Autonomous Navigation in Three-Dimensional Urban Environments Using Wide-Field Integration of Optic Flow von Hyslop, Andrew M, Humbert, J. Sean

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Optic flow estimation on trajectories generated by bio-inspired closed-loop flight von Shoemaker, Patrick A., Hyslop, Andrew M., Humbert, J. Sean

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Ground Simulation of an Autonomous Satellite Rendezvous and Tracking System Using Dual Robotic Systems von Trube, Matthew J., Hyslop, Andrew M., Carignan, Craig R., Easley, Joseph W.

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TREM2 shedding by cleavage at the H157‐S158 bond is accelerated for the Alzheimer's disease‐associated H157Y variant von Thornton, Peter, Sevalle, Jean, Deery, Michael J, Fraser, Graham, Zhou, Ye, Ståhl, Sara, Franssen, Elske H, Dodd, Roger B, Qamar, Seema, Gomez Perez‐Nievas, Beatriz, Nicol, Louise SC, Eketjäll, Susanna, Revell, Jefferson, Jones, Clare, Billinton, Andrew, St George‐Hyslop, Peter H, Chessell, Iain, Crowther, Damian C

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Latrepirdine improves cognition and arrests progression of neuropathology in an Alzheimer's mouse model von Steele, J W, Lachenmayer, M L, Ju, S, Stock, A, Liken, J, Kim, S H, Delgado, L M, Alfaro, I E, Bernales, S, Verdile, G, Bharadwaj, P, Gupta, V, Barr, R, Friss, A, Dolios, G, Wang, R, Ringe, D, Fraser, P, Westaway, D, St George-Hyslop, P H, Szabo, P, Relkin, N R, Buxbaum, J D, Glabe, C G, Protter, A A, Martins, R N, Ehrlich, M E, Petsko, G A, Yue, Z, Gandy, S

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TREM2 Variants in Alzheimer's Disease von Guerreiro, Rita, Wojtas, Aleksandra, Bras, Jose, Carrasquillo, Minerva, Rogaeva, Ekaterina, Majounie, Elisa, Cruchaga, Carlos, Sassi, Celeste, Kauwe, John S.K, Younkin, Steven, Hazrati, Lilinaz, Collinge, John, Pocock, Jennifer, Lashley, Tammaryn, Williams, Julie, Lambert, Jean-Charles, Amouyel, Philippe, Goate, Alison, Rademakers, Rosa, Morgan, Kevin, Powell, John, St. George-Hyslop, Peter, Singleton, Andrew, Hardy, John

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Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease von Naj, Adam C, Jun, Gyungah, Beecham, Gary W, Wang, Li-San, Vardarajan, Badri Narayan, Buros, Jacqueline, Gallins, Paul J, Buxbaum, Joseph D, Crane, Paul K, Larson, Eric B, Bird, Thomas D, De Jager, Philip L, Schneider, Julie A, Younkin, Steven G, Cruchaga, Carlos, Kauwe, John S K, Nowotny, Petra, Hardy, John, Myers, Amanda J, Barmada, Michael M, Baldwin, Clinton T, Arnold, Steven E, Barber, Robert, Beach, Thomas, Bowen, James D, Boxer, Adam, Carlson, Chris S, Carney, Regina M, Carroll, Steven L, Clark, David G, Cummings, Jeffrey L, DeKosky, Steven T, Diaz-Arrastia, Ramon, Dickson, Dennis W, Faber, Kelley M, Fallon, Kenneth B, Farlow, Martin R, Ferris, Steven, Ganguli, Mary, Gearing, Marla, Ghetti, Bernardino, Gilbert, John R, Gilman, Sid, Glass, Jonathan D, Growdon, John H, Hamilton, Ronald L, Harrell, Lindy E, Head, Elizabeth, Honig, Lawrence S, Hulette, Christine M, Johnson, Nancy, Karydas, Anna, Kaye, Jeffrey A, Kim, Ronald, Lah, James J, Levey, Allan I, Lieberman, Andrew P, Mack, Wendy J, Marson, Daniel C, Martiniuk, Frank, Mash, Deborah C, McDavid, Andrew N, McKee, Ann C, Mesulam, Marsel, Miller, Bruce L, Miller, Carol A, Parisi, Joseph E, Perl, Daniel P, Peskind, Elaine, Rajbhandary, Ruchita A, Reisberg, Barry, Ringman, John M, Roberson, Erik D, Rosenberg, Roger N, Sano, Mary, Seeley, William, Shelanski, Michael L, Slifer, Michael A, Smith, Charles D, Sonnen, Joshua A, Spina, Salvatore, Tanzi, Rudolph E, Troncoso, Juan C, Weintraub, Sandra, Welsh-Bohmer, Kathleen A, Woltjer, Randall L, Cantwell, Laura B, Lunetta, Kathryn L, Kamboh, M Ilyas, Saykin, Andrew J, Reiman, Eric M, Morris, John C, Goate, Alison M, Blacker, Deborah, Tsuang, Debby W, Hakonarson, Hakon, Kukull, Walter A, Haines, Jonathan L, Pericak-Vance, Margaret A, Farrer, Lindsay A

