Browse by Schools (by year)

2009. An association study of common variation at theMAPTlocus with late-onset Alzheimer's disease. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (8) , pp. 1152-1155. 10.1002/ajmg.b.30951

Alam, Masih-Ul, Kirton, John Paul, Wilkinson, Fiona L., Towers, Emily, Sinha, Smeeta, Rouhi, Mansour, Vizard, Thomas Neill, Sage, Andrew P., Martin, David, Ward, Donald T., Alexander, Marie Yvonne, Riccardi, Daniela

and Canfield, Ann E. 2009. Calcification is associated with loss of functional calcium-sensing receptor in vascular smooth muscle cells. Cardiovascular Research 81 (2) , pp. 260-268. 10.1093/cvr/cvn279

Ali, K. W., Cossburn, M., Linnane, S. and Hamandi, Khalid 2009. Tuberculous encephalopathy [Conference abstract]. Journal of Neurology, Neurosurgery and Psychiatry 80 (1) , pp. 97-128. 10.1136/jnnp.2008.163279

Anney, Richard

and Lasky-Su, J. 2009. S.18.05 Molecular-genetics of aggression and antisocial behaviour in clinical populations [Conference abstract]. European Neuropsychopharmacology 19 , S203-S203. 10.1016/S0924-977X(09)70264-0

Aragona, Massimiliano, Onesti, Emanuela, Tomassini, Valentina

, Conte, Antonella, Gupta, Shiva, Gilio, Francesca, Pantano, Patrizia, Pozzilli, Carlo and Inghilleri, Maurizio 2009. Psychopathological and cognitive effects of therapeutic cannabinoids in multiple sclerosis: a double-blind, placebo controlled, crossover study. Clinical Neuropharmacology 32 (1) , pp. 41-47. 10.1097/WNF.0B013E3181633497

Armstrong, J. D., Malik, B., Pocklington, Andrew

, Emes, R. and Grant, S. 2009. Evolution of the synapse proteome [Conference abstract]. Journal of Neurogenetics 23 , S34-S35.

Aziz, N. A., Jurgens, C. K., Landwehrmeyer, G. B., van Roon-Mom, W.M.C., van Ommen, G. J.B., Stijnen, T., Roos, R. A.C., Bisson, Jonathan Ian

2009. Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease. Neurology 73 (16) , pp. 1280-1285. 10.1212/WNL.0b013e3181bd1121

Azuma, Rayna, Daly, Eileen M., Campbell, Linda E., Stevens, Angela F., Deeley, Quinton, Giampietro, Vincent, Brammer, Michael J., Glaser, Beate, Ambery, Fiona Z., Morris, Robin G., Williams, Steven C. R., Owen, Michael John

, Murphy, Declan G. M. and Murphy, Kieran C. 2009. Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study. Journal of Neurodevelopmental Disorders 1 (1) , pp. 46-60. 10.1007/s11689-009-9008-9

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Baker, G., Jacoby, A., Kerr, Michael Patrick and Appleton, R. 2009. Introduction [Editorial]. Epilepsy & Behavior 15 (2) , S3-S4. 10.1016/j.yebeh.2009.04.019

Ball, H. A., Samaan, Z., Brewster, S., Craddock, Nicholas John

, Gill, M., Korszun, A., Maier, W., Middleton, L., Mors, O., Owen, Michael John

, Perry, Jonathan, Preisig, M., Rice, J., Rietschel, M., Jones, L., Jones, Ian Richard

, Farmer, A. E. and McGuffin, P. 2009. Depression, migraine with aura and migraine without aura: their familiality and interrelatedness. Cephalagia 29 (8) , pp. 848-854. 10.1111/j.1468-2982.2008.01808.x

Ban, Maria, Goris, An, Lorentzen, Åslaug R., Baker, Amie, Mihalova, Tania, Ingram, Gillian, Booth, David R., Heard, Robert N., Stewart, Graeme J., Bogaert, Elke, Dubois, Bénédicte, Harbo, Hanne F., Celius, Elisabeth G., Spurkland, Anne, Strange, Richard, Hawkins, Clive, Robertson, Neil

, Dudbridge, Frank, Wason, James, De Jager, Philip L., Hafler, David, Rioux, John D., Ivinson, Adrian J., McCauley, Jacob L., Pericak-Vance, Margaret, Oksenberg, Jorge R., Hauser, Stephen L., Sexton, David, Haines, Jonathan and Sawcer, Stephen 2009. Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. European Journal of Human Genetics 17 (10) , pp. 1309-1313. 10.1038/ejhg.2009.41

