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Number of items: 292.

A

Aberg, Karolina A., Liu, Youfang, Bukszár, Jozsef, McClay, Joseph L., Khachane, Amit N., Andreassen, Ole A., Blackwood, Douglas, Corvin, Aiden, Djurovic, Srdjan, Gurling, Hugh, Ophoff, Roel, Pato, Carlos N., Pato, Michele T., Riley, Brien, Webb, Todd, Kendler, Kenneth, O'Donovan, Michael Conlon, Craddock, Nicholas John, Kirov, George, Owen, Michael John, Rujescu, Dan, St Clair, David, Werge, Thomas, Hultman, Christina M., Delisi, Lynn E., Sullivan, Patrick and van den Oord, Edwin J. 2013. A comprehensive family-based replication study of schizophrenia genes. JAMA Psychiatry 70 (6) , pp. 573-581. 10.1001/jamapsychiatry.2013.288

Agha, Sharifah Shameem, Zammit, Stanley, Thapar, Anita and Langley, Kate 2013. Are parental ADHD problems associated with a more severe clinical presentation and greater family adversity in children with ADHD? European Child & Adolescent Psychiatry 22 (6) , pp. 369-377. 10.1007/s00787-013-0378-x

Ahuja, Alka, Martin, Joanna, Langley, Kate and Thapar, Anita 2013. Intellectual disability in children with attention deficit hyperactivity disorder. The Journal of Pediatrics 163 (3) , 890-895.e1. 10.1016/j.jpeds.2013.02.043
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Ali, K., Nannapaneni, R. and Hamandi, Khalid 2013. The isolated fourth ventricle. BMJ Case Reports 2013 , pii: bcr2013008791. 10.1136/bcr-2013-008791

Ali, Khalid W. and Robertson, Neil 2013. Lessons from preclinical disease. Journal of Neurology 260 (8) , pp. 2193-5. 10.1007/s00415-013-7055-3

Almeida, J. R. C., Mourao-Miranda, J., Aizenstein, H. J., Versace, A., Kozel, F. A., Lu, H., Marquand, A., LaBarbara, E. J., Brammer, M., Trivedi, M., Kupfer, D. J. and Phillips, M. L. 2013. Pattern recognition analysis of anterior cingulate cortex blood flow to classify depression polarity. British Journal of Psychiatry 203 (4) , pp. 310-1. 10.1192/bjp.bp.112.122838

Anderson, J. T. and Robertson, Neil 2013. Risk factors and cerebrovascular disease [Journal Article]. Journal of Neurology 260 (2) , pp. 692-694. 10.1007/s00415-013-6835-0

Andreassen, Ole A., Djurovic, Srdjan, Thompson, Wesley K., Schork, Andrew J., Kendler, Kenneth S., O'Donovan, Michael Conlon, Rujescu, Dan, Werge, Thomas, van de Bunt, Martijn, Morris, Andrew P., McCarthy, Mark I., Roddey, J. Cooper, McEvoy, Linda K., Desikan, Rahul S. and Dale, Anders M. 2013. Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors. American Journal of Human Genetics 92 (2) , pp. 197-209. 10.1016/j.ajhg.2013.01.001

Annovazzi, Pietro, Tomassini, Valentina, Bodini, Benedetta, Boffa, Laura, Calabrese, Massimiliano, Cocco, Eleonora, Cordioli, Cinzia, Luca, Giovanna, Frisullo, Giovanni, Gallo, Antonio, Malucchi, Simona, Paolicelli, Damiano, Pesci, Ilaria, Radaelli, Marta, Ragonese, Paolo, Roccatagliata, Luca, Tortorella, Carla, Vercellino, Marco, Zipoli, Valentina, Gasperini, Claudio, Rodegher, Mariaemma and Solaro, Claudio 2013. A cross-sectional, multicentre study of the therapeutic management of multiple sclerosis relapses in Italy. Neurological Sciences 34 (2) , pp. 197-203. 10.1007/s10072-012-0981-5

Arun, Tarunya, Tomassini, Valentina, Sbardella, Emilia, de Ruiter, Michiel, Matthews, Lucy, Leite, Maria Isabel, Gelineau-Morel, Rose, Cavey, Ana, Vergo, Sandra, Craner, Matt, Fugger, Lars, Rovira, Alex, Jenkinson, Mark and Palace, Jacqueline 2013. Targeting ASIC1 in primary progressive multiple sclerosis: evidence of neuroprotection with amiloride. Brain 136 (1) , pp. 106-115. 10.1093/brain/aws325

Asher, Laura, Zammit, Stanley, Sullivan, Sarah, Dorrington, Sarah, Heron, Jon and Lewis, Glyn 2013. The relationship between psychotic symptoms and social functioning in a non-clinical population of 12year olds. Schizophrenia Research 150 (2-3) , pp. 404-9. 10.1016/j.schres.2013.08.031

B

Baker, Jessica H., Sisk, Cheryl L., Thornton, Laura M., Brandt, Harry, Crawford, Steven, Fichter, Manfred M., Halmi, Katherine A., Johnson, Craig, Jones, Ian Richard, Kaplan, Allan S., Mitchell, James E., Strober, Michael, Treasure, Janet, Woodside, D. Blake, Berrettini, Wade H., Kaye, Walter H., Bulik, Cynthia M. and Klump, Kelly L. 2013. Primary amenorrhea in anorexia nervosa: impact on characteristic masculine and feminine traits. European Eating Disorders Review 22 (1) , pp. 32-38. 10.1002/erv.2263

Baker, Jessica H., Thornton, Laura M., Strober, Michael, Brandt, Harry, Crawford, Steve, Fichter, Manfred M., Halmi, Katherine A., Johnson, Craig, Jones, Ian Richard, Kaplan, Allan S., Klump, Kelly L., Mitchell, James E., Treasure, Janet, Woodside, D. Blake, Berrettini, Wade H., Kaye, Walter H. and Bulik, Cynthia M. 2013. Temporal sequence of comorbid alcohol use disorder and anorexia nervosa. Addictive Behaviors 38 (3) , pp. 1704-1709. 10.1016/j.addbeh.2012.10.005

