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Number of items: 121.

A

Arranz, M. J., Munro, J., Collier, D. A., Kirov, George and Kerwin, R. W. 1998. Genetic variation in the 5-HT3 receptor gene: No association with schizophrenia or drug response. Schizophrenia Research 29 (1-2) , pp. 127-128.

Arranz, M. J., Munro, J., Li, T., Collier, D. A., Kirov, George and Kerwin, R. W. 1998. A polymorphism in the promoter region of the dopamine D2 receptor gene (DRD2) and drug response: Association studies. Schizophrenia Research 29 (1-2) , p. 127.

Arranz, M. J., Munro, J., Owen, Michael John, Spurlock, G., Sham, P. C., Zhao, J., Kirov, George, Collier, D. A. and Kerwin, R. W. 1998. Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine. Molecular Psychiatry 3 (1) , pp. 61-66. 10.1038/sj.mp.4000348

Arranz, M. J., Munro, J., Sham, P., Kirov, George, Murray, R. M., Collier, D. A. and Kerwin, R. W. 1998. Meta-analysis of studies on genetic variation in 5-HT2A receptors and clozapine response. Schizophrenia Research 32 (2) , pp. 93-99. 10.1016/S0920-9964(98)00032-2

Asherson, P., Mant, R., Williams, Nigel Melville, Cardno, A., Jones, L., Murphy, Kevin, Collier, D. A., Nanko, S., Craddock, Nicholas John, Morris, S., Muir, W., Blackwood, B., McGuffin, P. and Owen, Michael John 1998. A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorder. Molecular Psychiatry 3 (4) , pp. 310-320. 10.1038/sj.mp.4000399

B

Ball, D., Hill, L., Eley, T. C., Chorney, M. J., Chorney, K., Thompson, L. A., Detterman, D. K., Benbow, C., Lubinski, D., Owen, Michael John, McGuffin, P. and Plomin, R. 1998. Dopamine markers and general cognitive ability. NeuroReport 9 (2) , pp. 347-349. 10.1097/00001756-199801260-00031

Bandmann, O., Valente, E. M., Holmans, Peter Alan, Surtees, R. A., Walters, J. H., Wevers, R. A., Marsden, C. D. and Wood, N. W. 1998. Dopa-responsive dystonia: a clinical and molecular genetic study. Annals of Neurology 44 (4) , pp. 649-656. 10.1002/ana.410440411

Bano, S., Morgan, C. J., Badawy, A. A.-B., Colombo, G., Buckland, Paul Robert, McGuffin, P., Fadda, F. and Gessa, G. L. 1998. Trypophan metabolism in male Sardinian alcohol-preferring (sP)and non-preferning (sNP) rats. Alcohol and Alcoholism 33 (3) , pp. 220-225. 10.1093/oxfordjournals.alcalc.a008385

Bennett, P., Mulcahy, T., Owen, Michael John, Craddock, Nicholas John and Gill, M. 1998. The Wellcome Trust UK-Irish Bipolar Sib-pair Study: Chromosome 21. American Journal of Medical Genetics 81 (6) , p. 541.

Beyer, Stephen Richard and Kilsby, Mark Stephen 1998. Financial costs and benefits of two supported employment agencies in Wales. Journal of Applied Research in Intellectual Disabilities 11 (4) , pp. 303-319. 10.1111/j.1468-3148.1998.tb00039.x

Birkett, J. T. P., Kirov, George, Powell, J., Murray, R. M., Kerwin, R. W. and Collier, D. A. 1998. No association between a variable number of tandem repeat (VNTR) in the 3 ' untranslated region of the dopamine transporter gene (DAT1) and bipolar affective disorder. American Journal of Medical Genetics 81 (6) , pp. 500-501.

Bisson, Jonathan Ian 1998. Understanding post-traumatic stress: a psychosocial perspective on PTSD and treatment. British Journal of Psychiatry 172 (3) , pp. 285-286.

Bisson, Jonathan Ian, Searle, Margaret M. and Srinivasan, Michael 1998. Follow-up study of British military hostages and their families held in Kuwait during the Gulf War. British Journal of Medical Psychology 71 (3) , pp. 247-252. 10.1111/j.2044-8341.1998.tb00989.x

Blake, Derek J, Nawrotzki, R., Loh, N. Y., Gorecki, D. C. and Davies, K. E. 1998. beta-dystrobrevin, a member of the dystrophin-related protein family. Proceedings of the National Academy of Sciences of the United States of America 95 (1) , pp. 241-246. 10.1073/pnas.95.1.241

Blake, Derek J, Nawrotzki, Ralph, Loh, Nellie Y., Gorecki, Dariusz C. and Davies, Kay E. 1998. β-dystrobrevin, a member of the dystrophin-related protein family. Proceedings of the National Academy of Sciences of the United States of America 95 (1) , pp. 241-246.

