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  • Cardiff University (98523)
    • MRC Centre for Neuropsychiatric Genetics and Genomics (CNGG) (4861)
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Number of items at this level: 4860.

2019

Addicoat, Alishia, Thapar, Ajay, Riglin, Lucy, Thapar, Anita and Collishaw, Stephan 2019. Adult mood problems in children with neurodevelopmental problems: evidence from a prospective birth cohort followed to age 50. Social Psychiatry and Psychiatric Epidemiology 10.1007/s00127-019-01727-5
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Al-Ansari, A. and Robertson, N. P. 2019. Autoimmune encephalitis: frequency and prognosis. Journal of Neurology 266 (5) , pp. 1287-1289. 10.1007/s00415-019-09273-5
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Baker, Emily, Sims, Rebecca, Leonenko, Ganna, Frizzati, Aura, Harwood, Janet, Grozena, Detelina, Morgan, Kevin, Passmore, Peter, Holmes, Clives, Powell, John, Brayne, Carol, Gill, Michael, Mead, Simon, Bossu, Paola, Spalletta, Gianfranco, Goate, Alison, Crunchaga, Carlos, Maier, Wolfgang, Heun, Reinhard, Jessen, Frank, Peters, Oliver, Dichgans, Martin, Frolich, Lutz, Ramirez, Alfredo, Jones, Lesley, Hardy, John, Ivanov, Dobril, Hill, Matthew, Holmans, Peter, Allen, Nicholas, Morgan, Paul, Seshadri, Sudha, Schellenberg, Gerard, Amouvel, Philippe, Williams, Julie and Escott-Price, Valentina 2019. Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer’s disease. PLoS ONE 14 (7) , e0218111. 10.1371/journal.pone.0218111
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Barker, Roger A., Farrell, K., Guzman, N., He, X., Lazic, S., Moore, S., Morris, R., Tyers, P., Wijeyekoon, R., Daft, D., Hewitt, S., Dayal, V., Foltynie, T., Kefalopoulou, Z., Mahlknecht, P., Lao-Kaim, N., Piccini, P., Bjartmarz, H., Björklund, A., Lindvall, O., Nelander-Wahlestedt, J., Parmar, M., Paul, G., Widner, H., Church, A., Dunnett, S., Peall, K., Rosser, A., Gurruchaga, J., Palfi, S., Piroth, T. and Winkler, C. 2019. Designing stem-cell-based dopamine cell replacement trials for Parkinson's disease. Nature Medicine 25 (7) , pp. 1045-1053. 10.1038/s41591-019-0507-2
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Benn, Caroline, Davis, John, Dawson, Lee, Dawson, Gerry, Evans, Alison, Fox, Nick, Gallacher, John, Hutton, Mike, Isaac, John, Jones, Declan, Jones, Lesley, Libri, Vincenzo, Lovestone, Simon, Mauricio, Rui, Moody, Catherine, Noble, Wendy, Perry, Hugh, Pickett, James, Reynolds, David, Ritche, Craig, Rohrer, John, Routledge, Carol, Rowe, James, Snyder, Heather, Spires-Jones, Tara, Swartz, Jina, Truyen, Luc and Whiting, Paul 2019. Tackling gaps in developing life-changing treatments for dementia. Alzheimer's & Dementia: Translational Research & Clinical Interventions 5 , pp. 241-253. 10.1016/j.trci.2019.05.001
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Bergen, Sarah E., Ploner, Alexander, Howrigan, Daniel, O'Donovan, Michael C., Smoller, Jordan W., Sullivan, Patrick F., Sebat, Jonathan, Neale, Benjamin and Kendler, Kenneth S. 2019. Joint contributions of rare copy number variants and common SNPs to risk for schizophrenia. American Journal of Psychiatry 176 (1) , pp. 29-35. 10.1176/appi.ajp.2018.17040467
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Bhargava, Raghav, Daughters, Katie L and Rees, D. Aled 2019. Oxytocin therapy in hypopituitarism: challenges and opportunities. Clinical Endocrinology 90 (2) , pp. 257-264. 10.1111/cen.13909
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Bondjiers, Krustina, Hyland, Philip, Roberts, Neil, Bisson, Jonathan, Willebrand, Mimmie and Arnberg, Filip 2019. Validation of a clinician-administered diagnostic measure of ICD-11 PTSD and Complex PTSD: The International Trauma Interview in a Swedish sample. European Journal of Psychotraumatology
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Brown, J. William L., Coles, Alasdair, Horakova, Dana, Havrdova, Eva, Izquierdo, Guillermo, Prat, Alexandre, Girard, Marc, Duquette, Pierre, Trojano, Maria, Lugaresi, Alessandra, Bergamaschi, Roberto, Grammond, Pierre, Alroughani, Raed, Hupperts, Raymond, McCombe, Pamela, Van Pesch, Vincent, Sola, Patrizia, Ferraro, Diana, Grand'Maison, Francois, Terzi, Murat, Lechner-Scott, Jeannette, Flechter, Schlomo, Slee, Mark, Shaygannejad, Vahid, Pucci, Eugenio, Granella, Franco, Jokubaitis, Vilija, Willis, Mark, Rice, Claire, Scolding, Neil, Wilkins, Alastair, Pearson, Owen R, Ziemssen, Tjalf, Hutchinson, Michael, Harding, Katharine, Jones, Joanne, McGuigan, Christopher, Butzkueven, Helmut, Kalincik, Tomas and Robertson, Neil 2019. Association of initial disease-modifying therapy with later conversion to secondary progressive multiple sclerosis. Journal of the American Medical Association 321 (2) , pp. 175-187. 10.1001/jama.2018.20588

Calabrese, Massimiliano, Gasperini, Claudio, Tortorella, Carla, Schiavi, Gianmarco, Frisullo, Giovanni, Ragonese, Paolo, Fantozzi, Roberta, Prosperini, Luca, Annovazzi, Pietro, Cordioli, Cinzia, Di Filippo, Massimiliano, Ferraro, Diana, Gajofatto, Alberto, Malucchi, Simona, Lo Fermo, Salvatore, De Luca, Giovanna, Stromillo, Maria L., Cocco, Eleonora, Gallo, Antonio, Paolicelli, Damiano, Lanzillo, Roberta, Tomassini, Valentina, Pesci, Ilaria, Rodegher, Maria E. and Solaro, Claudio 2019. "Better explanations" in multiple sclerosis diagnostic workup: a 3-year longitudinal study. Neurology 92 (22) , -. 10.1212/WNL.0000000000007573
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Cameron, Darren, Blake, Derek J., Bray, Nicholas J. and Hill, Matthew J. 2019. Transcriptional changes following cellular knockdown of the schizophrenia risk gene SETD1A are enriched for common variant association with the disorder. Molecular Neuropsychiatry 5 (2) , pp. 109-114. 10.1159/000497181
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Carnegie, Rebecca, Zheng, Jie, Sallis, Hannah, Jones, Hannh, Wade, Kaitlin, Jonathan, Evans, Zammit, Stan, Munafò, Marcus and Richards, Martin 2019. Mendelian randomization for nutritional psychiatry. Lancet Psychiatry , -.
