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Number of items: 128.

A

Abraham, Richard, Myers, Amanda, Wavrant-DeVrieze, Fabienne, Hamshere, Marian Lindsay, Thomas, Hollie Victoria, Marshall, Helen, Compton, Danielle, Spurlock, Gillian, Turic, Dragana, Hoogendoorn, Bastiaan, Kwon, Jennifer M., Petersen, Ronald C., Tangalos, Eric, Norton, Joanne, Morris, John C., Bullock, Roger, Liolitsa, Danae, Lovestone, Simon, Hardy, John, Goate, Alison, O'Donovan, Michael Conlon, Williams, Julie, Owen, Michael John and Jones, Lesley 2001. Substantial linkage disequilibrium across the insulin-degrading enzyme locus but no association with late-onset Alzheimer's disease. Human Genetics 109 (6) , pp. 646-652. 10.1007/s00439-001-0614-1

Armstrong, R. J., Harrower, T. P., Hurelbrink, C. B., McLaughin, M., Ratcliffe, E. L., Tyers, P., Richards, A, Dunnett, S. B., Rosser, Anne Elizabeth and Barker, R. A. 2001. Porcine neural xenografts in the immunocompetent rat: immune response following grafting of expanded neural precursor cells. Neuroscience 106 (1) , pp. 201-216. 10.1016/S0306-4522(01)00273-1

Armstrong, R. J., Rosser, Anne Elizabeth, Dunnett, S. B. and Barker, R. A. 2001. Neural stem cell technology as a novel treatment for Parkinson's disease. Methods in molecular medicine 62 , pp. 289-307. 10.1385/1-59259-142-6:289

Ashcroft, R., Fraser, William, Kerr, Michael Patrick and Ahmed, Z. 2001. Are antipsychotic drugs the right treatment for challenging behaviour in learning disability?: The place of a randomised trial. J Med Ethics 27 (5) , pp. 338-343.

B

Barker, R. A. and Rosser, Anne Elizabeth 2001. Neural transplantation therapies for Parkinson's and Huntington's diseases. Drug Discovery Today 6 (11) , pp. 575-582. 10.1073/pnas.0904239106

Benson, Matthew A., Newey, Sarah E., Martin-Rendon, Enca, Hawkes, Richard and Blake, Derek J. 2001. Dysbindin, a novel coiled-coil-containing protein that interacts with the dystrobrevins in muscle and brain. Journal of Biological Chemistry 276 (26) , pp. 24232-24241. 10.1074/jbc.M010418200

Berrios, G. E., Wagle, A. C., Markova, I. S., Wagle, S. A., Ho, L. W., Rubinsztein, D. C., Whittaker, J., Ffrench-Constant, C., Kershaw, A., Rosser, Anne Elizabeth, Bak, T. and Hodges, J. R. 2001. Psychiatric symptoms and CAG repeats in neurologically asymptomatic Huntington's disease gene carriers. Psychiatry Research 102 (3) , pp. 217-215.

Blake, Derek J, Brockington, M, Muntoni, F and Benson, M. A. 2001. Golgi-localisation of fukutin and fukutin-related protein: implications for muscular dystrophy. Molecular Biology of the Cell 12 , 85A-85A.

Bowen, Timothy, Williams, Nigel Melville, Norton, Nadine, Spurlock, G., Wittekindt, O. H., Morris-Rosendahl, D. J., Williams, Hywel John, Brzustowicz, L., Hoogendoorn, Bastiaan, Zammit, Stanley, Jones, G, Sanders, Rebecca, Jones, L. A., McCarthy, G., Jones, S., Bassett, A., Cardno, A. G., Owen, Michael John and O'Donovan, Michael Conlon 2001. Mutation screening of the KCNN3 gene reveals a rare frameshift mutation [Letter]. Molecular Psychiatry 6 (3) , pp. 259-260. 10.1038/sj.mp.4000128

Braddock, David, Emerson, Eric, Felce, David John and Stancliffe, Roger J. 2001. Living circumstances of children and adults with mental retardation or developmental disabilities in the United States, Canada, England and Wales, and Australia. Mental Retardation and Developmental Disabilities Research Reviews 7 (2) , pp. 115-121. 10.1002/mrdd.1016

Bray, Nicholas John and Owen, Michael John 2001. Searching for schizophrenia genes. Trends in Molecular Medicine 7 (4) , pp. 169-174.

Brickington, M., Blake, Derek J., Prandini, P., Brown, S. C., Torelli, S., Benson, M. A., Ponting, C.P., Estournet, B., Romero, N., Voit, T., Sewry, C. A., Guincheney, P. and Muntoni, F. 2001. A novel glycosyltransferase is mutated in a form of congenital muscular dystrophy with secondary laminin alpha 2 deficiency and abnormal glycosylation of alpha-dystroglycan. American Journal of Human Genetics 69 (4) , p. 229.