Boutell, J. M., Wood, J. D., Harper, P. S. and Jones, Lesley 1998. Huntingtin interacts with cystathionine beta-synthase. Human Molecular Genetics 7 (3) , pp. 371-378. 10.1093/hmg/7.3.371

Bowen, Timothy, Guy, Carol, Craddock, Nicholas John, Cardno, A. G., Williams, Nigel Melville, Spurlock, G., Murphy, K. C., Jones, L. A., Gray, M., Sanders, Rebecca, McCarthy, G, Chandy, K. G., Fantino, E, Kalman, K, Gutman, G. A., Gargus, J. J., Williams, Julie, McGuffin, P., Owen, Michael John and O'Donovan, Michael Conlon 1998. Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia. Molecular Psychiatry 3 (3) , pp. 266-269. 10.1038/sj.mp.4000400

Bowen, Timothy, Norton, N, Jacobsen, N. J., Guy, Carol, Daniels, J. K., Sanders, Rebecca, Cardno, A. G., Jones, L. A., Murphy, Kevin, McGuffin, P, Craddock, Nicholas John, O'Donovan, Michael Conlon and Owen, Michael John 1998. Linked polymorphisms upstream of exons 1 and 2 of the human cholecystokinin gene are not associated with schizophrenia or bipolar disorder. Molecular Psychiatry 3 (1) , pp. 67-71. 10.1038/sj.mp.4000293

C

Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Asherson, P., Owen, Michael John and McGuffin, P. 1998. Sibling pairs with schizophrenia or schizoaffective disorder: associations of subtypes, symptoms and demographic variables. Psychological Medicine 28 (4) , pp. 815-823. 10.1017/S0033291798006783

Cardno, A. G., McCandless, F., Bowen, Timothy, Guy, Carol, Jones, L. A., Murphy, Kevin, McGuffin, P., Owen, Michael John, Craddock, Nicholas John and O'Donovan, Michael Conlon 1998. Association between functional psychosis and expanded CAG/CTG repeats is not explained by health stratification [comparative study]. Psychiatric Genetics 8 (1) , pp. 29-32. 10.1097/00041444-199800810-00005

Cardno, A. G., Murphy, K. C., Jones, L. A., Cobb, A. M., Gray, J., McGuffin, P. and Owen, Michael John 1998. Polydactyly and psychosis. Five cases of co-occurrence. British Journal of Psychiatry 172 , pp. 184-185. 10.1192/bjp.172.2.184

Chataway, J., Feakes, R., Coraddu, F., Gray, J., Deans, J., Fraser, M., Robertson, Neil, Broadley, S., Jones, H., Clayton, D., Goodfellow, P., Sawcer, S. and Compston, A. 1998. The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen. Brain 121 (10) , pp. 1869-1887. 10.1093/brain/121.10.1869

Chorney, M.J., Chorney, K., Seese, N., Owen, Michael John, Daniels, J., McGuffin, P., Thompson, L.A., Detterman, D.K., Benbow, C., Lubinski, D., Eley, T. and Plomin, R. 1998. A Quantitative Trait Locus Associated With Cognitive Ability in Children. Psychological Science 9 (3) , pp. 159-166. 10.1111/1467-9280.00032

Collishaw, Stephan, Maughan, B. and Pickles, A. 1998. Infant adoption: psychosocial outcomes in adulthood. Social Psychiatry and Psychiatric Epidemiology 33 (2) , pp. 57-65. 10.1007/s001270050023

Craddock, Nicholas John and Lendon, C. 1998. New susceptibility gene for Alzheimer's disease on chromosome 12? The Lancet 352 (9142) , pp. 1720-1721. 10.1016/S0140-6736(98)00075-0

Currie, Craig John, Morgan, Christopher L., Peters, John R. and Kerr, Michael Patrick 1998. The demand for hospital services for patients with epilepsy. Epilepsia 39 (5) , pp. 537-544. 10.1111/j.1528-1157.1998.tb01417.x

D

Daniels, J., Holmans, Peter Alan, Williams, Nigel Melville, Turic, D., McGuffin, P., Plomin, R. and Owen, Michael John 1998. A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies. American Journal of Human Genetics 62 (5) , pp. 1189-1197. 10.1086/301816

Daniels, J., McGuffin, P., Owen, Michael John and Plomin, R. 1998. Molecular genetic studies of cognitive ability. Human Biology 70 (2) , pp. 281-296.

David, A. S., Kemp, R., Kirov, George, Everitt, B. and Hayward, P. 1998. Improving insight and compliance: Predictions and consequences. Schizophrenia Research 29 (1-2) , pp. 34-35. 10.1016/S0920-9964(97)88375-2

Deb, S., Braganza, J., Owen, Michael John, Kehoe, P., Williams, H. and Norton, N. 1998. No significant association between a PS-1 intronic polymorphism and dementia in Down's syndrome. Alzheimers Reports 1 (6) , pp. 365-368.

