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Number of items: 121.

Amelsvoort, T. V., Daly, E., Critchley, H., Robertson, D., Murphy, K., Simmons, A., Owen, Michael John

, Henry, J. and Murphy, D. G. M. 1999. An MRI and fMRI study on the effect of deletions on chromosome 22 on brain. Biological psychiatry 45 (8) , 110S-111S.

Andrews, T. C., Weeks, R. A., Turjanski, N., Gunn, R. N., Watkins, L. H., Shakian, B., Hodges, J. R., Rosser, Anne Elizabeth

, Wood, N. W. and Brooks, D. J. 1999. Huntington's disease progression. PET and clinical observations. Brain 122 (12) , pp. 2353-2363. 10.1093/brain/122.12.2353

Bandmann, O., Vaughan, J., Holmans, Peter Alan

, Marsden, C. D. and Wood, N. W. 1999. Toxins, genetics, and Parkinson's disease: the role of N-acetyltransferase 2. Advances in Neurology -New York- Raven Press- 80 , pp. 199-204.

Bano, S, Morgan, C. J., Badawy, A. A., Buckland, Paul Robert and McGuffin, P. M. 1999. Inhibition of rat liver tryptophan pyrrolase activity by fluoxetine. Pakistan Journal of Pharmaceutical Sciences 12 (2) , pp. 11-16.

Bennett, P., Middle, F., Mulcahy, T., Jones, Ian Richard

, McCandless, F., Heron, J., Segurado, R., Gill, M., Craddock, Nicholas John

and Grp, WTB. 1999. The Wellcome Trust UK-Irish Bipolar Sib-pair genome screen: First stage report: Chromosomes 1, 3, 4, 7, 8, 12, 13, 14, 15, 16, X. Molecular Psychiatry 4 , S22.

Beyer, Stephen Richard

, Kilsby, Mark Stephen and Shearn, Julia 1999. The organisation and outcomes of supported employment in Britain. Journal of Vocational Rehabilitation 12 (3) , pp. 137-146.

Birkett, J. T. P., Kirov, George

, Arranz, M. J., Murray, R. M., Collier, D. A. and Kerwin, R. W. 1999. Association between a 2030-G/A substitution in the human myo-inositol monophosphatase gene (IMPA) and bipolar disorder and schizophrenia. Molecular Psychiatry 4 , S103-S103.

Bisson, Jonathan Ian

1999. Rethinking the trauma of war. British Journal of Psychiatry 175 (3) , p. 295.

Blake, Derek J.

, Hawkes, Richard, Benson, Matthew A. and Beesley, Phillip W. 1999. Different dystrophin-like complexes are expressed in neurons and glia. Journal of Cell Biology 147 (3) , pp. 645-658. 10.1083/jcb.147.3.645

Blake, Derek J

, Benson, M. A., Hawkes, R. and Beesley, P. W. 1999. Dystrophin-binding proteins in the brain. Journal of Neurochemistry 73 , S93-S93.

Blank, Martina, Koulen, Peter, Blake, Derek J.

and Kröger, Stephan 1999. Dystrophin and beta-dystroglycan in photoreceptor terminals from normal and mdx3Cv mouse retinae. European Journal of Neuroscience 11 (6) , pp. 2121-2133. 10.1046/j.1460-9568.1999.00636.x

Bolonna, A. A., Markoff, A. J., Munro, J., Kirov, George

and Kerwin, R. W. 1999. An investigation of a structural polymorphism in the mGluR7 gene in association with schizophrenia. Schizophrenia Research 36 (1-3) , p. 99.

Borglum, A. D., Bruun, T. G., Hampson, M., Kjeldsen, T. E., Lodge, P., Ewald, H., Mors, O., Kirov, George

, Muir, W., Murray, V., Russ, C., Freeman, B., Blackwood, D., Collier, D. A. and Kruse, T. A. 1999. Association study of the DOPA decarboxylase gene in bipolar affective disorder and schizophrenia. Molecular Psychiatry 4 , S103-S104.

