Prediction model for prevalence and incidence of advanced age-related macular degeneration based on genetic, demographic, and environmental variables von Seddon, Johanna M, Reynolds, Robyn, Maller, Julian, Fagerness, Jesen A, Daly, Mark J, Rosner, Bernard

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Variation in complement factor 3 is associated with risk of age-related macular degeneration von Daly, Mark J, Seddon, Johanna M, Maller, Julian B, Fagerness, Jesen A, Reynolds, Robyn C, Neale, Benjamin M

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Variation near complement factor I is associated with risk of advanced AMD von FAGERNESS, Jesen A, MALLER, Julian B, NEALE, Benjamin M, REYNOLDS, Robyn C, DALY, Mark J, SEDDON, Johanna M

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Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC) von Neale, Benjamin M, Fagerness, Jesen, Reynolds, Robyn, Sobrin, Lucia, Parker, Margaret, Raychaudhuri, Soumya, Tan, Perciliz L, Oh, Edwin C, Merriam, Joanna E, Souied, Eric, Bernstein, Paul S, Li, Binxing, Frederick, Jeanne M, Zhang, Kang, Brantley, Milam A. Jr, Lee, Aaron Y, Zack, Donald J, Campochiaro, Betsy, Campochiaro, Peter, Ripke, Stephan, Smith, R. Theodore, Barile, Gaetano R, Katsanis, Nicholas, Allikmets, Rando, Daly, Mark J, Seddon, Johanna M

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Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder von Stewart, S. Evelyn, Fagerness, Jesen A., Platko, Jill, Smoller, Jordan W., Scharf, Jeremiah M., Illmann, Cornelia, Jenike, Eric, Chabane, Nadia, Leboyer, Marion, Delorme, Richard, Jenike, Michael A., Pauls, David L.

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ARMS2/HTRA1 Locus Can Confer Differential Susceptibility to the Advanced Subtypes of Age-Related Macular Degeneration von Sobrin, Lucia, Reynolds, Robyn, Yu, Yi, Fagerness, Jesen, Leveziel, Nicolas, Bernstein, Paul S, Souied, Eric H, Daly, Mark J, Seddon, Johanna M

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Heritability and Genome-Wide Association Study to Assess Genetic Differences between Advanced Age-related Macular Degeneration Subtypes von Sobrin, Lucia, MD, MPH, Ripke, Stephan, MD, Yu, Yi, PhD, Fagerness, Jesen, JD, Bhangale, Tushar R., PhD, Tan, Perciliz L., BSc, Souied, Eric H., MD, PhD, Buitendijk, Gabriëlle H.S., MD, MSc, Merriam, Joanna E., MD, PhD, Richardson, Andrea J., BSc, Raychaudhuri, Soumya, MD, PhD, Reynolds, Robyn, MPH, Chin, Kimberly A., BA, Lee, Aaron Y., MD, Leveziel, Nicolas, MD, PhD, Zack, Donald J., MD, PhD, Campochiaro, Peter, MD, Smith, R. Theodore, MD, PhD, Barile, Gaetano R., MD, Hogg, Ruth E., PhD, Chakravarthy, Usha, MD, PhD, Behrens, Timothy W., MD, Uitterlinden, André G., PhD, van Duijn, Cornelia M., PhD, Vingerling, Johannes R., MD, PhD, Brantley, Milam A., MD, PhD, Baird, Paul N., PhD, Klaver, Caroline C.W., MD, PhD, Allikmets, Rando, PhD, Katsanis, Nicholas, PhD, Graham, Robert R., PhD, Ioannidis, John P.A., MD, DSc, Daly, Mark J., PhD, Seddon, Johanna M., MD, ScM

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The Corticotropin-Releasing Hormone Gene and Behavioral Inhibition in Children at Risk for Panic Disorder von Smoller, Jordan W., Yamaki, Lesley H., Fagerness, Jesen A., Biederman, Joseph, Racette, Stephanie, Laird, Nan M., Kagan, Jerome, Snidman, Nancy, Faraone, Stephen V., Hirshfeld-Becker, Dina, Tsuang, Ming T., Slaugenhaupt, Susan A., Rosenbaum, Jerrold F., Sklar, Pamela B.