Dierks, Thomas, Linden, David Edmund Johannes, Hertel, Andreas, Günther, Thomas, Lanfermann, Heinrich, Niesen, Andreas, Frölich, Lutz, Zanella, Friedhelm E., Hör, Gustav, Goebel, Rainer and Maurer, Konrad 1998. Multimodal imaging of residual function and compensatory resource allocation in cortical atrophy: a case study of parietal lobe function in a patient with Huntington's disease. Psychiatry Research: Neuroimaging 84 (1) , pp. 27-35. 10.1016/S0925-4927(98)00040-7

Dorey, P., Pocklington, Andrew, Tateo, R. and Watts, G. 1998. TBA and TCSA with boundaries and excited states. Nuclear Physics B 525 (3) , pp. 641-663. 10.1016/S0550-3213(98)00339-3

F

Felce, David John 1998. The determinants of staff and resident activity in residential services for people with severe intellectual disability: Moving beyond size, building design, location and number of staff. Journal of Intellectual and Developmental Disability 23 (2) , pp. 103-119. 10.1080/13668259800033621

Felce, David John, Lowe, K., Perry, Jonathan, Baxter, Helen Ann, Jones, E., Hallam, A. and Beecham, J. 1998. Service support to people in Wales with severe intellectual disability and the most severe challenging behaviours: processes, outcomes and costs. Journal of Intellectual Disability Research 42 (5) , pp. 390-408. 10.1046/j.1365-2788.1998.00153.x

Fisher, P. J., Turic, D., Asherson, P., Ball, D., Benbow, C., Chorney, M., Chorney, K., Craig, I., Eley, T., Hill, L., Lubinski, D., Williams, Nigel Melville, McGuffin, P., Plomin, R. and Owen, Michael John 1998. DNA pooling for genomic scanning - Application to an association study. American Journal of Medical Genetics 81 (6) , p. 469.

G

Gill, M. and Craddock, Nicholas John 1998. The Wellcome Trust UK-Irish bipolar sib-pair study: Sample and study design. American Journal of Medical Genetics 81 (6) , p. 461.

Goebel, R., Linden, David Edmund Johannes, Lanfermann, H., Zanella, F. E. and Singer, W. 1998. Functional imaging of mirror and inverse reading reveals separate coactivated networks for oculomotion and spatial transformations. Neuroreport 9 (4) , pp. 713-719.

H

Hall, F. S., Wilkinson, Lawrence Stephen, Humby, Trevor, Inglis, W., Kendall, D. A., Marsden, C. A. and Robbins, T. W. 1998. Isolation rearing in rats: Pre- and postsynaptic changes in striatal dopaminergic systems. Pharmacology, Biochemistry and Behavior 59 (4) , pp. 859-872. 10.1016/S0091-3057(97)00510-8

Hateboer, N., Lazarou, L., Holmans, Peter Alan, Williams, A. J. and Ravine, D. 1998. Inter-family variability of phenotype in autosomal dominant polycystic kidney disease type 1. European Journal of Human Genetics 6 (1) , p. 71.

Healey, A., Knapp, M., Astin, J., Beecham, J., Kemp, R., Kirov, George and David, A 1998. Cost-effectiveness evaluation of compliance therapy for people with psychosis. British Journal of Psychiatry 172 , pp. 420-424. 10.1192/bjp.172.5.420

Hill, L., Asherson, P., Ball, D., Craig, I., Daniels, J., Eley, T., Freeman, B., Ninomiya, T., Fisher, P., Turic, D., Williams, Nigel Melville, Chorney, M., Chorney, K., Lubinski, D., Benbow, C., Thompson, L. A., Detterman, D. K., Owen, Michael John, McGuffin, P. and Plomin, R. 1998. QTLs for general cognitive ability in children: DNA pooling for chromosome 22. American Journal of Medical Genetics 81 (6) , p. 486.

Holmans, Peter Alan 1998. Affected sib-pair methods for detecting linkage to dichotomous traits: review of the methodology. Human biology 70 (6) , pp. 1025-1040.

Holmans, Peter Alan and Craddock, Nicholas John 1998. Efficient strategies for genome scanning with affected sib pairs - Reply. American Journal of Human Genetics 62 (1) , pp. 205-207. 10.1086/301683

Holmes, C., Russ, C., Kirov, George, Aitchison, K. J., Powell, J. F., Collier, D. A. and Lovestone, S. 1998. Apolipoprotein E: depressive illness, depressive symptoms, and Alzheimer's disease. Biological psychiatry 43 (3) , pp. 159-164. 10.1016/S0006-3223(97)00326-0

J

Johnson, E. O., van den Bree, Marianne Bernadette, Gupman, A. E. and Pickens, R. W. 1998. Extension of a typology of alcohol dependence based on relative genetic and environmental loading. Alcoholism-Clinical and Experimental Research 22 (7) , pp. 1421-1429. 10.1111/j.1530-0277.1998.tb03930.x

Jones, Ian Richard and Craddock, Nicholas John 1998. Ethical issues in genetics of mental disorders. The Lancet 352 (9142) , p. 1788. 10.1016/S0140-6736(05)79871-8

Jones, Ian Richard, McCandless, F., Morey, J., Benjamin, J., Brockington, I. and Craddock, Nicholas John 1998. Molecular genetic approaches to puerperal psychosis. American Journal of Medical Genetics 81 (6) , p. 544.