Borglum, A. D., Bruun, T. G., Kjeldsen, T. E., Ewald, H., Mors, O., Kirov, George

, Russ, C, Freeman, B., Collier, D. A. and Kruse, T. A. 1999. Two novel variants in the DOPA decarboxylase gene: association with bipolar affective disorder. Molecular Psychiatry 4 (6) , pp. 545-551. 10.1038/sj.mp.4000559

Boutell, J. M., Thomas, P., Neal, J. W., Weston, V. J., Duce, J., Harper, P. S. and Jones, Lesley

1999. Aberrant interactions of transcriptional repressor proteins with the Huntington's disease gene product, huntingtin. Human Molecular Genetics 8 (9) , pp. 1647-1655. 10.1093/hmg/8.9.1647

Bowen, Timothy

, Kirov, George

, Gill, M., Spurlock, Gillian, Vallada, H. P., Murray, R. M., McGuffin, P., Collier, D. A., Owen, Michael John

and Craddock, Nicholas John

1999. Linkage studies of bipolar disorder with chromosome 18 markers. American Journal of Medical Genetics 15 (88) , pp. 503-509. 10.1002/(SICI)1096-8628(19991015)88:5<503::AID-AJMG13>3.0.CO;2-U

Bray, Nicholas John

, Cardno, A. G., Fitzpatrick, E. R., Buckland, Paul Robert and Owen, Michael John

1999. Embryonic NCAM and schizophrenia: Genetic analysis of regulatory enzymes. Molecular Psychiatry 4 , S32-S32.

Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Asherson, P., Owen, Michael John

and McGuffin, P. 1999. Dimensions of psychosis in affected sibling pairs. Schizophrenia Bulletin 25 (4) , pp. 841-850.

Cardno, Alastair G., Bowen, Timothy

, Guy, Carol, Jones, Lisa A., McCarthy, Geraldine, Williams, Nigel Melville

, Murphy, Kieran C., Spurlock, Gillian, Gray, Marion, Sanders, Rebecca, Craddock, Nicholas John

, McGuffin, Peter, Owen, Michael John

and O'Donovan, Michael Conlon

1999. CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia. Biological Psychiatry 45 (12) , pp. 1592-1596. 10.1016/s0006-3223(99)00033-5

Craddock, Nicholas John

1999. Chromosome Workshop: chromosomes 11, 14, and 15. American Journal of Medical Genetics 88 (3) , pp. 244-254. 10.1002/(SICI)1096-8628(19990618)88:3<244::AID-AJMG7>3.0.CO;2-1

Craddock, Nicholas John

and Gill, M. 1999. The Wellcome Trust UK-Irish Bipolar Sib-pair Study: First stage genome screen. Molecular Psychiatry 4 , S21-S21.

Craddock, Nicholas John

and Jones, Ian Richard

1999. Genetics of bipolar disorder [review]. Journal of Medical Genetics 36 (8) , pp. 585-594. 10.1136/jmg.36.8.585

Craddock, Nicholas John

, Jones, Ian Richard

and Kent, L. 1999. Neurogenetic determinism and the new euphenics. Psychosocial and ethical issues in psychiatric genetics require constructive debate [letter]. BMJ 318 (7196) , p. 1488. 10.1136/bmj.318.7196.1488

Dalal, Brian, Larkin, Emmet, Leese, Morven and Taylor, Pamela Jane

1999. Clozapine treatment of long-standing schizophrenia and serious violence: a two-year follow-up study of the first 50 patients treated with clozapine in Rampton high security hospital. Criminal Behaviour and Mental Health 9 (2) , pp. 168-178. 10.1002/cbm.304

Davison, S., Jamieson, E. and Taylor, Pamela Jane

1999. Route of discharge for special (high-security) hospital patients with personality disorder. Relationship with re-conviction. British Journal of Psychiatry 175 (3) , pp. 224-227. 10.1192/bjp.175.3.224

Di Salle, F., Formisano, E., Linden, David Edmund Johannes

, Goebel, R., Bonavita, S., Pepino, A., Smaltino, F. and Tedeschi, G. 1999. Exploring brain function with magnetic resonance imaging. European Journal of Radiology 30 (2) , pp. 84-94. 10.1016/S0720-048X(99)00047-9

Dierks, Thomas, Linden, David Edmund Johannes

, Jandl, Martin, Formisano, Elia, Goebel, Rainer, Lanfermann, Heinrich and Singer, Wolf 1999. Activation of Heschl's Gyrus during Auditory Hallucinations. Neuron 22 (3) , pp. 615-621. 10.1016/S0896-6273(00)80715-1

Edwards, Adrian G.