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A novel Alzheimer disease locus located near the gene encoding tau protein von Jun, G, Ibrahim-Verbaas, C A, Vronskaya, M, Chung, J, Naj, A C, Kunkle, B W, Wang, L-S, Bis, J C, Bellenguez, C, Harold, D, Destefano, A L, Grenier-Boley, B, Sims, R, Smith, A V, Chouraki, V, Hamilton-Nelson, K L, Ikram, M A, Fievet, N, Martin, E R, Kamatani, Y, Valladares, O, Laza, A R, Zelenika, D, Choi, S-H, Boland, A, Becker, T, Kukull, W A, van der Lee, S J, Pasquier, F, Cruchaga, C, Beekly, D, Fitzpatrick, A L, Hanon, O, Gill, M, Gudnason, V, Campion, D, Love, S, Bennett, D A, Amin, N, Berr, C, Tsolaki, Magda, Buxbaum, J D, Lopez, O L, Deramecourt, V, Fox, N C, Cantwell, L B, Tárraga, L, Dufouil, C, Hardy, J, Crane, P K, Eiriksdottir, G, Hannequin, D, Clarke, R, Evans, D, Mosley, T H, Letenneur, L, Brayne, C, Maier, W, De Jager, P, Dartigues, J-F, Hampel, H, de Bruijn, R F A G, Tzourio, C, Pastor, P, Larson, E B, O'Donovan, M C, Montine, T J, Nalls, M A, Mead, S, Reiman, E M, Jonsson, P V, St George-Hyslop, P H, Boada, M, Passmore, P, Wendland, J R, Schmidt, R, Morgan, K, Powell, J F, Carasquillo, M, Jakobsdóttir, J, Kauwe, J S K, Rujescu, D, Nöthen, M M, Hofman, A, Jones, L, Haines, J L, Psaty, B M, Van Broeckhoven, C, Holmans, P, Launer, L J, Mayeux, R, Goate, A M, Escott-Price, V, Seshadri, S, Pericak-Vance, M A, Amouyel, P, Williams, J, van Duijn, C M, Schellenberg, G D, Farrer, L A

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Genetic variants in the SHISA6 gene are associated with delayed cognitive impairment in two family datasets von Ramos, Jairo, Caywood, Laura J., Prough, Michael B., Clouse, Jason E., Herington, Sharlene D., Slifer, Susan H., Fuzzell, M. Denise, Fuzzell, Sarada L., Hochstetler, Sherri D., Miskimen, Kristy L., Main, Leighanne R., Osterman, Michael D., Zaman, Andrew F., Whitehead, Patrice L., Adams, Larry D., Laux, Renee A., Song, Yeunjoo E., Foroud, Tatiana M., Mayeux, Richard P., St. George‐Hyslop, Peter, Ogrocki, Paula K., Lerner, Alan J., Vance, Jeffery M., Cuccaro, Michael L., Haines, Jonathan L., Pericak‐Vance, Margaret A., Scott, William K.