Jones, Ian Richard and Sullivan, G. 1998. Physical dependence on zopiclone: case reports. British Medical Journal (BMJ) 316 (7125) , p. 117. 10.1136/bmj.316.7125.117

K

Kaneva, R., Milanova, V., Onchev, G., Stoyanova, V., Chakarova, C. H., Nikolova, A., Hallmayer, J., Belemezova, M., Milenska, T., Kirov, George, Kremensky, I., Kalaydjieva, L. and Jablensky, A. 1998. A linkage study of affective disorders in two Bulgarian Gypsy families: results for candidate regions on chromosomes 18 and 21. Psychiatric Genetics 8 (4) , pp. 245-249. 10.1097/00041444-199808040-00008

Kehoe, P. G., Williams, H., Holmans, Peter Alan, Wilcock, G., Cairns, N. J., Neal, J. and Owen, Michael John 1998. The butyrylcholinesterase K variant and susceptibility to Alzheimer's disease. Journal of Medical Genetics 35 (12) , pp. 1034-1035. 10.1136/jmg.35.12.1034

Kemp, R., Kirov, George, Everitt, B., Hayward, P. and David, A. 1998. Randomised controlled trial of compliance therapy. 18-month follow-up. British Journal of Psychiatry 172 , pp. 413-419. 10.1192/bjp.172.5.413

Kerr, Michael Patrick 1998. Achieving health gain for people with intellectual disabilities. In: Kerr, Michael Patrick ed. Innovations in Health Care for People with Intellectual Disabilities, Chorley: Lisieux Hall, pp. 1-8.

Kerr, Michael Patrick 1998. Topiramate: uses in people with an intellectual disability who have epilepsy. Journal of Intellectual Disability Research 42 (1) , pp. 74-79.

Kirov, George 1998. Thyroid disorders in lithium-treated patients. Journal of affective disorders 50 (1) , pp. 33-40.

Kirov, George, Jones, Ian Richard, McCandless, F., Craddock, Nicholas John and Owen, Michael John 1998. Family-based association studies of candidate genes in bipolar disorder. American Journal of Medical Genetics 81 (6) , pp. 476-477.

Kirov, George, Kemp, R., Kirov, K. and David, A. S. 1998. Religious faith after psychotic illness. Psychopathology 31 (5) , pp. 234-245. 10.1159/000029045

Kirov, George, Murphy, K. C., Arranz, M. J., Jones, Ian Richard, McCandless, F., Kunugi, H., Murray, R. M., McGuffin, P., Collier, D. A., Owen, Michael John and Craddock, Nicholas John 1998. Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder. Molecular Psychiatry 3 (4) , pp. 342-345. 10.1038/sj.mp.4000385

Koppel, S. M. and Thapar, Ajay Kumar 1998. Treating blood needle phobia. Hospital Medicine 59 (9) , pp. 730-732.

L

Lawrence, Andrew David, Hodges, J. R., Rosser, Anne Elizabeth, Kershaw, A., Ffrench-Constant, C., Rubinsztein, D. C., Robbins, T. W. and Sahakian, B. J. 1998. Evidence for specific cognitive deficits in preclinical Huntington's disease. Brain 121 (7) , pp. 1329-1341. 10.1093/brain/121.7.1329

Lendon, C. L., Lynch, T., Norton, J., McKeel, D. W., Busfield, F., Craddock, Nicholas John, Chakraverty, S., Gopalakkrishnan, G., Shears, S. D., Grimmett, W., Wilhelmsen, K. C., Hansen, L., Morris, J. C. and Goate, A. M. 1998. Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22. Neurology 50 (6) , pp. 1546-1555. 10.1212/wnl.50.6.1546

Li, T., Vallada, H. P., Liu, X., Xie, T., Tang, X., Zhao, J., O'Donovan, Michael Conlon, Murray, R. M., Sham, P. C. and Collier, D. A. 1998. Analysis of CAG/CTG repeat size in Chinese subjects with schizophrenia and bipolar affective disorder using the repeat expansion detection method. Biological psychiatry 44 (11) , pp. 1160-1165. 10.1016/S0006-3223(97)00492-7

Linden, David Edmund Johannes 1998. The myth of upright vision. A psychophysical and functional imaging study of adaptation to inverting spectacles. Perception 352 (9142) , p. 1788. 10.1068/p2820

Linden, David Edmund Johannes 1998. Visual perception: myths and mechanisms. Trends in Neurosciences 21 (6) , pp. 225-226. 10.1016/S0166-2236(98)01271-5

Loh, N. Y., Ambrose, H. J., Guay-Woodford, L. M., DasGupta, S., Nawrotzki, R. A., Blake, Derek J and Davies, K. E. 1998. Genomic organization and refined mapping of the mouse beta-dystrobrevin gene. Mammalian Genome 9 (11) , pp. 857-862.

