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Number of items: 124.

A

Ahmed, Z., Bowley, C., Kerr, Michael Patrick and Grp, EG. 2000. Developing international guidelines for the management of the adult with epilepsy and intellectual disability - evidence based treatment. Journal of Intellectual Disability Research 44 , p. 191.

Ahmed, Z., Fraser, William, Kerr, Michael Patrick, Kiernan, C., Emerson, E., Robertson, J., Felce, David John, Allen, David G., Baxter, Helen Ann and Thomas, J. 2000. Reducing antipsychotic medication in people with a learning disability. British Journal of Psychiatry 176 , pp. 42-46. 10.1192/bjp.176.1.42

Armstrong, R. J., Watts, C., Svendsen, C. N., Dunnett, S. B. and Rosser, Anne Elizabeth 2000. Survival, neuronal differentiation, and fiber outgrowth of propagated human neural precursor grafts in an animal model of Huntington's disease. Cell Transplantation 9 (1) , pp. 55-64.

Arseneault, L., Moffitt, T. E., Caspi, A., Taylor, Pamela Jane and Silva, P. A. 2000. Mental disorders and violence in a total birth cohort: results from the Dunedin Study. Archives of General Psychiatry 57 (10) , pp. 979-986. 10.1001/archpsyc.57.10.979

Austin, J., Buckland, Paul Robert, Cardno, Alastair G., Williams, Nigel Melville, Spurlock, Gillian, Hoogendoorn, Bastiaan, Zammit, Stanley, Jones, G., Sanders, R., Jones, L., McCarthy, G., Jones, S., Bray, Nicholas John, McGuffin, Peter, Owen, Michael John and O'Donovan, Michael Conlon 2000. The high affinity neurotensin receptor gene (NTSR1): comparative sequencing and association studies in schizophrenia. Molecular Psychiatry 5 (5) , pp. 552-557. 10.1038/sj.mp.4000761

Austin, J., Hoogendoorn, Bastiaan, Buckland, Paul Robert, Jones, Ian Richard, McCandless, F., Williams, Nigel Melville, Middle, F., Owen, Michael John, Craddock, Nicholas John and O'Donovan, Michael Conlon 2000. Association analysis of the proneurotensin gene and bipolar disorder. Psychiatric Genetics 10 (1) , pp. 51-54. 10.1097/00041444-200010010-00009

Austin, J., Hoogendoorn, Bastiaan, Buckland, Paul Robert, Speight, G., Cardno, A., Bowen, Timothy, Williams, Nigel Melville, Spurlock, G., Sanders, R., Jones, L., Murphy, Kevin, McCarthy, G., McGuffin, P., Owen, Michael John and O'Donovan, Michael Conlon 2000. Comparative sequencing of the proneurotensin gene and association studies in schizophrenia. Molecular Psychiatry 5 (2) , pp. 208-212. 10.1038/sj.mp.4000693

B

Bandmann, O., Vaughan, J. R., Holmans, Peter Alan, Marsden, C. D. and Wood, N. W. 2000. Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease. Movement Disorders 15 (1) , pp. 30-35. 10.1002/1531-8257(200001)15:13.0.CO;2-V

Bennett, P., Middle, F., Jones, Ian Richard, Heron, J., Gill, M. and Craddock, Nicholas John 2000. The Wellcome Trust UK-Irish Bipolar Sib-pair Genome Screen: Complete first stage analysis of chromosomes 1, 3, 4, 7, 8, 12, 13, 14, 15, 16, X, and second stage progress report. American Journal of Medical Genetics 96 (4) , p. 549.

Beyer, Stephen Richard, Hill-Tout, J., Adams, D., Johanson-Brown, S., Davies, H. and Shiers, B. 2000. Into work: Stockport Employment Services Horizon Project: final evaluation report. [Project Report]. Stockport, UK: Stockport Borough Council.

Beyer, Stephen Richard and Kilsby, Mark Stephen 2000. Impact of agency organization on supported employment effectiveness [Abstract]. Journal of Intellectual Disability Research 44 (3-4) , pp. 207-208. 10.1046/j.1365-2788.2000.d01-124.x

Beyer, Stephen Richard and Kilsby, Mark Stephen 2000. Impact of agency organization on supported employment effectiveness. Journal of Applied Research in Intellectual Disabilities 44 , pp. 207-208. 10.1046/j.1468-3148.2000.00005.x

Bisson, Jonathan Ian, Shepherd, Jonathan Paul, Joy, Diamond and Probert, R. 2000. Randomised controlled trial of a brief early psychological intervention following acute physical injury. Journal of Psychosomatic Research 48 (3) , p. 224.