Barnard, Steve and Beyer, Stephen Richard

2009. Barriers to using personalised technology with people with learning disabilities. Journal of Assistive Technologies 3 (3) , pp. 50-57. 10.1108/17549450200900025

Barrett, Jeffrey C, Lee, James C, Lees, Charles W, Prescott, Natalie J, Anderson, Carl A, Phillips, Anne, Wesley, Emma, Parnell, Kirstie, Zhang, Hu, Drummond, Hazel, Nimmo, Elaine R, Massey, Dunecan, Blaszczyk, Kasia, Elliott, Timothy, Cotterill, Lynn, Dallal, Helen, Lobo, Alan J, Mowat, Craig, Sanderson, Jeremy D, Jewell, Derek P, Newman, William G, Edwards, Cathryn, Ahmad, Tariq, Mansfield, John C, Satsangi, Jack, Parkes, Miles, Mathew, Christopher G, Donnelly, Peter, Peltonen, Leena, Blackwell, Jenefer M, Bramon, Elvira, Brown, Matthew A, Casas, Juan P, Corvin, Aiden, Craddock, Nicholas John

, Deloukas, Panos, Duncanson, Audrey, Jankowski, Janusz, Markus, Hugh S, Mathew, Christopher G, McCarthy, Mark I, Palmer, Colin N A, Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J, Samani, Nilesh, Trembath, Richard C, Viswanathan, Ananth C, Wood, Nicholas, Spencer, Chris C A, Barrett, Jeffrey C, Bellenguez, Céline, Davison, Daniel, Freeman, Colin, Strange, Amy, Donnelly, Peter, 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, Perez, Marc L, Potter, Simon C, Ravindrarajah, Radhi, Ricketts, Michelle, Waller, Matthew, Weston, Paul, Widaa, Sara, Whittaker, Pamela, Deloukas, Panos, Peltonen, Leena, Mathew, Christopher G, Blackwell, Jenefer M, Brown, Matthew A, Corvin, Aiden, McCarthy, Mark I, Spencer, Chris C A, Attwood, Antony P, Stephens, Jonathan, Sambrook, Jennifer, Ouwehand, Willem H, McArdle, Wendy L, Ring, Susan M and Strachan, David P 2009. Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region. Nature Genetics 41 (12) , pp. 1330-1334. 10.1038/ng.483

Beavis, Janine M., Meek, Andrea Janine, Felce, David John and Kerr, Michael Patrick 2009. A prospective multi-centre open label study of the use of levetiracetam as add-on treatment in patients with epilepsy and intellectual disabilities. Seizure - European Journal of Epilepsy 18 (4) , pp. 279-284. 10.1016/j.seizure.2008.11.001

Betcheva, Elitza T., Mushiroda, Taisei, Takahashi, Atsushi, Kubo, Michiaki, Karachanak, Sena K., Zaharieva, Irina T., Vazharova, Radoslava V., Dimova, Ivanka I., Milanova, Vihra K., Tolev, Todor, Kirov, George

, Kamatani, Naoyuki, Nakamura, Yusuke and Toncheva, Draga I. 2009. Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population. Journal of Human Genetics 54 (2) , pp. 98-107. 10.1038/jhg.2008.14

Beyer, Stephen Richard

2009. Evaluation of the London Borough of Newham Employment Initiative: Final evaluation report. London, UK: Department of Health Valuing People Support Team.

Beyer, Stephen Richard

2009. A review of the literature on the ethical issues associated with assistive technology. London: Social Care Institute for Excellence.

Beyer, Stephen Richard

2009. Scoping study on existing courses and qualifications for job coaches. London, UK: Department of Health, Valuing Employment Now Team.

Beyer, Stephen Richard

and Robinson, Carol 2009. A review of the research literature on supported employment: a report for the cross-Government learning disability employment strategy team. [Project Report]. London: Department of Health. Available at: http://www.dh.gov.uk/prod_consum_dh/groups/dh_digi...

