Imidazole Initiates Exsheathing of L3 Teladorsagia circumcincta von Brown, Simon, Neale, Jennifer D, Nava-Tirado, Magnolia, Simpson, Heather V, Pedley, Kevin C, Simcock, David C

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Thermotolerance of L3 Ostertagia (Teladorsagia) circumcincta and some of its enzymes von Walker, L.R, Simcock, D.C, Neale, J.D, Simpson, H.V, Brown, S

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Imidazole Initiates Exsheathing of L3Teladorsagia circumcincta von Brown, Simon, Neale, Jennifer D, Nava-Tirado, Magnolia, Simpson, Heather V, Pedley, Kevin C, Simcock, David C

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IMIDAZOLE INITIATES EXSHEATHING OF L^sub 3^ TELADORSAGIA CIRCUMCINCTA von Brown, Simon, Neale, Jennifer D, Nava-Tirado, Magnolia, Simpson, Heather V, Pedley, Kevin C, Simcock, David C

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Imidazole Initiates Exsheathing of L 3 Teladorsagia circumcincta von Brown, Simon, Neale, Jennifer D., Nava-Tirado, Magnolia, Simpson, Heather V., Pedley, Kevin C., Simcock, David C.

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Thermotolerance of L 3 Ostertagia ( Teladorsagia) circumcincta and some of its enzymes von Walker, Lisa R., Simcock, David C., Neale, Jennifer D., Simpson, Heather V., Brown, Simon

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THE COMMUNITY EARTH SYSTEM MODEL: A Framework for Collaborative Research von Hurrell, James W., Holland, M. M., Gent, P. R., Ghan, S., Kay, Jennifer E., Kushner, P. J., Lamarque, J.-F., Large, W. G., Lawrence, D., Lindsay, K., Lipscomb, W. H., Long, M. C., Mahowald, N., Marsh, D. R., Neale, R. B., Rasch, P., Vavrus, S., Vertenstein, M., Bader, D., Collins, W. D., Hack, J. J., Kiehl, J., Marshall, S.

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Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations von Howrigan, Daniel P., Rose, Samuel A., Samocha, Kaitlin E., Fromer, Menachem, Cerrato, Felecia, Chen, Wei J., Churchhouse, Claire, Chambert, Kimberly, Chandler, Sharon D., Daly, Mark J., Dumont, Ashley, Genovese, Giulio, Hwu, Hai-Gwo, Laird, Nan, Kosmicki, Jack A., Moran, Jennifer L., Roe, Cheryl, Singh, Tarjinder, Wang, Shi-Heng, Faraone, Stephen V., Glatt, Stephen J., McCarroll, Steven A., Tsuang, Ming, Neale, Benjamin M.

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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population von Robinson, Elise B, St Pourcain, Beate, Anttila, Verneri, Kosmicki, Jack A, Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E, Sanders, Stephan J, Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V, Werge, Thomas, Hougaard, David M, Neale, Benjamin M, Evans, David M, Skuse, David, Mortensen, Preben Bo, Børglum, Anders D, Ronald, Angelica, Smith, George Davey, Daly, Mark J

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Exome sequencing and the genetic basis of complex traits von Kiezun, Adam, Garimella, Kiran, Do, Ron, Stitziel, Nathan O, Neale, Benjamin M, McLaren, Paul J, Gupta, Namrata, Sklar, Pamela, Sullivan, Patrick F, Moran, Jennifer L, Hultman, Christina M, Lichtenstein, Paul, Magnusson, Patrik, Lehner, Thomas, Shugart, Yin Yao, Price, Alkes L, de Bakker, Paul I W, Purcell, Shaun M, Sunyaev, Shamil R

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Identification of common genetic risk variants for autism spectrum disorder von Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond K., Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Awashti, Swapnil, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, De Rubeis, Silvia, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashley L., Goldstein, Jacqueline I., Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina M., Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer L., Nyegaard, Mette, Nærland, Terje, Palmer, Duncan S., Palotie, Aarno, Pedersen, Carsten Bøcker, Pedersen, Marianne Giørtz, dPoterba, Timothy, Poulsen, Jesper Buchhave, Pourcain, Beate St, Qvist, Per, Rehnström, Karola, Reichenberg, Abraham, Reichert, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Davey Smith, George, Stefansson, Hreinn, Steinberg, Stacy, Stevens, Christine R., Sullivan, Patrick F., Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Stefansson, Kari, Geschwind, Daniel H., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J., Børglum, Anders D.

