Modeling the impulse response between pairs of EMG signals to estimate conduction delay distribution von Hassan, T., McIntosh, K. C. D., Gabriel, D. A., Clancy, E. A.

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Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions von Howard, David M., Adams, Mark J., Clarke, Toni-Kim, Hafferty, Jonathan D., Gibson, Jude, Shirali, Masoud, Coleman, Jonathan R. I., Hagenaars, Saskia P., Ward, Joey, Wigmore, Eleanor M., Alloza, Clara, Shen, Xueyi, Barbu, Miruna C., Xu, Eileen Y., Whalley, Heather C., Marioni, Riccardo E., Porteous, David J., Davies, Gail, Deary, Ian J., Hemani, Gibran, Berger, Klaus, Teismann, Henning, Rawal, Rajesh, Arolt, Volker, Baune, Bernhard T., Dannlowski, Udo, Domschke, Katharina, Tian, Chao, Hinds, David A., Trzaskowski, Maciej, Byrne, Enda M., Ripke, Stephan, Smith, Daniel J., Sullivan, Patrick F., Wray, Naomi R., Breen, Gerome, Lewis, Cathryn M., McIntosh, Andrew M.

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The effects of a neuregulin 1 variant on white matter density and integrity von McIntosh, A M, Moorhead, T W J, Job, D, Lymer, G K S, Muñoz Maniega, S, McKirdy, J, Sussmann, J E D, Baig, B J, Bastin, M E, Porteous, D, Evans, K L, Johnstone, E C, Lawrie, S M, Hall, J

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Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general population von Clarke, T-K, Lupton, M K, Fernandez-Pujals, A M, Starr, J, Davies, G, Cox, S, Pattie, A, Liewald, D C, Hall, L S, MacIntyre, D J, Smith, B H, Hocking, L J, Padmanabhan, S, Thomson, P A, Hayward, C, Hansell, N K, Montgomery, G W, Medland, S E, Martin, N G, Wright, M J, Porteous, D J, Deary, I J, McIntosh, A M

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DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan von Porteous, D J, Thomson, P A, Millar, J K, Evans, K L, Hennah, W, Soares, D C, McCarthy, S, McCombie, W R, Clapcote, S J, Korth, C, Brandon, N J, Sawa, A, Kamiya, A, Roder, J C, Lawrie, S M, McIntosh, A M, St Clair, D, Blackwood, D H

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Probing the Symmetry Energy with the Spectral Pion Ratio von Estee, J, Lynch, W G, Tsang, C Y, Barney, J, Jhang, G, Tsang, M B, Wang, R, Kaneko, M, Lee, J W, Isobe, T, Kurata-Nishimura, M, Murakami, T, Ahn, D S, Atar, L, Aumann, T, Baba, H, Boretzky, K, Brzychczyk, J, Cerizza, G, Chiga, N, Fukuda, N, Gasparic, I, Hong, B, Horvat, A, Ieki, K, Inabe, N, Kim, Y J, Kobayashi, T, Kondo, Y, Lasko, P, Lee, H S, Leifels, Y, Łukasik, J, Manfredi, J, McIntosh, A B, Morfouace, P, Nakamura, T, Nakatsuka, N, Nishimura, S, Otsu, H, Pawłowski, P, Pelczar, K, Rossi, D, Sakurai, H, Santamaria, C, Sato, H, Scheit, H, Shane, R, Shimizu, Y, Simon, H, Snoch, A, Sochocka, A, Sumikama, T, Suzuki, H, Suzuki, D, Takeda, H, Tangwancharoen, S, Toernqvist, H, Togano, Y, Xiao, Z G, Yennello, S J, Zhang, Y, Cozma, M D

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Chromospheric Alfvénic Waves Strong Enough to Power the Solar Wind von De Pontieu, B, McIntosh, S.W, Carlsson, M, Hansteen, V.H, Tarbell, T.D, Schrijver, C.J, Title, A.M, Shine, R.A, Tsuneta, S, Katsukawa, Y, Ichimoto, K, Suematsu, Y, Shimizu, T, Nagata, S

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Gene Ontology Consortium: going forward

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Prevalence of small-scale jets from the networks of the solar transition region and chromosphere von Tian, H., DeLuca, E. E., Cranmer, S. R., De Pontieu, B., Peter, H., Martínez-Sykora, J., Golub, L., McKillop, S., Reeves, K. K., Miralles, M. P., McCauley, P., Saar, S., Testa, P., Weber, M., Murphy, N., Lemen, J., Title, A., Boerner, P., Hurlburt, N., Tarbell, T. D., Wuelser, J. P., Kleint, L., Kankelborg, C., Jaeggli, S., Carlsson, M., Hansteen, V., McIntosh, S. W.