Biglan, Kevin M., Ross, Christopher A., Langbehn, Douglas R., Aylward, Elizabeth H., Stout, Julie C., Queller, Sarah, Carlozzi, Noelle E., Duff, Kevin, Beglinger, Leigh J., Paulsen, Jane S. and Rosser, Anne Elizabeth

2009. Motor abnormalities in premanifest persons with Huntington's disease: The PREDICT-HD study. Movement Disorders 24 (12) , pp. 1763-1772. 10.1002/mds.22601

Bisson, Jonathan Ian

, Hampton, Victoria L., Rosser, Anne Elizabeth

and Holm, Søren 2009. Developing a care pathway for advance decisions and powers of attorney: qualitative study. British Journal of Psychiatry 194 (1) , pp. 55-61. 10.1192/bjp.bp.107.048900

Bisson, Jonathan Ian

, Tavakoly, Behrooz, Witteveen, Anke B., Ajdukovic, Dean, Jehel, Louis, Johansen, Venke J., Nordanger, Dag, Garcia, Francisco O., Punamaki, Raija-Leena, Schnyder, Ulrich, Sezgin, A. Ufuk, Wittmann, Lutz and Olff, Miranda 2009. TENTS guidelines: development of post-disaster psychosocial care guidelines through a Delphi process. British Journal of Psychiatry 196 (1) , pp. 69-74. 10.1192/bjp.bp.109.066266

Blom, Elin S., Giedraitis, Vilmantas, Arepalli, Sampath, Hamshere, Marian Lindsay

, Adighibe, Omanma, Goate, Alison, Williams, Julie

, Lannfelt, Lars, Hardy, John, Vrièze, Fabienne and Glaser, Anna 2009. Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs. BMC Medical Genetics 10 , pp. 1-6. 10.1186/1471-2350-10-122

Boivin, Jacky

, Hay, Dale F.

, Harold, Gordon Thomas, Lewis, Allyson, van den Bree, Marianne Bernadette

and Thapar, Anita

2009. Associations between maternal older age, family environment and parent and child wellbeing in families using assisted reproductive techniques to conceive. Social Science & Medicine 68 (11) , pp. 1948-1955. 10.1016/j.socscimed.2009.02.036

Booth, David R., Heard, Robert N., Stewart, Graeme J., Goris, An, Dobosi, Rita, Dubois, Bénédicte, Lorentzen, Åslaug R., Celius, Elisabeth G., Harbo, Hanne F., Spurkland, Anne, Olsson, Tomas, Kockum, Ingrid, Link, Jenny, Hillert, Jan, Ban, Maria, Baker, Amie, Sawcer, Stephen, Compston, Alastair, Mihalova, Tania, Strange, Richard, Hawkins, Clive, Ingram, Gillian, Robertson, Neil

, De Jager, Philip L., Hafler, David A., Barcellos, Lisa F., Ivinson, Adrian J., Pericak-Vance, Margaret, Oksenberg, Jorge R., Hauser, Stephen L., McCauley, Jacob L., Sexton, David and Haines, Jonathan 2009. The expanding genetic overlap between multiple sclerosis and type I diabetes. Genes and Immunity 10 (1) , pp. 11-14. 10.1038/gene.2008.83

Borg, Kristian, Stucka, Rolf, Locke, Matthew, Melin, Eva, Åhlberg, Gabrielle, Klutzny, Ursula, Von Der Hagen, Maja, Huebner, Angela, Lochmüller, Hanns, Wrogemann, Klaus, Thornell, Lars-Eric, Blake, Derek J.

and Schoser, Benedikt 2009. Intragenic deletion of TRIM32 in compound heterozygotes with sarcotubular myopathy/LGMD2H. Human Mutation 30 (10) , E831-E844. 10.1002/humu.21063

Bromage, D. I., McLauchlan, Duncan J. and Nightingale, A. K. 2009. Do cardiologists and cardiac surgeons need ethics? Achieving happiness for a drug user with endocarditis. Heart 95 (11) , pp. 885-887. 10.1136/hrt.2008.163782

Busse, Monica

, Wiles, Charles Mark and Rosser, Anne Elizabeth

2009. Mobility and falls in people with Huntington's disease. Journal of Neurology Neurosurgery and Psychiatry 80 (1) , pp. 88-90. 10.1136/jnnp.2008.147793

Butler, Amy W., Ng, Mandy Y.M., Hamshere, Marian Lindsay

, Forabosco, Paola, Wroe, Richard, Al-Chalabi, Ammar, Lewis, Cathryn M. and Powell, John F. 2009. Meta-analysis of linkage studies for Alzheimer's disease-A web resource. Neurobiology of Aging 30 (7) , pp. 1037-1047. 10.1016/j.neurobiolaging.2009.03.013