Blake, Derek J. and Kröger, Stephan 2000. The neurobiology of Duchenne muscular dystrophy: learning lessons from muscle? Trends in Neurosciences 23 (3) , pp. 92-99. 10.1016/S0166-2236(99)01510-6

Bowen, Timothy, Ashworth, Lindsay, Kirov, George, Guy, Carol, Jones, Ian Richard, McCandless, Fiona, Craddock, Nicholas John, O'Donovan, Michael Conlon and Owen, Michael John 2000. No evidence of association from transmission disequilibrium analysis of the hKCa3 gene in bipolar disorder. Bipolar Disorders 2 (4) , pp. 328-331. 10.1034/j.1399-5618.2000.020406.x

Bowen, Timothy, Guy, Carol, Cardno, A. G., Vincent, J. B., Kennedy, J. L., Jones, L. A., Gray, M, Sanders, Rhys, McCarthy, G, Murphy, K. C., Owen, Michael John and O'Donovan, Michael Conlon 2000. Repeat sizes at CAG/CTG loci CTG18.1, ERDA1 and TGC13-7a in schizophrenia. Psychiatric Genetics 10 (1) , pp. 33-37. 10.1097/00041444-200010010-00006

Bowley, C. and Kerr, Michael Patrick 2000. Epilepsy and intellectual disability. Journal of Intellectual Disability Research 44 (5) , pp. 529-543. 10.1046/j.1365-2788.2000.00270.x

Bray, Nicholas John, Jacobsen, N., Spurlock, Gillian, Austin, Jehanine, Williams, Hywel and Owen, Michael John 2000. A functional and positional candidate gene for schizophrenia. American Journal of Medical Genetics 96 (4) , pp. 461-462.

Bray, Nicholas John, Williams, Nigel Melville, Bowen, Timothy, Cardno, A. G., Gray, M., Jones, L. A., Murphy, K. C., Sanders, R., Spurlock, G., O'Donovan, Michael Conlon and Owen, Michael John 2000. No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia. Psychiatric Genetics 10 (2) , pp. 83-86. 10.1097/00041444-200010020-00005

Buckland, J., Pennington, D. J., Bruno, L. and Owen, Michael John 2000. Co-ordination of the expression of the protein tyrosine kinase p56(lck) with the pre-T cell receptor during thymocyte development. European Journal of Immunology 30 (1) , pp. 8-18. 10.1002/1521-4141(200001)30:1<8::AID-IMMU8>3.0.CO;2-8

Butler, J., Kerr, Michael Patrick and Todd, Stuart Philip 2000. Epilepsy - The plain facts. Journal of Intellectual Disability Research 44 , p. 227.

Butwell, M., Jamieson, E., Leese, M. and Taylor, Pamela Jane 2000. Trends in special (high-security) hospitals: 2: Residency and discharge episodes, 1986-1995. British Journal of Psychiatry 176 (3) , pp. 260-265. 10.1192/bjp.176.3.260

C

Cardno, A. G., O'Donovan, Michael Conlon and Owen, Michael John 2000. Genetic risk factors for schizophrenia. International Journal of Mental Health 29 (3) , pp. 13-38.

Carr, Deborah and Felce, David John 2000. Application of stimulus equivalence to language intervention for individuals with severe linguistic disabilities. Journal of Intellectual and Developmental Disability 25 (3) , pp. 181-205.

Collins, P., Wilkinson, Lawrence Stephen, Everitt, B. J., Robbins, T. W. and Roberts, A. C. 2000. The effect of dopamine depletion from the caudate nucleus of the common marmoset (Callithrix jacchus) on tests of prefrontal cognitive function. Behavioral Neuroscience 114 (1) , pp. 3-17. 10.1037/0735-7044.114.1.3

Collishaw, Stephan and Hole, G. J. 2000. Featural and configurational processes in the recognition of faces of different familiarity. Perception 29 (8) , pp. 893-909. 10.1068/p2949

Coyle, Natasha, Jones, Ian Richard, Robertson, Emma, Lendon, Corinne and Craddock, Nicholas John 2000. Variation at the serotonin transporter gene influences susceptibility to bipolar affective puerperal psychosis. The Lancet 356 (9240) , pp. 1490-1491. 10.1016/S0140-6736(00)02877-4

Craddock, Nicholas John 2000. Psychiatric genetics. British Journal of Psychiatry 177 (6) , p. 571. 10.1192/bjp.177.6.571

D

Deb, S., Braganza, J., Norton, N., Williams, H., Kehoe, P. G., Williams, Julie and Owen, Michael John 2000. APOE epsilon 4 influences the manifestation of Alzheimer's disease in adults with Down's syndrome. British Journal of Psychiatry 176 , pp. 468-472. 10.1192/bjp.176.5.468

Deb, S., Braganza, J., Norton, N., Williams, H., Kehoe, P. G., Williams, Julie and Owen, Michael John 2000. Presence of the Apolipoprotein E e4 allele is associated with the manifestation of Alzheimer dementia in adults with Down syndrome. Journal of Intellectual Disability Research 44 , p. 259.

Deb, S., Williams, Julie and Owen, Michael John 2000. Apolipoprotein E, Alzheimer's disease and Down's syndrome - Reply. British Journal of Psychiatry 177 , pp. 469-470.