Loh, Nellie Y., Ambrose, Helen J., Guay-Woodford, Lisa M., DasGupta, Srimita, Nawrotzki, Ralph A., Blake, Derek J. and Davies, Kay E. 1998. Genomic organization and refined mapping of the mouse β-dystrobrevin gene. Mammalian Genome 9 (11) , pp. 857-862. 10.1007/s003359900883

Lowe, K., Felce, David John, Perry, J., Baxter, Helen Ann and Jones, E. 1998. The characteristics and residential situations of people with severe intellectual disability and the most severe challenging behaviour in Wales. Journal of Intellectual Disability Research 42 (5) , pp. 375-389. 10.1046/j.1365-2788.1998.00154.x

M

Maughan, B, Collishaw, Stephan and Pickles, A. 1998. School achievement and adult qualifications among adoptees: a longitudinal study. Journal of Child Psychology and Psychiatry 39 (5) , pp. 669-685. 10.1111/1469-7610.00367

McCandless, F., Jones, I., Harper, K. and Craddock, Nicholas John 1998. Intrafamilial association of pericentric inversion of chromosome 9, inv (9)(p11-q21), and rapid cycling bipolar disorder. Psychiatric Genetics 8 (4) , pp. 259-262. 10.1097/00041444-199808040-00011

McGuffin, Peter and Thapar, Anita 1998. Genetics and Antisocial Personality Disorder. In: Millon, Theodore, Simonsen, Erik, Birket-Smith, Morton and Davis, Roger D eds. Psychopathy: Antisocial, Criminal and Violent Behavior, New York: The Guilford Press, pp. 215-230.

Murphy, K. C., Jones, R. G., Griffiths, E., Thompson, P. W. and Owen, Michael John 1998. Chromosome 22q11 deletions - An under-recognized cause of idiopathic learning disability? Schizophrenia Research 29 (1-2) , p. 132. 10.1016/S0920-9964(97)88634-3

Murphy, K. C., Jones, R. G., Griffiths, E., Thompson, P. W. and Owen, Michael John 1998. Chromosome 22qII deletions. An under-recognised cause of idiopathic learning disability. British Journal of Psychiatry 172 , pp. 180-183. 10.1192/bjp.172.2.180

Murphy, K. C. and Owen, Michael John 1998. The behavioural phenotype in velo-cardio-facial syndrome. Schizophrenia Research 29 (1-2) , p. 132.

Murphy, K. C. and Owen, Michael John 1998. Chromosome 22qII deletions and aggressive behaviour. British Journal of Psychiatry 173 , pp. 353-354. 10.1192/bjp.173.4.353b

Murphy, K. C., Williams, Nigel Melville, Cardno, A. G., Jones, L. A., Holmans, Peter Alan, McGuffin, P. and Owen, Michael John 1998. A linkage study of chromosome 22q in SIB-pairs with schizophrenia. Schizophrenia Research 29 (1-2) , pp. 131-132. 10.1016/S0920-9964(97)88632-X

N

Nawrotzki, Ralph, Loh, Nellie Y., Ruegg, M. A., Davies, Kay E. and Blake, Derek J. 1998. Characterisation of alpha-dystrobrevin in muscle. Journal of Cell Science 111 (17) , pp. 2595-2605.

O

O'Donovan, Michael Conlon, Oefner, P. J., Roberts, S. C., Austin, J., Hoogendoorn, B., Guy, C., Speight, G., Upadhyaya, M., Sommer, S. S. and McGuffin, P. 1998. Blind analysis of denaturing high-performance liquid chromatography as a tool for mutation detection. Genomics 52 (1) , pp. 44-49. 10.1006/geno.1998.5411

O'Mahony, E., Jones, Ian Richard, Gill, M. and Craddock, Nicholas John 1998. Wellcome trust UK/Irish bipolar sib pair study: Clinical similarities in siblings. American Journal of Medical Genetics 81 (6) , p. 546.

Oretti, R. G., O'Donovan, Michael Conlon, McGuffin, Peter and Buckland, Paul Robert 1998. Tryptophan pyrrolase gene expression in an alcohol preferring and non-preferring mouse strain. Addiction Biology 3 (1) , pp. 71-77. 10.1080/13556219872362

Owen, Michael John 1998. Psychiatric disorders in Wolfram syndrome heterozygotes. Molecular Psychiatry 3 (1) , pp. 12-13.