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Castle, Dan and Robertson, Neil P. 2019. Alternatives to intravenous immunoglobulin treatment in chronic inflammatory demyelinating polyradiculoneuropathy. Journal of Neurology 266 (9) , pp. 2338-2340. 10.1007/s00415-019-09485-9
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Castle, Daniel and Robertson, Neil P. 2019. Treatment of progressive multifocal leukoencephalopathy. Journal of Neurology 266 (10) , pp. 2587-2589. 10.1007/s00415-019-09501-y
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Castle, Daniel, Wynford-Thomas, Ray, Loveless, Sam, Bentley, Emily, Howell, Owain W and Tallantyre, Emma C 2019. Using biomarkers to predict clinical outcomes in multiple sclerosis. Practical Neurology 19 (4) , pp. 342-349. 10.1136/practneurol-2018-002000
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Cavenagh, Alice, Chatterjee, Sohini and Davies, William 2019. Behavioural and psychiatric phenotypes in female carriers of genetic mutations associated with X-linked ichthyosis. PLoS ONE 14 (2) , e0212330. 10.1371/journal.pone.0212330
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Charney, Alexander W., Stahl, Eli A., Green, Elaine K., Chen, Chia-Yen, Moran, Jennifer L., Chambert, Kimberly, Belliveau, Richard A., Forty, Liz, Gordon-Smith, Katherine, Lee, Phil H., Bromet, Evelyn J., Buckley, Peter F., Escamilla, Michael A., Fanous, Ayman H., Fochtmann, Laura J., Lehrer, Douglas S., Malaspina, Dolores, Marder, Stephen R., Morley, Christopher P., Nicolini, Humberto, Perkins, Diana O., Rakofsky, Jeffrey J., Rapaport, Mark H., Medeiros, Helena, Sobell, Janet L., Backlund, Lena, Bergen, Sarah E., Juréus, Anders, Schalling, Martin, Lichtenstein, Paul, Knowles, James A., Burdick, Katherine E., Jones, Ian, Jones, Lisa A., Hultman, Christina M., Perlis, Roy, Purcell, Shaun M., McCarroll, Steven A., Pato, Carlos N., Pato, Michele T., Di Florio, Arianna, Craddock, Nick, Landén, Mikael, Smoller, Jordan W., Ruderfer, Douglas M. and Sklar, Pamela 2019. Contribution of rare copy number variants to bipolar disorder risk Is limited to schizoaffective cases. Biological Psychiatry 86 (2) , pp. 110-119. 10.1016/j.biopsych.2018.12.009
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Chu, Alexander L., Stochl, Jan, Lewis, Glyn, Zammit, Stanley, Jones, Peter B. and Khandaker, Golam M. 2019. Longitudinal association between inflammatory markers and specific symptoms of depression in a prospective birth cohort. Brain, Behavior, and Immunity 76 , pp. 74-81. 10.1016/j.bbi.2018.11.007
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Ciosi, Marc, Maxwell, Alastair, Cumming, Sarah, Hensman Moss, Davina, Alshammari, Asma, Flower, Michael, Durr, Alexandra, Leavitt, Blair, Roos, Raymund, Holmans, Peter, Jones, Lesley, Langbehn, Douglas, Kwak, Seung, Tabrizi, Sarah and Monckton, Darren 2019. A genetic association study of glutamine-encoding DNA sequence structures, somatic CAG expansion, and DNA repair gene variants, with Huntington disease clinical outcomes. EBioMedicine 10.1016/j.ebiom.2019.09.020
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Clifton, Nicholas E, Hannon, Eilis, Harwood, Janet C, Di Florio, Arianna, Thomas, Kerrie L, Holmans, Peter A., Walters, James TR, O'Donovan, Michael, Owen, Michael J, Pocklington, Andrew J and Hall, Jeremy 2019. Dynamic expression of genes associated with schizophrenia and bipolar disorder across development. Translational Psychiatry 9 , -. 10.1038/s41398-019-0405-x
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Collins, Stephan C., Mikhaleva, Anna, Vrcelj, Katarina, Vancollie, Valerie E., Wagner, Christel, Demeure, Nestor, Whitley, Helen, Kannan, Meghna, Balz, Rebecca, Anthony, Lauren F. E., Edwards, Andrew, Moine, Hervé, White, Jacqueline K., Adams, David J., Reymond, Alexandre, Lelliott, Christopher J., Webber, Caleb and Yalcin, Binnaz 2019. Large-scale neuroanatomical study uncovers 198 gene associations in mouse brain morphogenesis. Nature Communications 10 (1) , -. 10.1038/s41467-019-11431-2
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Collishaw, Stephan, Furzer, Emma, Thapar, Ajay K. and Sellers, Ruth 2019. Brief report: a comparison of child mental health inequalities in three UK population cohorts. European Child and Adolescent Psychiatry 10.1007/s00787-019-01305-9
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Cunningham, Adam, Hill, Liam, Mon-Williams, Mark, Peall, Kathryn, Linden, David, Hall, Jeremy, Owen, Michael and van den Bree, Marianne 2019. Using kinematic analyses to explore sensorimotor control impairments in children with 22q11.2 deletion Syndrome. Journal of Neurodevelopmental Disorders 11 , 8. 10.1186/s11689-019-9271-3
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Czamara, Darina, Eraslan, Gökçen, Page, Christian M., Lahti, Jari, Lahti-Pulkkinen, Marius, Hämäläinen, Esa, Kajantie, Eero, Laivuori, Hannele, Villa, Pia M., Reynolds, Rebecca M., Nystad, Wenche, Håberg, Siri E., London, Stephanie J., O'Donnell, Kieran J., Garg, Elika, Meaney, Michael J., Entringer, Sonja, Wadhwa, Pathik D., Buss, Claudia, Jones, Meaghan J., Lin, David T. S., MacIsaac, Julie L., Kobor, Michael S., Koen, Nastassja, Zar, Heather J., Koenen, Karestan C., Dalvie, Shareefa, Stein, Dan J., Kondofersky, Ivan, Müller, Nikola S., Theis, Fabian J., Räikkönen, Katri, Binder, Elisabeth B., Craddock, Nick, Escott-Price, Valentina, Owen, Michael J. and O'Donovan, Michael C. 2019. Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nature Communications 10 , 2548. 10.1038/s41467-019-10461-0
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D'Ambrosio, Enrico, Dahoun, Tarik, Pardinas, Antonio F., Veronese, Mattia, Bloomfield, Michael A.P., Jauhar, Sameer, Bonoldi, Ilaria, Rogdaki, Maria, Froudist-Walsh, Sean, Walters, James T. R. and Howes, Oliver D. 2019. The effect of a genetic variant at the schizophrenia associated AS3MT/BORCS7 locus on striatal dopamine function: A PET imaging study. Psychiatry Research: Neuroimaging 291 , pp. 34-41. 10.1016/j.pscychresns.2019.07.005
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Davies, Jennifer, Wilkinson, Lawrence, Isles, Anthony and Humby, Trevor 2019. Prader-Willi syndrome imprinting centre deletion mice have impaired baseline and 5-HT2CR-mediated response inhibition. Human Molecular Genetics 28 (18) , pp. 3013-3023. 10.1093/hmg/ddz100