Brockington, Martin, Blake, Derek J., Prandini, Paola, Brown, Susan C., Torelli, Silvia, Benson, Matthew A., Ponting, Chris P., Estournet, Brigitte, Romero, Norma B., Mercuri, Eugenio, Voit, Thomas, Sewry, Caroline A., Guicheney, Pascale and Muntoni, Francesco 2001. Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin 2 deficiency and abnormal glycosylation of -dystroglycan. American Journal of Human Genetics 69 (6) , pp. 1198-1209. 10.1086/324412

Brockington, Martin, Prandini, P., Brown, Susan C., Sewry, Caroline A., Blake, Derek J. and Muntoni, Francesco 2001. A new gene encoding a fukutin-like protein and its analysis in patients with congenital muscular dystrophy [Abstract]. Neuromuscular Disorders 11 (6-7) , p. 635.

Buckland, Paul Robert 2001. Genetic association studies of alcoholism--problems with the candidate gene approach. Alcohol and Alcoholism 36 (2) , pp. 99-103. 10.1093/alcalc/36.2.99

C

Campbell, L. E., Stevens, A. F., Morris, R., Karmiloff-Smith, A., Siminoff, E., Owen, Michael John, Murphy, D. G. M. and Murphy, K. C. 2001. Neuropsychological profile of children with Velo-cardio-facial syndrome (VCFS). Journal of Medical Genetics 38 , S39-S39.

Campbell, S. M., Hann, M., Hacker, J., Burns, C., Oliver, D., Thapar, Ajay Kumar, Mead, N., Safran, D. G. and Roland, M. O. 2001. Identifying predictors of high quality care in English general practice: observational study. BMJ 323 (7316) , pp. 784-787. 10.1136/bmj.323.7316.784

Caseras, Xavier, Torrubia, R. and Farré, J. M. 2001. Is the Behavioural Inhibition System the core vulnerability for cluster C personality disorders? Personality and Individual Differences 31 (3) , pp. 349-359. 10.1016/S0191-8869(00)00141-0

Chadsey, Janis and Beyer, Stephen Richard 2001. Social relationships in the workplace. Mental Retardation and Developmental Disabilities Research Reviews 7 (2) , pp. 128-133. 10.1002/mrdd.1018

Chataway, J, Mander, A, Robertson, Neil, Sawcer, S, Deans, J, Fraser, M, Broadley, S, Clayton, D and Compston, A 2001. Multiple sclerosis in sibling pairs: an analysis of 250 families. Journal of Neurology, Neurosurgery and Psychiatry 71 (6) , pp. 757-761. 10.1136/jnnp.71.6.757

Corvin, A., O'Mahony, E., O'Regan, M., Comerford, C., O'Connell, R., Craddock, Nicholas John and Gill, M. 2001. Cigarette smoking and psychotic symptoms in bipolar affective disorder. British Journal of Psychiatry 179 (1) , pp. 35-38. 10.1192/bjp.179.1.35

Coyle, N. E., Lambert, J. C., Middle, F., Robertson, E., Jones, Ian Richard, Craddock, Nicholas John and Lendon, C. 2001. Is the estrogen regulated expression of the serotonin transporter gene modulated by the VNTR polymorphism: A possible mechanism for increased risk for bipolar affective puerperal psychosis? American Journal of Medical Genetics 105 (7) , p. 619.

Craddock, Nicholas John, Dave, Subodh and Greening, Jayne 2001. Association studies of bipolar disorder. Bipolar Disorders 3 (6) , pp. 284-298. 10.1034/j.1399-5618.2001.30604.x

Craddock, Nicholas John and Jones, Ian Richard 2001. Molecular genetics of bipolar disorder. British Journal of Psychiatry 178 (41) , pp. 128-133. 10.1192/bjp.178.41.s128

Crawford, P., Brown, S., Kerr, Michael Patrick and David, Parke Clinical Trials 2001. A randomized open-label study of gabapentin and lamotrigine in adults with learning disability and resistant epilepsy. Seizure - European Journal of Epilepsy 10 (2) , pp. 107-115. 10.1053/seiz.2000.0474

D

Davies, William, Isles, Anthony Roger and Wilkinson, Lawrence Stephen 2001. Imprinted genes and mental dysfunction. Annals of Medicine 33 (6) , pp. 428-436. 10.3109/07853890108995956

Davison, S., Leese, M. and Taylor, Pamela Jane 2001. Examination of the screening properties of the personality diagnostic questionnaire 4+ (PDQ-4+) in a prison population. Journal of Personality Disorders 15 (2) , pp. 180-194. 10.1521/pedi.15.2.180.19212

Davison, Sophie and Taylor, Pamela Jane 2001. Psychological distress and severity of personality disorder symptomatology in prisoners convicted of violent and sexual offences. Psychology, Crime & Law 7 (1-4) , pp. 263-273. 10.1080/10683160108401797

Di Salle, Francesco, Formisano, Elia, Seifritz, Erich, Linden, David Edmund Johannes, Scheffler, Klaus, Saulino, Claudio, Tedeschi, Gioacchino, Zanella, Friedhelm E., Pepino, Alessandro, Goebel, Rainer and Marciano, Elio 2001. Functional fields in human auditory cortex revealed by time-resolved fMRI without interference of EPI noise. Neuroimage 13 (2) , pp. 328-338. 10.1006/nimg.2000.0683

E

Elvidge, Gareth, Jones, Ian Richard, McCandless, Fiona, Asherson, Phil, Owen, Michael John and Craddock, Nicholas John 2001. Allelic variation of aBalI polymorphism in the DRD3 gene does not influence susceptibility to bipolar disorder: Results of analysis and meta-analysis. American Journal of Medical Genetics 105 (4) , pp. 307-311. 10.1002/ajmg.1353