Bannister, Christian, Poole, Christopher David, Jenkins-Jones, Sara, Morgan, Christopher L., Currie, Craig and Elwyn, Glyn 2013. Orals: validation of UKPDS risk engine predictions among patients with type 2 diabetes routinely managed in UK primary care. Diabetes 62 (Supp 1) , A71-A71. 10.2337/db13-1-387

Barch, Deanna M., Bustillo, Juan, Gaebel, Wolfgang, Gur, Raquel, Heckers, Stephan, Malaspina, Dolores, Owen, Michael John, Schultz, Susan, Tandon, Rajiv, Tsuang, Ming, Van Os, Jim and Carpenter, William 2013. Logic and justification for dimensional assessment of symptoms and related clinical phenomena in psychosis: Relevance to DSM-5 [Editorial Material]. Schizophrenia Research 150 (1) , pp. 15-20. 10.1016/j.schres.2013.04.027

Barker, R. A., Mason, S. L., Harrower, T. P., Swain, R. A., Ho, A. K., Sahakian, B. J., Mathur, R., Elneil, S., Thornton, S., Hurrelbrink, C., Armstrong, R. J., Tyers, P., Smith, E., Carpenter, A., Piccini, P., Tai, Y. F., Brooks, D. J., Pavese, N., Watts, C., Pickard, J. D., Rosser, Anne Elizabeth, Dunnett, Stephen Bruce, Simpson, S., Moore, J., Morrison, P., Esmonde, T., Chada, N., Craufurd, D., Snowdon, J., Thompson, J., Harper, P., Glew, R. and Harper, R. 2013. The long-term safety and efficacy of bilateral transplantation of human fetal striatal tissue in patients with mild to moderate Huntington's disease. Journal of Neurology, Neurosurgery & Psychiatry 84 (6) , pp. 657-665. 10.1136/jnnp-2012-302441

Bauer, P., Balding, D. J., Klunemann, H. H., Linden, D. E. J., Ory, D. S., Pineda, M., Priller, J., Sedel, F., Muller, A., Chadha-Boreham, H., Welford, R. W. D., Strasser, D. S., Patterson, M. C. and Linden, David 2013. Genetic screening for Niemann-Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM study. Human Molecular Genetics 22 (21) , pp. 4349-56. 10.1093/hmg/ddt284

Beecham, Ashley H, Patsopoulos, Nikolaos A, Xifara, Dionysia K, Davis, Mary F, Kemppinen, Anu, Cotsapas, Chris, Shah, Tejas S, Spencer, Chris, Booth, David, Goris, An, Oturai, Annette, Saarela, Janna, Fontaine, Bertrand, Hemmer, Bernhard, Martin, Claes, Zipp, Frauke, D'Alfonso, Sandra, Martinelli-Boneschi, Filippo, Taylor, Bruce, Harbo, Hanne F, Kockum, Ingrid, Hillert, Jan, Olsson, Tomas, Ban, Maria, Oksenberg, Jorge R, Hintzen, Rogier, Barcellos, Lisa F, Agliardi, Cristina, Alfredsson, Lars, Alizadeh, Mehdi, Anderson, Carl, Andrews, Robert, Søndergaard, Helle Bach, Baker, Amie, Band, Gavin, Baranzini, Sergio E, Barizzone, Nadia, Barrett, Jeffrey, Bellenguez, Céline, Bergamaschi, Laura, Bernardinelli, Luisa, Berthele, Achim, Biberacher, Viola, Binder, Thomas M C, Blackburn, Hannah, Bomfim, Izaura L, Brambilla, Paola, Broadley, Simon, Brochet, Bruno, Brundin, Lou, Buck, Dorothea, Butzkueven, Helmut, Caillier, Stacy J, Camu, William, Carpentier, Wassila, Cavalla, Paola, Celius, Elisabeth G, Coman, Irène, Comi, Giancarlo, Corrado, Lucia, Cosemans, Leentje, Cournu-Rebeix, Isabelle, Cree, Bruce A C, Cusi, Daniele, Damotte, Vincent, Defer, Gilles, Delgado, Silvia R, Deloukas, Panos, di Sapio, Alessia, Dilthey, Alexander T, Donnelly, Peter, Dubois, Bénédicte, Duddy, Martin, Edkins, Sarah, Elovaara, Irina, Esposito, Federica, Evangelou, Nikos, Fiddes, Barnaby, Field, Judith, Franke, Andre, Freeman, Colin, Frohlich, Irene Y, Galimberti, Daniela, Gieger, Christian, Gourraud, Pierre-Antoine, Graetz, Christiane, Graham, Andrew, Grummel, Verena, Guaschino, Clara, Hadjixenofontos, Athena, Hakonarson, Hakon, Halfpenny, Christopher, Hall, Gillian, Hall, Per, Hamsten, Anders, Harley, James, Harrower, Timothy, Hawkins, Clive, Hellenthal, Garrett, Hillier, Charles, Hobart, Jeremy, Hoshi, Muni, Hunt, Sarah E, Jagodic, Maja, Jel?i?, Ilijas, Jochim, Angela, Kendall, Brian, Kermode, Allan, Kilpatrick, Trevor, Koivisto, Keijo, Konidari, Ioanna, Korn, Thomas, Kronsbein, Helena, Langford, Cordelia, Larsson, Malin, Lathrop, Mark, Lebrun-Frenay, Christine, Lechner-Scott, Jeannette, Lee, Michelle H, Leone, Maurizio A, Leppä, Virpi, Liberatore, Giuseppe, Lie, Benedicte A, Lill, Christina M, Lindén, Magdalena, Link, Jenny, Luessi, Felix, Lycke, Jan, Macciardi, Fabio, Männistö, Satu, Manrique, Clara P, Martin, Roland, Martinelli, Vittorio, Mason, Deborah, Mazibrada, Gordon, McCabe, Cristin, Mero, Inger-Lise, Mescheriakova, Julia, Moutsianas, Loukas, Myhr, Kjell-Morten, Nagels, Guy, Nicholas, Richard, Nilsson, Petra, Piehl, Fredrik, Pirinen, Matti, Price, Siân E, Quach, Hong, Reunanen, Mauri, Robberecht, Wim, Robertson, Neil, Rodegher, Mariaemma, Rog, David, Salvetti, Marco, Schnetz-Boutaud, Nathalie C, Sellebjerg, Finn, Selter, Rebecca C, Schaefer, Catherine, Shaunak, Sandip, Shen, Ling, Shields, Simon, Siffrin, Volker, Slee, Mark, Sorensen, Per Soelberg, Sorosina, Melissa, Sospedra, Mireia, Spurkland, Anne, Strange, Amy, Sundqvist, Emilie, Thijs, Vincent, Thorpe, John, Ticca, Anna, Tienari, Pentti, van Duijn, Cornelia, Visser, Elizabeth M, Vucic, Steve, Westerlind, Helga, Wiley, James S, Wilkins, Alastair, Wilson, James F, Winkelmann, Juliane, Zajicek, John, Zindler, Eva, Haines, Jonathan L, Pericak-Vance, Margaret A, Ivinson, Adrian J, Stewart, Graeme, Hafler, David, Hauser, Stephen L, Compston, Alastair, McVean, Gil, De Jager, Philip, Sawcer, Stephen J and McCauley, Jacob L 2013. Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nature Genetics 45 (11) , pp. 1353-60. 10.1038/ng.2770