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Cantwell, R., Jones, Ian Richard

and Oates, M. 2009. Response to the Editor:. British Journal of Psychiatry 195 (4) , p. 369. 10.1192/bjp.195.4.369

Carrera, Noa

, Sanjuán, Julio, Moltó, María Dolores, Carracedo, Ángel and Costas, Javier 2009. Recent adaptive selection at MAOB and ancestral susceptibility to schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (3) , pp. 369-374. 10.1002/ajmg.b.30823

Carrillo-de-la-Peña, María, Baillès, Eva, Caseras, Xavier

, Martínez, Àlvar, Ortet, Generós and Pérez, Jorge 2009. Formative assessment and academic achievement in pre-graduate students of health sciences. Advances in Health Sciences Education 14 (1) , pp. 61-67. 10.1007/s10459-007-9086-y

Carroll, Liam S. and Owen, Michael John

2009. Genetic overlap between autism, schizophrenia and bipolar disorder [Review]. Genome Medicine 1 (10) , p. 102. 10.1186/gm102

Carroll, Liam Stuart, Kendall, Kimberley

and Williams, Nigel Melville

2009. Evidence that putative ADHD low risk alleles atSNAP25may increase the risk of schizophrenia. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (7) , pp. 893-899. 10.1002/ajmg.b.30915

Cichon, S., Craddock, Nicholas John

, Daly, M. J., Faraone,, S. V., Gejman, P. V., Kelsoe, J., Lehner, T., Levinson, D. F., Moran, A. P., Sklar, P., Sullivan, P. F., Boomsma, D. I., Geus, E. J. C. de, Posthuma, D. and Willemsen, G. 2009. Genomewide association studies: history, rationale, and prospects for psychiatric disorders. American Journal of Psychiatry 166 (5) , pp. 540-556. 10.1176/appi.ajp.2008.08091354

Clare, Linda, van Paasschen, Jorien, Evans, Suzannah J., Parkinson, Caroline, Woods, Robert T. and Linden, David Edmund Johannes

2009. Goal-oriented cognitive rehabilitation for an individual with Mild Cognitive Impairment: Behavioural and neuroimaging outcomes. Neurocase 15 (4) , pp. 318-331. 10.1080/13554790902783116

Coba, Marcelo P., Pocklington, Andrew

, Collins, Mark O., Kopanitsa, Maksym V., Uren, Rachel T., Swamy, Sajani, Croning, Mike D. R., Choudhary, Jyoti S. and Grant, Seth G. N. 2009. Neurotransmitters drive combinatorial multistate postsynaptic density networks. Science Signaling 2 (68) , ra19. 10.1126/scisignal.2000102

Cohen-Woods, S., Gaysina, D., Craddock, Nicholas John

, Farmer, A., Gray, J., Gunasinghe, C., Hoda, F., Jones, L., Knight, J., Korszun, A., Owen, Michael John

, Sterne, A., Craig, I. W. and McGuffin, P. 2009. Depression Case Control (DeCC) Study fails to support involvement of the muscarinic acetylcholine receptor M2 (CHRM2) gene in recurrent major depressive disorder. Human Molecular Genetics 18 (8) , pp. 1504-1509. 10.1093/hmg/ddp051

Collishaw, Stephan

, Goodman, Robert, Ford, Tamsin, Rabe-Hesketh, Sophia and Pickles, Andrew 2009. How far are associations between child, family and community factors and child psychopathology informant-specific and informant-general? Journal of Child Psychology and Psychiatry 50 (5) , pp. 571-580. 10.1111/j.1469-7610.2008.02026.x

Conroy, Judith, Cochrane, Lynne, Anney, Richard

, Sutcliffe, James S., Carthy, Paula, Dunlop, Adam, Mullarkey, Marice, O'hlci, Bronagh, Green, Andrew J., Ennis, Sean, Gill, Michael and Gallagher, Louise 2009. Fine mapping and association studies in a candidate region for autism on chromosome 2q31-q32. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (4) , pp. 535-544. 10.1002/ajmg.b.30854

Conte, Antonella, Bettolo, Chiara Marini, Onesti, Emanuela, Frasca, Vittorio, Iacovelli, Elisa, Gilio, Francesca, Giacomelli, Elena, Gabriele, Maria, Aragona, Massimiliano, Tomassini, Valentina

