variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration von Kanda, Atsuhiro, Chen, Wei, Othman, Mohammad, Branham, Kari E.H, Brooks, Matthew, Khanna, Ritu, He, Shirley, Lyons, Robert, Abecasis, Gonçalo R, Swaroop, Anand

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High-Resolution Imaging with Adaptive Optics in Patients with Inherited Retinal Degeneration von Duncan, Jacque L, Zhang, Yuhua, Gandhi, Jarel, Nakanishi, Chiaki, Othman, Mohammad, Branham, Kari E. H, Swaroop, Anand, Roorda, Austin

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CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration von Swaroop, Anand, Abecasis, Gonçalo R, Li, Mingyao, Atmaca-Sonmez, Pelin, Othman, Mohammad, Branham, Kari E H, Khanna, Ritu, Wade, Michael S, Li, Yun, Liang, Liming, Zareparsi, Sepideh

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Strong Association of the Y402H Variant in Complement Factor H at 1q32 with Susceptibility to Age-Related Macular Degeneration von Zareparsi, Sepideh, Branham, Kari E.H., Li, Mingyao, Shah, Sapna, Klein, Robert J., Ott, Jurg, Hoh, Josephine, Abecasis, Gonçalo R., Swaroop, Anand

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Madeline 2.0 PDE: a new program for local and web-based pedigree drawing von Trager, Edward H., Khanna, Ritu, Marrs, Adrian, Siden, Lawrence, Branham, Kari E.H., Swaroop, Anand, Richards, Julia E.

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Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype von SOFAT, Reecha, CASAS, Juan P, KHAN, Jane C, SHAHID, Humma, SWAROOP, Anand, ABECASIS, Gonçalo, BRANHAM, Kari E. H, ZAREPARSI, Sepideh, BERGEN, Arthur A, KLAVER, Caroline Cw, BAAS, Dominique C, KANG ZHANG, WEBSTER, Andrew R, YUHONG CHEN, GIBBS, Daniel, WEBER, Bernhard H. F, KEILHAUER, Claudia N, FRITSCHE, Lars G, LOTERY, Andrew, CREE, Angela J, GRIFFITHS, Helen L, BHATTACHARYA, Shomi S, CHEN, Li L, BIRD, Alan C, JENKINS, Sharon A, PETO, Tune, LATHROP, Mark, LEVEILLARD, Thierry, GORIN, Michael B, WEEKS, Daniel E, CAROLINA ORTUBE, Maria, FERRELL, Robert E, JAKOBSDOTTIR, Johanna, CONLEY, Yvette P, MANN, Samantha S, RAHU, Mati, SELAND, Johan H, SOUBRANE, Gisele, TOPOUZIS, Fotis, VIOQUE, Jesus, TOMAZZOLI, Laura, YOUNG, Ian, WHITTAKER, John, CHAKRAVARTHY, Usha, DE JONG, Paulus T.v M, YATES, John Rw, SMEETH, Liam, FLETCHER, Astrid, HINGORANI, Aroon D, MOORE, Anthony T, SEPP, Tiina, CIPRIANI, Valentina, BUNCE, Catey

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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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RP2 Phenotype and Pathogenetic Correlations in X-Linked Retinitis Pigmentosa von Jayasundera, Thiran, Branham, Kari E. H, Othman, Mohammad, Rhoades, William R, Karoukis, Athanasios J, Khanna, Hemant, Swaroop, Anand, Heckenlively, John R

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Genetic susceptibility to age-related macular degeneration: a paradigm for dissecting complex disease traits von Swaroop, Anand, Branham, Kari EH, Chen, Wei, Abecasis, Goncalo

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Discordant Phenotypes in Fraternal Twins Having an Identical Mutation in Exon ORF15 of the RPGR Gene von Walia, Saloni, Fishman, Gerald A, Swaroop, Anand, Branham, Kari E. H, Lindeman, Martin, Othman, Mohammad, Weleber, Richard G

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Association of Apolipoprotein E Alleles with Susceptibility to Age-Related Macular Degeneration in a Large Cohort from a Single Center von Zareparsi, Sepideh, Reddick, Adam C, Branham, Kari E. H, Moore, Kathryn B, Jessup, Laurie, Thoms, Susan, Smith-Wheelock, Michael, Yashar, Beverly M, Swaroop, Anand