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Davies, William and Wilkinson, Lawrence 2019. Editorial overview: special issue on epigenetics and genomic imprinting. Current Opinion in Behavioral Sciences 25 , iii-v. 10.1016/j.cobeha.2018.12.006
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Di Florio, Arianna, Gordon-Smith, Katherine, Forty, Liz, Kosorok, Michael R., Fraser, Christine, Perry, Amy, Bethell, Andrew, Craddock, Nick, Jones, Lisa and Jones, Ian R. 2019. Stratification of the risk of bipolar disorder recurrences in pregnancy and postpartum. British Journal of Psychiatry 213 (3) , pp. 542-547. 10.1192/bjp.2018.92
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Douglas, Katie, Groves, Samantha, Porter, Richard, Jorden, Jenny, Wilson, Lynere, Melzer, Tracy, Wise, Richard, Bisson, Jonathan and Bell, Caroline 2019. Traumatic imagery following glucocorticoid administration in earthquake-related post-traumatic stress disorder: A preliminary functional magnetic resonance imaging study. Australian and New Zealand Journal of Psychiatry 10.1177/0004867419851860
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Drakesmith, Mark, Parker, Greg D., Smith, Jacqueline, Linden, Stefanie C., Rees, Elliott, Williams, Nigel, Owen, Michael J., van den Bree, Marianne, Hall, Jeremy, Jones, Derek K. and Linden, David E. J. 2019. Genetic risk for schizophrenia and developmental delay is associated with shape and microstructure of midline white-matter structures. Translational Psychiatry 9 (1) , 102. 10.1038/s41398-019-0440-7
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Duarte, Rodrigo R.R., Bachtel, Nathaniel D., Côtel, Marie-Caroline, Lee, Sang H., Selvackadunco, Sashika, Watson, Iain A., Hovsepian, Gary A., Troakes, Claire, Breen, Gerome D., Nixon, Douglas F., Murray, Robin M., Bray, Nicholas J., Eleftherianos, Ioannis, Vernon, Anthony C., Powell, Timothy R. and Srivastava, Deepak P. 2019. The psychiatric risk gene NT5C2 regulates adenosine monophosphate-activated protein kinase signaling and protein translation in human neural progenitor cells. Biological Psychiatry 86 (2) , pp. 120-130. 10.1016/j.biopsych.2019.03.977
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Eggink, Hendriekje, Coenen, Maraike A., de Jong, Ronald, Toonen, Rivka F., Eissens, Melanie H., Veenstra, Wencke S., Peall, Kathryn J., Sival, Deborah A., Elema, Agnes and Tijssen, Marina AJ. 2019. Motor and non-motor determinants of health-related quality of life in young dystonia patients. Parkinsonism & Related Disorders 58 , pp. 50-55. 10.1016/j.parkreldis.2018.08.008
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Egmond, Martje E., Contarino, Maria Fiorella, Lugtenberg, Coen H.A., Peall, Kathryn J., Brouwer, Oebele F., Fung, Victor S.C., Roze, Emmanuel, Stewart, Roy E., Willemsen, Michel A., Wolf, Nicole I., Koning, Tom J. and Tijssen, Marina A. 2019. Variable interpretation of the dystonia consensus classification items compromises its solidity. Movement Disorders 34 (3) , pp. 317-320. 10.1002/mds.27627
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Ellis, Natalie, Grubb, Carla-Marie, Mustoe, Sophie, Watkins, Eleanor, Codling, David, Fitch, Sarah, Stirland, Lucy, Quraishy, Munzir, Jenkinson, Josie and Harrison, Judith 2019. Venous thromboembolism risk in psychiatric in-patients: a multicentre cross-sectional study. BJPsych Bulletin , p. 1. 10.1192/bjb.2019.25
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Escott-Price, Valentina, Baker, Emily, Shoai, Maryam, Leonenko, Ganna, Myers, Amanda J., Huentelman, Matt and Hardy, John 2019. Genetic analysis suggests high misassignment rates in clinical Alzheimer's cases and controls. Neurobiology of Aging 77 , pp. 178-182. 10.1016/j.neurobiolaging.2018.12.002
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Escott-Price, Valentina, Bracher-Smith, Matthew, Menzies, Georgina, Walters, James, Kirov, George, Owen, Michael J. and O'Donovan, Michael C. 2019. Genetic liability to schizophrenia is negatively associated with educational attainment in UK Biobank. Journal of Molecular Psychiatry , -. 10.1038/s41380-018-0328-6
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Favre, Pauline, Pauling, Melissa, Stout, Jacques, Hozer, Franz, Sarrazin, Samuel, Abé, Christoph, Alda, Martin, Alloza, Clara, Alonso-Lana, Silvia, Andreassen, Ole A., Baune, Bernhard T., Benedetti, Francesco, Busatto, Geraldo F., Canales-Rodríguez, Erick J., Caseras, Xavier, Chaim-Avancini, Tiffany Moukbel, Ching, Christopher R. K., Dannlowski, Udo, Deppe, Michael, Eyler, Lisa T., Fatjo-Vilas, Mar, Foley, Sonya F., Grotegerd, Dominik, Hajek, Tomas, Haukvik, Unn K., Howells, Fleur M., Jahanshad, Neda, Kugel, Harald, Lagerberg, Trine V., Lawrie, Stephen M., Linke, Julia O., McIntosh, Andrew, Melloni, Elisa M. T., Mitchell, Philip B., Polosan, Mircea, Pomarol-Clotet, Edith, Repple, Jonathan, Roberts, Gloria, Roos, Annerine, Rosa, Pedro G. P., Salvador, Raymond, Sarró, Salvador, Schofield, Peter R., Serpa, Mauricio H., Sim, Kang, Stein, Dan J., Sussmann, Jess E., Temmingh, Henk S., Thompson, Paul M., Verdolini, Norma, Vieta, Eduard, Wessa, Michele, Whalley, Heather C., Zanetti, Marcus V., Leboyer, Marion, Mangin, Jean-François, Henry, Chantal, Duchesnay, Edouard and Houenou, Josselin 2019. Widespread white matter microstructural abnormalities in bipolar disorder: evidence from mega- and meta-analyses across 3033 individuals. Neuropsychopharmacology 10.1038/s41386-019-0485-6