, Robling, Michael Richard

, Wilkinson, Clare Elizabeth, Matthews, S. J., Stott, Nigel C. H., Austoker, J., McKell-Redwood, D., Mansel, Robert Edward

, Russell, I. T. and Thapar, Ajay Kumar

1999. The presentation and management of breast symptoms in general practice in South Wales. The BRIDGE Study Group. British Journal of General Practice 49 (447) , pp. 811-812.

Emilien, Gérard, Maloteaux, Jean-Marie, Geurts, Muriel and Owen, Michael John

1999. Dopamine receptors and schizophrenia: contribution of molecular genetics and clinical neuropsychology. The International Journal of Neuropsychopharmacology 2 (3) , p. 197. 10.1017/S1461145799001479

Felce, David John 1999. The Gerry Simon Lecture, 1998: Enhancing the Quality of Life of People Receiving Residential Support. British Journal of Learning Disabilities 27 (1) , pp. 4-9. 10.1111/j.1468-3156.1999.tb00075.x

Felce, David John, Lowe, K., Perry, Jonathan, Jones, E., Baxter, Helen Ann and Bowley, C. 1999. The quality of residential and day services for adults with intellectual disabilities in eight local authorities in England: Objective data gained in support of a Social Services Inspectorate inspection. Journal of Applied Research in Intellectual Disabilities 12 (4) , pp. 273-293. 10.1111/j.1468-3148.1999.tb00084.x

Fisher, P. J., Hill, L., Turic, D., Asherson, P., Benbow, C., Chorney, K., Chorney, M., Craig, I., Lubinski, D., McGuffin, P., Owen, Michael John

and Plomin, R. 1999. A high resolution genome scan made possible with DNA pooling. Molecular Psychiatry 4 (1) , S10-S10.

Fisher, P. J., Turic, D., Williams, Nigel Melville

, McGuffin, P., Asherson, P., Ball, D., Craig, I., Eley, T., Hill, L., Chorney, K., Chorney, M. J., Benbow, C. P., Lubinski, D., Plomin, R. and Owen, Michael John

1999. DNA pooling identifies QTLs on chromosome 4 for general cognitive ability in children. Human Molecular Genetics 8 (5) , pp. 915-922. 10.1093/hmg/8.5.915

Franks, Emily, Guy, Carol, Jacobsen, N., Bowen, Timothy

, Owen, Michael John

, O'Donovan, Michael Conlon

and Craddock, Nicholas John

1999. Eleven trinucleotide repeat loci that map to chromosome 12 excluded from involvement in the pathogenesis of bipolar disorder. American Journal of Medical Genetics 88 (1) , pp. 67-70. 10.1002/(SICI)1096-8628(19990205)88:1<67::AID-AJMG12>3.0.CO;2-#

Frontoni, M., Monti, M. S., Tomassini, Valentina

and Giubilei, F. 1999. Aspects of autonomic dysfunctions in multiple sclerosis. Giornale di Neuropsicofarmacologia 21 (1) , pp. 7-13.

Guy, Carol, Bowen, Timothy

, Jones, Ian Richard

, McCandless, F., Owen, Michael John

, Craddock, Nicholas John

and O'Donovan, Michael Conlon

1999. CTG18.1 and ERDA-1 CAG/CTG repeat size in bipolar disorder. Neurobiology of Disease 6 (4) , pp. 302-307. 10.1006/nbdi.1999.0249

Guy, Carol, Bowen, Timothy

, Williams, Nigel Melville

, Jones, I. R., McCandless, F, McGuffin, P, Owen, Michael John

, Craddock, Nicholas John

and O'Donovan, Michael Conlon

1999. No association between a polymorphic CAG repeat in the human potassium channel gene hKCa3 and bipolar disorder. American Journal of Medical Genetics 88 (1) , pp. 57-60. 10.1002/(sici)1096-8628(19990205)88:1%3C57::aid-ajmg10%3E3.0.co;2-6

Hall, F. S., Wilkinson, Lawrence Stephen

, Humby, Trevor

and Robbins, T. W. 1999. Maternal deprivation of neonatal rats produces enduring changes in dopamine function. Synapse 32 (1) , pp. 37-43. 10.1002/(SICI)1098-2396(199904)32:1<37::AID-SYN5>3.0.CO;2-4

Hateboer, N., Lazarou, L. P., Williams, A. J., Holmans, Peter Alan

and Ravine, D. 1999. Familial phenotype differences in PKD11. Kidney International 56 (1) , pp. 34-40. 10.1046/j.1523-1755.1999.00541.x

Hayward, B., McCarthy, L. and Kerr, Michael Patrick 1999. Integrating a specialised epilepsy clinic for adults with a learning disability with community nursing services - Towards common standards? Epilepsia 40 , p. 105.

