Shifting the paradigm of type 1 diabetes: a narrative review of disease modifying therapies von O'Donovan, Alexander J, Gorelik, Seth, Nally, Laura M

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Voluntary Age Regression Entering "Headspace" in a Child With Post-traumatic Stress Disorder von O'Donovan, Alexander J, Cardiel Sam, Hector, Lagman, Jasmin G

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A Three-Way Accuracy Comparison of the Dexcom G5, Abbott Freestyle Libre Pro, and Senseonics Eversense CGM Devices in an Outpatient Study of Subjects with Type 1 Diabetes von JAFRI, RABAB Z., BALLIRO, COURTNEY A., EL-KHATIB, FIRAS, MAHENO, MICHELE, HILLARD, MALLORY A., O'DONOVAN, ALEXANDER J., SELAGAMSETTY, RAJENDRANATH, ZHENG, HUI, DAMIANO, EDWARD, RUSSELL, STEVEN J.

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Differential Effects of the Insulin-Only and Bihormonal Configurations of the Bionic Pancreas on Mean Glucose and Hypoglycemia during the Daytime and Nighttime von SHERWOOD, JORDAN, BALLIRO, COURTNEY A., JAFRI, RABAB Z., EL-KHATIB, FIRAS, MAHENO, MICHELE, HILLARD, MALLORY A., O'DONOVAN, ALEXANDER J., SELAGAMSETTY, RAJENDRANATH, ZHENG, HUI, DAMIANO, EDWARD, RUSSELL, STEVEN J.

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Voluntary Age Regression Entering "Headspace" in a Child With Post-traumatic Stress Disorder von O'Donovan, Alexander J, Cardiel Sam, Hector, Lagman, Jasmin G

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Contrasting genetic architectures of schizophrenia and other complex diseases using fast variance-components analysis von Loh, Po-Ru, Bhatia, Gaurav, Gusev, Alexander, Finucane, Hilary K, Bulik-Sullivan, Brendan K, Pollack, Samuela J, de Candia, Teresa R, Lee, Sang Hong, Wray, Naomi R, Kendler, Kenneth S, O'Donovan, Michael C, Neale, Benjamin M, Patterson, Nick, Price, Alkes L

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Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC von Hamshere, M L, Walters, J T R, Smith, R, Richards, A L, Green, E, Grozeva, D, Jones, I, Forty, L, Jones, L, Gordon-Smith, K, Riley, B, O'Neill, T, Kendler, K S, Sklar, P, Purcell, S, Kranz, J, Morris, D, Gill, M, Holmans, P, Craddock, N, Corvin, A, Owen, M J, O'Donovan, M C

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Analysis of copy number variations at 15 schizophrenia-associated loci von REES, Elliott, WALTERS, James T. R, O'DONOVAN, Michael C, OWEN, Michael J, KIROV, George, GEORGIEVA, Lyudmila, ISLES, Anthony R, CHAMBERT, Kimberly D, RICHARDS, Alexander L, MAHONEY-DAVIES, Gerwyn, LEGGE, Sophie E, MORAN, Jennifer L, MCCARROLL, Steven A

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Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia von Bergen, Sarah E, Ploner, Alexander, Howrigan, Daniel, O’Donovan, Michael C, Smoller, Jordan W, Sullivan, Patrick F, Sebat, Jonathan, Neale, Benjamin, Kendler, Kenneth S

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The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay von Kirov, George, Rees, Elliott, Walters, James T.R, Escott-Price, Valentina, Georgieva, Lyudmila, Richards, Alexander L, Chambert, Kimberly D, Davies, Gerwyn, Legge, Sophie E, Moran, Jennifer L, McCarroll, Steven A, O’Donovan, Michael C, Owen, Michael J

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The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia von Richards, Alexander L., Pardinas, Antonio F., Frizzati, Aura, Tansey, Katherine E., Lynham, Amy J., Holmans, Peter, Legge, Sophie E., Savage, Jeanne E., Agartz, Ingrid, Andreassen, Ole A., Blokland, Gabriella A. M., Corvin, Aiden, Cosgrove, Donna, Degenhardt, Franziska, Djurovic, Srdjan, Espeseth, Thomas, Ferraro, Laura, Gayer-Anderson, Charlotte, Giegling, Ina, van Haren, Neeltje E., Hartmann, Annette M., Hubert, John J., Jonsson, Erik G., Konte, Bettina, Lennertz, Leonhard, Loohuis, Loes M. Olde, Melle, Ingrid, Morgan, Craig, Morris, Derek W., Murray, Robin M., Nyman, Hakan, Ophoff, Roel A., van Os, Jim, Petryshen, Tracey L., Quattrone, Diego, Rietschel, Marcella, Rujescu, Dan, Rutten, Bart P. F., Streit, Fabian, Strohmaier, Jana, Sullivan, Patrick F., Sundet, Kjetil, Wagner, Michael, Escott-Price, Valentina, Owen, Michael J., Donohoe, Gary, O'Donovan, Michael C., Walters, James T. R.