DeLisi, L. E., Craddock, Nicholas John, Detera-Wadleigh, S., Foroud, T., Gejman, P., Kennedy, J. L., Lendon, C., Macciardi, F., McKeon, P., Mynett-Johnson, L., Nurnberger, J., Paterson, A., Schwab, S., van Broeckhoven, C., Wildenauer, D. and Crow, T. J. 2000. Update on chromosomal locations for psychiatric disorders: report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics, Monterey, California, October 14-18, 1999. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 96 (3) , pp. 434-449. 10.1002/1096-8628(20000612)96:3%3C434::aid-ajmg40%3E3.0.co;2-c

Dierks, Thomas, Jelic, Vesna, Pascual-Marqui, Roberto D., Wahlund, Lars-Olof, Julin, Per, Linden, David Edmund Johannes, Maurer, Konrad, Winblad, Bengt and Nordberg, Agneta 2000. Spatial pattern of cerebral glucose metabolism (PET) correlates with localization of intracerebral EEG-generators in Alzheimer's disease. Clinical Neurophysiology 111 (10) , pp. 1817-1824. 10.1016/S1388-2457(00)00427-2

E

Elvidge, G. P., Owen, Michael John and Craddock, Nicholas John 2000. Mutational analysis of purinergic receptor, P2X4: A positional candidate susceptibility gene for bipolar disorder. American Journal of Medical Genetics 96 (4) , p. 493.

Espie, C. and Kerr, Michael Patrick 2000. Epilepsy and learning disability: implications for quality of life. In: Baker, G. and Jacoby, A. eds. Quality of life in Epilepsy: Beyond Seizure Counts in Assessment and Treatment, Psychology Press, pp. 145-160.

F

Farmer, A. E., Owen, Michael John and McGuffin, P. 2000. Bioethics and genetic research in psychiatry. British Journal of Psychiatry 176 , pp. 105-108. 10.1192/bjp.176.2.105

Felce, David John, Bowley, Clare, Baxter, Helen Ann, Jones, Edwin, Lowe, Kathy and Emerson, Eric 2000. The effectiveness of staff support: evaluating Active Support training using a conditional probability approach. Research in Developmental Disabilities 21 (4) , pp. 243-255. 10.1016/S0891-4222(00)00040-8

Felce, David John, Jones, E., Lowe, K. and Bowley, C. 2000. Evaluation of the dissemination of Active Support training in staffed housing services for people with severe intellectual disabilities. Journal of Intellectual Disability Research 44 (3-4) , pp. 280-281. 10.1046/j.1365-2788.2000.d01-124.x

Felce, David John, Lowe, K. and Jones, E. 2000. Resident outcomes in staffed community residences. Journal of Intellectual Disability Research 44 , p. 281.

Felce, David John, Lowe, K. and Jones, E. 2000. Staff performance in staffed community residences. Journal of Intellectual Disability Research 44 , p. 281.

Felce, David John, Lowe, Kathy, Beecham, Jennifer and Hallam, Angela 2000. Exploring the relationships between costs and quality of services for adults with severe intellectual disabilities and the most severe challenging behaviours in Wales: A multivariate regression analysis. Journal of Intellectual and Developmental Disability 25 (4) , pp. 307-326. 10.1080/13668250020019593

Feng, J., Zheng, J., Bennett, W. P., Heston, L. L., Craddock, Nicholas John and Sommer, S. S. 2000. Five missense variants in the amino-terminal domain of the glucocorticoid receptor: no association with puerperal psychosis or schizophrenia. American Journal of Medical Genetics 96 (3) , pp. 412-417. 10.1002/1096-8628(20000612)96:3<412::AID-AJMG33>3.0.CO;2-C

Fitzpatrick, E., Spurlock, G., Coleman, Sharon Louise, Owen, Michael John and Buckland, Paul Robert 2000. Association studies of polymorphisms in the promoter region of the dopamine D4 receptor and the D2 receptor [Abstract]. American Journal of Medical Genetics 96 (4) , p. 530. 10.1002/1096-8628(20000807)96:4<515::AID-AJMG6>3.0.CO;2-U

Fruin, David and Felce, David John 2000. Evidence on Service Quality for the Social Services Inspectorate Inspection Process: Piloting the Application of Research. Tizard Learning Disability Review 5 (3) , pp. 5-13. 10.1108/13595474200000022

G

Guggenheim, J. A., Kirov, George and Hodson, S. A. 2000. The heritability of high myopia: a reanalysis of Goldschmidt's data. Journal of Medical Genetics 37 (3) , pp. 227-231. 10.1136/jmg.37.3.227

H

Harris, J. M, Cumming, A. M., Craddock, Nicholas John, St Clair, D. and Lendon, C. L. 2000. Human leucocyte antigen-A2 increases risk of Alzheimer's disease but does not affect age of onset in a Scottish population. Neuroscience Letters 294 (1) , pp. 37-40. 10.1016/S0304-3940(00)01539-1

Henry, J. C., van Amelsvoort, T., Morris, R. G., Owen, Michael John, Murphy, K. C. and Murphy, D. G. M. 2000. The neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS). American Journal of Medical Genetics 96 (4) , p. 474.

