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Number of items: 97.

A

Ahmed, Zed, O'Brien, G., Betts, T., Kerr, Michael Patrick and Fraser, William 1997. Learning disabilities: moving forward--a focus on epilepsy, Birmingham, England, 29 June 1996. Journal of Intellectual Disability Research 41 (4) , pp. 355-360. 10.1111/j.1365-2788.1997.tb00720.x

Ambrose, Helen J., Blake, Derek J., Nawrotzki, Ralph A. and Davies, Kay E. 1997. Genomic organization of the mouse dystrobrevin gene: comparative analysis with the dystrophin gene. Genomics 39 (3) , pp. 359-369. 10.1006/geno.1996.4515

Andrew, M. and Owen, Michael John 1997. Hyperekplexia: abnormal startle response due to glycine receptor mutations. British Journal of Psychiatry 170 , pp. 106-108. 10.1192/bjp.170.2.106

Arranz, M. J., Erdmann, J., Kirov, George, Rietschel, M., Sodhi, M., Albus, M., Ball, D., Maier, W., Davies, N., Franzek, E., Abusaad, I., Weigelt, B., Murray, R., Shimron-Abarbanell, D., Kerwin, R., Propping, P., Sham, P., Nothen, N. M. and Collier, D. M. 1997. 5-HT2A receptor and bipolar affective disorder: association studies in affected patients. Neuroscience Letters 224 (2) , pp. 95-98. 10.1016/S0304-3940(97)13456-5

Arranz, M. J., Munro, J., Kirov, George, Kerwin, R. W. and Collier, D. A. 1997. Novel polymorphisms detected in the 5-HT3 receptor gene: Association studies with schizophrenia and clozapine response. American Journal of Medical Genetics 74 (6) , p. 615.

Arranz, M.J., Munro, J., Sham, P., Zhao, J., Kirov, George, Sodhi, M., Spurlock, G., Owen, Michael John, Collier, D.A. and Kerwin, R. 1997. Polymorphisms in the 5-HT2A receptor gene and promoter region associated with clozapine response. Schizophrenia Research 24 (1-2) , p. 90. 10.1016/S0920-9964(97)82243-8

B

Baboolal, K., Ravine, D., Daniels, J., Williams, Nigel Melville, Holmans, Peter Alan, Coles, G. A. and Williams, J. D. 1997. Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney disease. Kidney International 52 (3) , pp. 607-613. 10.1038/ki.1997.373

Bandmann, O., Vaughan, J., Holmans, Peter Alan, Marsden, C. D. and Wood, N. W. 1997. Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease. The Lancet 350 (9085) , pp. 1136-1139. 10.1016/S0140-6736(97)03495-8

Beyer, Stephen Richard and Felce, David John 1997. Making progress together: The interplay between research and services. In: Fraser, W., Sines, D. and Kerr, M. eds. Hallas’ The Care of People with Intellectual Disabilities, London: Butterworth/Heinemann, pp. 42-60.

Bisson, Jonathan Ian 1997. Post-traumatic stress counselling [Comment]. British Journal of Hospital Medicine 57 (3) , p. 112.

Bisson, Jonathan Ian and Jenkins, P. L. 1997. Psychological debriefing for victims of acute burn trauma - reply. British Journal of Psychiatry 171 (6) , p. 583. 10.1192/bjp.171.6.583a

Bisson, Jonathan Ian, Jenkins, P. L., Alexander, J. and Bannister, C. 1997. Randomised controlled trial of psychological debriefing for victims of acute burn trauma. The British Journal of Psychiatry 171 (1) , pp. 78-81. 10.1192/bjp.171.1.78

Bisson, Jonathan Ian, Shepherd, Jonathan Paul and Dhutia, Manish 1997. Psychological sequelae of facial trauma. The Journal of Trauma 43 (3) , pp. 469-500.

Blake, Derek J, Loh, N. Y., Beesley, P. and Davies, K. E. 1997. The function dystrophin-related and -associated proteins in the brain. Journal of Neurochemistry 69 (S) , S123-S123.

Blake, Derek J, Nawrotzki, R., Loh, N. Y. and Davies, K. E. 1997. A novel dystrophin-associated protein in brain. American Journal of Human Genetics 61 (4) , A8-A8.