Belleau, Emily L., Phillips, Mary, Birmaher, Boris, Axelson, David A. and Ladouceur, Cecile D. 2013. Aberrant executive attention in unaffected youth at familial risk for mood disorders. Journal of affective disorders 147 (1-3) , pp. 397-400. 10.1016/j.jad.2012.08.020

Betcheva, E., Yosifova, A., Mushiroda, T., Kubo, M., Takahashi, A., Karachanak, S., Zaharieva, I., Hadjidekova, S., Dimova, I., Vazharova, R., Stoyanov, D., Milanova, V., Tolev, T., Kirov, George, Kamatani, N., Toncheva, D. and Nakamura, Y. 2013. Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene. Psychiatric Genetics 23 (1) , pp. 11-19. 10.1097/YPG.0b013e3283586343

Betcheva, Elitza T., Yosifova, Adelina G., Mushiroda, Taisei, Kubo, Michiaki, Takahashi, Atsushi, Karachanak, Sena K., Zaharieva, Irina T., Hadjidekova, Savina P., Dimova, Ivanka I., Vazharova, Radoslava V., Stoyanov, Drozdstoy S., Milanova, Vihra K., Tolev, Todor, Kirov, George, Kamatani, Naoyuki, Toncheva, Draga I. and Nakamura, Yusuke 2013. Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene [Article]. Psychiatric Genetics 23 (1) , pp. 11-19. 10.1097/YPG.0b013e3283586343

Bettencourt, Conceição, Morris, Huw R., Singleton, Andrew B., Hardy, John and Houlden, Henry 2013. Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to l-DOPA treatment. Journal of Neurology 260 (9) , pp. 2414-6. 10.1007/s00415-013-7044-6

Beyer, Stephen Richard and Perry, Jonathan 2013. Promoting independence through the use of assistive technology. Tizard Learning Disability Review 18 (4) , pp. 179-185. 10.1108/TLDR-03-2013-0028

Bisson, Jonathan Ian 2013. Disseminating and implementing evidence-based practice. European Journal of Psychotraumatology 4 10.3402/ejpt.v4i0.21252

Bisson, Jonathan Ian 2013. What happened to harmonization of the PTSD diagnosis? The divergence of ICD11 and DSM5 [Editorial Material]. Epidemiology and Psychiatric Sciences 22 (03) , pp. 205-207. 10.1017/S2045796013000164

Bisson, Jonathan Ian, Roberts, Neil Patrick, Andrew, Martin, Cooper, Rosalind and Lewis, Catrin 2013. Psychological therapies for chronic post-traumatic stress disorder (PTSD) in adults. Cochrane Database Syst Rev. 2013 10.1002/14651858.CD003388.pub4

Blackmore, E., Rubinow, D., O'Connor, T., Liu, X., Tang, W., Craddock, Nicholas John and Jones, Ian Richard 2013. Reproductive outcomes and risk of subsequent illness in women diagnosed with postpartum psychosis. Bipolar Disorders 15 (4) , pp. 394-404. 10.1111/bdi.12071

Bode, A., Wood, S.-E., Mullins, J. G. L., Keramidas, A., Cushion, T. D., Thomas, Rhys Huw, Pickrell, W. O., Drew, C. J. G., Masri, A., Jones, E. A., Vassallo, G., Born, A. P., Alehan, F., Aharoni, S., Bannasch, G., Bartsch, M., Kara, B., Krause, A., Karam, E. G., Matta, S., Jain, V., Mandel, H., Freilinger, M., Graham, G. E., Hobson, E., Chatfield, S., Vincent-Delorme, C., Rahme, J. E., Afawi, Z., Berkovic, S. F., Howell, O. W., Vanbellinghen, J.-F., Rees, M. I., Chung, S.-K. and Lynch, J. W. 2013. New hyperekplexia mutations provide insight into glycine receptor assembly, trafficking, and activation mechanisms. Journal of Biological Chemistry 288 (47) , pp. 33745-33759. 10.1074/jbc.M113.509240