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Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approach von SOBRIN, Lucia, MALLER, Julian B, NEALE, Benjamin M, REYNOLDS, Robyn C, FAGERNESS, Jesen A, DALY, Mark J, SEDDON, Johanna M

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Clinical and Genetic Dissection of Anger Expression and CREB1 Polymorphisms in Major Depressive Disorder von Perlis, Roy H, Purcell, Shaun, Fagerness, Jesen, Cusin, Cristina, Yamaki, Lesley, Fava, Maurizio, Smoller, Jordan W

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Association of SNPs and haplotypes in APOL1, 2 and 4 with schizophrenia von Takahashi, Sakae, Cui, Yu-hu, Han, Yong-hua, Fagerness, Jesen A, Galloway, Brian, Shen, Yu-cun, Kojima, Takuya, Uchiyama, Makoto, Faraone, Stephen V, Tsuang, Ming T

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Reply to Cipriani et al von Fagerness, Jesen A, Yu, Yi, Maller, Julian B, Neale, Benjamin M, Reynolds, Robyn C, Daly, Mark J, Seddon, Johanna M

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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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Pharmacogenomic and pharmacogenetic-guided therapy as a tool in precision medicine: current state and factors impacting acceptance by stakeholders von HESS, GREGORY P., FONSECA, EILEEN, SCOTT, RACHEL, FAGERNESS, JESEN

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Association of variants in the LIPC and ABCA1 genes with intermediate and large drusen and advanced age-related macular degeneration von Yu, Yi, Reynolds, Robyn, Fagerness, Jesen, Rosner, Bernard, Daly, Mark J, Seddon, Johanna M

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Identification of common variants associated with human hippocampal and intracranial volumes von Vasquez, Alejandro Arias, Toro, Roberto, Bartecek, Richard, Bergmann, Ørjan, Bernard, Manon, Chakravarty, M Mallar, Grimm, Oliver, Homuth, Georg, Lopez, Lorna M, Hansell, Narelle K, Kim, Sungeun, Laje, Gonzalo, Lee, Phil H, Liu, Xinmin, Loth, Eva, Lourdusamy, Anbarasu, Mattingsdal, Morten, Mohnke, Sebastian, Maniega, Susana Muñoz, O'Brien, Carol, Pütz, Benno, Rasmussen, Jerod, Risacher, Shannon L, Rose, Emma J, Ryten, Mina, Sprooten, Emma, Teumer, Alexander, Trabzuni, Daniah, Turner, Jessica, van Eijk, Kristel, van Erp, Theo G M, van Tol, Marie-Jose, Wolf, Christiane, Aleman, Andre, Alhusaini, Saud, Binder, Elisabeth B, Brohawn, David G, Cantor, Rita M, Czisch, Michael, de Almeida, Marcio A A, Delanty, Norman, Dyer, Thomas D, Erk, Susanne, Fox, Peter T, Freimer, Nelson B, Hagler, Donald J, Hoogman, Martine, Johnson, Matthew P, Kasperaviciute, Dalia, Kent, Jack W, Kochunov, Peter, Lancaster, Jack L, Liewald, David C, Matarin, Mar, Mattheisen, Manuel, Moses, Eric K, Mühleisen, Thomas W, Nöthen, Markus M, Puls, Ralf, Reinvang, Ivar, Savitz, Jonathan, Schnack, Hugo G, Seiferth, Nina, Valdés Hernández, Maria C, Van Haren, Neeltje E M, Veltman, Joris A, Völzke, Henry, Westlye, Lars T, Whelan, Christopher D, Cavalleri, Gianpiero L, Dale, Anders M, Drevets, Wayne C, Heinz, Andreas, Le Hellard, Stephanie, Macciardi, Fabio, Montgomery, Grant W, Starr, John M, Gudnason, Vilmundur, Tzourio, Christophe, Vernooij, Meike W, Launer, Lenore J, Andreassen, Ole A, Bastin, Mark E, Blangero, John, Brunner, Han G, Buckner, Randy L, Coppola, Giovanni, de Zubicaray, Greig I, Fernández, Guillén, Glahn, David C, Hardy, John, Kahn, René S, McIntosh, Andrew M, Nichols, Thomas E, Ophoff, Roel A, Pausova, Zdenka, Potkin, Steven G, Smoller, Jordan W, Martin, Nicholas G, Thompson, Paul M