Hennessey, A., Robertson, Neil

, Swingler, R. and Compston, D. A. 1999. Urinary, faecal and sexual dysfunction in patients with multiple sclerosis. Journal of Neurology 246 (11) , pp. 1027-1032. 10.1007/s004150050508

Hill, L., Chorney, M. J., Chorney, K., Craig, I., Fisher, P., Owen, Michael John

, McGuffin, P. and Plomin, R. 1999. IGF2R and cognitive ability. Molecular Psychiatry 4 , S108-S108.

Hill, L., Craig, I. W., Asherson, P., Ball, D., Eley, T., Ninomiya, T., Fisher, P. J., Turic, D., McGuffin, P., Owen, Michael John

, Chorney, K., Chorney, M. J., Benbow, C. P., Lubinski, D., Thompson, L. A. and Plomin, R. 1999. DNA pooling and dense marker maps: a systematic search for genes for cognitive ability. NeuroReport 10 (4) , pp. 843-848. 10.1097/00001756-199903170-00032

Holzfeind, Paul J., Ambrose, Helen J., Newey, Sarah E., Nawrotzki, Ralph A., Blake, Derek J.

and Davies, Kay E. 1999. Tissue-selective Expression of alpha-Dystrobrevin is Determined by Multiple Promoters. Journal of Biological Chemistry 274 (10) , pp. 6250-6258. 10.1074/jbc.274.10.6250

Hoogendoorn, Bastiaan

, Owen, Michael John

, Oefner, P. J., Williams, Nigel Melville

, Austin, J. and O'Donovan, Michael Conlon

1999. Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography. Human Genetics 104 (1) , pp. 89-93. 10.1007/s004390050915

Humby, Trevor

, Laird, Fiona M., Davies, William

and Wilkinson, Lawrence Stephen

1999. Visuospatial attentional functioning in mice: interactions between cholinergic manipulations and genotype. European Journal of Neuroscience 11 (8) , pp. 2813-2823. 10.1046/j.1460-9568.1999.00701.x

Jacobsen, N. J., Franks, E. K., Owen, Michael John

and Craddock, Nicholas John

1999. Mutational analysis of phospholipase A2A: a positional candidate susceptibility gene for bipolar disorder. Molecular Psychiatry 4 (3) , pp. 274-279. 10.1038/sj.mp.4000476

Jacobsen, N. J., Lyons, I., Hoogendoorn, Bastiaan

, Burge, S., Kwok, P. Y., O'Donovan, Michael Conlon

, Craddock, Nicholas John

and Owen, Michael John

1999. ATP2A2 mutations in Darier's disease and their relationship to neuropsychiatric phenotypes. Human Molecular Genetics 8 (9) , pp. 1631-1636. 10.1093/hmg/8.9.1631

Jones, L. A., Sanders, R. D., Cardno, A. G., Owen, Michael John

and Williams, Julie

1999. Sustained and selective attention as quantitative measures of schizophrenia liability. Molecular Psychiatry 4 , S117-S117.

Jones, Alistair C., Austin, Jehannine, Hansen, Nancy, Hoogendoorn, Bastiaan

, Oefner, Peter J., Cheadle, Jeremy Peter

and O'Donovan, Michael Conlon

1999. Optimal temperature selection for mutation detection by denaturing HPLC and comparison to single-stranded conformation polymorphism and heteroduplex analysis. Clinical Chemistry 45 (8) , pp. 1133-1140.