Owen, Michael John and Craddock, Nicholas John 1998. Chromosome 11 workshop. Psychiatric Genetics 8 (2) , pp. 89-92.

Owen, Michael John and McGuffin, P. 1998. The programmed alliance of two disciplines. La Recherche 311 , pp. 38-39.

P

Padareva, V., Djoumaliisky, S., Touleshkov, N. and Kirov, George 1998. Modification of blowing agent system based on sodium bicarbonate with activated natural zeolite. Journal of Materials Science Letters 17 (2) , pp. 107-109.

Perry, Jonathan, Beyer, Stephen Richard, Felce, David John and Todd, Stuart Philip 1998. Strategic service change: development of core services in Wales, 1983-1995. Journal of Applied Research in Intellectual Disabilities 11 (1) , pp. 15-33. 10.1111/j.1468-3148.1998.tb00031.x

Poulton, K., Holmes, J., Hever, T., Trumper, A., Fitzpatrick, H., McGuffin, P., Owen, Michael John, Worthington, J., Ollier, W., Harrington, R. and Thapar, Anita 1998. A molecular genetic study of hyperkinetic disorder/attention deficit hyperactivity disorder. American Journal of Medical Genetics 81 (6) , p. 458.

R

Rapley, M., Ridgway, J. and Beyer, S. 1998. Staff:staff and staff:client reliability of the Schalock & Keith (1993) Quality of Life Questionnaire. Journal of Intellectual Disability Research 42 (1) , pp. 37-42. 10.1046/j.1365-2788.1998.00066.x

Rapley, M., Ridgway, J. and Beyer, Stephen Richard 1998. Staff: staff and staff: client reliability of the Schalock & Keith (1993) Quality of Life Questionnaire. Journal of Intellectual Disability Research 42 (1) , pp. 37-42. 10.1046/j.1365-2788.1998.00066.x

Rapley, Mark and Beyer, Stephen Richard 1998. Daily activity, community participation and Quality of Life in an ordinary housing network: a two-year follow-up. Journal of Applied Research in Intellectual Disabilities 11 (1) , pp. 34-43. 10.1111/j.1468-3148.1998.tb00032.x

Robertson, Neil, Deans, J. and Compston, D. A. 1998. Myasthenia gravis: a population based epidemiological study in Cambridgeshire, England. Journal of Neurology, Neurosurgery & Psychiatry 65 (4) , pp. 492-496. 10.1136/jnnp.65.4.492

Robertson, Neil, Shaunak, S. and Compston, D. A. 1998. Urgent neurology out-patient referrals from primary health care physicians. QJM: An International Journal of Medicine 91 (4) , pp. 309-313. 10.1093/qjmed/91.4.309

Robertson, Neil Patrick, Wharton, S., Anderson, J. and Scolding, N. J. 1998. Adult polyglucosan body disease associated with an extrapyramidal syndrome. Journal of Neurology, Neurosurgery & Psychiatry 65 (5) , pp. 788-790. 10.1136/jnnp.65.5.788

Rose, S. and Taylor, Pamela Jane 1998. Selected characteristics of people on long-term sick leave. Psychiatric Bulletin 22 (7) , pp. 428-432. 10.1192/pb.22.7.428

Rose, Suzanna and Bisson, Jonathan Ian 1998. Brief early psychological interventions following trauma: A systematic review of the literature. Journal of Traumatic Stress 11 (4) , pp. 697-710. 10.1023/A:1024441315913

Rosenblatt, A., Ranen, N. G., Rubinsztein, D. C., Stine, O. C., Margolis, R. L., Wagster, M. V., Becher, M. W., Rosser, Anne Elizabeth, Leggo, J., Hodges, J. R., ffrench-Constant, C. K., Sherr, M., Franz, M. L., Abbott, M. H. and Ross, C. A. 1998. Patients with features similar to Huntington's disease, without CAG expansion in huntingtin. Neurology 51 (1) , pp. 215-220. 10.1212/WNL.51.1.215

S

Singhrao, S. K., Thomas, P., Wood, D. J., MacMillan, J. C., Neal, J. W., Harper, P. S. and Jones, Lesley 1998. Huntingtin protein colocalizes with lesions of neurodegenerative diseases: An investigation in Huntington's, Alzheimer's, and Pick's diseases. Experimental Neurology 150 (2) , pp. 213-222. 10.1006/exnr.1998.6778

Spurlock, G., Heils, A., Holmans, Peter Alan, Williams, J., D'Souza, U. M., Cardno, A., Murphy, K. C., Jones, L., Buckland, Paul Robert, McGuffin, P., Lesch, K. .P and Owen, Michael John 1998. A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter. Molecular Psychiatry 3 (1) , pp. 42-49. 10.1038/sj.mp.4000342