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Clinical significance of SF3B1 mutations in myelodysplastic syndromes and myelodysplastic/myeloproliferative neoplasms von Malcovati, Luca, Papaemmanuil, Elli, Bowen, David T., Boultwood, Jacqueline, Della Porta, Matteo G., Pascutto, Cristiana, Travaglino, Erica, Groves, Michael J., Godfrey, Anna L., Ambaglio, Ilaria, Gallì, Anna, Da Vià, Matteo C., Conte, Simona, Tauro, Sudhir, Keenan, Norene, Hyslop, Ann, Hinton, Jonathan, Mudie, Laura J., Wainscoat, James S., Futreal, P. Andrew, Stratton, Michael R., Campbell, Peter J., Hellström-Lindberg, Eva, Cazzola, Mario

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Transethnic genome-wide scan identifies novel Alzheimer's disease loci von Jun, Gyungah R, Chung, Jaeyoon, Mez, Jesse, Barber, Robert, Beecham, Gary W, Bennett, David A, Buxbaum, Joseph D, Byrd, Goldie S, Carrasquillo, Minerva M, Crane, Paul K, Cruchaga, Carlos, De Jager, Philip, Ertekin-Taner, Nilufer, Evans, Denis, Fallin, M. Danielle, Foroud, Tatiana M, Friedland, Robert P, Goate, Alison M, Graff-Radford, Neill R, Hendrie, Hugh, Hall, Kathleen S, Hamilton-Nelson, Kara L, Inzelberg, Rivka, Kamboh, M. Ilyas, Kauwe, John S.K, Kukull, Walter A, Kunkle, Brian W, Kuwano, Ryozo, Larson, Eric B, Logue, Mark W, Manly, Jennifer J, Martin, Eden R, Montine, Thomas J, Mukherjee, Shubhabrata, Naj, Adam, Reiman, Eric M, Reitz, Christiane, Sherva, Richard, St. George-Hyslop, Peter H, Thornton, Timothy, Younkin, Steven G, Vardarajan, Badri N, Wang, Li-San, Wendlund, Jens R, Winslow, Ashley R, Haines, Jonathan, Mayeux, Richard, Pericak-Vance, Margaret A, Schellenberg, Gerard, Lunetta, Kathryn L, Farrer, Lindsay A

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Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation von Hague, Stephen, Rogaeva, Ekaterina, Hernandez, Dena, Gulick, Cindy, Singleton, Amanda, Hanson, Melissa, Johnson, Janel, Weiser, Roberto, Gallardo, Marisol, Ravina, Bernard, Gwinn-Hardy, Katrina, Crawley, Anthony, St. George-Hyslop, Peter H., Lang, Anthony E., Heutink, Peter, Bonifati, Vincenzo, Hardy, John, Singleton, Andrew

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Heritability and genetic variance of dementia with Lewy bodies von Guerreiro, Rita, Escott-Price, Valentina, Hernandez, Dena G., Kun-Rodrigues, Celia, Ross, Owen A., Orme, Tatiana, Neto, Joao Luis, Carmona, Susana, Dehghani, Nadia, Eicher, John D., Shepherd, Claire, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G., Scholz, Sonja W., Troncoso, Juan C., Pletnikova, Olga, Dawson, Ted, Rosenthal, Liana, Ansorge, Olaf, Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Clark, Lorraine, Honig, Lawrence S., Marder, Karen, Lemstra, Afina, Rogaeva, Ekaterina, St. George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Serrano, Geidy E., Beach, Thomas G., Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, Tienari, Pentti J., Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad F., Petersen, Ronald C., Ferman, Tanis J., Graff-Radford, Neill, Cairns, Nigel J., Morris, John C., Pickering-Brown, Stuart, Mann, David, Halliday, Glenda M., Hardy, John, Trojanowski, John Q., Dickson, Dennis W., Singleton, Andrew, Stone, David J., Bras, Jose