Jones, E., Perry, Jonathan, Lowe, K., Felce, David John, Toogood, S., Dunstan, Frank David John

, Allen, David G. and Pagler, J. 1999. Opportunity and the promotion of activity among adults with severe intellectual disability living in community residences: the impact of training staff in active support. Journal of Intellectual Disability Research 43 (3) , pp. 164-178. 10.1046/j.1365-2788.1999.00177.x

Jones, Ian Richard

, Coyle, N., Robertson, E., Middle, F., McCandless, F., Lendon, C., Brockington, I. and Craddock, Nicholas John

1999. Puerperal psychosis: Evidence for familiality of the puerperal trigger. Molecular Psychiatry 4 , S26-S26.

Jones, Ian Richard

, Owen, Michael John

and Craddock, Nicholas John

1999. Further evidence of familial cosegregation of major affective disorder and Darier's disease. Molecular Psychiatry 4 , S73-S73.

Jones, Lesley

1999. The localization and interactions of huntingtin. Philosophical Transactions of the Royal Society of London Series B - Biological Sciences 354 (1386) , pp. 1021-1027. 10.1098/rstb.1999.0454

Jonsson, E. G., Norton, N., Gustavsson, J. P., Oreland, L., Owen, Michael John

and Sedvall, G. C. 1999. Monoamine oxidase a promoter polymorphism and relationships to monoamine metabolite concentrations in CSF. Molecular Psychiatry 4 , S97-S98.

Kehoe, P., Wavrant-De Vrieze, F., Crook, R., Wu, W. S., Holmans, Peter Alan

, Fenton, I., Williams, Nigel Melville

, Lovestone, S., Perez-Tur, J., Hutton, M., Chartier-Harlin, M. C., Shears, S., Roehl, K., Booth, J., Van Voorst, W., Ramic, D., Williams, Julie

, Goate, A., Hardy, J. and Owen, Michael John

1999. A full genome scan for late onset Alzheimer's disease. Human Molecular Genetics 8 (2) , pp. 237-245. 10.1093/hmg/8.2.237

Kehoe, P. G., Russ, C., McIlory, S., Williams, H., Powell, J., McGleenon, B., Liddell, M., Plomin, R., Dynan, K., Williams, Nigel Melville

, Neal, J., Cairns, N. J., Wilcock, G., Passmore, P., Lovestone, S., Williams, Julie

and Owen, Michael John

1999. Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease. Nature Genetics 21 (1) , pp. 71-72. 10.1038/5009

Kehoe, P., Krawczak, M., Harper, P. S., Owen, Michael John

and Jones, Lesley

1999. Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length. Journal of Medical Genetics 36 (2) , pp. 108-111. 10.1136/jmg.36.2.108

Kerr, Michael Patrick, Kane, K., Moorat, A. and Team, L. S. S. 1999. Switch to monotherapy with lamictal compared to valproate. Epilepsia 40 , p. 284.

Kerwin, R and Owen, Michael John

1999. Genetics of novel therapeutic targets in schizophrenia. The British journal of psychiatry. Supplement. 38 , pp. 1-4.

Kirov, George

, Jones, Ian Richard

, McCandless, F., Craddock, Nicholas John

and Owen, Michael John

1999. Family-based association studies of bipolar disorder with candidate genes involved in dopamine neurotransmission: DBH, DAT1, COMT, DRD2, DRD3 and DRD5. Molecular Psychiatry 4 (6) , pp. 558-565.

Kirov, George

and Murray, R. M. 1999. Ethnic differences in the presentation of bipolar affective disorder. European Psychiatry 14 (4) , pp. 199-204.

Kirov, George

, Norton, N., Jones, Ian Richard

, McCandless, F., Craddock, Nicholas John

and Owen, Michael John

1999. A functional polymorphism in the promoter of monoamine oxidase A gene and bipolar affective disorder. International Journal of Neuropsychopharmacology 2 (4) , pp. 293-298. 10.1017/s1461145799001601

Kirov, George

and Owen, Michael John

1999. Identification of new microsatellite markers on chromosome 4p16. American Journal of Human Genetics 65 (4) , A257-A257.