Bolonna, A. A., Makoff, A. J., Collier, D. A., Kirov, George, Arranz, M. J. and Kerwin, R. W. 1997. Analysis of the NMDA receptor in schizophrenia. American Journal of Medical Genetics 74 (6) , p. 631.

Bolonna, A.A., Makoff, A.J., Collier, D.A., Kirov, George, Munro, J., Arranz, M.J. and Kerwin, R.W. 1997. An investigation of the GLUR6 receptor gene (GRIK2) in schizophrenia. Schizophrenia Research 24 (1-2) , p. 93. 10.1016/S0920-9964(97)82252-9

Bond, L., Kerr, Michael Patrick, Dunstan, Frank David John and Thapar, Anita 1997. Attitudes of general practitioners towards health care for people with intellectual disability and the factors underlying these attitudes. Journal of Intellectual Disability Research 41 (5) , pp. 391-400. 10.1111/j.1365-2788.1997.tb00726.x

Boutell, J. M., Krusche, L. A., Harper, P. S. and Jones, Lesley 1997. Generation of clones with varying trinucleotide repeat sires using intrinsic instability in E-coli. American Journal of Human Genetics 61 (4) , A404-A404.

Buckland, Paul Robert, D'Souza, Ursula, Maher, Nazir A. and McGuffin, Peter 1997. The effects of antipsychotic drugs on the mRNA levels of serotonin 5HT2A and 5HT2C receptors. Molecular Brain Research 48 (1) , pp. 45-52. 10.1016/S0169-328X(97)00076-4

Buckland, Paul Robert, Marshall, Rupert, Watkins, Peter and McGuffin, Peter 1997. Does phenylethylamine have a role in schizophrenia?: LSD and PCP up-regulate aromatic l-amino acid decarboxylase mRNA levels. Molecular Brain Research 49 (1-2) , pp. 266-270. 10.1016/S0169-328X(97)00160-5

C

Craddock, B. and Craddock, Nicholas John 1997. Contractures in neuroleptic malignant syndrome [letter]. American Journal of Psychiatry 154 (3) , p. 436.

Craddock, Nicholas John 1997. No association between bipolar disorder and alleles at a functional polymorphism in the COMT gene. Biomed European Bipolar Collaborative Group. British Journal of Psychiatry 170 (6) , pp. 526-528. 10.1192/bjp.170.6.526

Craddock, Nicholas John, Jones, Ian Richard, McCandless, F., Kirov, George and Cardno, A. G. 1997. Dimensional classification for use in biological studies of bipolar disorder. American Journal of Medical Genetics 74 (6) , p. 588.

Craddock, Nicholas John, McKeon, P., Moorhead, S., Guy, Carol, Harrison, D., Mynett-Johnson, L., Claffey, E., Feldman, E., McGuffin, P., Owen, Michael John and O'Donovan, Michael Conlon 1997. Expanded CAG/CTG repeats in bipolar disorder: no correlation with phenotypic measures of illness severity. Biological psychiatry 42 (10) , pp. 876-881. 10.1016/s0006-3223(96)00516-1

Craddock, Nicholas John, van Erdewegh, P. and Reich, T. 1997. Single major locus models for bipolar disorder are implausible. American Journal of Medical Genetics Part A 74 (1) , p. 18. 10.1002/(sici)1096-8628(19970221)74:1%3C18::aid-ajmg4%3E3.3.co;2-i

D

D'souza, U., McGuffin, P. and Buckland, Paul Robert 1997. Antipsychotic regulation of dopamine D1, D2 and D3 receptor mRNA. Neuropharmacology 36 (11-12) , pp. 1689-1696. 10.1016/S0028-3908(97)00163-9

Daniels, J. K., Spurlock, G., Williams, Nigel Melville, Cardno, A. G., Jones, L. A., Murphy, K. C., Asherson, P., Holmans, Peter Alan, Fenton, I., McGuffin, P. and Owen, Michael John 1997. Linkage study of chromosome 6p in sib-pairs with schizophrenia. American Journal of Medical Genetics 74 (3) , pp. 319-323. 10.1002/(SICI)1096-8628(19970531)74:3<319::AID-AJMG14>3.0.CO;2-R

Davies, S. J., Norton, N., Daniels, J. K. and Owen, Michael John 1997. Parietal foramina and multiple exostoses - familial inheritance of a molecular deletion. American Journal of Human Genetics 61 (4) , A95-A95.