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Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis von Grotzinger, Andrew D., Mallard, Travis T., Akingbuwa, Wonuola A., Ip, Hill F., Adams, Mark J., Lewis, Cathryn M., McIntosh, Andrew M., Grove, Jakob, Dalsgaard, Søren, Lesch, Klaus-Peter, Strom, Nora, Meier, Sandra M., Mattheisen, Manuel, Børglum, Anders D., Mors, Ole, Breen, Gerome, Lee, Phil H., Kendler, Kenneth S., Smoller, Jordan W., Tucker-Drob, Elliot M., Nivard, Michel G.

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Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117) von Clarke, T-K, Adams, M J, Davies, G, Howard, D M, Hall, L S, Padmanabhan, S, Murray, A D, Smith, B H, Campbell, A, Hayward, C, Porteous, D J, Deary, I J, McIntosh, A M

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Subcortical volumetric abnormalities in bipolar disorder von Hibar, D P, Westlye, L T, van Erp, T G M, Rasmussen, J, Leonardo, C D, Faskowitz, J, Haukvik, U K, Hartberg, C B, Doan, N T, Agartz, I, Dale, A M, Gruber, O, Krämer, B, Trost, S, Liberg, B, Abé, C, Ekman, C J, Ingvar, M, Landén, M, Fears, S C, Freimer, N B, Bearden, C E, Sprooten, E, Glahn, D C, Pearlson, G D, Emsell, L, Kenney, J, Scanlon, C, McDonald, C, Cannon, D M, Almeida, J, Versace, A, Caseras, X, Lawrence, N S, Phillips, M L, Dima, D, Delvecchio, G, Frangou, S, Satterthwaite, T D, Wolf, D, Houenou, J, Henry, C, Malt, U F, Bøen, E, Elvsåshagen, T, Young, A H, Lloyd, A J, Goodwin, G M, Mackay, C E, Bourne, C, Bilderbeck, A, Abramovic, L, Boks, M P, van Haren, N E M, Ophoff, R A, Kahn, R S, Bauer, M, Pfennig, A, Alda, M, Hajek, T, Mwangi, B, Soares, J C, Nickson, T, Dimitrova, R, Sussmann, J E, Hagenaars, S, Whalley, H C, McIntosh, A M, Thompson, P M, Andreassen, O A

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CANDELS OBSERVATIONS OF THE STRUCTURAL PROPERTIES OF CLUSTER GALAXIES AT z = 1.62 von PAPOVICH, C, BASSETT, R, YICHENG GUO, FABER, S. M, FARRAH, D, FERGUSON, H. C, FINKELSTEIN, K. D, HAUSSLER, B, KOCEVSKI, D. D, KOEKEMOER, A. M, KOO, D. C, MCGRATH, E. J, LOTZ, J. M, MCLURE, R. J, MCINTOSH, D. H, MOMCHEVA, I, NEWMAN, J. A, RUDNICK, G, WEINER, B, WILLMER, C. N. A, WUYTS, S, VAN DER WEL, A, TRAN, K.-V, FINKELSTEIN, S. L, BELL, E. F, CONSELICE, C. J, DEKEL, A, DUNLOP, J. S

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A major role for common genetic variation in anxiety disorders von Purves, Kirstin L., Coleman, Jonathan R. I., Meier, Sandra M., Rayner, Christopher, Davis, Katrina A. S., Cheesman, Rosa, Bækvad-Hansen, Marie, Børglum, Anders D., Wan Cho, Shing, Jürgen Deckert, J., Gaspar, Héléna A., Bybjerg-Grauholm, Jonas, Hettema, John M., Hotopf, Matthew, Hougaard, David, Hübel, Christopher, Kan, Carol, McIntosh, Andrew M., Mors, Ole, Bo Mortensen, Preben, Nordentoft, Merete, Werge, Thomas, Nicodemus, Kristin K., Mattheisen, Manuel, Breen, Gerome, Eley, Thalia C.

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Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium von van Erp, T G M, Hibar, D P, Rasmussen, J M, Glahn, D C, Pearlson, G D, Andreassen, O A, Agartz, I, Westlye, L T, Haukvik, U K, Dale, A M, Melle, I, Hartberg, C B, Gruber, O, Kraemer, B, Zilles, D, Donohoe, G, Kelly, S, McDonald, C, Morris, D W, Cannon, D M, Corvin, A, Machielsen, M W J, Koenders, L, de Haan, L, Veltman, D J, Satterthwaite, T D, Wolf, D H, Gur, R C, Gur, R E, Potkin, S G, Mathalon, D H, Mueller, B A, Preda, A, Macciardi, F, Ehrlich, S, Walton, E, Hass, J, Calhoun, V D, Bockholt, H J, Sponheim, S R, Shoemaker, J M, van Haren, N E M, Pol, H E H, Ophoff, R A, Kahn, R S, Roiz-Santiañez, R, Crespo-Facorro, B, Wang, L, Alpert, K I, Jönsson, E G, Dimitrova, R, Bois, C, Whalley, H C, McIntosh, A M, Lawrie, S M, Hashimoto, R, Thompson, P M, Turner, J A