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Ferraro, Laura, La Cascia, Caterina, Quattrone, Diego, Sideli, Lucia, Matranga, Domenica, Capuccio, Veronica, Tripoli, Giada, Gayer-Anderson, Charlotte, Morgan, Craig, Sami, Musa B, Sham, Pak, de Haan, Lieuwe, Velthorst, Eva, Jongsma, Hannah E, Kirkbride, James B, Rutten, Bart P F, Richards, Alexander L, Roldan, Laura, Arango, Celso, Bernardo, Miquel, Bobes, Julio, Sanjuan, Julio, Santos, Jose Luis, Arrojo, Manuel, Tarricone, Ilaria, Tortelli, Andrea, Szöke, Andrei, Del-Ben, Cristina Marta, Selten, Jean-Paul, Lynskey, Michael, Jones, Peter B, Van Os, Jim, La Barbera, Daniele, Amoretti, Silvia, Baudin, Grégoire, Beards, Stephanie, Berardi, Domenico, Bonetto, Chiara, Cabrera, Bibiana, Carracedo, Angel, Charpeaud, Thomas, Costas, Javier, Cristofalo, Doriana, Cuadrado, Pedro, Ferchiou, Aziz, Franke, Nathalie, Frijda, Flora, García Bernardo, Enrique, Garcia-Portilla, Paz, González Peñas, Javier, González, Emiliano, Hubbard, Kathryn, Jamain, Stéphane, Jiménez-López, Estela, Lasalvia, Antonio, Leboyer, Marion, López Montoya, Gonzalo, Lorente-Rovira, Esther, M Díaz-Caneja, Covadonga, Marcelino Loureiro, Camila, Marrazzo, Giovanna, Martínez, Covadonga, Matteis, Mario, Messchaart, Elles, Moltó, Ma Dolores, Moreno, Carmen, Juan, Nacher, Olmeda, Ma Soledad, Parellada, Mara, Pignon, Baptiste, Rapado, Marta, Richard, Jean-Romain, Rodríguez Solano, José Juan, Rossi Menezes, Paulo, Ruggeri, Mirella, Sáiz, Pilar A, Sánchez-Gutierrez, Teresa, Sánchez, Emilio, Sartorio, Crocettarachele, Schurhoff, Franck, Seminerio, Fabio, Shuhama, Rosana, Stilo, Simona A, Termorshuizen, Fabian, Tosato, Sarah, Tronche, Anne-Marie, van Dam, Daniella, van der Ven, Elsje, Murray, Robin M and Di Forti, Marta 2019. Premorbid adjustment and IQ in patients with first-episode psychosis: a multisite case-control study of their relationship with cannabis use. Schizophrenia Bulletin , -. 10.1093/schbul/sbz077
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Flowers, Michael, Lomeilkaite, Vilila, Ciosi, Marc, Morales, Fernando, Lo, Kitty, Hensman Moss, Davina, Jones, Lesley, Holmans, Peter, Monckton, Darren and Tabrizi, Sarah 2019. MSH3 modifies somatic instability and disease severity in Huntington’s and myotonic dystrophy type 1. Brain 142 (7) , pp. 1876-1886. 10.1093/brain/awz115
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Fonville, Leon, Drakesmith, Mark, Zammit, Stanley, Lewis, Glyn, Jones, Derek and David, Anthony S 2019. MRI indices of cortical development in young people with psychotic experiences: influence of genetic risk and persistence of symptoms. Schizophrenia Bulletin 45 (1) , pp. 169-179. 10.1093/schbul/sbx195
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Garay, Samantha M., Savory, Katrina A., Sumption, Lorna A., Penketh, Richard J.A., Jones, Ian R., Janssen, Anna B. and John, Rosalind M. 2019. Seasonal variation in salivary cortisol but not symptoms of depression and trait anxiety in pregnant women undergoing an elective caesarean section. Psychoneuroendocrinology 108 , pp. 14-19. 10.1016/j.psyneuen.2019.05.029
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Germuska, Michael, Chandler, Hannah L., Stickland, Rachael, Foster, Catherine, Fasano, Fabrizio, Okell, T.W., Steventon, Jessica, Tomassini, Valentina, Murphy, Kevin and Wise, Richard 2019. Dual-calibrated fMRI measurement of absolute cerebral metabolic rate of oxygen consumption and effective oxygen diffusivity. NeuroImage 184 , pp. 717-728. 10.1016/j.neuroimage.2018.09.035
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Goold, Robert, Flower, Michael, Moss, Davina Hensman, Medway, Christopher, Wood-Kaczmar, Alison, Andre, Ralph, Farshim, Pamela, Bates, Gill P, Holmans, Peter, Jones, Lesley and Tabrizi, Sarah J 2019. FAN1 modifies Huntington's disease progression by stabilising the expanded HTT CAG repeat. Human Molecular Genetics 28 (4) , pp. 650-661. 10.1093/hmg/ddy375
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Gorman, Kathleen M., Meyer, Esther, Grozeva, Detelina, Spinelli, Egidio, McTague, Amy, Sanchis-Juan, Alba, Carss, Keren J., Bryant, Emily, Reich, Adi, Schneider, Amy L., Pressler, Ronit M., Simpson, Michael A., Debelle, Geoff D., Wassmer, Evangeline, Morton, Jenny, Sieciechowicz, Diana, Jan-Kamsteeg, Eric, Paciorkowski, Alex R., King, Mary D., Cross, J. Helen, Poduri, Annapurna, Mefford, Heather C., Scheffer, Ingrid E., Haack, Tobias B., McCullagh, Gary, Millichap, John J., Carvill, Gemma L., Clayton-Smith, Jill, Maher, Eamonn R., Raymond, F. 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Grove, Jakob, Ripke, Stephan, Als, Thomas D., Mattheisen, Manuel, Walters, Raymond, Won, Hyejung, Pallesen, Jonatan, Agerbo, Esben, Andreassen, Ole A., Anney, Richard, Belliveau, Rich, Bettella, Francesco, Buxbaum, Joseph D., Bybjerg-Grauholm, Jonas, B?kved-Hansen, Marie, Cerrato, Felecia, Chambert, Kimberly, Christensen, Jane H., Churchhouse, Claire, Dellenvall, Karin, Demontis, Ditte, Rubeis, Silvia De, Devlin, Bernie, Djurovic, Srdjan, Dumont, Ashle, Goldstein, Jacqueline, Hansen, Christine S., Hauberg, Mads Engel, Hollegaard, Mads V., Hope, Sigrun, Howrigan, Daniel P., Huang, Hailiang, Hultman, Christina, Klei, Lambertus, Maller, Julian, Martin, Joanna, Martin, Alicia R., Moran, Jennifer, Robinson, Elise B., Roeder, Kathryn, Roussos, Panos, Saemundsen, Evald, Sandin, Sven, Satterstrom, F. Kyle, Smith, George Davey, Stefansson, Hreinn, Stefansson, Kari, Steinberg, Stacy, Stevens, Christine, Sullivan, Patrick F, Turley, Patrick, Walters, G. Bragi, Xu, Xinyi, Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Mors, Ole, Mortensen, Preben Bo, Neale, Benjamin M., Daly, Mark J. and Brglum, Anders D. 2019. Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics 51 , pp. 431-444. 10.1038/s41588-019-0344-8
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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. and Bras, Jose 2019. Heritability and genetic variance of dementia with Lewy bodies. Neurobiology of Disease 127 , pp. 492-501. 10.1016/j.nbd.2019.04.004
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Darlay, Rebecca, Ayers, Kristin L., Mells, George F., Hall, Lynsey S., Liu, Jimmy Z., Almarri, Mohamed A., Alexander, Graeme J., Jones, David E., Sandford, Richard N., Anderson, Carl A. and Cordell, Heather J. 2018. Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitis. PLoS Genetics 14 (12) , e1007833. 10.1371/journal.pgen.1007833
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Davies, Jonathan, Sullivan, Sarah and Zammit, Stanley 2018. Adverse life outcomes associated with adolescent psychotic experiences and depressive symptoms. Social Psychiatry and Psychiatric Epidemiology 53 (5) , pp. 497-507. 10.1007/s00127-018-1496-z
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Davis, Katrina A. S., Coleman, Jonathan R. I., Adams, Mark, Allen, Naomi, Breen, Gerome, Cullen, Breda, Dickens, Chris, Fox, Elaine, Graham, Nick, Holliday, Jo, Howard, Louise M., John, Ann, Lee, William, McCabe, Rose, McIntosh, Andrew, Pearsall, Robert, Sudlow, Cathie, Ward, Joey, Zammit, Stan and Hotopf, Matthew 2018. Mental health in UK Biobank: development, implementation and results from an online questionnaire completed by 157 366 participants. Bjpsych Open 4 (03) , pp. 83-90. 10.1192/bjo.2018.12