Holmes, J., Payton, A., Barrett, J. H., Hever, T., Fitzpatrick, H., Trumper, A. L., Harrington, R., McGuffin, P., Owen, Michael John, Ollier, W., Worthington, J. and Thapar, Anita 2000. A family-based and case-control association study of the dopamine D4 receptor gene and dopamine transporter gene in attention deficit hyperactivity disorder. Molecular Psychiatry 5 (5) , pp. 523-530. 10.1038/sj.mp.4000751

Hoogendoorn, Bastiaan, Norton, Nadine, Kirov, George, Williams, Nigel Melville, Hamshere, Marian Lindsay, Spurlock, Gillian, Austin, Jehannine, Stephens, Mark, Buckland, Paul Robert, Owen, Michael John and O'Donovan, Michael Conlon 2000. Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools. Human Genetics 107 (5) , pp. 488-493. 10.1007/s004390000397

Hurelbrink, C. B., Armstrong, R. J., Barker, R. A., Dunnett, S. B. and Rosser, Anne Elizabeth 2000. Hibernated human fetal striatal tissue: successful transplantation in a rat model of Huntington's disease. Cell Transplantation 9 (6) , pp. 743-749.

I

Isles, Anthony Roger and Wilkinson, Lawrence Stephen 2000. Imprinted genes, cognition and behaviour. Trends in Cognitive Sciences 4 (8) , pp. 309-318. 10.1016/S1364-6613(00)01504-7

J

Jacobsen, N. J., Franks, E. K., Craddock, Nicholas John and Owen, Michael John 2000. Genomic characterisation and mutational analysis of CUX2, a potential regulator of NCAM expression, mapping to chromosome 12q23-q24.1. American Journal of Medical Genetics 96 (4) , pp. 493-494.

Jamieson, E., Buttwell, M., Taylor, Pamela Jane and Leese, M. 2000. Trends in special (high-security) hospitals. 1: Referrals and admissions. British Journal of Psychiatry 176 , pp. 253-259. 10.1192/bjp.176.3.253

Jamieson, Elizabeth, Davison, Sophie and Taylor, Pamela Jane 2000. Reconviction of special (high security) hospital patients with personality disorder: its relationship with route of discharge and time at risk. Criminal Behaviour and Mental Health 10 (2) , pp. 88-99. 10.1002/cbm.348

Jones, A. L., Sheen, N. J. L., North, R. V. and Morgan, James Edwards 2000. Reproducibility of the Humphrey Optical Coherence Tomography Scanner. Investigative Ophthalmology and Visual Science 41 (4) , S290-S290.

Jones, Ian Richard 2000. SES12.02 Genetics of puerperal psychosis. European Psychiatry 15 , s276-s276. 10.1016/S0924-9338(00)94198-1

Jones, Ian Richard, Middle, F., McCandless, F., Coyle, N., Robertson, E., Brockington, I., Lendon, C. and Craddock, Nicholas John 2000. Molecular genetic studies of bipolar disorder and puerperal psychosis at two polymorphisms in the estrogen receptor alpha gene (ESR 1). American Journal of Medical Genetics 96 (6) , pp. 850-853. 10.1002/1096-8628(20001204)96:6<850::aid-ajmg31>3.0.co;2-1

Jones, L. A., Cardno, A. G., Murphy, K. C., Sanders, R. D., Gray, M. Y., McCarthy, G., McGuffin, P., Owen, Michael John and Williams, Julie 2000. The kings schizotypy questionnaire as a quantitative measure of schizophrenia liability. Schizophrenia Research 45 (3) , pp. 213-221. 10.1016/S0920-9964(99)00183-8

Jones, Lesley, Herbert, D., Rutter, A. J., Dancer, J. E. and Harwood, J. L. 2000. Novel inhibitors of the condensing enzymes of the type II fatty acid synthase of pea (Pisum sativum). Biochemical Journal 347 (1) , pp. 205-209. 10.1042/bj3470205

Jonsson, E. G., Norton, N., Gustavsson, J. P., Oreland, L., Owen, Michael John and Sedvall, G. C. 2000. A promoter polymorphism in the monoamine oxidase A gene and its relationships to monoamine metabolite concentrations in CSF of healthy volunteers. Journal of Psychiatric Research 34 (3) , pp. 239-244. 10.1016/S0022-3956(00)00013-3

Joy, D. L. A., Shepherd, J. P. and Bisson, Jonathan Ian 2000. Randomised trial of early, brief psychological intervention to prevent Posttraumatic Stress Disorder following injury. Journal of Dental Research 79 , p. 607.

Joy, Deborah, Probert, Rachel, Bisson, Jonathan Ian and Shepherd, Jonathan Paul 2000. Post-traumatic stress reactions after injury. Journal of Trauma 48 (3) , pp. 490-494.