Dawson, E., Kirov, George, Hutchison, G., Murray, R. and Powell, J. F. 1997. The brain cannabinoid receptor gene and bipolar affective disorders. American Journal of Medical Genetics 74 (6) , pp. 613-614.

E

Elmslie, F. V., Rees, M., Williamson, M. P., Kerr, Michael Patrick, Kjeldsen, M. J., Pang, K. A., Sundqvist, A., Friis, M. L., Chadwick, D., Richens, A., Covanis, A., Santos, M., Arzimanoglou, A., Panayiotopoulos, C. P., Curtis, D., Whitehouse, W. P. and Gardiner, R. M. 1997. Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q. Human Molecular Genetics 6 (8) , pp. 1329-1334. 10.1093/hmg/6.8.1329

Espie, C. A., Kerr, Michael Patrick, Paul, A., O'Brien, G., Betts, T., Clark, J., Jacoby, A. and Baker, G. 1997. Learning disability and epilepsy. 2, a review of available outcome measures and position statement on development priorities. Seizure - European Journal of Epilepsy 6 (5) , pp. 337-350. 10.1016/S1059-1311(97)80033-7

F

Felce, David John 1997. Defining and applying the concept of quality of life. Journal of Intellectual Disability Research 41 (2) , pp. 126-135. 10.1111/j.1365-2788.1997.tb00689.x

Felce, David John and Perry, Jonathan 1997. A PASS 3 evaluation of community residences in Wales. Mental Retardation- American Association on Mental Retardation 35 (3) , pp. 170-176. 10.1352/0047-6765(1997)035%3C0170:apeocr%3E2.0.co;2

G

Gray, M. and Jones, Ian Richard 1997. Type II diabetes mellitus presenting as the Charles Bonnet syndrome. Journal of the Royal Society of Medicine 90 (9) , p. 503.

Guy, Carol, Bowen, Timothy, Daniels, J. K., Speight, G., McKeon, P., Mynett-Johnson, L., Claffey, E., McGuffin, P., Owen, Michael John, Craddock, Nicholas and O'Donovan, Michael Conlon 1997. Exclusion of expansion of 50 CAG/CTG trinucleotide repeats in bipolar disorder. American Journal of Psychiatry 154 (8) , pp. 1146-1147.

H

Hall, F. S., Humby, Trevor, Wilkinson, Lawrence Stephen and Robbins, T. W. 1997. The effects of isolation-rearing of rats on behavioural responses to food and environmental novelty. Physiology & Behavior 62 (2) , pp. 281-290. 10.1016/S0031-9384(97)00115-7

Hall, F. S., Humby, Trevor, Wilkinson, Lawrence Stephen and Robbins, T. W. 1997. The effects of isolation-rearing on preference by rats for a novel environment. Physiology & Behavior 62 (2) , pp. 299-303. 10.1016/S0031-9384(97)00117-0

Hall, F. S., Humby, Trevor, Wilkinson, Lawrence Stephen and Robbins, T. W. 1997. The effects of isolation-rearing on sucrose consumption in rats. Physiology & Behavior 62 (2) , pp. 291-297. 10.1016/S0031-9384(97)00116-9

Hateboer, N., Dijk, M., Torra, R., Bogdanova, N., Davies, F., Lazarou, L., Breuning, M., SaggarMalik, A. K., Jeffery, S., Millan, J. L. S., Martinez, I., Walker, R., Holmans, Peter Alan, Ravine, D. and Coles, G. A. 1997. Phenotype PKD2 vs. PKD1; results from the European concerted action. Journal of the American Society of Nephrology 8 , A1722-A1722.

Hateboer, N., Torra, R., Estivill, E., Bogdanova, N., Davies, F., Lazarou, L., vonDijk, M., Breuning, M., SaggarMalik, A., Jeffery, S., SanMillan, J. L., Martinez, I., Walker, R., Holmans, Peter Alan and Ravine, D. 1997. PKD2: The phenotype defined. Kidney International 52 (4) , p. 1122.