Bourne, C., Aydemir, Ö., Balanzá-Martínez, V., Bora, E., Brissos, S., Cavanagh, J., Clark, L., Cubukcuoglu, Z., Dias, V., Dittmann, S., Ferrier, I., Fleck, D., Frangou, S., Gallagher, P., Jones, L., Kieseppä, T., Martínez-Aran, A., Melle, I., Moore, P., Mur, M., Pfennig, A., Raust, A., Senturk, V., Simonsen, C., Smith, D., Bio, D., Soeiro-de-Souza, M., Stoddart, S., Sundet, K., Szöke, A., Thompson, J., Torrent, C., Zalla, T., Craddock, Nicholas John, Andreassen, O., Leboyer, M., Vieta, E., Bauer, M., Worhunsky, P., Tzagarakis, C., Rogers, R., Geddes, J. and Goodwin, G. 2013. Neuropsychological testing of cognitive impairment in euthymic bipolar disorder: an individual patient data meta-analysis. Acta Psychiatrica Scandinavica 128 (3) , pp. 149-162. 10.1111/acps.12133

Brayne, Carol, Barker, Roger A., Harold, Denise, Ince, Paul G., Sawa, George M., Williams, Julie, Williams-Gray, Caroline H. and Wharton, Stephen B. 2013. From molecule to clinic and community for neurodegeneration: research to bridge translational gaps. Journal of Alzheimer's Disease 33 (Supp 1) , S385-S396. 10.3233/JAD-2012-129006

Brennan, Sarah C., Finney, Brenda, Lazarou, Maria, Rosser, Anne Elizabeth, Scherf, Caroline, Adriaensen, Dirk, Kemp, Paul J. and Riccardi, Daniela 2013. Fetal calcium regulates branching morphogenesis in the developing human and mouse lung: involvement of voltage-gated calcium channels. PLoS ONE 8 (11) , e80294. 10.1371/journal.pone.0080294
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Brydges, Nichola, Whalley, Heather C., Jansen, Maurits A., Merrifield, Gavin D., Wood, Emma R., Lawrie, Stephen M., Wynne, Sara-Madge, Day, Mark, Fleetwood-Walker, Sue, Steele, Douglas, Marshall, Ian, Hall, Jeremy and Holmes, Megan C. 2013. Imaging conditioned fear circuitry using awake rodent fMRI. PLoS ONE 8 (1) , e54197. 10.1371/journal.pone.0054197
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Busse, Monica, Quinn, Lori, Hamana, Katy, Jones, Karen, Collett, Jonathan, Playle, Rebecca Anne, Kelly, Mark James, Simpson, Sharon Anne, Backx, Karianne, Wasley, David, Dawes, Helen and Rosser, Anne Elizabeth 2013. A randomized feasibility study of a 12-week community-based exercise program for people with Huntington's Disease. Journal of Neurologic Physical Therapy 37 (4) , pp. 149-158. 10.1097/NPT.0000000000000016

C

Caseras, Xavier, Lawrence, Natalia Sophie, Murphy, Kevin, Wise, Richard Geoffrey and Phillips, Mary Louise 2013. Ventral striatum activity in response to reward: differences between bipolar I and II disorders. American Journal of Psychiatry 170 (5) , pp. 533-541. 10.1176/appi.ajp.2012.12020169
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Caseras, Xavier, Murphy, Kevin, Mataix-Cols, David, López-Solà, Marina, Soriano-Mas, Carles, Ortriz, Hector, Pujol, Jesus and Torrubia, Rafael 2013. Anatomical and functional overlap within the insula and anterior cingulate cortex during interoception and phobic symptom provocation. Human Brain Mapping 34 (5) , pp. 1220-1229. 10.1002/hbm.21503

Casey, B. J., Craddock, Nicholas John, Cuthbert, Bruce N., Hyman, Steven E., Lee, Francis S. and Ressler, Kerry J. 2013. DSM-5 and RDoC: progress in psychiatry research? Nature Reviews Neuroscience 14 (11) , pp. 810-4. 10.1038/nrn3621

Cenydd, L. A., John, N. W., Phillips, N. I. and Gray, William Peter 2013. A tablet-based neurosurgery training tool. Medicine Meets Virtual Reality 20, Studies in health technology and informatics, IoS Press, pp. 20-23.

Chapman, J., Rees, Elliott, Harold, Denise, Ivanov, Dobril, Gerrish, Amy, Sims, Rebecca, Hollingworth, P, Stretton, A., Holmans, Peter Alan, Owen, Michael John, O'Donovan, Michael Conlon, Williams, Julie and Kirov, George 2013. A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk. Human Molecular Genetics 22 (4) , pp. 816-824. 10.1093/hmg/dds476

Chapuis, J, Hansmannel, F, Gistelinck, M, Mounier, A, Van Cauwenberghe, C, Kolen, K V, Geller, F, Sottejeau, Y, Harold, D, Dourlen, P, Grenier-Boley, B, Kamatani, Y, Delepine, B, Demiautte, F, Zelenika, D, Zommer, N, Hamdane, M, Bellenguez, C, Dartigues, J-F, Hauw, J-J, Letronne, F, Ayral, A-M, Sleegers, K, Schellens, A, Broeck, L V, Engelborghs, S, De Deyn, P P, Vandenberghe, R, O'Donovan, Michael Conlon, Owen, Michael John, Epelbaum, J, Mercken, M, Karran, E, Bantscheff, M, Drewes, G, Joberty, G, Campion, D, Octave, J-N, Berr, C, Lathrop, M, Callaerts, P, Mann, D, Williams, Julie, Buée, L, Dewachter, I, Van Broeckhoven, C, Amouyel, P, Moechars, D, Dermaut, B and Lambert, J-C 2013. Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology [Article]. Molecular Psychiatry 18 (11) , pp. 1225-1234. 10.1038/mp.2013.1