Spurlock, G., Williams, Julie, McGuffin, P., Aschauer, H. N., Lenzinger, E., Fuchs, K., Sieghart, W. C., Meszaros, K., Fathi, N., Laurent, C., Mallet, J., Macciardi, F., Pedrini, S., Gill, M., Hawi, Z., Gibson, S., Jazin, E. E., Yang, H. T., Adolfsson, R., Pato, C. N., Dourado, A. M. and Owen, Michael John 1998. European Multicentre Association Study of Schizophrenia: a study of the DRD2 Ser311Cys and DRD3 Ser9Gly polymorphisms. American Journal of Medical Genetics 81 (1) , pp. 24-28. 10.1002/(SICI)1096-8628(19980207)81:1<24::AID-AJMG5>3.0.CO;2-N

Spurlock, Gillian, Williams, Nigel Melville, Williams, Hywel and Owen, Michael John 1998. Polymorphism screening of the human type 1 sigma (sigma) receptor (a candidate gene for schizophrenia) using a modified dideoxy fingerprinting technique. American Journal of Medical Genetics 81 (6) , pp. 525-526.

Straub, R. E., Vallada, H., Curtis, D., Sham, P., Kunugi, H., Zhao, J. H., Murray, R., McGuffin, P., Nanko, S., Owen, Michael John, Gill, M., Collier, D. A., Antonarakis, S., Housman, D., Kazazian, H., Nestadt, G., Pulver, A. E., MacLean, C. J., Walsh, D., Kendler, K. S., DeLisi, L., Polymeropoulos, M., Coon, H., Byerley, W., Lofthouse, R., Gershon, E., Goldin, L., Freedman, R., Laurent, C., Bodeau-Pean, S., d'Amato, T., Jay, M., Campion, D., Mallet, J., Wildenauer, D. B., Lerer, B., Albus, M., Ackenheil, M., Ebstein, R. P., Hallmayer, J., Maier, W., Gurling, H., Curtis, D., Kalsi, G., Brynjolfsson, J., Sigmundson, T., Petursson, H., Blackwood, D., Muri, W., StClair, D., He, L., Maguire, S., Moises, H. W., Hwu, H. G., Yang, L., Wiese, C., Kristbjarnarson, H., Levinson, D. F., Mowry, B. J., Donis-Keller, H., Hayward, N. K., Crowe, R. R., Silverman, J. M., Nancarrow, D. J. and Read, C. M. 1998. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12. Schizophrenia Collaborative Linkage Group for Chromosome 22. Schizophrenia Research 32 (2) , pp. 115-121. 10.1016/S0920-9964(98)00048-6

Svendsen, C. N., ter Borg, M. G., Armstrong, R. J., Rosser, Anne Elizabeth, Chandran, S., Ostenfeld, T. and Caldwell, M. A. 1998. A new method for the rapid and long term growth of human neural precursor cells. Journal of Neuroscience Methods 85 (2) , pp. 141-152. 10.1016/S0165-0270(98)00126-5

T

Taylor, Pamela Jane 1998. When symptoms of psychosis drive serious violence. Social Psychiatry and Psychiatric Epidemiology 33 (S1) , pp. 47-54.

Taylor, Pamela Jane, Leese, M., Williams, D., Butwell, M., Daly, R. and Larkin, E. 1998. Mental disorder and violence. A special (high security) hospital study. British Journal of Psychiatry 172 (3) , pp. 218-226. 10.1192/bjp.172.3.218

Thapar, Ajay Kumar, Stott, N. C., Richens, A. and Kerr, Michael Patrick 1998. Attitudes of GPs to the care of people with epilepsy. Family Practice 15 (5) , pp. 437-442. 10.1093/fampra/15.5.437

Thapar, Anita 1998. Attention deficit hyperactivity disorder: unravelling the molecular genetics. Molecular Psychiatry 3 (5) , pp. 370-372. 10.1038/sj.mp.4000452

Thapar, Anita 1998. Behavioural phenotypes. Psychological Medicine 28 (2) , pp. 493-494.

Thapar, Anita, Harold, Gordon Thomas and McGuffin, P 1998. Life events and depressive symptoms in childhood--shared genes or shared adversity? A research note. Journal of Child Psychology and Psychiatry 39 (8) , pp. 1153-1158. 10.1111/1469-7610.00419

Thapar, Anita and McGuffin, P. 1998. A twin study of depressive symptoms in childhood. British Journal of Psychiatry 165 (2) , pp. 259-265. 10.1192/bjp.165.2.259

Thapar, Anita and McGuffin, P. 1998. Validity of the shortened Mood and Feelings Questionnaire in a community sample of children and adolescents: a preliminary research note. Psychiatry Research 81 (2) , pp. 259-268. 10.1016/S0165-1781(98)00073-0

Thapar, Anita and McGuffin, Peter 1998. Genetics and learning disability. In: Kerr, Michael Patrick ed. Innovations in Health Care for People with Intellectual Disabilites, Lisieux Hall Publications,