Kirov, George

, Owen, Michael John

, Jones, I., McCandless, F. and Craddock, Nicholas John

1999. Tryptophan hydroxylase gene and manic-depressive illness [letter]. Archives of General Psychiatry 56 (1) , pp. 98-99. 10.1001/archpsyc.56.1.98

Kirov, George

, Rees, M., Jones, Ian Richard

, McCandless, F, Owen, Michael John

and Craddock, Nicholas John

1999. Bipolar disorder and the serotonin transporter gene: a family-based association study. Psychological Medicine -London- 29 (5) , pp. 1249-1254. 10.1017/s003329179900882x

Li, T., Liu, X., Sham, P. C., Aitchison, K. J., Cai, G., Arranz, M. J., Deng, H., Liu, J., Kirov, George

, Murray, R. M. and Collier, D. A. 1999. Association analysis between dopamine receptor genes and bipolar affective disorder. Psychiatry Research 86 (3) , pp. 193-201. 10.1016/S0165-1781(99)00034-7

Linden, David Edmund Johannes

1999. Gabriele Zerbi's De cautelis medicorum and the Tradition of Medical Prudence. Bulletin of the History of Medicine 73 (1) , pp. 19-37. 10.1353/bhm.1999.0035

Linden, David Edmund Johannes

1999. The natural and the supernatural in melancholic genius. A debate in sixteenth century Spanish medicine and its antecedents. Medizinhistorisches Journal 34 (3-4) , pp. 227-243.

Linden, David Edmund Johannes

, Kallenbach, Ulrich, Heinecke, Armin, Singer, Wolf and Goebel, Rainer 1999. The myth of upright vision. A psychophysical and functional imaging study of adaptation to inverting spectacles. Perception 28 (4) , pp. 469-481. 10.1068/p2820

Linden, David Edmund Johannes

, Prvulovic, D., Formisano, E., Völlinger, M., Zanella, F. E., Goebel, R. and Dierks, T. 1999. The Functional Neuroanatomy of Target Detection: An fMRI Study of Visual and Auditory Oddball Tasks. Cerebral Cortex 9 (8) , pp. 815-823. 10.1093/cercor/9.8.815

Maughan, B., Collishaw, Stephan

and Pickles, A. 1999. Mild mental retardation: psychosocial functioning in adulthood. Psychological Medicine 29 (2) , pp. 351-366. 10.1017/S0033291798008058

McCarthy, G., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Gray, M. Y., McGuffin, P. and Owen, Michael John

1999. Familial aggregation of clinical variables in a sibling pair study of schizophrenia. Molecular Psychiatry 4 , S121-S121.

McCarthy, G., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Gray, M. Y., McGuffin, P. and Owen, Michael John

1999. Intra-pair correlations of symptom dimensions in a sibling pair study of schizophrenia. Molecular Psychiatry 4 , S26-S27.

McNamara, B., Boniface, S. J., Ray, J., Scolding, N. J. and Robertson, Neil

1999. Paraneoplastic sensory neuropathy and Purkinje cell antibodies [Letter]. Muscle & Nerve 22 (10) , pp. 1466-1467. 10.1002/(SICI)1097-4598(199910)22:10<1466::AID-MUS20>3.0.CO;2-D

Middle, F. A., Jones, Ian Richard

, MacCandless, F., Khanim, F., Barrett, T., Owen, Michael John

, Lendon, C. L. and Craddock, Nicholas John

1999. Association studies between bipolar disorder and a polymorphism in the Wolfram gene. Molecular Psychiatry 4 , S76-S76.

Morgan, Christopher L., Kerr, Michael Patrick and Ahmed, Z. 1999. Material deprivation and epilepsy. Epilepsia 40 , p. 197.

Murphy, K. C., Jones, L. A. and Owen, Michael John

1999. High rates of schizophrenia in velo-cardio-facial syndrome. American Journal of Human Genetics 65 (4) , A336-A336.

Murphy, K. C. and Owen, Michael John

1999. No association between polymorphisms of catechol-O-methyltransferase (COMT) or monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome. Journal of Medical Genetics 36 , S78-S78.

Murphy, K., Thompson, P. W., Davies, S. J., Groves, P., Owen, Michael John

and Stuart, G. 1999. The prevalence of chromosome 22q11 deletions in an adult congenital heart disease population. Journal of Medical Genetics 36 , S59-S59.

Norton, N., Bray, Nicholas John

, Williams, Nigel Melville

, Cardno, A. C., Murphy, K. C., Jones, L. A., Sanders, R. D., McCarthy, G., McGuffin, P. and Owen, Michael John

1999. No evidence for association between schizophrenia and MAO-A promoter polymorphism. Molecular Psychiatry 4 , S96-S96.