Joy, Diamond, Shepherd, Jonathan Paul and Bisson, Jonathan Ian 2000. Randomised trial of early, brief psychological intervention to prevent post traumatic stress disorder following injury. Journal of Dental Research 79 (1s) , p. 607.

K

Kent, L., Green, E., Fitzgerald, M., Hawi, Z., Gill, M., Thapar, Anita, Holmes, J., Asherson, P., Gould, A., Taylor, E., Payton, T. and Craddock, Nicholas John 2000. Nicotinic acetylcholine receptor 7 subunit gene and attention deficit hyperactivity disorder. American Journal of Medical Genetics 96 (4) , p. 490.

Kerr, Michael Patrick and Grp, EG 2000. Developing international guidelines for the management of the adult with epilepsy and intellectual disability: Towards a framework for care. Journal of Intellectual Disability Research 44 , pp. 344-345.

Kerr, Michael Patrick, Merrick, J. and Crowther, M. 2000. An international database for the management of epilepsy in people with an intellectual disability: EUROPIE-ID. Journal of Intellectual Disability Research 44 , p. 345.

Kerr, Michael Patrick and Merrick, Joav 2000. A review of the use of Topiramate in people with intellectual disability. International Journal of Adolescent Medicine and Health 12 (Supple) , pp. 87-102. 10.1515/IJAMH.2000.12.S1.87

Khastgir, S. P., Pocklington, Andrew and Sasaki, R. 2000. Quantum Calogero-Moser models: integrability for all root systems. Journal of Physics A: Mathematical and General 33 (49) , pp. 9033-9064. 10.1088/0305-4470/33/49/303

Kington, J. M., Jones, L. A., Watt, A. A., Hopkin, E. J. and Williams, Julie 2000. Impaired eye expression recognition in schizophrenia. Journal of Psychiatric Research 34 (4-5) , pp. 341-347.

Kirov, George, Nikolov, I., Milanova, V., Roglev, M. and Jivkov, L. 2000. Comparison between clinical and demographic characteristics of bipolar patients collected in two different countries. American Journal of Medical Genetics 96 (4) , p. 506.

Kirov, George, Stephens, M. and Owen, Michael John 2000. Examining the 4p16 region for association with bipolar disorder using DNA pooling. American Journal of Medical Genetics 96 (4) , p. 548.

Kirov, George, Stephens, M., Williams, Nigel Melville, O'Donovan, Michael Conlon and Owen, Michael John 2000. Automated genotyping of single-nucleotide polymorphisms by extension of fluorescently labelled primers: analysis of individual and pooled DNA samples. Balkan Journal of Medical Genetics 3 , pp. 23-28.

Kirov, George, Williams, Nigel Melville, Sham, P., Craddock, Nicholas John and Owen, Michael John 2000. Pooled genotyping of microsatellite markers in parent-offspring trios. Genome Research 10 (1) , pp. 105-115.

L

Levinson, D. F., Holmans, Peter Alan, Straub, R. E., Owen, Michael John, Wildenauer, D. B., Gejman, P. V., Pulver, A. E., Laurent, C., Kendler, K. S., Walsh, D., Norton, N., Williams, Nigel Melville, Schwab, S. G., Lerer, B., Mowry, B. J., Sanders, A. R., Antonarakis, S. E., Blouin, J. L., DeLeuze, J. F. and Mallet, J. 2000. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III. American Journal of Human Genetics 67 (3) , pp. 652-663. 10.1086/303041

Loh, Nellie Y., Newey, Sarah E., Davies, Kay E. and Blake, Derek J. 2000. Assembly of multiple dystrobrevin-containing complexes in the kidney. Journal of Cell Science 113 (15) , pp. 2715-2724.

M

McCarthy, G. M., Cardno, A. G., Jones, L. A., Murphy, K. C., Sanders, R. D., Gray, M. Y., McGuffin, P. and Owen, Michael John 2000. Investigating familiality of subtypes in schizophrenia. American Journal of Medical Genetics 96 (4) , pp. 473-474.

Middle, F., Jones, Ian Richard, McCandless, F., Barrett, T., Khanim, F., Owen, Michael John, Lendon, C. and Craddock, Nicholas John 2000. Bipolar disorder and variation at a common polymorphism (A1832G) within exon 8 of the Wolfram gene. American Journal of Medical Genetics 96 (2) , pp. 154-157. 10.1002/(sici)1096-8628(20000403)96:2%3C154::aid-ajmg5%3E3.0.co;2-f

Middle, Fiona, Jones, Ian, Robertson, Emma, Lendon, Corinne and Craddock, Nicholas John 2000. Tumour necrosis factor [alpha] and bipolar affective puerperal psychosis. Psychiatric Genetics 10 (4) , pp. 195-198. 10.1097/00041444-200010040-00008

Millar, David Stuart, Elliston, L., Deex, P., Krawczak, M., Wacey, A. I., Reynaud, J., Nieuwenhuis, H. K., Bolton-Maggs, P., Mannucci, P. M., Reverter, J. C., Cachia, P., Pasi, K. J., Layton, D. M. and Cooper, David Neil 2000. Molecular analysis of the genotype-phenotype relationship in factor X deficiency. Human Genetics -Berlin- 106 (2) , pp. 249-257. 10.1007/s004390051035