F

Felce, David John and Emerson, Eric 2001. Living with support in a home in the community: Predictors of behavioral development and household and community activity. Mental Retardation and Developmental Disabilities Research Reviews 7 (2) , pp. 75-83. 10.1002/mrdd.1011

Felce, David John and Emerson, Eric 2001. Overview: Community living. Mental Retardation and Developmental Disabilities Research Reviews 7 (2) , pp. 73-74. 10.1002/mrdd.1010

Felce, David John, Lowe, K., Beecham, J. and Hallam, A. 2001. 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 (vol 25, pg 307, 2000). Journal of Intellectual and Developmental Disability 26 (1) , p. 109.

Feng, J., Craddock, Nicholas John, Jones, Ian Richard, Cook, E. H. Jr, Goldman, D., Heston, L. L., Peltonen, L., DeLisi, L. E. and Sommer, S. S. 2001. Systematic screening for mutations in the glycine receptor alpha2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseases. Psychiatric Genetics 11 (1) , pp. 45-48.

Feng, J., Zheng, J., Gelernter, J., Kranzler, H., Cook, E., Goldman, D., Jones, Ian Richard, Craddock, Nicholas John, Heston, L. L., Delisi, L., Peltonen, L., Bennett, W. P. and Sommer, S. S. 2001. An in-frame deletion in the alpha2C adrenergic receptor is common in African-Americans. Molecular Psychiatry 6 (2) , pp. 168-172. 10.1038/sj.mp.4000817

Feng, Jinong, Craddock, Nicholas John, Jones, Ian R., Cook, Edwin H., Goldman, David, Heston, Leonard L., Peltonen, Leena, DeLisi, Lynn E. and Sommer, Steve S. 2001. Systematic screening for mutations in the glycine receptor alpha2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseases. Psychiatric Genetics 11 (1) , pp. 45-48. 10.1097/00041444-200103000-00009

Feng, Jinong, Yan, Jin, Michaud, Shawneen, Craddock, Nicholas John, Jones, Ian Richard, Cook, Edwin H., Goldman, David, Heston, Leonard L., Peltonen, Leena, Delisi, Lynn E. and Sommer, Steve S. 2001. Scanning of estrogen receptor α (ERα) and thyroid hormone receptor α (TRα) genes in patients with psychiatric diseases: Four missense mutations identified in ERα gene. American Journal of Medical Genetics 105 (4) , pp. 369-374. 10.1002/ajmg.1364

G

Green, Elaine Karen, Elvidge, G., Jones, Ian Richard, Owen, Michael John and Craddock, Nicholas John 2001. Mutational analysis of 2 positional candidate susceptibility genes for bipolar disorder: PAH and LHX5. American Journal of Medical Genetics 105 (7) , pp. 610-611.

H

Hamshere, Marian Linsday, Giles, Peter, Krawczak, M. and Owen, Michael John 2001. Statistical analysis of genotypic association data with HAPMAXII. AMERICAN JOURNAL OF HUMAN GENETICS 69 (4) , p. 390.

Harper, Peter, Evans, R, Elliston, Linda, Ironside, J. W., Jones, Lesley and Lazarou, L. 2001. Huntington's disease intermediate allele and new variant CJD. American Journal of Human Genetics 69 (4) , p. 547.

Hatton, Chris, Emerson, Eric, Robertson, Janet, Gregory, Nicola, Kessissoglou, Sophie, Perry, Jonathan, Felce, David John, Lowe, Kathy, Noonan Walsh, Patricia and Linehan, Christine 2001. The adaptive behavior scale-residential and community (part I): towards the development of a short form. Research in Developmental Disabilities 22 (4) , pp. 273-288. 10.1016/S0891-4222(01)00072-5

Heron, J., Jones, L., Jones, Ian Ricahrd, McCandless, F. and Craddock, Nicholas John 2001. Specificity of schizotypal traits: Findings from a Bipolar sample. American Journal of Medical Genetics 105 (7) , p. 607.

Hillier, C. and Robertson, Neil 2001. Practical management of headache in primary care medicine. British Journal of Hospital Medicine 62 (11) , pp. 634-641.

Holmans, Peter Alan 2001. Likelihood-ratio affected sib-pair tests applied to multiply affected sibships: issues of power and type I error rate. Genetic Epidemiology 20 (1) , pp. 44-56. 10.1002/1098-2272(200101)

Hupperts, R., Broadley, S., Mander, A., Clayton, D., Compston, D. A. and Robertson, Neil Patrick 2001. Patterns of disease in concordant parent-child pairs with multiple sclerosis. Neurology 57 (2) , pp. 290-295.

Hurelbrink, C. B., Armstrong, R. J., Luheshi, L. M., Dunnett, Stephen, Rosser, Anne Elizabeth and Barker, R. A. 2001. Death of dopaminergic neurons in vitro and in nigral grafts: reevaluating the role of caspase activation. Exp Neurol 171 (1) , pp. 46-58.

I

Isles, Anthony Roger 2001. Reversible regulation of mouse genes. Trends Genet 17 (8) , p. 441.