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Dent, Claire L., Humby, Trevor, Lewis, Katie, Ward, Andrew, Fischer-Colbrie, Reiner, Wilkinson, Lawrence S., Wilkins, Jon F. and Isles, Anthony R. 2018. Impulsive choice in mice lacking paternal expression of Grb10 suggests intra-genomic conflict in behavior. Genetics 209 (1) , pp. 233-239. 10.1534/genetics.118.300898
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Di Florio, Arianna, Alexander, Danny, Schmidt, Peter J. and Rubinow, David R. 2018. Progesterone and plasma metabolites in women with and in those without premenstrual dysphoric disorder. Depression and Anxiety 35 (12) , pp. 1168-1177. 10.1002/da.22827
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Dimitriadis, Stavros, Liparas, D and Tsolaki, Magda N 2018. Random forest feature selection, fusion and ensemble strategy: combining multiple morphological MRI measures to discriminate among healthy elderly, MCI, cMCI and Alzheimer's disease patients: from the Alzheimer's disease neuroimaging initiative (ADNI) database. Journal of Neuroscience Methods 302 , pp. 14-23. 10.1016/j.jneumeth.2017.12.010
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Donohoe, G., Holland, J., Mothersill, D., McCarthy-Jones, S., Cosgrove, D., Harold, D., Richards, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, Gill, M., Corvin, A. and Morris, D. W. 2018. Genetically predicted complement component 4A expression: effects on memory function and middle temporal lobe activation. Psychological Medicine 48 (10) , pp. 1608-1615. 10.1017/S0033291717002987
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Duncan, Laramie E, Ratanatharathorn, Andrew, Aiello, Allison E, Almli, Lynn M and Bisson, Jonathan 2018. Largest GWAS of PTSD (N=20,070) yields genetic overlap with schizophrenia and sex differences in heritability. Molecular Psychiatry 23 , pp. 666-673. 10.1038/mp.2017.77
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English, Jane A., Lopez, Lorna M., O’Gorman, Aoife, Föcking, Melanie, Hryniewiecka, Magdalena, Scaife, Caitriona, Sabherwal, Sophie, Wynne, Kieran, Dicker, Patrick, Rutten, Bart P. F., Lewis, Glynn, Zammit, Stanley, Cannon, Mary, Cagney, Gerard and Cotter, David R. 2018. Blood-Based Protein Changes in Childhood Are Associated With increased risk for later psychotic disorder: evidence from a nested case–control study of the ALSPAC Longitudinal Birth Cohort. Schizophrenia Bulletin 44 (2) , pp. 297-306. 10.1093/schbul/sbx075
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Foley, Sonya F, Bracher-Smith, Matthew, Tansey, Katherine E, Harrison, Judith, Parker, Greg D and Caseras, Xavier 2018. Fractional anisotropy of the uncinate fasciculus and cingulum in bipolar disorder type I, type II, their unaffected siblings and healthy controls. British Journal of Psychiatry 213 (3) , pp. 548-554. 10.1192/bjp.2018.101
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Forrest, Marc P, Hill, Matthew, Kavanagh, David, Tansey, Katherine, Waite, Adrian and Blake, Derek 2018. The psychiatric risk gene transcription factor 4 (TCF4) regulates neurodevelopmental pathways associated with schizophrenia, autism, and intellectual disability. Schizophrenia Bulletin 44 (5) , pp. 1100-1110. 10.1093/schbul/sbx164
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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 and Bras, Jose 2018. Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study. The Lancet Neurology 17 (1) , pp. 64-74. 10.1016/S1474-4422(17)30400-3
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Gyöngyösi, Mariann, Haller, Paul M., Blake, Derek J. and Martin Rendon, Enca 2018. Meta-analysis of cell therapy studies in heart failure and acute myocardial infarction. Circulation Research 123 (2) , pp. 301-308. 10.1161/CIRCRESAHA.117.311302
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Harding, Katharine, Anderson, Valerie, Williams, Owain, Willis, Mark, Butterworth, Sara, Tallantyre, Emma, Joseph, Fady, Wardle, Mark, Pickersgill, Trevor and Robertson, Neil 2018. A contemporary study of mortality in the multiple sclerosis population of south east Wales. Multiple Sclerosis and Related Disorders 25 , pp. 186-191. 10.1016/j.msard.2018.08.001
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Hoare, Thomas, Vidgen, Andrew and Roberts, Neil 2018. In their own words: a synthesis of the qualitative research on the experiences of adults seeking asylum. a systematic review of qualitative findings in forced migration. Medicine, Conflict and Survival 33 (4) , p. 273. 10.1080/13623699.2017.1419902
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Holmans, Peter and Stone, Tim 2018. Using genomic data to find disease-modifying loci in Huntington's Disease (HD). Methods in Molecular Biology 1780 , pp. 443-461. 10.1007/978-1-4939-7825-0_20

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Jones, Hannah J., Gage, Suzanne H., Heron, Jon, Hickman, Matthew, Lewis, Glyn, Munafò, Marcus R. and Zammit, Stanley 2018. Association of combined patterns of tobacco and cannabis use in adolescence with psychotic experiences. JAMA Psychiatry 75 (3) , pp. 240-246. 10.1001/jamapsychiatry.2017.4271
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Lawrence, Daniel, Davies, Tracey-Lee, Bagshaw, Ruth, Hewlett, Paul, Taylor, Pamela and Watt, Andrew 2018. External validity and anchoring heuristics: application of DUNDRUM-1 to secure service gatekeeping in South Wales. BJPsych Bulletin 42 (01) , pp. 10-18. 10.1192/bjb.2017.6
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Zhao, Yingjie, Guo, Tingwei, Fiksinski, Ania, Breetvelt, Elemi, McDonald-McGinn, Donna M., Crowley, Terrence B., Diacou, Alexander, Schneider, Maude, Eliez, Stephan, Swillen, Ann, Breckpot, Jeroen, Vermeesch, Joris, Chow, Eva W. C., Gothelf, Doron, Duijff, Sasja, Evers, Rens, van Amelsvoort, Thérèse A., Van Den Bree, Marianne, Owen, Michael, Niarchou, Maria, Bearden, Carrie E., Ornstein, Claudia, Pontillo, Maria, Buzzanca, Antonino, Vicari, Stefano, Armando, Marco, Murphy, Kieran C., Murphy, Clodagh, Garcia-Minaur, Sixto, Philip, Nicole, Campbell, Linda, Morey-Cañellas, Jaume, Raventos, Jasna, Rosell, Jordi, Heine-Suner, Damian, Shprintzen, Robert J., Gur, Raquel E., Zackai, Elaine, Emanuel, Beverly S., Wang, Tao, Kates, Wendy R., Bassett, Anne S., Vorstman, Jacob A. S., Morrow, Bernice E., International 22q11.2, Brain and Behavior Consortium and Chawner, Samuel 2018. Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects. American Journal of Medical Genetics Part A 176 (10) , pp. 2172-2181. 10.1002/ajmg.a.40359