Morgan, Christopher L., Ahmed, Z. and Kerr, Michael Patrick 2000. Health care provision for people with a learning disability. Record-linkage study of epidemiology and factors contributing to hospital care uptake. British Journal of Psychiatry 176 , pp. 37-41. 10.1192/bjp.176.1.37

Morgan, Christopher L., Ahmed, Z. and Kerr, Michael Patrick 2000. Social deprivation and prevalence of epilepsy and associated health usage. Journal of Neurology, Neurosurgery & Psychiatry 69 (1) , pp. 13-17. 10.1136/jnnp.69.1.13

Morgan, Christopher L., Ahmed, Z. and Kerr, Michael Patrick 2000. Social deprivation and prevalence of epilepsy and associated health usage - The authors reply. Journal of Neurology, Neurosurgery & Psychiatry 69 (6) , p. 838.

Morris, D. W., Robinson, L., Turic, D., Duke, M., Webb, V., Milham, C., Hopkin, E., Pound, K., Fernando, S., Easton, M., Hamshere, Marian Lindsay, Williams, Nigel Melville, McGuffin, P., Stephenson, Jessica, Krawczak, M., Owen, Michael John, O'Donovan, Michael and Williams, Julie 2000. Family-based association mapping provides evidence for a gene for reading disability on chromosome 15q. Human Molecular Genetics 9 (5) , pp. 843-848. 10.1093/hmg/9.5.843

Murphy, K. C. and Owen, Michael John 2000. Evidence for association between polymorphisms of the catechol-O-methyltransferase (COMT) and monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome. American Journal of Medical Genetics 96 (4) , p. 476.

Murphy, K. C., Williams, Nigel Melville, Cardno, A. G., Jones, L. A., Holmans, Peter Alan, Thompson, P., Thonas, N., McGuffin, P. and Owen, Michael John 2000. Chromosome 22q, velo-cardio-facial syndrome (VCFS) and schizophrenia. Journal of Medical Genetics 37 , S58-S58.

Murphy, K.C., Jones, L.A. and Owen, Michael John 2000. High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS). Schizophrenia Research 41 (1) , p. 29. 10.1016/S0920-9964(00)90364-5

Murphy, K.C. and Owen, Michael John 2000. No association between polymorphisms of catechol-o-methyltransferase (COMT) or monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome. Schizophrenia Research 41 (1) , p. 96. 10.1016/S0920-9964(00)90531-0

Myers, A., Holmans, Peter Alan, Marshall, H., Kwon, J., Meyer, D., Ramic, D., Shears, S., Booth, J., DeVrieze, F. W., Crook, R., Hamshere, Marian Lindsay, Abraham, R., Tunstall, N., Rice, Frances, Carty, S., Lillystone, S., Kehoe, P., Rudrasingham, V., Jones, Lesley, Lovestone, S., Perez-Tur, J., Williams, Julie, Owen, Michael John, Hardy, J. and Goate, A. M. 2000. Susceptibility locus for Alzheimer's disease on chromosome 10. Science 290 (5500) , pp. 2304-2305. 10.1126/science.290.5500.2304

N

Neuman, R. J., Saccone, N. L., Holmans, Peter Alan, Rice, J. P. and Sun, L. 2000. Clustering methods applied to allele sharing data. Genetic Epidemiology 19 (1) , pp. 57-63. 10.1002/1098-2272(2000)19:1+<::AID-GEPI9>3.0.CO;2-D

Newey, Sarah E., Benson, Matthew A., Ponting, Chris P., Davies, Kay E. and Blake, Derek J. 2000. Alternative splicing of dystrobrevin regulates the stoichiometry of syntrophin binding to the dystrophin protein complex. Current Biology 10 (20) , pp. 1295-1298. 10.1016/S0960-9822(00)00760-0

Newlin, D. B., Miles, D. R., van den Bree, Marianne Bernadette, Gupman, A. E. and Pickens, R. W. 2000. Environmental transmission of DSM-IV substance use disdorders in adoptive and step families. Alcoholism-Clinical and Experimental Research 24 (12) , pp. 1785-1794. 10.1111/j.1530-0277.2000.tb01982.x

O

O'Mahony, E., Corvin, A., O'Connell, R., Comerford, C., Larsen, B., Jones, Ian Richard, McCandless, F., Kirov, George, Craddock, Nicholas John and Gill, M. J. 2000. Clinical similarities in siblings with bipolar disorder. American Journal of Medical Genetics 96 (4) , p. 514.