Heads, Tracey C., Taylor, Pamela Jane and Leese, Morven 1997. Childhood experiences of patients with schizophrenia and a history of violence: a special hospital sample. Criminal Behaviour and Mental Health 7 (2) , pp. 117-130. 10.1002/cbm.157

Holmans, Peter Alan and Craddock, Nicholas John 1997. Efficient strategies for genome scanning using maximum-likelihood affected-sib-pair analysis. American Journal of Human Genetics 60 (3) , pp. 657-666.

J

Jones, Ian Richard and Craddock, Nicholas John 1997. The crisis in psychiatry [letter]. The Lancet 349 (9064) , p. 1550.

Jones, Ian Richard, Scourfield, J., McCandless, F. and Craddock, Nicholas John 1997. Testing for bipolar susceptibility genes: The patient's perspective. American Journal of Medical Genetics 74 (6) , p. 594.

Jones, Lesley, Boutell, J. M., Wood, J. D. and Harper, P. S. 1997. Two proteins which interact with the N-terminus of huntingtin. American Journal of Human Genetics 61 (4) , A311-A311.

Jones, Lesley, Middle, F., Guy, Carol, Spurlock, G., Cairns, N. J., McGuffin, P., Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 1997. No evidence for expanded polyglutamine sequences in bipolar disorder and schizophrenia. Molecular Psychiatry 2 (6) , pp. 478-482. 10.1038/sj.mp.4000297

Jones, Lesley, Wood, J. D. and Harper, P. S. 1997. Huntington disease: advances in molecular and cell biology. Journal of Inherited Metabolic Disease 20 (2) , pp. 125-138. 10.1023/A:1005340302695

Jones, R. G. and Kerr, Michael Patrick 1997. A randomized control trial of an opportunistic health screening tool in primary care for people with intellectual disability. Journal of Intellectual Disability Research 41 (5) , pp. 409-415. 10.1111/j.1365-2788.1997.tb00728.x

Jonsson, E. G., Goldman, D., Spurlock, G., Gustavsson, J. P., Nielsen, D. A., Linnoila, M., Owen, Michael John and Sedvall, G. C. 1997. Tryptophan hydroxylase and catechol-O-methyltransferase gene polymorphisms: relationships to monoamine metabolite concentrations in CSF of healthy volunteers. European Archives of Psychiatry and Clinical Neuroscience 247 (6) , pp. 297-230. 10.1007/BF02922258

K

Kerr, Michael Patrick 1997. Down's syndrome - Psychological, psychobiological and socio-educational perspectives - Rondal,J, Perera,J, Nadel,L, Comblain,A. British Journal of Psychiatry 170 , pp. 584-585.

Kerr, Michael Patrick 1997. Primary health care for people with an intellectual disability. Journal of Intellectual Disability Research 41 (5) , pp. 363-364. 10.1111/j.1365-2788.1997.tb00722.x

Kerr, Michael Patrick 1997. Psychological disturbances in epilepsy. Journal of Applied Research in Intellectual Disabilities 10 (3) , pp. 266-268.

Kerr, Michael Patrick and Epsie, C. A. 1997. Learning disability and epilepsy. 1, towards common outcome measures. Seizure - European Journal of Epilepsy 6 (5) , pp. 331-336. 10.1016/S1059-1311(97)80032-5

Kirov, George and Murray, R. 1997. The molecular genetics of schizophrenia: progress so far. Molecular Medicine Today 3 (3) , pp. 124-130. 10.1016/S1357-4310(96)10060-5

Kirov, George, Murray, R. M., Seth, R. V. and Feeney, S. 1997. Observations on switching patients with schizophrenia to risperidone treatment. Risperidone Switching Study Group. Acta Psychiatrica Scandinavica 95 (5) , pp. 439-443. 10.1111/j.1600-0447.1997.tb09659.x

Kunugi, H., Vallada, H. P., Hoda, F., Kirov, George, Gill, M., Aitchison, K. J., Ball, D., Arranz, M. J., Murray, R. M. and Collier, D. A. 1997. No evidence for an association of affective disorders with high- or low-activity allele of catechol-o-methyltransferase gene. Biological psychiatry 42 (4) , pp. 282-285. 10.1016/S0006-3223(96)00366-6