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Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study von Guerreiro, Rita, Ross, Owen A, Kun-Rodrigues, Celia, Hernandez, Dena G, Orme, Tatiana, Eicher, John D, Shepherd, Claire E, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G, Scholz, Sonja W, Troncoso, Juan C, Pletnikova, Olga, Ansorge, Olaf, Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Clark, Lorraine, Honig, Lawrence S, Marder, Karen, Lemstra, Afina, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Serrano, Geidy E, Beach, Thomas G, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, Tienari, Pentti J, Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad F, Petersen, Ronald C, Ferman, Tanis J, Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel J, Morris, John C, Pickering-Brown, Stuart, Mann, David, Halliday, Glenda M, Hardy, John, Trojanowski, John Q, Dickson, Dennis W, Singleton, Andrew, Stone, David J, Bras, Jose

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Cholinergic Neuron Gene Expression Differences Captured by Translational Profiling In A Mouse Model of Alzheimer’s Disease von McKeever, Paul M, Kim, TaeHyung, Hesketh, Andrew R, MacNair, Laura, Miletic, Denise, Favrin, Giorgio, Oliver, Stephen G, Zhang, Zhaolei, St George-Hyslop, Peter, Robertson, Janice

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Bioinspired Visuomotor Convergence von Humbert, J.S., Hyslop, A.M.

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Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseases von Guerreiro, Rita, Escott-Price, Valentina, Darwent, Lee, Parkkinen, Laura, Ansorge, Olaf, Hernandez, Dena G, Nalls, Michael A, Clark, Lorraine, Honig, Lawrence, Marder, Karen, van der Flier, Wiesje, Holstege, Henne, Louwersheimer, Eva, Lemstra, Afina, Scheltens, Philip, Rogaeva, Ekaterina, St George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Ortega-Cubero, Sara, Pastor, Pau, Ferman, Tanis J, Graff-Radford, Neill R, Ross, Owen A, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Maetzler, Walter, Berg, Daniela, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Compta, Yaroslau, Revesz, Tamas, Lees, Andrew, Cairns, Nigel J, Halliday, Glenda M, Mann, David, Pickering-Brown, Stuart, Powell, John, Lunnon, Katie, Lupton, Michelle K, Dickson, Dennis, Hardy, John, Singleton, Andrew, Bras, Jose

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Assessment of the genetic variance of late-onset Alzheimer’s disease von Ridge, Perry G, Hoyt, Kaitlyn B, Boehme, Kevin, Mukherjee, Shubhabrata, Crane, Paul K, Haines, Jonathan L, Mayeux, Richard, Farrer, Lindsay A, Pericak-Vance, Margaret A, Schellenberg, Gerard D, Kauwe, John S.K

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A comprehensive screening of copy number variability in dementia with Lewy bodies von Kun-Rodrigues, Celia, Orme, Tatiana, Carmona, Susana, Hernandez, Dena G., Ross, Owen A., Eicher, John D., Shepherd, Claire, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G., Scholz, Sonja W., Troncoso, Juan C., Pletnikova, Olga, Dawson, Ted, Rosenthal, Liana, Ansorge, Olaf, Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Clark, Lorraine, Honig, Lawrence S., Marder, Karen, Lemstra, Afina, Rogaeva, Ekaterina, St. George-Hyslop, Peter, Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Serrano, Geidy E., Beach, Thomas G., Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, Tienari, Pentti J., Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad F., Petersen, Ronald C., Ferman, Tanis J., Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel J., Morris, John C., Pickering-Brown, Stuart, Mann, David, Halliday, Glenda M., Hardy, John, Trojanowski, John Q., Dickson, Dennis W., Singleton, Andrew, Stone, David J., Guerreiro, Rita, Bras, Jose

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Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia von Swarup, Vivek, Hinz, Flora I., Rexach, Jessica E., Noguchi, Ken-ichi, Toyoshiba, Hiroyoshi, Oda, Akira, Hirai, Keisuke, Sarkar, Arjun, Seyfried, Nicholas T., Cheng, Chialin, Haggarty, Stephen J., Grossman, Murray, Van Deerlin, Vivianna M., Trojanowski, John Q., Lah, James J., Levey, Allan I., Kondou, Shinichi, Geschwind, Daniel H.

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