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Extremely low-coverage sequencing and imputation increases power for genome-wide association studies von Pasaniuc, Bogdan, Rohland, Nadin, McLaren, Paul J, Garimella, Kiran, Zaitlen, Noah, Li, Heng, Gupta, Namrata, Neale, Benjamin M, Daly, Mark J, Sklar, Pamela, Sullivan, Patrick F, Bergen, Sarah, Moran, Jennifer L, Hultman, Christina M, Lichtenstein, Paul, Magnusson, Patrik, Purcell, Shaun M, Haas, David W, Liang, Liming, Sunyaev, Shamil, Patterson, Nick, de Bakker, Paul I W, Reich, David, Price, Alkes L

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Copy number variation in schizophrenia in Sweden von Szatkiewicz, J P, O'Dushlaine, C, Chen, G, Chambert, K, Moran, J L, Neale, B M, Fromer, M, Ruderfer, D, Akterin, S, Bergen, S E, Kähler, A, Magnusson, P K E, Kim, Y, Crowley, J J, Rees, E, Kirov, G, O'Donovan, M C, Owen, M J, Walters, J, Scolnick, E, Sklar, P, Purcell, S, Hultman, C M, McCarroll, S A, Sullivan, P F

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LD Score regression distinguishes confounding from polygenicity in genome-wide association studies von Bulik-Sullivan, Brendan K, Loh, Po-Ru, Finucane, Hilary K, Ripke, Stephan, Yang, Jian, Patterson, Nick, Daly, Mark J, Price, Alkes L, Neale, Benjamin M

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Six Months of Hybrid Closed-Loop Versus Manual Insulin Delivery With Fingerprick Blood Glucose Monitoring in Adults With Type 1 Diabetes: A Randomized, Controlled Trial von McAuley, Sybil A, Lee, Melissa H, Paldus, Barbora, Vogrin, Sara, de Bock, Martin I, Abraham, Mary B, Bach, Leon A, Burt, Morton G, Cohen, Neale D, Colman, Peter G, Davis, Elizabeth A, Hendrieckx, Christel, Holmes-Walker, D Jane, Kaye, Joey, Keech, Anthony C, Kumareswaran, Kavita, MacIsaac, Richard J, McCallum, Roland W, Sims, Catriona M, Speight, Jane, Stranks, Stephen N, Sundararajan, Vijaya, Trawley, Steven, Ward, Glenn M, Jenkins, Alicia J, Jones, Timothy W, O'Neal, David N

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Sentinel responses to droughts, wildfires, and floods: effects of UV radiation on lakes and their ecosystem services von Williamson, Craig E, Erin P Overholt, Jennifer A Brentrup, Rachel M Pilla, Taylor H Leach, S Geoffrey Schladow, Joseph D Warren, Samuel S Urmy, Steven Sadro, Sudeep Chandra, Patrick J Neale

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Barriers and enablers to the implementation of protocol-based imaging in pancreatic cancer: A qualitative study using the theoretical domains framework von Maharaj, Ashika D, Evans, Sue M, Zalcberg, John R, Ioannou, Liane J, Graco, Marnie, Croagh, Daniel, Pilgrim, Charles H C, Dodson, Theresa, Goldstein, David, Philip, Jennifer, Kench, James G, Merrett, Neil D, Neale, Rachel E, White, Kate, Evans, Peter, Leong, Trevor, Green, Sally E

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Interrupting prolonged sitting in type 2 diabetes: nocturnal persistence of improved glycaemic control von Dempsey, Paddy C., Blankenship, Jennifer M., Larsen, Robyn N., Sacre, Julian W., Sethi, Parneet, Straznicky, Nora E., Cohen, Neale D., Cerin, Ester, Lambert, Gavin W., Owen, Neville, Kingwell, Bronwyn A., Dunstan, David W.