Oretti, R. G., Bano, S., Azani, M. O., Badawy, A. A. -B., Morgan, C. J., McGuffin, P. and Buckland, Paul Robert 2000. Rat liver tryptophan pyrrolase activity and gene expression during alcohol withdrawal. Alcohol and Alcoholism 35 (5) , pp. 427-434. 10.1093/alcalc/35.5.427

Owen, Michael John 2000. Molecular genetic studies of schizophrenia. Brain research. Brain research reviews 31 (2-3) , pp. 179-186. 10.1016/S0165-0173(99)00035-1

Owen, Michael John, Cardno, A. G. and O'Donovan, Michael Conlon 2000. Psychiatric genetics: back to the future. Molecular Psychiatry 5 (1) , pp. 22-31. 10.1038/sj.mp.4000702

P

Paolillo, A., Pozzilli, C., Gasperini, C., Giugni, E., Mainero, C., Giuliani, S, Tomassini, Valentina, Millefiorini, E. and Bastianello, S. 2000. Brain atrophy in relapsing-remitting multiple sclerosis: relationship with 'black holes', disease duration and clinical disability. Journal of the Neurological Sciences 174 (2) , pp. 85-91.

Payton, A., Holmes, J., Barrett, J., Hever, T., Fitzpatrick, H., Trumper, A., Harrington, R., McGuffin, P., Owen, Michael John, Ollier, W., Worthington, J. and Thapar, Anita 2000. A family based candidate gene association study of Attention Deficit Hyperactivity Disorder. American Journal of Medical Genetics 96 (4) , p. 489.

Perry, Jonathan, Lowe, Kathy, Felce, David John and Jones, Susan 2000. Characteristics of staffed community housing services for people with learning disabilities: a stratified random sample of statutory, voluntary and private agency provision. Health and Social Care in the Community 8 (5) , pp. 307-315. 10.1046/j.1365-2524.2000.00255.x

R

Rees, M. I., Lewis, T. M., Mortier, G., Snell, R. G., Schofield, P. R. and Owen, Michael John 2000. A transient hyperekplexia phenotype associated with compound heterozygote mutations in the human beta-subunit of the inhibitory glycine receptor (GLRB). American Journal of Human Genetics 67 (4) , p. 391.

Rees, M. I., Watts, P., Fenton, I., Clarke, A., Snell, R. G., Owen, Michael John and Gray, J. 2000. Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3). Human Genetics 106 (2) , pp. 206-209. 10.1007/s004390051029

Robertson, E., Jones, Ian Richard, Benjamin, J., Murdoch, C., Pelios, G., Brockington, I. and Craddock, Nicholas John 2000. Approaches to the ascertainment, recruitment and clinical assessment of women with puerperal psychosis. Archives of Women's Mental Health 3 (2) , p. 59. 10.1007/s007370070007

Robertson, Neil 2000. Enumerating neurology. Brain 123 (4) , pp. 663-664. 10.1093/brain/123.4.663

Rosser, Anne Elizabeth 2000. Stem cell research--will further work be permitted? NeuroReport 11 (18) , A15.

Rosser, Anne Elizabeth, Ostendeld, T. and Svendsen, C. N. 2000. Invited commentary: treatment of diseases of the central nervous system using encapsulated cells, by A. F. Hottinger and P. Aebischer (Advances and Technical Standards in Neurosurgery vol. 25). Advances and technical standards in neurosurgery 26 , pp. 125-128.

Rosser, Anne Elizabeth, Tyers, P. and Dunnett, S. B. 2000. The morphological development of neurons derived from EGF- and FGF-2-driven human CNS precursors depends on their site of integration in the neonatal rat brain. European Journal of Neuroscience 12 (7) , pp. 2405-2413. 10.1046/j.1460-9568.2000.00135.x

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Schalock, R., Brown, R. T., Cummins, R., Mattkka, L, Felce, David John and Brown, I. 2000. Conceptualization, measurement and application of the concept of quality of life: a consensus document symposium. Presented at: New Millennium Research to Practice - Conference Abstracts: 11th World Congress of the International Association for the Scientific Study of Intellectual Disabilities (IASSID),, Seattle, Washington, USA, 1-6 August 2000. New Millennium Research to Practice - Conference Abstracts: 11th World Congress of the International Association for the Scientific Study of Intellectual Disabilities (IASSID), 1-6 August 2000 Seattle, Washington, USA. New Millennium Research to Practice - Conference Abstracts: 11th World Congress of the International Association for the Scientific Study of Intellectual Disabilities (IASSID) , vol. 3-4. Journal of Intellectual Disability Research: Wiley-Blackwell, p. 452. 10.1046/j.1365-2788.2000.d01-124.x

Sham, P. C., Sterne, A., Purcell, S., Cherny, S., Webster, M., Rijsdijk, F., Asherson, P., Ball, D., Craig, I., Eley, T., Goldberg, D., Gray, J., Mann, A., Owen, Michael John and Plomin, R. 2000. GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings. Twin Research 3 (4) , pp. 316-322. 10.1375/136905200320565292

Shearn, Julia, Beyer, Stephen Richard and Felce, David John 2000. The cost-effectiveness of supported employment for people with severe intellectual disabilities and high support needs: a pilot study. Journal of Applied Research in Intellectual Disabilities 13 (1) , pp. 29-37. 10.1046/j.1468-3148.2000.00005.x

Snell, R. G., Miller, J., Owen, Michael John and Rees, M. I. 2000. Genomic structure of postsynaptic organizational protein, Gephyrin, and mutation analysis in hyperekplexia and startle phenotypes. American Journal of Human Genetics 67 (4) , p. 385.