, Pantano, Patrizia, Pozzilli, Carlo and Inghilleri, Maurizio 2009. Cannabinoid-induced effects on the nociceptive system: A neurophysiological study in patients with secondary progressive multiple sclerosis. European Journal of Pain 13 (5) , pp. 472-477. 10.1016/j.ejpain.2008.05.014

Costas, Javier, Carrera, Noa

, Domínguez, Eduardo, Vilella, Elisabet, Martorell, Lourdes, Valero, Joaquín, Gutiérrez-Zotes, Alfonso, Labad, Antonio and Carracedo, Ángel 2009. A common haplotype of DRD3 affected by recent positive selection is associated with protection from schizophrenia. Human Genetics 124 (6) , pp. 607-613. 10.1007/s00439-008-0584-7

Craddock, Nicholas John

, Kendler, Kenneth, Neale, Michael, Nurnberger, John, Purcell, Shaun, Rietschel, Marcella, Perlis, Roy, Santangelo, Susan L., Schulze, Thomas, Smoller, Jordan W. and Thapar, Anita

2009. Dissecting the phenotype in genome-wide association studies of psychiatric illness (Editorial). British Journal of Psychiatry 195 (2) , pp. 97-99. 10.1192/bjp.bp.108.063156

Craddock, Nicholas John

, Wilkinson, Lawrence Stephen

2009. Psychosis genetics: modeling the relationship between Schizophrenia, Bipolar Disorder, and Mixed (or "Schizoaffective") Psychoses. Schizophrenia Bulletin 35 (3) , pp. 482-490. 10.1093/schbul/sbp020

Craddock, Nicholas John

and Sklar, Pamela 2009. Genetics of bipolar disorder: successful start to a long journey. Trends in Genetics 25 (2) , pp. 99-105. 10.1016/j.tig.2008.12.002

Creighton, S., Semaka, A., Hughes, Alis, Collins, J. A. and Hayden, M. R. 2009. The Huntington disease predictive testing experience in British Columbia, Canada [Conference Abstract]. Clinical Genetics 76 , p. 118. 10.1111/j.1399-0004.2009.01267.x

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Dallosso, Anthony Richard, Jones, Siân, Azzopardi, Duncan Lee, Escott-Price, Valentina

, Al-Tassan, Nada A., Williams, Geraint Trefor

, Idziaszczyk, Shelley Alexis, Davies, D. Rhodri, Milewski, Peter, Williams, Sally, Beynon, John, Sampson, Julian Roy

and Cheadle, Jeremy Peter

2009. The APC Variant p.Glu1317Gln predisposes to colorectal adenomas by a novel mechanism of relaxing the target for tumorigenic somatic APC mutations. Human Mutation 30 (10) , pp. 1412-1418. 10.1002/humu.21089

Davies, D, Rosser, Anne Elizabeth

and Sarangi, S 2009. Carers' Participation in Decision Making in a Huntingdon's disease management clinic. Journal of Medical Genetics 46 , S107-S107.

Davies, William

, Humby, Trevor

, Kong, Wendy, Otter, Tamara Leonie, Burgoyne, Paul S. and Wilkinson, Lawrence Stephen

2009. Converging pharmacological and genetic evidence indicates a role for steroid sulfatase in attention. Biological Psychiatry 66 (4) , pp. 360-367. 10.1016/j.biopsych.2009.01.001

de la Prida, Liset Menendez, Vaudano, Anna E., Laufs, Helmut, Kiebel, Stefan J., Carmichael, David W., Hamandi, Khalid, Guye, Maxime, Thornton, Rachel, Rodionov, Roman, Friston, Karl J., Duncan, John S. and Lemieux, Louis 2009. Causal hierarchy within the thalamo-cortical network in spike and wave discharges. PLoS ONE 4 (8) , e6475. 10.1371/journal.pone.0006475

De Silva, R., Giunti, P., Greenfield, J., Fletcher, N., Hadjivassiliou, M., Harrison, E., Hunt, B., Lowit, A., Morrison, P., Robertson, Neil

, Schapira, T., Surtees, R., Talbot, K., Baxter, P., Bates, C., Cassidy, E., Evans, M., Farrell, A., Hourihan, S., Pantazis, A. and Rodriguez, I. 2009. Management of ataxias: guidelines on best clinical practice. [Documentation]. London: Ataxia. Available at: https://www.acpin.net/pdfs/Ataxia_Guidelines.pdf