Chase, Henry W., Nusslock, Robin, Almeida, Jorge R. C., Forbes, Erika E., LaBarbara, Edmund J. and Phillips, Mary L. 2013. Dissociable patterns of abnormal frontal cortical activation during anticipation of an uncertain reward or loss in bipolar versus major depression. Bipolar Disorders 15 (8) , pp. 839-854. 10.1111/bdi.12132

Cohen, Sabrina Rachel, Haddon, Josephine Elizabeth, George, David Noel and Honey, Robert Colin 2013. Pavlovian-to-instrumental transfer: paradoxical effects of the Pavlovian relationship explained. Journal of Experimental Psychology: Animal Behavior Processes 39 (1) , pp. 14-23. 10.1037/a0030594

Colasanti, Alessandro, Owen, David R., Grozeva, Detelina, Rabiner, Eugenii A., Matthews, Paul M., Craddock, Nicholas John and Young, Allan H. 2013. Bipolar disorder is associated with the rs6971 polymorphism in the gene encoding 18kDa Translocator Protein (TSPO). Psychoneuroendocrinology 38 (11) , pp. 2826-9. 10.1016/j.psyneuen.2013.07.007

Cooper, Miriam and Rajyaguru, Priya 2013. Authors' reply [Correspondence]. British Journal of Psychiatry 203 (2) , pp. 154-155. 10.1192/bjp.203.2.154a

Cossburn, Mark D., Harding, Katharine, Ingram, Gillian, El-Shanawany, Tariq, Heaps, Adrian, Pickersgill, Trevor Paul, Jolles, Stephen and Robertson, Neil 2013. Clinical relevance of differential lymphocyte recovery after alemtuzumab therapy for multiple sclerosis. Neurology 80 (1) , pp. 55-61. 10.1212/WNL.0b013e31827b5927

Costas, Javier, Suárez-Rama, Jose Javier, Carrera, Noa, Paz, Eduardo, Páramo, Mario, Agra, Santiago, Brenlla, Julio, Ramos-Ríos, Ramón and Arrojo, Manuel 2013. Role of DISC1 Interacting Proteins in Schizophrenia Risk from Genome-Wide Analysis of Missense SNPs. Annals of Human Genetics , pp. 504-12. 10.1111/ahg.12037

Craddock, Nicholas John 2013. Where's our Higgs? [Editorial Material]. New Scientist 218 (2914) , pp. 30-31. 10.1016/S0262-4079(13)61054-4

Craddock, Nicholas John and Sklar, P. 2013. Genetics of bipolar disorder. The Lancet 381 (9878) , pp. 1654-1662. 10.1016/S0140-6736(13)60855-7

Cruchaga, Carlos, Kauwe, John S. K., Harari, Oscar, Jin, Sheng Chih, Cai, Yefei, Karch, Celeste M., Benitez, Bruno A., Jeng, Amanda T., Skorupa, Tara, Carrell, David, Bertelsen, Sarah, Bailey, Matthew, McKean, David, Shulman, Joshua M., De Jager, Philip L., Chibnik, Lori, Bennett, David A., Arnold, Steve E., Harold, Denise, Sims, Rebecca, Gerrish, Amy, Williams, Julie, Van Deerlin, Vivianna M., Lee, Virginia M.-Y., Shaw, Leslie M., Trojanowski, John Q., Haines, Jonathan L., Mayeux, Richard, Pericak-Vance, Margaret A., Farrer, Lindsay A., Schellenberg, Gerard D., Peskind, Elaine R., Galasko, Douglas, Fagan, Anne M., Holtzman, David M., Morris, John C. and Goate, Alison M. 2013. GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease. Neuron 78 (2) , pp. 256-268. 10.1016/j.neuron.2013.02.026

D

Dalton, Anthony, Khalil, Hanan, Busse, Monica, Rosser, Anne Elizabeth, Van Deursen, Robert William Martin and ÓLaighin, Gearóid 2013. Analysis of gait and balance through a single triaxial accelerometer in presymptomatic and symptomatic Huntington's disease. Gait & Posture 37 (1) , pp. 49-64. 10.1016/j.gaitpost.2012.05.028

Davies, William 2013. Using mouse models to investigate sex-linked genetic effects on brain, behaviour and vulnerability to neuropsychiatric disorders. Brain Research Bulletin 92 , pp. 12-20. 10.1016/j.brainresbull.2011.06.018
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Delio, Maria, Guo, Tingwei, McDonald-McGinn, Donna M., Zackai, Elaine, Herman, Sean, Kaminetzky, Mark, Higgins, Anne Marie, Coleman, Karlene, Chow, Carolyn, Jarlbrzkowski, Maria, Bearden, Carrie E., Bailey, Alice, Vangkilde, Anders, Olsen, Line, Olesen, Charlotte, Skovby, Flemming, Werge, Thomas M., Templin, Ludivine, Busa, Tiffany, Philip, Nicole, Swillen, Ann, Vermeesch, Joris R., Devriendt, Koen, Schneider, Maude, Dahoun, Sophie, Eliez, Stephan, Schoch, Kelly, Hooper, Stephen R., Shashi, Vandana, Samanich, Joy, Marion, Robert, van Amelsvoort, Therese, Boot, Erik, Klaassen, Petra, Duijff, Sasja N., Vorstman, Jacob, Yuen, Tracy, Silversides, Candice, Chow, Eva, Bassett, Anne, Frisch, Amos, Weizman, Abraham, Gothelf, Doron, Niarchou, Maria, van den Bree, Marianne Bernadette, Owen, Michael John, Suñer, Damian Heine, Andreo, Jordi Rosell, Armando, Marco, Vicari, Stefano, Digilio, Maria Cristina, Auton, Adam, Kates, Wendy R., Wang, Tao, Shprintzen, Robert J., Emanuel, Beverly S. and Morrow, Bernice E. 2013. Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes. American Journal of Human Genetics 92 (3) , pp. 439-447. 10.1016/j.ajhg.2013.01.018

de Candia, Teresa R., Lee, S. Hong, Yang, Jian, Browning, Brian L., Gejman, Pablo V., Levinson, Douglas F., Mowry, Bryan J., Hewitt, John K., Goddard, Michael E., O'Donovan, Michael Conlon, Purcell, Shaun M., Posthuma, Danielle, Visscher, Peter M., Wray, Naomi R. and Keller, Matthew C. 2013. Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. American Journal of Human Genetics 93 (3) , pp. 463-470. 10.1016/j.ajhg.2013.07.007