Speight, G., Turic, Dragana, Austin, Jehannine, Hoogendoorn, Bastiaan, Cardno, Alistair, Jones, L., Murphy, K. C., Sanders, R., McCarthy, G., Jones, Ian Richard, McCandless, F., McGuffin, P., Craddock, Nicholas John, Owen, Michael John, Buckland, Paul Robert and O'Donovan, Michael Conlon 2000. Comparative sequencing and association studies of aromatic L-amino acid decarboxylase in schizophrenia and bipolar disorder. Molecular Psychiatry 5 (3) , pp. 327-331. 10.1038/sj.mp.4000717

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Taylor, Pamela Jane 2000. Balancing policy development and research evidence: are we falling short? Acta Psychiatrica Scandinavica 102 (1) , pp. 1-2. 10.1034/j.1600-0447.2000.102001001.x

Thapar, Anita, Harrington, R. and McGuffin, P. 2000. Examining the genetic basis of ADHD related behaviours and conduct problems. American Journal of Medical Genetics 96 (4) , p. 470.

Thapar, Anita, Harrington, R., Ross, K. and McGuffin, P. 2000. Does the definition of ADHD affect heritability? Journal of the American Academy of Child & Adolescent Psychiatry 39 (12) , pp. 1528-1536. 10.1097/00004583-200012000-00015

Todd, Stuart Philip, Felce, David John, Beyer, Stephen Richard, Shearn, Julia, Perry, Jonathan and Kilsby, Mark Stephen 2000. Strategic planning and progress under the All Wales Strategy: reflecting the perceptions of stakeholders. Journal of Intellectual Disability Research 44 (1) , pp. 31-44. 10.1046/j.1365-2788.2000.00248.x

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Tunstall, N., Owen, Michael John, Williams, Julie, Rice, Frances, Carty, S., Lillystone, S., Fraser, L., Kehoe, P., Neill, D., Rudrasingham, V., Sham, P. and Lovestone, S. 2000. Familial influence on variation in age of onset and behavioural phenotype in Alzheimer's disease. British Journal of Psychiatry 176 , pp. 156-159. 10.1192/bjp.176.2.156

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Van Amelsvoort, T., Daly, E., Critchley, H., Robertson, D., Henry, D., Suckling, J., Owen, Michael John, Murphy, K. C. and Murphy, D. G. M. 2000. Brain abnormalities associated with deletions at 22q11: Implicatons for psychosis. American Journal of Medical Genetics 96 (4) , p. 551.

van Amelsvoort, T., Daly, E., Critchley, H., Robertson, D., Henry, J. C., Suckling, J., Owen, Michael John, Murphy, K. C. and Murphy, D. G. M. 2000. Brain abnormalities associated with deletions at 22q11: Implications for psychosis. Journal of Medical Genetics 37 , S26-S26.

Vincent, John B., Qiu-Ping, Yuan, Schalling, Martin, Adolfsson, R., Azevedo, M. Helena, Macedo, Antonio, Bauer, Amy, Dalla Torre, Camille, Medeiros, Helena M., Pato, Carlos N., Bowen, Timothy, Guy, Carol, Owen, Michael John, O'Donovan, Michael Conlon, Paterson, Andrew D., Petronis, Arturas and Kennedy, James L. 2000. Long repeat tracts at SCA8 in major psychosis. American Journal of Medical Genetics 96 (6) , pp. 873-876. 10.1002/1096-8628(20001204)96:6<873::AID-AJMG37>3.0.CO;2-9

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Walters, S. E., Williams, Nigel Melville, Spurlock, Gillian, Sanders, R. D., McCarthy, G. M., Cardno, A. G. and Owen, Michael John 2000. Identification of a polymorphism in the human NURR1 gene and investigation of an association with schizophrenia. American Journal of Medical Genetics 96 (4) , p. 535.

Watkins, L. H. A., Rogers, R. D., Lawrence, Andrew David, Sahakian, B. J., Rosser, Anne Elizabeth and Robbins, T. W. 2000. Impaired planning but intact decision making in early Huntington's disease: implications for specific fronto-striatal pathology. Neuropsychologia 38 (8) , pp. 1112-1125. 10.1016/S0028-3932(00)00028-2

Watts, Patrick, Rees, Mark I., Clarke, Angus John, Beck, Lyn, Lane, Carol M., Owen, Michael John and Gray, Jonathon 2000. Linkage analysis in an autosomal dominant 'zonular nuclear pulverulent' congenital cataract, mapped to chromosome 13q11-13. Eye 14 (2) , pp. 172-175. 10.1038/eye.2000.48

This list was generated on Thu Nov 14 11:23:14 2019 GMT.