Kunugi, H., Vallada, H. P., Sham, P. C., Hoda, F., Arranz, M. J., Li, T., Nanko, S., Murray, R. M., McGuffin, P., Owen, Michael John, Gill, M. and Collier, D. A. 1997. Catechol-O-methyltransferase polymorphisms and schizophrenia: a transmission disequilibrium study in multiply affected families. Psychiatric Genetics 7 (3) , pp. 97-101. 10.1097/00041444-199723000-00001

L

Lendon, C. L., Talbot, C. J., Craddock, Nicholas John, Han, S. W., Wragg, M., Morris, J. C. and Goate, A. M. 1997. Genetic association studies between dementia of the Alzheimer's type and three receptors for apolipoprotein E in a Caucasian population. Neuroscience Letters 222 (3) , pp. 187-190. 10.1016/s0304-3940(97)13381-x

Lennox, N. G. and Kerr, Michael Patrick 1997. Primary health care and people with an intellectual disability: the evidence base. Journal of Intellectual Disability Research 41 (5) , pp. 365-372. 10.1111/j.1365-2788.1997.tb00723.x

Li, T., Holmes, C., Sham, P. C., Vallada, H., Birkett, J., Kirov, George, Lesch, K. P., Powell, J., Lovestone, S. and Collier, D. 1997. Allelic functional variation of serotonin transporter expression is a susceptibility factor for late onset Alzheimer's disease. NeuroReport 8 (3) , pp. 683-686. 10.1097/00001756-199702100-00021

Loh, N. Y., Blake, Derek J, Nawrotzki, R., Ambrose, H. J. and Davies, K. E. 1997. Beta-dystrobrevin; a new member of the dystrophin-related protein family. American Journal of Human Genetics 61 (4) , A177-A177.

M

McCandless, F., Jones, Ian Richard and Craddock, Nicholas John 1997. Bipolar disorder and sensation seeking. American Journal of Medical Genetics 74 (6) , p. 591.

McCandless, F., Jones, Ian Richard and Craddock, Nicholas John 1997. Intrafamilial association of pericentric inversion of chromosome 9 and rapid cycling bipolar II disorder. American Journal of Medical Genetics 74 (6) , pp. 590-591.

Metzinger, Laurent, Blake, Derek J., Squier, Marian V., Anderson, Louise V. B., Deconinck, Anne E., Nawrotzki, Ralph, Hilton-Jones, David and Davies, Kay E. 1997. Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy. Human Molecular Genetics 6 (7) , pp. 1185-1191. 10.1093/hmg/6.7.1185

Murphy, K. C., Jones, R. G., Griffiths, E., Thompson, P. W. and Owen, Michael John 1997. Chromosome 22q11 deletions: An underrecognized cause of idiopathic learning disability? American Journal of Medical Genetics 74 (6) , p. 567.

Murphy, K. C. and Owen, Michael John 1997. The behavioral phenotype in velo-cardio-facial syndrome. American Journal of Medical Genetics 74 (6) , p. 660.

O

O'Donovan, Michael Conlon and Guy, C 1997. Bias in the genomic distribution of CAG and CTG trinucleotide repeats. American Journal of Medical Genetics 74 (1) , pp. 62-64. 10.1002/(SICI)1096-8628(19970221)74:1<62::AID-AJMG14>3.0.CO;2-P

Owen, Michael John, Holmans, Peter Alan and McGuffin, P. 1997. Association studies in psychiatric genetics. Molecular Psychiatry 2 (4) , pp. 270-273. 10.1038/sj.mp.4000292

Owen, Michael John and McGuffin, P. 1997. Genetics and psychiatry. British Journal of Psychiatry 171 , pp. 201-202. 10.1192/bjp.171.3.201

P

Petrill, S. A., Plomin, R., McClearn, G. E., Smith, D. L., Vignetti, S., Chorney, M. J., Chorney, K., Thompson, L. A., Detterman, D. K., Benbow, C., Lubinski, D., Daniels, J., Owen, Michael John and McGuffin, P. 1997. No association between general cognitive ability and the A1 allele of the D2 dopamine receptor gene. Behavior Genetics 27 (1) , pp. 29-31. 10.1023/A:1025659124405