Isles, Anthony Roger 2001. When is a clone not a clone? Trends Genet 17 (8) , p. 441.

Isles, Anthony Roger, Baum, M. J., Ma, D., Keverne, E. B. and Allen, Nicholas Denby 2001. Urinary odour preferences in mice. Nature 409 (6822) , pp. 783-784. 10.1038/35057323

Isles, Anthony Roger, Baum, Michael J., Ma, Dan, Keverne, Eric B. and Allen, Nicholas Denby 2001. Genetic imprinting: urinary odour preferences in mice. Nature 409 (6822) , pp. 783-784. 10.1038/35057323

Isles, Anthony Roger, Ma, Dan, Milsom, Chloe, Skynner, Michael J., Cui, Wei, Clark, John, Keverne, Eric B. and Allen, Nicholas Denby 2001. Conditional ablation of neurones in transgenic mice. Journal of Neurobiology 47 (3) , pp. 183-193. 10.1002/neu.1026

J

Jacobsen, N. J. O., Franks, E. K. E., Elvidge, G., Jones, Ian Richard, McCandless, F., O'Donovan, Michael Conlon, Owen, Michael John and Craddock, Nicholas John 2001. Exclusion of the Darier's disease gene, ATP2A2, as a common susceptibility gene for bipolar disorder. Molecular Psychiatry 6 (1) , pp. 92-97. 10.1038/sj.mp.4000774

Jacobsen, Nick J. O., Elvidge, Gareth, Franks, Emily K. E., O'Donovan, Michael Conlon, Craddock, Nicholas John and Owen, Michael John 2001. CUX2, a potential regulator of NCAM expression: Genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder. American Journal of Medical Genetics 105 (3) , pp. 295-300. 10.1002/ajmg.1325

Jain, M., Armstrong, R. J., Barker, R. A. and Rosser, Anne Elizabeth 2001. Cellular and molecular aspects of striatal development. Brain Research Bulletin 55 (4) , pp. 553-540.

Jones, A. L., Aldebasi, Y. H., Drasdo, N., North, R. V. and Morgan, James Edwards 2001. Survival of the S-cone retinal pathway in normotensive glaucoma. Investigative Ophthalmology and Visual Science 42 (4) , S147-S147.

Jones, E., Felce, David John, Lowe, K., Bowley, C., Pagler, J., Gallagher, B. and Roper, A. 2001. Evaluation of the dissemination of active support training in staffed community residences. American Journal on Mental Retardation 106 (4) , pp. 344-358. 10.1352/0895-8017(2001)106<0344:EOTDOA>2.0.CO;2

Jones, Edwin, Felce, David John, Lowe, Kathy, Bowley, Clare, Pagler, Jane, Strong, Gwyneth, Gallagher, Barry, Roper, Adrian and Kurowska, Katrina 2001. Evaluation of the dissemination of active support training and training trainers. Journal of Applied Research in Intellectual Disabilities 14 (2) , pp. 79-99. 10.1046/j.1468-3148.2001.00064.x

Jones, Gaynor, Zammit, Stanley, Norton, Nadine, Hamshere, Marian Lindsay, Jones, S. J., Milham, C., Sanders, R. D., McCarthy, G. M., Jones, L. A., Cardno, Alastair G., Gray, M., Murphy, K. C. and Owen, Michael John 2001. Aggressive behaviour in patients with schizophrenia is associated with catechol-O-methyltransferase genotype. British Journal of Psychiatry 179 (4) , pp. 351-355. 10.1192/bjp.179.4.351

Jones, Ian Richard and Craddock, Nicholas John 2001. Candidate gene studies of bipolar disorder. Annals of Medicine 33 (4) , pp. 248-256. 10.3109/07853890108998753

Jones, Ian Richard and Craddock, Nicholas John 2001. Familiality of the puerperal trigger in bipolar disorder: results of a family study. American Journal of Psychiatry 158 (6) , pp. 913-917.

Jones, Ian Richard, Kent, L., Paul, M. and Craddock, Nicholas John 2001. Clinical implications of psychiatric genetics in the new millennium -- nightmare or nirvana? Psychiatric Bulletin 25 (4) , pp. 129-131. 10.1192/pb.25.4.129

Jones, Ian Richard, Lendon, C., Coyle, N., Robertson, E., Brockington, I. and Craddock, Nicholas John 2001. Molecular genetic approaches to puerperal psychosis. Progress in Brain Research 133 , pp. 321-331. 10.1016/S0079-6123(01)33024-8

Jones, Ian Richard, Robertson, E., Middle, F., Morey, J., Coyle, N., Lendon, C. L. and Craddock, Nicholas John 2001. Association between vulnerability to puerperal triggering in bipolar disorder and a common polymorphism in the COMT gene. American Journal Of Medical Genetics Part A 105 (7) , p. 570.

Jones, L .A., Jones, Ian Richard and Craddock, Nicholas John 2001. Efficient recruitment for molecular genetic studies of major psychiatric disorders. American Journal of Medical Genetics Part A 105 (7) , p. 644.

Jones, L. A., Cardno, A. G., Sanders, R. D., Owen, Michael John and Williams, Julie 2001. Sustained and selective attention as measures of genetic liability to schizophrenia. Schizophrenia Research 48 (2-3) , pp. 263-267.

