Realization of the Manipulation of Ultracold Atoms with a Reconfigurable Nanomagnetic System of Domain Walls von West, Adam D, Weatherill, Kevin J, Hayward, Thomas J, Fry, Paul W, Schrefl, Thomas, Gibbs, Mike R. J, Adams, Charles S, Allwood, Dan A, Hughes, Ifan G

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Transverse Field-Induced Nucleation Pad Switching Modes During Domain Wall Injection von Bryan, Matthew T., Fry, Paul W., Schrefl, Thomas, Gibbs, Mike R. J., Allwood, Dan A., Im, Mi-Young, Fischer, Peter

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The Effect of Injection Layers on a Room Temperature Organic Spin Valve von Dhandapani, Dhana, Morley, Nicola A., Gibbs, Mike R. J., Kreouzis, Theo, Shakya, Pabrita, Desai, Pratik, Gillin, William P.

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Texture and magnetic properties of hard magnetic RE–Fe–B thin films deposited on a Nb buffer layer von Tang, S.L., Gibbs, Mike R.J., Liu, Zong-Wu, Davies, Hywel A.

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Materials Optimization for Magnetic MEMS von Gibbs, M.R.J.

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Enterprise in physical science von Gibbs, Mike R J

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Observation of changing of magnetic properties and microstructure of metallic glass Fe78Si9B13 with annealing von SAHINGOZ, Recep, EROL, Mustafa, GIBBS, Mike R. J

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Moment canting and structural anisotropy in amorphous alloys: experiments using synchrotron Mössbauer radiation von PANKHURST, Quentin A, COHEN, Neil S, FERNANDEZ BARQUIN, Luis, GIBBS, Mike R. J, SMIRNOV, Gennadii V

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Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain von Hernandez, Dena G, Nalls, Mike A, Moore, Matthew, Chong, Sean, Dillman, Allissa, Trabzuni, Daniah, Gibbs, J. Raphael, Ryten, Mina, Arepalli, Sampath, Weale, Michael E, Zonderman, Alan B, Troncoso, Juan, O'Brien, Richard, Walker, Robert, Smith, Colin, Bandinelli, Stefania, Traynor, Bryan J, Hardy, John, Singleton, Andrew B, Cookson, Mark R

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Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource von Iwaki, Hirotaka, Leonard, Hampton L., Makarious, Mary B., Bookman, Matt, Landin, Barry, Vismer, David, Casey, Bradford, Gibbs, J. Raphael, Hernandez, Dena G., Blauwendraat, Cornelis, Vitale, Daniel, Song, Yeajin, Kumar, Dinesh, Dalgard, Clifton L., Sadeghi, Mahdiar, Dong, Xianjun, Misquitta, Leonie, Scholz, Sonja W., Scherzer, Clemens R., Nalls, Mike A., Biswas, Shameek, Singleton, Andrew B.

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Genome‐Wide Analysis of Structural Variants in Parkinson Disease von Billingsley, Kimberley J., Ding, Jinhui, Jerez, Pilar Alvarez, Illarionova, Anastasia, Levine, Kristin, Grenn, Francis P., Makarious, Mary B., Moore, Anni, Vitale, Daniel, Reed, Xylena, Hernandez, Dena, Torkamani, Ali, Ryten, Mina, Hardy, John, Chia, Ruth, Scholz, Sonja W., Traynor, Bryan J., Dalgard, Clifton L., Ehrlich, Debra J., Tanaka, Toshiko, Ferrucci, Luigi, Beach, Thomas G., Serrano, Geidy E., Quinn, John P., Bubb, Vivien J., Collins, Ryan L, Zhao, Xuefang, Walker, Mark, Pierce‐Hoffman, Emma, Brand, Harrison, Talkowski, Michael E., Casey, Bradford, Cookson, Mark R, Markham, Androo, Nalls, Mike A., Mahmoud, Medhat, Sedlazeck, Fritz J, Blauwendraat, Cornelis, Gibbs, J. Raphael, Singleton, Andrew B.