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Zutt, Rodi, Elting, Jan W., van Zijl, Jonathan C., van der Hoeven, J. Han, Roosendaal, Christiaan M., Gelauff, Jeannette M., Peall, Kathryn J. and Tijssen, Marina A. J. 2018. Electrophysiologic testing aids diagnosis and subtyping of myoclonus. Neurology 90 (8) , e647-e657. 10.1212/WNL.0000000000004996
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Abdul Rahim, Mohammad Izzat and Thomas, Rhys Huw 2017. Gamification of medication adherence in epilepsy. Seizure - European Journal of Epilepsy 52 , pp. 11-14. 10.1016/j.seizure.2017.09.008
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Absoud, Michael, Brex, Peter, Ciccarelli, Olga, Diribe, Onyinye, Giovannoni, Gavin, Hellier, Jennifer, Howe, Rosemary, Holland, Rachel, Kelly, Joanna, McCrone, Paul, Murphy, Caroline, Palace, Jackie, Pickles, Andrew, Pike, Michael, Robertson, Neil, Jacob, Anu and Lim, Ming 2017. A multicentre randomiSed controlled TRial of IntraVEnous immunoglobulin compared with standard therapy for the treatment of transverse myelitis in adults and children (STRIVE). Health Technology Assessment 21 , 31. 10.3310/hta21310
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Abu-Akel, Ahmad, Clark, Jennifer, Perry, Amy, Wood, Stephen J., Forty, Elizabeth, Craddock, Nicholas John, Jones, Ian Richard, Gordon-Smith, Katherine and Jones, Lisa 2017. Autistic and schizotypal traits and global functioning in bipolar I disorder. Journal of affective disorders 207 , pp. 268-275. 10.1016/j.jad.2016.09.059
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Adam, Manal A. and Isles, Anthony R. 2017. EHMT1/GLP; biochemical function and association with brain disorders. Epigenomes 1 (3) , 15. 10.3390/epigenomes1030015
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Agha, Sharifah, Zammit, Stanley, Thapar, Anita and Langley, Kate 2017. Maternal psychopathology and offspring clinical outcome: a four year follow-up of boys with ADHD. European Child and Adolescent Psychiatry 26 (2) , pp. 253-262. 10.1007/s00787-016-0873-y
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Agha, Sharifah, Zammit, Stanley, Thapar, Anita and Langley, Kate 2017. Parent psychopathology and neurocognitive functioning in children with ADHD. Journal of Attention Disorders 10.1177/1087054717718262
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Al-Ansari, Aseel and Robertson, Neil 2017. Creutzfeldt-Jacob disease: new directions in diagnosis and therapeutics. Journal of Neurology 264 (5) , pp. 1029-1031. 10.1007/s00415-017-8473-4
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Allardyce, Judith, Leonenko, Ganna, Hamshere, Marian L., Pardinas, Antonio, Forty, Liz, Knott, Sarah, Gordon Smith, Katherine, Porteus, David J., Haywood, Caroline, Di Florio, Arianna, Jones, Lisa, McIntosh, Andrew M, Owen, Michael, Holmans, Peter, Walters, James, Craddock, Nicholas, Jones, Ian, O’Donovan, Michael C. and Escott-Price, Valentina 2017. Psychosis and the level of mood incongruence in Bipolar Disorder are related to genetic liability for Schizophrenia. bioRxiv
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Andreassen, Ole A, Hibar, Derrek P, Westlye, Lars T and Caseras, Xavier 2017. Cortical abnormalities in bipolar disorder: An MRI analysis of 6,503 individuals from the ENIGMA-Bipolar Disorder Working Group. Molecular Psychiatry 23 , pp. 932-942. 10.1038/mp.2017.73
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Antonakakis, Marios, Dimitriadis, Stavros, Zervakis, Michalis, Papanicolaou, Andrew C. and Zouridakis, George 2017. Reconfiguration of dominant coupling modes in mild traumatic brain injury mediated by δ-band activity: a resting state MEG study. Neuroscience 356 , pp. 275-286. 10.1016/j.neuroscience.2017.05.032
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Bassett, Anne S., Lowther, Chelsea, Merico, Daniele, Costain, Gregory, Chow, Eva W. C., van Amelsvoort, Therese, McDonald-McGinn, Donna, Gur, Raquel E., Swillen, Ann, Van Den Bree, Marianne, Murphy, Kieran, Gothelf, Doron, Bearden, Carrie E., Eliez, Stephan, Kates, Wendy, Philip, Nicole, Sashi, Vandana, Campbell, Linda, Vorstman, Jacob, Cubells, Joseph, Repetto, Gabriela M., Simon, Tony, Boot, Erik, Heung, Tracy, Evers, Rens, Vingerhoets, Claudia, van Duin, Esther, Zackai, Elaine, Vergaelen, Elfi, Devriendt, Koen, Vermeesch, Joris, Owen, Michael, Murphy, Clodagh, Michaelovosky, Elena, Kushan, Leila, Schneider, Maude, Fremont, Wanda, Busa, Tiffany, Hooper, Stephen, McCabe, Kathryn, Duijff, Sasja, Isaev, Karin, Pellecchia, Giovanna, Wei, John, Gazzellone, Matthew J., Scherer, Stephen W., Emanuel, Beverly S., Guo, Tingwei, Morrow, Bernice E. and Marshall, Christian R. 2017. Rare genome-wide copy number variation and expression of schizophrenia in 22q11.2 deletion syndrome. American Journal of Psychiatry 174 (11) , pp. 1054-1063. 10.1176/appi.ajp.2017.16121417
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Benson, Matthew A., Tinsley, Caroline L., Waite, Adrian, Carlisle, Francesca, Sweet, Steve M. M., Ehler, Elisabeth, George, Christopher, Lai, Francis, Martin-Rendon, Enca and Blake, Derek 2017. Ryanodine receptors are part of the myospryn complex in cardiac muscle. Scientific Reports 7 (1) , 6312. 10.1038/s41598-017-06395-6
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Bevan Jones, Rhys, Thomas, Julia, Lewis, Jamie Thornton, Read, Simon Mark and Jones, Ian 2017. Translation: From bench to brain – Using the visual arts and metaphors to engage and educate. Research for All 1 (2) , pp. 265-283. 10.18546/RFA.01.2.04
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Bevan-Jones, Rhys, Thapar, Anita, Stone, Zoe, Thapar, Ajay, Jones, Ian R., Smith, Daniel and Simpson, Sharon 2017. Psychoeducational interventions in adolescent depression: A systematic review. Patient Education and Counseling 10.1016/j.pec.2017.10.015
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Beyer, Stephen 2017. Economic impact of inclusion in the open labour market for persons with disabilities. Éditions universitaires européennes.