Di Florio, Arianna and Craddock, Nicholas John 2013. The genomics revolution in psychiatry: a lesson from bipolar disorder. Dusunen Adam 26 (2) , pp. 119-121. 10.5350/DAJPN20132602001

Di Florio, Arianna, Forty, Elizabeth, Gordon-Smith, Katherine, Heron, Jess, Jones, Lisa, Craddock, Nicholas John, Jones, Ian Richard and Dunajewski, Katherine 2013. Perinatal episodes across the mood disorder spectrum. JAMA Psychiatry 70 (2) , pp. 168-175. 10.1001/jamapsychiatry.2013.279

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Edwards, Rhiannon Tudor, Linck, Pat, Hounsome, Natalia, Raisanen, Lawrence Matthew, Williams, Nefyn, Moore, Laurence Anthony Russell and Murphy, Simon 2013. Cost-effectiveness of a national exercise referral programme for primary care patients in Wales: results of a randomised controlled trial. BMC Public Health 13 (1) , 1021. 10.1186/1471-2458-13-1021
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Escott-Price, Valentina, Harold, Denise, Russo, Giancarlo, Vedernikov, Alexey, Sharma, Manu, Saad, Mohamad, Holmans, Peter Alan, Bras, Jose M., Bettella, Francesco, Keller, Margaux F., Nicolaou, Nayia, Simón-Sánchez, Javier, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Peter, Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Owen, Michael John, O’Donovan, Michael Conlon, Williams, Julie, Morris, Huw and Williams, Nigel Melville 2013. Analysis of genome-wide association studies of Alzheimer disease and of Parkinson disease to determine if these 2 diseases share a common genetic risk. JAMA Neurology 70 (10) , pp. 1268-1276. 10.1001/jamaneurol.2013.448

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Fratta, Pietro, Poulter, Mark, Lashley, Tammaryn, Rohrer, Jonathan D., Polke, James M., Beck, Jon, Ryan, Natalie, Hensman, Davina, Mizielinska, Sarah, Waite, Adrian James, Lai, Mang-Ching, Gendron, Tania F., Petrucelli, Leonard, Fisher, Elizabeth M. C., Revesz, Tamas, Warren, Jason D., Collinge, John, Isaacs, Adrian M. and Mead, Simon 2013. Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia. Acta Neuropathologica 126 (3) , pp. 401-409. 10.1007/s00401-013-1147-0
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Gibson, Greg, Schork, Andrew J., Thompson, Wesley K., Pham, Phillip, Torkamani, Ali, Roddey, J. Cooper, Sullivan, Patrick F., Kelsoe, John R., O'Donovan, Michael Conlon, Furberg, Helena, Schork, Nicholas J., Andreassen, Ole A. and Dale, Anders M. 2013. All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs. PLoS Genetics 9 (4) , e1003449. 10.1371/journal.pgen.1003449
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Graf, M., Wermuth, P., Hafeli, D., Weisert, A., Reagu, Shuja, Pfluger, M., Taylor, Pamela Jane, Dittmann, V. and Jones, Roland Morgan 2013. Prevalence of mental disorders among detained asylum seekers in deportation arrest in Switzerland and validation of the Brief Jail Mental Health Screen BJMHS. International Journal of Law and Psychiatry 36 (3-4) , pp. 201-206. 10.1016/j.ijlp.2013.04.009

Green, E., Gordon-Smith, K., Burge, S., Grozeva, D., Munro, C., Tavadia, S., Jones, L. and Craddock, Nicholas John 2013. NovelATP2A2mutations in a large sample of individuals with Darier disease. The Journal of Dermatology 40 (4) , pp. 259-266. 10.1111/1346-8138.12082

Green, Elaine, Gordon-Smith, Katherine, Burge, Susan M., Grozever, Detelina, Munro, Colin S., Tavadia, Sherine, Jones, Lisa, Craddock, Nicholas John and Dunajewski, Katherine 2013. NovelATP2A2mutations in a large sample of individuals with Darier disease [Article]. The Journal of Dermatology 40 (4) , pp. 259-266. 10.1111/1346-8138.12082

Green, Elaine Karen, Grozeva, Detelina Valentinova, Forty, Elizabeth, Gordon-Smith, K., Russell, Elen, Farmer, A., Hamshere, Marian Lindsay, Jones, Ian Richard, Jones, L., McGuffin, P., Moran, J. L., Purcell, S., Sklar, P., Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2013. Association at SYNE1 in both bipolar disorder and recurrent major depression. Molecular Psychiatry 18 , pp. 614-617. 10.1038/mp.2012.48

Green, Elaine Karen, Hamshere, Marian L., Forty, Elizabeth, Gordon-Smith, K., Fraser, Christine, Russell, Elen Elizabeth, Grozeva, Detelina Valentinova, Kirov, George, Holmans, Peter Alan, Moran, J. L., Purcell, S., Sklar, P., Owen, Michael John, O'Donovan, Michael Conlon, Jones, L., Jones, Ian Richard and Craddock, Nicholas John 2013. Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample. Molecular Psychiatry 18 (12) , pp. 1302-1307. 10.1038/mp.2012.142

Grosset, Donald, Naveed, Malek, Aquino, Camila Catherine, Fox, Susan H., Williams, Susannah, Rosser, Anne Elizabeth and Hughes, Alis 2013. Journal Watch: Our panel of experts highlight the most important research articles across the spectrum of topics relevant to the field of neurodegenerative disease management. Neurodegenerative Disease Management 3 (4) , pp. 303-305. 10.2217/nmt.13.39