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Genetic comorbidities in Parkinson's disease von Nalls, Mike A, Saad, Mohamad, Noyce, Alastair J, Keller, Margaux F, Schrag, Anette, Bestwick, Jonathan P, Traynor, Bryan J, Gibbs, J Raphael, Hernandez, Dena G, Cookson, Mark R, Morris, Huw R, Williams, Nigel, Gasser, Thomas, Heutink, Peter, Wood, Nick, Hardy, John, Martinez, Maria, Singleton, Andrew B

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Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies von Vallerga, Costanza L, Tan, Manuela, Kia, Demis A, Xue, Angli, Young, Emily, Sharma, Manu, Krohn, Lynne, Siitonen, Ari, Iwaki, Hirotaka, Leonard, Hampton, Botia, Juan A, Martinez, Maria, Jankovic, Joseph, Sutherland, Margaret, Majamaa, Kari, Andreassen, Ole A, Gan-Or, Ziv, Gasser, Thomas, Heutink, Peter, Gratten, Jacob, Alvarez, Ignacio, Alvarez, Victoria, Bandres-Ciga, Sara, Bergareche Yarza, Jesús Alberto, Billingsley, Kimberley, Bonilla-Toribio, Marta, Botía, Juan A, Boungiorno, María Teresa, Bras, Jose, Bubb, Vivien, Buiza-Rueda, Dolores, Cerdan, Debora, Chelban, Viorica, Corvol, Jean-Christophe, Craig, David W, Danjou, Fabrice, Diez-Fairen, Monica, Escott-Price, Valentina, Ezquerra, Mario, Fernández, Manel, Fernández-Santiago, Rubén, Gan-Or, Ziv, Garcia, Ciara, García-Ruiz, Pedro, Hernandez, Dena G, Hoenicka, Janet, Infante, Jon, Jesús, Silvia, Kaiyrzhanov, Rauan, Kia, Demis A, Leonard, Hampton L, Lewis, Patrick, Lopez-Sendon, Jose Luis, Lovering, Ruth, Lubbe, Steven, Majamaa, Kari, Manzoni, Claudia, Marti, Maria Jose, Méndez-del-Barrio, Carlota, Middlehurst, Ben, Mínguez, Adolfo, Muñoz, Esteban, Pagola, Ana Gorostidi, Pastor, Pau, Perez Errazquin, Francisco, Periñán-Tocino, Teresa, Reed, Xylena, Rezola, Elisabet Mondragon, Rodriguez, Antonio Sanchez, Ruiz-Martínez, Javier, Sadykova, Dinara, Shashkin, Chingiz, Sierra, María, Simón-Sánchez, Javier, Singleton, Andrew B, Suarez-Sanmartin, Esther, Tabernero, Cesar, Tolosa, Eduard, van Hilten, Jacobus J, Vargas-González, Laura, Wood, Nicholas W, Zimprich, Alexander, Reich, Stephen, Savitt, Joseph, Bryc, Katarzyna, Hicks, Barry, Jiang, Yunxuan, McCreight, Jennifer C., McIntyre, Matthew H., Noblin, Elizabeth S., Sathirapongsasuti, J. Fah, Tung, Joyce, Anderson, Tim, Bentley, Steven, Kennedy, Martin, Mellick, George, Sidorenko, Julia, Silburn, Peter A., Visscher, Peter M., Yang, Jian

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Differences in the Presentation and Progression of Parkinson's Disease by Sex von Iwaki, Hirotaka, Blauwendraat, Cornelis, Leonard, Hampton L., Makarious, Mary B., Kim, Jonggeol J., Liu, Ganqiang, Maple‐Grødem, Jodi, Corvol, Jean‐Christophe, Pihlstrøm, Lasse, Nimwegen, Marlies, Smolensky, Luba, Amondikar, Ninad, Hutten, Samantha J., Frasier, Mark, Nguyen, Khanh‐Dung H., Rick, Jacqueline, Eberly, Shirley, Faghri, Faraz, Auinger, Peggy, Scott, Kirsten M., Wijeyekoon, Ruwani, Van Deerlin, Vivianna M., Hernandez, Dena G., Gibbs, Raphael J., Day‐Williams, Aaron G., Brice, Alexis, Alves, Guido, Noyce, Alastair J., Tysnes, Ole‐Bjørn, Evans, Jonathan R., Breen, David P., Estrada, Karol, Wegel, Claire E., Danjou, Fabrice, Simon, David K., Andreassen, Ole A., Ravina, Bernard, Toft, Mathias, Heutink, Peter, Bloem, Bastiaan R., Weintraub, Daniel, Barker, Roger A., Williams‐Gray, Caroline H., Warrenburg, Bart P., Van Hilten, Jacobus J., Scherzer, Clemens R., Singleton, Andrew B., Nalls, Mike A.