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Bhugra, Dinesh, Tasman, Allan, Pathare, Soumitra, Priebe, Stefan, Smith, Shubulade, Torous, John, Arbuckle, Melissa R, Langford, Alex, Alarcón, Renato D, Chiu, Helen Fung Kum, First, Michael B, Kay, Jerald, Sunkel, Charlene, Thapar, Anita, Udomratn, Pichet, Baingana, Florence K, Kestel, Dévora, Ng, Roger Man Kin, Patel, Anita, Picker, Livia De, McKenzie, Kwame Julius, Moussaoui, Driss, Muijen, Matt, Bartlett, Peter, Davison, Sophie, Exworthy, Tim, Loza, Nasser, Rose, Diana, Torales, Julio, Brown, Mark, Christensen, Helen, Firth, Joseph, Keshavan, Matcheri, Li, Ang, Onnela, Jukka-Pekka, Wykes, Til, Elkholy, Hussien, Kalra, Gurvinder, Lovett, Kate F, Travis, Michael J and Ventriglio, Antonio 2017. The WPA-Lancet Psychiatry Commission on the future of psychiatry. The Lancet Psychiatry 4 (10) , pp. 775-818. 10.1016/S2215-0366(17)30333-4
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Blokland, Gabriëlla A. M., Mesholam-Gately, Raquelle I., Toulopoulou, Timothea, del Re, Elisabetta C., Lam, Max, DeLisi, Lynn E., Donohoe, Gary, Walters, James, Seidman, Larry J. and Petryshen, Tracey L. 2017. Heritability of neuropsychological measures in Schizophrenia and non-psychiatric populations: a systematic review and meta-analysis. Schizophrenia Bulletin 43 (4) , pp. 788-800. 10.1093/schbul/sbw146
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Bowles, Kathryn R., Stone, Timothy C., Holmans, Peter Alan, Allen, Nicholas Denby, Dunnett, Stephen Bruce and Jones, Lesley 2017. SMAD transcription factors are altered in cell models of HD and regulate HTT expression. Cellular Signalling 31 , pp. 1-14. 10.1016/j.cellsig.2016.12.005
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Casanova Dias, Marisa, Abbara, Aula, Gilbert, Rosie, van Schalkwyk, May CI, Rees, Claire P., Ryland, Howard, Leather, Andrew J. M., Williams, Bhanu and Crisp, Nigel 2017. Equipping doctors for global health challenges. Journal of the Royal Society of Medicine 110 (1) , pp. 5-8. 10.1177/0141076816686349
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Chao, Michael J., Gillis, Tammy, Atwal, Ranjit S., Srinidhi Mysore, Jayalakshmi, Arjomand, Jamshid, Harold, Denise, Holmans, Peter Alan, Jones, Lesley, Orth, Michael, Myers, Richard H., Kwak, Seung, Wheeler, Vanessa C., MacDonald, Marcy E., Gusella, James F. and Lee, Jong-Min 2017. Haplotype-based stratification of Huntington's disease. European Journal of Human Genetics 25 , pp. 1202-1209. 10.1038/ejhg.2017.125
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Charney, A W, Ruderfer, D M, Stahl, E A, Moran, J L, Chambert, K, Belliveau, R A, Forty, L, Gordon-Smith, K, Di Florio, Arianna, Lee, P H, Bromet, E J, Buckley, P F, Escamilla, M A, Fanous, A H, Fochtmann, L J, Lehrer, D S, Malaspina, D, Marder, S R, Morley, C P, Nicolini, H, Perkins, D O, Rakofsky, J J, Rapaport, M H, Medeiros, H, Sobell, J L, Green, E K, Backlund, L, Bergen, S E, Juréus, A, Schalling, M, Lichtenstein, P, Roussos, P, Knowles, J A, Jones, Ian, Jones, L A, Hultman, C M, Perlis, R H, Purcell, S M, McCarroll, S A, Pato, C N, Pato, M T, Craddock, Nicholas, Landén, M, Smoller, J W and Sklar, P 2017. Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder. Translational Psychiatry 7 (1) , e993. 10.1038/tp.2016.242
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Chawner, Samuel, Doherty, Joanne L., Moss, Hayley, Niarchou, Maria, Walters, James, Owen, Michael J. and Van Den Bree, Marianne Bernadette 2017. Childhood cognitive development in 22q11.2 deletion syndrome: case–control study. British Journal of Psychiatry 211 (4) , pp. 223-230. 10.1192/bjp.bp.116.195651
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Clifton, Nicholas, Pocklington, Andrew, Scholz, B., Rees, Elliott, Walters, James, Kirov, George, O'Donovan, Michael, Owen, Michael, Wilkinson, Lawrence, Thomas, Kerrie and Hall, Jeremy 2017. Schizophrenia copy number variants and associative learning. Molecular Psychiatry 22 (2) , pp. 178-182. 10.1038/mp.2016.227
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Connolly, Siobhan, Anney, Richard, Gallagher, Louise and Heron, Elizabeth A. 2017. A genome-wide investigation into parent-of-origin effects in autism spectrum disorder identifies previously associated genes including SHANK3. European Journal of Human Genetics 25 (2) , pp. 234-239. 10.1038/ejhg.2016.153
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Copeland, Lauren, Meek, Andrea, Kerr, Mike, Robling, Michael, Hood, Kerry and McNamara, Rachel 2017. Measurement of side effects of anti-epileptic drugs (AEDs) in adults with intellectual disability: A systematic review. Seizure - European Journal of Epilepsy 51 , pp. 61-73. 10.1016/j.seizure.2017.07.013
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Cosgrove, D, Harold, D, Mothersill, O, Anney, Richard, Hill, Martin, Bray, Nicholas, Blokland, G, Petryshen, T, Donnelly, Peter, Bates, Lesley, Barroso, Ines, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, Palmer, Colin N A, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas W, Spencer, Chris C A, Band, Gavin, Bellenguez, Céline, Freeman, Colin, Hellenthal, Garrett, Giannoulatou, Eleni, Hopkins, Lucinda, Pirinen, Matti, Pearson, Richard, Strange, Amy, Su, Zhan, Vukcevic, Damjan, Langford, Cordelia, Hunt, Sarah E, Edkins, Sarah, Gwilliam, Rhian, Blackburn, Hannah, Bumpstead, Suzannah J, Dronov, Serge, Gillman, Matthew, Gray, Emma, Hammond, Naomi, Jayakumar, Alagurevathi, McCann, Owen T, Liddle, Jennifer, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Waller, Matthew, Weston, PaulWeston, Widaa, SaraWidaa, Whittaker, Pamela, Richards, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, Gill, M, Corvin, A, Morris, D W and Donohoe, G 2017. MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls. Translational Psychiatry 7 (1) , e1012. 10.1038/tp.2016.286
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Cosgrove, Donna, Mothersill, Omar, Kendall, Kimberley, Konte, Bettina, Harold, Denise, Giegling, Ina, Hartmann, Annette, Richards, Alexander, Mantripragada, Kiran, Owen, Michael, O'Donovan, Michael, Gill, Michael, Rujescu, Dan, Walters, James, Corvin, Aiden, Morris, Derek W and Donohoe, Gary 2017. Cognitive characterization of schizophrenia risk variants involved in synaptic transmission: evidence of CACNA1C's role in working memory. Neuropsychopharmacology 42 , pp. 2612-2622. 10.1038/npp.2017.123