Petrill, Stephen A., Ball, David, Eley, Thalia, Hill, Linzy, Plomin, Robert, Mcclearn, Gerald E., Smith, Deborah L., Chorney, Karen, Chorney, Michael, Hershz, Milton S., Detterman, Douglas K., Thompson, Lee A., Benbow, Camilla, Lubinski, David, Daniels, Johanna, Owen, Michael John and McGuffin, Peter 1997. Failure to replicate a QTL association between a DNA marker identified by EST00083 and IQ. Intelligence 25 (3) , pp. 179-184. 10.1016/S0160-2896(97)90041-6

Ponting, Christopher P., Phillips, Christopher, Davies, Kay E. and Blake, Derek J. 1997. PDZ domains: targeting signalling molecules to sub-membranous sites. Bioessays 19 (6) , pp. 469-479. 10.1002/bies.950190606

R

Rees, M., Norton, N., Jones, Ian Richard, McCandless, F., Scourfield, J., Holmans, Peter Alan, Moorhead, S., Feldman, E., Sadler, S., Cole, T., Redman, K., Farmer, A., McGuffin, P., Owen, Michael John and Craddock, Nicholas John 1997. Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT). Molecular Psychiatry 2 (5) , pp. 398-402. 10.1038/sj.mp.4000256

Robertson, Neil, O'Riordan, J. I., Chataway, J., Kingsley, D. P., Miller, D. H., Clayton, D. and Compston, D. A. 1997. Offspring recurrence rates and clinical characteristics of conjugal multiple sclerosis. The Lancet 349 (9065) , pp. 1587-1590. 10.1016/S0140-6736(96)07317-5

Rosser, Anne Elizabeth, Tyers, P., ter Borg, M., Dunnett, S. B. and Svendsen, C. N. 1997. Co-expression of MAP-2 and GFAP in cells developing from rat EGF responsive precursor cells. Brain research. Developmental brain research 98 (2) , pp. 291-295. 10.1016/S0165-3806(96)00189-7

S

Scourfield, J., McGuffin, P. and Thapar, Anita 1997. Genes and social skills. Bioessays 19 (12) , pp. 1125-1127. 10.1002/bies.950191212

Singhrao, S. K., Thomas, P., Wood, J. D., Harper, P. S., Neal, J. W. and Jones, Lesley 1997. Huntingtin is associated with intracellular neuropathology in Huntington's, Alzheimer's and Pick's disease. American Journal of Human Genetics 61 (4) , A321-A321.

Sodhi, Monsheel S., Kirov, George, Aitchison, Katherine J., Arranz, Maria J., Collier, David A. and Kerwin, Robert W. 1997. Allelic variation of the 5-HT2C receptor in psychosis. Schizophrenia Research 24 (1-2) , p. 90. 10.1016/S0920-9964(97)82246-3

Speight, G., Guy, Carol, Bowen, Timothy, Asherson, P., McGuffin, P., Craddock, Nicholas John, Owen, Michael John and O'Donovan, Michael Conlon 1997. Exclusion of CAG/CTG trinucleotide repeat loci which map to chromosome 4 in bipolar disorder and schizophrenia. American Journal of Medical Genetics 74 (2) , pp. 204-206. 10.1002/(SICI)1096-8628(19970418)74:2<204::AID-AJMG19>3.0.CO;2-M

Spurlock, Gillian, Williams, Julie, McGuffin, Peter, Mallet, Jacques, Nöthen, Markus, Gill, Michael, Aschauer, Harald, Adlfsson, Rolf, Macciardi, Fabio and Owen, Michael John 1997. Meta-analysis of association studies between schizophrenia and polymorphisms of the 5-hydroxytryptamine type 2A receptor gene. Schizophrenia Research 24 (1-2) , p. 91. 10.1016/S0920-9964(97)82247-5

Sullivan, Gary and Jones, Ian Richard 1997. Membership course or masters course? Psychiatric Bulletin 21 (7) , pp. 449-450. 10.1192/pb.21.7.449

Svendsen, C. N., Caldwell, M. A., Shen, J., ter Borg, M. G., Rosser, Anne Elizabeth, Tyres, P., Karmiol, S. and Dunnett, S. B. 1997. Long-term survival of human central nervous system progenitor cells transplanted into a rat model of Parkinson's disease. Experimental Neurology 148 (1) , pp. 135-146. 10.1006/exnr.1997.6634

Svendsen, C. N., Skepper, J., Rosser, Anne Elizabeth, ter Borg, M. G., Tyres, P. and Ryken, T. 1997. Restricted growth potential of rat neural precursors as compared to mouse. Brain research. Developmental brain research 99 (2) , pp. 253-258. 10.1016/S0165-3806(97)00002-3

T

Thapar, Anita, Harrington, R. and McGuffin, P. 1997. A genetic study of hyperactivity and related traits. American Journal of Medical Genetics 74 (6) , pp. 571-572.