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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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Genome-wide association study of Tourette's syndrome von Scharf, J M, Yu, D, Mathews, C A, Neale, B M, Stewart, S E, Fagerness, J A, Evans, P, Gamazon, E, Edlund, C K, Service, S K, Tikhomirov, A, Osiecki, L, Illmann, C, Pluzhnikov, A, Konkashbaev, A, Davis, L K, Han, B, Crane, J, Moorjani, P, Crenshaw, A T, Parkin, M A, Reus, V I, Lowe, T L, Rangel-Lugo, M, Chouinard, S, Dion, Y, Girard, S, Cath, D C, Smit, J H, King, R A, Fernandez, T V, Leckman, J F, Kidd, K K, Kidd, J R, Pakstis, A J, State, M W, Herrera, L D, Romero, R, Fournier, E, Sandor, P, Barr, C L, Phan, N, Gross-Tsur, V, Benarroch, F, Pollak, Y, Budman, C L, Bruun, R D, Erenberg, G, Naarden, A L, Lee, P C, Weiss, N, Kremeyer, B, Berrío, G B, Campbell, D D, Cardona Silgado, J C, Ochoa, W C, Mesa Restrepo, S C, Muller, H, Valencia Duarte, A V, Lyon, G J, Leppert, M, Morgan, J, Weiss, R, Grados, M A, Anderson, K, Davarya, S, Singer, H, Walkup, J, Jankovic, J, Tischfield, J A, Heiman, G A, Gilbert, D L, Hoekstra, P J, Robertson, M M, Kurlan, R, Liu, C, Gibbs, J R, Singleton, A, Hardy, J, Strengman, E, Ophoff, R A, Wagner, M, Moessner, R, Mirel, D B, Posthuma, D, Sabatti, C, Eskin, E, Conti, D V, Knowles, J A, Ruiz-Linares, A, Rouleau, G A, Purcell, S, Heutink, P, Oostra, B A, McMahon, W M, Freimer, N B, Cox, N J, Pauls, D L

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Two-component system cross-regulation integrates Bacillus anthracis response to heme and cell envelope stress von Mike, Laura A, Choby, Jacob E, Brinkman, Paul R, Olive, Lorenzo Q, Dutter, Brendan F, Ivan, Samuel J, Gibbs, Christopher M, Sulikowski, Gary A, Stauff, Devin L, Skaar, Eric P

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Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance von Lubbe, Steven J, Escott-Price, Valentina, Gibbs, J Raphael, Nalls, Mike A, Bras, Jose, Price, T Ryan, Nicolas, Aude, Jansen, Iris E, Mok, Kin Y, Pittman, Alan M, Tomkins, James E, Lewis, Patrick A, Noyce, Alastair J, Lesage, Suzanne, Sharma, Manu, Schiff, Elena R, Levine, Adam P, Brice, Alexis, Gasser, Thomas, Hardy, John, Heutink, Peter, Wood, Nicholas W, Singleton, Andrew B, Williams, Nigel M, Morris, Huw R

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NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases von Nalls, Mike A, Bras, Jose, Hernandez, Dena G, Keller, Margaux F, Majounie, Elisa, Renton, Alan E, Saad, Mohamad, Jansen, Iris, Guerreiro, Rita, Lubbe, Steven, Plagnol, Vincent, Gibbs, J. Raphael, Schulte, Claudia, Pankratz, Nathan, Sutherland, Margaret, Bertram, Lars, Lill, Christina M, DeStefano, Anita L, Faroud, Tatiana, Eriksson, Nicholas, Tung, Joyce Y, Edsall, Connor, Nichols, Noah, Brooks, Janet, Arepalli, Sampath, Pliner, Hannah, Letson, Chris, Heutink, Peter, Martinez, Maria, Gasser, Thomas, Traynor, Bryan J, Wood, Nick, Hardy, John, Singleton, Andrew B

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Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease von Beilina, Alexandria, Rudenko, Iakov N., Kaganovich, Alice, Civiero, Laura, Chau, Hien, Kalia, Suneil K., Kalia, Lorraine V., Lobbestael, Evy, Chia, Ruth, Ndukwe, Kelechi, Ding, Jinhui, Nalls, Mike A., Olszewski, Maciej, Hauser, David N., Kumaran, Ravindran, Lozano, Andres M., Baekelandt, Veerle, Greene, Lois E., Taymans, Jean-Marc, Greggio, Elisa, Cookson, Mark R.

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