Jones, Lesley, Duce, J., Elliston, Linda and Harper, Peter 2001. The involvement of transcriptional repressor proteins in Huntington's disease. Journal of Medical Genetics 38 (Suppl1) , S65-S65.

Jones, R. G., Morley-Canellas, J., Owen, Michael John and Murphy, K. C. 2001. Chromosome 22q11 deletions and severe learning disability [comment]. The British Journal of Psychiatry 179 (5) , pp. 466-467. 10.1192/bjp.179.5.466-a

Jurewicz, I, Owen, R.J, O'Donovan, Michael Conlon and Owen, Michael John 2001. Searching for susceptibility genes in schizophrenia. European Neuropsychopharmacology 11 (6) , pp. 395-398. 10.1016/S0924-977X(01)00116-X

K

Kent, L., Hardy, E., Hawzi, Z., Fitzgerald, M., Kirley, A., Gill, M. and Craddock, Nicholas John 2001. A significant association of serotonin transporter polymorphism haplotypes in attention deficit hyperactivity disorder (ADHD). Presented at: The IXth World Congress of Psychiatric Genetics, Saint Louis, Missouri, Saint Louis, Missouri, American Journal of Medical Genetics. Abstracts for the IXth World Congress of Psychiatric Genetics , vol. 7. Wiley, pp. 574-575. 10.1002/ajmg.1592

Kent, L., Hardy, E., Hawzi, Z., Fitzgerald, M., Kirley, A., Gill, M. and Craddock, Nicholas John 2001. A significant association of serotonin transporter polymorphism haplotypes in attention deficit hyperactivity disorder (ADHD). American Journal of Medical Genetics 105 (7) , pp. 574-575.

Kent, L., Middle, S., Hawi, Z., Fitzgerald, M., Gill, M., Feehan, C. and Craddock, Nicholas John 2001. Nicotinic acetylcholine receptor alpha4 subunit gene polymorphism and attention deficit hyperactivity disorder. Psychiatric Genetics 10 (2) , pp. 107-115.

Kent, Lindsey, Green, Elaine, Holmes, Jane, Thapar, Anita, Gill, Michael, Hawi, Ziarah, Fitzgerald, Michael, Asherson, Philip, Curran, Sarah, Mills, John, Payton, Anthony and Craddock, Nicholas John 2001. No association between CHRNA7 microsatellite markers and attention-deficit hyperactivity disorder. American Journal of Medical Genetics 105 (8) , pp. 686-689. 10.1002/ajmg.1553

Kent, Lindsey, Middle, Fiona, Hawi, Ziarah, Fitzgerald, Michael, Gill, Michael, Feehan, Cathy and Craddock, Nicholas John 2001. Nicotinic acetylcholine receptor [alpha]4 subunit gene polymorphism and attention deficit hyperactivity disorder. Psychiatric Genetics 11 (1) , pp. 37-40. 10.1097/00041444-200103000-00007

Kerr, Michael Patrick and Bowley, C. 2001. Evidence-based prescribing in adults with learning disability and epilepsy. Epilepsia 42 (1) , pp. 44-45. 10.1046/j.1528-1157.2001.00515.x

Kerr, Michael Patrick and Bowley, C. 2001. Multidisciplinary and multiagency contributions to care for those with learning disability who have epilepsy. Epilepsia 42 (1) , pp. 55-58. 10.1046/j.1528-1157.2001.00519.x

Kerr, Michael Patrick, Scheepers, M., Besag, F., Bowley, C., Brown, S., Espie, C., Foley, Joshua, Paul, Alison, Webb, J. O., Ahmed, Z., Baker, G., Betts, Thomas, Bjorkman, M., Cornaggia, C., Iivanainen, M., Wallace, R., Kaski, M., Koot, H., Marson, A., Mohammed, N., Prasher, V. and Visser, F. 2001. Clinical guidelines for the management of epilepsy in adults with an intellectual disability. SEIZURE EUROPEAN JOURNAL OF EPILEPSY 10 (6) , pp. 401-409.

Kirov, George, Lowry, C. A., Stephens, M., Oldfield, S., O'Donovan, Michael Conlon, Lightman, S. L. and Owen, Michael John 2001. Screening ABCG1, the human homologue of the Drosophila white gene, for polymorphisms and association with bipolar affective disorder. Molecular Psychiatry 6 (6) , pp. 671-677. 10.1038/sj.mp.4000899

Kirov, George, Stehens, M. and Owen, Michael John 2001. Screening of three candidate genes in the bipolar candidate region on chromosome 21q22.3. American Journal of Medical Genetics 105 (7) , p. 612.