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Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration von Chen, Wei, Stambolian, Dwight, Edwards, Albert O, Branham, Kari E, Othman, Mohammad, Jakobsdottir, Johanna, Tosakulwong, Nirubol, Pericak-Vance, Margaret A, Campochiaro, Peter A, Klein, Michael L, Tan, Perciliz L, Conley, Yvette P, Kanda, Atsuhiro, Kopplin, Laura, Li, Yanming, Augustaitis, Katherine J, Karoukis, Athanasios J, Scott, William K, Agarwal, Anita, Kovach, Jaclyn L, Schwartz, Stephen G, Postel, Eric A, Brooks, Matthew, Baratz, Keith H, Brown, William L, Brucker, Alexander J, Orlin, Anton, Brown, Gary, Ho, Allen, Regillo, Carl, Donoso, Larry, Tian, Lifeng, Kaderli, Brian, Hadley, Dexter, Hagstrom, Stephanie A, Peachey, Neal S, Klein, Ronald, Klein, Barbara E.K, Gotoh, Norimoto, Yamashiro, Kenji, Ferris III, Frederick, Fagerness, Jesen A, Reynolds, Robyn, Farrer, Lindsay A, Kim, Ivana K, Miller, Joan W, Cortón, Marta, Carracedo, Angel, Sanchez-Salorio, Manuel, Pugh, Elizabeth W, Doheny, Kimberly F, Brion, Maria, DeAngelis, Margaret M, Weeks, Daniel E, Zack, Donald J, Chew, Emily Y, Heckenlively, John R, Yoshimura, Nagahisa, Iyengar, Sudha K, Francis, Peter J, Katsanis, Nicholas, Seddon, Johanna M, Haines, Jonathan L, Gorin, Michael B, Abecasis, Gonçalo R, Swaroop, Anand

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Genome-wide association study of obsessive-compulsive disorder von Stewart, S E, Yu, D, Scharf, J M, Neale, B M, Fagerness, J A, Arnold, P D, Evans, P D, Gamazon, E R, McGrath, L, Haddad, S, Crane, J, Hezel, D, Illman, C, Mayerfeld, C, Konkashbaev, A, Liu, C, Pluzhnikov, A, Tikhomirov, A, Rauch, S L, Maier, W, Ruhrmann, S, Grabe, H-J, Lennertz, L, Wagner, M, Bellodi, L, Cavallini, M C, Richter, M A, Cook, E H, Kennedy, J L, Rosenberg, D, Stein, D J, Hemmings, S M J, Azzam, A, Chavira, D A, Fournier, E, Garrido, H, Sheppard, B, Umaña, P, Murphy, D L, Wendland, J R, Veenstra-VanderWeele, J, Denys, D, Blom, R, Deforce, D, Van Nieuwerburgh, F, Walitza, S, Egberts, K, Renner, T, Miguel, E C, Cappi, C, Hounie, A G, Conceição do Rosário, M, Sampaio, A S, Vallada, H, Lanzagorta, N, Camarena, B, Delorme, R, Leboyer, M, Pato, C N, Pato, M T, Voyiaziakis, E, Heutink, P, Cath, D C, Posthuma, D, Smit, J H, Samuels, J, Bienvenu, O J, Cullen, B, Fyer, A J, Grados, M A, Greenberg, B D, McCracken, J T, Riddle, M A, Wang, Y, Coric, V, Leckman, J F, Pittenger, C, Eapen, V, Black, D W, Ophoff, R A, Strengman, E, Cusi, D, Turiel, M, Frau, F, Macciardi, F, Gibbs, J R, Cookson, M R, Singleton, A, Hardy, J, Crenshaw, A T, Parkin, M A, Mirel, D B, Conti, D V, Purcell, S, Nestadt, G, Hanna, G L, Jenike, M A, Knowles, J A, Cox, N, Pauls, D L

