman, Mohammad, Karoukis, Athanasios J, Sharma, Nisha, Moncrief, Ashley, Mahmood, Mahdi N, Sieving, Paul A, Swaroop, Anand, Heckenlively, John R, Jayasundera, Thiran

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