L

Lawrence, Andrew David, Rosser, Anne Elizabeth and Sahakian, B. J. 2001. Cognition. In: Fawcett, J. W., Rosser, Anne Elizabeth and Dunnett, Stephen Bruce eds. Brain Damage, Brain Repair, Oxford: Oxford University Press, pp. 243-254. (10.1093/acprof:oso/9780198523376.003.0018)

Lázaro, Carlos, Caseras, Xavier, Whizar-Lugo, Victor M., Wenk, Roberto, Baldioceda, Fernando, Bernal, Rodrigo, Ovalle, Abdiel, Torrubia, Rafael and Baños, J. E. 2001. Psychometric properties of a Spanish version of the McGill pain questionnaire in several Spanish-speaking countries. The Clinical Journal of Pain 17 (4) , pp. 365-374. 10.1097/00002508-200112000-00012

Lendon, Corinne and Craddock, Nicholas John 2001. Is LBP-1c/CP2/LSF a disease-modifying gene for Alzheimer's disease? The Lancet 358 (9287) , pp. 1029-1030. 10.1016/S0140-6736(01)06228-6

Lendon, Corinne and Craddock, Nicholas John 2001. Susceptibility gene(s) for Alzheimer's disease on chromosome 10. Trends in Neurosciences 24 (10) , pp. 557-559. 10.1016/S0166-2236(00)01912-3

Liddell, M., Lovestone, S. and Owen, Michael John 2001. Advising relatives of risk of Alzheimer's disease - Authors' reply. British Journal of Psychiatry 179 (1) , pp. 73-74. 10.1192/bjp.179.1.73

Liddell, M. B., Lovestone, S. and Owen, Michael John 2001. Genetic risk of Alzheimer's disease: advising relatives. British Journal of Psychiatry 178 (1) , pp. 7-11. 10.1192/bjp.178.1.7

Loh, Nellie Y., Nebenius-Oosthuizen, Daniela, Blake, Derek J., Smith, Andrew J. H. and Davies, Kay E. 2001. Role of β-dystrobrevin in nonmuscle dystrophin-associated protein complex-like complexes in kidney and liver. Molecular and Cellular Biology 21 (21) , pp. 7442-7448. 10.1128/MCB.21.21.7442-7448.2001
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M

Marangi, P. Angelo, Forsayeth, John R., Mittaud, Peggy, Erb-Vögtli, Susanne, Blake, Derek J., Moransard, Martijn, Sander, Andreas and Fuhrer, Christian 2001. Acetylcholine receptors are required for agrin-induced clustering of postsynaptic proteins. The EMBO Journal 20 (24) , pp. 7060-7073. 10.1093/emboj/20.24.7060

McEntagart, M., Norton, N., Williams, H., Teare, M. D., Dunstan, Melanie, Baker, P., Houlden, H., Reilly, M., Wood, N., Harper, P. S., Futreal, P. A., Williams, Nigel Melville and Rahman, N. 2001. Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14. American Journal of Human Genetics 68 (5) , pp. 1270-1276. 10.1086/320122

Miles, D. R., van den Bree, Marianne Bernadette, Gupman, A. E., Newlin, D. B., Glantz, M. D. and Pickens, R. W. 2001. A twin study on sensation seeking, risk taking behavior and marijuana use. Drug and Alcohol Dependence 62 (1) , pp. 57-68. 10.1002/ajmg.b.32352

Mohan, D., Jamieson, E. and Taylor, Pamela Jane 2001. The use of trial leave for restricted special hospital patients. Criminal Behaviour and Mental Health 11 (1) , pp. 55-62. 10.1002/cbm.369

Mooslehner, K. A., Chan, P. M., Xu, W. M., Liu, L. Z., Smadja, C., Humby, Trevor, Allen, Nicholas Denby, Wilkinson, Lawrence Stephen and Emson, P. C. 2001. Mice with Very Low Expression of the Vesicular Monoamine Transporter 2 Gene Survive into Adulthood: Potential Mouse Model for Parkinsonism. Molecular and Cellular Biology 21 (16) , pp. 5321-5331. 10.1128/MCB.21.16.5321-5331.2001
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Morgan, Christopher L., Scheepers, M. I. A. and Kerr, Michael Patrick 2001. Mortality in patients with intellectual disability and epilepsy. Current Opinion in Psychiatry 14 (5) , pp. 471-475. 10.1097/00001504-200109000-00008

Murphy, K. C. and Owen, Michael John 2001. Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia. British Journal of Psychiatry 179 (5) , pp. 397-402. 10.1192/bjp.179.5.397

N

Newey, S. E., Gramolini, A. O., Wu, J., Holzfeind, P., Jasmin, B. J., Davies, K. E. and Blake, Derek J. 2001. A novel mechanism for modulating synaptic gene expression: differential localization of alpha-dystrobrevin transcripts in skeletal muscle. Molecular and Cellular Neuroscience 17 (1) , pp. 127-140. 10.1212/01.wnl.0000302174.08951.cf.

Newey, S. E., Howman, E. V., Ponting, C. P., Benson, M. A., Nawrotzki, R., Loh, N. Y., Davies, K. E. and Blake, Derek J 2001. Syncoilin, a novel member of the intermediate filament superfamily that interacts with alpha-dystrobrevin in skeletal muscle. Journal of Biological Chemistry 276 (9) , pp. 6645-6655. 10.1074/jbc.M008305200

Newey, Sarah E., Gramolini, Anthony O., Wu, Jun, Holzfiend, Paul, Jasmin, Bernard J., Davies, Kay E. and Blake, Derek J. 2001. A novel mechanism for modulating synaptic gene expression: differential localization of α-dystrobrevin transcripts in skeletal muscle. Molecular and Cellular Neuroscience 17 (1) , pp. 127-140. 10.1006/mcne.2000.0918

Newey, Sarah E., Howman, Emily V., Ponting, Chris P., Benson, Matthew A., Nawrotzki, Ralph, Loh, Nellie Y., Davies, Kay E. and Blake, Derek J. 2001. Syncoilin, a novel member of the intermediate filament superfamily that interacts with α-dystrobrevin in skeletal muscle. Journal of Biological Chemistry 276 (9) , pp. 6645-6655. 10.1074/jbc.M008305200

O

Owen, Michael John 2001. Simple and complex genetics of Alzheimer's disease. Journal of Medical Genetics 38 , S29-S29.