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Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements von Wang, Feng, Wang, Hui, Tuan, Han-Fang, Nguyen, Duy H., Sun, Vincent, Keser, Vafa, Bowne, Sara J., Sullivan, Lori S., Luo, Hongrong, Zhao, Ling, Wang, Xia, Zaneveld, Jacques E., Salvo, Jason S., Siddiqui, Sorath, Mao, Louise, Wheaton, Dianna K., Birch, David G., Branham, Kari E., Heckenlively, John R., Wen, Cindy, Flagg, Ken, Ferreyra, Henry, Pei, Jacqueline, Khan, Ayesha, Ren, Huanan, Wang, Keqing, Lopez, Irma, Qamar, Raheel, Zenteno, Juan C., Ayala-Ramirez, Raul, Buentello-Volante, Beatriz, Fu, Qing, Simpson, David A., Li, Yumei, Sui, Ruifang, Silvestri, Giuliana, Daiger, Stephen P., Koenekoop, Robert K., Zhang, Kang, Chen, Rui

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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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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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Detailed clinical characterisation, unique features and natural history of autosomal recessive RDH12-associated retinal degeneration von Fahim, Abigail T, Bouzia, Zaina, Branham, Kari H, Kumaran, Neruban, Vargas, Mauricio E, Feathers, Kecia L, Perera, N Dayanthi, Young, Kelly, Khan, Naheed W, Heckenlively, John R, Webster, Andrew R, Pennesi, Mark E, Ali, Robin R, Thompson, Debra A, Michaelides, Michel

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A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants von Fritsche, Lars G, Igl, Wilmar, Grassmann, Felix, Sengupta, Sebanti, Bragg-Gresham, Jennifer L, Burdon, Kathryn P, Hebbring, Scott J, Wen, Cindy, Zack, Donald, Souied, Eric, Scholl, Hendrik P N, Bala, Elisa, Lee, Kristine E, Hunter, David J, Sardell, Rebecca J, Cipriani, Valentina, Hoffman, Joshua D, Schick, Tina, Guymer, Robyn H, Johnson, Matthew P, Jiang, Yingda, Buitendijk, Gabriëlle H S, Zhan, Xiaowei, Kwong, Alan M, Brooks, Matthew, Branham, Kari E, Foerster, Johanna R, Souzeau, Emmanuelle, McAllister, Ian L, Isaacs, Timothy, Hall, Janette, Lake, Stewart, Mackey, David A, Constable, Ian J, Craig, Jamie E, Yang, Zhenglin, Su, Zhiguang, Luo, Hongrong, Chen, Daniel, Ouyang, Hong, Mao, Guanping, Ferreyra, Henry, Stark, Klaus, Brandl, Caroline, Morrison, Margaux A, Morgan, Denise J, Park, Kyu Hyung, Farrer, Lindsay A, Li, Mingyao, Curcio, Christine A, Mohand-Saïd, Saddek, Benchaboune, Mustapha, Cree, Angela J, Rennie, Christina A, Goverdhan, Srinivas V, Grunin, Michelle, Campochiaro, Peter, Katsanis, Nicholas, Blanché, Hélène, Igo, Robert P, Truitt, Barbara, Peachey, Neal S, Klein, Ronald, Postel, Eric A, Courtenay, Monique D, Schwartz, Stephen G, Liew, Gerald, Tan, Ava G, Gopinath, Bamini, Merriam, John C, Smith, R Theodore, Shahid, Humma, Moore, Anthony T, McGrath, J Allie, Brantley, Milam A, Agarwal, Anita, Saksens, Nicole T M, de Jong, Eiko K, Cain, Melinda S, Richardson, Andrea J, Martin, Tammy M, Doheny, Kimberly F, Romm, Jane, Hayward, Caroline, Klein, Michael L, Baird, Paul N, Fauser, Sascha, Yates, John R W, Allikmets, Rando, Schaumberg, Debra A, Klein, Barbara E K, Hagstrom, Stephanie A, Lotery, Andrew J, Léveillard, Thierry, Hewitt, Alex W, Swaroop, Anand, Chew, Emily Y, Pericak-Vance, Margaret A, DeAngelis, Margaret, Heid, Iris M

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Next-generation genetic testing for retinitis pigmentosa von Neveling, Kornelia, Collin, Rob W.J., Gilissen, Christian, van Huet, Ramon A.C., Visser, Linda, Kwint, Michael P., Gijsen, Sabine J., Zonneveld, Marijke N., Wieskamp, Nienke, de Ligt, Joep, Siemiatkowska, Anna M., Hoefsloot, Lies H., Buckley, Michael F., Kellner, Ulrich, Branham, Kari E., den Hollander, Anneke I., Hoischen, Alexander, Hoyng, Carel, Klevering, B. Jeroen, van den Born, L. Ingeborgh, Veltman, Joris A., Cremers, Frans P.M., Scheffer, Hans

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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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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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