Grozeva, Detelina, Kirov, George, Conrad, Donald F, Barnes, Chris P, Hurles, Matthew, Owen, Michael John, O'Donovan, Michael Conlon and Craddock, Nicholas John 2013. Reduced burden of very large and rare CNVs in bipolar affective disorder. Bipolar Disorders 15 (8) , pp. 893-8. 10.1111/bdi.12125

Guerreiro, Rita, Wojtas, Aleksandra, Bras, Jose, Carrasquillo, Minerva, Rogaeva, Ekaterina, Majounie, Elisa, Cruchaga, Carlos, Sassi, Celeste, Kauwe, John S.K., Younkin, Steven, Hazrati, Lilinaz, Collinge, John, Pocock, Jennifer, Lashley, Tammaryn, Williams, Julie, Lambert, Jean-Charles, Amouyel, Philippe, Goate, Alison, Rademakers, Rosa, Morgan, Kevin, Powell, John, St. George-Hyslop, Peter, Singleton, Andrew and Hardy, John 2013. TREM2Variants in Alzheimer's disease. New England Journal of Medicine 368 (2) , pp. 117-127. 10.1056/NEJMoa1211851

Guha, Saurav, Rees, Elliott, Darvasi, Ariel, Ivanov, Dobril, Ikeda, Masashi, Bergen, Sarah E., Magnusson, Patrik K., Cormican, Paul, Morris, Derek, Gill, Michael, Cichon, Sven, Rosenfeld, Jeffrey A., Lee, Annette, Gregersen, Peter K., Kane, John M., Malhotra, Anil K., Rietschel, Marcella, Nöthen, Markus M., Degenhardt, Franziska, Priebe, Lutz, Breuer, René, Strohmaier, Jana, Ruderfer, Douglas M., Moran, Jennifer L., Chambert, Kimberly D., Sanders, Alan R., Shi, Jianxin, Kendler, Kenneth, Riley, Brien, O’Neill,, Tony, Walsh, Dermot, Malhotra, Dheeraj, Corvin, Aiden, Purcell, Shaun, Sklar, Pamela, Iwata, Nakao, Hultman, Christina M., Sullivan, Patrick F., Sebat, Jonathan, McCarthy, Shane, Gejman, Pablo V., Levinson, Douglas F., Owen, Michael John, O'Donovan, Michael Conlon, Lencz, Todd and Kirov, George 2013. Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry 70 (3) , pp. 253-260. 10.1001/2013.jamapsychiatry.71

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Hamshere, Marian Lindsay, Langley, Kate, Martin, Joanna, Agha, Sharifah Shameem, Stergiakouli, Evangelia, Anney, Richard, Buitelaar, Jan, Faraone, Stephen V., Lesch, Klaus-Peter, Neale, Benjamin M., Franke, Barbara, Sonuga-Barke, Edmund, Asherson, Philip, Merwood, Andrew, Kuntsi, Jonna, Medland, Sarah E., Ripke, Stephan, Steinhausen, Hans-Christoph, Freitag, Christine, Reif, Andreas, Renner, Tobias J., Romanos, Marcel, Romanos, Jasmin, Warnke, Andreas, Meyer, Jobst, Palmason, Haukur, Vasquez, Alejandro Arias, Lambregts-Rommelse, Nanda, Roeyers, Herbert, Biederman, Joseph, Doyle, Alysa E., Hakonarson, Hakon, Rothenberger, Aribert, Banaschewski, Tobias, Oades, Robert D., McGough, James J., Kent, Lindsey, Williams, Nigel Melville, Owen, Michael John, Holmans, Peter Alan, O'Donovan, Michael Conlon and Thapar, Anita 2013. High loading of polygenic risk for ADHD in children with comorbid aggression. American Journal of Psychiatry 170 (8) , pp. 909-916. 10.1176/appi.ajp.2013.12081129

Hamshere, Marian Lindsay, Stergiakouli, Evangelia, Langley, Kate, Martin, Joanna, Holmans, Peter Alan, Kent, L., Owen, Michael John, Gill, M., Thapar, Anita, O'Donovan, Michael Conlon and Craddock, Nicholas John 2013. Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia. British Journal of Psychiatry 203 (2) , pp. 107-111. 10.1192/bjp.bp.112.117432
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Hamshere, Marian Lindsay, Walters, James Tynan Rhys, Smith, Rhodri, Richards, Alexander, Green, Elaine Karen, Grozeva, Detelina Valentinova, Jones, Ian Richard, Forty, Elizabeth, Jones, L., Gordon-Smith, Katherine, Riley, B., O'Neill, T., Kendler, K. S., Sklar, P., Purcell, S, Kranz, J., Morris, D., Gill, M., Holmans, Peter Alan, Craddock, Nicholas John, Corvin, A., Owen, Michael John and O'Donovan, Michael Conlon 2013. Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC. Molecular Psychiatry 18 (6) , pp. 708-712. 10.1038/mp.2012.67

Harding, Katharine 2013. The spirit catches you and you fall down. Practical Neurology 14 (1) , p. 67. 10.1136/practneurol-2013-000728

Harding, Katharine, Liang, Kate, Cossburn, Mark D., Ingram, Gillian, Hirst, Claire Louise, Pickersgill, Trevor, te Water Naude, Johann, Wardle, Mark, Ben-Shlomo, Y. and Robertson, Neil 2013. Long-term outcome of paediatric-onset multiple sclerosis: a population-based study. Journal of Neurology, Neurosurgery & Psychiatry 84 (2) , pp. 141-147. 10.1136/jnnp-2012-303996

Harding, Katharine and Robertson, Neil 2013. Assessment of long-term outcome in neurological disease. Journal of Neurology 260 (6) , pp. 1693-5. 10.1007/s00415-013-6966-3