Thijs, R. D. and Kerr, Michael Patrick 1998. The outcome of prescribing novel anticonvulsants in an outpatient setting: factors affecting response to medication. Seizure - European Journal of Epilepsy 7 (5) , pp. 379-383. 10.1016/S1059-1311(05)80006-8

Thomas, P., Wilkinson, F., Nguyen, T. M., Harper, P. S., Neal, J. W., Morris, G. E. and Jones, Lesley 1998. Full length huntingtin is not detected in intranuclear inclusions in Huntington's disease brain. Biochemical Society Transactions 26 (3) , S243. 10.1042/bst026s243

V

Vallada, H. P., Vasques, L., Curtis, D, Zatz, M., Kirov, George, Lauriano, V., Gentil, V., Murray, R. M., McGuffin, P., Owen, Michael John, Gill, M., Craddock, Nicholas John and Collier, D. A. 1998. Linkage analysis between bipolar affective disorder and markers on chromosome X. Psychiatric Genetics 8 (3) , pp. 183-186. 10.1097/00041444-199800830-00008

van den Bree, Marianne Bernadette, Johnson, E. O., Neale, M. C. and Pickens, R. W. 1998. Genetic and environmental influences on drug use and abuse/dependence in male and female twins. Drug and Alcohol Dependence 52 (3) , pp. 231-241. 10.1016/S0376-8716(98)00101-X

van den Bree, Marianne Bernadette, Johnson, E. O., Neale, M. C., Svikis, D. S., McGue, M. and Pickens, R. W. 1998. Genetic analysis of diagnostic systems of alcoholism in males. Biological psychiatry 43 (2) , pp. 139-145. 10.1016/S0006-3223(97)00225-4

van den Bree, Marianne Bernadette, Svikis, D. S. and Pickens, R. W. 1998. Genetic influences in antisocial personality and drug use disorders. Drug and Alcohol Dependence 49 (3) , pp. 177-187. 10.1016/S0376-8716(98)00012-X

Vater, Ruth, Young, Carol, Anderson, Louise V. B., Lindsay, Susan, Blake, Derek J., Davies, Kay E., Zuellig, Richard and Slater, Clarke R. 1998. Utrophin mRNA expression in muscle is not restricted to the neuromuscular junction. Molecular and Cellular Neuroscience 10 (5-6) , pp. 229-242. 10.1006/mcne.1998.0661

W

Wilkinson, Lawrence Stephen, Humby, Trevor, Killcross, Andrew Simon, Torres, EM, Everitt, B. J. and Robbins, T. W. 1998. Dissociations in dopamine release in medial prefrontal cortex and ventral striatum during the acquisition and extinction of classical aversive conditioning in the rat. European Journal of Neuroscience 10 (3) , pp. 1019-1026. 10.1046/j.1460-9568.1998.00119.x

Williams, Julie, Spurlock, G., Holmans, Peter Alan, Mant, R., Murphy, K., Jones, L., Cardno, A., Asherson, P., Blackwood, D., Muir, W., Meszaros, K., Aschauer, H., Mallet, J., Laurent, C., Pekkarinen, P., Seppala, J., Stefanis, C. N., Papadimitriou, G. N., Macciardi, F., Verga, M., Pato, C., Azevedo, H., Crocq, M. A., Gurling, H. and Owen, Michael John 1998. A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia. Molecular Psychiatry 3 (2) , pp. 141-149.

Williams, Nigel Melville, Fenton, I. and Owen, Michael John 1998. PsycheMap - An interactive Internet-based database of psychiatric genetics linkage, association, and genome mapping projects. American Journal of Medical Genetics 81 (6) , pp. 463-464.

Williams, Nigel Melville, Kirov, George, Craddock, Nicholas John and Owen, Michael John 1998. Screening the critical region on chromosome 4p with DNA pooling for association with bipolar disorder. American Journal of Medical Genetics 81 (6) , p. 486.

Wright, P., Dawson, E., Donaldson, P. T., Underhill, J. A., Sham, P. C., Zhao, J., Gill, M., Nanko, S., Owen, Michael John, McGuffin, P. and Murray, R. M. 1998. A transmission/disequilibrium study of the DRB1*04 gene locus on chromosome 6p21.3 with schizophrenia. Schizophrenia Research 32 (2) , pp. 75-80. 10.1016/S0920-9964(98)00050-4

Wu, W. S., Holmans, Peter Alan, Wavrant-DeVrieze, F., Shears, S., Kehoe, P., Crook, R., Booth, J., Williams, Nigel Melville, Perez-Tur, J., Roehl, K., Fenton, I., Chartier-Harlin, M. C., Lovestone, S., Williams, Julie, Hutton, M., Hardy, J., Owen, Michael John and Goate, A. 1998. Genetic studies on chromosome 12 in late-onset Alzheimer disease. JAMA - The Journal of the American Medical Association 280 (7) , pp. 619-622. 10.1001/jama.280.7.619

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