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Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett’s oesophagus and provides insights into clinical heter... von Ong, Jue-Sheng, An, Jiyuan, Han, Xikun, Law, Matthew H, Nandakumar, Priyanka, Schumacher, Johannes, Gockel, Ines, Bohmer, Anne, Jankowski, Janusz, Palles, Claire, Olsen, Catherine M, Neale, Rachel E, Fitzgerald, Rebecca, Thrift, Aaron P, Vaughan, Thomas L, Buas, Matthew F, Hinds, David A, Gharahkhani, Puya, Kendall, Bradley J, MacGregor, Stuart, Fitzgerald, Rebecca, Buas, Matt, Gammon, Marilie D, Corley, Douglas A, Shaheen, Nicholas J, Hardie, Laura J, Bird, Nigel C, Reid, Brian J, Chow, Wong-Ho, Risch, Harvey A, Ye, Weimin, Liu, Geoffrey, Romero, Yvonne, Bernstein, Leslie, Wu, Anna H, Schumacher, Johannes, Gockel, Ines, Bohmer, Anne, Jankowski, Janusz, Palles, Claire, Whiteman, David C, Agee, Michelle, Aslibekyan, Stella, Auton, Adam, Bell, Robert K, Bryc, Katarzyna, Clark, Sarah K, Elson, Sarah L, Fletez-Brant, Kipper, Fontanillas, Pierre, Furlotte, Nicholas A, Gandhi, Pooja M, Heilbron, Karl, Hicks, Barry, Hinds, David A, Huber, Karen E, Jewett, Ethan M, Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K, Luff, Marie K, McCreight, Jennifer C, McIntyre, Matthew H, McManus, Kimberly F, Mountain, Joanna L, Mozaffari, Sahar V, Nandakumar, Priyanka, Noblin, Elizabeth S, Northover, Carrie AM, O'Connell, Jared, Petrakovitz, Aaron A, Pitts, Steven J, David Poznik, G., Fah Sathirapongsasuti, J, Shastri, Anjali J, Shelton, Janie F, Shringarpure, Suyash, Tian, Chao, Tung, Joyce Y, Tunney, Robert J, Vacic, Vladimir, Wang, Xin, Zare, Amir S

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Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains von Demontis, Ditte, Walters, G. Bragi, Athanasiadis, Georgios, Walters, Raymond, Therrien, Karen, Nielsen, Trine Tollerup, Farajzadeh, Leila, Voloudakis, Georgios, Bendl, Jaroslav, Zeng, Biau, Zhang, Wen, Grove, Jakob, Als, Thomas D., Duan, Jinjie, Satterstrom, F. Kyle, Bybjerg-Grauholm, Jonas, Bækved-Hansen, Marie, Gudmundsson, Olafur O., Magnusson, Sigurdur H., Baldursson, Gisli, Davidsdottir, Katrin, Haraldsdottir, Gyda S., Agerbo, Esben, Hoffman, Gabriel E., Dalsgaard, Søren, Martin, Joanna, Ribasés, Marta, Boomsma, Dorret I., Soler Artigas, Maria, Roth Mota, Nina, Howrigan, Daniel, Medland, Sarah E., Zayats, Tetyana, Rajagopal, Veera M., Nordentoft, Merete, Mors, Ole, Hougaard, David M., Mortensen, Preben Bo, Daly, Mark J., Faraone, Stephen V., Stefansson, Hreinn, Roussos, Panos, Franke, Barbara, Werge, Thomas, Neale, Benjamin M., Stefansson, Kari, Børglum, Anders D.

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