Clinical and anatomical heterogeneity in autistic spectrum disorder: a structural MRI study von Toal, F., Daly, E. M., Page, L., Deeley, Q., Hallahan, B., Bloemen, O., Cutter, W. J., Brammer, M. J., Curran, S., Robertson, D., Murphy, C., Murphy, K. C., Murphy, D. G. M.

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Brain morphometry volume in autistic spectrum disorder: a magnetic resonance imaging study of adults von Hallahan, B., Daly, E. M., McAlonan, G., Loth, E., Toal, F., O'Brien, F., Robertson, D., Hales, S., Murphy, C., Murphy, K. C., Murphy, D. G. M.

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Annotation: Velo-cardio-facial syndrome von Murphy, K.C.

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Genotype and psychological phenotype in tuberous sclerosis von Lewis, J C, Thomas, H V, Murphy, K C, Sampson, J R

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Dose-dependent expression of claudin-5 is a modifying factor in schizophrenia von Greene, C, Kealy, J, Humphries, M M, Gong, Y, Hou, J, Hudson, N, Cassidy, L M, Martiniano, R, Shashi, V, Hooper, S R, Grant, G A, Kenna, P F, Norris, K, Callaghan, C K, Islam, M dN, O’Mara, S M, Najda, Z, Campbell, S G, Pachter, J S, Thomas, J, Williams, N M, Humphries, P, Murphy, K C, Campbell, M

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Chemotherapy with mitoxantrone plus prednisone or prednisone alone for symptomatic hormone-resistant prostate cancer: a Canadian randomized trial with palliative end points von Tannock, I F, Osoba, D, Stockler, M R, Ernst, D S, Neville, A J, Moore, M J, Armitage, G R, Wilson, J J, Venner, P M, Coppin, C M, Murphy, K C

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Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome von van Amelsvoort, T., Zinkstok, J., Figee, M., Daly, E., Morris, R., Owen, M. J., Murphy, K. C., De Haan, L., Linszen, D. H., Glaser, B., Murphy, D. G. M.

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An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS) von Henry, J.C, van Amelsvoort, T, Morris, R.G, Owen, M.J, Murphy, D.G.M, Murphy, K.C

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A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter von SPURLOCK, G, HEILS, A, LESCH, K. P, OWEN, M. J, HOLMANS, P, WILLIAMS, J, D'SOUZA, U. M, CARDNO, A, MURPHY, K. C, JONES, L, BUCKLAND, P. R, MCGUFFIN, P

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A Systematic Genomewide Linkage Study in 353 Sib Pairs with Schizophrenia von Williams, N.M., Norton, N., Williams, H., Ekholm, B., Hamshere, M.L., Lindblom, Y., Chowdari, K.V., Cardno, A.G., Zammit, S., Jones, L.A., Murphy, K.C., Sanders, R.D., McCarthy, G., Gray, M.Y., Jones, G., Holmans, P., Nimgaonkar, V., Adolfson, R., Ösby, U., Terenius, L., Sedvall, G., O'Donovan, M.C., Owen, M.J.

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A psychoeducational intervention increases use of a delirium protocol by Neurologists and Neurosurgeons in patients with brain disorders von Patel, S., Carey, C., Cotter, D., Murphy, K. C.

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Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia von Murphy, K. C., Owen, M. J.

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A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs von Williams, N. M., Rees, M. I., Holmans, P., Norton, N., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., McCarthy, G., Gray, M. Y., Fenton, I., McGuffin, P., Owen, M. J.

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Neuropsychiatric manifestations in a patient with prolonged COVID-19 encephalopathy: case report and literature review von O’Leary, J., McAndrew, J., Shukralla, A., Murphy, K.C.

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Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype von Jones, G., Zammit, S., Norton, N., Hamshere, M. L., Jones, S. J., Milham, C., Sanders, R. D., McCarthy, G. M., Jones, L. A., Cardno, A. G., Gray, M., Murphy, K. C., Owen, M. J.

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Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder von KIROV, G, MURPHY, K. C, CRADDOCK, N, ARRANZ, M. J, JONES, I, MCCANDLES, F, KUNUGI, H, MURRAY, R. M, MCGUFFIN, P, COLLIER, D. A, OWEN, M. J

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Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137 von Cummings, E., Donohoe, G., Hargreaves, A., Moore, S., Fahey, C., Dinan, T.G., McDonald, C., O’Callaghan, E., O’Neill, F.A., Waddington, J.L., Murphy, K.C., Morris, D.W., Gill, M., Corvin, A.

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Chromosome 22q11 deletions, velo-cardio-facial syndrome and early-onset psychosis: Molecular genetic study von IVANOV, D, KIROV, G, NORTON, N, WILLIAMS, H.J, WILLIAMS, N.M, NIKOLOV, I, TZWETKOVA, R, STAMBOLOVA, S. M, MURPHY, K. C, TONCHEVA, D, THAPAR, A, O'DONOVAN, M.C, OWEN, M.J

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Psychiatric and psychosocial morbidity 1 year after epilepsy surgery von Patel, S., Clancy, M., Barry, H., Quigley, N., Clarke, M., Cannon, M., Delanty, N., Murphy, K. C., Cotter, D.

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Association between PRODH and schizophrenia is not confirmed von WILLIAMS, H. J, WILLIAMS, N, NIKOLOV, I, KEHAIOV, I, THAPAR, A, MURPHY, K. C, KIROV, G, OWEN, M. J, O'DONOVAN, M. C, SPURLOCK, G, NORTON, N, IVANOV, D, MCCREADIE, R. G, PREECE, A, SHARKEY, V, JONES, S, ZAMMIT, S

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