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The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data von Vasquez, Alejandro Arias, Renteria, Miguel E., Agartz, Ingrid, Apostolova, Liana G., Bastin, Mark E., Bauer, Michael, Bearden, Carrie E., Binder, Elisabeth B., Bøen, Erlend, Bowman, Ian J., Brohawn, David G., Buitelaar, Jan, Carless, Melanie A., Ching, Christopher R. K., Conrod, Patricia, Depondt, Chantal, de Zubicaray, Greig I., Djurovic, Srdjan, Duggirala, Ravindranath, Dyer, Thomas D., Ekman, Carl Johan, Emsell, Louise, Fears, Scott, Fedko, Iryna, Fox, Peter T., Francks, Clyde, Frodl, Thomas, Frouin, Vincent, Godlewska, Beata, Haukvik, Unn K., Hickie, Ian B., Hoekstra, Pieter J., Homuth, Georg, Hulshoff Pol, Hilleke E., Hwang, Kristy S., Kim, Sungeun, Kochunov, Peter, Krämer, Bernd, Kwok, John B. J., Laje, Gonzalo, Landman, Bennett A., Lauriello, John, Li, Chiang-shan, Liberg, Benny, Liu, Xinmin, Macciardi, Fabio, Malt, Ulrik F., Mattheisen, Manuel, Meyer-Lindenberg, Andreas, Melle, Ingrid, Mohnke, Sebastian, Morris, Derek W., Mueller, Bryon A., Mühleisen, Thomas W., Müller-Myhsok, Bertram, Nichols, Thomas E., Oosterlaan, Jaap, Pandolfo, Massimo, Papmeyer, Martina, Pausova, Zdenka, Penninx, Brenda W., Peterson, Charles P., Potkin, Steven G., Rasmussen, Jerod, Rijpkema, Mark, Risacher, Shannon L., Roiz-Santiañez, Roberto, Romanczuk-Seiferth, Nina, Rujescu, Dan, Salami, Alireza, Scanlon, Cathy, Schmaal, Lianne, Schnack, Hugo G., Schork, Andrew J., Seidman, Larry, Shen, Li, Smoller, Jordan W., Sponheim, Scott R., Starr, John M., Sussmann, Jessika, Sämann, Philipp G., Teumer, Alexander, Toga, Arthur W., Trabzuni, Daniah, Turner, Jessica, Van den Heuvel, Martijn, van Eijk, Kristel, van Erp, Theo G. M., van Haren, Neeltje E. M., van ‘t Ent, Dennis, van Tol, Marie-Jose, Valdés Hernández, Maria C., Versace, Amelia, Weale, Michael E., Westlye, Lars T., Whelan, Christopher D., Wittfeld, Katharina, Zilles, David, Freimer, Nelson B., Lawrence, Natalia S.

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Common variants at 12q14 and 12q24 are associated with hippocampal volume von Bis, Joshua C, DeCarli, Charles, Smith, Albert Vernon, van der Lijn, Fedde, Crivello, Fabrice, Fornage, Myriam, Debette, Stephanie, Shulman, Joshua M, Schmidt, Helena, Srikanth, Velandai, Schuur, Maaike, Yu, Lei, Choi, Seung-Hoan, Sigurdsson, Sigurdur, Verhaaren, Benjamin F J, DeStefano, Anita L, Lambert, Jean-Charles, Jack, Jr, Clifford R, Struchalin, Maksim, Stankovich, Jim, Ibrahim-Verbaas, Carla A, Fleischman, Debra, Zijdenbos, Alex, den Heijer, Tom, Mazoyer, Bernard, Coker, Laura H, Enzinger, Christian, Danoy, Patrick, Amin, Najaf, Arfanakis, Konstantinos, van Buchem, Mark A, de Bruijn, Renée F A G, Beiser, Alexa, Dufouil, Carole, Huang, Juebin, Cavalieri, Margherita, Thomson, Russell, Niessen, Wiro J, Chibnik, Lori B, Gislason, Gauti K, Hofman, Albert, Pikula, Aleksandra, Amouyel, Philippe, Freeman, Kevin B, Phan, Thanh G, Oostra, Ben A, Stein, Jason L, Medland, Sarah E, Vasquez, Alejandro Arias, Hibar, Derrek P, Wright, Margaret J, Franke, Barbara, Martin, Nicholas G, Thompson, Paul M, Nalls, Michael A, Uitterlinden, Andre G, Au, Rhoda, Elbaz, Alexis, Beare, Richard J, van Swieten, John C, Lopez, Oscar L, Harris, Tamara B, Chouraki, Vincent, Breteler, Monique M B, De Jager, Philip L, Becker, James T, Vernooij, Meike W, Knopman, David, Fazekas, Franz, Wolf, Philip A, van der Lugt, Aad, Gudnason, Vilmundur, Longstreth, Jr, W T, Brown, Matthew A, Bennett, David A, van Duijn, Cornelia M, Mosley, Thomas H, Schmidt, Reinhold, Tzourio, Christophe, Launer, Lenore J, Ikram, M Arfan, Seshadri, Sudha

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