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The Interface Region Imaging Spectrograph (IRIS) von De Pontieu, B., Title, A. M., Lemen, J. R., Kushner, G. D., Akin, D. J., Allard, B., Berger, T., Boerner, P., Cheung, M., Chou, C., Drake, J. F., Duncan, D. W., Freeland, S., Heyman, G. F., Hoffman, C., Hurlburt, N. E., Lindgren, R. W., Mathur, D., Rehse, R., Sabolish, D., Seguin, R., Schrijver, C. J., Tarbell, T. D., Wülser, J.-P., Wolfson, C. J., Yanari, C., Mudge, J., Nguyen-Phuc, N., Timmons, R., van Bezooijen, R., Weingrod, I., Brookner, R., Butcher, G., Dougherty, B., Eder, J., Knagenhjelm, V., Larsen, S., Mansir, D., Phan, L., Boyle, P., Cheimets, P. N., DeLuca, E. E., Golub, L., Gates, R., Hertz, E., McKillop, S., Park, S., Perry, T., Podgorski, W. A., Reeves, K., Saar, S., Testa, P., Tian, H., Weber, M., Dunn, C., Eccles, S., Jaeggli, S. A., Kankelborg, C. C., Mashburn, K., Pust, N., Springer, L., Carvalho, R., Kleint, L., Marmie, J., Mazmanian, E., Pereira, T. M. D., Sawyer, S., Strong, J., Worden, S. P., Carlsson, M., Hansteen, V. H., Leenaarts, J., Wiesmann, M., Aloise, J., Chu, K.-C., Bush, R. I., Scherrer, P. H., Brekke, P., Martinez-Sykora, J., Lites, B. W., McIntosh, S. W., Uitenbroek, H., Okamoto, T. J., Gummin, M. A., Auker, G., Jerram, P., Pool, P., Waltham, N.

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Expansion of the Gene Ontology knowledgebase and resources

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708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits von Thomson, P A, Parla, J S, McRae, A F, Kramer, M, Ramakrishnan, K, Yao, J, Soares, D C, McCarthy, S, Morris, S W, Cardone, L, Cass, S, Ghiban, E, Hennah, W, Evans, K L, Rebolini, D, Millar, J K, Harris, S E, Starr, J M, MacIntyre, D J, McIntosh, A M, Watson, J D, Deary, I J, Visscher, P M, Blackwood, D H, McCombie, W R, Porteous, D J

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Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium von van Erp, T G M, Hibar, D P, Rasmussen, J M, Glahn, D C, Pearlson, G D, Andreassen, O A, Agartz, I, Westlye, L T, Haukvik, U K, Dale, A M, Melle, I, Hartberg, C B, Gruber, O, Kraemer, B, Zilles, D, Donohoe, G, Kelly, S, McDonald, C, Morris, D W, Cannon, D M, Corvin, A, Machielsen, M W J, Koenders, L, de Haan, L, Veltman, D J, Satterthwaite, T D, Wolf, D H, Gur, R C, Gur, R E, Potkin, S G, Mathalon, D H, Mueller, B A, Preda, A, Macciardi, F, Ehrlich, S, Walton, E, Hass, J, Calhoun, V D, Bockholt, H J, Sponheim, S R, Shoemaker, J M, van Haren, N E M, Hulshoff Pol, H E, Ophoff, R A, Kahn, R S, Roiz-Santiañez, R, Crespo-Facorro, B, Wang, L, Alpert, K I, Jönsson, E G, Dimitrova, R, Bois, C, Whalley, H C, McIntosh, A M, Lawrie, S M, Hashimoto, R, Thompson, P M, Turner, J A

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Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders von Singh, Tarjinder, Kurki, Mitja I, Curtis, David, Purcell, Shaun M, Crooks, Lucy, McRae, Jeremy, Suvisaari, Jaana, Chheda, Himanshu, Blackwood, Douglas, Breen, Gerome, Pietiläinen, Olli, Gerety, Sebastian S, Ayub, Muhammad, Blyth, Moira, Cole, Trevor, Collier, David, Coomber, Eve L, Craddock, Nick, Daly, Mark J, Danesh, John, DiForti, Marta, Foster, Alison, Freimer, Nelson B, Geschwind, Daniel, Johnstone, Mandy, Joss, Shelagh, Kirov, Georg, Körkkö, Jarmo, Kuismin, Outi, Holmans, Peter, Hultman, Christina M, Iyegbe, Conrad, Lönnqvist, Jouko, Männikkö, Minna, McCarroll, Steve A, McGuffin, Peter, McIntosh, Andrew M, McQuillin, Andrew, Moilanen, Jukka S, Moore, Carmel, Murray, Robin M, Newbury-Ecob, Ruth, Ouwehand, Willem, Paunio, Tiina, Prigmore, Elena, Rees, Elliott, Roberts, David, Sambrook, Jennifer, Sklar, Pamela, Clair, David St, Veijola, Juha, Walters, James T R, Williams, Hywel, Sullivan, Patrick F, Hurles, Matthew E, O'Donovan, Michael C, Palotie, Aarno, Owen, Michael J, Barrett, Jeffrey C

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