P

Paolillo, A., Bastianello, S., Tomassini, Valentina, Gasperini, C., Giugni, E., Mainero, C., Horsfield, M. A. and Pozzilli, C. 2001. MRI measures and clinical disability: A six-year follow up study in relapsing-remitting multiple sclerosis patients under interferon beta therapy. Neurology 56 (8) , A461-A461.

Pavese, N., Andrews, T. C., Brooks, D. J., Rosser, Anne Elizabeth, Barker, R. A., Dunnett, S. B., Sahakian, B. and Piccini, P. 2001. Huntington's disease progression measured with serial [11C]-raclopride PET and the UHDRS. Neurology 56 (8) , A385-A385.

Payton, A., Holmes, J., Barrett, J. H., Hever, T., Fitzpatrick, H., Trumper, A. L., Harrington, R., O'Donovan, Michael Conlon, Owen, Michael John, Ollier, W., Worthington, J. and Thapar, Anita 2001. Examining for association between candidate gene polymorphisms in the dopamine pathway and attention-deficit hyperactivity disorder: a family-based study. Neuroscience Letters 105 (5) , pp. 464-470. 10.1002/ajmg.1407

Payton, A., Holmes, J., Harrington, R., McGuffin, P., Owen, Michael John, Ollier, W., Worthington, J. and Thapar, Anita 2001. Susceptibility genes for a trait measure of attention deficit hyperactivity disorder: a pilot study in a non-clinical sample of twins. Psychiatry Research 105 (3) , 273 -278. 10.1016/S0165-1781(01)00342-0

Pickens, R. W., Preston, K. L., Miles, D. R., Gupman, A. E., Johnson, E. O., Newlin, D. B., Soriano, J., van den Bree, Marianne Bernadette and Umbricht, A. 2001. Family history influence on drug abuse severity and treatment outcome. Drug and Alcohol Dependence 61 (3) , pp. 261-270. 10.1016/S0376-8716(00)00146-0

Plomin, R., Hill, L., Craig, I. W., McGuffin, P., Purcell, S., Sham, P., Lubinski, D., Thompson, L. A., Fisher, P. J., Turic, D. and Owen, Michael John 2001. A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groups. Behaviour Genetics 31 (6) , pp. 497-509. 10.1023/A:1013385125887

R

Rakebrandt, F., Turner, J. M., Ansari, E. E., Smith, G. M., Jones, A. L., Erichsen, J. T., North, R. V. and Morgan, James Edwards 2001. Comparison of histological primate retinal nerve fibre layer and full retinal thickness using optical coherence tomography. Investigative Ophthalmology and Visual Science 42 (4) , S133-S133.

Rees, M. I., Baer, K., Ward, H., Coleman, Sharon Louise, Evans, I. L., Miller, J., Waldvogel, H., Faull, R. L. M., Owen, Michael John and Snell, R. G. 2001. A missense mutation of human Gephyrin (GPHN) is associated with Hyperekplexia and transcript isoform analysis re-defines the genomic structure of GPHN. American Journal of Human Genetics 69 (4) , p. 627.

Rees, M. I., Lewis, T. M., Vafa, B., Ferrie, C., Corry, P., Muntoni, F, Jungbluth, H., Stephenson, J. B., Kerr, Michael Patrick, Snell, R. G., Schofield, P.R. and Owen, Michael John 2001. Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia. Hum Genet 109 (3) , pp. 267-270.

Reid, S. J., Rees, M. I., van Roon-Mom, W. M. C., Jones, Lesley, McDonald, M. E., Sutherland, G. T., Owen, Michael John, Dragunow, M. and Snell, R. G. 2001. Expression and population studies of the TATA-box binding protein polyglutamine region at normal and expanded lengths. American Journal of Human Genetics 69 (4) , p. 424.

Rice, Frances, Harold, Gordon Thomas and Thapar, Anita 2001. Extreme depressive symptoms in children and adolescents. Behavior Genetics 31 (5) , p. 467.

S

Schanda, H and Taylor, Pamela Jane 2001. Inpatient violence: frequency, risk factors, preventive strategies. Fortschr Neurol Psychiatr 69 (10) , pp. 443-452. 10.1055/s-2001-17560

Sklar, P., Schwab, S. G., Williams, Nigel Melville, Daly, M., Schaffner, S., Maier, W., Albus, M., Trixler, M., Eichhammer, P., Lerer, B., Hallmayer, J., Norton, N., Williams, H., Zammit, Stanley, Cardno, A. G., Jones, S. and McCarthy, G. 2001. Association analysis of NOTCH4 loci in schizophrenia using family and population-based controls. Nature Genetics 28 (2) , pp. 126-128. 10.1038/88836

Sommer, S. .S, Feng, J., Yan, J., Craddock, Nicholas John, Jones, Ian Richard, Cook, E. H. and Goldman, D. 2001. Mutation scanning of steroid receptor gene family in patients with schizophrenia and other psychiatric disease. American Journal of Medical Genetics 105 (7) , pp. 622-623.