Nothen, M. M., Cichon, S., Rohleder, H., Hemmer, S., Franzek, E., Fritze, J., Albus, M., Borrmann-Hassenbach, M., Kreiner, R., Weigelt, B., Minges, J., Lichtermann, D., Maier, W., Craddock, Nicholas John

, Fimmers, R., Holler, T., Baur, M. P., Rietschel, M. and Propping, P. 1999. Evaluation of linkage of bipolar affective disorder to chromosome 18 in a sample of 57 German families. Molecular Psychiatry 4 (1) , pp. 76-84. 10.1038/sj.mp.4000454

O'Donovan, Michael Conlon

and Owen, Michael John

1999. Candidate-gene association studies of schizophrenia. American Journal of Human Genetics 65 (3) , pp. 587-592. 10.1086/302560

Owen, Michael John

1999. Evidence of novel loci in late onset Alzheimer's disease. Molecular Psychiatry 4 (1) , S9-S9.

Owen, Michael John

and Cardno, A. G. 1999. Psychiatric genetics: progress, problems, and potential. The Lancet 354 (1) , SI11-SI14. 10.1016/S0140-6736(99)90242-8

Petouni, M., Bolonna, A. A., Arranz, M. J., Martinez, M. J., Collier, D. A., Kirov, George

and Kerwin, R. W. 1999. Association study between genetic variants in the alpha- adrenergic receptor genes and bipolar affective disorder. Molecular Psychiatry 4 , S112-S112.

Phillips, Sarah L., Heads, Tracey C., Taylor, Pamela Jane

and Hill, G. Mary 1999. Sexual offending and antisocial sexual behavior among patients with schizophrenia. The Journal of Clinical Psychiatry 60 (3) , pp. 170-175. 10.4088/JCP.v60n0304

Rees, M. I., Fenton, I., Williams, Nigel Melville

, Holmans, Peter Alan

, Norton, N., Cardno, A., Asherson, P., Spurlock, G., Vallada, H., Dawson, E., Li, M. W., Collier, D. A., Powell, J. F., Nanko, S., Gill, M., McGuffin, P. and Owen, Michael John

1999. Autosome search for schizophrenia susceptibility genes in multiply affected families. Molecular Psychiatry 4 (4) , pp. 353-359. 10.1038/sj.mp.4000521

Robertson, Neil

1999. An Atlas of Multiple Sclerosis [Book Review]. Journal of Neurology, Neurosurgery & Psychiatry 67 (1) , p. 132. 10.1136/jnnp.67.1.132a

Robertson, Neil

, Compston, D. A. and Kirkpatrick, P. 1999. Moyamoya disease presenting as Valsalva related partial seizures. Journal of Neurology, Neurosurgery & Psychiatry 66 (1) , p. 111. 10.1136/jnnp.66.1.111

Rodgers, B., Pickles, A., Power, C., Collishaw, Stephan

and Maughan, B. 1999. Validity of the Malaise Inventory in general population samples. Social Psychiatry and Psychiatric Epidemiology 34 (6) , pp. 333-341. 10.1007/s001270050153

Rosser, Anne Elizabeth

1999. Cell transplantation for neurological disorders. Journal of Neurology, Neurosurgery & Psychiatry 67 (6) , 833C. 10.1136/jnnp.67.6.833c

Rudrasingham, V., Wavrant-De Vrieze, F., Lambert, J. C., Chakraverty, S., Kehoe, P., Crook, R., Amouyel, P., Wu, W., Rice, Frances

, Perez-Tur, J., Frigard, B., Morris, J. C., Carty, S., Petersen, R., Cottel, D. and Tunstall, N. 1999. Alpha-2 macroglobulin gene and Alzheimer disease. Nature Genetics 22 (1) , pp. 17-19. 10.1038/8726

Sakuntabhai, A., Ruiz-Perez, V., Carter, S., Jacobsen, N., Burge, S., Monk, S., Smith, M., Munro, C. S., O'Donovan, Michael Conlon

, Craddock, Nicholas John

, Kucherlapati, R., Rees, J. L., Owen, Michael

, Lathrop, G. M., Monaco, A. P., Strachan, T. and Hovnanian, A. 1999. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Nature Genetics 21 (3) , pp. 271-277.

Sanders, R. D., Norton, Nadine, Williams, Julie

and Owen, Michael John

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