Clustering of metabolic comorbidity in schizophrenia: A genetic contribution? by Gough, S, O'Donovan, M

Clustering of metabolic comorbidity in schizophrenia: a genetic contribution? by Gough, S, O'Donovan, M

The mentally handicapped person with epilepsy: a comparative study investigating psychosocial functioning. by Espie, C, Pashley, A, Bonham, K, Sourindhrin, I, O'Donovan, M

Diagnosis and management of rectal syphilis—case report by Afzal, Z, Hussein, A, O’Donovan, M, Bowden, D, Davies, RJ, Buczacki, S

OC-017 Autofluorescence-targeted Optical Biopsy Accurately Diagnoses Dysplasia In Barrett's Oesophagus And Can Detect The Field Of Molecular Change. by Di Pietro, M, Bird-Lieberman, E, Liu, X, O'Donovan, M, Fitzgerald, R

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

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

Randomized crossover study comparing efficacy of transnasal endoscopy with that of standard endoscopy to detect Barrett's esophagus. by Shariff, M, Bird-Lieberman, E, O'Donovan, M, Abdullahi, Z, Liu, X, Blazeby, J, Fitzgerald, R

LTD is involved in the formation and maintenance of rat hippocampal CA1 place-cell fields by Donovan M. Ashby, Stan B. Floresco, Anthony G. Phillips, Alexander McGirr, Jeremy K. Seamans, Yu Tian Wang

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Shifting the Forensic Anthropological Paradigm to Incorporate the Transgender and Gender Diverse Community by Donovan M. Adams, Samantha H. Blatt, Taylor M. Flaherty, Jaxson D. Haug, Mariyam I. Isa, Amy R. Michael, Ashley C. Smith

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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

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

Molecular imaging using fluorescent lectins permits rapid endoscopic identification of dysplasia in Barrett's esophagus. by Bird-Lieberman, E, Neves, A, Lao-Sirieix, P, O'Donovan, M, Novelli, M, Lovat, L, Eng, W, Mahal, L, Brindle, K, Fitzgerald, R

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

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

Inhibitory medial zona incerta pathway drives exploratory behavior by inhibiting glutamatergic cuneiform neurons by Sandeep Sharma, Cecilia A. Badenhorst, Donovan M. Ashby, Stephanie A. Di Vito, Michelle A. Tran, Zahra Ghavasieh, Gurleen K. Grewal, Cole R. Belway, Alexander McGirr, Patrick J. Whelan

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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

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

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

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