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A Deletion in the Canine POMC Gene Is Associated with Weight and Appetite in Obesity-Prone Labrador Retriever Dogs von Raffan, Eleanor, Dennis, Rowena J., O’Donovan, Conor J., Becker, Julia M., Scott, Robert A., Smith, Stephen P., Withers, David J., Wood, Claire J., Conci, Elena, Clements, Dylan N., Summers, Kim M., German, Alexander J., Mellersh, Cathryn S., Arendt, Maja L., Iyemere, Valentine P., Withers, Elaine, Söder, Josefin, Wernersson, Sara, Andersson, Göran, Lindblad-Toh, Kerstin, Yeo, Giles S.H., O’Rahilly, Stephen

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Comparison of Genetic Liability for Sleep Traits Among Individuals With Bipolar Disorder I or II and Control Participants von Lewis, Katie J. S, Richards, Alexander, Karlsson, Robert, Leonenko, Ganna, Jones, Samuel E, Jones, Hannah J, Gordon-Smith, Katherine, Forty, Liz, Escott-Price, Valentina, Owen, Michael J, Weedon, Michael N, Jones, Lisa, Craddock, Nick, Jones, Ian, Landén, Mikael, O’Donovan, Michael C, Di Florio, Arianna

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De novo mutations identified by exome sequencing implicate rare missense variants in SLC6A1 in schizophrenia von Rees, Elliott, Han, Jun, Morgan, Joanne, Carrera, Noa, Escott-Price, Valentina, Pocklington, Andrew J., Duffield, Madeleine, Hall, Lynsey S., Legge, Sophie E., Pardiñas, Antonio F., Richards, Alexander L., Roth, Julian, Lezheiko, Tatyana, Kondratyev, Nikolay, Kaleda, Vasilii, Golimbet, Vera, Parellada, Mara, González-Peñas, Javier, Arango, Celso, Gawlik, Micha, Kirov, George, Walters, James T. R., Holmans, Peter, O’Donovan, Michael C., Owen, Michael J.

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A Population-Based Study of Genetic Variation and Psychotic Experiences in Adolescents von ZAMMIT, Stanley, HAMSHERE, Marian, OWEN, Michael J, O'DONOVAN, Michael C, DWYER, Sarah, GEORGIVA, Lyudmila, TIMPSON, Nic, MOSKVINA, Valentina, RICHARDS, Alexander, EVANS, David M, LEWIS, Glyn, JONES, Peter

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Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia von Legge, S E, Hamshere, M L, Ripke, S, Pardinas, A F, Goldstein, J I, Rees, E, Richards, A L, Leonenko, G, Jorskog, L F, Chambert, K D, Collier, D A, Genovese, G, Giegling, I, Holmans, P, Jonasdottir, A, Kirov, G, McCarroll, S A, MacCabe, J H, Mantripragada, K, Moran, J L, Neale, B M, Stefansson, H, Rujescu, D, Daly, M J, Sullivan, P F, Owen, M J, O'Donovan, M C, Walters, J T R

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A rationale for determining, testing, and controlling specific impurities in pharmaceuticals that possess potential for genotoxicity von Müller, Lutz, Mauthe, Robert J., Riley, Christopher M., Andino, Marta M., Antonis, David De, Beels, Chris, DeGeorge, Joseph, De Knaep, Alfons G.M., Ellison, Dean, Fagerland, Jane A., Frank, Rebecca, Fritschel, Betsy, Galloway, Sheila, Harpur, Ernie, Humfrey, Charles D.N., Jacks, Alexander S., Jagota, Nirdosh, Mackinnon, John, Mohan, Ganapathy, Ness, Daniel K., O’Donovan, Michael R., Smith, Mark D., Vudathala, Gopi, Yotti, Larry

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Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain von Richards, A L, Jones, L, Moskvina, V, Kirov, G, Gejman, P V, Levinson, D F, Sanders, A R, Purcell, S, Visscher, P M, Craddock, N, Owen, M J, Holmans, P, O'Donovan, M C

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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1 von Rees, Elliott, Walters, James T R, Chambert, Kimberly D, O'Dushlaine, Colm, Szatkiewicz, Jin, Richards, Alexander L, Georgieva, Lyudmila, Mahoney-Davies, Gerwyn, Legge, Sophie E, Moran, Jennifer L, Genovese, Giulio, Levinson, Douglas, Morris, Derek W, Cormican, Paul, Kendler, Kenneth S, O'Neill, Francis A, Riley, Brien, Gill, Michael, Corvin, Aiden, Sklar, Pamela, Hultman, Christina, Pato, Carlos, Pato, Michele, Sullivan, Patrick F, Gejman, Pablo V, McCarroll, Steven A, O'Donovan, Michael C, Owen, Michael J, Kirov, George

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Application of transfer learning to predict drug-induced human in vivo gene expression changes using rat in vitro and in vivo data von O'Donovan, Shauna D, Cavill, Rachel, Wimmenauer, Florian, Lukas, Alexander, Stumm, Tobias, Smirnov, Evgueni, Lenz, Michael, Ertaylan, Gokhan, Jennen, Danyel G. J, van Riel, Natal A. W, Driessens, Kurt, Peeters, Ralf L. M, de Kok, Theo M. C. M

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