Thapar, Anita and McGuffin, P. 1997. Anxiety and depressive symptoms in childhood--a genetic study of comorbidity. Journal of Child Psychology and Psychiatry 38 (6) , pp. 651-656. 10.1111/j.1469-7610.1997.tb01692.x

Thapar, Anita and McGuffin, P. 1997. Genetic basis of bad behaviour in adolescents. The Lancet 350 (9075) , pp. 411-412. 10.1016/S0140-6736(05)64134-7

Thapar, Anita and McGuffin, Peter 1997. Anxiety and depressive symptoms in childhood - a genetic study of comorbidity. Journal of Child Psychology and Psychiatry 38 (6) , pp. 651-656. 10.1111/j.1469-7610.1997.tb01692

Thomas, Nicholas Stuart Tudor, Davies, K., Webb, T., Williams, Nigel Melville, Price, W., Owen, Michael John, Pereira, J., Kerr, A., Anvret, M., Hanefeld, E. and Clarke, Angus John 1997. Molecular genetic studies in familial Rett syndrome. European Child & Adolescent Psychiatry 6 (Supp 1) , p. 94.

V

Vallada, H. P., Vasques, L., Curtis, D., Kirov, George, Gentil, V., Zatz, M., Murray, R. M., McGuffin, P., Owen, Michael John, Gill, M., Craddock, Nicholas John and Collier, D. A. 1997. Linkage studies in bipolar affective disorder with markers on chromosome Xq25-27. American Journal of Medical Genetics 74 (6) , pp. 679-680.

W

Watts, C., Dunnett, S. B. and Rosser, Anne Elizabeth 1997. Effect of embryonic donor age and dissection on the DARPP-32 content of cell suspensions used for intrastriatal transplantation. Experimental Neurology 148 (1) , pp. 271-280. 10.1006/exnr.1997.6646

Wilkinson, Lawrence Stephen 1997. The nature of interactions involving prefrontal and striatal dopamine systems. Journal of Psychopharmacology 11 (2) , pp. 143-150. 10.1177/026988119701100207

Wilkinson, Lawrence Stephen, Dias, R, Thomas, K.L, Augood, S.J, Everitt, B.J, Robbins, T.W and Roberts, A.C 1997. Contrasting effects of excitotoxic lesions of the prefrontal cortex on the behavioural response to d-amphetamine and presynaptic and postsynaptic measures of striatal dopamine function in monkeys. Neuroscience 80 (3) , pp. 717-730. 10.1016/S0306-4522(97)00075-4

Williams, Julie, McGuffin, P., Nothen, . and Owen, Michael John 1997. A meta analysis of association between the 5-HT2a receptor, T102C polymorphism and schizophrenia. American Journal of Medical Genetics 74 (6) , p. 612.

Williams, Julie, McGuffin, Peter, Nothen, Markus and Owen, Michael John 1997. Meta-analysis of association between the 5-HT2a receptor T102C polymorphism and schizophrenia. The Lancet 349 (9060) , p. 1221. 10.1016/S0140-6736(05)62413-0

Williams, Nigel Melville, Cardno, A. G., Murphy, K. C., Jones, L. A., Asherson, P., McGuffin, P. and Owen, Michael John 1997. Association between schizophrenia and a microsatellite polymorphism at the dopamine D5 receptor gene. Psychiatric Genetics 7 (2) , pp. 83-85. 10.1097/00041444-199722000-00005

Williams, Nigel Melville, Jones, L. A., Murphy, K. C., Cardno, A. G., Asherson, P., Williams, Julie, McGuffin, P. and Owen, Michael John 1997. No evidence for an allelic association between schizophrenia and markers D22S278 and D22S283. American Journal of Medical Genetics 74 (1) , pp. 37-39. 10.1002/(SICI)1096-8628(19970221)74:1<37::AID-AJMG8>3.0.CO;2-S

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