Doe, Christine M., Relkovic, Dinko, Garfield, Alastair S., Dalley, J. W., Theobald, D. E.H., Humby, Trevor

and Isles, Anthony Roger

2009. Loss of the imprinted snoRNA mbii-52 leads to increased 5htr2c pre-RNA editing and altered 5HT2CR-mediated behaviour. Human Molecular Genetics 18 (12) , pp. 2140-2148. 10.1093/hmg/ddp137

Donohoe, Gary, Walters, James Tynan Rhys

, Morris, Derek W., Quinn, Emma M., Róisín, Judge, Norton, Nadine, Giegling, Ina, Hartmann, Annette M., Möller, Hans-Jürgen, Muglia, Pierandrea, Williams, Hywel John

, Escott-Price, Valentina

, Peel, Rosemary, O’Donoghue, Theresa, Owen, Michael John

, Gill, Michael and Rujescu, Dan 2009. Influence of NOS1 on verbal intelligence and working memory in both patients with schizophrenia and healthy control subjects. Archives of General Psychiatry 66 (10) , pp. 1045-1054. 10.1001/archgenpsychiatry.2009.139

Dwyer, Sarah Lynne, Carroll, Liam Stuart, Mantripragada, Kiran Kumar

and Williams, Nigel Melville

2009. Mutation screening of the DTNBP1 exonic sequence in 669 schizophrenics and 710 controls using high-resolution melting analysis. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153B (3) , pp. 766-774. 10.1002/ajmg.b.31045

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Escott-Price, Valentina

, Holmans, Peter Alan

, Nikolov, Ivan, Pahwa, Jaspreet Singh, Green, Elaine Karen, Wellcome Trust Case Control Consortium, Owen, Michael John

2009. Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk. Molecular Psychiatry 14 (3) , pp. 252-260. 10.1038/mp.2008.133

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Felce, David John, Kerr, Michael Patrick and Hastings, R. P. 2009. A general practice-based study of the relationship between indicators of mental illness and challenging behaviour among adults with intellectual disabilities. Journal of Intellectual Disability Research 53 (3) , pp. 243-254. 10.1111/j.1365-2788.2008.01131.x

Filippini, Nicola, Rao, Anil, Wetten, Sally, Gibson, Rachel A., Borrie, Michael, Guzman, Danilo, Kertesz, Andrew, Loy-English, Inge, Williams, Julie

, Nichols, Thomas, Whitcher, Brandon and Matthews, Paul M. 2009. Anatomically-distinctgeneticassociations of APOE ɛ4 alleleload with regionalcorticalatrophy in Alzheimer's disease. NeuroImage 44 (3) , pp. 724-728. 10.1016/j.neuroimage.2008.10.003

Forty, Elizabeth, Jones, Lisa, Jones, Ian Richard

, Cooper, Carly, Russell, Elen, Farmer, Anne, McGuffin, Peter and Craddock, Nicholas John

2009. Is depression severity the sole cause of psychotic symptoms during an episode of unipolar major depression? A study both between and within subjects. Journal of Affective Disorders 114 (1-3) , pp. 103-109. 10.1016/j.jad.2008.06.012

Forty, Elizabeth, Jones, Lisa, Jones, Ian Richard

, Smith, Daniel J., Caesar, Sian, Fraser, Christine, Gordon-Smith, Katherine, Hyde, Sally and Craddock, Nicholas John

2009. Polarity at illness onset in bipolar I disorder and clinical course of illness. Bipolar Disorders 11 (1) , pp. 82-88. 10.1111/j.1399-5618.2008.00654.x

Forty, Elizabeth, Smith, Daniel J., Jones, Lisa, Jones, Ian Richard

, Caesar, Sian, Cooper, Carly, Fraser, Christine, Gordon-Smith, Katherine, Hyde, Sally, Farmer, Anne, McGuffin, Peter and Craddock, Nicholas John

2009. Clinical characteristics of unipolar disorder and bipolar disorder according to the lifetime presence of recurrent panic attacks. Bipolar Disorders 11 (3) , pp. 307-315. 10.1111/j.1399-5618.2009.00676.x

Forty, Elizabeth, Smith, Daniel J., Jones, Lisa, Jones, Ian Richard

, Caesar, Sian, Fraser, Christine, Gordon-Smith, Katherine and Craddock, Nicholas John

2009. Identifying hypomanic features in major depressive disorder using the hypomania checklist (HCL-32). Journal of Affective Disorders 114 (1-3) , pp. 68-73. 10.1016/j.jad.2008.07.017