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Crawshaw, Ania and Harding, Katharine 2017. The Selfish Gene. Practical Neurology 17 (3) , p. 244. 10.1136/practneurol-2017-001645
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Crawshaw, Ania and Harding, Katharine 2017. A portrait of the brain by Adam Zeman [Book Club]. Practical Neurology 17 , p. 419. 10.1136/practneurol-2017-001746

Crawshaw, Ania A. and Robertson, Neil P. 2017. The role of TSPO PET in assessing neuroinflammation. Journal of Neurology 264 (8) , pp. 1825-1827. 10.1007/s00415-017-8565-1
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Davies, William 2017. Understanding the pathophysiology of postpartum psychosis: challenges and new approaches. World Journal of Psychiatry 7 (2) , pp. 77-88. 10.5498/wjp.v7.i2.77
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De Giglio, Laura, Marinelli, Fabiana, Barletta, Valeria T., Pagano, Veronica A., De Angelis, Floriana, Fanelli, Fulvia, Petsas, Nikolaos, Pantano, Patrizia, Tomassini, Valentina and Pozzilli, Carlo 2017. Effect on cognition of estroprogestins combined with Interferon beta in multiple sclerosis: analysis of secondary outcomes from a randomized controlled trial. CNS Drugs 31 (2) , pp. 161-168. 10.1007/s40263-016-0401-0
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Deans, P.J. Michael, Raval, Pooja, Sellers, Katherine J., Gatford, Nicholas J.F., Halai, Sanjay, Duarte, Rodrigo R.R., Shum, Carole, Warre-Cornish, Katherine, Kaplun, Victoria E., Cocks, Graham, Hill, Matthew, Bray, Nicholas, Price, Jack and Srivastava, Deepak P. 2017. Psychosis risk candidate ZNF804A localizes to synapses and regulates neurite formation and dendritic spine structure. Biological psychiatry 82 (1) , pp. 49-61. 10.1016/j.biopsych.2016.08.038
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Demaerel, Wolfram, Hestand, Matthew S., Vergaelen, Elfi, Swillen, Ann, López-Sánchez, Marcos, Pérez-Jurado, Luis A., McDonald-McGinn, Donna M., Zackai, Elaine, Emanuel, Beverly S., Morrow, Bernice E., Breckpot, Jeroen, Devriendt, Koenraad, Vermeesch, Joris R., Antshel, Kevin, Arango, Celso, Armando, Marco, Bassett, Anne, Bearden, Carrie, Boot, Erik, Bravo-Sanchez, Marta, Breetvelt, Elemi, Busa, Tiffany, Butcher, Nancy, Campbell, Linda, Carmel, Miri, Chow, Eva, Crowley, T. Blaine, Cubells, Joseph, Cutler, David, Demaerel, Wolfram, Digilio, Maria Cristina, Duijff, Sasja, Eliez, Stephan, Emanuel, Beverly, Epstein, Michael, Evers, Rens, Fernandez Garcia-Moya, Luis, Fiksinski, Ania, Fraguas, David, Fremont, Wanda, Fritsch, Rosemarie, Garcia-Minaur, Sixto, Golden, Aaron, Gothelf, Doron, Guo, Tingwei, Gur, Ruben, Gur, Raquel, Heine-Suner, Damian, Hestand, Matthew, Hooper, Stephen, Kates, Wendy, Kushan, Leila, Laorden-Nieto, Alejandra, Maeder, Johanna, Marino, Bruno, Marshall, Christian, McCabe, Kathryn, McDonald-McGinn, Donna, Michaelovosky, Elena, Morrow, Bernice, Moss, Edward, Mulle, Jennifer, Murphy, Declan, Murphy, Kieran, Murphy, Clodagh, Niarchou, Maria, Ornstein, Claudia, Owen, Michael J., Philip, Nicole, Repetto, Gabriela, Schneider, Maude, Shashi, Vandana, Simon, Tony, Swillen, Ann, Tassone, Flora, Unolt, Marta, van Amelsvoort, Therese, van den Bree, Marianne, Van Duin, Esther, Vergaelen, Elfi, Vermeesch, Joris, Vicari, Stefano, Vingerhoets, Claudia, Vorstman, Jacob, Warren, Steve, Weinberger, Ronnie, Weisman, Omri, Weizman, Abraham, Zackai, Elaine, Zhang, Zhengdong and Zwick, Michael 2017. Nested inversion polymorphisms predispose chromosome 22q11.2 to meiotic rearrangements. American Journal of Human Genetics 101 (4) , pp. 616-622. 10.1016/j.ajhg.2017.09.002
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DeMichele-Sweet, M A A, Weamer, E A, Klei, L, Vrana, D T, Hollingshead, D J, Seltman, H J, Sims, Rebecca, Foroud, T, Hernandez, I, Moreno-Grau, S, Tárraga, L, Boada, M, Ruiz, A, Williams, Julie, Mayeux, R, Lopez, O L, Sibille, E L, Kamboh, M I, Devlin, B and Sweet, R A 2017. Genetic risk for schizophrenia and psychosis in Alzheimer disease. Molecular Psychiatry 23 , pp. 963-972. 10.1038/mp.2017.81
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Dimitriadis, Stavros 2017. A high performing EEG approach for the automated scoring of the sleep stages of neonates. Clinical Neurophysiology 128 (6) , pp. 1039-1040. 10.1016/j.clinph.2017.04.001
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Dimitriadis, Stavros, Antonakakis, Marios, Simos, Panagiotis, Fletcher, Jack M. and Papanicolaou, Andrew C. 2017. Data-driven topological filtering based on orthogonal minimal spanning trees: application to multi-group MEG resting-state connectivity. Brain Connectivity 7 (10) , pp. 661-670. 10.1089/brain.2017.0512
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Dimitriadis, Stavros, Salis, Christos, Tarnanas, Ioannis and Linden, David Edmund Johannes 2017. Topological filtering of dynamic functional brain networks unfolds informative chronnectomics: a novel data-driven thresholding scheme based on Orthogonal Minimal Spanning Trees (OMSTs). Frontiers in Neuroinformatics 11 , 28. 10.3389/fninf.2017.00028
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Escott-Price, Valentina and Jones, Lesley 2017. Genomic profiling and diagnostic biomarkers in Alzheimer's disease. The Lancet Neurology 16 (8) , pp. 582-583. 10.1016/S1474-4422(17)30202-8
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Escott-Price, Valentina, Myers, Amanda J, Huentelman, Matt and Hardy, John 2017. Polygenic risk score analysis of pathologically confirmed alzheimer's disease. Annals of Neurology 82 (2) , pp. 311-314. 10.1002/ana.24999
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Escott-Price, Valentina, Shoai, Maryam, Pither, Richard, Williams, Julie and Hardy, John 2017. Polygenic score prediction captures nearly all common genetic risk for Alzheimer's disease. Neurobiology of Aging 49 , 214.e7-214.e11. 10.1016/j.neurobiolaging.2016.07.018
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Eyre, Olga, Langley, Kate, Stringaris, Argyris, Leibenluft, Ellen, Collishaw, Stephan and Thapar, Anita 2017. Irritability in ADHD: associations with depression liability. Journal of Affective Disorders 215 , pp. 281-287. 10.1016/j.jad.2017.03.050
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