Showing 1 - 20 results of 34 for search 'O'Donovan, M', query time: 0.08s
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Clustering of metabolic comorbidity in schizophrenia: A genetic contribution? by Gough, S, O'Donovan, M
Published 2005Journal article -
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Clustering of metabolic comorbidity in schizophrenia: a genetic contribution? by Gough, S, O'Donovan, M
Published 2005Journal article -
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The mentally handicapped person with epilepsy: a comparative study investigating psychosocial functioning. by Espie, C, Pashley, A, Bonham, K, Sourindhrin, I, O'Donovan, M
Published 1989Journal article -
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Adverse effects from antidepressant treatment: randomised controlled trial of 601 depressed individuals. by Crawford, A, Lewis, S, Nutt, D, Peters, T, Cowen, P, O'Donovan, M, Wiles, N, Lewis, G
Published 2014Journal article -
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Adverse effects from antidepressant treatment: Randomised controlled trial of 601 depressed individuals by Crawford, A, Lewis, S, Nutt, D, Peters, T, Cowen, P, O'Donovan, M, Wiles, N, Lewis, G
Published 2014Journal article -
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Severity of depression and response to antidepressants: GENPOD randomised controlled trial. by Wiles, N, Mulligan, J, Peters, T, Cowen, P, Mason, V, Nutt, D, Sharp, D, Tallon, D, Thomas, L, O'Donovan, M, Lewis, G
Published 2012Journal article -
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GENetic and clinical predictors of treatment response in depression: the GenPod randomised trial protocol. by Thomas, L, Mulligan, J, Mason, V, Tallon, D, Wiles, N, Cowen, P, Nutt, D, O'Donovan, M, Sharp, D, Peters, T, Lewis, G
Published 2008Journal article -
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Multicentre cohort study to define and validate pathological assessment of response to neoadjuvant therapy in oesophagogastric adenocarcinoma by Noble, F, Lloyd, MA, Turkington, R, Griffiths, E, O'Donovan, M, O'Neill, JR, Mercer, S, Parsons, SL, Fitzgerald, RC, Underwood, TJ, Occams Consortium
Published 2017Journal article -
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Polymorphism of the 5-HT transporter and response to antidepressants: randomised controlled trial. by Lewis, G, Mulligan, J, Wiles, N, Cowen, P, Craddock, N, Ikeda, M, Grozeva, D, Mason, V, Nutt, D, Sharp, D, Tallon, D, Thomas, L, O'Donovan, M, Peters, T
Published 2011Journal article -
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Further evidence that KIAA0319 is associated with developmental dyslexia by Harold, D, Paracchini, S, Scerri, T, Dennis, M, Cope, N, Hill, G, Moskvina, V, Walter, J, Richardson, A, Owen, M, Stein, J, Green, E, O'Donovan, M, Williams, J, Monacco, A
Published 2006Conference item -
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Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia. by Harold, D, Paracchini, S, Scerri, T, Dennis, M, Cope, N, Hill, G, Moskvina, V, Walter, J, Richardson, A, Owen, M, Stein, J, Green, E, O'Donovan, M, Williams, J, Monaco, A
Published 2006Journal article -
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Linkage disequilibrium structure of KIAA0319 and DCDC2, two candidate susceptibility genes for developmental dyslexia by Harold, D, Paracchini, S, Scerri, T, Dennis, M, Cope, N, Hill, G, Moskvina, V, Walter, J, Richardson, A, Owen, M, Stein, J, Green, E, O'Donovan, M, Williams, J, Monaco, A
Published 2006Journal article -
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Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. by Shifman, S, Johannesson, M, Bronstein, M, Chen, S, Collier, D, Craddock, N, Kendler, K, Li, T, O'Donovan, M, O'Neill, F, Owen, M, Walsh, D, Weinberger, DR, Sun, C, Flint, J, Darvasi, A
Published 2008Journal article -
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Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. by Sakuntabhai, A, Ruiz-Perez, V, Carter, S, Jacobsen, N, Burge, S, Monk, S, Smith, M, Munro, C, O'Donovan, M, Craddock, N, Kucherlapati, R, Rees, J, Owen, M, Lathrop, G, Monaco, A, Strachan, T, Hovnanian, A
Published 1999Journal article -
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Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors. by Andreassen, O, Djurovic, S, Thompson, W, Schork, A, Kendler, K, O'Donovan, M, Rujescu, D, Werge, T, van de Bunt, M, Morris, A, McCarthy, M, Roddey, J, McEvoy, L, Desikan, R, Dale, A
Published 2013Journal article -
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Population-based study reveals new risk-stratification biomarker panel for Barrett's esophagus. by Bird-Lieberman, E, Dunn, J, Coleman, H, Lao-Sirieix, P, Oukrif, D, Moore, C, Varghese, S, Johnston, B, Arthur, K, McManus, D, Novelli, MR, O'Donovan, M, Cardwell, C, Lovat, L, Murray, L, Fitzgerald, R
Published 2012Journal article -
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Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort by Strawbridge, R, Ward, J, Cullen, B, Tunbridge, E, Hartz, S, Bierut, L, Horton, A, Bailey, M, Graham, N, Ferguson, A, Lyall, D, Mackay, D, Pidgeon, L, Cavanagh, J, Pell, J, O'Donovan, M, Escott-Price, V, Harrison, P, Smith, D
Published 2018Journal article