Fowler, Tom Alan, Langley, Kate

, Ross, Kenny, Wilkinson, Lawrence Stephen

and Thapar, Anita

2009. Psychopathy trait scores in adolescents with childhood ADHD: the contribution of genotypes affecting MAOA, 5HTT and COMT activity. Psychiatric Genetics 19 (6) , pp. 312-319. 10.1097/YPG.0b013e3283328df4

Fowler, Tom Alan, Langley, Kate

, Whittinger, Naureen, Ross, Kenny, van Goozen, Stephanie Helena Maria

and Thapar, Anita

2009. Psychopathy traits in adolescents with childhood attention-deficit hyperactivity disorder. British Journal of Psychiatry 194 (1) , pp. 62-67. 10.1192/bjp.bp.107.046870

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Gerrish, Amy, Williams, Hywel John

, Escott-Price, Valentina

and Williams, Nigel Melville

2009. An examination of MUTED as a schizophrenia susceptibility gene [Letter]. Schizophrenia Research 107 (1) , pp. 110-111. 10.1016/j.schres.2008.08.011

Glaser, Beate and Holmans, Peter Alan

2009. Comparison of methods for combining case-control and family-based association studies. Human Heredity 68 (2) , pp. 106-116. 10.1159/000212503

Goodwin, G., Jones, Ian Richard

and Thapar, Anita

2009. Evidence-based guidelines for treating bipolar disorder: revised second edition--recommendations from the British Association for Psychopharmacology. Journal of Psychopharmacology 23 (4) , pp. 346-388. 10.1177/0269881109102919

Green, Elaine Karen, Grozeva, Detelina

, Raybould, Rachel, Elvidge, Gareth, Macgregor, Stuart, Craig, Ian, Farmer, Anne, McGuffin, Peter, Forty, Elizabeth, Jones, Lisa, Jones, Ian Richard

2009. P2RX7: A bipolar and unipolar disorder candidate susceptibility gene? American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 150B (8) , pp. 1063-1069. 10.1002/ajmg.b.30931

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Haenschel, Corinna, Bittner, Robert A., Waltz, James, Haertling, Fabian, Wibral, Michael, Singer, Wolf, Linden, David Edmund Johannes

and Rodriguez, Eugenio 2009. Cortical oscillatory activity is critical for working memory as revealed by deficits in early-onset schizophrenia. Journal of Neuroscience 29 (30) , pp. 9481-9489. 10.1523/JNEUROSCI.1428-09.2009

Hall, Jeremy

, Romaniuk, Liana, McIntosh, Andrew M., Steele, J. Douglas, Johnstone, Eve C. and Lawrie, Stephen M. 2009. Associative learning and the genetics of schizophrenia [Review]. Trends in Neurosciences 32 (6) , pp. 359-365. 10.1016/j.tins.2009.01.011

Hamshere, Marian Lindsay

, Gordon-Smith, Katherine, Forty, Elizabeth, Jones, Lisa, Caesar, Sian, Fraser, Christine, Hyde, Sally, Tredget, John, Kirov, George

, Jones, Ian Richard

and Smith, Daniel J. 2009. Age-at-onset in bipolar-I disorder: mixture analysis of 1369 cases identifies three distinct clinical sub-groups. Journal of affective disorders 116 (1-2) , pp. 23-29. 10.1016/j.jad.2008.10.021

Hamshere, Marian Lindsay

, Green, Elaine Karen, Jones, Ian Richard

, Jones, L., Escott-Price, Valentina

, Grozeva, Detelina

, Nikolov, Ivan, Vukcevic, D., Caesar, S., Gordon-Smith, K., Fraser, Christine, Russell, Elen, Breen, G., St Clair, D., Collier, D. A., Young, A. H., Ferrier, I. N., Farmer, A., McGuffin, P., Holmans, Peter Alan

2009. Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. British Journal of Psychiatry 195 (1) , pp. 23-29. 10.1192/bjp.bp.108.061424

Hamshere, Marian Lindsay

, Schulze, Thomas G., Schumacher, Johannes, Corvin, Aiden, Owen, Michael John

, Jamra, Rami Abou, Propping, Peter, Maier, Wolfgang, Orozco y Diaz, Guillermo, Mayoral, Fermin, Rivas, Fabio, Jones, Ian Richard

, Jones, Lisa, Kirov, George

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