Stephens, M, Kirov, George and Owen, Michael John 2001. ADARB1, a brain specific member of the RNA-specific adenosine deaminase family and bipolar affective disorder. American Journal of Medical Genetics 105 (7) , p. 622.

T

Thapar, Ajay Kumar, Richens, A., Roland, M., Jacoby, A., Russell, I., Roberts, C., Porter, E. and Wall, S. 2001. Are serum anticonvulsant levels in people with epilepsy appropriately monitored? Journal of Evaluation in Clinical Practice 7 (3) , pp. 335-338. 10.1046/j.1365-2753.2001.00289.x

Thapar, Anita, Harrington, R. and McGuffin, P. 2001. Examining the comorbidity of ADHD related behaviours and conduct problems using a twin study design. British Journal of Psychiatry 179 (3) , pp. 224-229. 10.1192/bjp.179.3.224

Thapar, Anita and Holmes, J. 2001. Genes really do matter. The Psychologist 14 (3) , pp. 146-147.

Thomas, Rhys Huw, Lewis, D. J., Griffiths, E. J. and Suleiman, M. S. 2001. Ischaemic preconditioning by metabolic inhibition in isolated perfused cardiac myocytes [Conference Abstract]. The Journal of Physiology 531 (Suppl.) , 191P-191P.

Tomassini, Valentina, Giugni, E., Mainero, C., Onesti, E., Giuliani, S., Paolillo, A., Bastianello, S., Salvetti, M. and Pozzilli, C. 2001. Relationship between sex hormones and MRI activity in relapsing-remitting Multiple Sclerosis. Neurology 56 (8) , A254-A255.

Torrubia, Rafael, Ávila, César, Moltó, Javier and Caseras, Xavier 2001. The sensitivity to punishment and sensitivity to reward questionnaire (SPSRQ) as a measure of Gray's anxiety and impulsivity dimensions. Personality and Individual Differences 31 (6) , pp. 837-862. 10.1016/S0191-8869(00)00183-5

Tredget, John 2001. The aetiology, presentation and treatment of personality disorders. Journal of Psychiatric and Mental Health Nursing 8 (4) , pp. 347-356.

Tredget, John 2001. A systematic desensitisation programme for agoraphobia. Nurs Times 97 (33) , pp. 39-40.

Turic, D., Fisher, P. J., Plomin, R. and Owen, Michael John 2001. No association between apolipoprotein E polymorphisms and general cognitive ability in children. Neuroscience Letters 299 (1-2) , pp. 97-100. 10.1016/S0304-3940(00)01789-4

V

van Amelsvoort, T., Daly, E., Robertson, D., Suckling, J., Ng, V., Critchley, H., Owen, Michael John, Henry, J., Murphy, K. C. and Murphy, D. G. 2001. Structural brain abnormalities associated with deletion at chromosome 22q11. British Journal of Psychiatry (178) , pp. 412-419. 10.1192/bjp.178.5.412

W

Wang, Edward Chung Yern, Kitson, Jeremy, Thern, Anette, Williamson, Jill, Farrow, Stuart N. and Owen, Michael John 2001. Genomic structure, expression, and chromosome mapping of the mouse homologue for the WSL-1 (DR3, Apo3, TRAMP, LARD, TR3, TNFRSF12) gene. Immunogenetics 53 (1) , pp. 59-63. 10.1007/s002510000290

Wang, Edward Chung Yern, Thern, Anette, Denzel, Angela, Kitson, Jeremy, Farrow, Stuart N. and Owen, Michael John 2001. DR3 regulates negative selection during thymocyte development. Molecular and cellular biology 21 (10) , pp. 3451-61. 10.1128/MCB.21.10.3451-3461.2001
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Ward, Beatrice O, Billinton, Andrew and Wilkinson, Lawrence Stephen 2001. Learning, remembering and applying an arbitrary non-matching to position rule in mice. Behavioural Brain Research 125 (1-2) , pp. 229-236. 10.1016/S0166-4328(01)00304-7

Wickham, H., Walsh, C., Asherson, P., Taylor, C., Sigmundson, T., Gill, M., Owen, Michael John, McGuffin, P., Murray, R. and Sham, P. 2001. Familiality of symptom dimensions in schizophrenia. Schizophrenia Research 47 (2-3) , pp. 223-232. 10.1016/S0920-9964(00)00098-0

Williams, H., Kirov, George, Meyer, J., Lesch, K. P. and Owen, Michael John 2001. Further analysis of KIAA0027 in schizophrenic patients. American Journal of Medical Genetics 105 (7) , p. 561.

Williams, H. J., Murphy, K. C., Spurlock, G. and Owen, Michael John 2001. No association between a promoter polymorphism of the UFD1L gene and schizophrenia in individuals with or without velo-cardio-facial syndrome (VCFS). Schizophrenia Research 49 , p. 81.

This list was generated on Wed Nov 13 12:21:34 2019 GMT.