Harding, Katharine and Robertson, Neil 2013. Traumatic brain injury: risk factors and prognostic assessment. Journal of Neurology 260 (10) , pp. 2691-3. 10.1007/s00415-013-7106-9

Harold, Gordon Thomas, Leve, Leslie D., Barrett, Douglas, Elam, Kit, Neiderhiser, Jenae M., Natsuaki, Misaki N., Shaw, Daniel S., Reiss, David and Thapar, Anita 2013. Biological and rearing mother influences on child ADHD symptoms: revisiting the developmental interface between nature and nurture. Journal of Child Psychology and Psychiatry 54 (10) , pp. 1038-46. 10.1111/jcpp.12100

Harold, Gordon Thomas, Leve, Leslie D., Elam, Kit K., Thapar, Anita, Neiderhiser, Jenae M., Natsuaki, Misaki N., Shaw, Daniel S. and Reiss, David 2013. The nature of nurture: Disentangling passive genotype-environment correlation from family relationship influences on children's externalizing problems [Article]. Journal of Family Psychology 27 (1) , pp. 12-21. 10.1037/a0031190

Harris, M., Farquhar, F., Healy, David, Le Noury, J. C., Linden, Stefanie, Hughes, J. A. and Roberts, A. P. 2013. The morbidity and mortality linked to melancholia: two cohorts compared, 1875-1924 and 1995-2005. History of Psychiatry 24 (1) , pp. 3-14. 10.1177/0957154X12450131

Harrison, David John, Busse, Monica, Openshaw, Rebecca, Rosser, Anne Elizabeth, Dunnett, Stephen Bruce and Brooks, Simon Philip 2013. Exercise attenuates neuropathology and has greater benefit on cognitive than motor deficits in the R6/1 Huntington's disease mouse model. Experimental Neurology 248 , pp. 457-469. 10.1016/j.expneurol.2013.07.014
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Hodgson, Kate, Shelton, Katherine Helen, van den Bree, Marianne Bernadette and Los, Férenc J. 2013. Psychopathology in young people experiencing homelessness: A systematic review. American Journal of Public Health 103 (6) , e24-e37. 10.2105/AJPH.2013.301318

Holmans, Peter Alan, Escott-Price, Valentina, Jones, Lesley, Sharma, Manu, Vedernikov, Alexey, Buchel, Finja, Sadd, Mohamad, Bras, Jose M., Bettella, Francesco, Nicolaou, Nayia, Simón-Sánchez, Javier, Mittag, Florian, Gibbs, J. Raphael, Schulte, Claudia, Durr, Alexandra, Guerreiro, Rita, Hernandez, Dena, Brice, Alexis, Stefánsson, Hreinn, Majamaa, Kari, Gasser, Thomas, Heutink, Peter, Wood, Nicholas W., Martinez, Maria, Singleton, Andrew B., Nalls, Michael A., Hardy, John, Morris, Huw Rees and Williams, Nigel Melville 2013. A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease. Human Molecular Genetics 22 (5) , pp. 1039-1049. 10.1093/hmg/dds492

Hubers, Anna A.M., van Duijn, Erik, Roos, Raymund A.C., Craufurd, David, Rickards, Hugh, Bernhard Landwehrmeyer, G., van der Mast, Rose C., Giltay, Erik J., Bisson, Jonathan Ian, Owen, Michael John, Price, Kathleen, Robertson, Neil and Rosser, Anne Elizabeth 2013. Suicidal ideation in a European Huntington's disease population. Journal of Affective Disorders 151 (1) , pp. 248-58. 10.1016/j.jad.2013.06.001

Hudson, G., Nalls, M., Evans, J. R., Breen, D. P., Winder-Rhodes, S., Morrison, K. E., Morris, H. R., Williams-Gray, C. H., Barker, R. A., Singleton, A. B., Hardy, J., Wood, N. E., Burn, D. J. and Chinnery, P. F. 2013. Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease [Article]. Neurology 80 (22) , pp. 2042-2048. 10.1212/WNL.0b013e318294b434

Humby, Trevor, Eddy, Jessica B., Good, Mark Andrew, Reichelt, Amy C. and Wilkinson, Lawrence Stephen 2013. A novel translational assay of response inhibition and impulsivity: effects of prefrontal cortex lesions, drugs used in ADHD, and serotonin 2C receptor antagonism. Neuropsychopharmacology 38 (11) , pp. 2150-2159. 10.1038/npp.2013.112
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Hummel, Alegra, Shelton, Katherine Helen, Heron, Jon, Moore, Laurence Anthony Russell and van den Bree, Marianne Bernadette 2013. A systematic review of the relationships between family functioning, pubertal timing and adolescent substance use. Addiction 108 (3) , pp. 487-496. 10.1111/add.12055

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Jones, Derek K, and Linden, David Edmund Johannes 2013. Abstracts of Presentations at the International Conference on Basic and Clinical Multimodal Imaging (BaCI), a Joint Conference of the International Society for Neuroimaging in Psychiatry (ISNIP), the International Society for Functional Source Imaging (ISFSI), the International Society for Bioelectromagnetism (ISBEM), the International Society for Brain Electromagnetic Topography (ISBET), and the EEG and Clinical Neuroscience Society (ECNS), in Geneva, Switzerland, September 5-8, 2013. Clinical EEG and Neuroscience 44 (4) , E1. 10.1177/1550059413507209

Jones, Emma L., Mok, Kin, Hanney, Marisa, Harold, Denise, Sims, Rebecca, Williams, Julie and Ballard, Clive 2013. Evidence that PICALM affects age at onset of Alzheimer's dementia in Down syndrome. Neurobiology of Aging 34 (10) , p. 2441. 10.1016/j.neurobiolaging.2013.03.018

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This list was generated on Mon Nov 11 10:57:11 2019 GMT.